CA2991984A1

CA2991984A1 - Peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory diseases

Info

Publication number: CA2991984A1
Application number: CA2991984A
Authority: CA
Inventors: Ashok Bhandari; Gregory BOURNE; Xiaoli Cheng; Brian Troy FREDERICK; Jie Zhang; Dinesh V. Patel; David Liu
Original assignee: Protagonist Therapeutics Inc
Current assignee: Protagonist Therapeutics Inc
Priority date: 2015-07-15
Filing date: 2016-07-15
Publication date: 2017-01-19
Also published as: EA035733B1; EP3341011A4; HK1257747A1; HK1259149A1; PE20180571A1; WO2017011820A2; EA201890325A1; BR112018000691A2; PH12018500086A1; UA123772C2; AU2016293619B2; WO2017011820A3; ECSP18002929A; CL2018000128A1; SG10201912066SA; SV2018005614A; IL256827A; AU2016293619A1; CO2018000349A2; CL2018003322A1

Abstract

The present invention provides novel peptide inhibitors of the interleukin-23 receptor, and related compositions and methods of using these peptide inhibitors to treat or prevent a variety of diseases and disorders, including inflammatory bowel diseases.

Description

TO TREAT INFLAMMATORY DISEASES
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application claims priority to and is a continuation-in-part of U.S. Application No.
14/800,627 filed on July 15, 2015, and also claims priority to International Patent Application PCT/US2015/040658 filed on July 15, 2015, U.S. Provisional Application No.
62/264,820 filed on December 8, 2015, and U.S. Provisional Application No. 62/281,123 filed on January 20, 2016, all of which are incorporated by reference herein in theirentireties.
SEQUENCE LISTING

[0002] The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on July 15, 2016, is named PRTH-002-03WO SL.txt and is 504 KB in size FIELD OF THE INVENTION

[0003] The present invention relates to novel peptide inhibitors of the interleukin-23 receptor, and their use to treat or prevent a variety of diseases and disorders, including inflammatory bowel disease, Crohn's disease and psoriasis.
BACKGROUND

[0004] The interleukin-23 (IL-23) cytokine has been implicated as playing a crucial role in the pathogenesis of autoimmune inflammation and related diseases and disorders, such as multiple sclerosis, asthma, rheumatoid arthritis, psoriasis, and inflammatory bowel diseases (IBDs), e.g., ulcerative colitis and Crohn's disease. Studies in acute and chronic mouse models of IBD
revealed a primary role of IL-23R and downstream effector cytokines in disease pathogenesis.
IL-23R is expressed on various adaptive and innate immune cells including Th17 cells, T cells, natural killer (NK) cells, dendritic cells, macrophages, and innate lymphoid cells, which are found abundantly in the intestine. At the intestine mucosal surface, the gene expression and protein levels of IL-23R are found to be elevated in IBD patients. It is believed that IL-23 mediates this effect by promoting the development of a pathogenic CD4+ T cell population that produces IL-6, IL-17, and tumor necrosis factor (TNF).
100051 Production of IL-23 is enriched in the intestine, where it is believed to play a key role in regulating the balance between tolerance and immunity through T-cell-dependent and T-cell-independent pathways of intestinal inflammation through effects on T-helper 1 (Thl) and Th17-associated cytokines, as well as restraining regulatory T-cell responses in the gut, favoring inflammation. In addition, polymorphisms in the IL-23 receptor (IL-23R) have been associated with susceptibility to IBDs, further establishing the critical role of the IL-23 pathway in intestinal homeostasis.
[0006] Psoriasis, a chronic skin disease affecting about 2%-3% of the general population has been shown to be mediated by the body's T cell inflammatory response mechanisms. 11-23 has one of several interleukins implicated as a key player in the pathogenesis of psoriasis, purportedly by maintaining chronic autoimmune inflammation via the induction of interleukin-17, regulation of T memory cells, and activation of macrophages. Expression of IL-23 and IL-23R has been shown to be increased in tissues of patients with psoriasis, and antibodies that neutralize IL-23 showed IL-23-dependent inhibition of psoriasis development in animal models of psoriasis.
[0007] IL-23 is a heterodimer composed of a unique p19 subunit and the p40 subunit of IL-12, which is a cytokine involved in the development of interferon-y (IFN-y)-producing T helper 1 (TH1) cells. Although IL-23 and IL-12 both contain the p40 subunit, they have different phenotypic properties. For example, animals deficient in IL-12 are susceptible to inflammatory autoimmune diseases, whereas IL-23 deficient animals are resistant, presumably due to a reduced number of CD4+ T cells producing IL-6, IL-17, and TNF in the CNS of IL-23-deficient animals.
IL-23 binds to IL-23R, which is a heterodimeric receptor composed of IL-12R31 and IL-23R
subunits. Binding of IL-23 to IL-23R activates the Jak-stat signaling molecules, Jak2, Tyk2, and Statl, Stat 3, Stat 4, and Stat 5, although Stat4 activation is substantially weaker and different DNA-binding Stat complexes form in response to IL-23 as compared with IL-12.

associates constitutively with Jak2 and in a ligand-dependent manner with Stat3. In contrast to IL-12, which acts mainly on naive CD4(+) T cells, IL-23 preferentially acts on memory CD4(+) T cells.
[0008] Efforts have been made to identify therapeutic moieties that inhibit the IL-23 pathway, for use in treating IL-23-related diseases and disorders. A number of antibodies that bind to IL-23 or IL-23R have been identified, including ustekinumab, a humanized antibody that binds IL-23, which has been approved for the treatment of psoriasis. More recently, polypeptide inhibitors that bind to IL-23R and inhibit the binding of IL-23 to IL-23R have been identified (see, e.g., US Patent Application Publication No. US2013/0029907). Clinical trials in Crohn's Disease or psoriasis with ustekinumab and briakinumab (which target the common p40 subunit) and tildrakizumab, guselkumab, MEDI2070, and BI-655066 (which target the unique p19 subunit of IL-23) highlight the potential of IL-23 signaling blockade in treatment of human inflammatory diseases. While these findings are promising, challenges remain with respect to identifying stable and selective agents that preferentially target the IL-23 pathway in the intestine, which can be used for the treatment of intestinal inflammation, such as intestinal bowel diseases, including Crohn's disease, ulcerative colitis and related disorders.
[0009] Clearly, there remains a need in the art for new therapeutics targeting the IL-23 pathway, which may be used to treat and prevent IL-23-asociated diseases, including those associated with autoimmune inflammation in the intestinal tract. In addition, compounds and methods for specific targeting of IL-23R from the luminal side of the gut may provide therapeutic benefit to IBD patients suffering from local inflammation of the intestinal tissue. The present invention addresses these needs by providing novel peptide inhibitors that bind IL-23R
to inhibit IL-23 binding and signaling and which are suitable for oral administration.
BRIEF SUMMARY OF THE INVENTION
[0010] The present invention provides inter alia novel peptide inhibitors of IL-23R and related methods of use.
In a first aspect, the present invention provides a peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Xa): X1-X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Xa), wherein:
Xl, X2 and X3 are any amino acid or absent X4 is any amino acid or chemical moiety capable of forming a bond with X9;
X5, X6, X7 and X8 are any amino acid;
X9 is any amino acid or chemical moiety capable of forming a bond with X4;
X10, X11, X12, X13, X14 and X15 are any amino acid; and X16, X17, X18, X19 and X20 are any amino acid or absent;
wherein the peptide inhibitor is cyclized via a bond between X4 and X9, and wherein the peptide inhibitor inhibits the binding of an interleukin-23 (IL-23) to an IL-23 receptor.
[0011] In certain embodiments of Xa:
[0012] X1 is absent; X2 is absent; X3 is absent; X4 is Cys, Abu or Pen; X5 is Ala, E -MeOrn, E-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn, Gln, Arg, Ser or Thr;
X6 is Asp or Thr; X7 is Trp or 6-Chloro-Trp; X8 is Glu, Gln or Val; X9 is Cys, Abu or Pen; X10 is 2-Nal, a Phe analog, Tyr, or a Tyr analog; X11 is 1-Nal, 2-Nal, Phe(3,4-dimethoxy), 5-HydroxyTrp, Phe(3,4-C12), Trp or Tyr(3-tBu); X12 is 3-Pal, Acpc, Acbc, Acvc, Achc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, Cav, Cha, Cit, Cpa, D-Asn, Glu, His, hLeu, hArg, Lys, Leu, Octgly, Orn, 4-amino-4-carboxy-piperidine, Arg, Ser, Thr or MP; X13 is Cit, Asp, Dab, Dap, Phe, His, Dap(Peg2-Ac), Dap(pyroglutaric acid), Glu, HomoArg, Lys, Lys(Ac), Lys(Benzoic acid), Lys(glutaric acid), Lys(IVA), Lys(Peg4-isoGlu-Palm), Lys(pyroglutaric acid), Lys(succinic acid), Asn, Orn, Gln, Arg, Thr or Val; X14 is Asp, Dab(Ac), Dap(Ac), Phe, His, Lys(Ac), Met, Asn(isobutyl), Gln, Arg, Tyr or Asp(1,4-diaminobutane); and X15 is Ala, f3Ala, Glu, Gly, Asn, Gln, Arg or Ser.
[0013] In certain embodiments of Xa: X1 is absent; X2 is absent; X3 is absent;
X4 is Cys, Abu or Pen; X5 is Ala, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, Orn, Gln, Arg, Ser or Thr; X6 is Asp or Thr; X7 is Trp or 6-Chloro-Trp; X8 is Gin or Val; X9 is Cys, Abu or Pen; X10 is 2-Nal, a Phe analog, Tyr, or a Tyr analog; X11 is 1-Nal, 2-Nal, Phe(3,4-dimethoxy),

5-HydroxyTrp, Phe(3,4-C12), Trp or Tyr(3-tBu); X12 is 3-Pal, Acpc, Acbc, Acvc, Achc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, Cav, Cha, Cit, Cpa, D-Asn, His, hLeu, hArg, Lys, Leu, Octgly, Orn, 4-amino-4-carboxy-piperidine, or THP; X13 is Cit, Asp, Dab, Dap, Phe, His, Dap(Peg2-Ac), Dap(pyroglutaric acid), Glu, hArg, Lys, Lys(Ac), Lys(Benzoic acid), Lys(glutaric acid), Lys(IVA), Lys(Peg4-isoGlu-Palm), Lys(pyroglutaric acid), Lys-(succinic acid), Asn, Orn,G1n, Arg, Thr or Val;
X14 is Dab(Ac), Dap(Ac), Phe, His, Lys(Ac), Met, Asn, Gin, Arg, or Tyr; and X15 is Ala, betaAla, Gly, Asn, Gin, or Ser.
[0014] In certain embodiments of Xa: X1 is absent; X2 is absent; X3 is absent;
X4 is Cys, Abu or Pen; X5 is Dap, Dap(Ac), Gly, Lys, Gin, Arg, Ser,Thr or Asn; X6 is Thr; X7 is Trp or 6-Chloro-Trp; X8 is Gin; X9 is Cys, Abu or Pen; X10 is 2-Nal, a Phe analog, Tyr, or a Tyr analog;
X11 is 1-Nal, 2-Nal, Phe(3,4-dimethoxy), Phe(3,4-C12), or Trp; X12 is Acpc, Acbc, Acvc, Achc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, hLeu, Lys, Leu, Arg or THP; X13 is Cit, Asp, Dap, Dap(Peg2-Ac), Dap(pyroglutaric acid), Glu, hArg, Lys, Lys(Ac), Lys(Benzoic acid), Lys(glutaric acid), Lys(IVA), Lys(Peg4-isoGlu-Palm), Lys(pyroglutaric acid), Lys-(succinic acid), Asn, Orn,G1n, Arg, or Val;
X14 is Dab(Ac), Dap(Ac), His, Lys(Ac), Asn, Gin, or Tyr; and X15 is Ala, betaAla, Gly, Asn, Gin, or Ser.
[0015] In certain embodiments of Xa: X1 is absent; X2 is absent; X3 is absent;
X4 is Cys, Abu or Pen; X5 is Dap, Dap(Ac), Gin, Ser, Thr or Asn; X6 is Thr; X7 is Trp; X8 is Gin; X9 is Cys, Abu or Pen; X10 is a Phe analog, Tyr, or a Tyr analog; X11 is 2-Nal or Trp;
X12 is Acpc, Acbc, Acvc, Achc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, hLeu, Leu, or THP; X13 is Cit, Asp, Glu, Lys, Lys(Ac), Asn, or Gin; X14 is Dab(Ac), Asn, or His; and X15 is Ala, betaAla, Gly, Asn, or Gin.
[0016] In certain embodiments of Xa: X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Met, Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Sec, 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choropropanoic acid, 4-chlorobutyric acid, 3-chloroisobutyric acid, Abu, f3-azido-Ala-OH, propargylglycine, 2-(3 '-butenyl)glycine, 2-allylglycine, 2-(3 '-butenyl)glycine, 2- (4'-pentenyl)glycine, 2-(5'-hexenyl)glycine, or Abu; X7 is Trp, Glu, Gly, Ile, Asn, Pro, Arg, Thr or OctGly, or a corresponding a-methyl amino acid form of any of the foregoing; X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Asp, Leu, Val, Phe, or Ser, Sec, Abu, f3-azido-Ala-OH, propargylglycine, 2-2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, Ala, hCys, Abu, Met, MeCys, (D)Tyr or 2-(5'-hexenyl)glycine; X10 is Tyr, Phe(4-0Me), 1-Nal, 2-Na!, Aic, a-MePhe, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, His, hPhe(3,4-dimethoxy), hTyr, N-Me-Tyr, Trp, Phe(4-CONH2), Phe(4-phenoxy), Thr, Tic, Tyr(3-tBu), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-NH2), Phe(4-F), Phe(3,5-F2), Phe(4-CH2CO2H), Phe(penta-F), Phe(3,4-C12), Phe(4-CF3), Phe(4-0CH3), Bip, Cha, 4-PyridylAlanine, f3hTyr, OctGly, Phe(4-N3), Phe(4-Br), Phe[4-(2-aminoethoxy)]
or Phe, a Phe analog, a Tyr analog, or a corresponding a-methyl amino acid form of any of the foregoing; X11 is 2-Na!, 1-Nal, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe (3,4-F2), Phe(4-CO2H), f3hPhe(4-F), Me-Trp, 4-phenylcyclohexyl, Phe(4-CF3), a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Trp, Tyr, Phe(4-0Me), Phe(4-Me), Trp(2,5,7-tri-tert-Butyl), Phe(4-0ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino, Phe(4-0Bz1), Octgly, Glu(Bz1), 4-Phenylbenzylalanine, Phe[4-(2-aminoethoxy)], 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, 1,2,3,4-tetrahydro-norharman, Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(2,3 -C12), Phe(2,3-F2), Phe(4-F), 4-phenylcyclohexylalanine, Bip, or a corresponding a-methyl amino acid form of any of the foregoing; X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acvc, Acbc, Agp, Aib, a-DiethylGly, MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Aibõ D-Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Tyr, Aib, a-MeLeu,a-MeOrn, R-Aib, f3-Ala, f3hAla, PhArg, PhLeu, f3hVal, f3-spiro-pip, Glu, hArg, Ile, Lys, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gin, Ser, Thr, Tie, t-butyl-Gly, or a corresponding a-methyl amino acid form of any of the foregoing; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Arg, Orn, Val, f3hAla, Lys(Ac), (D)Asn, (D)Leu, (D)Phe, (D)Thr, Ala, a-MeLeu, Aib, f3-Ala, f3-Glu, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, hLeu, Asn, Ogl, Pro, Gin, Ser, f3-spiro-pip, Thr, Tba, Tie or Aib, Cit, hArg, Lys, Asn, Orn, Gin or a corresponding a-methyl amino acid form of any of the foregoing; X14 is Phe, Tyr, Glu, Gly, His, Lys, Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr,

6 Ticf3hPhe, Arg, Lys(Ac), His; Dap(Ac), Dab(Ac), Asp or a corresponding a-methyl amino acid form of any of the foregoing; X15 is Gly, Ser, Thr, Gin, Ala, (D)Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Thr, Aea, Asp, Asn, Glu, Phe, Gly, Lys, Leu, Pro, Arg, f3-Ala, Sarc, or a corresponding a-methyl amino acid form of any of the foregoing; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, Gly, Ser, Pro, Asn, Thr or absent, or a corresponding a-methyl amino acid form of any of the foregoing; and X17 is Leu, Lys, Arg, Glu, Ser, Gly, Gin or absent, or a corresponding a-methyl amino acid form of any of the foregoing.
[0017] In certain embodiments of peptide inhibitors of Xa, the bond is a disulfide bond, a thioether bond, a lactam bond, a triazole ring, a selenoether bond, a diselenide bond, or an olefin bond.
[0018] In particular embodiments of peptide inhibitors of Xa, X4 is Cys and X9 is Cys, and the bond is a disulfide bond. In particular embodiments, X4 is Pen and X9 is Pen, and the bond is a disulfide bond. In certain embodiments: X7 is Trp; X10 is Phe, Tyr, a Phe analog, or a Tyr analog; X11 is Trp, 1-Nal or 2-Nal; and X12 is Aib, a-Me-Lys, a-Me-Leu, Achc, Acvc, Acpc, Acbc or THP. In certain embodiments: X7 is Trp; X10 is Phe, Tyr, a Phe analog, or a Tyr analog; X11 is Trp, 1-Nal or 2-Nal; and X12 is Aib, a-Me-Lys or a-Me-Leu. In particular embodiments, the peptide inhibitor comprises any of the following the amino acid sequences:
Pen-Q-T-W-Q-Pen-[Phe(4-0Me)]-[2-Nal]-[a-Me-Lys]-E-N-G; Pen-N-T-W-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[Aib]-[Lys(Ac)]-N-N; Pen-Q-T-W-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[a-MeLeu]-[Lys(Ac)]-N-N; or Pen-Q-T-W-Q-[Pen]-[Phe(4-CONH2)]-[2-Nall-[a-MeLys]-[Lys(Ac)]-N-N, wherein the peptide inhibitor comprises a disulfide bond between the two Pen amino acids.
[0019] In particular embodiments of peptide inhibitors of Xa, X4 is an amino acid, aliphatic acid, alicyclic acid or modified 2- methyl aromatic acid having a carbon side chain capable of forming a thioether bind with X9; X9 is a sulfur-containing amino acid capable of forming a thioether bond with X4, and the bond between X4 and X9 is a thioether bond. In certain embodiments, X4 is Abu, 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-chloro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid; and X9 is Abu, Cys, Pen, hCys, D-Pen, D-Cys, or D-hCys.In certain

7 embodiments, X4 is Abu; and X9 is Cys. In certain embodiments, X7 is Trp; X10 is Phe, Tyr, a Phe analog, or a Tyr analog; X11 is Trp, 1-Nal or 2-Nal; and X12 is a-Me-Lys, a-Me-Leu, Me-Ser, a-Me-Val, Achc, Acvc, Acpc, Acbc, or [4-amino-4-carboxy-tetrahydropyran]. In certain embodiments, X7 is Trp; X10 is Phe, Tyr, a Phe analog, or a Tyr analog; X11 is Trp, 1-Nal or 2-Nal; and X12 is a-Me-Lys or [4-amino-4-carboxy-tetrahydropyran]. In particular embodiments, the peptide inhibitor comprises any of the following amino acid sequences: [Abu]-Q-T-W-Q-C-[Phe(4-0Me)]-[2-Nal]-[a-MeLys]-E-N-G;
[Abu]-Q-T-W-Q-C-[Phe(4-(2-aminoethoxy))]-W-[a-MeLys]-E-N-G; or [Abu]-Q-T-W-Q-C-[Phe[4-(2-aminoethoxy)]]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-E-N-N, wherein the peptide inhibitor comprises a thioether bond between the Abu and the C.
[0020] In certain embodiments of peptide inhibitors of Xa: X4 is Pen, Cys or hCys; X5 is any amino acid; X6 is any amino acid; X7 is Trp, Bip, Gln, His, Glu(Bz1), 4-Phenylbenzylalanine, Tic, Phe[4-(2-aminoethoxy)], Phe(3,4-C12), Phe(4-0Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-Me-Trp, 1,2,3,4 -tetrahydro-norharman, Phe(4-CO2H), Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(4-CF3), Phe(4-tBu), f33-diPheAla, Glu, Gly, Ile, Asn, Pro, Arg, Thr or Octgly, or a corresponding a-methyl amino acid form of any of the foregoing; X8 is any amino acid; X9 is Pen, Cys or hCys; X10 is 1-Nal, 2-Nal, Aic, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, Phe, His, Trp, Thr, Tic, Tyr, 4-pyridylAla, Octgly, a Phe analog or a Tyr analog (optionally, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), or Phe(4-0Bz1)), or a corresponding a-methyl amino acid form of any of the foregoing; X11 is 2-Nal, 1-Nal, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe (3,4-F2), Phe(4-CO2H), f3hPhe(4-F), a-Me-Trp, 4-phenylcyclohexyl, Phe(4-CF3), a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Trp, Tyr, Phe(4-0Me), Phe(4-Me), Trp(2,5,7-tri-tert-Butyl), Phe(4-0ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino, Phe(4-0Bz1), Octgly, Glu(Bz1), 4-Phenylbenzylalanine, Phe[4-(2-aminoethoxy)], 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, 1,2,3,4-tetrahydro-norharman, Phe(4-CONH2), Phe(3,4-0Me2) Phe(2,3-C12), Phe(2,3-F2), Phe(4-F), 4-phenylcyclohexylalanine or Bip, or a corresponding a-methyl amino acid form of any of the foregoing; X12 is a-MeLys, a-MeOrn, a-MeLeu, a-MeVal, 4-amino-4-carboxy-tetrahydropyran, Achc, Acpc, Acbc, Acvc, MeLeu, Aib, (D)Ala, (D)Asn, (D)Leu, (D)Asp,

8 (D)Phe, (D)Thr, 3-Pal, Aib, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, hArg, hLeu, Ile, Lys, Leu, Asn, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Arg, Ser, Thr or Tle, or a corresponding a-methyl amino acid form of any of the foregoing; X13 is Lys(Ac), (D)Asn, (D)Leu, (D)Thr, (D)Phe, Ala, Aib, a-MeLeu, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Lys, Arg, Orn, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, Lys, Leu, Asn, Ogl, Pro, Gln, Asp, Arg, Ser, spiro-pip, Thr, Tba, Tlc, Val or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing; X14 is Asn, Glu, Phe, Gly, His, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Tic or Tyr, Lys(Ac), Orn or a corresponding a-methyl amino acid form of any of the foregoing; X15 is Gly, (D)Ala, (D)Asn, (D)Asp, Asn, (D)Leu, (D)Phe, (D)Thr, Ala, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gln, Arg or Ser, f3-Ala, Arg or a corresponding a-methyl amino acid form of any of the foregoing; X16 is absent, Gly, Ala, Asp, Ser, Pro, Asn or Thr, or a corresponding a-methyl amino acid form of any of the foregoing; X17 is absent, Glu, Ser, Gly or Gln, or a corresponding a-methyl amino acid form of any of the foregoing; X18 is absent or any amino acid; X19 is absent or any amino acid; and X20 is absent or any amino acid. In particular embodiments, the bond between X4 and X9 is a disulfide bond. In certain embodiments, Xl, X2, and X3 are absent.In certain embodiments, X17, X19 and X20 are absent. In certain embodiments, one or both of X4 or X9 is Pen. In certain embodiments, both X4 and X9 are Pen. In particular embodiments, X18 is (D)-Lys. In certain embodiments, the peptide inhibitors comprise one or more, two or more, three or more, or four of the following: X5 is Arg, Asn, Gln, Dap, Orn; X6 is Thr or Ser; X7 is Trp, 2-Nal, 1-Nal, Phe(4-0Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(Bz1) or Phe(4-Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp or 1,2,3,4 -tetrahydro-norharman; and X8 is Gln, Val, Phe, Glu, Lys. In certain embodiments, the peptide inhibitors comprise one or more, two or more, three or more, four or more, five or more, six or more, or seven of the following: X10 is Tyr, Phe(4-0Bz1), Phe(4-0Me), Phe(4-CONH2), Phe(3,4-C12), Phe(4-tBu), Phe(4-NH2), Phe(4-Br), Phe(4-CN), Phe(4-CO2H), Phe(4-(2aminoethoxy)) or Phe(4-guanadino); X11 is Trp, 2-Nal, 1-Nal, Phe(4-0Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(Bz1) or Phe(4-Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp or 1,2,3,4 -tetrahydro-norharman; X12 is Arg, a-MeLys a-MeLeu, Aib or a-MeOrn;
X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is Gly, Sr or Ala; and X16 is absent or

9 AEA. In certain embodiments, X4 and X9 are Pen; X5 is Gin; X6 is Thr; X7 is Trp; X8 is Gin;
X10 is Tyr, Phe(4-0Me) or 2-Nal; X11 is Trp, 2-Nal or 1-Nal; X12 is Arg, aMeLys or a-MeOrn; X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is Gly; and X16 is absent. In certain embodiments, one or more of Xl, X2 and X3 are absent; and one or more, two or more, three or more, or four of X17, X18, X19 and X20 are absent.
[0021] In certain embodiments of peptide inhibitors of Xa: X4 is Abu, Pen, or Cys; X7 is Trp, Bip, Gin, His, Glu(Bz1), 4-Phenylbenzylalanine, Tic, Phe[4-(2-aminoethoxy)], Phe(3,4-C12), Phe(4-0Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp, 1,2,3,4 -tetrahydro-norharman, Phe(4-CO2H), Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(4-CF3), f33-diPheAla, Phe(4-tBu), Glu, Gly, Ile, Asn, Pro, Arg, Thr or Octgly, or a corresponding a-methyl amino acid form of any of the foregoing; X9 is Abu, Pen, or Cys; X10 is 1-Nal, 2-Nal, Aic, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, Phe, His, Trp, Thr, Tic, Tyr, 4-pyridylAla, Octgly a Phe analog or a Tyr analog, or a corresponding a-methyl amino acid form of any of the foregoing; X11 is 2-Nal, 1-Nal, 2,4-dimethylPhe, Bip, 4-phenylcyclohexyl, Glu(Bz1), 4-Phenylbenzylalanine, Tic, Phe[4-(2-aminoethoxy)], Phe(3,4-C12), Phe(3,4-F2), f3hPhe(4-F), Phe(4-0Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp, 1,2,3,4 -tetrahydro-norharman, Phe(4-CO2H), Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(4-CF3), Phe(2,3-C12), Phe(2,3-F2),Phe(4-F), 4-phenylcyclohexylalanine, a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Bip, Nva(5-phenyl), Phe, His, hPhe, Tqa, Trp, Tyr, Phe(4-Me), Trp(2,5,7-tri-tertButyl), Phe(4-0Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(4-0Bz1), or Octgly, or a corresponding a-methyl amino acid form of any of the foregoing; X12 is a-MeLys, a-MeOrn, a-MeLeu, MeLeu, Aib, (D)Ala, (D)Asn, (D)Leu, (D)Asp, (D)Phe, (D)Thr, 3-Pal, Aib, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, hArg, hLeu, Ile, Lys, Leu, Asn, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gin, Arg, Ser, Thr or Tie, or a corresponding a-methyl amino acid form of any of the foregoing; X13 is Lys(Ac), (D)Asn, (D)Leu, (D)Thr, (D)Phe, Ala, Aib, a-MeLeu, f3Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Arg, Orn, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, Lys, Leu, Asn, Ogl, Pro, Gin, Asp, Arg, Ser, spiro-pip, Thr, Tba, Tic, Val or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing; X14 is Asn, Glu, Phe, Gly, His, Lys, Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr, Tic or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing; X15 is Gly, (D)Ala, (D)Asn, (D)Asp, Asn, (D)Leu, (D)Phe, (D)Thr, Ala, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gln, Arg or Ser, or a corresponding a-methyl amino acid form of any of the foregoing, or X15 is Gly, (D)Ala, (D)Asn, (D)Asp, Asn, (D)Leu, (D)Phe, (D)Thr, Ala, Asn, Ser, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gln, Arg or Ser, or a corresponding a-methyl amino acid form of any of the foregoing; X16 is absent, Gly, Ala, Asp, Ser, Pro, Asn or Thr, or a corresponding a-methyl amino acid form of any of the foregoing; and X17 is absent, Glu, Ser, Gly or Gln, or a corresponding a-methyl amino acid form of any of the foregoing. In particular embodiments, the peptide inhibitor is cyclized via an intramolecular bond between X4 and X9.In certain embodiments, one or more of Xl, X2, and X3 are absent. In certain embodiments, one or more of X17, X19 and X20 are absent.In certain embodiments, one of X4 or X9 is Abu, and the other of X4 or X9 is not Abu.In certain embodiments, the peptide inhibitors comprise one or more, two or more, three or more, or four of the following: X5 is Arg, Gln, Dap or Orn;
X6 is Thr or Ser;
X7 is Trp, 2-Nal, 1-Nal, Phe(4-0Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(4-0Bz1), Phe(4-Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, or a-MeTrp, 1,2,3,4 -tetrahydro-norharman; and X8 is Gln, Val, Phe, Glu or Lys. In certain embodiments, the peptide inhibitors comprise one or more, two or more, three or more, four or more, five or more, six or more, or seven of the following: X10 is Tyr, Phe(4-0Bz1), Phe(4-0Me), Phe(4-CONH2), Phe(3,4-C12), Phe(4-tBu), Phe(4-NH2), Phe(4-Br), Phe(4-CN), Phe(4-CO2H), Phe(4-(2aminoethoxy)) or Phe(4-guanadino); X11 is Trp, 2-Nal, 1-Nal, Phe(4-0Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(Bz1) or Phe(4-Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp or 1,2,3,4 -tetrahydro-norharman; X12 is Arg, hLeu, (D)Asn, Aib, a-MeLys, a-MeLeu or a-MeOrn; X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is Gly, Ser or Ala, or X15 is Asn, Gly, Ser, f3Ala or Ala; and X16 is absent or AEA.
[0022] In particular embodiments of any of the peptide inhibitors, X4 and X9 are Pen. In particular embodiments, X4 and X9 form a disulfide bond.
[0023] In particular embodiments, X4 is Abu and X9 is Cys. In particular embodiments, X4 and X9 form a thioether bond.

In particular embodiments, the peptide inhibitor comprises an amino acid sequence of any one of SEQ ID NOS: 365-370, 857-1029. In particular embodiments, the peptide inhibitor is cyclized via a bond between X4 and X9, and the peptide inhibitor inhibits the binding of an interleukin-23 (IL-23) to an IL-23 receptor.
[0024] In certain embodiments of peptide inhibitors of Xa, the peptide inhibitor comprises an amino acid sequence set forth in any of Formulas (V), (Va), (Vb), (Vc), (Vd), (Ve), (Vf), (Vg) and (Vh).
100251 In certain embodiments of peptide inhibitors of Xa, the peptide inhibitor comprises any of the following amino acid sequences:
[Palm] - [isoGlu] - [PEG4] - [Pen] -NTWQ- [Pen] - [Phe [4- (2-aminoethoxy)] -[2-Nal] - [Aib] - [Ly s (Ac)] -E12;
Ac- [Pen] -NTWQ- [Pen]- [Phe [4- (2-amino ethoxy)]- [2-Nal] - [Aib] - [Lys (PEG4 - s oGlu-Palm)] -NN-NH2;
Ac- [Pen]-QTWQ - [Pen] -Phe(4-CONH2)- [2-Nal] - [a -MeLy s (Ac)] - [Lys(Ac)] -NN-NH2;
[Octany1]-[IsoGlu]-[PEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
[0 ctanyl] - [PEG4] - [Pen] -NTWQ- [Pen] - [Phe [4 -(2 -aminoethoxy)] - [2-Nal] - [Aib] - [Ly s(Ac)]-NN-NH2;
[Palm] - [PEG4]- [Pen] -NTWQ- [Pen] - [Phe [4 -(2 -aminoethoxy)] - [2-Nal] -[Aib] - [Lys (Ac)] -NN-NH2;
Ac- [Pen] -NTWQ- [Pen]- [Phe[4-(2-aminoethoxY)] - [2-Nal] - [Ail* [Lys (PEG4-0 ctanyl)] -NN-NH2;
Ac- [Pen] -NTWQ- [Pen]- [Phe [442-amino ethoxY)] - [2-Nal] - [Aib] - [Lys (PEG4 -Palm)] -NN-NH2;
Ac- [Pen] -NTWQ- [Pen] - [Phe [4 -(2-amino ethoxy)-(PEG4 -Palm)] - [2-Nal] -[Aib] - [Ly s (Ac)]NN-NH2;

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-Laury1)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(PEG4-Palm)-[Lys(Ac)]-NN-NH2;

Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(PEG4-Laury1)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-IsoGlu-Palm)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-IsoGLu-Laury1)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(PEG4-IsoGlu-Palm)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(PEG4-IsoGlu-Laury1)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(IVA)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(Biotin)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(Octany1)]-[Lys(A0]-NN-NH2;
Ac-[Pen]-[Lys(IVA)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Na1]-[Aib]-[Lys(Ac)]-[Lys(IVA)]-N-NH2;
Ac-[Pen]-[Lys(Biotin)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(Biotin)]-N-NH2;
Ac-[Pen]-[Lys(Octany1)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(octany1)]-N-NH2;
Ac-[Pen]-[Lys(Palm)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]--[A113]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-Lys(Palm)]-N-NH2;
Ac-[Pen]-[Lys(PEG8)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(PEG8)]-N-NH2;
Ac-[Pen]-K(Pegll-Palm)TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-[Lys(Pegll-palm)]-N-NH2;
Ac-[Pen]-[Cit]-TW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]--[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-[Lys(Ac)]-TW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[Phe(3,4-0CH3)2]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[Phe(2,4-CH3)2]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[Phe(3-CH3)]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[Phe(4-CH3)]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac[(D)Arg]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal] - [Aib]-[Lys(Ac)]-N-[j3Ala]-NH2;

Ac-[(D)Tyr]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-N-[f3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(A0]-QN-NE12;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(Ac)]-N-NE12;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-N-[Lys(Ac)]-NE12;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(A0]-QQ-NE12;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-Q-[f3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-N-[Cit]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[A1b]-[1-Ys(A0]-[Cit]-NNH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Cit]-Q-NE12;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Cit]-[Lys(Ac)]-NE12;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(Ac)]-[Cit]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-QN-[13Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-E-[Cit]-Q-NE12;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[A113]-[Cit]-N-[Cit]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)] - [2-Nall-[Aib]-[Cn]-Q-[Cit]-M12;
Ac-[Pen]-[Cit]-TWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-P-Nall-[A113]-QNN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-ENQ-NH2;

Ac-[Pen]-GPWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[A113]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-PGWQ-[Pen]-[Phe[4-(2-aminoethcxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWN-[Pen]-[Phe[4-(2-aminoethcxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NSWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[A113]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-N-[Aib]-WQ-[Pen]-[Phe[4-(2-aminoethcxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTW-[Aib]-[Pen]-[Phe[4-(2-aminoethoxY)] - [2-NalHAibl-[Lys(Ac)]N-[Aib]-NH2;
Ac-[Pen]-QTW- [Ly s(Ac)] - [Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-[Lys(Ac)]-TWQ-[Pen]-[Phe[4-(2-aminoethcxY)]-[2-Nal]--[A113]-[Lys(Ac)]NNNH2;
Ac-[Pen]-QVWQ-[Pen]-[Phe[4-(2-aminoethcxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[2-Nal]-Q-[Pen]-[Phe[4-(2-aminoethcxY)]-[2-Nal]-[A113]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[1-Nal]-Q-[Pen]-[Phe[4-(2-aminoethcxY)]-[2-Nal]-[A113]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[a-MeLeu]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[a-MeLeu]-[Lys(Ac)]-N-[f3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]-N-[f3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-N-[f3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethcxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-1_,N-NH2;

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-GN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-SN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Aib]-N-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(A0]-FN-NH2;
Ac-[Pen]-NTW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Tic]-[(3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[nLeu]-[[3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-G-[(3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-R-[f3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]¨[A113]-[Lys(Ac)]-W-[PAla]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]--[Aib]-[Lys(Ac)]-S-[(3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]--[Aib]-[Lys(Ac)]-L-[f3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]--[Ab]-[Lys(Ac)]-[MB]-[(3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-[N-MeAla]-[f3Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-[2-Nal*H3Alal-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxY)]-[2-Nal]-[Aib]-[Lys(Ac)]-F-[f3Ala]-NH2;
Ac-[(D)Arg]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[ 4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]NNNH2;
Biotin-[PEG4]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;

Ac-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)l-NN-NH2;
Ac-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)l-NN-NH2;
Ac-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)l-NN-NH2;
Ac-E-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyranFENN-NH2;
Ac-RD)Asp]-[(D)Arg]-cyclo[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-carboxy-tetrahydropyran]-ENN-NH2;
Ac-R-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyranFENN-NH2;
inoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-F-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyranFENN-NH2;
Ac-RD)Phe]-[(D)Arg]-cyclo[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-carboxy-tetrahydropyran]-ENN-NH2;
Ac42-Nall-RD)Arg]-cyclo[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-T-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyranFENN-NH2;
Ac-L-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyranFENN-NH2;

Ac-[(D)Gln]-[(D)Arg]-cycloMbuFQTWQCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-[(D)Asn]-[(D)Arg]-cyclo[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-cyclo[[Abu] -QTWQC]- [Phe[4-(2-aminoethoxy)-(PEG4-Alexa488)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
[Alexa488]-[PEG4]-cyclo[[Abu] -QTWQC] - [Phe[4-(2-aminoethoxy)]-42-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
[Alexa647]-[PEG4]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-carboxy-tetrahydropyran]-ENN-NH2;
[Alexa-647]-[PEG4]-[(D)Arg]-cyclo[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(A0]-NN-NH2;
[Alexa647]- [PEG12]- [(D)Arg]-cyclo[ [Abu]-QTWQC] -[Phe[4-(2-aminoethoxy)]- [2-Nall - [4-amino-4-carboxy-tetrahydropyran]- [Lys(Ac)]-NN-NH2; and [Alexa488]-[PEG4]-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]- [Lys(Ac)]-NN-NH2, [0026] wherein the peptide inhibitor is cyclized via a disulfide bond between two Pen residues or by a thioether bond between Abu and a Cys residue, and wherein the peptide inhibitor inhibits the binding of an interleukin-23 (IL-23) to an IL-23 receptor.
[0027] In particular embodiments, any of the peptide inhibitors described herein comprise one or more half-life extension moiety and/or one or more linker moiety conjugated to the peptide inhibitor. In particular embodiments, the half-life extension moiety is conjugated to the peptide inhibitor via one or more linker moieties.
[0028] In certain embodiments, any of the peptide inhibitors described hereinfurther comprise a conjugated chemical substituent. In particular embodiments, the conjugated chemical substituent is a lipophilic substituent or a polymeric moiety, e.g., Ac, Palm, gamaGlu-Palm, isoGlu-Palm, PEG2-Ac, PEG4-isoGlu-Palm, (PEG)5-Palm, succinic acid, glutaric acid, pyroglutaric acid, benzoic acid, IVA, octanoic acid, 1,4 diaminobutane, isobutyl, or biotin. In certain embodiments, the conjugated chemical substituent is a polyethylene glycol with a molecular mass of 400 Da to 40,000 Da.
[0029] In another aspect, the present invention includes peptide inhibitors comprising the structure of Formula I:
R1-X-R2 (I) or a pharmaceutically acceptable salt or solvate thereof, wherein Rl is a bond, hydrogen, a C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl, a C 1 -C6 alkyl, a C 1 -C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing;
R2 is a bond, OH or NH2; and X is any of the peptide sequences described herein, e.g., Xa, I, Ia-It, II, ha-lid, III, Illa-Ille, IV, IVa-IVb, V, or Va-Vh.
[0030] In a related aspect, the present invention includes a peptide dimer inhibitor of an interleukin-23 receptor, wherein the peptide dimer inhibitor comprises two peptide monomer subunits connected via one or more linker moieties, wherein each peptide monomer subunit has a sequence or structure set forth herein. In certain embodiments, one or both peptide monomer subunit is cyclized via an intramolecular bond between X4 and X9. In certain embodiments, one or both intramolecular bond is a disulfide bond, a thioether bond, a lactam bond, a selenoether, diselenide, or an olefin bond. In certain embodiments, the linker is any of those shown in Table 2 or described herein. In certain embodiments, the linker moiety is a diethylene glycol linker, an iminodiacetic acid (IDA) linker, a P-Ala-iminodiaceticacid (f3-Ala-IDA) linker, or a PEG linker.
In particular embodiments, the N-terminus of each peptide monomer subunit is connected by the linker moiety. In particular embodiments, the C-terminus of each peptide monomer subunit is connected by the linker moiety. In certain embodiments, the linker connects an internal amino acid residue of at least one of the peptide monomer subunits to the N-terminus, C-terminus, or an internal amino acid residue of the other peptide monomer subunit.
[0031] In a further related aspect, the present invention includes a polynucleotide comprising a sequence encoding a peptide inhibitor of the present invention or one or both peptide monomer subunit of a peptide dimer inhibitor of the present invention. The present invention also includes a vector comprising the polynucleotide.
[0032] In another aspect, the present invention includes a pharmaceutical composition comprising a peptide inhibitor or a peptide dimer inhibitor of the present invention, and a pharmaceutically acceptable carrier, excipient, or diluent. In particular embodiments, the pharmaceutical composition comprises an enteric coating. In certain embodiments, the enteric coating protects and releases the pharmaceutical composition within a subject's lower gastrointestinal system.
[0033] In another aspect, the present invention includes a method for treating or preventing a disease associated with IL-23 signalling, including but not limited to an Inflammatory Bowel Disease (IBD), ulcerative colitis, Crohn's disease, Celiac disease (nontropical Sprue), enteropathy associated with seronegative arthropathies, microscopic colitis, collagenous colitis, eosinophilic gastroenteritis, colitis associated with radio- or chemo-therapy, colitis associated with disorders of innate immunity as in leukocyte adhesion deficiency-1, chronic granulomatous disease, glycogen storage disease type 1 b, Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, and Wiskott-Aldrich Syndrome, pouchitis resulting after proctocolectomy and ileoanal anastomosis, gastrointestinal cancer, pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, pericholangitis, chronic bronchitis, chronic sinusitis, asthma, psoriasis, or graft versus host disease in a subject, comprising providing to the subject an effective amount of a peptide inhibitor or pharmaceutical composition of the present invention.
In certain embodiments, the inflammatory bowel disease is ulcerative colitis or Crohn's disease.
In particular embodimnts, the peptide inhibitor or the peptide dimer inhibitor inhibits binding of an interleukin-23 (IL-23) to the interleukin-23 receptor (IL-23R). In certain embodiments, the pharmaceutical composition is provided to the subject by an oral, intravenous, peritoneal, intradermal, subcutaneous, intramuscular, intrathecal, inhalation, vaporization, nebulization, sublingual, buccal, parenteral, rectal, intraocular, inhalation, vaginal, or topical route of administration. In particular embodiments, the pharmaceutical composition is provided orally for treating Inflammatory Bowel Disease (IBD), ulcerative colitis, Crohn's disease. In certain embodiments, the pharmaceutical composition is provided to the subject topically, parenterally, intravenously, subcutaneously, peritonealy, or intravenously for treating psoriasis.
BRIEF DESCRIPTION OF THE DRAWINGS
[0034] FIG. 1 Figure 1 provides an example of a rat IL-23 dose-response curve as measured by levels of IL-17A in the rat splenoctye assay.
[0035] Figure 2 is a graph showing IL-12-dependent production of IFNy from human PBMCs treated with the indicated amounts of Compound A or Compound B.
[0036] Figure 3 shows results for DAI values from Day 7. Statistical analysis for significance was determined using Student's t-test (GraphPad Prism). Differences were noted as signficant *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.
[0037] Figure 4 shows an alignment of the amino acid sequences of human IL23R, mouse IL-23R, rat IL23R, chimp IL-23R, dog IL-23R and cow IL-23R, with highly conserved amino acid residues shaded. The region of mouse IL-23R lacking in the other IL-23R
species shown is shown, and a region of IL23R that may be bound by certain peptide inhibitors of the present invention is indicated by a dashed line.
[0038] Figure 5 is a table outlining the study design for TNBS induced colitis in rats.
[0039] Figures 6A-6D are graphs showing colon weight to length (Figure 6A), colon wall thickness (Table 6B, colon macroscopic score (Table 6C) or myeloperoxidase (MPO) abundance in proximal colon extracts quantified by ELISA, following sham treatment, vehicle treatment, or treatment with the indicated amounts of anti-IL23p19 antibody or Compound C.
Values are shown as mean +SD. Statistical significance assessed by one-way ANOVA: *<0.05;
**<0.01;
***p<0.001; ****p<0.0001; ns, not significant.

[0040] Figure 7 provides micrographs of colon lesions found in animals following sham treatment (upper left panel), vehicle treatment (upper right panel) showing transmural inflammation, presence of necrotic tissue, and mucosa devoid of crypts, anti-IL23p19 antibody (lower left panel), or 160 mg/kg/d Compound C (lower right panel) showing restriction of lesions to the mucosa.
[0041] Figures 8A-8E are graphs showing inflammation (Figure 8A), mucosal necrosis (Figure 8B), grand loss (Figure 8C), colon wall thickness (Figure 8D) and histological score (Figure 8E) following vehicle treatment, treatment with anti-IL23p19 antibody, or treatment with the indicated amount of Compound C
[0042] Figure 9 shows the concentration of Compound C in the plasma and proximal colon determined one hour post last PO dose (left panel), and fold above IC75 of its activity as determined by the rat splenocyte assay (middle panel) and the rat IL23R ELISA
assay (right panel).
[0043] Figure 10 provides a schematic diagram depicting the structure of certain peptide inhibitors and illustrating representative types of bonds between X4 and X9.
[0044] FIGS. 11A-11E show pharmacokinetic data for the IL-23R peptide inhibitor Peptide 993 (SEQ ID NO: 993). FIG. 11A shows the concentration of Peptide 993 in serum (nIVI) measured at different time points up to 24 hours after oral administration of Peptide 993. FIGS. 11B-11D
show the concentration of Peptide 993 (in nIVI) in samples taken from the Peyer's Patch (FIG.
11B), small intestine (FIG. 11C), and the colon (FIG. 11D). The dashed line indicates 350 mIVI.
Fig 11E shows the amount of Peptide 993 detected in feces 24 hours after oral administration (%
dose).
[0045] FIGS. 12A-12D summarize experiments comparing systemic treatments with prodnisolone or anti-IL-23p19 neutralizing antibody with treatment with Peptide 993 by oral administration in the TNBS model of acute colitis. FIG. 12A shows the change in body weight (percentage) from day 0 to day 7 from sham, vehicle, and Peptide 993 treated rats. FIG. 12B
shows the ratio of colon weight to colon length in mg/cm of colons harvested from rats at day 7.
FIG. 12C shows the colon macroscopic score of colons harvested from rats at day 7. FIG. 12D.

shows the sum of histopathology scores for colons taken from sham, vehicle, and Peptide 993 treated rats. For all experiments, statistical comparisons between groups were performed with a 1-Way ANOVA followed by a post hoc test: * p< 0.05; ** p< 0.01; *** p< 0.001;
**** p<
0.0001; ns, not significant.
[0046] FIGS. 13A-13C summarizes experiments comparing systemic treatments with prodnisolone or anti-IL-23p19 neutralizing antibody with treatment with Peptide 1185 by oral administration in the TNBS model of acute colitis. FIG. 13A shows the change in body weight (percentage) from day 0 to day 7 from sham, vehicle, and Peptide 1185 treated rats. FIG. 13B
shows the ratio of colon weight to colon length in mg/cm of colons harvested from rats at day 7.
FIG. 13C shows the colon macroscopic score of colons harvested from rats at day 7. For all experiments, statistical comparisons between groups were performed with a 1-Way ANOVA
followed by a post hoc test: * p< 0.05; ** p< 0.01; *** p< 0.001; **** p<
0.0001; ns, not significant.
[0047] FIGS. 14A-14D summarizes experiments comparing systemic treatments with prodnisolone or anti-IL-23p19 neutralizing antibody with treatment with Peptide 980 by oral administration in the TNBS model of acute colitis. FIG. 14A shows the change in body weight (percentage) from day 0 to day 7 from sham, vehicle, and Peptide 980 treated rats. FIG. 14B
shows the ratio of colon weight to colon length in mg/cm of colons harvested from rats at day 7.
FIG. 13C shows the colon macroscopic score of colons harvested from rats at day 7. FIG. 14D.
shows the sum of histopathology scores for colons taken from sham, vehicle, and Peptide 980 treated rats. For all experiments, statistical comparisons between groups were performed with a 1-Way ANOVA followed by a post hoc test: * p< 0.05; ** p< 0.01; *** p< 0.001;
**** p<
0.0001; ns, not significant.
[0048] FIGS. 15A-15E show levels of disease and IL-23 directed biomarkers measured in colons from rats in the sham (not TNBS-exposed) experimental group, or TNBS-exposed experimental groups that received treatment with vehicle or Peptide 993. Data is shown for MPO (FIG. 15A), IL-6 (FIG. 15B), IL-1 beta (FIG. 15C), IL-22 (FIG. 15D), and (FIG.15E). For all experiments, statistical comparisons between groups were performed with a 1-Way ANOVA followed by a post hoc test: * p< 0.05; ** p< 0.01; *** p< 0.001;
**** p<
0.0001; ns, not significant.
[0049] FIGS. 16A-16B show levels of disease and IL-23 directed biomarkers measured in colons from rats in the sham (not TNBS-exposed) experimental group, or TNBS-exposed experimental groups that received treatment with vehicle or Peptide 980. Data is shown for MPO (FIG. 16A) and IL-22 (FIG. 16B). For all experiments, statistical comparisons between groups were performed with a 1-Way ANOVA followed by a post hoc test: * p<
0.05; ** p<
0.01; *** p< 0.001; **** p< 0.0001; ns, not significant [0050] FIGS. 17A-17D show Schild analysis of inhibitor peptides. FIG. 17A
shows a graph depicting the % Emax response as a function of increasing concentrations of IL-23 in the presence of Peptide 993 in concentrations of 0 nM (closed circles), 0.3 nM
(closed squares), 1 nM (triangles), 3 nM (inverted triangles), 10 nM (diamonds), 30 nM (open circles), or 100 nM
(open squares). Properties of the curves are listed below the graph. FIG. 17B
depicts results from the same set of experiments, and shows a graph displaying Log(dose ratio') as a function of Peptide 993 concentration (M) on a logarithmic scale. Properties of the resulting linear function are displayed below the graph. FIG. 17C shows a graph depicting the %
Emax response as a function of increasing concentrations of IL-23 in the presence of the peptide of SEQ ID NO:
1169 in concentrations of 0 nM (closed circles), 0.3 nM (closed squares), 1 nM
(triangles), 3 nM
(inverted triangles), 10 nM (diamonds), 30 nM (open circles), or 100 nM (open squares).
Properties of the curves are listed below the graph. FIG. 17D shows a graph depicting the %
Emax response as a function of increasing concentrations of IL-23 in the presence of the peptide of SEQ ID NO: 1211 in concentrations of 0 nM (closed circles), 0.3 nM (closed squares), 1 nM
(triangles), 3 nM (inverted triangles), 10 nM (diamonds), 30 nM (open circles), or 100 nM (open squares). Properties of the curves are listed below the graph.
[0051] FIGS. 18A-18B show pharmacokinetic data for the IL-23R peptide inhibitor Peptide 1185. FIG. 18A shows the concentration of Peptide 1185 in serum and in samples taken from small intestine and the colon. Fig 18B shows the amount of Peptide 1185 detected in urine and feces 24 hours after oral administration (% dose).

[0052] FIGS. 19A and 19B show pharmacokinetic data for the IL-23R peptide inhibitor Peptide 980. FIG. 19A shows the concentration of Peptide 980 in serum and in samples taken from small intestine and the colon. Fig 19B shows the amount of Peptide 980 detected in urine and feces 24 hours after oral administration (% dose).
DETAILED DESCRIPTION OF THE INVENTION
[0053] Unless otherwise defined herein, scientific and technical terms used in this application shall have the meanings that are commonly understood by those of ordinary skill in the art.
Generally, nomenclature used in connection with, and techniques of, chemistry, molecular biology, cell and cancer biology, immunology, microbiology, pharmacology, and protein and nucleic acid chemistry, described herein, are those well-known and commonly used in the art.
[0054] As used herein, the following terms have the meanings ascribed to them unless specified otherwise.
[0055] Throughout this specification, the word "comprise" or variations such as "comprises"
or "comprising" will be understood to imply the inclusion of a stated integer (or components) or group of integers (or components), but not the exclusion of any other integer (or components) or group of integers (or components).
[0056] The singular forms "a," "an," and "the" include the plurals unless the context clearly dictates otherwise.
[0057] The term "including" is used to mean "including but not limited to."
"Including" and "including but not limited to" are used interchangeably.
[0058] The terms "patient," "subject," and "individual" may be used interchangeably and refer to either a human or a non-human animal. These terms include mammals such as humans, primates, livestock animals (e.g., bovines, porcines), companion animals (e.g., canines, felines) and rodents (e.g., mice and rats).
[0059] The term "peptide," as used herein, refers broadly to a sequence of two or more amino acids joined together by peptide bonds. It should be understood that this term does not connote a specific length of a polymer of amino acids, nor is it intended to imply or distinguish whether the polypeptide is produced using recombinant techniques, chemical or enzymatic synthesis, or is naturally occurring.
[0060] The recitations "sequence identity", "percent identity", "percent homology", or, for example, comprising a "sequence 50% identical to," as used herein, refer to the extent that sequences are identical on a nucleotide-by-nucleotide basis or an amino acid-by-amino acid basis over a window of comparison. Thus, a "percentage of sequence identity" may be calculated by comparing two optimally aligned sequences over the window of comparison, determining the number of positions at which the identical nucleic acid base (e.g., A, T, C, G, I) or the identical amino acid residue (e.g., Ala, Pro, Ser, Thr, Gly, Val, Leu, Ile, Phe, Tyr, Trp, Lys, Arg, His, Asp, Glu, Asn, Gln, Cys and Met) occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison (i.e., the window size), and multiplying the result by 100 to yield the percentage of sequence identity.
[0061] Calculations of sequence similarity or sequence identity between sequences (the terms are used interchangeably herein) can be performed as follows. To determine the percent identity of two amino acid sequences, or of two nucleic acid sequences, the sequences can be aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes). In certain embodiments, the length of a reference sequence aligned for comparison purposes is at least 30%, preferably at least 40%, more preferably at least 50%, 60%, and even more preferably at least 70%, 80%, 90%, 100% of the length of the reference sequence. The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position.
[0062] The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.

[0063] The comparison of sequences and determination of percent identity between two sequences can be accomplished using a mathematical algorithm. In some embodiments, the percent identity between two amino acid sequences is determined using the Needleman and Wunsch, (1970, J. Mol. Biol. 48: 444-453) algorithm which has been incorporated into the GAP
program in the GCG software package, using either a Blossum 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6. In yet another preferred embodiment, the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package, using an NVVSgapdna.CMP
matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6. Another exemplary set of parameters includes a Blossum 62 scoring matrix with a gap penalty of 12, a gap extend penalty of 4, and a frameshift gap penalty of 5. The percent identity between two amino acid or nucleotide sequences can also be determined using the algorithm of E. Meyers and W. Miller (1989, Cabios, 4: 11-17) which has been incorporated into the ALIGN
program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4.
[0064] The peptide sequences described herein can be used as a "query sequence" to perform a search against public databases to, for example, identify other family members or related sequences. Such searches can be performed using the NBLAST and )(BLAST
programs (version 2.0) of Altschul, et al., (1990, J. Mol. Biol, 215: 403-10). BLAST nucleotide searches can be performed with the NBLAST program, score = 100, wordlength = 12 to obtain nucleotide sequences homologous to nucleic acid molecules of the invention. BLAST protein searches can be performed with the )(BLAST program, score = 50, wordlength = 3 to obtain amino acid sequences homologous to protein molecules of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al. (Nucleic Acids Res. 25:3389-3402, 1997). When utilizing BLAST and Gapped BLAST
programs, the default parameters of the respective programs (e.g., )(BLAST and NBLAST) can be used.
[0065] The term "conservative substitution" as used herein denotes that one or more amino acids are replaced by another, biologically similar residue. Examples include substitution of amino acid residues with similar characteristics, e.g., small amino acids, acidic amino acids, polar amino acids, basic amino acids, hydrophobic amino acids and aromatic amino acids. See, for example, the table below. In some embodiments of the invention, one or more Met residues are substituted with norleucine (Nle) which is a bioisostere for Met, but which, as opposed to Met, is not readily oxidized. Another example of a conservative substitution with a residue normally not found in endogenous, mammalian peptides and proteins is the conservative substitution of Arg or Lys with, for example, ornithine, canavanine, aminoethylcysteine or another basic amino acid.
In some embodiments, one or more cysteines of a peptide analogue of the invention may be substituted with another residue, such as a serine. For further information concerning phenotypically silent substitutions in peptides and proteins, see, for example, Bowie et.al.
Science 247, 1306-1310, 1990. In the scheme below, conservative substitutions of amino acids are grouped by physicochemical properties. I: neutral, hydrophilic, II: acids and amides, III:
basic, IV: hydrophobic, V: aromatic, bulky amino acids.
I II III IV V
AN H M F
S DR L
TEK I
P Q V
[0066] In the scheme below, conservative substitutions of amino acids are grouped by physicochemical properties. VI: neutral or hydrophobic, VII: acidic, VIII:
basic, IX: polar, X:
aromatic.
VI VII VIII IX X
A E H M F
L D R S Y
T W
V

[0067] The term "amino acid" or "any amino acid" as used here refers to any and all amino acids, including naturally occurring amino acids (e.g., a-amino acids), unnatural amino acids, modified amino acids, and non-natural amino acids. It includes both D- and L-amino acids.
Natural amino acids include those found in nature, such as, e.g., the 23 amino acids that combine into peptide chains to form the building-blocks of a vast array of proteins.
These are primarily L
stereoisomers, although a few D-amino acids occur in bacterial envelopes and some antibiotics.
The 20 "standard," natural amino acids are listed in the above tables. The "non-standard,"
natural amino acids are pyrrolysine (found in methanogenic organisms and other eukaryotes), selenocysteine (present in many noneukaryotes as well as most eukaryotes), and N-formylmethionine (encoded by the start codon AUG in bacteria, mitochondria and chloroplasts).
"Unnatural" or "non-natural" amino acids are non-proteinogenic amino acids (i.e., those not naturally encoded or found in the genetic code) that either occur naturally or are chemically synthesized. Over 140 unnatural amino acids are known and thousands of more combinations are possible. Examples of "unnatural" amino acids include f3-amino acids (f33 and f32), homo-amino acids, proline and pyruvic acid derivatives, 3-substituted alanine derivatives, glycine derivatives, ring-substituted phenylalanine and tyrosine derivatives, linear core amino acids, diamino acids, D-amino acids, alpha-methyl amino acids and N-methyl amino acids. Unnatural or non-natural amino acids also include modified amino acids. "Modified" amino acids include amino acids (e.g., natural amino acids) that have been chemically modified to include a group, groups, or chemical moiety not naturally present on the amino acid. According to certain embodiments, a peptide inhibitor comprises an intramolecular bond between two amino acid residues present in the peptide inhibitor. It is understood that the amino acid residues that form the bond will be altered somewhat when bonded to each other as compared to when not bonded to each other.
Reference to a particular amino acid is meant to encompass that amino acid in both its unbonded and bonded state. For example, the amino acid residue homoSerine (hSer) or homoSerine(C1) in its unbonded form may take the form of 2-aminobutyric acid (Abu) when participating in an intramolecular bond according to the present invention. The present invention inclues both peptide inhibitors containing cross-links between X4 and X9, as well as the peptide inhibitors that do not contain cross-links between X4 and X9, e.g., before cross-link formation. As such, the names hSer and Abu are intended to indicate the same amino acids and are used interchangeably.

[0068] For the most part, the names of naturally occurring and non-naturally occurring aminoacyl residues used herein follow the naming conventions suggested by the IUPAC
Commission on the Nomenclature of Organic Chemistry and the IUPAC-IUB
Commission on Biochemical Nomenclature as set out in "Nomenclature of a-Amino Acids (Recommendations, 1974)" Biochemistry, 14(2), (1975). To the extent that the names and abbreviations of amino acids and aminoacyl residues employed in this specification and appended claims differ from those suggestions, they will be made clear to the reader. Some abbreviations useful in describing the invention are defined below in the following Table 1A.
[0069] Table 1A. Abbreviations of Non-Natural Amino Acids and Chemical Moieties (for amino acid derivatives, all L unless stated) Abbreviation Definition Ac- Acetyl Hy Hydrogen (Free N-terminal) Dap L-Diaminopropionic acid Dab L-Diaminobutyric acid Orn L-Ornathine Pen L-Penicillamine Sarc Sarcosine Cit L-Citrulline Cav L-Cavanine Phe-(4-Guanidino) 4-Guanidine-L-Phenylalanine N-MeArg N-Methyl-L-Arginine N-MeTrp N-Methyl-L-Tryptophan N-MeGln N-Methyl-L-Glutamine N-MeAla N-Methyl-L-Alanine N-MeLys N-Methyl-Lysine N-MeAsn N-Methyl-L-Asparagine 6-ChloroTrp 6-Chloro-L-Tryptophan 5-HydroxyTrp 5-Hydroxy-L-Tryptophan 1,2,3,4-tetrahydro-norharman L-1,2,3,4-tetrahydro-norharman 2-Na!
L-2-Napthylalanine (also referred to as 2-Nap) 1-Na!
L-1-Napthylalanine (also referred to as 1-Nap) Phe(4-0Me) 4-Methoxy-L-phenylalanine Abu 2-Aminobutyric acid B ip L-4,4' -B ipheny la lan in e f3Ala beta-Alanine PhTyr beta homo-L-Tyrosine PhTrp beta homo-L-Trptophan f3hAla beta homo-L-Alanine phLeu, beta homo-L-Leucine PhVal beta homo-L-Valine Aib 2-aminoisobutyric acid Azt L-azetidine-2-carboxylic acid (3S)-1,2,3,4-Tetrahydroisoquinoline-7-hydroxy-3-carboxylic Tic Acid Phe(4-0Me) 4-methoxy-L-phenylalanine N-Me-Lys N-Methyl-L-Lysine N-Me-Lys(Ac) N-E-Acetyl-D-lysine CONH2 Carboxamide COOH Acid 3-Pal L-3-Pyridylalanine Phe(4-F) 4-Fluoro-L-Phenylalanine DMT 2,6-DimethylTyrosine Phe(4-0Me) 4-Methoxyphenylalanine hLeu L-homoLeucine hArg L-homoArginine a-MeLys alpha-methyl-L-Lysine a-MeOrn alpha-methyl-L-Ornathine a-MeLeu alpha-methyl-L-Leucine a-MeTrp alpha-methyl-L-Tryptophan a-MePhe alpha-methyl-L-Phenylalanine a-MeTyr alpha-methyl-L-Tyrosine a¨DiethylGly a-DiethylGlycine Lys(Ac) N-c-acetyl-L-Lysine DTT Dithiothreotol Nle L-Norleucine fihTrp L-0-homoTrypophan f3hPhe L-P-homophenylalanine f3hPro L-P-homoproline Phe(4-CF3) 4-Trifluoromethyl-L-Phenylalanine P-Glu L-P-Glutamic acid f3hG1u L-0-homog1utamic acid 2-2-Indane 2-Aminoindane-2-carboxylic acid 1-1-Indane 1-Aminoindane-1-carboxylic acid hCha L-homocyclohexylalanine Cyclobutyl L-cyclobutylalanine f3hPhe L-P-homo-phenylalanine Gla Gama-Carboxy-L-Glutamic acid Cpa Cyclopentyl-L-alanine Cha Cyclohexyl-L-alanine Octgly L-Octylglycine t-butyl-Ala 3-(tert-buty1)-L-Ala-OH
t-butyl-Gly tert-butyl-glycine AEP 3-(2-aminoethoxy)propanoic acid AEA (2-aminoethoxy)acetic acid Phe(4-Phenoxy)] 4-Phenoxy-L-phenylalanine Phe(4-0Bz1) O-Benzyl-L-tyrosine Phe(4-CONH2) 4-Carbamoyl-L-phenylalanine Phe(4-CO2H) 4-Carboxy-L-phenylalanine Phe(3,4-C12) 3,4 dichloro-L-phenylalanine Tyr(3-t-Bu) 3-t-butyl-L-tyrosine Phe(t-Bu) t-butyl-L-phenylalanine Phe[4-(2-aminoethoxy)]
co2H

4-(2-aminoethoxy)-L-phenylalanine Phe(4-CN) 4-cyano-L-phenylalanine Phe(4-Br) 4-bromo-L-phenylalanine Phe(4-NH2) 4-amino-L-phenylalanine Phe(4-Me) 4-methyl-L-phenylalanine 4-Pyridylalanine 4-L-Pyridylalanine H
N
4-amino-4-carboxy-piperidine X
H2N co2H
4-amino-4-carboxy-piperidine hPhe(3,4-dimethoxy) 3,4-dimethoxy-L-homophenylalanine Phe(2,4-Me2) 2,4-dimethyl-L-phenylalanine Phe(3,5-F2) 3,5-difluoro-L-phenylalanine Phe(penta-F) pentafluoro-L-phenylalanine 2,5,7-tert butyl Trp 2,5,7-Tris-tert-butyl-L-tryptophan Tic NH
L-1,2,3,4,-tetrahydro-isoquinoline-3-carboxylic acid Phe(4-0Ally1) 0-Allyl-L-Tyrosine Phe(4-N3) 4-azidophenylalanine Achc q H2N co2H
1-aminocyclohexanecarboxylic acid Acvc R
H2N co2H
1-aminocyclopentanecarboxylic acid Acbc H2N co2H
1-aminocyclobutanecarboxylic acid Acpc H2N co2H

1-aminocyclopropylcarboxylic acid 4-amino-4-carboxy-tetrahydropyran (also referred as THP) H2N co2H
4-amino-4-carboxy-tetrahydropyran [0070] Throughout the present specification, unless naturally occurring amino acids are referred to by their full name (e.g. alanine, arginine, etc.), they are designated by their conventional three-letter or single-letter abbreviations (e.g. Ala or A for alanine, Arg or R for arginine, etc.).
Unless otherwise indicated, three-letter and single-letter abbreviations of amino acids refer to the L-isomeric form of the amino acid in question. The term "L-amino acid," as used herein, refers to the "L" isomeric form of a peptide, and conversely the term "D-amino acid"
refers to the "D"
isomeric form of a peptide (e.g., Dasp, (D)Asp or D-Asp; Dphe, (D)Phe or D-Phe). Amino acid residues in the D isomeric form can be substituted for any L-amino acid residue, as long as the desired function is retained by the peptide. D-amino acids may be indicated as customary in lower case when referred to using single-letter abbreviations.
[0071] In the case of less common or non-naturally occurring amino acids, unless they are referred to by their full name (e.g. sarcosine, ornithine, etc.), frequently employed three- or four-character codes are employed for residues thereof, including, Sar or Sarc (sarcosine, i.e. N-methylglycine), Aib (a-aminoisobutyric acid), Dab (2,4-diaminobutanoic acid), Dapa (2,3-diaminopropanoic acid), y-Glu (y-glutamic acid), Gaba (y-aminobutanoic acid), 3-Pro (pyrrolidine-3-carboxylic acid), and 8Ado (8-amino-3,6-dioxaoctanoic acid), Abu (2-amino butyric acid), f3hPro (f3-homoproline), PhPhe (P-homophenylalanine) and Bip (3,r3 diphenylalanine), and Ida (Iminodiacetic acid).
[0072] As is clear to the skilled artisan, the peptide sequences disclosed herein are shown proceeding from left to right, with the left end of the sequence being the N-terminus of the peptide and the right end of the sequence being the C-terminus of the peptide.
Among sequences disclosed herein are sequences incorporating a "Hy-" moiety at the amino terminus (N-terminus) of the sequence, and either an "-OH" moiety or an "-NH2" moiety at the carboxy terminus (C-terminus) of the sequence. In such cases, and unless otherwise indicated, a "Hy-" moiety at the N-terminus of the sequence in question indicates a hydrogen atom, corresponding to the presence of a free primary or secondary amino group at the N-terminus, while an "-OH"
or an "¨NH2"
moiety at the C-terminus of the sequence indicates a hydroxy group or an amino group, corresponding to the presence of an amido (CONH2) group at the C-terminus, respectively. In each sequence of the invention, a C-terminal "¨OH" moiety may be substituted for a C-terminal "¨NH2" moiety, and vice-versa.
[0073] The term "DRP," as used herein, refers to disulfide rich peptides.
[0074] The term "dimer," as used herein, refers broadly to a peptide comprising two or more monomer subunits. Certain dimers comprise two DRPs. Dimers of the present invention include homodimers and heterodimers. A monomer subunit of a dimer may be linked at its C- or N-terminus, or it may be linked via internal amino acid residues. Each monomer subunit of a dimer may be linked through the same site, or each may be linked through a different site (e.g., C-terminus, N-terminus, or internal site).
[0075] The term "NH2," as used herein, can refer to a free amino group present at the amino terminus of a polypeptide. The term "OH," as used herein, can refer to a free carboxy group present at the carboxy terminus of a peptide. Further, the term "Ac," as used herein, refers to Acetyl protection through acylation of the C- or N-terminus of a polypeptide.
In certain peptides shown herein, the NH2 locates at the C-terminus of the peptide indicates an amino group.
[0076] The term "carboxy," as used herein, refers to ¨CO2H.
[0077] The term "isostere replacement," as used herein, refers to any amino acid or other analog moiety having chemical and/or structural properties similar to a specified amino acid.
[0078] The term "cyclized," as used herein, refers to a reaction in which one part of a polypeptide molecule becomes linked to another part of the polypeptide molecule to form a closed ring, such as by forming a disulfide bridge or other similar bond.

[0079] The term "subunit," as used herein, refers to one of a pair of polypeptide monomers that are joined to form a dimer peptide composition.
[0080] The term "linker moiety," as used herein, refers broadly to a chemical structure that is capable of linking or joining together two peptide monomer subunits to form a dimer.
[0081] The term "pharmaceutically acceptable salt," as used herein, represents salts or zwitterionic forms of the peptides or compounds of the present invention which are water or oil-soluble or dispersible, which are suitable for treatment of diseases without undue toxicity, irritation, and allergic response; which are commensurate with a reasonable benefit/risk ratio, and which are effective for their intended use. The salts can be prepared during the final isolation and purification of the compounds or separately by reacting an amino group with a suitable acid.
Representative acid addition salts include acetate, adipate, alginate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsulfonate, digluconate, glycerophosphate, hemisulfate, heptanoate, hexanoate, formate, fumarate, hydrochloride, hydrobromide, hydroiodide, 2 -hydroxyethansulfonate (isethionate), lactate, maleate, mesitylenesulfonate, methanesulfonate, naphthylenesulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, pamoate, pectinate, persulfate, 3 -phenylproprionate, picrate, pivalate, propionate, succinate, tartrate, trichloroacetate, trifluoroacetate, phosphate, glutamate, bicarbonate, para-toluenesulfonate, and undecanoate. Also, amino groups in the compounds of the present invention can be quaternized with methyl, ethyl, propyl, and butyl chlorides, bromides, and iodides; dimethyl, diethyl, dibutyl, and diamyl sulfates; decyl, lauryl, myristyl, and steryl chlorides, bromides, and iodides; and benzyl and phenethyl bromides. Examples of acids which can be employed to form therapeutically acceptable addition salts include inorganic acids such as hydrochloric, hydrobromic, sulfuric, and phosphoric, and organic acids such as oxalic, maleic, succinic, and citric. A pharmaceutically acceptable salt may suitably be a salt chosen, e.g., among acid addition salts and basic salts. Examples of acid addition salts include chloride salts, citrate salts and acetate salts. Examples of basic salts include salts where the cation is selected among alkali metal cations, such as sodium or potassium ions, alkaline earth metal cations, such as calcium or magnesium ions, as well as substituted ammonium ions, such as ions of the type N(R1)(R2)(R3)(R4)+, where R1, R2, R3 and R4 independently will typically designate hydrogen, optionally substituted C1-6-alkyl or optionally substituted C2-6-alkenyl.

Examples of relevant C1-6-alkyl groups include methyl, ethyl, 1-propyl and 2-propyl groups.
Examples of C2-6-alkenyl groups of possible relevance include ethenyl, 1-propenyl and 2-propenyl. Other examples of pharmaceutically acceptable salts are described in "Remington's Pharmaceutical Sciences", 17th edition, Alfonso R. Gennaro (Ed.), Mark Publishing Company, Easton, PA, USA, 1985 (and more recent editions thereof), in the "Encyclopaedia of Pharmaceutical Technology", 3rd edition, James Swarbrick (Ed.), Informa Healthcare USA
(Inc.), NY, USA, 2007, and in J. Pharm. Sci. 66: 2 (1977). Also, for a review on suitable salts, see Handbook of Pharmaceutical Salts: Properties, Selection, and Use by Stahl and Wermuth (Wiley-VCH, 2002). Other suitable base salts are formed from bases which form non-toxic salts.
Representative examples include the aluminum, arginine, benzathine, calcium, choline, diethylamine, diolamine, glycine, lysine, magnesium, meglumine, olamine, potassium, sodium, tromethamine, and zinc salts. Hemisalts of acids and bases may also be formed, e.g., hemisulphate and hemicalcium salts.
[0082] The term "N(alpha)Methylation", as used herein, describes the methylation of the alpha amine of an amino acid, also generally termed as an N-methylation.
[0083] The term "sym methylation" or "Arg-Me-sym", as used herein, describes the symmetrical methylation of the two nitrogens of the guanidine group of arginine. Further, the term "asym methylation" or "Arg-Me-asym" describes the methylation of a single nitrogen of the guanidine group of arginine.
[0084] The term "acylating organic compounds", as used herein refers to various compounds with carboxylic acid functionality that are used to acylate the N-terminus of an amino acid or a monomer or dimer, e.g., a monomer subunit prior to forming a C-terminal dimer.
Non-limiting examples of acylating organic compounds include cyclopropylacetic acid, 4-Fluorobenzoic acid, 4-fluorophenylacetic acid, 3-Phenylpropionic acid, Succinic acid, Glutaric acid, Cyclopentane carboxylic acid, 3,3,3-trifluoropropeonic acid, 3-Fluoromethylbutyric acid, Tetrahedro-2H-Pyran-4-carboxylic acid.
[0085] The term "alkyl" includes a straight chain or branched, noncyclic or cyclic, saturated aliphatic hydrocarbon containing from 1 to 24 carbon atoms. Representative saturated straight chain alkyls include, but are not limited to, methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, and the like, while saturated branched alkyls include, without limitation, isopropyl, sec-butyl, isobutyl, tert-butyl, isopentyl, and the like. Representative saturated cyclic alkyls include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like, while unsaturated cyclic alkyls include, without limitation, cyclopentenyl, cyclohexenyl, and the like.
[0086] The term "mammal" refers to any mammalian species such as a human, mouse, rat, dog, cat, hamster, guinea pig, rabbit, livestock, and the like.
[0087] As used herein, a "therapeutically effective amount" of the peptide inhibitor of the invention is meant to describe a sufficient amount of the peptide inhibitor to treat an IL-23/IL-23R-related disease, including but not limited to any of the diseases and disorders described herein (for example, to reduce inflammation associated with IBD). In particular embodiments, the therapeutically effective amount will achieve a desired benefit/risk ratio applicable to any medical treatment.
[0088] An "analog" of an amino acid, e.g., a "Phe analog" or a "Tyr analog"
means an analog of the referenced amino acid. A variety of amino acid analogs are known and available in the art, including Phe and Tyr analogs. In certain embodiments, an amino acid analog, e.g., a Phe analog or a Tyr analog comprises one, two, three, four or five substitutions as compared to Phe or Tyr, respectively. In certain embodiments, the substitutions are present in the side chains of the amino acids. In certain embodiments, a Phe analog has the structure Phe(R2), wherein R2 is a Hy, OH, CH3, CO2H, CONH2, CONH2OCH2CH2NH2, t-Bu, OCH2CH2NH2, phenoxy, OCH3, 0Allyl, Br, Cl, F, NH2, N3, or guanadino. In certain embodiments, R2 is CONH2OCH2CH2NH2, OCH3, CONH2, OCH3 or CO2H. Examples of Phe analogs include, but are not limited to: hPhe, Phe(4-0Me), a-Me-Phe, hPhe(3,4-dimethoxy), Phe(4-CONH2), Phe(4-phenoxy), Phe(4-guanadino), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-0Bz1), Phe(4-NH2), BhPhe(4-F), Phe(4-F), Phe(3,5 DiF), Phe(CH2CO2H), Phe(penta-F), Phe(3,4-C12), Phe (3,4-F2), Phe(4-CF3), RR-diPheAla, Phe(4-N3), Phe[4-(2-aminoethoxy)], 4-Phenylbenzylalanine, Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(4-CF3), Phe(2,3-C12), and Phe(2,3-F2). Examples of Tyr analogs include, but are not limited to: hTyr, N-Me-Tyr, Tyr(3-tBu), Tyr(4-N3) and f3hTyr.

Peptide Inhibitors of IL-23R
[0089] Genome-wide association studies (GWAS) have demonstrated significant association of the IL-23 receptor (IL-23R) gene with inflammatory bowel disease (IBD), suggesting that perturbation of IL-23 signaling could be relevant to the pathogenesis of the disease. The present invention provides compositions and methods to modulate the IL-23 pathway through selective antagonism of IL-23R by oral treatment with peptides that are stable and restricted to the gastrointestinal (GI) tissue. Novel inhibitory peptides that are uniquely resistant to oxidative/reductive conditions and proteolytic degradation in a variety of assays that mimic the various compartments of the GI environment were identified. Functionally, these peptides potently neutralize IL-23-mediated signaling in a transformed human cell line and in human primary cells. The binding of IL-23R is selective, since the peptides do not block the interaction between IL-6 to IL-6R or antagonize the IL-12 signaling pathway. Furthermore, these orally delivered peptides are efficacious in attenuating colitis in a 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced acute rat model of IBD, as shown by a significant reduction in the ratio of colon weight to length, colon macroscopic score, neutrophil infiltration, and histopathology comparable to that of the control anti-IL-23p19 mAb.
[0090] The present invention relates generally to peptides that have IL-23R
antagonist activity, including both peptide monomers and peptide dimers. In certain embodiments, this invention demonstrates a new paradigm for treatment of IBD and other diseases and disorders by oral delivery of antagonists of IL-23. IBD represents a local inflammation of the intestinal tissue;
therefore, advantageous therapeutic agents would act from the luminal side of the intestine, yielding high drug concentrations in diseased tissue, minimizing systemic availability and resulting in improved efficacy and safety when compared to systemic approaches. Oral administration of the compounds of the present invention is expected to maximize drug levels in diseased intestinal tissues while limiting drug concentrations in circulation, thereby providing efficacious, safe, and durable delivery for life-long treatment of IBD and other diseases and disorders.
[0091] In certain embodiments, the present invention relates to various peptides, or peptide dimers comprising hetero- or homo-monomer subunits, that form cyclized structures through disulfide or other bonds. In certain embodiments, the disulfide or other bonds are intramolecular bonds. The cyclized structure of the peptide monomer inhibitors and the monomer subunits of the peptide dimer inhibitors has been shown to increase potency and selectivity of the peptide inhibitors. In certain embodiments, a peptide dimer inhibitor may include one or more intermolecular bonds linking the two monomer peptide subunits within the peptide dimer inhibitor, e.g., an intermolecular bridge between two cysteine residues, one in each peptide monomer subunit.
[0092] The present invention provides peptide inhibitors that bind to IL-23R, which may be monomers or dimers. In particular embodiments, the peptide inhibitors inhibit the binding of IL-23 to IL-23R. In certain embodiments, the IL-23R is human IL-23R, and the IL-23 is human IL-23. In certain embodiments, a peptide inhibitor of the present invention reduces IL-23 binding to IL-23R by at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, or at least 90% as compared to a negative control peptide. Methods of determining binding are known in the art and include ELISA assays, as described in the accompanying Examples.
[0093] In certain embodiments, a peptide inhibitor of the present invention has an IC50 of > 1 mM, < 1 mM, 500 nM to 1000 nM, < 500 nIVI, <250 nIVI, < 100 nIVI, < 50 nM, <25 nIVI, < 10 <5 nM, <2 nM, < 1 nM, or < 5 mM, e.g., for inhibiting binding of IL-23 to IL-23R (e.g., human IL-23 and human IL-23R). Methods of determining activity are known in the art and include any of those described in the accompanying Examples.
[0094] In certain embodiments, a peptide inhibitor of the present invention has increased stability, increased gastrointestinal stability, or increased stability in stimulated intestinal fluid (SIF) or simulated gastric fluid (SGF), and/or under redox conditions (e.g., DTT) as compared to a control peptide. In certain embodiments, a control peptide is an unrelated peptide of the same or similar length. In particular embodiments, a control peptide is a peptide having the identical or a highly related amino acid sequence (e.g., > 90% sequence identity) as the peptide inhibitor.
In particular embodiments, a control peptide is a peptide having the identical or a highly related amino acid sequence (e.g., > 90% sequence identity) as the peptide inhibitor, but which does not have a cyclized structure, e.g., through an intramolecular bond between two amino acid residues within the control peptide, or which is not dimerized, or which does not comprise a conjugate for stabilization. In particular embodiments, the only difference between the peptide inhibitor and the control peptide is that the peptide inhibitor comprises one or more amino acid substitutions that introduce one or more amino acid residues into the peptide inhibitor, wherein the introduced amino residue(s) forms an intrasulfide disulfide or thioether bond with another amino acid residue in the peptide inhibitor. One example of a control for a peptide dimer inhibitor is a monomer having the same sequence as one of the monomer subunits present in the peptide dimer inhibitor. One example of a control for a peptide inhibitor comprising a conjugate is a peptide having the same sequence but not including the conjugated moiety. In certain embodiments, a control peptide is a peptide (e.g., a naturally-occurring peptide) corresponding to a region of IL-23 that binds to IL-23R.
[0095] Methods of determining the stablity of a peptide are known in the art.
In certain embodiments, the stability of a peptide inhibitor is determined using an SIF
assay, e.g., as described in Example 3. In certain embodiments, the stability of a peptide inhibitor is determined using an SGF assay, e.g., as described in Example 3. In particular embodiments, a peptide inhibitor has a half-life (e.g., in SIF or SGF or DTT) under a given set of conditions (e.g., temperature) of greater than 1 minute, greater than 10 minutes, greater than 20 minutes, greater than 30 minutes, greater than 60 minutes, greater than 90 minutes, greater than 120 minutes, greater than 3 hours, or greater than four hours when exposed to SIF or SGF or DTT. In certain embodiments, the temperature is about 25 C, about 4 C, or about 37 C, and the pH is a physiological pH, or a pH about 7.4.
[0096] In some embodiments, the half-life is measured in vitro using any suitable method known in the art, e.g., in some embodiments, the stability of a peptide of the present invention is determined by incubating the peptide with pre-warmed human serum (Sigma) at 37 C. Samples are taken at various time points, typically up to 24 hours, and the stability of the sample is analyzed by separating the peptide or peptide dimer from the serum proteins and then analyzing for the presence of the peptide or peptide dimer of interest using LC-MS.
[0097] In some embodiments, a peptide inhibitor of the present invention exhibits improved solubility or improved aggregation characteristics as compared to a control peptide. Solubility may be determined via any suitable method known in the art. In some embodiments, suitable methods known in the art for determining solubility include incubating peptides in various buffers (Acetate pH4.0, Acetate pH5.0, Phos/Citrate pH5.0, Phos Citrate pH6.0, Phos pH 6.0, Phos pH 7.0, Phos pH7.5, Strong PBS pH 7.5, Tris pH7.5, Tris pH 8.0, Glycine pH 9.0, Water, Acetic acid (pH 5.0 and other known in the art) and testing for aggregation or solubility using standard techniques. These include, but are not limited to, visual precipitation, dynamic light scattering, Circular Dichroism and fluorescent dyes to measure surface hydrophobicity, and detect aggregation or fibrillation, for example. In some embodiments, improved solubility means the peptide is more soluble in a given liquid than is a control peptide.
In some embodiments, improved aggregation means the peptide has less aggregation in a given liquid under a given set of conditions than a control peptide.
[0098] In certain embodiments advantageous for achieving high compound concentrations in intestinal tissues when delivered orally, peptide inhibitors of the present invention are stable in the gastrointestinal (GI) environment. Proteolytic metabolism in the GI tract is driven by enzymes (including pepsins, trypsin, chymotrypsin, elastase, aminopeptidases, and carboxypeptidase A/B) that are secreted from the pancreas into the lumen or are produced as brush border enzymes. Proteases typically cleave peptides and proteins that are in an extended conformation. In the reducing environment of intestinal fluids, disulfide bonds may be broken, resulting in a linear peptide and rapid proteolysis. This luminal redox environment is largely determined by the Cys/CySS redox cycle. In enterocytes, relevant activities include numerous digestive enzymes such as CYP450 and UDP-glucuronsyl-transferase. Finally, bacteria, present in the large intestine at concentration ranging from 1010 to 1012 CFU/ml, constitute another metabolic barrier. In certain embodiments, the peptide inhibitors are stable to various pHs that range from strongly acidic in the stomach (pH 1.5-1.9), trending towards basic in the small intestine (pH 6-7.5), and then weakly acidic in the colon (pH 5-7). Such peptide inhibitors are stable during their transit through the various GI compartments, a process that has been estimated to take 3-4 h in the intestine and 6-48 h in the colon.
[0099] In some embodiments, the peptide inhibitors of the present invention have less degradation, e.g., over a period of time (i.e., more degradation stability), e.g., greater than or about 10% less, greater than or about 20% less, greater than or about 30%
less, greater than or about 40 less, or greater than or about 50% less degradation than a control peptide. In some embodiments, degradation stability is determined via any suitable method known in the art. In some embodiments, the degradation is enzymatic degradation. For example, in certain embodiments, the peptide inhibitors have reduced susceptibility to degradation by trypsin, chhrmotrypsin or elastase. In some embodiments, suitable methods known in the art for determining degradation stability include the method described in Hawe et al., J Pharm Sci, VOL. 101, No. 3, 2012, p 895-913, incorporated herein in its entirety. Such methods are in some embodiments used to select potent peptide sequences with enhanced shelf lifes.
In particular embodiments, peptide stability is determined using a SIF assay or SGF assay as described herein.
1001001In certain embodiments, peptide inhibitors of the present invention inhibit or reduce IL-23-mediated inflammation. In related embodiments, peptide inhibibitors of the present invention inhibit or reduce IL-23-mediated secretion of one or more cytokines, e.g., by binding to IL-23R
on the cell surface, thus inhibiting IL-23 binding to the cell. In particular embodiments, peptide inhibitors of the present invention inhibit or reduce IL-23-mediated activation of Jak2, Tyk2, Statl, Stat3, Stat4, or Stat5. Methods of determining inhibition of cytokine secretion and inhibition of signaling molecules are known in the art. For example, inhibiton of IL-23/IL-23R
signaling may be determined by measuring inhibition of phospho-Stat3 levels in cell lysates, as decribed in the accompanying Examples, including Example 2.
1001011In certain embodiments, peptide inhibitors of the present invention inhibit or reduce IL-23-mediated inflammation. In related embodiments, peptide inhibibitors of the present invention inhibit or reduce IL-23-mediated secretion of one or more cytokines, e.g., by binding to IL-23R
on the cell surface, thus inhibiting IL-23 binding to the cell. In particular embodiments, peptide inhibitors of the present invention inhibit or reduce IL-23-mediated activation of Jak2, Tyk2, Statl, Stat3, Stat4, or Stat5. Methods of determining inhibition of cytokine secretion and inhibition of signaling molecules are known in the art. For example, inhibiton of IL-23/IL-23R
signaling may be determined by measuring inhibition of phospho-Stat3 levels in cell lysates, as decribed in the accompanying Examples, including Example 2.
1001021In certain embodiments, peptide inhibitors have increased redox stability as compared to a control peptide. A variety of assays that may be used to determine redox stability are known and available in the art. Any of these may be used to determine the redox stability of peptide inhibitors of the present invention.
1001031In certain embodiments, the present invention provides various peptide inhibitors that bind or associate with the IL-23R, in vitro or in vivo, to disrupt or block binding between IL-23 and IL-23R. In certain embodiments, the peptide inhibitors bind and/or inhibit human IL-23R.
In certain embodiments, the peptide inhibitors bind and/or inhibit both human and rodent IL-23R. In certain embodiments, the peptide inhibitors bind and/or inhibit both human and rat IL-23R. In particular embodiments, the peptide inhibitors inhibit rat IL-23R at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or at least 95% as well as they bind or inhibit human IL-23R, e.g., as determined by an assay described herein. In certain embodiments, the peptide inhibitors preferentially bind and/or inhibit human and/or rat IL-23R
as compared to mouse IL-23R. In particular embodiments, the peptide inhibitors preferentially bind to rat IL-23R as compared to mouse IL-23R. In particular embodiments, the peptide inhibitors preferentially bind to human IL-23R as compared to mouse IL-23R. In certain embodiments, binding of a peptide inhibitor to mouse IL-23R is less than 75%, less than 50%, less than 40%, less than 30%, less than 20%, or less than 10% of binding of the same peptide inhibitor to human IL-23R and/or rat IL-23R. In certain embodiments of peptide inhibitors that preferentially bind and/or inhibit human IL-23R and/or rat IL-23R as compared to mouse IL-23R, the peptide inhibitor binds to a region of IL-23R that is disrupted by the presence of additional amino acids present in mouse IL-23R but not human IL-23R or rat IL-23. In one embodiment, the additional amino acids present in the mouse IL-23R are in the region corresponding to about amino acid residue 315 to about amino acid residue 340 of the mouse IL23R protein, e.g., amino acid region NVVQPWSSPFVHQTSQETGKR (see, e.g., Figure 4). In particular embodiments, the peptide inhibitors bind to a region of human IL-23R from about amino acid 230 to about amino acid residue 370.
1001041In certain embodiments, peptide inhibitors show GI-restricted localization following oral administration. In particular embodiments, greater than 50%, greater than 60%, greater than 70%, greater than 80%, or greater than 90% of orally administered peptide inhibitor is localized to gastrointestinal organs and tissues. In particular embodiments, blood plasma levels of orally administered peptide inhibitor are less than 20%, less than 10%, less than 5%, less than 2%, less than 1% or less than 0.5% the levels of peptide inhibitor found in the small intestine mucosa, colon mucosa, or proximal colon.
1001051The various peptide inhibitors of the invention may be constructed solely of natural amino acids. Alternatively, the peptide inhibitors may include non-natural amino acids including, but not limited to, modified amino acids. In certain embodiments, modified amino acids include natural amino acids that have been chemically modified to include a group, groups, or chemical moiety not naturally present on the amino acid. The peptide inhibitors of the invention may additionally include one or more D-amino acids. Still further, the peptide inhibitors of the invention may include amino acid analogs.
1001061In certain embodiments, peptide inhibitors of the present invention include one or more modified or unnatural amino acids. For example, in certain embodiments, a peptide inhibitor includes one or more of Dab, Dap, Pen, Sarc, Cit, Cav, hLeu, 2-Nal, D-1-Nal, D-2-Nal, Phe(4-0Me), f3hTrp, a-MePhe, a-MeTyr, a-MeTrp, f3-HPhe, Phe(4-CF3), 2-2-Indane, 1-1-Indane, Cyclobutyl, f3-hPhe, Gla, Phe(4-NH2), hPhe, 1-Nal, Nle, homoamino acids, D-amino acids, 4,4'-Biphenylalanine (Bip), cyclobutyl-Ala, hCha, f3hPhe, f3G1u, Phe(4-Guanidino), Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)], Phe(4-CONH2), Phe(4-Me), Tyr(Bz1), or Tyr(Me), Phe(3,4-diF2), Phe(3,4-C12), Phe(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)], Phe(Br), Phe(4-CONH2), Phe(C1), Phe(4-CN), Phe(4-guadino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Tyr, Tyr(Bz1), or Tyr(Me), Phe(3,4-dimethoxy), 5-HydroxyTrP, Phe(3,4-C12), Tyr(3-tBu), and various N-methylated amino acids and alpha-methyl amino acids.
In some embodiments of the present invention, a peptide inhibitor includes one or more non-natural amino acids shown in Table 1A. One having skill in the art will appreciate that other modified or unnatural amino acids, and various other substitutions of natural amino acids with modified or unnatural amino acids, may be made to achieve similar desired results, and such substitutions are within the teaching and spirit of the present invention. In certain embodiments, peptide inhibitors of the present invention include any of those described herein, including but not limited to any of those comprising an amino acid sequence or peptide inhibitor structure shown in any one of the tables herein, the accompanying sequence listing or the accompanying figures, wherein one or more residues is substituted with a modified or unnatural amino acid.

1001071 The present invention also includes any of the peptide inhibitors described herein in either a free or a salt form. Thus, embodiments of any of the peptide inhibitors described herein (and related methods of use thereof) include a pharmaceutically acceptable salt of the peptide inhibitor.
1001081 The present invention also includes variants of any of the peptide inhibitors described herein, including but not limited to any of those comprising a sequence shown in any one of the tables herein, the accompanying sequence listing or the accompanying figures, wherein one or more L-amino acid residue is substituted with the D isomeric form of the amino acid residue, e.g., an L-Ala is substituted with a D-Ala.
1001091In particular embodiments of the peptide inhibitors described herein, they comprise one or more unnatural or non-natural amino acid residue.
1001101 The present invention also includes any of the peptide monomer inhibitors described herein linked to a linker moiety, including any of the specific linker moieties described herein. In particular embodiments, a linker is attached to an N-terminal or C-terminal amino acid, while in other embodiments, a linker is attached to an internal amino acid. In particular embodiments, a linker is attached to two internal amino acids, e.g., an internal amino acid in each of two monomer subunits that form a dimer. In some embodiments of the present invention, a peptide inhibitor is attached to one or more linker moieties shown.
1001111 The present invention also includes peptides and peptide dimers comprising a peptide having at least 90%, at least 95%, at least 98%, or at least 99% sequence identity to the peptide sequence of a peptide inhibitor described herein. In particular embodiments, peptide inhibitors of the present invention comprise a core peptide sequence and one or more N-terminal and/or C-terminal modification (e.g., Ac and NH2) and/or one or more conjugated linker moiety and/or half-life extension moiety. As used herein, the core peptide sequence is the amino acid sequence of the peptide absent such modifications and conjugates. For example, for the peptide inhibitor:
[Palm] - [isoGlu] - [PEG4] - [Pen] -NTWQ- [Pen] - [Phe [4- (2-aminoethoxy)] -[2-Nal] - [Aib] - [Ly s (Ac)] -NN-NH2, the core peptide sequence is: [Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN.

1001121In certain embodiments, a peptide inhibitor or a monomer subunit of a peptide inhibitor of the present invention comprises, consists essentially of, or consists of 7 to 35 amino acid residues, 8 to 35 amino acid residues, 9 to 35 amino acid residues, 10 to 35 amino acid residues, 7 to 25 amino acid residues, 8 to 25 amino acid residues, 9 to 25 amino acid residues, 10 to 25 amino acid residues, 7 to 20 amino acid residues, 8 to 20 amino acid residues, 9 to 20 amino acid residues, 10 to 20 amino acid residues, 7 to 18 amino acid residues, 8 to 18 amino acid residues, 9 to 18 amino acid residues, or 10 to 18 amino acid residues, and, optionally, one or more additional non-amino acid moieties, such as a conjugated chemical moiety, e.g., a PEG or linker moiety. In particular embodiments, a peptide inhibitor of the present invention (or a monomer subunit thereof), including but not limited to those of any embodiments of Formula X, Formula I, Formula II, Formula III, Formula IV, or Formula V is greater than 10, greater than 12, greater than 15, greater than 20, greater than 25, greater than 30 or greater than 35 amino acids, e.g., 35 to 50 amino acids. In certain embodiments, a peptide inhibitor (or a monomer subunit thereof) is less than 50, less than 35, less than 30, less than 25, less than 20, less than 15, less than 12, or less than 10 amino acids. In particular embodiments, a monomer subunit of a peptide inhibitor (or a peptide monomer inhibitor) comprises or consists of 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, or 35 amino acid residues. In particular embodiments, a monomer subunit of a peptide inhibitor of the present invention comprises or consists of 10 to 18 amino acid residues and, optionally, one or more additional non-amino acid moieties, such as a conjugated chemical moiety, e.g., a PEG or linker moiety. In various embodiments, the monomer subunit comprises or consists of 7 to 35 amino acid residues, 7 to 20 amino acid residues, 8 to 20 amino acid residues, 9 to 20 amino acid residues, 10 to 20 amino acid residues, 8 to 18 amino acid residues, 8 to 19 amino acid residues, 8 to 18 amino acid residues, 9 to 18 amino acid residues, or 10 to 18 amino acid residues. In particular embodiments of any of the various Formulas described herein, X comprises or consists of 7 to 35 amino acid residues, 8 to 35 amino acid residues, 9 to 35 amino acid residues,

10 to 35 amino acid residues, 7 to 25 amino acid residues, 8 to 25 amino acid residues, 9 to 25 amino acid residues, 10 to 25 amino acid residues, 7 to 18 amino acid residues, 8 to 18 amino acid residues, 9 to 18 amino acid residues, or 10 to 18 amino acid residues.
[00113] Certain illustrative peptide inhibitors described herein comprise 12 or more amino acid residues. However, the present invention also includes peptide inhibitors comprising a fragment of any of the peptide sequences described herein, including peptide inhibitors having 7, 8, 9, 10, or 11 amino acid residues. For example, peptide inhibitors of the present invention include peptides comprising or consisting of X4-X9, X4-X10, X4-X11, X4-X12, X4-X13, X4-X14, X4-X15, or X4-X16. In particular embodiments, the present invention includes peptide inhibitors having any of the sequences described herein, including but not limited to, those shown in any of the formulas described herein, the sequence listing, or any of the tables provided herein, wherein one or more of X10, X11, X12, X13, X14, X15, or X16 is absent. In particular embodiments, one or more of X13, X14, X15 or X16 is absent.
[00114] In particular embodiments of the present invention, the peptide inhibitors, or X regions thereof, are not present within an antibody. In particular embodiments, the peptide inhibitors, or X regions thereof, are not present within a VH or VL region of an antibody.
1001151In particular embodiments of the peptide inhibitors described herein, they comprise one or more unnatural or non-natural amino acid residue.
1001161In particular embodiments, peptide inhibitors of the present invention are cyclized via a cyclic amide bond, a disulfide bond, or a thioether bond. In particular embodiments, the bond is an intramolecular bond between two amino acid residues within the peptide inhibitor or a monomer subunit thereof.
Peptide Inhibitors [00117] Peptide inhibitors of the present invention include peptides having any of the amino acid sequences described herein, compounds having any of the structures described herein, including compounds comprising any of the peptide sequences described herein, and dimers of any of such peptides and compounds. Peptide inihibitors on the present invention include both peptides not having and those having a bond between X4 and X9, e.g., before and after a cross-link is introduced between X4 and X9. Illustrative peptides of the invention comprise an amino acid sequence or structure described in any of the accompanying tables, Examples, figures and sequence listing.
Si 1001181In certain embodiments, the present invention includes a peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Xa):
X1 -X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Xa) wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is any amino acid or chemical moiety capable of forming a bond with X9;
X5 is any amino acid;
X6 is any amino acid;
X7 is any amino acid;
X8 is any amino acid;
X9 is any amino acid or chemical moiety capable of forming a bond with X4;
X10 is any amino acid;
X11 is any amino acid;
X12 is any amino acid;
X13 is any amino acid;
X14 is any amino acid;
X15 is any amino acid, X16 is any amino acid or absent;

X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, 1001191wherein X4 and X9 are capable of forming a bond with each other. In particular embodiments, the bond is a disulfide bond, a thioether bond, a lactam bond, a triazole ring, a selenoether bond, a diselenide bond, or an olefin bond. In particular embodiments, the bond is a disulfide bond or a thioether bond. In certain embodiments, the peptide inhibitor is cyclized via the bond between X4 and X9. In certain embodiments, the peptide inhibitor inhibits the binding of an interleukin-23 (IL-23) to an IL-23 receptor. In particular embodiments, when X4 is not an amino acid, then X1 , X2, and X3 are absent. In certain embodiments, X1 is a D-amino acid or absent. In certain embodiments, X2 is a D-amino acid or absent. In certain embodiments, X3 is a D-amino acid or absent. In certain embodiments, X16 is a D-amino acid or absent. In certain embodiments, X17 is a D-amino acid or absent. In certain embodiments, X18 is a D-amino acid or absent. In certain embodiments, X19 is a D-amino acid or absent. In certain embodiments, X20 is a D-amino acid or absent.
[00120] In one embodiment of the peptide inhibitor of Formula Xa, X1 is absent;
X2 is absent;
X3 is Glu, D-Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, (D)Gln or absent;
X4 is Cys, Abu or Pen;
X5 is Ala, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn, Gln, Arg, Ser or Thr;
X6 is Asp or Thr;

X7 is Trp or 6-Chloro-Trp;
X8 is Glu, Gin or Val;
X9 is Cys, Abu or Pen;
X10 is 2-Nal, a Phe analog, Tyr, or a Tyr analog, wherein in particular embodiments, X10 is 2-Nal, Phe(3,4-diF2), Phe(3,4-C12), Phe(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)], Phe(Br), Phe(4-CONH2), Phe(C1), Phe(4-CN), Phe(4-guadino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Tyr, Tyr(Bz1), or Tyr(Me);
X11 is 1-Nal, 2-Nal, Phe(3,4-dimethoxy), 5-HydroxyTrp, Phe(3,4-C12), Trp or Tyr(3-tBu);
X12 is 3-Pal, Acpc, Acbc, Acvc, Achc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a- a-MeOrn, a-MeSer, a-MeVal, Cav, Cha, Cit, Cpa, D-Asn, Glu, His, hLeu, hArg, Lys, Leu, Octgly, Orn, piperidine, Arg, Ser, Thr or THP;
X13 is Cit, Asp, Dab, Dap, Phe, His, Dap(Peg2-Ac), Dap(pyroglutaric acid), Glu, hArg, Lys, Lys(Ac), Lys(Benzoic acid), Lys(glutaric acid), Lys(IVA), Lys(Peg4-isoGlu-Palm), Lys(pyroglutaric acid), Lys-succinic acid, Asn, Orn,G1n, Arg, Thr or Val;
X14 is Asp, Dab(Ac), Dap(Ac), Phe, His, Lys(Ac), Met, Asn(isobutyl), Gin, Arg, Tyr or Asp(1,4-diaminobutane);
X15 is Ala, betaAla, Glu, Gly, Asn, Gin, Arg or Ser, X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.

10012111N certain embodiments, X3 is absent. In particular embodiments, X16, X17, X18, X19 and X20 are absent. In particular embodiments, X4 and X9 are Cys, and X4 and X9 are linked via a disulfide bond. In particular embodiments, X4 is Abu and X9 is Pen, and X4 and X9 are linked via a thioether bond. In particular embodiments, X4 is Abu and X9 is Cys, and X4 and X9 are linked via a thioether bond.
[00122] In another embodiment of the peptide inhibitor of Formula Xa, X1 is absent;
X2 is absent;
X3 is Glu, D-Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, (D)Gln or absent;
X4 is Cys, Abu or Pen;
X5 is Ala, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, Orn, Gln, Arg, Ser or Thr;
X6 is Asp or Thr;
X7 is Trp or 6-Chloro-Trp;
X8 is Gln or Val;
X9 is Cys, Abu or Pen;
X10 is 2-Nal, a Phe analog, Tyr, or a Tyr analog, wherein in particular embodiments, X10 is 2-Nal, Phe(3,4-diF2), Phe(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)], Phe(Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guadino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Tyr, Tyr(Bz1), or Tyr(Me);
X11 is 1-Nal, 2-Nal, Phe(3,4-dimethoxy), 5-HydroxyTrp, Phe(3,4-C12), Trp or Tyr(3-tBu);

X12 is 3-Pal, Acpc, Acbc, Acvc, Achc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, Cav, Cha, Cit, Cpa, D-Asn, His, hLeu, hArg, Lys, Leu, Octgly, Orn, 4-amino-4-carboxy-piperidine, or MP;
X13 is Cit, Asp, Dab, Dap, Phe, His, Dap(Peg2-Ac), Dap(pyroglutaric acid), Glu, hArg, Lys, Lys(Ac), Lys(Benzoic acid), Lys(glutaric acid), Lys(IVA), Lys(Peg4-isoGlu-Palm), Lys(pyroglutaric acid), Lys-succinic acid, Asn, Orn,G1n, Arg, Thr or Val;
X14 is Dab(Ac), Dap(Ac), Phe, His, Lys(Ac), Met, Asn, Gln, Arg, or Tyr;
X15 is Ala, f3Ala, Gly, Asn, Gln, or Ser, X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1001231In some embodiments, X3 is absent. In particular embodiments, X16, X17, X18, X19 and X20 are absent. In particular embodiments, X4 and X9 are Cys, and X4 and X9 are linked via a disulfide bond. In particular embodiments, X4 is Abu and X9 is Pen, and X4 and X9 are linked via a thioether bond. In particular embodiments, X4 is Abu and X9 is Cys, and X4 and X9 are linked via a thioether bond.
[00124] In another embodiment of the peptide inhibitor of Formula Xa, X1 is absent;
X2 is absent;
X3 is Glu, D-Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, (D)Gln or absent;
X4 is Cys, Abu or Pen;

X5 is Dap, Dap(Ac), Gly, Lys, Gin, Arg, Ser,Thr or Asn;
X6 is Thr;
X7 is Trp or 6-Chloro-Trp;
X8 is Gin;
X9 is Cys, Abu or Pen;
X10 is 2-Nal, a Phe analog, Tyr, or a Tyr analog, wherein in particular embodiments, X10 is 2-Nal, Phe(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)], Phe(4-CONH2), Phe(4-Me), Phe(4-NH2), Tyr, Tyr(Bz1), or Tyr(Me);
X11 is 1-Nal, 2-Nal, Phe(3,4-dimethoxy), Phe(3,4-C12), or Trp;
X12 is Acpc, Acbc, Acvc, Achc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, hLeu, Lys, Leu, Arg or THP;
X13 is Cit, Asp, Dap, Dap(Peg2-Ac), Dap(pyroglutaric acid), Glu, hArg, Lys, Lys(Ac), Lys(Benzoic acid), Lys(glutaric acid), Lys(IVA), Lys(Peg4-isoGlu-Palm), Lys(pyroglutaric acid), Lys(succinic acid), Asn, Orn,G1n, Arg, or Val;
X14 is Dab(Ac), Dap(Ac), His, Lys(Ac), Asn, Gin, or Tyr;
X15 is Ala, betaAla, Gly, Asn, Gin, or Ser, X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.

1001251In some embodiments, X3 is absent. In particular embodiments, X16, X17, X18, X19 and X20 are absent. In particular embodiments, X4 and X9 are Cys, and X4 and X9 are linked via a disulfide bond. In particular embodiments, X4 is Abu and X9 is Pen, and X4 and X9 are linked via a thioether bond. In particular embodiments, X4 is Abu and X9 is Cys, and X4 and X9 are linked via a thioether bond.
[00126] In another embodiment of the peptide inhibitor of Formula Xa, X1 is absent;
X2 is absent;
X3 is Glu, D-Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, (D)Gln or absent;
X4 is Cys, Abu or Pen;
X5 is Dap, Dap(Ac), Gln, Ser, Thr or Asn;
X6 is Thr;
X7 is Trp;
X8 is Gln;
X9 is Cys, Abu or Pen;
X10 is a Phe analog, Tyr, or a Tyr analog, wherein in particular embodiments, X10 is Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)], Phe(4-CONH2), Phe(4-Me), Tyr, Tyr(Bz1), or Tyr(Me);
X11 is 2-Nal or Trp;
X12 is Acpc, Acbc, Acvc, Achc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, hLeu, Leu, or THP;
X13 is Cit, Asp, Glu, Lys, Lys(Ac), Asn, or Gln;

X14 is Dab(Ac), Asn, or His;
X15 is Ala, betaAla, Gly, Asn, or Gln;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1001271In some embodiments, X3 is absent. In particular embodiments, X16, X17, X18, X19 and X20 are absent. In particular embodiments, X4 and X9 are Cys, and X4 and X9 are linked via a disulfide bond. In particular embodiments, X4 is Abu and X9 is Pen, and X4 and X9 are linked via a thioether bond. In particular embodiments, X4 is Abu and X9 is Cys, and X4 and X9 are linked via a thioether bond.
1001281In particular embodiments, the peptide inhibitor comprises the amino acid sequence set forth in any of the various formula described herein, e.g., Ia-It, Illa-Ille, or IV.
1001291In certain embodiments, the present invention includes a peptide inhibitor of an interleukin-23 receptor, wherein the peptide inhibitor has the structure of Formula I:
R1-X-R2 (I) [00130] or a pharmaceutically acceptable salt or solvate thereof, 100131] wherein 1Z1 is a bond, hydrogen, an Cl -C6 alkyl, a C6-C12 aryl, a C6-C12 aryl Cl -C6 alkyl, a Cl -C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing;
1001321R2 is a bond, OH or NH2; and 1001331X is an amino acid sequence, e.g., an amino acid comprising 7 to 35 amino acid residues.
In certain embodiments, R2 is OH or NH2.
[00134] In certain embodiments, X comprises a sequence of Formula Xa.
[00135] In particular embodiments of formula (I), X comprises the sequence of Formula Ia:
X1 -X2-X3-X4-X5-X6-W-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Ia) wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Met, Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Sec, 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, Abu, f3-azido-Ala-OH, propargylglycine, 2-(3'-butenyl)glycine, 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, 2-(5'-hexenyl)glycine or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Serõ a-MeOrn, a-MeSer, CitDap, Dab, Dap (Ac), Gly, Lys, Asn, N-Me-Gln, N-Me-Arg, Orn or Gln, X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Asp, Leu, Val, Phe, Ser, Sec, Abu, f3-azido-Ala-OH, propargylglycine, 2-2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, or 2-(5'-hexenyl)glycine;

X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Na!, 2-Na!, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu) X12 is His, Phe, Arg, N-Me-His, or Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln;
X14 is Phe, Tyr f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac), or Asp;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
In particular embodiments of Ia: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib or D-Sarc; X10 is Tyr or Phe;
X11 is Trp, 1-Na! or 2-Na!; X12 is His, Phe, Arg, N-Me-His, or Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib; X14 is Phe, Tyr or f3hPhe; X15 is Gly, Ser, Thr, Gln, Ala or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
[00136] In particular embodiments, X4 is present.

1001371 In certain embodiments, the peptide inhibitor is cyclized.
1001381 In certain embodiments, the peptide inhibitor is linear or not cyclized.
1001391In certain embodiments, the peptide inhibitor is cyclized, or contains an intramolecular bond, between X4 and X9.
1001401 In certain embodiments of Formula I, X comprises the sequence of Formula Ib:
X1 -X2-X3-X4-X5-X6-W-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Ib), [00141] wherein:
X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Sec, 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, Abu, f3-azido-Ala-OH, propargylglycine, 2-(3'-butenyl)glycine, 2-2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, 2-(5'-hexenyl)glycine, or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, a-MeOrn, a-MeSer, CitDap, Dab, Dap (Ac), Gly, Lys, Asn, N-Me-Gln, N-Me-Arg, Orn or Gln;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Asp, Sec, Abu, f3-azido-Ala-OH, propargylglycine, 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, or 2-(5'-hexenyl)glycine;

X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr X11 is Trp, 1-Na!, 2-Na!, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12), Tyr(3-t-Bu) X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAlaAib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln X14 is Phe, Tyr, or f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp;
X15 is Gly, Ser, Thr, Gln, Ala, or Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid, or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1001421In particular embodiments of Ib: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib or D-Sarc; X10 is Tyr or Phe; X11 is Trp, 1-Na! or 2-Na!; X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla or Aib; X14 is Phe, Tyr or f3hPhe; X15 is Gly, Ser, Thr, Gln, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
[00143] In particular embodiments, X4 is present.

[00144] In certain embodiments, the peptide inhibitor is cyclized.
1001451ln certain embodiments, the peptide inhibitor is linear or not cyclized.
1001461In certain embodiments, the peptide inhibitor is cyclized, or contains an intramolecular bond, between X4 and X9.
1001471 In certain embodiments of Formula I, X comprises the sequence of Formula Ic:

(Ic) [00148] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Met, Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Sec, 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, Abu, f3-azido-Ala-OH, propargylglycine, 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, 2-(5'-hexenyl)glycine, or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, a-MeOrn, a-MeSer, CitDap, Dab, Dap (Ac), Gly, Lys, Asn, N-Me-Gln, N-Me-Arg, Orn or Gln X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;

X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Asp, Sec, Abu, f3-azido-Ala-OH, propargylglycine, 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, or 2-(5'-hexenyl)glycine;
X11 is Trp, 1-Na!, 2-Na! Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu) X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala t-butyl-Gly;
4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1001491In particular embodiments of Ic, X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X11 is Trp, 1-Na!, or 2-Na!;
X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib; X14 is Phe, Tyr, or f3hPhe;
X15 is Gly, Ser, Thr, Gln, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
1001501ln particular embodiments, X4 is present.

1001511 In certain embodiments, the peptide inhibitor is cyclized.
[00152] In certain embodiments, the peptide inhibitor is linear or not cyclized.
1001531In certain embodiments, the peptide inhibitor is cyclized, or contains an intramolecular bond, between X4 and X9.
1001541 In certain embodiments of Formlua I, X comprises the sequence of Formula Id:

(Id) [00155] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, a-MeOrn, a-MeSer, CitDap, Dab, Dap (Ac), Gly, Lys, Asn, N-Me-Gln, N-Me-Arg, Orn or Gln;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;
X10 is Tyr Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12), Tyr(3-t-Bu) X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gin X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His, Dap(Ac), Dab(Ac) or Asp;
X15 is Gly, Ser, Thr, Gin, Ala, Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00156] wherein X4 and X9 are optionally linked by a intramolecular disulphide bridge.
1001571In certain embodiments of Id: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X10 is Tyr or Phe;
X11 is Trp, 1-Na!, or 2-Na!; X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib; X14 is Phe, Tyr, or f3hPhe; X15 is Gly, Ser, Thr, Gin, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
[00158] In certain embodiments of Formula I, X comprises the sequence of Formula le:

(le) [00159] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Pen, hCys, D-Pen, D-Cys, or D-hCys;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, a-MeOrn, a-MeSer, CitDap, Dab, Dap (Ac), Gly, Lys, Asn, N-Me-Gln, N-Me-Arg, Orn or Gln;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is Pen, hCys, D-Pen, D-Cys, D-hCys;
X10 is Tyr, Phe Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);
X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;

X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00160] wherein X4 and X9 are optionally linked by a intramolecular disulphide bridge.
1001611In certain embodiments of le: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X10 is Tyr or Phe;
X11 is Trp, 1-Nal, or 2-Nal; X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib; X14 is Phe, Tyr, or f3hPhe; X15 is Gly, Ser, Thr, Gln, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
[00162] In particular embodiments, X4 is present.
1001631 In certain embodiments, the peptide inhibitor is cyclized.
1001641 In certain embodiments, the peptide inhibitor is linear or not cyclized.
1001651In certain embodiments, the peptide inhibitor is cyclized, or contains an intramolecular bond, between X4 and X9.
1001661 In particular embodiments, X4 and X9 and both Pen.
1001671 In certain embodiments of Formula I, X comprises the sequence of Formula If:

(If) [00168] wherein X1 is any amino acid or absent;

X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, or Asp;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap (Ac), Gly, Lys, Asn, N-Me-Gln, N-Me-Arg, Orn or Gln;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, or Asp;
X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);
X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid or absent;

X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00169] wherein X4 and X9 are optionally cyclized through an intramolecular bond.
1001701In certain embodiments of If: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe; X8 is Val, Gln, Glu, or Lys; X9 is Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, or Asp; X10 is Tyr or Phe;; X11 is Trp, 1-Nal, or 2-Nal;
X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; ;X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib; X14 is Phe, Tyr, or f3hPhe;
X15 is Gly, Ser, Thr, Gln, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
10017111n certain embodiments, the intramolecular bond is a lactam bond.
1001721 In certain embodiments of Formula I, X comprises the sequence of Formula Ig:

(Ig) [00173] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is f3-azido-Ala-OH, or propargylglycine;

X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is f3-azido-Ala-OH or propargylglycine, ;
X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu) X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp;
X15 is Gly, Ser, Thr, Gln, Ala, or Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00174] wherein X4 and X9 are optionally cyclized through an intramolecular triazole ring.
1001751In particular embodiments of Ig: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe; X8 is Val, Gln, Glu, or Lys; X9 is f3-azido-Ala-OH or propargylglycine; X10 is Tyr or Phe; X11 is Trp, 1-Nal, or 2-Nal; X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib; X14 is Phe, Tyr, or f3hPhe; X15 is Gly, Ser, Thr, Gln, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
[00176] In certain embodiments of Formula I, X comprises the sequence of Formula Ih:

(Ih) [00177] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, or 2-(5'-hexenyl)glycine;
X5 is Ala, Arg, Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, or Asn;
X8 is Val, Gln, or Glu;
X9 is 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, or 2-(5'-hexenyl)glycine;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu) X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gin;
X15 is Gly, Ser, Thr, Gin, Ala, Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00178] wherein X4 and X9 are optionally cyclized via an intramolecular ring closing methasis to give the corresponding olefins.
1001791In particular embodiments of Ih: X5 is Ala, Arg, or Sarc; X6 is Asp, Thr, or Asn; X11 is Trp, 1-Nal, or 2-Nal; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, or Aib; X15 is Gly, Ser, Thr, Gin, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
[00180] In certain embodiments of Formula I, X comprises the sequence of Formula Ii:
X1 -X2-X3-X4-X5-X6-W-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Ii), [00181] wherein:
X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;

X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, or 3-chloro-isobutyric acid;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, or Abu;
X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu) X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid or absent;

X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00182] wherein X4 and X9 are optionally cyclized via an intramolecular thioether bond.
1001831In particular embodiments of Ii: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe; X10 is Tyr or Phe; X11 is Trp, 1-Nal, or 2-Nal;
X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib; X14 is Phe, Tyr, or f3hPhe; X15 is Gly, Ser, Thr, Gln, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
1001841 In certain embodiments of Formula I, X comprises the sequence of Formula Ij:
X1 -X2-X3-X4-X5-X6-W-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Ij), 1001851 wherein:
X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Sec, 2-chloromethylbenzoic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, or Abu;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;

X8 is Val, Gin, Glu, or Lys;
X9 is Sec or Abu;
X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-aminoethoxy), Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Na!, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);
X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc, Acpc, Acbc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gin;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp;
X15 is Gly, Ser, Thr, Gin, Ala, Sarc, f3-Ala, Glu, Arg or Asn;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00186] wherein X4 and X9 are optionally cyclized via an intramolecular thioseleno or diselenide bond.
1001871In particular embodiments of Ij: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X10 is Tyr or Phe; X11 is Trp, 1-Na!, or 2-Na!; X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, or Aib; X14 is Phe, Tyr, or f3hPhe; X15 is Gly, Ser, Thr, Gln, Ala, or Sarc; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
[00188] In certain embodiments of Formula I, X comprises the sequence of Formula Ik:
X1 -X2-X3-X4-X5-X6-W-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Ik), [00189] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Met, Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Asp, Leu, Val, Phe, or Ser;
X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Na!, 2-Na!, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);

X12 is His, Phe, Arg, N-Me-His, Val, D-His, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly,4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp or absent;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn or absent;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1001901In particular embodiments of Ik: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X10 is Tyr or Phe; X11 is Trp, 1-Nal, or 2-Na!; X12 is His, Phe, Arg, N-Me-His, Val, D-His, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib or absent; X14 is Phe, Tyr, PhPhe or absent; X15 is Gly, Ser, Thr, Gln, Ala, Sarc or absent; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, Leu, or absent; and X17 is Leu, Lys, Arg, or absent.
In certain embodiments of Formula I, X comprises or consists of the sequence of Formula Ii:
X1 -X2-X3-X4-X5-X6-W-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (I1), [00191] wherein X1 is any amino acid or absent;

X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Met, Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, Asn, or Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Asp, Leu, Val, Phe, or Ser;
X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Nal, 2-Nalõ Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);
X12 is His, Phe, Arg, N-Me-His, Val, D-His, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln or absent;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp or absent;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn or absent;
X16 is any amino acid or absent;

X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1001921In particular embodiments of Ii: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, or Sarc;
X10 is Tyr or Phe; X11 is Trp, 1-Nal, or 2-Nal; X12 is His, Phe, Arg, N-Me-His, Val, D-His, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Val, f3hAla, Aib or absent; X14 is Phe, Tyr, PhPhe or absent; X15 is Gly, Ser, Thr, Gln, Ala, Sarc or absent; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, Leu, or absent; and X17 is Leu, Lys, Arg, or absent.
10019311n certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln. In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, or Aib.
1001941In certain embodiments, X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp. In certain embodiments, X14 is Phe, Tyr, or f3hPhe.
1001951In certain embodiments, X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn. In certain embodiments, X15 is Gly, Ser, Thr, Gln, Ala, or Sarc.
[00196] In certain embodiments, X12 is alpha amino acid, e.g., 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Aib, a-MeGly(diethyl), a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal.
[00197] In certain embodiments, X13 is present.
[00198] In certain embodiments, X13 and X14 are present.
[00199] In certain embodiments, X13, X14 and X15 are present.
[00200] In particular embodiments, X4 is present.

1002011 In certain embodiments, the peptide inhibitor is cyclized.
[00202] In certain embodiments, the peptide inhibitor is linear or not cyclized.
1002031In certain embodiments, the peptide inhibitor is cyclized, or contains an intramolecular bond, between X4 and X9.
1002041In certain embodiments of the peptide inhibitor of Formula I, X
comprises or consists of the sequence of Formula Im:
X1 -X2-X3 -X4-X5-X6-W-X8-X9-Y-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Im), [00205] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Met, Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn, or Gln;
X6 is Asp, Thr, Asn, or Phe;
X8 is Val, Gln, Glu, or Lys;
X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Asp, Leu, Val, Phe, or Ser;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2); 5-Hydroxy-Trp, Phe(3,4-C12), or Tyr(3-t-Bu);
X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gin or absent;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac), or Asp or absent;
X15 is Gly, Ser, Thr, Gin, Ala, Sarc, f3-Ala, Glu, Arg or Asn or absent;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1002061In certain embodiments of Im: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, or Sarc; X11 is Trp, 1-Na!, or 2-Nal; X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib or absent;
X14 is Phe, Tyr, PhPhe or absent; X15 is Gly, Ser, Thr, Gin, Ala, Sarc or absent; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
1002071In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, or Aib. In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gin.
1002081 In certain embodiments, X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp. In certain embodiments, X14 is Phe, Tyr, or f3hPhe.
1002091in certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala, or Sarc, f3-Ala, Glu, Arg or Asn.
In certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala, or Sarc.

1002101 In certain embodiments, X12 is alpha amino acid, e.g., 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Aib, a-MeGly(diethyl), a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal.
[00211]In certain embodiments, X13 is present.
1002121 In certain embodiments, X13 and X14 are present.
[00213]In certain embodiments, X13, X14, and X15 are present.
1002141 In particular embodiments, X4 is present.
1002151In certain embodiments, the peptide inhibitor is cyclized.
1002161 In certain embodiments, the peptide inhibitor is linear or not cyclized.
1002171In certain embodiments, the peptide inhibitor is cyclized, or contains an intramolecular bond, between X4 and X9.
1002181 In certain embodiments of the peptide inhibitor of Formula I, X
comprises or consists of the sequence of Formula In:
X1-X2-X3-C-X5-X6-W-X8-C-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (In) [00219] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, Asn, or Phe;
X8 is Val, Gln, Glu, or Lys;

X10 is Tyr Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Na!, 2-Na!, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);
X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln or absent;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp or absent;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn or absent;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00220] wherein the Cys at position X4 and and the Cys at position X9 are optionally linked by a disulphide bridge.
1002211In certain embodiments of In: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr; X11 is Trp, 1-Na!, 2-Na!, Phe(3,4-OMe2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu); X12 is His, Phe, Arg, N-Me-His, Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln or absent; X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp or absent; X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn or absent; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
1002221In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln. In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, or Aib.
1002231In certain embodiments, X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp. In certain embodiments, X14 is Phe, Tyr, or f3hPhe.
1002241In certain embodiments, X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn. In certain embodiments, X15 is Gly, Ser, Thr, Gln, Ala, or Sarc.
1002251In certain embodiments, X12 is an alpha amino acid, e.g., 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal.
[00226] In certain embodiments, X13 is present.
[00227] In certain embodiments, X13 and X14 are present.
[00228] In certain embodiments, X13, X14 and X15 are present.
1002291In certain embodiments of the peptide inhibitor of Formula I, X
comprises or consists of the sequence of Formula lo:
X1 -X2-X3-C-X5-X6-W-X8-C-Y-X11-H-X13-X14-X15-X16-X17-X18-X19-X20 (lo) [00230] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, Asn, or Phe;
X8 is Val, Gln, Glu, or Lys;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln or absent;
X14 is Phe, Tyr, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp or absent;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg or Asn or absent;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00231] wherein the Cys at position X4 and and the Cys at position X9 are optionally linked by a disulphide bridge.
1002321In certain embodiments of To: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2), 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu); X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, Gin or absent; X14 is Phe, Tyr, Asn, Arg, Qln, Lys(Ac), His;
Dap(Ac), Dab(Ac) Asp or absent; X15 is Gly, Ser, Thr, Gin, Ala, Sarc, f3-Ala, Glu, Arg or Asn or absent; X16 is Asp, Glu, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
1002331In certain embodiments, X12 is an alpha amino acid, e.g., 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal.
[00234] In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gin. In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla or Aib.
1002351In certain embodiments, X14 is Phe, Tyr, Asn, Arg, Qln, Lys(Ac), His;
Dap(Ac), Dab(Ac) or Asp. In certain embodiments, X14 is Phe or Tyr.
1002361In certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala, Sarc, f3-Ala, Glu, Arg or Asn. In certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala or Sarc.
[00237] In certain embodiments, X13 is present.
[00238] In certain embodiments, X13 and X14 are present.
[00239] In certain embodiments, X13, X14 and X15 are present.
1002401In certain embodiments of the peptide inhibitor of Formula I, X
comprises or consists of the sequence of Formula Ip:
X1 -X2-X3-C-X5-X6-W-X8-C-Y-X11-H-X13-F-X15-X16-X17-X18-X19-X20 (Ip) [00241] wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;

X3 is any amino acid or absent;
X5 is Ala, Arg, Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gln;
X6 is Asp, Thr, or Asn;
X8 is Val, Gln, or Glu;
X11 is Trp, 1-Nal, 2-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, Gln or absent;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg Asn or absent;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, [00242] wherein the Cys at position X4 and and the Cys at position X9 are optionally linked by a disulphide bridge.
1002431In certain embodimetns of Ip: X5 is Ala, Arg, or Sarc; X11 is Trp, 1-Nal, or 2-Nal; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib or absent; X15 is Gly, Ser, Thr, Gln, Ala, Sarc or absent; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, or absent; and X17 is Leu, Lys, Arg, or absent.
[00244] In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gln. In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla or Aib.

1002451In certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala or Sarc, f3-Ala, Glu, Arg or Asn.
In certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala or Sarc.
[00246] In certain embodiments, X13 is present.
[00247] In certain embodiments, X13 and X14 are present.
[00248] In certain embodiments, X13, X14 and X15 are present.
1002491In certain embodiments of the peptide inhibitor of Formula I, X
comprises or consists of the sequence of Formula Iq:
X1 -X2-X3-C-X5-X6-W-X8-C-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Iq), wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, D-Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn or Gin;
X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, or D-Phe;
X8 is Val, Gin, Glu, or Lys;
X10 is Tyr, Phe, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp, 1-Nal, 2-Nalõ Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);

X12 is His, Phe, Arg, N-Me-His, Val, or D-His, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, Gln or absent;
X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac), Asp or absent;
X15 is Gly, Ser, Thr, Gln, Ala, Sarc, f3-Ala, Glu, Arg, Asn or absent;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, 1002501 wherein the Cys at position X4 and and the Cys at position X9 are optionally linked.
1002511In certain embodiments of Iq: X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X10 is Tyr or Phe;
X11 is Trp, 1-Nal, or 2-Na!; X12 is His, Phe, Arg, N-Me-His, Val, or D-His, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib or absent;
X14 is Phe, Tyr, PhPhe or absent; X15 is Gly, Ser, Thr, Gln, Ala, Sarc or absent; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, Leu, or absent; and X17 is Leu, Lys, Arg, or absent.
[00252] In certain embodiments, X12 is alpha amino acid, e.g., 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal.

[00253] In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gin. In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla or Aib.
1002541In certain embodiments, X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac), or Asp. In certain embodiments, X14 is Phe, Tyr or f3hPhe.
1002551In certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala, Sarc, f3-Ala, Glu, Arg or Asn. In certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala or Sarc.
[00256] In certain embodiments, X13 is present.
[00257] In certain embodiments, X13 and X14 are present.
[00258] In certain embodiments, X13, X14 and X15 are present.
[00259] In certain embodiments, Iq comprises or consists of the sequence of Formula Iq':
X1 -X2-X3-C-X5-X6-W-X8-C-X10-X11-X12-X13-X14-X15 (Iq'), wherein X1-X14 have the definition provided for Iq, and wherein the Cys at position X4 and and the Cys at position X9 are optionally linked.
1002601In certain embodiments of Iq': X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, or D-Sarc; X10 is Tyr or Phe;
X11 is Trp, 1-Nal, or 2-Nal; X12 is His, Phe, Arg, N-Me-His, Val, or D-His, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, or t-butyl-Gly; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Val, Aib or absent;
X14 is Phe, Tyr, PhPhe or absent; X15 is Gly, Ser, Thr, Gin, Ala, Sarc or absent; X16 is Asp, Glu, Ala, AEA, AEP, f3hAla, Gaba, Leu, or absent; and X17 is Leu, Lys, Arg, or absent.
[00261] In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, Aib, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, or Gin. In certain embodiments, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla or Aib.

1002621In certain embodiments, X14 is Phe, Tyr, f3hPhe, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp. In certain embodiments, X14 is Phe, Tyr or f3hPhe.
1002631In certain embodiments, X15 is Gly, Ser, Thr, Gin, Ala or Sarc, f3-Ala, Glu, Arg or Asn.
In certain embodiments, X14 is Phe, Tyr or f3hPhe.
1002641 In certain embodiments, X13 is present.
1002651 In certain embodiments, X13 and X14 are present.
1002661 In certain embodiments, X13, X14 and X15 are present.
1002671In certain embodiments of the peptide inhibitor of Formula I, X
comprises or consists of the sequence of Formula Ir:
X1 -X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Ir) wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Met, Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Sec, 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, Abu, f3-azido-Ala-OH, propargylglycine, 2-(3'-butenyl)glycine, 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, 2-(5'-hexenyl)glycine, Abu or absent;
X5 is any amino acid;
X6 is any amino acid;
X7 is Trp, Glu, Gly, Ile, Asn, Pro, Arg, Thr or OctGly, or a corresponding a-methyl amino acid form of any of the foregoing;

X8 is any amino acid;
X9 is Cys, Pen, hCys, D-Pen, D-Cys, D-hCys, Glu, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu, D-Lys, Asp, Leu, Val, Phe, or Ser, Sec, Abu, f3-azido-Ala-OH, propargylglycine, 2-2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, Ala, hCys, Abu, Met, MeCys, (D)Tyr or 2-(5'-hexenyl)glycine;
X10 is Tyr, Phe(4-0Me), 1-Nal, 2-Na!, Aic, a-MePhe, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, His, hPhe(3,4-dimethoxy), hTyr, N-Me-Tyr, Trp, Phe(4-CONH2), Phe(4-phenoxy), Thr, Tic, Tyr(3-tBu), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-NH2), Phe(4-F), Phe(3,5-F2), Phe(4-CH2CO2H), Phe(penta-F), Phe(3,4-C12), Phe(4-CF3), Bip, Cha, 4-PyridylAlanine, f3hTyr, OctGly, Phe(4-N3), Phe(4-Br), Phe[4-(2-aminoethoxy)] or Phe, a Phe analog, a Tyr analog, or a corresponding a-methyl amino acid form of any of the foregoing;
X11 is 2-Na!, 1-Nal, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe (3,4-F2), Phe(4-CO2H), f3hPhe(4-F), a-Me-Trp, 4-phenylcyclohexyl, Phe(4-CF3)õ Phe(3,4-0Me2), a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Trp, Tyr, Phe(4-0Me), Phe(4-Me), Trp(2,5,7-tri-tert-Butyl), Phe(4-0ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino, Phe(4-0Bz1), Octgly, Glu(Bz1), 4-Phenylbenzylalanine, Phe[4-(2-aminoethoxy)], 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, 1,2,3,4-tetrahydro-norharman, Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(2,3-C12), Phe(2,3-F2), Phe(4-F), 4-phenylcyclohexylalanine or Bip, or a corresponding a-methyl amino acid form of any of the foregoing;
X12 is His, Phe, Arg, N-Me-His, or Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, a-MeLys, D-Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Tyr, Aib, a-MeLeu, a-MeOrn, (3-Aib, f3-Ala, f3hAla, PhArg, PhLeu, f3hVal, f3-spiro-pip, Glu, hArg, Ile, Lys, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Ser, Thr, Tle or t-butyl-Gly, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys or a corresponding a-methyl amino acid form of any of the foregoing;

X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Asn, Cit, Lys, Arg, Orn, Val, f3hAla, Lys(Ac), (D)Asn, (D)Leu, (D)Phe, (D)Thr, Ala, a-MeLeu, Aib, f3-Ala, f3-Glu, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, hLeu, Asn, Ogl, Pro, Gln, Ser, f3-spiro-pip, Thr, Tba, Tle or Aib, or a corresponding a-methyl amino acid form of any of the foregoing;
X14 is Phe, Tyr, Glu, Gly, His, Lys, Leu, Met, Asn, Lys(Ac), Dap(Ac), Asp, Pro, Gln, Arg, Ser, Thr, Tic or f3hPhe, or a corresponding a-methyl amino acid form of any of the foregoing;
X15 is Gly, Ser, Thr, Gln, Ala, (D)Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Thr, Aea, Asp, Asn, Glu, Phe, Gly, Lys, Leu, Pro, Arg, f3-Ala, or Sarc, or a corresponding a-methyl amino acid form of any of the foregoing;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
[00268] In particular embodiments, the peptide is cyclized via X4 and X9.
1002691 In particular embodiments, X3 is Glu, D-Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Na!, Thr, Leu, (D)Gln.
1002701In certain embodiments of Ir: X11 is 2-Na!, 1-Nal, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe (3,4-F2), Phe(4-CO2H), f3hPhe(4-F), a-Me-Trp, 4-phenylcyclohexyl, Phe(4-CF3), a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Trp, Tyr, Phe(4-0Me), Phe(4-Me), Trp(2,5,7-tri-tert-Butyl), Phe(4-0ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino, Phe(4-0Bz1), Octgly, Glu(Bz1), 4-Phenylbenzylalanine, Phe[4-(2-aminoethoxy)], 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, 1,2,3,4-tetrahydro-norharman, Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(2,3-C12), Phe(2,3-F2), Phe(4-F), 4-phenylcyclohexylalanine or Bip, or a corresponding a-methyl amino acid form of any of the foregoing; X12 is His, Phe, Arg, N-Me-His, or Val, Cav, Cpa, Leu, Cit, hLeu, 3-Pal, t-butyl-Ala, a-MeLys, D-Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Tyr, Aib, a-MeLeu, a-MeOrn, (3-Aib, (3-Ala, (3hAla, (3hArg, (3hLeu, (3hVal, (3-spiro-pip, Glu, hArg, Ile, Lys, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Ser, Thr, Tle or t-butyl-Gly, or a corresponding a-methyl amino acid form of any of the foregoing; X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Arg, Orn, Val, (3hAla, Lys(Ac), (D)Asn, (D)Leu, (D)Phe, (D)Thr, Ala, a-MeLeu, Aib, (3-Ala, (3-Glu, (3hLeu, (3hVal, (3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, hLeu, Asn, Ogl, Pro, Gln, Ser, (3-spiro-pip, Thr, Tba, Tle or Aib, or a corresponding a-methyl amino acid form of any of the foregoing; X14 is Phe, Tyr, Glu, Gly, His, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Tic or (3hPhe, or a corresponding a-methyl amino acid form of any of the foregoing; X15 is Gly, Ser, Thr, Gln, Ala, (D)Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Thr, Aea, Asp, Asn, Glu, Phe, Gly, Lys, Leu, Pro, Arg or Sarc, or a corresponding a-methyl amino acid form of any of the foregoing; X16 is Asp, Glu, Ala, AEA, AEP, (3hAla, Gaba, Gly, Ser, Pro, Asn, Thr or absent, or a corresponding a-methyl amino acid form of any of the foregoing; and X17 is Leu, Lys, Arg, Glu, Ser, Gly, Gln or absent, or a corresponding a-methyl amino acid form of any of the foregoing.
[00271] In certain embodiments, both X4 and X9 are Pen. In particular embodiments, X4 and X9 are cyclized via a disulfide bond.
1002721In certain embodiments, X4 is Abu and X9 is Cys. In certain embodiments, X4 and X9 are cyclized via a thioether bond.
[00273] In particular embodiments, X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, Cys, Cit, Asp, Dab, Dap, Gly, His, hCys, Lys, Met, Asn, N-Me-Ala, N-Me-Asn, N-Me-Lys, N-Me-Gln, Orn, Pro, Pen, Gln, Val, aMe-Lys, aMe-Orn, or D-Sarc, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, or Gln. In certain embodiments, X5 is Gln or Asn. In particular embodiments, X5 is Ala, Arg, Glu, Phe, Leu, Thr, Ser, Aib, Sarc, D-Ala, D-Arg, D-Glu, D-Phe, D-Leu, D-Thr, D-Ser, D-Aib, Cys, Cit, Asp, Dab, Dap, Gly, His, hCys, Lys, Met, Asn, N-Me-Ala, N-Me-Asn, N-Me-Lys, N-Me-Gln, N-Me-Arg, Orn, Pro, Pen, Gln, Val, aMe-Lys, aMe-Orn, or D-Sarc.In certain embodiments, X5 is Gln.

1002741In particular embodiments, X6 is Asp, Thr, Asn, Phe, D-Asp, D-Thr, D-Asn, Glu, Arg, Ser or D-Phe. In particular embodiments, X6 is Thr.
1002751 In particular embodiments, X7 is Trp.
1002761In particular embodiments, X8 is Val, Gln, Glu, Phe, Asn, Pro, Arg, Thr, Trp or Lys. In particular embodiments, X8 is Gln.
1002771 In particular embodiments, X1 , X2 and X3 are absent.
1002781 In certain embodiments, X11 is a Trp analog.
1002791In particular embodiments, X10 is a Phe analog. In particular embodiments, X10 is Phe(4-0Me), Phe(4-CONH2), or Phe[4-(2-aminoethoxy)] (also referred to herein as Phe[4-2ae)]). In particular embodiments, X10 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)]
(also referred to herein as Phe[4-2ae)]).
1002801 In particular embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, X11 is 2-Nal.
1002811In certain embodiments, X12 is a-MeLys, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, or a-MeVal. In certain embodiments, X12 is a-MeLys.
1002821 In certain embodiments, X13 is Glu or Lys(Ac). In certain embodiments, X13 is Glu.
[00283] In certain embodiments, X14 is Asn.
1002841 In certain embodiments, X15 is Gly or Asn. In certain embodiments, X15 is Gly.
1002851 In certain embodiments, one or more, two or more, three or more, or four or more of X16, X17, X18, X19 and X20 are absent. In particular embodiments, X16, X17, X18, X19 and X20 are absent.
1002861In particular embodiments of Ir, X4 and X9 are Cys, X7 is Trp, and X18 is [(D)Lys]. In particular embodiments of Ir, X4 and X9 are Cys, X7 is Trp, X10 is Tyr, and X18 is [(D)Lys]. In particular embodiments of Ir, X4 and X9 are Cys, X7 is Trp, Xi, X2 and X3 are absent, X17 is absent, X18 is [(D)Lys], and X19 and X20 are absent. In particular embodiments of Ir, X4 and X9 are Cys, X7 and X11 are Trp, X10 is Tyr, and X18 is [(D)Lys. In certain embodiments, Xl, X2, and X3 are absent; and in certain embodiments, X17 is absent.
1002871In particular embodiments of Ir, X4 and X9 are Pen, and X12 is a-MeLys.
In particular embodiments of Ir, X4 and X9 are Pen, X12 is a-MeLys, and X16, X17, X18, X19 and X20 are absent. In particular embodiments of Ir, X4 and X9 are Pen, X12 is a-MeLys, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, X16, X17, X18, X19 and X20 are absent, and X7 is Trp. In particular embodiments of Ir, X4 and X9 are Pen, X12 is a-MeLys, X16, X17, X18, X19 and X20 are absent, and X7 is Trp. In particular embodiments of Ir, X4 and X9 are Pen, X7 is Trp, and X12 is a-MeLys. In certain embodiments, X1 , X2, and X3 are absent.
In particular embodiments, there is a disulfide bond between X4 and X9.
1002881In particular embodiments of Ir, X4 is Abu, X9 is Cys, and X12 is 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, or a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, or a-MeVal. In particular embodiments of Ir, X4 is Abu, X9 is Cys, and X12 is a-MeLys. In particular embodiments of Ir, X4 is Abu, X9 is Cys, X12 is a-MeLys, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, or a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, or a-MeVal and X16, X17, X18, X19 and X20 are absent. In particular embodiments of Ir, X4 is Abu, X9 is Cys, X12 is a-MeLys, and X16, X17, X18, X19 and X20 are absent. In particular embodiments of Ir, X4 is Abu, X9 is Cys, X12 is a-MeLys, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, or a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, or a-MeVal, X16, X17, X18, X19 and X20 are absent, and X7 is Trp. In particular embodiments of Ir, X4 is Abu, X9 is Cys, X12 is a-MeLys, X16, X17, X18, X19 and X20 are absent, and X7 is Trp.
In particular embodiments of Ir, X4 is Abu, X9 is Cys, X7 is Trp, and X12 is a-MeLys. In certain embodiments, X1 , X2, and X3 are absent. In particular embodiments, there is a thioether bond between X4 and X9.

1002891In certain embodiments of the peptide inhibitor of Formula I, X
comprises or consists of the sequence of Formula Is:
X1 -X2-X3-C-X5-X6-W-X8-C-X10-X11-X12-X13-X14-G-X16-X17-X18-X19-X20 (Is) wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X5 is any amino acid;
X6 is any amino acid;
X8 is any amino acid;
X10 is Tyr, 1-Nal 2-Nal, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1) or Tyr;
X11 is Trp 1-Nal, Phe(3,4-0Me2) 5-Hydroxy-Trp, Phe(3,4-C12) or Tyr(3-t-Bu);
X12 is Arg, Lys, His, hArg, Cit, Orn, 1-Nal, D-Ala, D-Leu, D-Phe, D-Asn, D-Asp, Agp, Leu, PhLeu, Aib, f3hAla, f3hVal, PhArg, hLeu, Dap, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, Cha, Cit, Cpa, (D)Asn, Glu, hArg, or Lys;
X13 is Cha, Ogl, Aib, Leu, Val, Dab, Glu, Lys, PhLeu, f3hAla, PhVal f3G1u, Lys(Ac), Cit, Asp, Dab, Dap, Glu, hArg, Lys, Asn, Orn, Lys(Ac), or Gln;
X14 is Phe, Tic, Asn Tyr, Asn, Arg, Qln, Lys(Ac), His; Dap(Ac), Dab(Ac) or Asp;
X16 is any amino acid;

X17 is absent;
X18 is D-Lys;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1002901In particular embodiments of Is: X10 is Tyr, 1-Na! or 2-Na!; X11 is Trp or 1-Na!; X12 is Arg, Lys, His, hArg, Cit, Orn, 1-Na!, D-Ala, D-Leu, D-Phe, D-Asn, D-Asp, Agp, Leu, PhLeu, Aib, f3hAla, f3hVal, PhArg, hLeu or Dap; X13 is Cha, Ogl, Aib, Leu, Val, Dab, Glu, Lys, PhLeu, f3hAla, PhVal or PGLu; X14 is Phe, Tic, Asn or Tyr; and X16 is AEA, Ala or f3Ala.
1002911In particular embodiments, X5 is Glu, Arg, Ala, N-Me-Arg, N-Me-Ala, N-Me-Gln, Orn, N-Me-Asn, N-Me-Lys, Ser, Gln, Orn, Asn or Dap. In particular embodiments, X5 is Glu, Arg, Ala, N-Me-Arg, N-Me-Ala, N-Me-Gln, Orn, N-Me-Asn, N-Me-Lys, Ser, Asn or Dap.
[00292] In particular embodiments, X6 is Asp or Thr.
[00293] In particular embodiments, X8 is Gln or Val.
1002941 In particular embodiments, the peptide of Is is cyclized via a disulfide bond between X4 and X9.
1002951In certain embodiments of the peptide inhibitor of Formula I, X
comprises or consists of the sequence of Formula It:
X1 -X2-X3-C-X5-X6-W-X8-C-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (It) wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;

X5 is any amino acid;
X6 is any amino acid;
X8 is any amino acid;
X10 is Tyr, 1-Na!, 2-Na!, Phe[4-(2-aminoethoxy)], Phe(4-CONH2), Phe(4-0Me);
X11 is Trp, 1-Na!, 2-Na!, Bipõ Phe(3,4-0Me2) 5-Hydroxy-Trp,;
X12 is Arg, His, 3-Pal, Leu, Thr, Gln, Asn, Glu, Ile, Phe, Ser, Lys, hLeu, a-MeLeu, D-Leu, D-Asn, h-Leu, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer or a-MeVal;
X13 is Thr, Glu, Tyr, Lys, Gln, Asn, Lys, Lys (Ac), Asp, Arg, Ala, Ser, Leu;
X14 is Phe, Tyr, Asn, Gly, Ser, Met, Arg, His, Lys, Leu or Gln;
X15 is Gly, Ser, Arg, Leu, Asp, Ala, f3-Ala, Glu, Arg or Asn;
X16 is absent or any amino acid;
X17 is absent or any amino acid;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1002961In certain embodiments of It: X10 is Tyr, 1-Na! or 2-Na!; X11 is Trp, 1-Na!, 2-Na! or Bip; X12 is Arg, His, 3-Pal, Leu, Thr, Gln, Asn, Glu, Ile, Phe, Ser, Lys, hLeu, a-MeLeu, D-Leu, D-Asn, or h-Leu; X13 is Thr, Glu, Tyr, Lys, Gln, Asn, Lys, Asp, Arg, Ala, Ser, Leu; X15 is Gly, Ser, Arg, Leu, Asp or Ala; X16 is absent or Asn, Glu, Phe, Ala, Gly, Pro, Asp, Gln, Ser, Thr, D-Glu or Lys; and X17 is absent or Pro, Arg, Glu, Asp, Ser, Gly or Gln.
10029711n particular embodiments, X5 is Ser, Asp, Asn, Gln, Ala, Met, Arg, His or Gly. In particular embodiments, X5 is Ser, Asp, Gln, Ala, Met, Arg, His or Gly.

1002981 In particular embodiments, X6 is any Asp, Ser or Thr.
1002991 In particular embodiments, X8 is Gln, Glu or Thr.
[00300] In particular embodiments, the peptide of It is cyclized via a disulfide bond between X4 and X9.
1003011In a further embodiment, the present invention includes a peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Va):

(Va) wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any D-amino acid or absent;
X4 is Cys, hCys, Pen, hPen, Abu, Ser, hSer or chemical moiety capable of forming a bond with X9;
X5 is Ala, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn, Gln, Arg, Ser or Thr;
X6 is Thr, Ser, Asp, Ile or any amino acid;
X7 is Trp, 6-Chloro-Trp, 1-Nap or 2-Nap;
X8 is Glu, Gln, Asn, Lys(Ac), Cit, Cav, Lys(N-c-(N-a-Palmitoyl-L-y-glutamy1)), or Lys(N-c-Palmitoyl;
X9 is Cys, hCys, Pen, hPen Abu, or any amino acid or chemical moiety capable of forming a bond with X4;

X10 is 2-Na!, a Phe analog, Tyr, or a Tyr analog;
X11 is 1-Na!, 2-Na!, Phe(3,4-dimethoxy), 5-HydroxyTrp, Phe(3,4-C12), Trp or Tyr(3-tBu);
X12 is Aib, 4-amino-4-carboxy-tetrahydropyran, any alpha-methylamino acid, alpha-ethyl-amino acid, Achc, Acvc, Acbc Acpc, 4-amino-4-carboxy-piperidine, 3-Pal, Agp, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a- a-MeOrn, a-MeSer, a-MeVal, Cav, Cha, Cit, Cpa, D-Asn, Glu, His, hLeu, hArg, Lys, Leu, Octgly, Orn, piperidine, Arg, Ser, Thr or THP;
X13 is Lys(Ac), Gln, Cit, Glu, or any amino acid;
X14 is Asn, Gln, Lys(Ac), Cit, Cav, Lys(N-c-(N-a-Palmitoyl-L-y-glutamy1)), Lys(N-c-Palmitoy1), or any amino acid;
X15 is f3-Ala, Asn, Gly, Gln, Ala, Ser, Aib or Cit;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, wherein X4 and X9 are capable of forming a bond with each other. In particular embodiments, the bond is a ether, disulfide bond or a thioether bond. In certain embodiments, the peptide inhibitor is cyclized via the bond between X4 and X9.
1003021 In certain embodiments, X1 is a D-amino acid or absent. In certain embodiments, X2 is a D-amino acid or absent.
1003031In certain embodiments, X16 is a D-amino acid or absent. In certain embodiments, X17 is a D-amino acid or absent. In certain embodiments, X18 is a D-amino acid or absent. In certain embodiments, X19 is a D-amino acid or absent. In certain embodiments, X20 is a D-amino acid or absent.
10030411n particular embodiments of Formula (Ia), X10 is 2-Nal, Phe(3,4-diF2), Phe(3,4-C12), Phe(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)], Phe(Br), Phe(4-CONH2), Phe(C1), Phe(4-CN), Phe(4-guadino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Tyr, Tyr(Bz1), or Tyr(Me). In certain embodiments of Formula (Ia), X10 is Phe(4-ZR), Phe(3-ZR), oe Phe(2-ZR), where R= CH2(CH2).Y and n=1-25, Z=NH, 0, CO, CONH, or CH2, and Y=NH2, CO2H, OH, or CH3.
1003051ln a further related embodiments, the present invention includes a peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Vb):
X1 -X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Vb) wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is D-Arg, D-Phe, any D amino acid or absent;
X4 is Cys, hCys, Pen, hPen, Abu, or a chemical moiety capable of forming a bond with X9;
X5 is Gln, Asn, Lys(Ac), Cit, Cav, Lys(N-6-(N-a-Palmitoyl-L-y-glutamy1)), or Lys(N-c-Palmitoyl);
X6 is Thr, Ser, Asp, Ile or any amino acid;
X7 is Trp, 1-Nap or 2-Nap;
X8 is Gln, Asn, Lys(Ac), Cit, Cav, Lys(N-6-(N-a-Palmitoyl-L-y-glutamy1)), or Lys(N-c-Palmitoyl;

X9 is Cys, hCys, Pen, hPen, Abu, any amino acid or a chemical moiety capable of forming a bond with X4;
X10 is Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)], Phe(4-CONH2), Phe(4-guadino), Phe(4-NH2), Tyr(Me) or Phe(4-ZR), where R= CH2(CH2).Y; n=1-25; Z= 0, CO, NH, CONH, or CH2; and Y=NH2, CO2H, OH, or CH3, X11 is 2-Nal or Trp;
X12 is Aib, 4-amino-4-carboxy-tetrahydropyran, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, acid, Achc, Acvc, Acbc Acpc, or 4-amino-4-carboxy-piperidine;
X13 is Lys(Ac), Gln, Cit, Glu, or any amino acid;
X14 is Asn, Gln, Lys(Ac), Cit, Cav, Lys(N-6-(N-a-Palmitoyl-L-y-glutamy1)), Lys(N-c-Palmitoyl), or any amino acid;
X15 is f3-Ala, Asn, Gln, Ala, Ser, or Aib;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, wherein X4 and X9 are capable of forming a bond with each other. In particular embodiments, the bond is a disulfide bond or a thioether bond. In certain embodiments, the peptide inhibitor is cyclized via the bond between X4 and X9.
[00306] In certain embodiments, X1 is a D-amino acid or absent. In certain embodiments, X2 is a D-amino acid or absent.

1003071In certain embodiments, X16 is a D-amino acid or absent. In certain embodiments, X17 is a D-amino acid or absent. In certain embodiments, X18 is a D-amino acid or absent. In certain embodiments, X19 is a D-amino acid or absent. In certain embodiments, X20 is a D-amino acid or absent.
1003081In another related embodiment, the present invention includes a peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Vc):
X1 -X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Vc) wherein X1 is absent;
X2 is absent;
X3 is D-Arg or absent;
X4 is Cys, Pen, Abu, or a chemical moiety capable of forming a bond with X9;
X5 is Gln, Asn, Lys(Ac), Cit, or Cav;
X6 is Thr or Ser;
X7 is Trp, 1-Nap or 2-Nap;
X8 is Gln, Asn, Lys(Ac), Cit, or Cav;
X9 is Cys, hCys, Pen, hPen, Abu, or any amino acid or chemical moiety capable of forming a bond with X4;
X10 is Phe[4-(2-aminoethoxy)], Phe(4-CONH2) or Phe(4-0R) where R= CH2(CH2)õY;
n=1-25;
and Y=NH2, CO2H, OH, or CH3;
X11 is Trp or 2-Nal;

X12 is Aib, 4-amino-4-carboxy-tetrahydropyran, a-MeLys, a-MeLys(Ac), a-MeLeu, Achc, Acvc, Acbc or Acpc;
X13 is Lys(Ac) or Glu;
X14 is Asn, Gin, Lys(Ac), Lys(N-c-(N-a-Palmitoyl-L-y-glutamy1)), or Lys(N-c-Palmitoy1);
X15 is Gly, f3-Ala, Asn, Gin, Ala, Ser, or Aib;
X16 is absent;
X17 is absent;
X18 is absent;
X19 is absent; and X20 is absent, wherein X4 and X9 are capable of forming a bond with each other. In particular embodiments, the bond is a disulfide bond or a thioether bond. In certain embodiments, the peptide inhibitor is cyclized via the bond between X4 and X9.
[00309] In certain embodiments, X1 is a D-amino acid or absent. In certain embodiments, X2 is a D-amino acid or absent.
1003101In certain embodiments, X16 is a D-amino acid or absent. In certain embodiments, X17 is a D-amino acid or absent. In certain embodiments, X18 is a D-amino acid or absent. In certain embodiments, X19 is a D-amino acid or absent. In certain embodiments, X20 is a D-amino acid or absent.
1003111In another related embodiment, the present invention includes a peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Vd):
X1 -X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Vd) wherein X1 is absent;
X2 is absent;
X3 is absent;
X4 is Pen or Abu;
X5 is Gin or Asn;
X6 is Thr or Ser;
X7 is Trp;
X8 is Gin or Asn;
X9 is Pen or Cys;
X10 is Phe[4-(2-aminoethoxy)] or Phe(4-CONH2);
X11 is Trp or 2-Nal;
X12 is Aib, 4-amino-4-carboxy-tetrahydropyran, a-MeLys, a-MeLeu, or Achc;
X13 is Lys(Ac) or Glu;
X14 is Asn, Gin or Lys(Ac);
X15 is Gly, Ala, Ser, f3-Ala, Asn, or Gin;
X16 is absent;
X17 is absent;
X18 is absent;
X19 is absent; and X20 is absent, wherein X4 and X9 are capable of forming a bond with each other. In particular embodiments, the bond is a disulfide bond or a thioether bond. In certain embodiments, the peptide inhibitor is cyclized via the bond between X4 and X9.
[00312] Any of the peptide inhibitors of the present invention (e.g., any of those of Formula I
(e.g., Ix, Ia-It) may be further defined, e.g., as described below. It is understood that each of the further defining features described herein may be applied to any peptide inhibitors where the amino acids designated at particular positions allow the presence of the further defining feature.
[00313] In certain embodiments, any of the Phe[4-(2-aminoethoxy)] residues present in a peptide inhibitor may be substituted by Phe[4-(2-acetylaminoethoxy)].
1003141 In certain embodiments, X1 -X20 are any of the amino acids shown in the corresponding position relative to the cyclized Pen-Pen or cyclized Abu-Cys residues of the illustrative peptide inhibitors set forth in Tables 2-5.
1003151 In certain embodiments, any of the peptides inhibitors described herein, including but not limited to those of Formulas (X), (Va), (Vb), Vc), (Vd), (Ve), (Vf), (Vg) or (Vh), further comprises a linker or spacer moiety between any two amino acid residues of the peptide. In particular embodiments, the linker or spacer moiety is a PEG moiety.
[00316] In certain embodiments, the peptide inhibitor is cyclized by a disulphide bridge.
1003171In certain embodiments, X10 is Tyr, Phe[4-(2-aminoethoxy)], Phe(4-CONH2) or Phe(4-0Me). In certain embodiments, X10 is Tyr.
1003181In certain embodiments, X11 is 2-Nal, Trp, or 5-Hydroxy-Trp. In certain embodiments, X11 is Trp.
1003191In certain embodiments, X10 is Tyr or Phe[4-(2-aminoethoxy)], and X11 is Trp or 2-Nal.
In certain embodiments, X10 is Tyr and X11 is Trp.

[00320] In particular embodiments, X4 and X9 are both Cys.
[00321] In particular embodiments, X4 is Cys, Pen, hCys, or absent.
[00322] In particular embodiments, X7 and X11 are not both W.
[00323] In particular embodiments, X7 and X11 are both W.
1003241In particular embodiments, X7 and X11 are both W, X10 is Y, and X4 and X9 are both Cys.
1003251In particular embodiments, X15 is Gly, Asn, f3-ala or Ser. In particular embodiments, X15 is Gly or Ser.
[00326] In particular embodiments, X16 is AEA or AEP.
1003271In particular embodiments, X10 is Tyr, Phe or Phe[4-(2-aminoethoxy). In particular embodiments, X10 is Tyr or Phe.
[00328] In particular embodiments, X11 is Trp or 2-Nal. In particular embodiments, X11 is Trp.
[00329] In particular embodiments, Xi, X2 and X3 are absent.
[00330] In particular embodiments, X18, X19 and X20 are absent.
[00331] In particular embodiments, Xi, X2, X3, X18, X19 and X20 are absent.
[00332] In particular embodiments, one or more of Xi, X2 or X3 are present.
1003331In particular embodiments of any of Ix, la-Ir, one of Xi, X2 and X3 is present and the other two are absent. In one embodiment, the Xi, X2 or X3 present is Ala.
1003341In certain embodiments, X3 is present. In particular embodiments, X3 is Glu, (D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, (D)G1n. In certain embodiments, X3 is (D)Arg or (D)Phe. In particular embodiments, X1 and X2 are absent and X3 is present.

1003351 In particular embodiments, two of Xl, X2 and X3 are present and the other one is absent.
In certain embodiments, the two present consist of SG, NK, DA, PE, QV or DR.
1003361 In particular embodiments, Xl, X2 and X3 are present. In certain embodiments, Xl, X2 and X3 consist of ADQ, KEN, VQE, GEE, DGF, NAB, ERN, RVG, KAN, or YED.
1003371In certain embodiments, the peptide comprises an AEP residue. In particular embodiments, any of X15, X16, X17, X18, X19 or X20 is AEP.
1003381In certain embodiments of any of the peptide inhibitors or peptide monomer subunits, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, Lys(Ac), f3hAla, or Aib. In certain embodiments of any of the peptide inhibitors or peptide monomer subunits, X13 is Thr, Sarc, Glu, Phe, Arg, Leu, Lys, f3hAla, or Aib. In certain embodiments, X14 is Phe, Asn, Tyr, or f3hPhe.
In certain embodiments, X14 is Phe, Tyr, or f3hPhe. In certain embodiments, X15 is Gly, Asn Ser, Thr, Gln, Ala, or Sarc. In certain embodiments, X15 is Gly, Ser, Thr, Gln, Ala, or Sarc. In certain embodiments, X12 is alpha amino acid, e.g., 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, or a-MeVal.
1003391 In certain embodiments, X13 is present.
1003401 In certain embodiments, X13 and 14 are present.
[00341]In certain embodiments, X13, X14 and X15 are present.
1003421In particular embodiments of any one of Ia-It, one or more of X16-X20 are present. In particular embodiments, two or more or three or more of X16-X20 are present.
In particular embodiments, X18 is [(D)Lys]. In particular embodiments, X17 is absent, and X18 is [(D)Lys].
In certain embodiments wherein X4 and X9 are optionally Cys, X4 and X9 are Cys, X7 is Trp, and X18 is [(D)Lys]. In particular embodiments wherein X4 and X9 are optionally Cys, X4 and X9 are Cys, X7 is Trp, X10 is Tyr or Phe[4-(2-aminoethoxy)], and X18 is [(D)Lys]. In particular embodiments wherein X4 and X9 are optionally Cys, X4 and X9 are Cys, X7 is Trp, X10 is Tyr, and X18 is [(D)Lys]. In particular embodiments wherein X4 and X9 are optionally Cys, X4 and X9 are Cys, X7 is Trp, Xl, X2 and X3 are absent, X17 is absent, X18 is [(D)Lys], and X19 and X20 are absent. In particular embodiments of Ir, X4 and X9 are Cys, X7 and X11 are Trp, X10 is Tyr, and X18 is [(D)Lys. In certain embodiments, Xi, X2, and X3 are absent;
and in certain embodiments, X17 is absent.
1003431In certain embodiments, any of the peptide inhibitors (or monomer subunits) described herein is cyclized. In particular embodiments, the peptide inhibitor is cyclized via a bond between two or more internal amino acids of the peptide inhibitor. In particular embodiments, cyclized peptide inhibitors are not cyclized via a bond between the N-terminal and C-terminal amino acids of the peptide inhibitor. In certain embodiments, one of the amino acid residues participating in the intramolecular bond cyclizing the peptide in the amino terminal amino acid residue. In certain embodiments, any of the peptide inhibitors in cyclized via a peptide bond between its N-terminal amino acid and its C-terminal amino acid.
[00344] In certain embodiments of any of the peptide inhibitors, or one or both monomer subunits thereof, the peptide inhibitor (or one or both monomer subunit thereof) is cyclized via an intramolecular bond between X4 and X9 or by a triazole ring. In particular embodiments, the intramolecular bond is any disulfide bond, a thioether bond, a lactam bond, a triazole, a selenoether bond, a diselendide bond, or an olefin bond.
1003451 In one embodiment, X4 and X9 of the peptide inhibitor (or one or both monomer subunits thereof) are Cys, Pen, hCys, D-Pen, D-Cys or D-hCys, and the intramolecular bond is a disulfide bond. In certain embodiments, both X4 and X9 are Cys, or both X4 and X9 are Pen, and the intramolecular bond is a disulfide bond.
1003461 In one embodiment, X4 and X9 of the peptide inhibitor (or one or both monomer subunits thereof) are Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu or D-Lys, and the intramolecular bond is a lactam bond.
1003471In one embodiment, X4 is Abu, 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, or 3-chloro-isobutyric acid; X9 is Abu, Cys, Pen, hCys, D-Pen, D-Cys or D-hCys; and the intramolecular bond is a thioether bond. In certain embodiments, X4 is Abu and X9 is Pen, and the intramolecular bond is a thioether bond. In particular embodiments, X4 is a 2-methylbenzoyl moiety capable of forming a thioether bond with X9, and X9 is selected from Cys, N-Me-Cys, D-Cys, hCys, Pen, and D-Pen. In particular embodiments, X4 is Abu and X9 is Cys, and the intramolecular bond is a thioether bond. In particular instances, a peptide monomer, dimer, or subunit thereof of any of the Formulas and peptides described herein, X4 is selected from the group consisting of modified Ser, modified hSer (e.g., Homo-Ser-C1), a suitable isostere, and corresponding D-amino acids. In other instances, X4 is an aliphatic acid having from one to four carbons and forming a thioether bond with X9. In some instances, X4 is a five-or six-membered alicyclic acid having a modified 2-methyl group that forms a thioether bond with X9. In some embodiments, X4 is a 2-methylbenzoyl moiety. In certain embodiments, X4 is selected from Cys, hCys, Pen, and a 2-methylbenzoyl moiety. In certain embodiments, X4 is selected from the group consisting of a modified Ser, a modified hSer, a suitable isostere, and corresponding D-amino acids. In one embodiment, X4 is a hSerC1 (before the thioether bond is formed with X9 whereby the Cl is removed) or a hSer precursor (e.g., homoSer(0-TBDMS). In other instances, X4 is an aliphatic acid having from one to four carbons and forming a thioether bond with X9.
In some instances, X4 is a five- or six-membered alicyclic acid having a modified 2-methyl group that forms a thioether bond with X9. In some instances, X4 is a 2-methylbenzoyl moiety.
In certain embodiments wherein X4 is not an amino acid but is a chemical moiety that binds to X9, Xl, X2, and X3 are absent, and X4 is conjugated to or bound to X5. In some embodiments, the amino acid directly carboxyl to X9 is an aromatic amino acid. In certain embodiments, X4 is an amino acid, while in other embodiments, X4 is another chemical moiety capable of binding to X9, e.g., to form a thioether bond. In particular embodiments, X4 is another chemical moiety selected from any of the non-amino acid moieties described herein for X4. In particular embodiments wherein X4 is another chemical moiety, Xl, X2 and X3 are absent, and the another chemical moiety is bound to or conjugated to X5. In certain embodiments, X4 is defined as a chemical moiety including a group such as a chloride, e.g., in 2-chloromethylbenzoic acid, 2-chloro-acetic acid, 3-choropropanoic acid, 4-chlorobutyric acid, 3-chloroisobutyric acid.
However, the skilled artisan will appreciate that once the peptide has undergone ring closing cyclization to form a thioether bond between X4 and X9, the chloride group is no longer present.
The description of chemical moieties at X4 that include a reactant group such as chloride thus means both the group with the chloride and also the group without the chloride, i.e., after formation of the bond with X9. The present invention also includes peptides comprising the same structure as shown in any of the other formulas or tables described herein, but where the thioether bond is in the reverse orientation. In such embodiments of the invention, it may generally be considered that the amino acid residues or other chemical moieties shown at X4 are instead present at X9, and the amino acid residues shown at X9 are instead present at X4, i.e., the amino acid residue comprising the sulfur of the resulting thioether bond is located at X4 instead of X9, and the amino acid residue or other moiety having a carbon side chain capable of forming a thioether bond with X4 is located at X9. In this reverse orientation, however, the amino acid or chemical moiety at position X9 is one that comprises a free amine. For example, in particular embodiments, the amino acid at X9 is a protected homoserine, such as, e.g., homoserine (OTBDMS). Thus, in particular reverse orientation embodiments of peptide inhibitors of any of the formulas described herein, X9 is an amino acid residue having a side chain with one or two carbons, and forming a thioether bond with X4, and X4 is selected from the group consisting of Cys, N-Me-Cys, D-Cys, HCys, Pen, and D-Pen. Specific examples of amino acid residues and other chemical moieties present at corresponding positions of other formulas and tables are described herein.
[00348] One of skill in the art will appreciate that certain amino acids and other chemical moieties are modified when bound to another molecule. For example, an amino acid side chain may be modified when it forms an intramolecular bridge with another amino acid side chain, e.g., one or more hydrogen may be removed or replaced by the bond. In addition, when hSer-C1 binds to an amino acid such as Cys or Pen via a thioether bond, the Cl moiety is released.
Accordingly, as used herein, reference to an amino acid or modified amino acid, such as hSer-C1, present in a peptide dimer of the present invention (e.g., at position X4 or position X9) is meant to include the form of such amino acid or modified amino acid present in the peptide both before and after forming the intramolecular bond.
1003491In certain embodiments, the peptide inhibitor of the peptide inhibitor (or one or both monomer subunits thereof) is cyclized through a triazole ring. In certain embodiments, the peptide inhibitor of the peptide inhibitor (or one or both monomer subunits thereof) is linear or not cyclized. In certain embodiments of any of the peptide inhibitors described herein, including both monomer peptide inhibitors and dimer peptide inhibitors, one (or both) peptide monomer subunits comprise or consist of a cyclized peptide having a structure or sequence set forth in any of Ix, Ia, Ib, Ic, Id, Ie, If, Ig, Ih, Ti, Ij, Ik, Ti, Im, In, To, Ip, Iq, Iq', Tr, Is or It, IIa-IId, Illa-Ille, Iva, or IVb.
1003501In certain embodiments of any of the peptide inhibitors or monomer subunits, X7 and X11 are both W.
1003511In certain embodiments of any of the peptide inhibitors or monomer subunits, X7 and X11 are not both W. In particular embodiments, X7 is W and X11 is not W.
[00352] In certain embodiments of any of the peptide inhibitors or monomer subunits, X4 and X9 are amino acid residues capable of forming an intramolecular bond between each other that is a thioether bond, a lactam bond, a triazole, a selenoether, a diselenide bond, or an olefin bond.
1003531In certain embodiments, X7 and X11 are both W, X10 is Y, Phe[4-(2-aminoethoxy) or Phe(CONH2), and X4 and X9 are amino acid residues capable of forming an intramolecular bond between each other that is a thioether bond, a lactam bond, a triazole, a selenoether, a diselenide bond, or an olefin bond. In certain embodiments, X7 and X11 are both W, X10 is Y, and X4 and X9 are amino acid residues capable of forming an intramolecular bond between each other that is a thioether bond, a lactam bond, a triazole, a selenoether, a diselenide bond, or an olefin bond.
[00354] In certain embodiments, X7 and X11 are both W, X10 is Y, and X4 and X9 are both C.
1003551In certain embodiments, X4 and X9 are each Cys, Pen, hCys, D-Pen, D-Cys or D-hCys, and the intramolecular bond is a disulfide bond.
1003561In certain embodiments, X4 and X9 are each Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu or D-Lys, and the intramolecular bond is a lactam bond.
1003571In certain embodiments, X4 and X9 are each f3-azido-Ala-OH or propargylglycine, and the peptide inhibitor (or monomer subunit) is cyclized through a triazole ring.
1003581In certain embodiments, X4 and X9 are each 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, or 2-(5'-hexenyl)glycinem and the peptide inhibitor (or monomer subunit) is cyclized via ring closing methasis to give the corresponding olefin / "stapled peptide."

1003591In certain embodiments, X4 is 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, or hSer(C1); X9 is hSer(C1), Cys, Pen, hCys, D-Pen, D-Cys or D-hCys;
and the intramolecular bond is a thioether bond. In certain embodiments, X4 is chloromethylbenzoic acid or hSer(C1); X9 is Cys or Pen, and the intramolecular bond is a thioether bond. In certain embodiments, X4 is Abu, and X9 is Cys or Pen.
[00360] In certain embodiments, X4 is 2-chloromethylbenzoic acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, Abu or Sec;
X9 is Abu or Sec;
and the intramolecular bond is a selenoether bond.
10036111n certain embodiments, the intramolecular bond between X4 and X9 is a diselenide bond.
[00362] In certain embodiments of any of the peptide inhibitors described herein that contain two amino acid residues, e.g., cysteine residues, joined by an intramolecular bond, e.g., disulphide bond, the two amino acid residues participating in the intramolecular bond are not both located at either the N-terminal or C-terminal position of the peptide inhibitor. In certain embodiments, neither of the two amino acid residues, e.g., cysteines, particpating in the intramolecular bond is located at the N-terminal or C-terminal position of the peptide inhibitor. In other words, in certain embodiments, at least one, or both, of the two amino acid residues, e.g., cysteines, participating in the intramolecular bond are internal amino acid residues of the peptide inhibitor.
In certain embodiments, neither of the two amino acid resiudes, e.g., cysteines, participating in the intramolecular bond is located at the C-terminal position of the peptide inhibitor. At certain embodiment, the two amino acid residues participating in the intramolecular bond are Cys, Pen, hCys, D-Pen, D-Cys or D-hCys residues. In certain embodiments, the two amino acid residues participating in the intramolecular bond are located at X4 and X9. In one embodiment, there is a disulfide bond between the amino acid resiudes, e.g., cysteines or Pen residues, at X4 and X9. In particular embodiments, both X4 and X9 are Pen. In certain embodiments, one or both peptide monomer subunits in the peptide inhibitor is cyclized via a disulfide bond between two Pen residues, e.g., at positions X4 and X9.

1003631In particular embodiments of any of the peptide inhibitors described herein, one or both peptide monomer subunits present in the peptide inhibitor, whether it is a monomer or a dimer, is cyclic or cyclized, e.g., by an intramolecular bond, such as a disulfide bond, between two cysteine residues present in the peptide monomer or peptide monomer subunit.
In certain embodiments, a peptide inhibitor comprises two or more cysteine residues. In some embodiments, the peptide inhibitor is cyclized via an intramolecular disulfide bond between the two cysteine residues. In particular embodiments of peptide inhibitors having any of the Formulas described herein, the two cysteines occur at positions X4 and X9. In other embodiments, one or both peptide monomer subunits in the peptide inhibitor is cyclized via a disulfide bond between two Pen residues, e.g., at positions X4 and X9.
1003641In some embodiments, a peptide inhibitor has a structure of any of the Formulas described herein (e.g., Formula I) and comprises a disulfide bond, e.g., an intramolecular disulfide bond, or a thioether bond. Illustrative examples of such peptide inhibitors are shown in Tables 3A-3H and 4A, 4B, 9, 11 or 15. Such disulfide bonded peptides may have a particular advantage in that the disulfide bonds enhance structural stability and can improve biological activity of many bioactive peptides. However, in certain situations, these bonds are labile to reducing agents. One of skill in the art will appreciate that disulfide is amenable to simple isosteric replacement. Illustrative examples of such replacements include, but are not limited to, thioethers, dithioethers, selenoethers, diselenides, triazoles, lacatams, alkane and alkene groups.
Accordingly, in certain embodiments of any of the peptide inhibitors described herein, one, two or more cysteine residues are substitued, e.g., with a thioether, dithioether, selenoether, diselenide, triazoles, lacatam, alkane or alkene group, including but not limited to any of those shown below or described herein. In particular embodiments, two of these substituted groups form a bond (e.g., an intramolecular bond), thus cyclizing the peptide inhibitor or one or both monomer subunits thereof.
1003651ln certain embodiments, a peptide inhibitor of the present invention comprises or consists of an amino acid sequence shown herein, e.g., in any one of Tables 3A-3H, 4A, 4B, 5A-5C, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15. In certain embodiments, a peptide inhibitor of the present invention has a structure shown herein, e.g., in any one of Tables 3A-3H, 4A, 4B, 5A-5C, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15.

1003661 In certain embodiments, the present invention includes a peptide inhibitor that comprises a core consensus sequence selected from one of the following (shown in N-terminal to C-terminal direction):
X1X2X2WX2X1X2W;
X1X2X2WX2X1X2 (1-Nal);
X1X2X2WX2X1X2 (2-Nal);
X1X2X2WX2X1YVV;
X iX2X2WX2X1Y(1 -Nal);
X1X2X2WX2X1Y(2-Nal);
X1X2X2WX2X1X2X2;
X1X2X2WX2X1X2X2X2X2X2-[(D)Lys];
X1X2X2WX2X1X3X2;
X1X2X2WX2X1X3 (1-Nal); and X iX2X2WX2X iX3(2-Nal) .
[00367] wherein W is tryptophan, Y is tyrosine, each the two X1 residues are amino acids or other chemical moieties capable of forming an intramolecular bond with each other;
each X2 is independently selected from all amino acids, which include, e.g., natural amino acids, L-amino acids, D-amino acids, non-natural amino acids, and unnatural amino acids; and X3 is any amino acid. In particular embodiments, X3 is Phe, a Phe analog (e.g., Phe[4-(2-aminoethoxy)] or Phe(4-CONH2)), Tyr, or a Tyr analog (e.g., Tyr(Me)). In particular embodiments, each X1 is selected from Cys, Pen and Abu. In particular embodiments, each X1 is Cys. In certain embodiments, each X1 is Pen. In certain embodiments, one X1 is Cys and the other X1 is Abu.
In particular embodiments, the N-terminal X1 is Abu and the C-terminal X1 is Cys. In particular embodiments, the N-terminal X1 is Cys and the C-terminal X1 is Abu. In particular embodiments, the residues between the two X1 residues are Gln, Thr, Trp and Gln. In particular embodiments, each X1 is selected from Cys, Pen and Abu; and X3 is Phe, a Phe analog (e.g., Phe[4-(2-aminoethoxy)] or Phe(4-carbomide)), Tyr, or a Tyr analog (e.g., Tyr(Me)). In particular embodiments, X3 is a Phe analog.

1003681In certain embodiments, peptide inhibitors of the present invention comprises any of the following consensus sequences, wherein X1 , X2, X3, X4, X5, X6, X7, X8, X9, X10, X11, X12, X13, X14 and X15 are defined as shown in any of the various Formula or peptide inhibitors described herein:
X1 -X2-X3-Pen-X5-X6-W-X8-Pen-X10-X11-X12-X13-X14-X15;
Pen-X5-X6-W-Q-Pen;
Pen-X5-X6-W-X8-Pen;
Pen-X5-X6-W-X8-Pen-[Phe(4-CONH2)];
Pen-X5-X6-W-X8-Pen-[Phe[4-(2-aminoethoxy)]];
X1 -X2-X3-Abu-X5-X6-W-X8-C-X9-X10-X11-X12-X13-X14-X15;
Abu-X5-X6-W-Q-C;
Abu-X5-X6-W-X8-C;
Abu-X5-X6-W-X8-C-[Phe(4-CONH2)]; or Abu-X5-X6-W-X8-C-[Phe[4-(2-aminoethoxy)]].
1003691In certain embodiments of any of the peptide inhibitors or monomer subunits, X7 and X11 are both W. In certain embodiments of any of the peptide inhibitors, X7 and X11 are both W, and X10 is Y. In certain embodiments, X7 and X11 are both W and X10 is Phe[4-(2-aminoethoxy)] or Phe(4-0Me) .
1003701In certain embodiments of any of the peptide inhibitors or monomer subunits, X7 and X11 are not both W.
1003711In certain embodiments of peptide inhibitors of Formula I, X4 and X9 are each Pen, and the intramolecular bond is a disulfide bond.

[00372] In certain embodiments, a peptide inhibitor of the present invention comprises or consists of an amino acid sequence shown in any one of the tables, sequence listing or the accompanying figures herein.
[00373] In certain embodiments of any of the peptide inhibitors described herein that contain two amino acid residues, e.g., Pen residues, joined by an intramolecular bond, e.g., disulphide bond, one or both of the two amino acid residues participating in the intramolecular bond are not located at either the N-terminal or C-terminal position of the peptide inhibitor. In certain embodiments, neither of the two amino acid residues, e.g., Pen, particpating in the intramolecular bond is located at the N-terminal or C-terminal position of the peptide inhibitor. In other words, in certain embodiments, at least one, or both, of the two amino acid residues, e.g., Pens, participating in the intramolecular bond are internal amino acid residues of the peptide inhibitor.
In certain embodiments, neither of the two amino acid residues, e.g., Pens, participating in the intramolecular bond is located at the C-terminal position of the peptide inhibitor.
1003741In some embodiments, wherein a peptide of the invention is conjugated to an acidic compound such as, e.g., isovaleric acid, isobutyric acid, valeric acid, and the like, the presence of such a conjugation is referenced in the acid form. So, for example, but not to be limited in any way, instead of indicating a conjugation of isovaleric acid to a peptide by referencing isovaleroyl (e.g., is ovaleroyl- [Pen]-QTWQ [Pen] - [Phe(4-0Me)]- [2-Nal] - [a-MeLys]-[Lys(Ac)]-NG-NH2 in some embodiments, the present application references such a conjugation as isovaleric acid-[Pen]- Q TWQ [Pen] - [Phe(4-0Me)] - [2-Nal] - [a-MeLys] - [Lys(Ac)]-NG-NH2.
1003751 The present invention further includes peptide inhibitors that selectively bind to an epitope or binding domain present within amino acid residues 230 ¨ 349 of the human IL23R
protein. In particular embodiments, the peptide inhibitor binds human IL23R
and not mouse IL-23R. In certain embodiments, the peptide inhibitor also binds to rat IL-23R.
[00376] In certain embodiments of peptide inhibitors of Formula I, X4 is Abu;
X9 is Cys, Pen, homocys, and the intramolecular bond is a thioether bond.
1003771In certain embodiments, peptide inhibitors do not include compounds, disclosed in PCT
Application No. PCT/U52014/030352 or PCT Application No. PCT/U52015/038370.

Illustrative Peptide Inhibitors Comprising Pen-Pen Disulfide Bonds 1003781In certain embodiments, the present invention includes a peptide inhibitor of an interleukin-23 receptor, wherein the peptide inhibitor has the structure of Formula II:
R1-X-R2 (II) [00379] or a pharmaceutically acceptable salt or solvate thereof, wherein Rl is a bond, hydrogen, a C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl, a C1-C6 alkyl, a C1-C20 alkanoyl, an alkylsulphonate, an acid, y-Glu or pG1u, appended to the N-terminus, and including PEGylated versions (e.g., 200 Da to 60,000 Da), alone or as a spacer of any of the foregoing;
[00380]R2 is a bond, OH or NH2; and 1003811X is an amino acid sequence of 8 to 20 amino acids or 8 to 35 amino acids.
1003821In particular embodiments of peptide inhibitor of Formula II, X
comprises or consists of the sequence of Formula Ha:
X1 -X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Ha) wherein X1 is absent or any amino acid;
X2 is absent or any amino acid;
X3 is absent or any amino acid;
X4 is Pen, Cys or homo-Cys;
X5 is any amino acid;
X6 is any amino acid;
X7 is Trp, Bip, Gln, His, Glu(Bz1), 4-Phenylbenzylalanine, Tic, Phe[4-(2-aminoethoxy)], Phe(3,4-C12), Phe(4-0Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-Me-Trp, 1,2,3,4 -tetrahydro-norharman, Phe(4-CO2H), Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(4-CF3), Phe(4-tBu), f3f3-diPheAla, Glu, Gly, Ile, Asn, Pro, Arg, Thr or Octgly, or a corresponding a-methyl amino acid form of any of the foregoing;
X8 is any amino acid;

X9 is Pen, Cys or hCys;
X10 is 1-Na!, 2-Na!, Aic, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, Phe, His, Trp, Thr, Tic, Tyr, 4-pyridylAla, Octgly, a Phe analog or a Tyr analog (optionally, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), or Phe(4-OBz1)), or a corresponding a-methyl amino acid form of any of the foregoing;
X11 is 2-Na!, 1-Na!, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe (3,4-F2), Phe(4-CO2H), f3hPhe(4-F), a-Me-Trp, 4-phenylcyclohexyl, Phe(4-CF3), a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Trp, Tyr, Phe(4-0Me), Phe(4-Me), Trp(2,5,7-tri-tert-Butyl), Phe(4-0ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino, Phe(4-0Bz1), Octgly, Glu(Bz1), 4-Phenylbenzylalanine, Phe[4-(2-aminoethoxy)], 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, 1,2,3,4-tetrahydro-norharman, Phe(4-CONH2), Phe(3,4-0Me2) Phe(2,3-C12), Phe(2,3-F2), Phe(4-F), 4-phenylcyclohexylalanine or Bip, or a corresponding a-methyl amino acid form of any of the foregoing;
X12 is a-MeLys, a-MeOrn, a-MeLeu, a-MeVal, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, MeLeu, Aib, (D)Ala, (D)Asn, (D)Leu, (D)Asp, (D)Phe, (D)Thr, 3-Pal, Aib, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, hArg, hLeu, Ile, Lys, Leu, Asn, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Arg, Ser, Thr or Tle, or a corresponding a-methyl amino acid form of any of the foregoing;
X13 is Lys(Ac), (D)Asn, (D)Leu, (D)Thr, (D)Phe, Ala, Aib, a-MeLeu, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Lys, Arg, Orn, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, Lys, Leu, Asn, Ogl, Pro, Gln, Asp, Arg, Ser, spiro-pip, Thr, Tba, Tlc, Val or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing;
X14 is Asn, Glu, Phe, Gly, His, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Tic or Tyr, Lys(Ac), Orn or a corresponding a-methyl amino acid form of any of the foregoing;
X15 is Gly, (D)Ala, (D)Asn, (D)Asp, Asn, (D)Leu, (D)Phe, (D)Thr, Ala, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gln, Arg or Ser, f3-Ala, Arg or a corresponding a-methyl amino acid form of any of the foregoing;
X16 is absent, Gly, Ala, Asp, Ser, Pro, Asn or Thr, or a corresponding a-methyl amino acid form of any of the foregoing;

X17 is absent, Glu, Ser, Gly or Gin, or a corresponding a-methyl amino acid form of any of the foregoing;
X18 is absent or any amino acid;
X19 is absent or any amino acid; and X20 is absent or any amino acid.
1003831In certain embodiments of Ha: X10 is 1-Nal, 2-Nal, Aic, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, Phe, His, Trp, Thr, Tic, Tyr, 4-pyridylAla, Octgly, a Phe analog or a Tyr analog, or a corresponding a-methyl amino acid form of any of the foregoing; X11 is 2-Nal, 1-Nal, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe (3,4-F2), Phe(4-CO2H), f3hPhe(4-F), a-Me-Trp, 4-phenylcyclohexyl, Phe(4-CF3), a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Trp, Tyr, Phe(4-0Me), Phe(4-Me), Trp(2,5,7-tri-tert-Butyl), Phe(4-0ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino, Phe(4-0Bz1), Octgly, Glu(Bz1), 4-Phenylbenzylalanine, Phe[4-(2-aminoethoxy)], 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, 1,2,3,4-tetrahydro-norharman, Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(2,3-C12), Phe(2,3-F2), Phe(4-F), 4-phenylcyclohexylalanine or Bip, or a corresponding a-methyl amino acid form of any of the foregoing; X12 is a-MeLys, a-MeOrn, a-MeLeu, MeLeu, Aib, (D)Ala, (D)Asn, (D)Leu, (D)Asp, (D)Phe, (D)Thr, 3-Pal, Aib, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, hArg, hLeu, Ile, Lys, Leu, Asn, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gin, Arg, Ser, Thr or Tie, or a corresponding a-methyl amino acid form of any of the foregoing; X13 is Lys(Ac), (D)Asn, (D)Leu, (D)Thr, (D)Phe, Ala, Aib, a-MeLeu, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Lys, Arg, Orn, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, Lys, Leu, Asn, Ogl, Pro, Gin, Asp, Arg, Ser, spiro-pip, Thr, Tba, Tic, Val or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing;
X14 is Asn, Glu, Phe, Gly, His, Lys, Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr, Tic or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing; and X15 is Gly, (D)Ala, (D)Asn, (D)Asp, Asn, (D)Leu, (D)Phe, (D)Thr, Ala, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gin, Arg or Ser, or a corresponding a-methyl amino acid form of any of the foregoing.

1003841In certain embodiments, X3 is present. In particular embodiments, X3 is Glu,(D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Na!, Thr, Leu, (D)Gln. In certain embodiments, X3 is (D)Arg or (D)Phe. In particular embodiments, X1 and X2 are absent and X3 is present.
1003851In certain embodiments, X5 is Gln, Ala, Cit, Asp, Dab, Dap, Cit Glu, Phe, Gly, His, hCys, Lys, Leu, Met, Asn, N-Me-Ala, N-Me-Asn, N-Me-Lys, a¨Me-Lys, a¨Me-Orn, N-Me-Gln, N-Me-Arg, a-MeSer, Orn, Pro, Arg, Ser, Thr, or Val. In certain embodiments, X5 is Gln, Ala, Cit, Asp, Dab, Dap, Glu, Phe, Gly, His, hCys, Lys, Leu, Met, Asn, N-Me-Ala, N-Me-Asn, N-Me-Lys, aMe-Lys, aMe-Orn, N-Me-Gln, N-Me-Arg, Orn, Pro, Arg, Ser, Thr, or Val. In certain embodiments, X5 is Gln or Asn.
[00386] In certain embodiments, X6 is Thr, Asp, Glu, Phe, Asn, Pro, Arg, or Ser.
[00387] In certain embodiments, X7 is Trp.
[00388] In certain embodiments, X8 is Gln, Glu, Phe, Lys, Asn, Pro, Arg, Val, Thr, or Trp.
[00389] In certain embodiments, X10 is a Tyr analog or a Phe analog. In particular embodiments, X10 is a Phe analog.
1003901In certain embodiments wherein X10 is a Phe analog, X10 is selected from hPhe, Phe(4-0Me), a-Me-Phe, hPhe(3,4-dimethoxy), Phe(4-CONH2), Phe(4-phenoxy), Phe(4-guanadino), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-0Bz1), Phe(4-NH2), Phe(4-F), Phe(3,5 DiF), Phe(CH2CO2H), Phe(penta-F), Phe(3,4-C12), Phe(4-CF3), f33-diPheAla, Phe(4-N3) and Phe[4-(2-aminoethoxy)]. In particular embodiments, X10 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)]. In particular embodiments, X10 is Phe(4-0Me), Phe(4-CONH2) or Phe[4-(2-aminoethoxy)]. In certain embodiments where X10 wherein X10 is a Phe analog, X10 is selected from hPhe, Phe(4-0Me), a-Me-Phe, hPhe(3,4-dimethoxy), Phe(4-CONH2), Phe(4-phenoxy), Phe(4-guanadino), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-0Bz1), Phe(4-NH2), Phe(4-F), Phe(3,5 DiF), Phe(CH2CO2H), Phe(penta-F), Phe(3,4-C12), Phe(4-CF3), f33-diPheAla, Phe(4-N3) and Phe[4-(2-aminoethoxy)]. In particular embodiments, X10 is Phe(4-0Me).
10039111n certain embodiments where X10 is a Tyr analog, X10 is selected from hTyr, a-MeTyr, N-Me-Tyr, Tyr(3-tBu), Phe(4-CONH2), Phe[4-(2-aminoethoxy)], and bhTyr. In certain embodiments where X10 is a Tyr analog, X10 is selected from hTyr, a-MeTyr, N-Me-Tyr, Tyr(3-tBu), and bhTyr.
1003921In certain embodiments, X10 is Tyr, Phe(4-0Me), Phe[4-(2-aminoethoxy)], Phe(4-CONH2), or 2-Nal. In certain embodiments, X10 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)]. In certain embodiments, X10 is not Tyr.
In certain embodiments, X11 is a Trp analog. In particular embodiments, X11 is 2-Nal or 1-Nal.
In certain embodiments, X11 is 2-Nal.
[00393] In certain embodiments, X12 is Aib, a-MeLys or a¨MeLeu.
[00394] In particular embodiments of a peptide inhibitor of Formula II, one or both of X4 or X9 is Pen. In particular embodiments, both X4 and X9 are Pen.
1003951In certain embodiments, the peptide inhibitor of Formula II is cyclized. In particular embodiments, the peptide inhibitor of Formula II is cyclized via an intramolecular bond between X4 and X9. In particular embodiments, the intramolecular bond is a disulfide bond. In particular embodiments, X4 and X9 are both Pen.
1003961In certain embodiments, the peptide inhibitor of Formula II is linear or not cyclized. In particular embodiments of the linear peptide inhibitor of Formula I, X4 and/or X9 are any amino acid.
[00397] In particular embodiments of a peptide inhibitor of Formula II, one or more, two or more, or all three of Xi, X2, and X3 are absent. In certain embodiments, X1 is absent. In certain embodiments, X1 and X2 are absent. In certain embodiments, Xi, X2 and X3 are absent.
[00398] In particular embodiments of a peptide inhibitor of Formula II, one or more, two or more, three or more, four or more, or all of X16, X17, X18, X19 and X20 are absent.
In particular embodiments of a peptide inhibitor of Formula I, one or more, two or more, three or more, or all of X17, X18, X19 and X20 are absent. In certain embodiments, one or more, two or more, or all three of X17, X19 and X20 are absent. In certain embodiments, one or more of Xi, X2 and X3 are absent; and one or more, two or more, three or more, or four of X17, X18, X19 and X20 are absent.
[00399] In particular embodiments of a peptide inhibitor of Formula II, X18 is (D)-Lys. In certain embodiments, X18 is (D)-Lys and X17 is absent.
1004001In particular embodiments of a peptide inhibitor of Formula II, the peptide inhibitor comprises one or more, two or more, three or more, or four of the following features: X5 is Asn, Arg or Gln; X6 is Thr; X7 is Trp; and X8 is Gln. In particular embodiments of a peptide inhibitor of Formula I, X4 is Pen; X5 is Gln, Asn or Arg; X6 is Thr; X7 is Trp, 5-hydroxy-Trp, 6-chloro-Trp, N-MeTrp, alpha-Me-Trp, or 1,2,3,4-tetrahydro-norharman; X8 is Gln; and X9 is Pen. In particular embodiments, X5 is Gln. In certain embodiments, Xl, X2 and X3 are absent. In particular embodiments, both X4 and X9 are Pen.
1004011In particular embodiments of a peptide inhibitor of Formula II, the peptide inhibitor comprises one or more, two or more, three or more, four or more, five or more, six or more, or seven of the following features: X10 is Tyr, a Phe analog, a Tyr analog or 2-Nal; X11 is Trp, 5-hydroxy-Trp, 6-chloro-Trp, N-MeTrp, alpha-Me-Trp, 1,2,3,4-tetrahydro-norharman, 2-Nal or 1-Nal; X12 is Aib, a-MeLys, a-MeOrn and a-MeLeu; X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is Gly, Ser or Ala; and X16 is absent or AEA. In certain embodiments, X10 is Tyr, Phe(4-0Me), Phe[4-(2-aminoethoxy)], Phe(CONH2), or 2-Nal. In certain embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, X10 is not Tyr. In certain embodiments, Xl, X2 and X3 are absent. In particular embodiments, both X4 and X9 are Pen.
1004021In particular embodiments of a peptide inhibitor of Formula II, the peptide inhibitor comprises one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, or eleven of the following features: X5 is Arg or Gln; X6 is Thr; X7 is Trp; X8 is Gln; X10 is a Phe analog; X11 is Trp, 2-Nal or 1-Nal;
X12 is Aib, a-MeLys or a-MeOrn; X13 is Lys, Glu or Lys(Ac); X14 is Asn; X15 is Gly, Ser or Ala; and X16 is absent or AEA. In certain embodiments, X10 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)]. In certain embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, Xl, X2 and X3 are absent. In particular embodiments, both X4 and X9 are Pen.

[00403] In particular embodiments of a peptide inhibitor of Formula II, the peptide is cyclized via X4 and X9; X4 and X9 are Pen; X5 is Gln; X6 is Thr; X7 is Trp; X8 is Gln; X10 is Tyr, a Phe analog or 2-Nal; X11 is Trp, 2-Nal or 1-Nal; X12 is Arg, a¨MeLys, a-MeOrn, or a-MeLeu;
X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is Gly, Ser or Ala; and X16 is absent. In certain embodiments, X10 is Tyr, Phe(4-0Me), Phe[4-(2-aminoethoxy)], Phe(4-0Me) or 2-Nal.
In certain embodiments, X10 is Phe(4-0Me). In certain embodiments, X10 is not Tyr. In certain embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, X1 , X2 and X3 are absent.
1004041 In particular embodiments of a peptide inhibitor of Formula II, the peptide is cyclized via X4 and X9; X4 and X9 are Pen; X5 is Gln; X6 is Thr; X7 is Trp; X8 is Gln; X10 is Tyr, Phe(4-OMe) or 2-Nal; X11 is Trp, 2-Nal or 1-Nal; X12 is Arg, a-MeLys or a-MeOrn; X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is Gly; and X16 is absent. In certain embodiments, X10 is Phe(4-0Me). In certain embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, Xi, X2 and X3 are absent.
1004051 In particular embodiments of a peptide inhibitor of Formula II, the peptide is cyclized via X4 and X9; X4 and X9 are Pen; X5 is Gln; X6 is Thr; X7 is Trp; X8 is Gln; X10 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)]; X11 is Trp, 2-Nal or 1-Nal; X12 is a¨MeLys, a-MeOrn, or a-MeLeu; X13 is Lys, Glu or Lys(Ac); X14 is Asn; X15 is Gly, Ser or Ala; and X16 is absent. In certain embodiments, X10 is Phe(4-0Me). In certain embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, Xi, X2 and X3 are absent.
[00406] In particular embodiments of a peptide inhibitor of Formula II, X10 is not Tyr.
1004071In certain embodiments, the present invention includes a peptide, optionally 8 to 35, 8 to 20, 8 to 16 or 8 to 12 amino acids in length, optionally cyclized, comprising or consisting of having a core sequence of Formula IIb:
Pen-Xaa5-Xaa6-Trp-Xaa8-Pen-Xaa10- [(2-Nal)] (II13) [00408] wherein Xaa5, Xaa6 and Xaa8 are any amino acid residue; and Xaal 0 is a Phe analogue, wherein the peptide inhibits binding of IL-23 to IL-23R. In particular embodiments, X10 is a Phe analog selected from a¨Me-Phe, Phe(4-0Me), Phe(4-0Bz1), Phe(4-0Me), Phe(4-CONH2), Phe(3,4-C12), Phe(4-tBu), Phe(4-NH2), Phe(4-Br), Phe(4-CN), Phe(4-CO2H), Phe[4-(2-aminoethoxy)] or Phe(4-guanadino). In particular embodiments, Xaal 0 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)]. In one embodiment, Xaal 0 is Phe(4-0Me). In certain embodiments, the peptide is cyclized via an intramolecular bond between Pen at Xaa4 and Pen at Xaa9. In particular embodiments, the peptide is a peptide inhibitor of Formula II, and wherein in certain embodiments, Xl, X2 and X3 are absent. In particular embodiments, the peptide inhibits the binding of IL-23 to IL-23R. In certain embodiments, a peptide of Formula IIb further comprises an amino acid bound to the N-terminal Pen residue. In particular embodiments, the bound amino acid is Glu,(D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, or (D)G1n. In certain embodiments, it is is (D)Arg or (D)Phe.
1004091In certain embodiments, the present invention includes a peptide, optionally 8 to 35, 8 to 20, 8 to 16, or 8 to 12 amino acids in length, optionally cyclized, comprising or consisting of a core sequence of Formula IIc:
Pen-Xaa5-Xaa6-Trp-Xaa8-Pen-Xaa10- [(2-Nal)] (IIc) 1004101 wherein Xaa5, Xaa6 and Xaa8 are any amino acid residue; and Xaal 0 is Tyr, a Phe analog, a-Me-Tyr, a-Me-Trp or 2-Nal, wherein the peptide inhibits binding of IL-23 to IL-23R.
In certain embodiments, X10 is Tyr, Phe(4-0Me), Phe[4-(2-aminoethoxy)], a-Me-Tyr, a¨Me-Phe, a-Me-Trp or 2-Nal. In certain embodiments, Xaal 0 is Tyr, Phe(4-0Me), Phe(CONH2), Phe[4-(2-aminoethoxy)] or 2-Nal. In certain embodiments, Xaal 0 is Tyr, Phe(4-0Me), Phe[4-(2-aminoethoxy)] or 2-Nal. In particular embodiments, Xaal 0 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)]. In one embodiment, Xaal 0 is Phe[4-(2-aminoethoxy)] or Phe(CONH2). In particular embodiments, Xaal 0 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)]. In one embodiment, Xaal 0 is Phe[4-(2-aminoethoxy)]. In certain embodiments, Xaal 0 is not Tyr.
In certain embodiments, the peptide is cyclized via an intramolecular bond between Pen at Xaa4 and Pen at Xaa9. In particular embodiments, the peptide is a peptide inhibitor of Formula II, and wherein in certain embodiments, Xl, X2 and X3 are absent. In particular embodiments, the peptide inhibits the binding of IL-23 to IL-23R. In certain embodiments, a peptide of Formula IIc further comprises an amino acid bound to the N-terminal Pen residue. In particular embodiments, the bound amino acid is Glu,(D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Na!, Thr, Leu, or (D)G1n. In certain embodiments, it is is (D)Arg or (D)Phe.
10041111n certain embodiments, the present invention includes a peptide, optionally 8 to 35, 8 to 20, 8 to 16 or 8 to 12 amino acids in length, optionally cyclized, comprising or consisting of a core sequence of Formula lid:
Pen-Xaa5-Xaa6-Trp-Xaa8-Pen- Phe [4 -(2 -aminoethoxy)] - [2-Na!] (lid) [00412] wherein Xaa5, Xaa6 and Xaa8 are any amino acid residue. In certain embodiments, the peptide comprises a disulfide bond between Xaa4 and Xaa9. In certain embodiments, the peptide is a peptide inhibitor of Formula I, and wherein in certain embodiments, X1 , X2 and X3 are absent. In particular embodiments, the peptide inhibits the binding of IL-23 to IL-23R. In certain embodiments, a peptide of Formula lid further comprises an amino acid bound to the N-terminal Pen residue. In particular embodiments, the bound amino acid is Glu,(D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Na!, Thr, Leu, or (D)G1n. In certain embodiments, it is is (D)Arg or (D)Phe.
[00413] In particular embodiments of a peptide inhibitor of Formula II, the peptide inhibitor has a structure shown in any of Tables 2, 3, 4A, 4B, 8, 11 or 15 or comprises an amino acid sequence set forth in Tables 2, 3, 4A, 4B, 8, 11 or 15.
Table 2. Illustrative Di-Pen Inhibitors [Palm]-[isoGluHPEG4HPenl-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(PEG4-isoGlu-Palm)]-Ac-[Per]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(Ac)HLys(Ac)]-NN-NH2 [Octanyl]-[lsoGluHPEG4HPerd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-NH2 [Octany1]-[PEG4HPerd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-[Palm]-[PEG4HPenl-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-N

Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(PEG4-Octany1)]-NN-Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(PEG4-Palm)]-NN-N

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-Palm)H2-NalHAibHLys(Ac)1NN-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-Lauryl)H2-NalHAibHLys(Ac)]-NN-Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal[a-MeLys(PEG4-Palm)-[Lys(Ac)]-NN-N H2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal[a-MeLys(PEG4-Lauryl)HLys(Ac)]-NN-NH2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-lsoGlu-Palm)H2-NalHAibHLys(Ac)]-NN-NH2 Ac-[Pen]-NTWQ-[Pen]- [Phe[4-(2-arninoethoxy)-(PEG4-IsoGLu-Lauryl)H2-NalHAibHLys(Ac)]-NN-NH2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(PEG4-IsoGlu-Palm)HLys(Ac)]-Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-a-Me-K(PEG4-IsoGlu-Lauryl)HLys(Ac)]-Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(IVA)HLys(Ac)]-NN-NH2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(Biotin)HLys(Ac)]-NN-NH2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[a-MeLys(Octanyl)HLys(Ac)]-NN-N H2 Ac-[Pen]Lys(IVA)]-TWQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-NN-N

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)HLys(IVA)1-N-N

Ac-[Pen]- [Lys(Biotin)l-TWQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)]-Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)HLys(Biotin)]-N-Ac-[Pen]-[Lys(octany1)]-TWQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)]-Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)HLys(octany1)]-Ac-[Pen]-[Lys(Palm)]-TWQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-Nall--[Aib]-[Lys(Ac)]-NN-N H2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)]-Lys(Palm)]-N-Ac-[Pen]- [Lys(PEG8)1-TWQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-NN-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)HLys(PEG8)]-N-NH2 Ac-[Pen]-K(Pegll-Palm)TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall--[Aib]-[Lys(Ac)HLys(Pegll-palm)]-N-NH2 Ac-[Pen]-[Citl-TW-[Cit]-[PenHPhe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-Ac-[Pen]-[Lys(Ac)]-TW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-NN-NH2 Ac-[Pen]-NT-[Phe(3,4-0CH3)2]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-NH2 Ac-[Pen]-NT-[Phe(2,4-CH3)2]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-NN-NH2 Ac-[Pen]-NT-[Phe(3-CH3)]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall--[Aib]-[Lys(Ac)]-NN-NH2 Ac-[Penl-NT-[Phe(4-CH3)]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-Ac[(D)Arg]-[Penl-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall--[Aib]-[Lys(Ac)]-N-[13Ala]-NH2 Ac-[(D)Tyr]-[Pen]-NTWQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)]-N-[13Ala]-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-QN-NH2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibHLys(Ac)HLys(Ac)]-N-N H2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)H2-NalHAibHLys(Ac)]-N-[Lys(Ac)]-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibHLys(Ac)]-QQ-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)H2-NalHAibHLys(Ac)1-Q-U3Alal-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)]-N-[Cit]-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)HCitl-NNH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)HCitl-Q-NH2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)HCitHLys(Ac)]-N

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Na IHAibl-[Lys(Ac)]-[Lys(Ac)]-[Citl-N H2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-QN-[13Alal-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-E-[Cit]-Q-NH2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-CitNCitNH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHCitl-Q-[Cit]-NH2 Ac-[Pen]-[Citl-TWQ-[Pen]-[Phe[4-(2-arninoethoxy)]-[2-NalHAibHLys(Ac)]-NN-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-NH2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-CINN-N H2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-ENCI-NH2 Ac-[Pen]-GPWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-NN-N H2 Ac-[Pen]-PGWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-NN-N H2 Ac-[Pen]-NTVVN-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-NH2 Ac-[Pen]-NSWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-NH2 Ac-[Pen]-N-[Aib]-WQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-NN-NH2 Ac-[Pen]-NTVV-[Aib]-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHAibHLys(Ac)]N-[Aib]-Ac-[Pen]-QTW-[Lys(Ac)]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-NN-Ac-[Pen]-[Lys(Ac)]-TWQ-[Pen]-[Phe[4-(2-arninoethoxy)]-[2-Nall--[Aib]-[Lys(Ac)]NNNH2 Ac-[Pen]-QVWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-NN-N H2 Ac-[Penl-NT-[2-Nal]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]- [AibHLys(Ac)]-NN-Ac-[Penl-NT-[1-Nal]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]- [AibHLys(Ac)]-NN-Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHa-MeLeuHLys(Ac)]-NN-N H2 Ac-[Pen]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-NalHa-MeLysHLys(Ac)]-NN-NH2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHa-MeLeuHLys(Ac)]-N-U3Alal-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHa-MeLysHLys(Ac)]-N-U3Alal-Ac-[Perd-NTWQ-[PenHPhe[4-(2-aminoethoxy)H2-Nall-[4-amino-4-carboxy-tetrahydropyranHLys(AcH-N-[13Ala]-NH2 Ac-[Per]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)1-[2-Nal]-[AibHLys(Ac)]-LN-NH2 Ac-[Per]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)1-[2-Nal]-[AibHLys(Ac)]-GN-N H2 Ac-[Per]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[AibHLys(Ac)]-SN-N H2 Ac-[Per]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-Nal]-[AibHLys(Ac)HAibl-N-NH2 Ac-[Per]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)1-[2-Nal]-[AibHLys(Ac)]-FN-N H2 Ac-[Per]-NTW-[Cit]-[PenHPhe[4-(2-aminoethoxy)]-[2-NalHAibHLys(Ac)]-NN-NH2 Ac-[Per]-NTVVQ-[Pen]-[Phe[4-(2_aminoethoxy)]-[2-Nal]-[AibHLys(Ac)HTicH13Alal-Ac-[Perd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibHLys(Ac)HnLeu]-[13Alal-NH2 Ac-[Perd-NTVVQ-[PenHPhe[4-(2_aminoethoxy)1-[2-NalHAibHLys(Ac)]-G-[13Alal-NH2 Ac-[Perd-NTVVQ-[PenHPhe[4-(2_aminoethoxy)1-[2-NalHAibHLys(Ac)]-R-[13Alal-N H2 Ac-[Perd-NTVVQ-[PenHPhe[4-(2-aminoethoxy)1-[2-Nall--[AibHLys(Ac)]-W-[13Alal-Ac-[Perd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-Nall--[AibHLys(Ac)]-S-[13Alal-NH2 Ac-[Perd-NTVVQ-[PenHPhe[4-(2_aminoethoxy)1-[2-Nall--[AibHLys(Ac)]-L-[13Alal-Ac-[Perd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-Nall--[AibHLys(Ac)HAIBHI3Alal-NH2 Ac-[Perd-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-Nall--[AibHLys(Ac)HN-MeAlal-U3Alal-NH2 Ac-[Perd-NTVVQ-[PenHPhe[4-(2_aminoethoxy)1-[2-NalHAibHLys(Ac)H2-NapH13Alal-NH2 Ac-[Perd-NTVVQ-[PenHPhe[4-(2_aminoethoxy)1-[2-NalHAibHLys(Ac)]-F-[13Alal-NH2 Ac-[(D)ArgHPerd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-Nall-[ 4-arnino-4-carboxy-tetrahydropyrard-[Lys(AcH-NN-NH2 Table 3. Illustrative Peptides Containing the Ac-[Pen]-)0(WX-[Pen]-)00(X Motif and Analogues Thereof Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NNW-NH
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]- [Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-GGG-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-RRR-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-FFF-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-EEE-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-QQQ-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-TTT-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-RG-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-FG-[Perd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyranHLys(AcH-Ac-EG-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-C1G-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(AcH-NN-NH2 Ac-TG-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Palm)]-Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(isoGlu-Palm)]-NN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(PEG11-Palm)]-NN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ahx-Palm)]-NN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(isoGlu-Ahx-Palm)]-NN-NH2 [Palm]-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(AcH-NN-N H2 [Palm-isoGlu]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(AcH-NN-NH2 [Palm-PEG11]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(AcH-NN-NH2 [Palm-Ahx]-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(AcH-NN-NH2 [Palm-Ahx-isoGlu]-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-Lys[Palml-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-Lys[isoGlu-Palm]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-Lys[PEG11-Palm]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-Lys[Ahx-Palm]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-Lys[isoGlu-Ahx-Palm]-NH2 Illustrative Peptide Inhibitors Comprising Thioether Bonds 10041411n certain embodiments, the present invention includes a peptide inhibitor of an interleukin-23 receptor, wherein the peptide inhibitor has the structure of Formula III:

R1-X-R2 (III) [00415] or a pharmaceutically acceptable salt or solvate thereof, [00416] wherein 1Z1 is a bond, hydrogen, a C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl, a C1-C6 alkyl, a C1-C20 alkanoyl, an alkylsulphonate, an acid, y-Glu or pG1u, appended to the N-terminus, and including PEGylated versions (e.g., 200 Da to 60,000 Da), alone or as a spacer of any of the foregoing;
1004171R2 is a bond, OH or NH2; and 1004181X is an amino acid sequence of 8 to 20 amino acids or 8 to 35 amino acids, [00419] In particular embodiments of peptide inhibitors of Formula III, X
comprises or consists of the sequence of Formula Ma:
X1 -X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Ma) wherein X1 is absent or any amino acid;
X2 is absent or any amino acid;
X3 is absent or any amino acid;
X4 is Abu, Pen, or Cys;
X5 is any amino acid;
X6 is any amino acid;
X7 is Trp, Bip, Gln, His, Glu(Bz1), 4-Phenylbenzylalanine, Tic, Phe[4-(2-aminoethoxy)], Phe(3,4-C12), Phe(4-0Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp, 1,2,3,4 -tetrahydro-norharman, Phe(4-CO2H), Phe(4-CONH2), Phe(3,4-(OCH3)2), Phe(4-CF3), f3f3-diPheAla, Phe(4-tBu), Glu, Gly, Ile, Asn, Pro, Arg, Thr or Octgly, or a corresponding a-methyl amino acid form of any of the foregoing;
X8 is any amino acid;
X9 is Abu, Pen, or Cys;
X10 is 1-Nal, 2-Nal, Aic, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, Phe, His, Trp, Thr, Tic, Tyr, 4-pyridylAla, Octgly a Phe analog or a Tyr analog (optionally, Phe(3,4-F2), Phe(3,4-C12), F(3-Me), Phe[4-(2-aminoethoxy)], Phe[4-(2-(acetyl-aminoethoxy)], Phe(4-Br), Phe(4-CONH2), Phe(4-C1), Phe(4-CN), Phe(4-guanidino), Phe(4-Me), Phe(4-NH2), Phe(4-N3), Phe(4-0Me), Phe(4-0Bz1)), or a corresponding a-methyl amino acid form of any of the foregoing;
X11 is 2-Na!, 1-Na!, 2,4-dimethylPhe, Bip, 4-phenylcyclohexyl, Glu(Bz1), 4-Phenylbenzylalanine, Tic, Phe[4-(2-aminoethoxy)], Phe(3,4-C12), Phe(3,4-F2), f3hPhe(4-F), Phe(4-0Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp, 1,2,3,4 -tetrahydro-norharman, Phe(4-CO2H), Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(4-CF3), Phe(2,3-C12), Phe(3,4-C12), Phe(2,3-F2),Phe(4-F), 4-phenylcyclohexylalanine, a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Bip, Nva(5-phenyl), Phe, His, hPhe, Tqa, Trp, Tyr, Phe(4-Me), Trp(2,5,7-tri-tertButyl), Phe(4-0Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(4-0Bz1), or Octgly, or a corresponding a-methyl amino acid form of any of the foregoing;
X12 is a-MeLys, a-MeOrn, a-MeLeu, MeLeu, Aib, (D)Ala, (D)Asn, (D)Leu, (D)Asp, (D)Phe, (D)Thr, 3-Pal, Aib, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, hArg, hLeu, Ile, Lys, Leu, Asn, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Arg, Ser, Thr or Tle, amino-4-carboxy-tetrahydropyran (THP), Achc Acpc, Acbc, Acvc, Aib, or a corresponding a-methyl amino acid form of any of the foregoing;
X13 is Lys Lys(Ac), (D)Asn, (D)Leu, (D)Thr, (D)Phe, Ala, Aib, a-MeLeu, f3Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Arg, Orn, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, Lys, Leu, Asn, Ogl, Pro, Gln, Asp, Arg, Ser, spiro-pip, Thr, Tba, Tlc, Val or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing;
X14 is Asn, Glu, Phe, Gly, His, Lys, Lys (Ac), Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Tic, Asp or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing;
X15 is Gly, (D)Ala, (D)Asn, (D)Asp, Asn, (D)Leu, (D)Phe, (D)Thr, Ala, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gln, Arg, f3-Ala, or Ser, or a corresponding a-methyl amino acid form of any of the foregoing;
X16 is absent, Gly, Ala, Asp, Ser, Pro, Asn or Thr, or a corresponding a-methyl amino acid form of any of the foregoing;
X17 is absent, Glu, Ser, Gly or Gln, or a corresponding a-methyl amino acid form of any of the foregoing;
X18 is absent or any amino acid;

X19 is absent or any amino acid; and X20 is absent or any amino acid.
1004201In certain embdoiments, X14 is Asn, Glu, Phe, Gly, His, Lys, Lys (Ac), Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr, Tic, or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing [00421]In certain embodiments of Ma: X7 is Trp, Bip, Gin, His, Glu(Bz1), 4-Phenylbenzylalanine, Tic, Phe[4-(2-aminoethoxy)], Phe(3,4-C12), Phe(4-0Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp, 1,2,3,4 -tetrahydro-norharman, Phe(4-CO2H), Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(4-CF3), f33-diPheAla, Phe(4-tBu), Glu, Gly, Ile, Asn, Pro, Arg, Thr or Octgly, or a corresponding a-methyl amino acid form of any of the foregoing; X10 is 1-Nal, 2-Nal, Aic, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, Phe, His, Trp, Thr, Tic, Tyr, 4-pyridylAla, Octgly a Phe analog or a Tyr analog, or a corresponding a-methyl amino acid form of any of the foregoing; X11 is 2-Nal, 1-Nal, 2,4-dimethylPhe, Bip, 4-phenylcyclohexyl, Glu(Bz1), 4-Phenylbenzylalanine, Tic, Phe[4-(2-aminoethoxy)], Phe(3,4-C12), Phe(3,4-F2), f3hPhe(4-F), Phe(4-0Me), 5-Hydroxy-Trp, 6-Chloro-Trp, N-MeTrp, a-MeTrp, 1,2,3,4 -tetrahydro-norharman, Phe(4-CO2H), Phe(4-CONH2), Phe(3,4-Dimethoxy), Phe(4-CF3), Phe(2,3-C12), Phe(2,3-F2),Phe(4-F), 4-phenylcyclohexylalanine, a-MePhe, f3hNal, f3hPhe, f3hTyr, f3hTrp, Bip, Nva(5-phenyl), Phe, His, hPhe, Tqa, Trp, Tyr, Phe(4-Me), Trp(2,5,7-tri-tertButyl), Phe(4-0Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(4-0Bz1), or Octgly, or a corresponding a-methyl amino acid form of any of the foregoing; X12 is a-MeLys, a-MeOrn, a-MeLeu, MeLeu, Aib, (D)Ala, (D)Asn, (D)Leu, (D)Asp, (D)Phe, (D)Thr, 3-Pal, Aib, f3-Ala, f3hGlu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, hArg, hLeu, Ile, Lys, Leu, Asn, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gin, Arg, Ser, Thr or Tie, or a corresponding a-methyl amino acid form of any of the foregoing; X13 is Lys(Ac), (D)Asn, (D)Leu, (D)Thr, (D)Phe, Ala, Aib, a-MeLeu, f3Ala, f3hGlu, f3hAla, PhLeu, f3hVal, (3-spiro-pip, Cha, Chg, Asp, Arg, Orn, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, Lys, Leu, Asn, Ogl, Pro, Gin, Asp, Arg, Ser, spiro-pip, Thr, Tba, Tic, Val or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing; X14 is Asn, Glu, Phe, Gly, His, Lys, Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr, Tic or Tyr, or a corresponding a-methyl amino acid form of any of the foregoing; and X15 is Gly, (D)Ala, (D)Asn, (D)Asp, Asn, (D)Leu, (D)Phe, (D)Thr, Ala, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gln, Arg or Ser, or a corresponding a-methyl amino acid form of any of the foregoing.
[00422] In certain embodiments, X3 is present. In particular embodiments, X3 is Glu,(D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, or (D)Gln. In certain embodiments, it is (D)Arg or (D)Phe.
1004231 In particular embodiments, X5 is Gln, Ala, Cys, Cit, Asp, Dab, Dap, Glu, Phe, Gly, His, hCys, Lys, Leu, Met, Asn, N-Me-Ala, N-M-Asn, N-Me-Lys, N-Me-Gln, N-Me-Arg, Orn, Pro, Pen, Gln, Arg, Ser, Thr, or Val.
1004241 In particular emodiments, X6 is Thr, Asp, Glu, Phe, Asn, Pro, Arg, Ser, or Thr.
1004251 In particular embodiments, X8 is Gln, Glu, Phe, Lys, Asn, Pro, Arg, Val, Thr, or Trp.
1004261 In certain embodiments, X10 is a Tyr analog or a Phe analog. In particular embodiments, X10 is Phe(4-0Me), Phe(CONH2) or Phe[4-(2-aminoethoxy)]. In certain embodiments, X10 is a Tyr analog or a Phe analog. In particular embodiments, X10 is Phe(4-0Me) or Phe[4-(2-aminoethoxy)].
1004271In certain embodiments where X10 is a the Phe analog, X10 is selected from hPhe, Phe(4-0Me), a-MePhe, hPhe(3,4-dimethoxy), Phe(4-CONH2), Phe(4-0-Bz1)), Phe(4-guanadino), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-NH2), Phe(4-F), Phe(3,5 DiF), Phe(CH2CO2H), Phe(penta-F), Phe(3,4-C12), Phe(4-CF3), f33-diPheAla, Phe(4-N3) and Phe[4-(2-aminoethoxy)]. In particular embodiments, X10 is Phe[4-(2-aminoethoxy)] or Phe(CONH2). In particular embodiments, X10 is Phe[4-(2-aminoethoxy)].
1004281In certain embodiments where X10 is a Tyr analog, X10 is selected from hTyr, N-Me-Tyr, Tyr(3-tBu), Phe(4-0Me) and bhTyr. In particular embodiments, X10 is Phe(4-0Me).
1004291In particular embodiments, X10 is Tyr, Phe(4-0Me), Phe(4-0Bz1), Phe(4-0Me), Phe(4-CONH2), Phe(3,4-C12), Phe(4-tBu), Phe(4-NH2), Phe(4-Br), Phe(4-CN), Phe(4-carboxy), Phe[4-(2aminoethoxy)] or Phe(4-guanadino). In particular embodiments, X10 is not Tyr.

1004301In certain embodiments, X11 is Trp or a Trp analog. In particular embodiments, X11 is 2-Nal or 1-Nal.
1004311In particular embodiments, the peptide inhibitor of Formula III is cyclized. In certain embodiments, the peptide inhibitor is cyclized via an intramolecular bond between X4 and X9.
In certain embodiments, the intramolecular bond is a thioether bond.
1004321In certain embodiments, the peptide inhibitor of Formula III is linear or not cyclized. In particular embodoiments of the linear peptide inhibitor of Formula III, X4 and/or X9 are any amino acid.
1004331In particular embodiments of a peptide inhibitor of Formula III, one or more, two or more, or all three of Xi, X2, and X3 are absent. In certain embodiments, X1 is absent. In certain embodiments, X1 and X2 are absent. In certain embodiments, Xi, X2 and X3 are absent.
1004341In particular embodiments of a peptide inhibitor of Formula III, one or more, two or more, three or more, four or more, or all of X16, X17, X18, X19 and X20 are absent. In particular embodiments of a peptide inhibitor of Formula III, one or more, two or more, three or more, or all of X17, X18, X19 and X20 are absent. In certain embodiments, one or more, two or more, or all three of X17, X19 and X20 are absent. In certain embodiments, one or more of Xi, X2 and X3 are absent; and one or more, two or more, three or more, or four of X17, X18, X19 and X20 are absent.
1004351 In particular embodiments of a peptide inhibitor of Formula III, one of X4 or X9 is Abu, and the other of X4 or X9 is not Abu. In certain embodiments, X4 is Abu and X9 is Cys.
1004361 In particular embodiments, a peptide inhibitor of Formula III
comprises one or more, two or more, three or more, or four of the following features: X5 is Arg or Gln;
X6 is Thr; X7 is Trp;
and X8 is Gln. In particular embodiments, X5 is Gln, X6 is Thr, X7 is Trp, and X8 is Gln. In certain embodiments, X5 is Gln. In certain embodiments, Xi, X2 and X3 are absent. In certain embodiments, X4 is Abu and X9 is Cys.
1004371 In particular embodiments, a peptide inhibitor of Formula III
comprises one or more, two or more, three or more, four or more, five or more, six or more, or seven of the following features: X10 is Tyr or a Phe analog; X11 is Trp, 2-Nal, 1-Nal, Phe(4-0-Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(4-0Bz1) or Phe(4-Me); X12 is Arg, hLeu, (D)Asn, or any alpha methyl amino acids including, Aib, a-MeLys, a-MeLeu or a-MeOrn; X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is f3-Ala, Gln, Gly, Ser, Ala; and X16 is absent or AEA. In particular embodiments, a peptide inhibitor of Formula III comprises one or more, two or more, three or more, four or more, five or more, six or more, or seven of the following features: X10 is Tyr or a Phe analog; X11 is Trp, 2-Nal, 1-Nal, Phe(4-0-Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(4-0Bz1) or Phe(4-Me); X12 is Arg, hLeu, (D)Asn, or any alpha methyl amino acids including, Aib, a-MeLys, a-MeLeu or a-MeOrn; X13 is Lys, Glu or Lys(Ac);
X14 is Phe or Asn; X15 is Gly, Ser, Ala; and X16 is absent or AEA. In certain embodiments, the Phe analog is Phe(4-0Bz1), Phe(4-0Me), Phe(4-CONH2), Phe(3,4-C12), Phe(4-tBu), Phe(4-NH2), Phe(4-Br), Phe(4-CN), Phe(4-carboxy), Phe[4-(2aminoethoxy)] or Phe(4-guanadino). In certain embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, X1 , X2 and X3 are absent. In certain embodiments, X4 is Abu and X9 is Cys.
[00438] In particular embodiments, a peptide inhibitor of Formula III
comprises one or more, two or more, three or more, four or more, five or more, six or more, or seven of the following features: X10 is Tyr or a Phe analog; X11 is Trp, 2-Nal, 1-Nal, Phe(4-0-Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(4-0Bz1) or Phe(4-Me); X12 is Arg, hLeu, (D)Asn, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal,; X13 is Lys, Glu or Lys(Ac);
X14 is Phe or Asn; X15 is Gly; and X16 is absent or AEA. In certain embodiments, the Phe analog is Phe(4-0Bz1), Phe(4-0Me), Phe(4-CONH2), Phe(3,4-C12), Phe(4-tBu), Phe(4-NH2), Phe(4-Br), Phe(4-CN), Phe(4-carboxy), Phe(4-(2aminoethoxy)) or Phe(4-guanadino). In certain embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, Xi, X2 and X3 are absent. In certain embodiments, X4 is Abu and X9 is Cys.
[00439] In particular embodiments, a peptide inhibitor of Formula III
comprises one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, or eleven of the following features: X5 is Arg or Gln; X6 is Thr; X7 is Trp; X8 is Gln; X10 is a Phe analog; X11 is Trp, 2-Nal, 1-Nal, Phe(4-0-Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(Bz1) or Phe(4-Me); X12 is Aib, a-MeLys, a-MeLeu, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Agp, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeSer, a-MeVal,a-MeOrn; X13 is Lys, Glu or Lys(Ac);
X14 is Phe or Asn; X15 is f3-ala, Gly, Ser, Ala; and X16 is absent or AEA. In particular embodiments, a peptide inhibitor of Formula III comprises one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, or eleven of the following features: X5 is Arg or Gln; X6 is Thr; X7 is Trp; X8 is Gln; X10 is a Phe analog; X11 is Trp, 2-Nal, 1-Nal, Phe(4-0-Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(Bz1) or Phe(4-Me); X12 is Aib, a-MeLys, a-MeLeu or a-MeOrn;
X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is Gly, Ser, Ala; and X16 is absent or AEA. In certain embodiments, the Phe analog is Phe(4-0Bz1), Phe(4-0Me), Phe[4-(2aminoethoxy)], Phe(4-CONH2), Phe(3,4-C12), Phe(4-tBu), Phe(4-NH2), Phe(4-Br), Phe(4-CN), Phe(4-CO2H), or Phe(4-guanadino). In certain embodiments, X11 is 2-Nal or 1-Nal. In certain embodiments, X1 , X2 and X3 are absent. In certain embodiments, X4 is Abu and X9 is Cys.
[00440] In particular embodiments, a peptide inhibitor of Formula III
comprises one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, or eleven of the following features: X5 is Arg or Gln; X6 isThr; X7 is Trp; X8 is Gln; X10 is Tyr or a Phe analog; X11 is Trp, 2-Nal, 1-Nal, Phe(4-0-Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(Bz1) or Phe(4-Me); X12 is Arg, hLeu, (D)Asn, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeSer, a-MeVal,; X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn;
X15 is f3-Ala, Asn or Gly; and X16 is absent or AEA. In particular embodiments, a peptide inhibitor of Formula III comprises one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, or eleven of the following features: X5 is Arg or Gln; X6 isThr; X7 is Trp; X8 is Gln; X10 is Tyr or a Phe analog; X11 is Trp, 2-Nal, 1-Nal, Phe(4-0-Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Phe(Bz1) or Phe(4-Me); X12 is Arg, hLeu, (D)Asn, a-MeLys, a-MeLeu or a-MeOrn, Aib; X13 is Lys, Glu or Lys(Ac); X14 is Phe or Asn; X15 is Gly; and X16 is absent or AEA. In certain embodiments, the Phe analog is Phe(4-0Bz1), Phe(40Me), Phe(4-CONH2), Phe(3,4-C12), Phe(4-tBu), Phe(4-NH2), Phe(4-Br), Phe(4-CN), Phe(4-CO2H), Phe(4-(2-aminoethoxy)) or Phe(4-guanidino). In certain embodiments, X11 is 2-Na! or 1-Nal. In certain embodiments, Xl, X2 and X3 are absent. n certain embodiments, X4 is Abu and X9 is Cys.
1004411In certain embodiments, the present invention includes a peptide of 8 to 20, 8 to 16 or 8 to 12 amino acids, optionally cyclized, comprising or consisting of a core sequence of Formula Xaa4-Xaa5-Xaa6-Trp-Xaa8-Xaa9-Xaa 1 0-Xaa11 (Tub) 1004421wherein Xaa4 and Xaa9 are each independently selected from Abu and Cys, wherein Xaa4 and Xaa9 are not both the same; Xaa5, Xaa6 and Xaa8 are any amino acid residue; Xaal 0 is Tyr, a Phe analog or 2-Na!, and Xaall is 2-Na! or Trp, wherein the peptide inhibits binding of IL-23 to IL-23R. In particular embodiments, Xaal 0 is Phe(4-0Me), 2-Na!, or Phe[4-(2-aminoethoxy)]. In one embodiment, Xaal0 is Phe(4-0Me). In one embodiment, Xaa7 is Phe[4-(2-aminoethoxy)]. In one embodiment, Xaal 1 is 2-Nal. In certain embodiments, the peptide is cyclized via Xaa4 and Xaa9. In particular embodiments, the Phe analog is Phe[4-(2aminoethoxy)] or Phe(4-0Me). In certain embodiments, Xaa4 is Abu and Xaa9 is Cys, and the peptide is cyclized via Xaa4 and Xaa9. In particular embodiments, the peptide is a peptide inhibitor of Formula III, and wherein in certain embodiments, Xl, X2 and X3 are absent. In particular embodiments, the peptide inhibits the binding of IL-23 to IL-23R.
In certain embodiments, a peptide of Formula Illb comprises a Glu,(D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Na!, Thr, Leu, or (D)Gln bound to Xaa4. In certain embodiments, it is (D)Arg or (D)Phe.
1004431In certain embodiments, the present invention includes a peptide of 8 to 20, 8 to 16 or 8 to 12 amino acids, optionally cyclized, comprising or consisting of a core sequence of Formula IIIc:
Abu-Xaa5-Xaa6-Trp-Xaa8-Cys-[Phe(4-0Me)]-(2-Nal) (IIIc) 1004441wherein Xaa5, Xaa6 and Xaa8 are any amino acid residue; and wherein the peptide inhibits binding of IL-23 to IL-23R. In certain embodiments, the peptide is cyclized via Abu at Xaa4 and Cys at Xaa9. In certain embodiments, the peptide is a peptide inhibitor of Formula III, and wherein in certain embodiments, Xl, X2 and X3 are absent. In particular embodiments, the peptide inhibits the binding of IL-23 to IL-23R. In certain embodiments, a peptide of Formula Mc comprises a Glu, (D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Na!, Thr, Leu, or (D)Gln bound to Abu. In certain embodiments, it is (D)Arg or (D)Phe.
1004451 In certain embodiments, the present invention includes a peptide of 8 to 20, 8 to 16 or 8 to 12 amino acids, optionally cyclized, comprising or consisting of a core sequence of Formula IIId:
Abu-Xaa5 -Xaa6 - Trp-Xaa8 -Cy s-Xaal0 - Trp (IIId) [00446] wherein Xaa5, Xaa6 and Xaa8 are any amino acid residue; Xaal 0 is a modified Phe; and wherein the peptide inhibits binding of IL-23 to IL-23R. In particular embodiments, the modified Phe is Phe(4-tBu), Phe(4-guanidino), Phe[4-(2-aminoethoxy)], Phe(4-CO2H), Phe(4-CN), Phe(4-Br), Phe(4-NH2), PHe(CONH2) or Phe(4-Me). In particular embodiments, the modified Phe is Phe(4-tBu), Phe(4-guanidino), Phe[4-(2-aminoethoxy)], Phe(4-CO2H), Phe(4-CN), Phe(4-Br), Phe(4-NH2), or Phe(4-Me). In one embodiment, Xaal 0 is Phe[4-(2-aminoethoxy)] or Phe(4-0Me). In one embodiment, Xaal 0 is Phe[4-(2-aminoethoxy)]. In certain embodiments, the peptide is cyclized via Abu at Xaa4 and Cys at Xaa9. In certain embodiments, the peptide is a peptide inhibitor of Formula III, and wherein in certain embodiments, Xl, X2 and X3 are absent. In particular embodiments, the peptide inhibits the binding of IL-23 to IL-23R. In certain embodiments, a peptide of Formula IIId comprises a Glu, (D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Na!, Thr, Leu, or (D)Gln bound to Abu. In certain embodiments, it is (D)Arg or (D)Phe.
1004471 In certain embodiments, the present invention includes a peptide, optionally 8 to 20, 8 to 16 or 8 to 12 amino acids, optionally cyclized, comprising or consisting of a core sequence of Formula Me:
Abu-Xaa5 -Xaa6 - Trp-Xaa8 -Cy s- Phe [4 -(2-aminoethoxy)] - [2-Na!] (Me) [00448] wherein Xaa5, Xaa6 and Xaa8 are any amino acid residue. In certain embodiments, the peptide is cyclized via Abu at Xaa4 and Cys at Xaa9. In certain embodiments, the peptide is a peptide inhibitor of Formula III, and wherein in certain embodiments, Xl, X2 and X3 are absent.
In particular embodiments, the peptide inhibits the binding of IL-23 to IL-23R. In certain embodiments, a peptide of Formula Illb comprises a Glu, (D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, or (D)Gln bound to Abu. In certain embodiments, it is (D)Arg or (D)Phe.
1004491In one embodiment, Xaa5 and Xaa8 is Gln. In one embodiment, Xaa6 is Thr. In certain embodiments, the peptide is cyclized via Abu at Xaa4 and Cys at Xaa9.
[00450] In particular embodiments of a peptide inhibitor of Formula III, the peptide inhibitor has a structure shown in any of Tables 5A-5C or comprises an amino acid sequence set forth in Tables 5A-5C.
1004511In certain aspects, the present invention provides a peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Vf):
X1 -X2-X3-Abu-X5-X6-X7-X8-Cys-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (VI), wherein:
X1 is absent;
X2 is absent or X2 is D-Asp, E, R, D-Arg, F, D-Phe, 2-Nal, T, L, D-Gln, or D-Asn;
X3 is D-Arg;
X5 is N, Q, Cit, Lys, or a Lys conjugate (e.g., Lys(IVA), Lys(biotin), Lys(octanyl), Lys(Palm), Lys(PEG), Lys(PEG8), Lys(PEG11-Palm), Lys(Ac));
X6 is T, S or V;
X7 is W, 1-Nal, or 2-Nal;
X8 is Q, Cit, N, Aib or Lys(Ac);
X10 is Phe[4-(2-aminoethoxy)], Phe[4-(2-acetylaminoethoxy)] or Phe(4-CONH2);
X11 is 2-Nal;

X12 is 4-amino-4-carboxy-tetrahydropyran, Aib, aMeLeu, aMeLys, or an aMeLys conjugate (e.g., aMeLys(Ac), aMeLys(PEG4-Palm), aMeLys(PEG4-Laury1), aMeLys(PEG4IsoGluPalm), aMeLys(PEG4IsoGluLaury1), aMeLys(IVA), aMeLys(bi otin), or aMeLys(octany1));
X13 is Q, E, Cit or a Lys conjugate (e.g., Lys(Ac), Lys(PEG4-isoGlu-Palm), Lys(PEG4-octanyl), Lys(PEG4-Palm), Lys(biotin), Lys(octanyl), Lys(Palm), Pys(PEG8), or Lys(PEG11-Palm));
X14 is N, Cit, Q, L, G, S, Aib, F, 2-Nap, N-Me-Ala, R, W, nLeu, Tic or a Lys conjugate (e.g., Lys(Ac));
X15 is N, Cit, Q, f3Ala, Lys(Ac) or Aib; and X16, X17, X18, X19 and X20 are absent.
In particular embodiments, X2 is D-Asp, E, R, D-Arg, F, D-Phe, 2-Nal, T, L, D-Gln, or D-Asn 1004521In certain aspects, the present invention provides a peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Vh):
X1 -X2-X3-Abu-X5-X6-X7-X8-Cys-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Vh), wherein:
X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any D-amino acid or absent;
X4 is Cys, hCys, Pen, hPen, Abu, Ser, hSer or chemical moiety capable of forming a bond with X9;

X5 is Ala, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn, Gln, Arg, Ser, Glu or Thr;
X6 is Thr, Ser, Asp, Ile or any amino acid;
X7 is Trp, 6-Chloro-Trp, 1-Nap or 2-Nap;
X8 is Glu, Gln, Asn, Lys(Ac), Cit, Cav, Lys(N-c-(N-a-Palmitoyl-L-y-glutamy1)), or Lys(N-c-Palmitoyl;
X9 is Cys, hCys, Pen, hPen Abu, or any amino acid or chemical moiety capable of forming a bond with X4;
X10 is 2-Nal, a Phe analog, Tyr, or a Tyr analog;
X11 is 1-Nal, 2-Nal, Phe(3,4-dimethoxy), 5-HydroxyTrp, Phe(3,4-C12), Trp or Tyr(3-tBu);
X12 is Aib, 4-amino-4-carboxy-tetrahydropyran, any alpha-methylamino acid, alpha-ethyl-amino acid, Achc, Acvc, Acbc Acpc, 4-amino-4-carboxy-piperidine, 3-Pal, Agp, -DiethylGly, a-MeLys, a-MeLys(Ac), a-MeLeu, a-MeOrn, a-MeSer, a-MeVal, Cav, Cha, Cit, Cpa, D-Asn, Glu, His, hLeu, hArg, Lys, Leu, Octgly, Orn, piperidine, Arg, Ser, Thr or THP;
X13 is Lys(Ac), Gln, Cit, Glu, or any amino acid;
X14 is Asn, Gln, Lys(Ac), Cit, Cav, Lys(N-c-(N-a-Palmitoyl-L-y-glutamy1)), Lys(N-c-Palmitoy1), Asp, or any amino acid;
X15 is f3-Ala, Asn, Gly, Gln, Ala, Ser, Aib, Asp or Cit;
X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent.
1004531In certain embodiments of any of the peptide inhibitors described herein, including but not limited to those of Formula (If) and (Ih), the peptide inhibitor is cyclized via a bond, e.g., a thioether bond, between X4 and X9. In certain embodiments, the peptide inhibitor inhibits the binding of an interleukin-23 (IL-23) to an IL-23 receptor.
1004541In certain embodiments, X1 , X2 and X3 are absent. In certain embodiments, X1 and X2 are absent. In certain embodiments, X1 is a D-amino acid or absent. In certain embodiments, X2 is a D-amino acid or absent.
1004551In certain embdoiments, X5 is Ala, a-MeOrn, a-MeSer, Cit, Dap, Dab, Dap(Ac), Gly, Lys, Asn, N-MeGln, N-MeArg, Orn, Gln, Arg, Ser, or Thr;
1004561 In certain embodiments, X5 is N, X6 is T, X7 is W, or X8 is Q. In certain embodiments, X5 is N, X6 is T, X7 is W, and X8 is Q.
1004571In certain embodiments, X5 is Q, X6 is T, X7 is W, or X8 is Q. In certain embodiments, X5 is Q, X6 is T, X7 is W, and X8 is Q.
1004581 In certain embodiments, X5 is N, X6 is T, X7 is W, and X8 is Cit.
1004591 In certain embodiments, X10 is Phe[4-(2-aminoethoxy)].
1004601In certain embodiments, X12 is 4-amino-4-carboxy-tetrahydropyran, Aib, aMeLeu, or aMeLys. In certain embodiments, X12 is 4-amino-4-carboxy-tetrahydropyran.
[00461]In certain embodiments, X13 is E or Lys(Ac). In certain embodiments, X13 is Lys(Ac).
1004621In certain embodiments, X14 is Asn, Gln, Lys(Ac), Cit, Cav, Lys(N-6-(N-a-Palmitoyl-L-y-glutamy1)), Lys(N-E-Palmitoy1), or any amino acid;
1004631 In certain embdoiments, X15 is f3-Ala, Asn, Gly, Gln, Ala, Ser, Aib, or Cit.
1004641 In certain embodiments, X14 is N.

1004651 In certain embodiments, X15 is N.
1004661In certain embodiments, X16 is a D-amino acid or absent. In certain embodiments, X17 is a D-amino acid or absent. In certain embodiments, X18 is a D-amino acid or absent. In certain embodiments, X19 is a D-amino acid or absent. In certain embodiments, X20 is a D-amino acid or absent.
1004671In certain embodiments, X2 is absent; X3 is absent; X5 is Q, X6 is T, X7 is W, and X8 is Q; X10 is Phe[4-(2-aminoethoxy)]; X12 is 4-amino-4-carboxy-tetrahydropyran, Aib, aMeLeu, or aMeLys; X13 is E or Lys(Ac); X14 is N; and X15 is N. In certain embodiments, X12 is 4-amino-4-carboxy-tetrahydropyran and X13 is Lys(Ac).
[00468] In certain embodiments, any of the amino acids of the peptide inhibitor are connected by a linker moiety, e.g., a PEG.
1004691 In certain embodiments, the N-terminus of the peptide inhibitor comprises an Ac group.
[00470] In certain embodiments, the C-terminus of the peptide inhibitor comprises an NH2 group.
1004711 In certain embodiments, the present invention includes a peptide comprising or consisting of an amino acid sequence shown in any of the Table 4s or Table 5s, or a peptide inhibitor comprising or consisting of a structure shown in any of the Table 4s or Table 5s (or a pharmaceutically acceptable salt thereof). In particular embodiments, the peptide does not include the conjugated moieties but does include the Abu residue. In particular embodiments, the peptide or inhibitor comprises a thioether bond between the two Abu and Cys residues, or between the two outermost amino acids within the brackets folloing the term "cyclo", which indicated the presence of a cyclic structure. In particular embodiments, the inhibitor is an acetate salt. The peptide sequence of illustrative inhibitors is shown in Tables 4 and 5 from N-term to C-term, with conjugated moieties, and N-terminal Ac and/or C-terminal NH2 groups indicated.
The cyclic structure is indicated by "Cyclo" as illustrated in Table 5, indicating the presence of a thioether bond between the bracketed Abu at X4 and Cys at X9.
Table 4. Illustrative Thioether Peptide Inhibitors Biotin-[PEG11-cyclo[[Abul-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyranHLys(Ac)]-NN-Ac-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-[Lys(Ac)]-NN-NFI2 Ac-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-[Lys(Ac)]-NN-NFI2 Ac-E-[(D)Argl-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-[4-amino-4-carboxy-tetrahydropyrard-Ac-[(D)Asp]-[(D)Argl-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-R-[(D)Argl-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-[4-amino-4-carboxy-tetrahydropyrard-Ac-[(D)Arg]-[(D)Argl-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-F-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyrar]-Ac-[(D)Phe]-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-N H2 Ac-[2-Nal]-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-T-[(D)Argl-cyclo[[Abul-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-[4-amino-4-carboxy-tetrahydropyrard-Ac-L-[(D)Argl-cyclo[[Abul-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-[4-amino-4-carboxy-tetrahydropyrard-Ac-[(D)G1n]-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-[(D)Asn]-[(D)Arg]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-cycloRAbul-QTWOC1-[Phe[4-(2-aminoethoxy)-(PEG4-Alexa488)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 [A1exa488]-[PEG4]-cycloRAbul-QTWOC1-[Phe[4-(2-aminoethoxy)] [2 Nal] [4 amino-4-carboxy-tetrahydropyran]-ENN-NH2 [Alexa647]-[PEG4]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 [Alexa-647]-[PEG4]-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-N H2 [A1exa647]-[PEG12]-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-N H2 [Alexa488]-[PEG4]-[(D)Arg]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-N H2 Table 5A. Illustrative Thioether Peptide Inhibitors _____________ S----Ac, N N--[Phe(4-0Me)]-[2-Nal]-XXXX-N H2 Ac-Cyclo-[[Abu]-XXWXC]-[Phe(4-0Me)[2-Na11-XXXX-NH2 Sequence Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-ENN-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-ENNE-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-ENNF-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-ENNK-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-ENNN-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-ENNT-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-ENNG-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyrar]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-Ac-GGG-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-RRR-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-FFF-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-EEE-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-000-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-TTT-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-RG-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-FG-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-EG-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-C1G-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-Ac-TG-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Palm)]-NN-NH2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(PEG11-Palm)]-NN-NH2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(isoGlu-Palm)]-NN-NH2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ahx-Palm)]-NN-NH2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(isoGlu-Ahx-Palm)]-NN-NH2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Lys(isoGlu-Ahx-Palm)]-NN-NH2 [Palm]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-[Palm-isoGlu]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyranl-ENN-N H2 [Palm-PEG11]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-N H2 [Palm-Ahx]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-N H2 [Palm-Ahx-isoGlu]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-N H2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-Lys[Palml-NH2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-Lys[Pegll-Palm]-NH2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-Lys[isoGlu-Palm]-NH2 Ac-cyclo[[Abu]-QTVVOC]-[Phe[4-(2-aminoethoxy)]-[2-NalH4-amino-4-carboxy-tetrahydropyranl-ENN-Lys[Ahx-Palml-NH2 Ac-cyclo[[Abu]-QTVVOC]-[Phe[4-(2-aminoethoxy)]-[2-NalH4-amino-4-carboxy-tetrahydropyranl-ENN-Lys[isoGlu-Ahx-Palml-NH2 Table 5B. Illustrative Thioether Peptides Ac-[D-Arg]- Cyclo4Abu-QTWOC1-[Phe(4-2ae)H2-NaIHTHH-ENN-NH2 Ac-[D-Arg]- Cyclo4Abu-QTWOC1-[Phe(4-2ae)H2-NaIHTHP11-END-NH2 Ac-[D-Arg]- Cyclo4Abu-QTWOC1-[Phe(4-2ae)H2-NaIHTHH-EDN-NH2 Ac-[D-Arg]- Cyclo4Abu-QTWEC1-[Phe(4-2ae)H2-NaIHTHH-ENN-NH2 Ac-[D-Arg]- Cyclo4Abu-ETWOC1-[Phe(4-2ae)H2-NaIHTHP1-ENN-NH2 Ac-[D-Arg]- Cyclo4Abu-QTWOC1-[Phe(4-2ae)H2-NaIHTHH-EDD-N H2 Ac-[D-Arg]- Cyclo4Abu-QTWEC1-[Phe(4-2ae)H2-NaIHTHH-END-NH2 Ac-[D-Arg]- Cyclo4Abu-ETWCIC1-[Phe(4-2ae)H2-Nall-[Tetrahydropyran-A1-END-N H2 Ac-[D-Arg]- Cyclo4Abu-QTWEC1-[Phe(4-2ae)H2-NaIHTHH-EDN-NH2 Ac-[D-Arg]- Cyclo4Abu-ETWCIC1-[Phe(4-2ae)H2-Nall-[Tetrahydropyran-A1-EDN-N H2 Ac-[D-Arg]- Cyclo4Abu-ETWEC1-[Phe(4-2ae)H2-NaIHTHP1-ENN-NH2 Ac-[D-Arg]- Cyclo4Abu-QTWOC1-[Phe(4-2ae)H2-NaIHTHH-ENN-NH2 Ac-[D-Arg]- Cyclo4Abu-QTWOC1-[Phe(4-2ae)H2-NaIHTHH-END-NH2 Ac-[D-Arg]- Cyclo4Abu-QTWCIC1-[Phe(4-2ae)H2-Nall-[Tetrahydropyran-A1-EDN-N H2 Ac-[D-Arg]- Cyclo4Abu-ETWEC1-[Phe(4-2ae)H2-NaIHTHP1-ENN-NH2 Ac-[D-Arg]- Cyclo4Abu-ETWOC1-[Phe(4-2ae)H2-NaIHTetrahydropan-Al-ENN-OH
Ilustrative Peptide Inhibitors Containing Cyclic Amides 10047211n certain embodiments, the present invention includes a peptide inhibitor of an interleukin-23 receptor, wherein the peptide inhibitor has the structure of Formula IV:
R1-X-R2 (IV) [00473] or a pharmaceutically acceptable salt or solvate thereof, [00474] wherein 1Z1 is a bond, hydrogen, an C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl C1-C6 alkyl, a Cl -C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing;
[00475] R2 is a bond, OH or NH2; and 1004761X is an amino acid sequence of 8 to 20 amino acids, comprising or consisting of the sequence of Formula IVa:

(IVO
[00477] wherein X1 is absent or any amino acid;
X2 is absent or any amino acid;
X3 is absent or any amino acid;
X4 is Dap, Dab, Glu, Asp, (D)-Asp or (D)-Dab;
X5 is Gln, Ala, Cys, Cit, Asp, Dab, Dap, Glu, Phe, Gly, His, hCys, Lys, Leu, Met, Asn, N-Me-Ala, N-M-Asn, N-Me-Lys, N-Me-Gln, N-Me-Arg, Orn, Pro, Pen, Gln, Arg, Ser, Thr, or Val;
X6 is Thr, Asp, Glu, Phe, Asn, Pro, Arg, Ser, or Thr;
X7 is Trp, Glu, Gly, Ile, Asn, Pro, Arg, Thr or OctGly;
X8 is Gln, Glu, Phe, Lys, Asnõ Pro, Arg, Thr, or Trp;
X9 is Dap, Dab, Glu, Asp, (D)-Asp or (D)-Dab;

X10 is Tyr(OMe)Phe(4-0Me), 1-Na!, 2-Na!, Aic, a-MePhe, Bip, (D)Cys, Cha, DMT, (D)Tyr), Glu, Phe, His, hPhe(3,4-dimethoxy), hTyr, N-Me-Tyr, Trp, Phe(4-CONH2), Phe(4-phenoxy), Thr, Tic, Tyr, Tyr(3-tBu), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-NH2), Phe(4-F), Phe(3,5-F2),Phe(penta-F), Phe(3,4-C12), Phe(4-CF3), Bip, Cha, 4-pyridylalanine, f3hTyr, OctGly, Phe(4-N3), Phe(4-Br) or Phe[4-(2-aminoethoxy)];
X11 is 2-Na!, 1-Na!, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe(3,5-F2), Phe(4-CONH2), Phe(4-F), 4-phenylcyclohexylalanine, Phe(4-CF3), a-MePhe, f3hPhe, f3hTyr, f3hTrp, BIP, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Trp, Tyr, Phe(4-0Me), Phe(4-Me), Trp(2,5,7-tri-tertButyl), Phe(4-0Ally1), Tyr(3-tBu), Phe(4-tBu), Phe(4-guanidino), Tyr(Bz1), or OctGly;
X12 is a-MeLys, a-MeOrn, a-MeLeu, Aib, (D)Ala, (D)Asn, (D)Leu, (D)Asp, (D)Phe, (D)Thr, 3-Pal, Aib, f3-Ala, f3-Glu, f3hAla, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, hArg, hLeu, Ile, Lys, Leu, Asn, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Arg, Ser, Thr Tle, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeSer, a-MeVal,;
X13 is Lys(Ac), (D)Asn, (D)Leu, (D)Thr, (D)Phe, Ala, Aib, a-MeLeu, Aib, f3-Ala, f3-Glu, f3hAla,f3hLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, Lys, Lys(Ac), Leu, Asn, Ogl, Pro, Gln, Arg, Ser, f3-spiro-pip, Thr, Tba, Tlc, Val or Tyr;
X14 is Asn, Glu, Phe, Gly, His, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Tic or Tyr;
X15 is f3-ala, Asn, Gly, (D)Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Thr, Ala, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gln, Arg or Ser;
X16 is absent, Gly, Ala, Asp, Ser, Pro, Asn or Thr;
X17 is absent, Glu, Ser, Gly or Gln;
X18 is absent or any amino acid;
X19 is absent or any amino acid; and X20 is absent or any amino acid.

10047811n certain embodiments of IVa: X12 is a-MeLys, a-MeOrn, a-MeLeu, Aib, (D)Ala, (D)Asn, (D)Leu, (D)Asp, (D)Phe, (D)Thr, 3-Pal, Aib, f3-Ala, f3-Glu, f3hAla, PhLeu, f3hVal, (3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeu, hArg, hLeu, Ile, Lys, Leu, Asn, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Arg, Ser, Thr or Tle; X13 is Lys(Ac), (D)Asn, (D)Leu, (D)Thr, (D)Phe, Ala, Aib, a-MeLeu, Aib, f3-Ala, f3-Glu, f3hAla,f3hLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, Glu, Phe, hLeuLys, Leu, Asn, Ogl, Pro, Gln, Arg, Ser, f3-spiro-pip, Thr, Tba, Tlc, Val or Tyr; X14 is Asn, Glu, Phe, Gly, His, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Tic or Tyr; and X15 is Gly, (D)Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Thr, Ala, AEA, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Gln, Arg or Ser.
1004791In particular embodiments of a peptide inhibitor of Formula (IV): X5 is Cys, Cit, Asp, Dab, Dap, Gly, His, hCys, Lys, Met, Asn, N-Me-Ala, N-Me-Asn, N-Me-Lys, N-Me-Gln, N-Me-Arg, Orn, Pro, Pen, Gln, Val; X6 is Glu, Arg, Ser; X7 is Trp, Glu, Gly, Ile, Asn, Pro, Arg, Thr or OctGly; X8 is Phe, Asn, Pro, Arg, Thr, Trp; X10 is Phe(4-0Me), 1-Nal, 2-Nal, Aic, a-MePhe, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, His, hPhe(3,4-dimethoxy), hTyr, N-Me-Tyr, Trp, Phe(4-CONH2), Phe-(4-phenoxy), Thr, Tic, Tyr(3-tBu), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-NH2), Phe(4-F), Phe(3,5-F2), PheCH2CO2H, Phe(penta-F), Phe(3,4-C12), Phe(4-CF3), Bip, Cha, 4-PyridylAlanine, f3hTyr, OctgGly, Tyr(4-N3), Phe(4-Br), Phe[4-(2-aminoethoxy)]; X11 is 2-Nal, 1-Nal, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe(3,5-F2), Phe(4-CONH2), Phe(4-F),4-phenylcyclohexyl, Phe(4-CF3), a-MePhe, Nal, f3hPhe, f3hTyr, f3hTrp, BIP, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Tyr, Phe(4-0Me), Phe(4-Me), Tyr(2,5,7-tri-tert-Butyl), Phe(4-0Ally1), Phe(3-tBu), Phe(4-tBu), Phe(4-guanidino), Tyr(Bz1), OctGly; X12 is a-Me-Lys, D-Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Tyr, Aib, a-MeLeu, a-MeOrn, Aib, f3-Ala, f3hAla, PhArg, PhLeu, f3hVal, f3-spiro-pip, Glu, hArg, Ile, Lys, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Ser, Thr, Tle, 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, a-DiethylGly, a-MeLys(Ac)õ a-MeSer, a-MeVal; X13 is Lys, Lys(Ac), (D)Asn, (D)Leu, (D)Phe, (D)Thr, Ala, a-MeLeu, Aib, (3-Ala, f3-Glu, PhLeu, f3hVal, f3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, hLeu, Asn, Ogl, Pro, Gln, Ser, Thr, Tba, Tle; X14 is Glu, Gly, His, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Tic; X15 is (D)Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Thr, Aea, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Asn, Arg or f3-Ala; X16 is Gly, Ser, Pro, Asn, Thr; or X17 is Glu, Ser, Gly, Gln.

1004801In particular embodiments of a peptide inhibitor of Formula (IV): X5 is Cys, Cit, Asp, Dab, Dap, Gly, His, hCys, Lys, Met, Asn, N-Me-Ala, N-Me-Asn, N-Me-Lys, N-Me-Gln, N-Me-Arg, Orn, Pro, Pen, Gln, Val; X6 is Glu, Arg, Ser; X7 is Trp, Glu, Gly, Ile, Asn, Pro, Arg, Thr or OctGly; X8 is Phe, Asn, Pro, Arg, Thr, Trp; X10 is Phe(4-0Me), 1-Nal, 2-Nal, Aic, a-MePhe, Bip, (D)Cys, Cha, DMT, (D)Tyr, Glu, His, hPhe(3,4-dimethoxy), hTyr, N-Me-Tyr, Trp, Phe(4-CONH2), Phe-(4-phenoxy), Thr, Tic, Tyr(3-tBu), Phe(4-tBu), Phe(4-CN), Phe(4-Br), Phe(4-NH2), Phe(4-F), Phe(3,5-F2), PheCH2CO2H, Phe(penta-F), Phe(3,4-C12), Phe(4-CF3), Bip, Cha, 4-PyridylAlanine, (3hTyr, OctgGly, Tyr(4-N3), Phe(4-Br), Phe[4-(2-aminoethoxy)]; X11 is 2-Nal, 1-Nal, 2,4-dimethylPhe, Bip, Phe(3,4-C12), Phe(3,5-F2), Phe(4-CONH2), Phe(4-F),4-phenylcyclohexyl, Phe(4-CF3), a-MePhe, Nal, (3hPhe, (3hTyr, (3hTrp, BIP, Nva(5-phenyl), Phe, His, hPhe, Tic, Tqa, Tyr, Phe(4-0Me), Phe(4-Me), Tyr(2,5,7-tri-tert-Butyl), Phe(4-0Ally1), Phe(3-tBu), Phe(4-tBu), Phe(4-guanidino), Tyr(Bz1), OctGly; X12 is a-Me-Lys, D-Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Tyr, Aib, a-MeLeu, a-MeOrn, Aib, (3-Ala, (3hAla, (3hArg, (3hLeu, (3hVal, (3-spiro-pip, Glu, hArg, Ile, Lys, N-MeLeu, N-MeArg, Ogl, Orn, Pro, Gln, Ser, Thr, Tle;
X13 is Lys(Ac), (D)Asn, (D)Leu, (D)Phe, (D)Thr, Ala, a-MeLeu, Aib, (3-Ala, (3-Glu, (3hLeu, (3hVal, (3-spiro-pip, Cha, Chg, Asp, Dab, Dap, a-DiethylGly, hLeu, Asn, Ogl, Pro, Gln, Ser, Thr, Tba, Tle; X14 is Glu, Gly, His, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Tic; X15 is (D)Ala, (D)Asn, (D)Asp, (D)Leu, (D)Phe, (D)Thr, Aea, Asp, Glu, Phe, Gly, Lys, Leu, Pro, Arg; X16 is Gly, Ser, Pro, Asn, Thr; or X17 is Glu, Ser, Gly, Gln.
1004811 In certain embodiments, the peptide inhibitor is cyclized. In particular embodiments, the peptide is cyclized through an intramolecular bond between X4 and X9. In particular embodiments, the intramolecular bond is an amide bond.
1004821 In certain embodiments, the peptide inhibitor is linear or not cyclized.
1004831In particular embodiments of a peptide inhibitor of Formula IV, one or more, two or more, or all three of Xl, X2, and X3 are absent.
1004841In certain embodiments, X3 is Glu, (D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, or (D)Gln. In certain embodiments, X3 is (D)Arg or (D)Phe.

1004851In particular embodiments of a peptide inhibitor of Formula IV, one or more, two or more, or all three of X17, X19 and X20 are absent.
1004861In particular embodiments of a peptide inhibitor of Formula IV, X4 is Dap, Dab, or (D)Dab, and X9 is Glu, (D)Asp, or Asp. In particular embodiments of a peptide inhibitor of Formula I, X4 is Glu, (D)Asp or Asp, and X9 is Dab, Dap or (D)Dab.
1004871In particular embodiments of a peptide inhibitor of Formula IV, X18 is (D)-Lys. In certain embodiments, X17 is absent and X18 is (D)-Lys.
1004881In particular embodiments of a peptide inhibitor of Formula IV, the peptide inhibitor includes one or more, two or more, three or more, or all four of the following features: X5 is Gln;
X6 isThr; X7 is Trp; and X8 is Gln.
1004891In particular embodiments of a peptide inhibitor of Formula IV, the peptide inhibitor includes one or more, two or more, three or more, four or more, five or more, six or more, or seven of the following features: X10 is Tyr, Phe[4-(2-aminoethoxy)], Phe(4-CONH2) or Phe(4-0Me); X11 is 2-Nal or Trp; X12 is 4-amino-4-carboxy-tetrahydropyran, Achc Acpc, Acbc, Acvc, Aib, a-DiethylGly, a-MeLys, a-MeLys(Ac), a-Me-Leu, a-MeOrn, a-MeSer, a-MeVal, or Arg; X13 is Glu or Lys(Ac); X14 is Asn; X15 is Gly, Asn, or f3-Ala; and X16 is AEA. In particular embodiments of a peptide inhibitor of Formula IV, the peptide inhibitor includes one or more, two or more, three or more, four or more, five or more, six or more, or seven of the following features: X10 is Tyr; X11 is Trp; X12 is Arg; X13 is Glu; X14 is Asn; X15 is Gly; and X16 is AEA.
1004901In particular embodiments of a peptide inhibitor of Formula IV, the peptide inhibitor includes one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more ten or more or all of the following features: X5 is Gln; X6 isThr; X7 is Trp; X8 is Gln; X10 is Tyr; X11 is Trp; X12 is Arg; X13 is Glu or Lys(Ac); X14 is Asn; X15 is Gly; and X16 is AEA. In particular embodiments of a peptide inhibitor of Formula IV, the peptide inhibitor includes one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more ten or more or all of the following features: X5 is Gin; X6 isThr; X7 is Trp; X8 is Gin; X10 is Tyr; X11 is Trp;
X12 is Arg; X13 is Glu; X14 is Asn; X15 is Gly; and X16 is AEA.
1004911In certain embodiments of a peptide inhibitor of Formula IV, the peptide is cyclized via X4 and X9; X5, X6, X7 and X8 are Gin, Thr, Trp, and Gin, respectively; and X10, X11, X12, X13, X14, X15, and X16 are Tyr, Trp, Arg, Glu, Asn, Gly, and AEA, respectively.
1004921In certain embodiments, the present invention includes a peptide of 8 to 20 amino acids, optionally cyclized, comprising or consisting of having a core sequence comprising:
Xaa4-Xaa5-Xaa6-Trp-Xaa8-Xaa9-[Phe(4-0Me)]-[ 2-Nail (Formula IVb) [00493] wherein Xaa4 and Xaa9 are each independently selected from Dap, Dab, Glu, Asp, (D)-Asp and(D)-Dab, wherein Xaa4 and Xaa9 are capable of forming an intramolecular bond, e.g., a cyclic amide; and Xaa5, Xaa6 and Xaa8 are any amino acid residue, wherein the peptide inhibits binding of IL-23 to IL-23R. In particular embodiments, the peptide inhibitor is a peptide inhibitor of Formula IV. In particular embodiments, the peptide inhibits the binding of IL-23 to 1004941In certain embodiments, of a peptide inhibitor of Formula IV, the peptide inhibitor has a structure shown in Table 7 or comprises an amino acid sequence set forth in Table 7.
1004951Certain illustrative peptide inhibitors of the present invention are also shown in any of Formulas (Va), (Vb), (Vc), (Vd), (Ve), (Vf), (Vg) and (Vh), and in Tables 2-5, which provide the amino acid sequence of selected peptide inhibitors. These peptide inhibitors are acetate salts.
Optional Characteristics of Peptide Inhibitors 1004961Any of the peptide inhibitors of the present invention may be further defined, e.g., as described below. It is understood that each of the further defining features described herein may be applied to any peptide inhibitors where the amino acids designated at particular positions allow the presence of the further defining feature.
1004971In certain embodiments of any of the peptide inhibitors described herein, the peptide inhibitor is cyclized.

1004981In certain embodiments of any of the peptide inhibitors described herein, the peptide inhibitor or monomer subunit thereof is linear or not cyclized. In certain embodiments where the peptide is linear or not cyclized, X4 and X9 can be any amino acid.
[00499] In certain embodiments, the peptide inhibitor is cyclized, e.g., through X4 and X9.
1005001 In various embodiments, Rl is a bond, hydrogen, a C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl Cl -C6 alkyl, or a Cl -C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing, e.g., acetyl. It is understood that the Rl may replace or be present in addition to the typical amine group located at the amino terminus of a peptide. It is further understood that Rl may be absent. In certain embodiments, the peptide inhibitor comprises an N-terminus selected from hydrogen, a C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl C1-C6 alkyl, or a C1-C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing, e.g., acetyl. In particular embodiments of any of the peptide inhibitors described herein, Rl or the N-terminal moiety is hydrogen. In certain embodiments, Rl is a bond, e.g., a covalent bond.
1005011In certain embodiments of any of the peptide inhibitors having any of the various Formulas set forth herein, Rl or the N-terminal moiety is selected from methyl, acetyl, formyl, benzoyl, trifluoroacetyl, isovaleryl, isobutyryl, octanyl, and the conjugated amides of lauric acid, hexadecanoic acid, and y-Glu-hexadecanoic acid. In one embodiment, Rl or the N-terminal moiety is pG1u. In certain embodiments, Rl is hydrogen. In particular embodiments, Rl is acetyl, whereby the peptide inhibitor is acylated at its N-terminus, e.g., to cap or protect an N-terminal amino acid residue, e.g., an N-terminal Pen or Abu residue.
1005021In certain embodiments of any of the peptide inhibitors described herein, Rl or the N-terminal moiety is an acid. In certain embodiments, Rl or the N-terminal moiety is an acid selected from acetic acid, formic acid, benzoic acid, trifluoroacetic acid, isovaleric acid, isobutyric acid, octanoic acid, lauric acid, hexadecanoic acid, 4-Biphenylacetic acid, 4-fluorophenylacetic acid, gallic acid, pyroglutamic acid, cyclopentanepropionic acid, glycolic acid, oxalic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, palmitic acid, benzoic acid, 3-(4-hydroxybenzoyl) benzoic acid, cinnamic acid, mandelic acid, 4-methylbicyclo(2.2.2)-oct-2-ene-1 -carboxylic acid, glucoheptonic acid, 3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid, an alkylsulfonic acid and an arylsulfonic acid.
1005031In particular embodiments, Rl or the N-terminal moiety is an alkylsulfonic acid selected from methanesulfonic acid, ethanesulfonic acid, 1,2-ethane-disulfonic acid, and 2-hydroxyethanesulfonic acid.
1005041In particular embodiments, Rl or the N-terminal moiety is an arylsulfonic acid selected from benzenesulfonic acid, 4- chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, and camphorsulfonic acid.
1005051In some embodiments, wherein a peptide of the present invention comprises a conjugation to an acidic compound such as, e.g., isovaleric acid, isobutyric acid, valeric acid, and the like, the presence of such a conjugation is referenced in the acid form.
So, for example, but not to be limited in any way, instead of indicating a conjugation of isovaleric acid to a peptide by referencing i s oval eroyl (e. g. , isovaleroyl- [Pen] - Q TWQ [Pen]- [Phe(4-0Me)]- [2-Nal] - [a-MeLys]-[Lys(Ac)]-NG-NH2, in some embodiments, the present application references such a conjugation as isovaleric acid-[Pen]-QTWQ[Pen]-[Phe(4-0Me)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]-NG-NH2.
Reference to the conjugation in its acid form is intended to encompass the form present in the peptide inhibitor.
1005061In certain embodiments, the peptide inhibitor comprises a C-terminus (e.g., R2 or the C-termial moiety) selected from a bond, OH or NH2. In certain embodiments, R2 is a bond. In various embodiments of any of the peptide inhibitors having any of the various Formulas set forth herein, R2 or the C-terminal moiety is OH or NH2. It is understood that the R2 or the C-terminal moiety may replace or be present in addition to the carboxyl group typically located at the carboxy terminus of a peptide. It is further understood that R2 may be absent.
1005071In particular embodiments of any of the peptide inhibitors having any of the various Formulae set forth herein, X comprises or consists of 7 to 35 amino acid residues, 8 to 35 amino acid residues, 9 to 35 amino acid residues, 10 to 35 amino acid residues, 7 to 25 amino acid residues, 8 to 25 amino acid residues, 9 to 25 amino acid residues, 10 to 25 amino acid residues, 7 to 20 amino acid residues, 8 to 20 amino acid residues, 9 to 20 amino acid residues, 7 to 18 amino acid residues, 8 to 18 amino acid residues, 9 to 18 amino acid residues, or 10 to 18 amino acid residues.
[00508] In certain embodiments of any of the Formulae set forth herein, X
either or both does not comprise or does not consist of an amino acid sequence set forth in US Patent Application Publication No. US2013/0029907. In certain embodiments of any of the Formulae set forth herein, X either or both does not comprise or does not consist of an amino acid sequence set forth in US Patent Application Publication No. US2013/0172272.
1005091In certain embodiments of any of the peptide inhibitors described herein, the peptide inhibitor, or each monomer subunit thereof, comprises or consists of at least 3, at least 4 at least 5, at least 6, or at least 7 amino acid residues carboxy terminal of the X9 amino acid residue. In particular embodiments of any of the peptide inhibitors described herein, the peptide inhibitor comprises 3 to 11,3 to 10,3 to 9,3 to 8,3 to 7,3 to 6,3 to 5,3 to 4, 3, 4, 5, 6, 7, 8, 9, 10, or 11 amino acid residues carboxy terminal of the X9 amino acid residue.
1005101In certain embodiments of any of the peptide inhibitors described herein, the peptide inhibitor, or each monomer subunit thereof, comprises or consists of 4 amino acid residues between X4 and X9. In one embodiment, both X4 and X9 are cysteines.
[00511]In certain embodiments, a peptide inhibitor of any of the Formulae described herein comprises the amino acid residues or moieties indicated as X4-X15. In particular embodiments, the peptide inhibitor does not include X1 -X3 or X16-X20. In certain embodiments, the peptide inhibitors include an N-terminal extension of one to three amino acid residues corresponding to any of X1 -X3. In particular embodiments, any one or more of X1 , X2 and X3, when present, are a D-amino acid. In certain embodiments, the peptide inhibitors include an C-terminal extension of one to five amino acid residues corresponding to any of X16-X20. In particular embodiments, any one or more of X16, X17, X18, X19 and X20, when present, are a D-amino acid.
Illustrative amino acid residues that may be present in the N-terminal and/or C-terminal extensions are shown in Tables 3 and 5. These tables each show a first peptide inhibitor, with derivates thereof comprising N-terminal extensions, C-terminal extensions, and/or conjugated moieties. The present invention includes derivatives of any fo the peptide inhibitors described herein comprising one or more such N-terminal extension, C-terminal extension, and/or conjugated moiety. In certain embodiments, any of the amino acid residues shown in the extended positions in Tables 3 and 5 may be present in any combination in a peptide inhibitor of the present invention. In particular embodiments, the N-terminal and/or C-terminal extensions are associated with an increased half-life, e.g., upon administration to a subject.
1005121In certain embodiments of any of the peptide inhibitors described herein, the peptide inhibitor, or each monomer subunit thereof, comprises the amino acid sequence motif, W-X-X-Y-W, e.g., at positions X7-X11. In certain embodiments, the peptide inhibitor, or each monomer subunit thereof, comprises the amino acid sequence motif, C-X-X-W-X-C-Y-W, e.g., at positions X4-X11. In certain embodiments, the peptide inhibitor, or each monomer subunit thereof, comprises the amino acid sequence motif, Pen-X-X-W-X-Pen-Y-W, e.g., at positions X4-X11. In certain embodiments of any of the peptide inhibitors described herein, the peptide inhibitor, or both monomer subunit thereof, does not comprise the amino acid sequence motif, W-X-X-Y-W, e.g., at positions X7-X11, where X is any amino acid.
1005131In certain embodiments of any of the Formula or peptide inhibitors described herein, the peptide inhibitor comprises one or more amino acid residues N-terminal to X4.
In particular embodiments, X3 is present. In certain embodiments, X3 is Glu, (D)Glu, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, or (D)G1n. In certain embodiments, X3 is (D)Arg or (D)Phe.
1005141In particular embodiments of any of the Formula or peptide inhibitors described herein, the peptide inhibitor comprises an amino acid at X2. In particular embodiments, X2 is Glu, (D)Asp, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, (D)G1n, or (D)Asn. In certain embodiments, X2 and X3 are present. In particular embodiments, X2 is Glu, (D)Asp, Arg, (D)Arg, Phe, (D)Phe, 2-Nal, Thr, Leu, (D)G1n, or (D)As, and X3 is (D)Arg.
1005151In certain embodiments, a peptide inhibitor of the present invention, or one or both monomer subunits thereof, comprises, optionally at its C-terminus, one of the following amino acid sequences:
ENG;
ENN;
[4-amino-4-carboxy-tetrahydropyran] -ENN;

[Lys(Ac)]-NN;
[a-MeLys]-ENG;
[a-MeLys]- [Lys(Ac)]-NN;
[a-MeLeu]- [Lys(Ac)]-NN
[a-MeLeu]-ENG;
[a-MeOrn]-[Lys(Ac)]-NG;
[a-MeLeu]-ENG;
Aib-[Lys(Ac)]-NG;
Aib-[Lys(Ac)]-NN;
NG-[AEA](D)-Lys];
[Dapa]-NG-[AEA] - [(D)-Lys];
[Orn]-NG-[AEA]-[(D)-Lys];
[a-MeLys]-ENN;
[4-amino-4-carboxy-tetrahydropyran]- [Lys(Ac)]-NN;
[Achc]-[Lys(Ac)]-NN; or [Acpc]-[Lys(Ac)]-NN.
[00516] In particular embodiments, one of these amino acid sequences constitutes the terminal C-terminal amino acids of the peptide. In particular embodiment, these amino acid sequences correspond to X13-X15 or X12-X15 or X14-X16 or X13-X17.
1005171In certain embodiments, a peptide inhibitor of the present invention, or one or both monomer subunits thereof, comprises, optionally at its C-terminus, one of the following amino acid sequences:
WQCY42-NalHa-MeLys];
WQC-[Phe(4-0Me)]-[2-Nal]-[a-MeLys];

WQC- [Phe(4-0Me)]- [2-Nall- [Al b];
WQ-[Pen]-[Phe(4-0Me)]- [2-Nall- [a-MeLys];
W-Xaa8-C-Phe[4-(2-aminoethoxy)] 42-Nall;
W-Xaa8-C-Phe[4-(2-aminoethoxy)] ;
W-Xaa8-C-Phe[4-(2-aminoethoxy)]; or 1005181 W-Xaa8-C-[Phe(4-0CH3)]. In particular embodiments, one of these amino acid sequences constitutes the terminal C-terminal amino acids of the peptide. In particular embodiment, these amino acid sequences correspond to X7 to X12 or X7 to X11 or X7 to X10.
1005191In certain embodiments of any of the peptide inhibitors described herein, including both peptide monomer inhibitors and monomer subunits of peptide dimer inhibitors, the peptide monomer inhibitor or monomer subunit is cyclized via a peptide bond between its N-terminal amino acid residue and its C-terminal amino acid residue. In particular embodiments, the peptide inhibitor (or monomer subunit thereof) comprises both an intramolecular bond between X4 and X9 and a peptide bond between its N-terminal amino acid residue and its C-terminal amino acid residue. In certain embodiments, the intramolecular bond is any of those described herein, e.g., a disulfide bond or a thioether bond.
[00520] In certain embodiments, the present invention includes a peptide inhibitor that comprises a core consensus sequence selected from one of the following (shown in N-terminal to C-terminal direction):
X1 -X2 -X3 -Pen-X5-X6-W-X8-Pen-X10-X11 -X12 -X13 -X14-X15;
Pen-X5-X6-W-Q-Pen;
Pen-X5-X6-W-X8-Pen;
Pen-X5 -X6-W-X8 -Pen- [Phe(4-CONH2)]; and Pen-X5-X6-W-X8-Pen- [Phe [4- (2-aminoethoxy)] , wherein the Pen residues arejoined by an intramolecular bond, e.g., disulphide bond. Xl, X2, X3, X5, X6, X8, X10, X11, X12, X13, X14, and X15 may be any amino acid. In some embodiment X5 is Arg, Asn, Gln, Dap, Orn; X6 is Thr or Ser; and X8 is Gln, Val, Phe, Glu, Lys.
In particular embodiments, Xl, X2, X3, X5, X6, X8, X10, X11, X12, X13, X14, and X15 are defined as described in any of the various Formulas and peptide inhibitors described herein.
1005211 In certain embodiments, the present invention includes a peptide inhibitor that comprises a core consensus sequence selected from one of the following (shown in N-terminal to C-terminal direction):
X1 -X2-X3-Abu-X5-X6-W-X8-C-X9-X10-X11-X12-X13-X14-X15;
Abu-X5-X6-W-Q-C;
Abu-X5-X6-W-X8-C;
Abu-X5-X6-W-X8-C-[Phe(4-CONH2)]; and Abu-X5-X6-W-X8-C-[Phe[4-(2-aminoethoxy)]], where Abu and C are linked through a intra moleculer thiother bond. Xl, X2, X3, X5, X6, X8, X10, X11, X12, X13, X14, and X15 may be any amino acid. In some embodiment X5 is Arg, Asn, Gln, Dap, Orn; X6 is Thr or Ser; and X8 is Gln, Val, Phe, Glu, Lys. In particular embodiments, Xl, X2, X3, X5, X6, X8, X10, X11, X12, X13, X14, and X15 are defined as described in any of the various Formulas and peptide inhibitors described herein.
1005221In certain embodiments, any of the peptide inhibitors described herein may be further cyclized via a peptide bond between its N-terminal amino acid residue and its C-terminal amino acid residue. In particular embodiments, the peptide inhibitor comprises a peptide bond between X3 or X4 and any one of X9, X10, X11, X12, X13, X14, X15, X16, X17, X18, X19 or X20. In particular embodiments, peptide inhibitors of the present invention comprise a peptide bond between their N-terminal and C-terminal amino acid residues, and they also comprise an intramolecular bond between X4 and X9. In certain embodiments, the intramolecular bond is a disulfide bond, a thioether bond, a lactam bond or any of the other bonds described herein.

Peptide Dimers 1005231In certain embodiments, the present invention includes dimers of the monomer peptide inhibitors described herein, including dimers of any of the monomer peptide inhibitors described herein or in the accompanyingtables, figures or sequences listing. These dimers fall within the scope of the general term "peptide inhibitors" as used herein. Illustrative dimers of the present invention are also shown in the accompanying tables, which indicate the dimerized monomer subnits in brackets followed by the linker. Unless otherwise indicated, the subunits are linked via their C-termini. The term "dimer," as in a peptide dimer, refers to compounds in which two peptide monomer subinits are linked. A peptide dimer inhibitor of the present invention may comprise two identical monomer subunits, resulting in a homodimer, or two non-identical monomer subunits, resulting in a heterodimer. A cysteine dimer comprises two peptide monomer subunits linked through a disulfide bond between a cysteine residue in one monomer subunit and a cysteine residue in the other monomer subunit.
1005241In some embodiments, the peptide inhibitors of the present invention may be active in a dimer conformation, in particular when free cysteine residues are present in the peptide. In certain embodiments, this occurs either as a synthesized dimer or, in particular, when a free cysteine monomer peptide is present and under oxidizing conditions, dimerizes.
In some embodiments, the dimer is a homodimer. In other embodiments, the dimer is a heterodimer.
1005251In certain embodiments, a peptide dimer inhibitor of the present invention is a peptide dimer comprising two peptide inhibitors of the invention, including but not limited to a homodimer or heterdimer comprising any of the peptide sequences shown herein, e.g., in Tables 3A-3H, 4A, 4B, 5A-5C, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15.
[00526] Certain amino acid sequences listed in Tables 3A-3H, 4A, 4B, 5A-5C, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15 are shown using one letter codes for amino acids. Where only the monomer peptide inhibitor sequences are shown; however it is understood that, in certain embodiments, these monomer peptide inhibitors, i.e., monomer subunits, are dimerized to form peptide dimer inhibitors, in accordance with the present teaching and as shown generally, e.g., in Tables 3A-3H, 4A, 4B, 5A-5C, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15.

[00527] In certain embodiments, monomer subunits of the present invention may be dimerized by a suitable linking moiety, e.g., a disulphide bridge between two cysteine residues, one in each peptide monomer subunit, or by another suitable linker moiety, including but not limited to those defined herein. Some of the monomer subunits are shown having C- and N-termini that both comprise free amine. Thus, to produce a peptide dimer inhibitor, the monomer subunit may be modified to eliminate either the C- or N-terminal free amine, thereby permitting dimerization at the remaining free amine. Further, in some instances, a terminal end of one or more monomer subunits is acylated with an acylating organic compound selected from the group consisting of:
Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Trifluoromethyl butyric, cy cl op entane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3 -Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, monomer subunits comprise both a free carboxy terminal and a free amino terminal, whereby a user may selectively modify the subunit to achieve dimerization at a desired terminus.
One having skill in the art therefore, will appreciate that the monomer subunits of the instant invention may be selectively modified to achieve a single, specific amine for a desired dimerization.
1005281It is further understood that the C-terminal residues of the monomer subunits disclosed herein are optionally amides. Further, it is understood that, in certain embodiments, dimerization at the C-terminus is facilitated by using a suitable amino acid with a side chain having amine functionality, as is generally understood in the art. Regarding the N-terminal residues, it is generally understood that dimerization may be achieved through the free amine of the terminal residue, or may be achieved by using a suitable amino acid side chain having a free amine, as is generally understood in the art.
1005291 The linker moieties connecting monomer subunits may include any structure, length, and/or size that is compatible with the teachings herein. In at least one embodiment, a linker moiety is selected from the non-limiting group consisting of cysteine, lysine, DIG, PEG4, PEG4-biotin, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, ADA, Boc-IDA, Glutaric acid, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, 1,2-phenylenediacetic acid, Triazine, Boc-Triazine, IDA-biotin, PEG4-Biotin, AADA, suitable aliphatics, aromatics, heteroaromatics, and polyethylene glycol based linkers having a molecular weight from approximately 400Da to approximately 40,000Da. Non-limiting examples of suitable linker moieties are provided in Table 2A.
Table 2A. Illustrative Linker Moieties Abbrivation Discription Structure DIG DIGlycolic acid, Bifunctional PEG linker with 4 PolyEthylene Glycol units a Bifunctional PEG linker with 13 PolyEthylene Glycol units Bifunctional PEG linker with 25 PolyEthylene Glycol units Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 1000Da Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 2000Da Bifunctional PEG linker with PolyEthylene PEG3.4K
Glycol Mol wt of 3400Da Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 5000Da DIG DIGlycolic acid (3-A1a-IDA (3-A1a-Iminodiacetic acid Y-Boc- (3 -Ala-Iminodiacetic acid Ala-IDA

Ac-(3 -Ala -Ac- (3 -Ala-Iminodiacetic acid IDA

Palmityl- (3 -Ala-Iminodiacetic acid Palm 0 )=3 GTA Glutaric acid PMA Pemilic acid oo AZA Azelaic acid DDA Dodecanedioic acid IPA Isopthalic aicd 1,3-PDA 1,3- Phenylenediacetic acid 1,4-PDA 1,4- Phenylenediacetic acid 0 1,2-PDA 1,2 - Phenylenediacetic acid N=<
Triazine Amino propyl Triazine di-acid ti¨c 114 N¨)1_0 Ni)-Boc- \ N=( Boc-Triazine di-acid N4 14 Triazine 14 4 Amino diacetic acid , 0 ADA (which may also referred to as Iminodiacetic 0/4J.L0 acid) n-Acetyl amino acetic acid AADA (which may also referred to as N-acetyl )0jL

Iminodiacetic acid) ,-, PEG4- PEG4-Biotin (Product number 10199, Biotin QuantaBioDesign) 'l .NC\r"\-1H-\''',.---\;,--ve'c,-%"./11,:,=, ---'N
IDA-Biotin N-Biotin- (3 -Ala-Iminodiacetic acid e ) c,..
OH

OH
Lys Lysine H2N

10053011n some embodiments, a peptide dimer inhibitor is dimerized via a linker moiety. In some embodiments, a peptide dimer inhibitor is dimerized via an intermolecular disulfide bond formed between two cysteine residues, one in each monomer subunit. In some embodiments, a peptide dimer inhibitor is dimerized via both a linker moiety and an intermolecular disulfide bond formed between two cysteine residues. In some embodiments, the intramolecular bond is a thioether, lactam, triazole, selenoether, diselenide or olefin, instead of the disulfide bond.
[00531] An illustrative diageam of one embodiments of a dimer is shown below:
o o NH2 NH2 it o o./ 0 0 0 0 .N

N N N

0 H.,....1-1OjciH H
N NH
HNN N [Nlj= 1\1,..,NH2 N
H H H H

-o NH2 111 NH -1) HN,Ire 01) NH

o/HH
0HO o o o o JNH2 0 OH
I-I...... H H
HN\/cN N ENIA N
N N N N N [gi r\h(rNH2 H H

H

-NH

HN

S S

Compound D .

[00532] One having skill in the art will appreciate that the linker (e.g., C-and N-terminal linker) moieties disclosed herein are non-limiting examples of suitable, and that the present invention may include any suitable linker moiety. Thus, some embodiments of the present invention comprises a homo- or heterodimer peptide inhibitor comprised of two monomer subunits selected from the peptides shown in any of tables herein or comprising or consisting of a sequence presented in any of tables herein, wherein the C- or N-termini of the respective monomer subunits (or internal amino acid residues) are linked by any suitable linker moiety to provide a dimer peptide inhibitor having IL-23R inhibitory activity. In certain embodiments, a linker binds to the N- or C-terminus of one monomer subunit and an internal amino acid residue of the other monomer subunit making up the dimer. In certain embodiments, a linker binds to an internal amino acid residue of one monomer subunit and an internal amino acid residue of the other monomer subunit making up the dimer. In further embodiments, a linker binds to the N-or C-terminus of both subunits.
1005331In particular embodiments, a peptide inhibitor of the present invention comprise two or more polypeptide sequences of monomer peptide inhibitors described herein.
1005341In one embodiment, a peptide dimer inhibitor of the present invention comprises two peptide monomer subunits connected via one or more linker moieties, wherein each peptide monomer subunit comprises or consists of 7 to 35 amino acid residues, 8 to 35 amino acid residues, 9 to 35 amino acid residues, 10 to 35 amino acid residues, 7 to 25 amino acid residues, 8 to 25 amino acid residues, 9 to 25 amino acid residues, 10 to 25 amino acid residues, 7 to 20 amino acid residues, 8 to 20 amino acid residues, 9 to 20 amino acid residues, 7 to 18 amino acid residues, 8 to 18 amino acid residues, 9 to 18 amino acid residues, or 10 to 18 amino acid residues and comprises the sequence of Formula Ia, as described herein.
1005351In particular embodiments, one or both of the monomer subunits comprise the sequence of any one of Formula Formula X, Formula I, II, III, IV or V as described herein.
1005361In certain embodiments, a peptide dimer inhibitor comprises two peptide monomer subunits connected via one or more linker moieties, wherein each peptide monomer subunit is 8-20 amino acids in length and comprises a sequence of any one of the formulas describd herein, e.g., Formula X, Formula I, II, III, IV or V. In certain embodiments, a peptide dimer inhibitor comprises two peptide monomer subunits connected via one or more linker moieties, wherein each peptide monomer subunit is 8-20 amino acids in length and comprises a sequence of any one of Formula X, Formula I, II, III, IV or V.
[00537] In certain embodiments, a peptide dimer inhibitor has the structure of Formula VI:
(R1-X-R2)2-L (VI) [00538] or a pharmaceutically acceptable salt or solvate thereof, [00539] wherein each Rl is independently absent, a bond (e.g., a covalent bond), or R1 is selected from hydrogen, a C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl C1-C6 alkyl, a C 1 -C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing;
[00540] each R2 is independently absent, a bond (e.g., a covalent bond), or selected from OH or NH2;
1005411L is a linker moiety; and [00542] each X is an independently selected peptide monomer subunit comprising or consisting of 7 to 35 amino acid residues, 8 to 35 amino acid residues, 9 to 35 amino acid residues, 10 to 35 amino acid residues, 7 to 25 amino acid residues, 8 to 25 amino acid residues, 9 to 25 amino acid residues, 10 to 25 amino acid residues, 7 to 20 amino acid residues, 8 to 20 amino acid residues, 9 to 20 amino acid residues, 7 to 18 amino acid residues, 8 to 18 amino acid residues, 9 to 18 amino acid residues, or 10 to 18 amino acid residues amino acids in length, each comprising or consisting of the sequence of Formula Ia, as described herein. In particular embodiments, each peptide monomer subunit comprises or consists of a sequence of Formula Ix, Ia, Ib, Ic, Id, Ie, If, Ig, Ih, Ti, Ij, Ik, Tl, Im, In, To, Ip, Iq, Iq', Is, It, IIa, IIb, IIc, IId, Ma, Mb, IIIc, IIId, Me, IVa, IVb, or Va-Vh as described herein.
1005431In certain embodiments, one or both peptide monomer subunit of a peptide dimer inhibitor is cyclized, e.g., via an intramolecular bond between X4 and X9. In certain embodiments wherein both peptide monomer subunits are cyclized, the intramolecular bond may be the same or different between the two peptide monomer subinits. In certain embodiments, one or both intramolecular bond is a disulfide bond, a thioether bond, a lactam bond, a selenoether, diselenide, or an olefin bond.
1005441In one embodiment, X4 and X9 of the one or both cyclized peptide monomer subunit is independently selected from Cys, Pen, hCys, D-Pen, D-Cys and D-hCys, and the intramolecular bond is a disulfide bond.
1005451In one embodiment, X4 and X9 of the one or both cyclized peptide monomer subunit is independently selected from Glu, Asp, Lys, Orn, Dap, Dab, D-Dap, D-Dab, D-Asp, D-Glu and D-Lys, and the intramolecular bond is a lactam bond.
1005461 In one embodiment, X4 and X9 of the one or both cyclized peptide monomer subunit are each independently selected from f3-azido-Ala-OH, propargylglycine, and the peptide dimer inhibitor is cyclized through a triazole ring. In one embodiment, X4 and X9 of the one or both cyclized peptide monomer subunit are each independently selected from 2-allylglycine, 2-(3'-butenyl)glycine, 2-(4'-pentenyl)glycine, 2-(5'-hexenyl)glycine, and the peptide dimer inhibitor is cyclized vi a ring closing methasis to give the corresponding olefins /
'stapled peptides'.
10054711n one embodiment, X4 of one or both cyclized peptide monomer subunit is 2-chloromethylbenzoic acid, mercapto-propanoic acid, mercapto-butyric acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, or hSer(C1), X9 of one or both cyclized peptide monomer subunit is hSer(C1), Cys, Pen, hCys, D-Pen, D-Cys or D-hCys, and the intramolecular bond is a thioether bond.
10054811n one embodiment, X4 of one or both cyclized peptide monomer subunit is 2-chloromethylbenzoic acid, 2-chloro-acetic acid, 3-choro-propanoic acid, 4-chloro-butyric acid, 3-chloro-isobutyric acid, hSer(C1), or Sec, X9 of one or both cyclized peptide monomer subunit is hSer(C1) or Sec, and the intramolecular bond is a selenoether bond.
1005491 In certain embodiments, one or both intramolecular bond is a diselenide bond.
1005501In certain embodiments, one or both peptide monomer subunits is linear or not cyclized.

1005511In particular embodiments, of the peptide dimer inhibitors, each X7 and each X11 are both W. In certain embodiments, each X7 and each X11 are both W, each X10 is Y, and each X4 and X9 are both C. In certain embodiments, each X7 and each X11 are both W, each X10 is Y, and each X4 and X9 are amino acids capable of forming an intramolecular bond that is a thioether bond, a lactam bond, a triazole, a selenoether, a diselenide bond, or an olefin bond.
1005521In certain embodiments of the peptide dimer inhibitors, one or both peptide monomer subunit has a structure shown herein, e.g., in Tables 3A-3I, or comprises an amino acid sequence shown herein, e.g., as set forth in Tables 3A-3I, or wherein the peptide dimer inhibitor has a structure shown herein, e.g., in Table 3F, or comprises an amino acid sequence shown herein, e.g., as set forth in Table 3F.
1005531In particular embodiments, each Rl is independently a bond (e.g., a covalent bond), or selected from hydrogen, a C 1 -C6 alkyl, a C6-C12 aryl, a C6-C12 aryl C 1 -C6 alkyl, a C1-C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing. In particular embodimetns, the N-terminus of each subunit includes a moiety selected from hydrogen, a C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl C 1 -C6 alkyl, a C1-C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing.
10055411n certain embodiments of any of the peptide inhibitors having any of the various Formulae set forth herein, each R1 (or N-terminal moiety) is selected from methyl, acetyl, formyl, benzoyl, trifluoroacetyl, isovaleryl, isobutyryl, octanyl, and the conjugated amides of lauric acid, hexadecanoic acid, and y-Glu-hexadecanoic acid.
1005551ln particular embodiments, each R2 (or C-terminal moiety) is independently a bond (e.g., a covalent bond), or selected from OH or NH2.
1005561In particular embodiments of any of the peptide inhibitors having any of the various Formulae set forth herein, each X comprises or consists of 7 to 35 amino acid residues, 8 to 35 amino acid residues, 9 to 35 amino acid residues, 10 to 35 amino acid residues, 7 to 25 amino acid residues, 8 to 25 amino acid residues, 9 to 25 amino acid residues, 10 to 25 amino acid residues, 7 to 18 amino acid residues, 8 to 18 amino acid residues, 9 to 18 amino acid residues, or 10 to 18 amino acid residues.

1005571In particular embodiments, one or both X comprises or consists of the sequence of any one of the formulas described herein. In certain embodiments of any of the peptide inhibitors, including dimers, or Formulae set forth herein, an X does not comprise or consist of an amino acid sequence set forth in US Patent Application Publication No.
US2013/0029907. In certain embodiments of any of the peptide inhibitors, including dimers, or formulas set forth herein, an X does not comprise or consist of an amino acid sequence set forth in US
Patent Application Publication No. US2013/0172272.
1005581 In particular embodiments of peptide inhibitors of the present invention (both monomers and dimers) comprising Cys at position X4 and Cys at position X9, the Cys at position X4 and and the Cys at position X9 are linked by a disulphide bridge.
1005591In particular embodiments of peptide inhibitors of the present invention, each X7 and each X11 are not both W.
1005601In particular embodiments of peptide inhibitors of the present invention, each X7 and each X11 are both W.
1005611In particular embodiments of peptide inhibitors of the present invention, each X7 and each X11 are both W, X10 is Y, and X4 and X9 are both C.
1005621In certain embodiments, at least two cysteine residues of the peptide dimer inhibitor are linked by a disulphide bridge, either intramolecular or intermolecular.
10056311n particular embodiments of either or both monomer subunit (e.g., Ix, Ia-It where permissible) present in a peptide dimer inhibitor, X4 and X9 are both Cys.
10056411n particular embodiments of either or both monomer subunit (e.g., Ix, Ia-It where permissible) present in a peptide dimer inhibitor, X7 and X11 are both W.
10056511n particular embodiments of either or both monomer subunit (e.g., Ia-It where permissible) present in a peptide dimer inhibitor, X7 and X11 are both W, X10 is Y, and X4 and X9 are both Cys.

10056611n particular embodiments of either or both monomer subunit (e.g., Ia-It where permissible) present in a peptide dimer inhibitor, X15 is Gly or Ser.
10056711n particular embodiments of either or both monomer subunit (e.g., Ia-It where permissible) present in a peptide dimer inhibitor, X16 is AEA or AEP.
10056811n particular embodiments of either or both monomer subunit (e.g., Ia-It where permissible) present in a peptide dimer inhibitor, X10 is Tyr or Phe, or an analog of Tyr or Phe.
10056911n particular embodiments of either or both monomer subunit (e.g., Ia-It where permissible) present in a peptide dimer inhibitor, X11 is Trp.
1005701In particular embodiments of any of the peptide dimer inhibitors described herein, either or both 1Z1 is hydrogen.
[00571] In particular embodiments of peptide dimer inhibitors of the present invention, the linker moiety (L) is any of the linkers described herein or shown in Table 2A or 2B.
In certain embodiments, L is a lysine linker, a diethylene glycol linker, an iminodiacetic acid (IDA) linker, a P-Ala-iminodiaceticacid (f3-Ala-IDA) linker, or a PEG linker.
1005721In various embodiments of any of the peptide dimer inhibitors, each of the peptide monomer subunits is attached to a linker moiety via its N-terminus, C-terminus, or an internal amino acid residue.
1005731In certain embodiments of any of the peptide dimer inhibitors, the N-terminus of each peptide monomer subunit is connected by a linker moiety.
1005741In certain embodiments of any of the peptide dimer inhibitors, the C-terminus of each peptide monomer subunit is connected by a linker moiety.
1005751In certain embodiments of any of the peptide dimer inhibitors, each peptide monomer subunit is connected by a linker moiety attached to an internal amino acid.

1005761In certain embodiements of peptide dimer inhibitors, the linker moiety is a diethylene glycol linker, an iminodiacetic acid (IDA) linker, a f3-Ala-iminodiaceticacid (j3-Ala-IDA) linker, or a PEG linker.
1005771In certain embodiments of the peptide dimer inhibitors, one or both peptide monomer subunit has a structure shown in any of the tables in the Examples or comprises an amino acid sequence set forth in any of the tables in the Examples.
1005781In certain embodiments of any of the peptide inhibitors, including dimers, or Formulae set forth herein, an X does not comprise or consist of an amino acid sequence set forth in US
Patent Application Publication No. US2013/0029907. In certain embodiments of any of the peptide inhibitors, including dimers, or Formulas set forth herein, an X does not comprise or consist of an amino acid sequence set forth in US Patent Application Publication No.
US2013/0172272.
1005791In particular embodiments of peptide inhibitors of the present invention, each X7 and each X11 are both W, X10 is Y, and X4 and X9 are both Pen.
In certain embodiments, at least two cysteine residues of the peptide dimer inhibitor are linked by a disulphide bridge, either intramolecular or intermolecular.
Peptide Inhibitor Conjugates and Biopolymers 1005801In certain embodiments, peptide inhibitors of the present invention, including both monomers and dimers, comprise one or more conjugated chemical substituents, such as lipophilic substituents and polymeric moieties, which may be referred to herein as half-life extension moieties. Without wishing to be bound by any particular theory, it is believed that the lipophilic substituent binds to albumin in the bloodstream, thereby shielding the peptide inhibitor from enzymatic degradation, and thus enhancing its half-life. In addition, it is believed that polymeric moieties enhance half-life and reduce clearance in the bloodstream.
1005811In additional embodiments, any of the peptide inhibitors, e.g. petides of Formulas (Va)-(Vh), further comprise a linker moiety attached to an amino acid residue present in the inhibitor, e.g., a linker moiety may be bound to a side chain of any amino acid of the peptide inhibitor, to the N-terminal amino acid of the peptide inhibitor, or to the C-terminal amino acid of the peptide inhibitor.
1005821In additional embodiments, any of the peptide inhibitors e.g. petides of Formulas (Va)-(Vh), further comprise half-life extension moiety attached to an amino acid residue present in the inhibitor, e.g., a half-life extension moiety may be bound to a side chain of any amino acid of the peptide inhibitor, to the N-terminal amino acid of the peptide inhibitor, or to the C-terminal amino acid of the peptide inhibitor.
1005831In additional embodiments, any of the peptide inhibitors e.g. petides of Formulas (Va)-(Vh), further comprise half-life extension moiety attached to a linker moiety that is attached to an amino acid residue present in the inhibitor, e.g., a half-life extension moiety may be bound to a linker moiety that is bound to a side chain of any amino acid of the peptide inhibitor, to the N-terminal amino acid of the peptide inhibitor, or to the C-terminal amino acid of the peptide inhibitor.
1005841In particular embodiments, an IL23R analogue comprises a half-life extension moiety having the structure shown below, wherein n=0 to 24 or n=14 to 24:
n=0 to 24 X kiy2:
X=CH3, CO2H, NH2, OH

1005851In certain embodiments, a IL23R analogue of the present invention comprises a half-life extension moiety shown in Table 7.
Table 7. Illustrative Half-Life Extension Moieties Half-Life Extension Moietys Cl SS.
C12 (Lauric acid) C14 (Mysteric acid) Sg{
C16 (Palm or Palmitic acid) C4 S'S
C18 (Stearic acid) C5 -SS:

C6 rPrN
OH C12 diacid C7 HO sr:
C14 diacid 3-53.
0 C16 diacid C18 diacid C20 diacid 10058611n certain embodiments, a half-life extension moiety is bound directly to a peptide inhibitor, while in other embodiments, a half-life extension moiety is bound to the peptide inhibitor via a linker moiety, e.g., any of those depicted in Tables 6 or 8.
[00587] Table 8. Illustrative Linker Moieties Linker Moiety Li IsoGlu Dapa N3-( Ahx Lipidic based linkers:

in N
n=1 to 24 N )211 H
.5*SjK
/ oo NIX

0 n=11 PEG11 (40 atoms) also known as PEG12 ''..s.. sJ.,..,..........,.... 0 ..,........$, A
N
\ n H

n=1 to 25 PEG based linkers s-CS5.0(3 A

H
OEG

H

IsoGlu-Ahx CO2H o IsoGlu-OEG-OEG

H
Nni...,....../=i.N o.,..õ.õ,-,...so.õ.....o.õ........õ,,,,o.....o.õ,....õ..-...Nc-CO2H o 1soGlu-PEG5 H

n=1-25 IsoGlu-PEGn L14 ;22''NNOC):31-H H
pAla-PEG2 N 1.
L15 H \ H
n=11 pAla-PEG11 (40 atoms) 1005881In particular embodiments, a peptide inhibitor of the present invention comprises any of the linker moieties shown in Table 8 and any of the half-life extension moieties shown in Table 7, including any of the following combinations shown in Table 9a.
Table 9a. Illustrative Combinations of Linkers and Half-Life Extension Moieties in Peptide Inhibitors Linker Half-Life Linker Half-Life Linker Half-Life Extension Extension Extension Moiety Moiety Moiety Li Cl Li C2 Li C3 L2 Cl L2 C2 L2 C3 L3 Cl L3 C2 L3 C3 L4 Cl L4 C2 L4 C3 L5 Cl L5 C2 L5 C3 L6 Cl L6 C2 L6 C3 L7 Cl L7 C2 L7 C3 L8 Cl L8 C2 L8 C3 L9 Cl L9 C2 L9 C3 L10 Cl L10 C2 L10 C3 L11 Cl L11 C2 L11 C3 L12 Cl L12 C2 L12 C3 L13 Cl L13 C2 L13 C3 L14 Cl L14 C2 L14 C3 L15 Cl L15 C2 L15 C3 Linker Half-Life Linker Half-Life Linker Half-Life Extension Extension Extension Moiety Moiety Moiety Li C4 Li C5 Li C6 Ll 1 C4 L11 C5 Ll 1 C6 Linker Half-Life Linker Half-Life Linker Half-Life Extension Extension Extension Moiety Moiety Moiety Li C7 Li C8 Li C9 Ll 1 C7 L11 C8 Ll 1 C9 Linker Half-Life Linker Half-Life Linker Half-Life Extension Extension Extension Moiety Moiety Moiety Li C10 L6 C10 L11 C10 10058911n some embodiments there may be multiple linkers present between the peptide the conjugated moiety, e.g., half-life extension moiety, e.g., as depicted in Table 9b.
Table 9b. Illustrative Combinations of Linkers and Half-Life Extension Moieties in Peptide Inhibitors Linker Half-Life Extension Linker Half-Life Extension Moiety Moiety 1005901Illustrative examples of peptide inhibitors of the present invention, including those having a conjugates linker and/or half-life extension moiety are shown below.
All amino acids are L amino acids unless otherwise stated. The present invention also includes salt forms of any of these peptide inhibitors, including, but not limited to, acetate salts thereof.

oNH2 o . NH
0 o N H2 z o o 0 cr 0 hl 40 0 ,.
H H
kil JL H
(N))LN N N

H H H

S H2P1 NH ) 1 HO 0 0 OH IN
0 o Example 1: cyclo[[Abt]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 o%..... NH2 *

0 0 I.:

H JL H
N H
NH JL
VY N h,yr N

H H H

H2N¨
s-NH ) 0 H
OH CD) NINH
\
,0 D

H
H2N N 0) HN
Example 1a: Ac-[(D)-Arg]-cyclo[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 0) NH2 = Oj 140 o Z o o o o 0 N
H
FN H H
Her N H rN LFNI4 N

Ht N
y t NH _\sI 0 r OH H WI NHAc 0 Ir'NH

Example 2: Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 half-Life Extension Moiety Linker ) NH ___________________________________ H
lik NH 0 NH2 0 , 4111 (0 _...,y H H N y Nyks N NrFij(N4 H H H H

NH .) 0 OH kil 0 Ir*NH
...,., 0 o Example 3: cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)-(Linker-Half-Life Extension Moiety)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NE12 Half-Life Extension Moiety __________________________________________ =
Linker ..= 1 NH _______________________________________ H
* 0 NH2 0 H)....1., H 2iii.....TK
N N
H H
N N

H ir N H H H
0 NH Os 0 0 -...1. 0 .....j NH ill OH i\11 ...,..
0 yCiNo 0 \......,H D

NH
H2N H y N,......._.....õ, 0),......
HN
Example 3a: Ac-[(D)-Arg]cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)-(Linker-Half-Life Extension Moiety)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NE-12 Ll NH 0.,....., NH2 0 7 0 0 0 1\pr rj......e.... 40 HH r 2 ......\...r, N).õ1.. N
N N N NH
H H H H

.....-IX NH ...) 0 OH 0 kil (''NH
....õ
0 o WI Hi IME
IIalf-Life Extension Moiety H2N o Example 4: cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyrari]-[Lys(Linker-Half-Life Extension Moiety)]-NN-NE-12 0%.....,. NH2 0 Ll . NH 111) Z

Nr N
H H H
N .........).1. N N H2 0....., N H 0 ,..= 0 0 ......(11...' 0 S
H2N-( OH kl WI HI OEM

..,...c Half-Life D Extension Moiety H
H2N y, N .................... )..,......

N H
Example 4a: Ac-[(D)-Arg]-cyclo[[Abu] -QTWQC] - [Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Linker-Half-Life Extension Moiety)]-NN-NE-12 Half-Life Extension Moiety NH2 Cen NH
0)õ, NH2 0 NH2 NH

0 0 0 0 .0 0 4 H H
kli NH2 N N NPIr \11......N N
H H H H H

X NH ill HO o 0 OH 0 PI ye ..õ
NH
0 o) Example 5: cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-[Lys(Linker-Half-Life Extension Moiety)]-1\1E12 1 la11-1 de NH2 EM , * NH :)_NH2 01-10 ' 0 H
H
N
N x.11,N N .,...,r1 f42 r....1A, N ,.....IN H2 N N

S

ki NH illl HO
OH 0 l 0 0 yeN H
....
0 \
\ ") .........NH
H
H2NyN....,.......... 0),...., HN
Example 5a: Ac[(D)-Arg]-cyclo[[Abu] -QTWQC] -[Phe[4-(2-aminoethoxy)] - [2-NalH4-amino-4-carboxy-tetrahydropyran]-ENN-[Lys(Linker-Half-Life Extension Moiety)]-NH2 LI
* 0,NH2 0 ) / VL
0 0 = 0 0 0 0 H H rH H N))LN r\ N N
N Nr NH2 H H H

S
*0 NH 40) HO 0 OH NI
_______________________ . , ______ .
INC) \H r Linker,1 Half-1i fe ,Extension moiety, H2N o Example 6: [Half-Life Extension Moiety-Linker]-[cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 0...õ N H2 1.---1 4Ik NH NH2 H
H H
,...T., N ....õ....,1, N
7rTILN NH2 H H H H
0,.............õ..NH 0 0 kl 0 0 0 y.......NH .40 HOO
OH oõ),........õ..
y...(INH
0 \O
D

H I
H2N ________________________________________ =
N r Linker Half-Lith Extension Moiety, NH
Example 6a: [Half-Life Extension Moiety-Linked-[(D)-Arg]-[cyclo[[Abt]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 * NH
0.õ......, NH2 0 0 Oj NH2 n 0 0 0 "......L0 0 H H H
N
N
N hi )( N
.="....k 0 'ICIL hl .....-y NiT)LF1 N H2 FIN -----y- H

_\s1 1lLi 0 'II NH
W
H
OH ())N NH
Ir NHAc H2N 1,===== 0 0 Linker Half-Life N
Extension Moiety , o Example 7: [Half-Life Extension Moiety-Linked-[Pen]-NTWQ-[Pen]-[Phe[4-(aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Half-Life Extension Moiety 0%...,NH2 0 0) NH NH2 NH
r CD, ../' 0 0 0 0 0 0 N....cr. H H Hj LN41 N N
ri4 NH2 .11....'N N
H H
0........., NH 0 0 0 0 NH2 0 S
I
rNH s III 0 OH ..,,,,IVI 411 NHAc 0 --i---NH

Example 8: Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-[Lys(Linker-Half-Life Extension Moiety)]-NE-12 Half-Life Extension Moiety MIE
NH
41 0 0.........) NH 0 NH2 NH2 , .a..., H 0 Nqr s...(11,....
N N N
N H. N N NH2 H H H H
.....:;xNH 0 0 0 0 NH2 S
I
Ilit 0 wil r----NHAc OH o.....õN
NH
H2N 0 o) Example 9: Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(aminoethoxy)-(Linker-Half-Life Extension Moiety)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NE12 NH
0) a a a a M*LN

NL

S
=
si Half-Life OH o N HN Linker Extension Moiety) H2N 0 oA
Example 10: Ac- [Pen] -NTWQ- [Pen]- [Phe[4-(aminoethoxy)] - [2-Na!]- [4-amino-4-carboxy-tetrahydropyran]-[Lys(Linker-Half-Life Extension moiety )]-NN-NE12.
10059111n certain embodiments, the half-life of a peptide inhibitor of the invention that includes a conjugated chemical substituent, i.e., a half-life extension moiety, is at least 100%, at least 120%, at least 150%, at least 200%, at least 250%, at least 300%, at least 400%, or at least 500%
of the half-life of the same peptide inhibitor but without the conjugated chemical substituent. In certain embodiments, the lipophilic substituents and/or polypermic moieties enhance the permeability of the peptide inhibitor through the epithelium and/or its retention in the lamina propria. In certain embodiments, the permeability through the epithelium and/or the retention in the lamina propria of a peptide inhibitor of the invention that includes a conjugated chemical substituent is at 100%, at least 120%, at least 150%, at least 200%, at least 250%, at least 300%, at least 400%, or at least 500% of the half-life of the same peptide inhibitor but without the conjugated chemical substituent.
1005921 In one embodiment, a side chain of one or more amino acid residues (e.g., Lys residues) in a peptide inhibitor of the invention is conjugated (e.g., covalently attached) to a lipophilic substituent. The lipophilic substituent may be covalently bonded to an atom in the amino acid side chain, or alternatively may be conjugated to the amino acid side chain via one or more spacers. The spacer, when present, may provide spacing between the peptide analogue and the lipophilic substituent. In particular embodiments, the peptide inhibitor comprises any of the conjugated moieties shown in Tables 2-5.

1005931In certain embodiments, the lipophilic substituent may comprise a hydrocarbon chain having from 4 to 30 C atoms, for example at least 8 or 12 C atoms, and preferably 24 C atoms or fewer, or 20 C atoms or fewer. The hydrocarbon chain may be linear or branched and may be saturated or unsaturated. In certain embodiments, the hydrocarbon chain is substituted with a moiety which forms part of the attachment to the amino acid side chain or the spacer, for example an acyl group, a sulfonyl group, an N atom, an 0 atom or an S atom. In some embodiments, the hydrocarbon chain is substituted with an acyl group, and accordingly the hydrocarbon chain may form part of an alkanoyl group, for example palmitoyl, caproyl, lauroyl, myristoyl or stearoyl.
1005941A lipophilic substituent may be conjugated to any amino acid side chain in a peptide inhibitor of the invention. In certain embodiment, the amino acid side chain includes a carboxy, hydroxyl, thiol, amide or amine group, for forming an ester, a sulphonyl ester, a thioester, an amide or a sulphonamide with the spacer or lipophilic substituent. For example, the lipophilic substituent may be conjugated to Asn, Asp, Glu, Gln, His, Lys, Arg, Ser, Thr, Tyr, Trp, Cys or Dbu, Dpr or Orn. In certain embodiments, the lipophilic substituent is conjugated to Lys. An amino acid shown as Lys in any of the formula provided herein may be replaced by, e.g., Dbu, Dpr or Orn where a lipophilic substituent is added.
[00595] In certain embodiments, the peptide inhibitors of the present invention may be modified, e.g., to enhance stability, increase permeability, or enhance drug like characteristics, through conjugation of a chemical moiety to one or more amino acid side chain within the peptide. For example, the N(epsilon) of lysine N(epsilon), the (3¨carboxyl of aspartic, or the y¨carboxyl of glutamic acid may be appropriately functionalized. Thus, to produce the modified peptide, an amino acid within the peptide may be appropriately modified. Further, in some instances, the side chain is acylated with an acylating organic compound selected from the group consisting of:
Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid glutaric acid or bile acids. One having skill is the art will appreciate that a series of conjugates can be linked, e.g., for example PEG4, isoglu and combinations thereof. One having skill is the art will appreciate that an amino acid with the peptide can be isosterically replaced, for example, Lys may be replaced for Dap, Dab, a-MeLys orOrn. Examples of modified residues within a peptide are shown in Table 1B.
Table 1B. Examples of modified Lysine, Asp and Asn within the peptide HN). H1\1) ) ) 14 Ne-Lys(Ac) Ne-Lys(Palm) EN1 ifH
HN ) H N) - [\11 HO2C 0 14 II

) 0 14 /
H2N rOH
H2N (OH

Ne-Lys-gamaGlu-Palm o Ne-Lys-isoGiu-Palm ) HNI)LV0l-----LNK 2 0 i 4 0 H 14 H2N4r0H
H2N rOH
Ne-Lys(PEG2-Ac) Ne-Lys(PEG4-isoGIu-PaIrn) HNO INI
HN )-H.r0H
-N-) 5 0 14 ) 0 ThrOH ThrOH

Ne-Lys(PEG)5-Palm Ne-Lys(succinic acid) HN).*LON HN)Lr EN-11 tO
ThrOH ThrOH

Ne-Lys(glutaric acid) Ne-Lys(Pyroglutaric acid) o 11 HN HN
H2N.r0H

N8-Lys(Benzoic acid) Ne-Lys(IVA) HN
HN

H2N.r0H
H2NrOH

Asp(1,4 diaminobutane) Ne-Lys(octanoic acid) HN)õ

HN-7¨tHH
H2NrOH
o 0 H2N rOH
Asn(isobutyl) 0 Ne-Lys(Biotin) 1005961In further embodiments of the present invention, alternatively or additionally, a side-chain of one or more amino acid residues in a peptide inhibitor of the invention is conjugated to a polymeric moiety, for example, in order to increase solubility and/or half-life in vivo (e.g. in plasma) and/or bioavailability. Such modifications are also known to reduce clearance (e.g.
renal clearance) of therapeutic proteins and peptides.
1005971As used herein, "Polyethylene glycol" or "PEG" is a polyether compound of general formula H-(0-CH2-CH2)n-OH. PEGS are also known as polyethylene oxides (PE0s) or polyoxyethylenes (POEs), depending on their molecular weight PEO, PEE, or POG, as used herein, refers to an oligomer or polymer of ethylene oxide. The three names are chemically synonymous, but PEG has tended to refer to oligomers and polymers with a molecular mass below 20,000 Da, PEO to polymers with a molecular mass above 20,000 Da, and POE to a polymer of any molecular mass. PEG and PEO are liquids or low-melting solids, depending on their molecular weights. Throughout this disclosure, the 3 names are used indistinguishably.
PEGS are prepared by polymerization of ethylene oxide and are commercially available over a wide range of molecular weights from 300 Da to 10,000,000 Da. While PEG and PEO with different molecular weights find use in different applications, and have different physical properties (e.g. viscosity) due to chain length effects, their chemical properties are nearly identical. The polymeric moiety is preferably water-soluble (amphiphilic or hydrophilic), non-toxic, and pharmaceutically inert. Suitable polymeric moieties include polyethylene glycols (PEG), homo- or co-polymers of PEG, a monomethyl-substituted polymer of PEG
(mPEG), or polyoxyethylene glycerol (POG). See, for example, Int. J. Hematology 68:1 (1998);
Bioconjugate Chem. 6:150 (1995); and Crit. Rev. Therap. Drug Carrier Sys.
9:249 (1992). Also encompassed are PEGS that are prepared for purpose of half life extension, for example, mono-activated, alkoxy-terminated polyalkylene oxides (P0A's) such as mono-methoxy-terminated polyethyelene glycols (mPEG's); bis activated polyethylene oxides (glycols) or other PEG
derivatives are also contemplated. Suitable polymers will vary substantially by weights ranging from about 200 Da to about 40,000 Da or from about 200 Da to about 60,000 Da are usually selected for the purposes of the present invention. In certain embodiments, PEGs having molecular weights from 200 to 2,000 or from 200 to 500 are used. Different forms of PEG may also be used, depending on the initiator used for the polymerization process ¨
a common common initiator is a monofunctional methyl ether PEG, or methoxypoly(ethylene glycol), abbreviated mPEG.

[00598]Lower-molecular-weight PEGS are also available as pure oligomers, referred to as monodisperse, uniform, or discrete. These are used in certain embodiments of the present invention.
[00599] PEGS are also available with different geometries: branched PEGS have three to ten PEG
chains emanating from a central core group; star PEGs have 10 to 100 PEG
chains emanating from a central core group; and comb PEGS have multiple PEG chains normally grafted onto a polymer backbone. PEGS can also be linear. The numbers that are often included in the names of PEGS indicate their average molecular weights (e.g. a PEG with n = 9 would have an average molecular weight of approximately 400 daltons, and would be labeled PEG 400.
[00600] As used herein, "PEGylation" is the act of covalently coupling a PEG
structure to the peptide inhibitor of the invention, which is then referred to as a "PEGylated peptide inhibitor".
In certain embodiments, the PEG of the PEGylated side chain is a PEG with a molecular weight from about 200 to about 40,000. In some embodiments, a spacer of a peptide of formula I, formula I', or formula I" is PEGylated. In certain embodiments, the PEG of a PEGylated spacer is PEG3, PEG4, PEGS, PEG6, PEG7, PEG8, PEG9, PEG10, or PEG11. In certain embodiments, the PEG of a PEGylated spacer is PEG3 or PEG8.
[00601] Other suitable polymeric moieties include poly-amino acids such as poly-lysine, poly-aspartic acid and poly-glutamic acid (see for example Gombotz, et al. (1995), Bioconjugate Chem., vol. 6: 332-351; Hudecz, et al. (1992), Bioconjugate Chem., vol. 3, 49-57 and Tsukada, et al. (1984), J. Natl. Cancer Inst., vol. 73, : 721-729. The polymeric moiety may be straight-chain or branched. In some embodiments, it has a molecular weight of 500-40,000 Da, for example 500-10,000 Da, 1000-5000 Da, 10,000-20,000 Da, or 20,000-40,000 Da.
1006021In some embodiments, a peptide inhibitor of the invention may comprise two or more such polymeric moieties, in which case the total molecular weight of all such moieties will generally fall within the ranges provided above.
1006031In some embodiments, the polymeric moiety is coupled (by covalent linkage) to an amino, carboxyl or thiol group of an amino acid side chain. Certain examples are the thiol group of Cys residues and the epsilon amino group of Lys residues, and the carboxyl groups of Asp and Glu residues may also be involved.
[00604] The skilled worker will be well aware of suitable techniques which can be used to perform the coupling reaction. For example, a PEG moiety bearing a methoxy group can be coupled to a Cys thiol group by a maleimido linkage using reagents commercially available from Nektar Therapeutics AL. See also WO 2008/101017, and the references cited above, for details of suitable chemistry. A maleimide-functionalised PEG may also be conjugated to the side-chain sulfhydryl group of a Cys residue.
[00605] As used herein, disulfide bond oxidation can occur within a single step or is a two step process. As used herein, for a single oxidation step, the trityl protecting group is often employed during assembly, allowing deprotection during cleavage, followed by solution oxidation. When a second disulfide bond is required, one has the option of native or selective oxidation. For selective oxidation requiring orthogonal protecting groups, Acm and Trityl is used as the protecting groups for cysteine. Cleavage results in the removal of one protecting pair of cysteine allowing oxidation of this pair. The second oxidative deprotection step of the cysteine protected Acm group is then performed. For native oxidation, the trityl protecting group is used for all cysteines, allowing for natural folding of the peptide. A skilled worker will be well aware of suitable techniques which can be used to perform the oxidation step.
[00606] Several chemical moieties, including poly(ethylene)glycol, react with functional groups present in the twenty naturally occurring amino acids, such as, for example, the epsilon amino group in lysine amino acid residues, the thiol present in cysteine amino acid residues, or other nucleophilic amino acid side chains. When multiple naturally occurring amino acids react in a peptide inhibitor, these non-specific chemical reactions result in a final peptide inhibitor that contains many isomers of peptides conjugated to one or more poly(ethylene)glycol strands at different locations within the peptide inhibitor.
[00607] One advantage of certain embodiments of the present invention includes the ability to add one or more chemical moiety (such as PEG) by incorporating one or more non-natural amino acid(s) that possess unique functional groups that react with an activated PEG
by way of chemistry that is unreactive with the naturally occurring amino acids present in the peptide inhibitor. For example, azide and alkyne groups are unreactive with all naturally occurring functional groups in a protein. Thus, a non-natural amino acid may be incorporated in one or more specific sites in a peptide inhibitor where PEG or another modification is desired without the undesirable non-specific reactions. In certain embodiments, the particular chemistry involved in the reaction results in a stable, covalent link between the PEG strand and the peptide inhibitor.
In addition, such reactions may be performed in mild aqueous conditions that are not damaging to most peptides. In certain embodiments, the non-natural amino acid residue is AHA.
[00608] Chemical moieties attached to natural amino acids are limited in number and scope. By contrast, chemical moieties attached to non-natural amino acids can utilize a significantly greater spectrum of useful chemistries by which to attach the chemical moiety to the target molecule.
Essentially any target molecule, including any protein (or portion thereof) that includes a non-natural amino acid, e.g., a non-natural amino acid containing a reactive site or side chain where a chemical moiety may attach, such as an aldehyde- or keto-derivatized amino acid, can serve as a substrate for attaching a chemical moiety.
1006091 Numerous chemical moieties may be joined or linked to a particular molecule through various known methods in the art. A variety of such methods are described in U.S. Patent No.
8,568,706. As an illustrative example, azide moieties may be useful in conjugating chemical moieties such as PEG or others described herein. The azide moiety serves as a reactive functional group, and is absent in most naturally occurring compounds (thus it is unreactive with the native amino acids of naturally occurring compounds). Azides also undergo a selective ligation with a limited number of reaction partners, and azides are small and can be introduced to biological samples without altering the molecular size of significantly. One reaction that allows incorporation or introduction of azides to molecules is the copper-mediated Huisgen [3+2]
cycloaddition of an azide. This reaction can be used for the selective PEGylation of peptide inhibitors. (Tornoe et al., J. Org. Chem. 67: 3057, 2002; Rostovtsev et al., Angew. Chem., Int.
Ed. 41: 596, 2002; and Wang et al., J. Am. Chem. Soc. 125: 3192, 2003, Speers et al., J. Am.
Chem. Soc., 2003, 125, 4686).

Illustrative Peptide Inhibitors and Peptide Dimer Inhibitors, and Methods of Making the Same [00610] The present invention thus provides various peptide inhibitors which bind or associate with IL-23, to disrupt or block binding between IL-23 and IL-23R.
[006111Illustrative peptide inhibitors and peptide dimer inhibitors of the present invention are shown in Tables 3A-3H, 4A, 4B, 5A-5C, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15 provides the amino acid sequence of selected monomer peptide inhibitors and peptide dimer inhibitors, and indicates the linker moiety present in the peptide dimer inhibitors. According to the protocols discussed herein, a number of the peptide inhibitors and peptide dimer inhibitors shown in the accompanying tables were synthesized and cyclyzed. Tables E3A-E3H, E4A, E4B, ESA-ESC, E6, E7, E8, E9, El 0, Ell, E12, E13, E14 or El 5 provide the IC50 values for selected monomer peptide inhibitors and peptide dimer inhibitors in inhibiting IL-23 binding to the IL-23R, or in inhibiting IL-23 signaling as determined by measuring changes in phospho-STAT3 levels, as described in the accompanying Examples. Illustrative peptide inhibitors of the present invention are shown in Formulas (V), and in Tables 2-5, which provide the amino acid sequence of selected peptide inhibitors. These peptide inhibitors are acetate salts.
[00612] The peptide inhibitors of the present invention may be synthesized by many techniques that are known to those skilled in the art. In certain embodiments, monomer subunits are synthesized, purified, and dimerized using the techniques described in the accompanying Examples. In certain embodiments, the present invention provides a method of producing a peptide inhibitor (or monomer subunit thereof) of the present invention, comprising chemically synthesizing a peptide comprising, consisting of, or consisting essentially of a peptide having an amino acid sequence described herein, including but not limited to any of the amino acid sequences set forth in any of Formulas I, II, III, IV, V or VI or tables herein. In other embodiments, the peptide is recombinantly synthesized, instead of being chemically synthesized.
In certain embodiments, the peptide inhibitor is a dimer, and the method comprises synthezing both monomer subunits of the peptide dimer inhibitor and then dimerizing the two monomer subunits to produce the peptide dimer inhibitor. In various embodiments, dimerization is accomplished via any of the various methods described herein. In particular embodiments, methods of producing a peptide inhibitor (or monomer subunit thereof) further comprise cyclizing the peptide inhibitor (or monomer subunit thereof) after its synthesis. In particular embodiments, cyclization is accomplished via any of the various methods described herein. In certain embodiments, the present invention provides a method of producing a peptide inhibitor (or monomer subunit thereof) of the present invention, comprising introducing an intramolecular bond, e.g., a disulfide, an amide, or a thioether bond between two amino acids residues within a peptide comprising, consisting of, or consisting essentially of a peptide having an amino acid sequence described herein, including but not limited to any of the amino acid sequences set forth in any of Formulas I, II, III, IV, V or VI, or the accompanying Examples, Tables, or Sequence Listing.
1006131In related embodiments, the present invention includes polynucleotides that encode a polypeptide having a sequence set forth in any one of Formulas I, II, III, IV, V or VI, or the accompanying Examples, Tables, or Sequence Listing.
1006141 In addition, the present invention includes vectors, e.g., expression vectors, comprising a polynucleotide of the present invention.
Methods of Treatment 1006151In certain embodiments, the present invention includes methods of inhibiting IL-23 binding to an IL-23R on a cell, comprising contacting the IL-23 with a peptide inhibitor of the present invention. In certain embodiments, the cell is a mammalian cell. In particular embodiments, the method is performed in vitro or in vivo. Inhibition of binding may be determined by a variety of routine experimental methods and assays known in the art.
1006161In certain embodiments, the present invention includes methods of inhibiting IL-23 signaling by a cell, comprising contacting the IL-23 with a peptide inhibitor of the present invention. In certain embodiments, the cell is a mammalian cell. In particular embodiments, the method is performed in vitro or in vivo. In particular embodiments, the inhibition of IL-23 signalling may be determined by measuring changes in phospho-STAT3 levels in the cell.
1006171In some embodiments, the present invention provides methods for treating a subject afflicted with a condition or indication associated with IL-21 or IL-23R
(e.g., activation of the IL-23/IL-23R signaling pathway), wherein the method comprises administering to the subject a peptide inhibitor of the present invention. In one embodiment, a method is provided for treating a subject afflicted with a condition or indication characterized by inappropriate, deregulated, or increased IL-23 or IL-23R activity or signaling, comprising administering to the individual a peptide inhibitor of the present invention in an amount sufficient to inhibit (partially or fully) binding of IL-23 to IL-23R in the subject. In particular embodiments, the inhibition of IL-23 binding to IL-23R occurs in particular organs or tissues of the subject, e.g., the stomach, small intestine, large intestine/colon, intestinal mucosa, lamina propria, Peyer's Patches, mesenteric lymph nodes, or lymphatic ducts.
1006181In some embodiments, methods of the present invention comprise providing a peptide inhibitor of the present invention to a subject in need thereof. In particular embodiments, the subject in need thereof has been diagnosed with or has been determined to be at risk of developing a disease or disorder associated with IL-23/IL-23R. In particular embodiments, the subject is a mammal.
1006191In certain embodiments, the disease or disorder is autoimmune inflammation and related diseases and disorders, such as multiple sclerosis, asthma, rheumatoid arthritis, inflammatory bowel diseases (IBDs), juvenile IBD, adolescent IBD, Crohn's disease, sarcoidosis, Systemic Lupus Erythematosus, ankylosing spondylitis (axial spondyloarthritis), psoriatic arthritis, or psoriasis. In particular embodiments, the disease or disorder is psoriasis (e.g., plaque psoriasis, guttate psoriasis, inverse psoriasis, pustular psoriasis, Palmo-Plantar Pustulosis, psoriasis vulgaris, or erythrodermic psoriasis), atopic dermatitis, acne ectopica, ulcerative colitis, Crohn's disease, Celiac disease (nontropical Sprue), enteropathy associated with seronegative arthropathies, microscopic colitis, collagenous colitis, eosinophilic gastroenteritis/esophagitis, colitis associated with radio- or chemo-therapy, colitis associated with disorders of innate immunity as in leukocyte adhesion deficiency-1, chronic granulomatous disease, glycogen storage disease type lb, Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, Wiskott-Aldrich Syndrome, pouchitis resulting after proctocolectomy and ileoanal anastomosis, gastrointestinal cancer, pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, primary biliary cirrhosis, viral-associated enteropathy, pericholangitis, chronic bronchitis, chronic sinusitis, asthma, uveitis, or graft versus host disease.

1006201In certain related embodiments, the present invention provides a method of selectively inhibiting IL-23 or IL-23R signaling (or the binding of IL-23 to IL-23R) in a subject in need thereof, comprising providing to the subject a peptide inhibitor of the present invention. In particular embodiments, the present invention includes a method of selectively inhibiting IL-23 or IL-23R signaling (or the binding of IL-23 to IL-23R) in the GI tract of a subject in need thereof, comprising providing to the subject a peptide inhibitor of the present invention by oral administration. In particular embodiments, exposure of the administered peptide inhibitor in GI
tissues (e.g., small intestine or colon) is at least 10-fold, at least 20-fold, at least 50-fold, or at least 100-fold greater than the exposure in the blood. In particular embodiments, the present invention includes a method of selectively inhibiting IL23 or IL23R signaling (or the binding of IL23 to IL23R) in the GI tract of a subject in need thereof, comprising providing to the subject a peptide inhibitor, wherein the peptide inhibitor does not block the interaction between IL-6 and IL-6R or antagonize the IL-12 signaling pathway. In a further related embodiment, the present invention includes a method of inhibiting GI inflammation and/or neutrophil infiltration to the GI, comprising providing to a subject in need thereof a peptide inhibitor of the present invention.In some embodiments, methods of the present invention comprise providing a peptide inhibitor of the present invention (i.e., a first therapeutic agent) to a subject in need thereof in combination with a second therapeutic agent. In certain embodiments, the second therapeutic agent is provided to the subject before and/or simultaneously with and/or after the peptide inhibitor is administered to the subject. In particular embodiments, the second therapeutic agent is an anti-inflammatory agent. In certain embodiments, the second therapeutic agent is a non-steroidal anti-inflammatory drug, steroid, or immune modulating agent. In another embodiment, the method comprises administering to the subject a third therapeutic agent.
In certain embodiments, the second therapeutic agent is an antibody that binds IL-23 or IL-23R.
1006211In particular embodiments, the peptide inhibitor, or the pharmaceutical composition comprising a peptide inhibitor, is suspended in a sustained-release matrix. A
sustained-release matrix, as used herein, is a matrix made of materials, usually polymers, which are degradable by enzymatic or acid-base hydrolysis or by dissolution. Once inserted into the body, the matrix is acted upon by enzymes and body fluids. A sustained-release matrix desirably is chosen from biocompatible materials such as liposomes, polylactides (polylactic acid), polyglycolide (polymer of glycolic acid), polylactide co-glycolide (copolymers of lactic acid and glycolic acid) polyanhydrides, poly(ortho)esters, polypeptides, hyaluronic acid, collagen, chondroitin sulfate, carboxylic acids, fatty acids, phospholipids, polysaccharides, nucleic acids, polyamino acids, amino acids such as phenylalanine, tyrosine, isoleucine, polynucleotides, polyvinyl propylene, polyvinylpyrrolidone and silicone. One embodiment of a biodegradable matrix is a matrix of one of either polylactide, polyglycolide, or polylactide co-glycolide (co-polymers of lactic acid and glycolic acid).
1006221In certain embodiments, the present invention includes pharmacetical compositions comprising one or more peptide inhibitors of the present invention and a pharmaceutically acceptable carrier, diluent or excipient. A pharmaceutically acceptable carrier, diluent or excipient refers to a non-toxic solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. Prevention of the action of microorganisms may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents such as sugars, sodium chloride, and the like.
1006231In certain embodiments, the compositions are administered orally, parenterally, intracisternally, intravaginally, intraperitoneally, intrarectally, topically (as by powders, ointments, drops, suppository, or transdermal patch), by inhalation (such as intranasal spray), ocularly (such as intraocularly) or buccally. The term "parenteral" as used herein refers to modes of administration which include intravenous, intramuscular, intraperitoneal, intrasternal, subcutaneous, intradermal and intraarticular injection and infusion.
Accordingly, in certain embodiments, the compositions are formulated for delivery by any of these routes of administration.
1006241In certain embodiments, pharmaceutical compositions for parenteral injection comprise pharmaceutically acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, or sterile powders, for reconstitution into sterile injectable solutions or dispersions just prior to use. Examples of suitable aqueous and nonaqueous carriers, diluents, solvents or vehicles include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), carboxymethylcellulose and suitable mixtures thereof, f3-cyclodextrin, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate.
Proper fluidity may be maintained, for example, by the use of coating materials such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants. Thes compositions may also contain adjuvants such as preservative, wetting agents, emulsifying agents, and dispersing agents. Prolonged absorption of an injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption, such as aluminum monostearate and gelatin.
1006251Injectable depot forms include those made by forming microencapsule matrices of the peptide inhibitor in one or more biodegradable polymers such as polylactide-polyglycolide, poly(orthoesters), poly(anhydrides), and (poly)glycols, such as PEG. Depending upon the ratio of peptide to polymer and the nature of the particular polymer employed, the rate of release of the peptide inhibitor can be controlled. Depot injectable formulations are also prepared by entrapping the peptide inhibitor in liposomes or microemulsions compatible with body tissues.
[00626] The injectable formulations may be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium just prior to use.
[00627] Topical administration includes administration to the skin or mucosa, including surfaces of the lung and eye. Compositions for topical lung administration, including those for inhalation and intranasal, may involve solutions and suspensions in aqueous and non-aqueous formulations and can be prepared as a dry powder which may be pressurized or non-pressurized. In non-pressurized powder compositions, the active ingredientmay be finely divided form may be used in admixture with a larger-sized pharmaceutically acceptable inert carrier comprising particles having a size, for example, of up to 100 micrometers in diameter. Suitable inert carriers include sugars such as lactose.
[00628] Alternatively, the composition may be pressurized and contain a compressed gas, such as nitrogen or a liquefied gas propellant. The liquefied propellant medium and indeed the total composition may bey such that the active ingredient does not dissolve therein to any substantial extent. The pressurized composition may also contain a surface active agent, such as a liquid or solid non-ionic surface active agent or may be a solid anionic surface active agent. It is preferred to use the solid anionic surface active agent in the form of a sodium salt.
[00629] A further form of topical administration is to the eye. A peptide inhibitor of the invention may be delivered in a pharmaceutically acceptable ophthalmic vehicle, such that the peptide inhibitor is maintained in contact with the ocular surface for a sufficient time period to allow the peptide inhibitor to penetrate the corneal and internal regions of the eye, as for example the anterior chamber, posterior chamber, vitreous body, aqueous humor, vitreous humor, cornea, iris/ciliary, lens, choroid/retina and sclera. The pharmaceutically acceptable ophthalmic vehicle may, for example, be an ointment, vegetable oil or an encapsulating material.
Alternatively, the peptide inhibitors of the invention may be injected directly into the vitreous and aqueous humour.
[00630] Compositions for rectal or vaginal administration include suppositories which may be prepared by mixing the peptide inhibitorss of this invention with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax, which are solid at room temperature but liquid at body temperature and, therefore, melt in the rectum or vaginal cavity and release the active compound.
[00631] Peptide inhibitors of the present invention may also be administered in liposomes or other lipid-based carriers. As is known in the art, liposomes are generally derived from phospholipids or other lipid substances. Liposomes are formed by mono- or multi-lamellar hydrated liquid crystals that are dispersed in an aqueous medium. Any non-toxic, physiologically acceptable and metabolizable lipid capable of forming liposomes can be used. The present compositions in liposome form can contain, in addition to a peptide inhibitor of the present invention, stabilizers, preservatives, excipients, and the like. In certain embodiments, the lipids comprise phospholipids, including the phosphatidyl cholines (lecithins) and serines, both natural and synthetic. Methods to form liposomes are known in the art.
[00632Wharmaceutical compositions to be used in the invention suitable for parenteral administration may comprise sterile aqueous solutions and/or suspensions of the peptide inhibitos made isotonic with the blood of the recipient, generally using sodium chloride, glycerin, glucose, mannitol, sorbitol, and the like.

1006331In some aspects, the invention provides a pharmaceutical composition for oral delivery.
Compositions and peptide inhibitors of the instant invention may be prepared for oral administration according to any of the methods, techniques, and/or delivery vehicles described herein. Further, one having skill in the art will appreciate that the peptide inhibitors of the instant invention may be modified or integrated into a system or delivery vehicle that is not disclosed herein, yet is well known in the art and compatible for use in oral delivery of peptides.
1006341In certain embodiments, formulations for oral administration may comprise adjuvants (e.g. resorcinols and/or nonionic surfactants such as polyoxyethylene oleyl ether and n-hexadecylpolyethylene ether) to artificially increase the permeability of the intestinal walls, and/or enzymatic inhibitors (e.g. pancreatic trypsin inhibitors, diisopropylfluorophosphate (DFF) or trasylol) to inhibit enzymatic degradation. In certain embodiments, the peptide inhibitor of a solid-type dosage form for oral administration can be mixed with at least one additive, such as sucrose, lactose, cellulose, mannitol, trehalose, raffinose, maltitol, dextran, starches, agar, alginates, chitins, chitosans, pectins, gum tragacanth, gum arabic, gelatin, collagen, casein, albumin, synthetic or semisynthetic polymer, or glyceride. These dosage forms can also contain other type(s) of additives, e.g., inactive diluting agent, lubricant such as magnesium stearate, paraben, preserving agent such as sorbic acid, ascorbic acid, alpha-tocopherol, antioxidants such as cysteine, disintegrators, binders, thickeners, buffering agents, pH
adjusting agents, sweetening agents, flavoring agents or perfuming agents.
1006351In particular embodiments, oral dosage forms or unit doses compatible for use with the peptide inhibitors of the present invention may include a mixture of peptide inhibitor and nondrug components or excipients, as well as other non-reusable materials that may be considered either as an ingredient or packaging. Oral compositions may include at least one of a liquid, a solid, and a semi-solid dosage forms. In some embodiments, an oral dosage form is provided comprising an effective amount of peptide inhibitor, wherein the dosage form comprises at least one of a pill, a tablet, a capsule, a gel, a paste, a drink, a syrup, ointment, and suppository. In some instances, an oral dosage form is provided that is designed and configured to achieve delayed release of the peptide inhibitor in the subject's small intestine and/or colon.

1006361 In one embodiment, an oral pharmaceutical composition comprising a peptide inhibitor of the present invention comprises an enteric coating that is designed to delay release of the peptide inhibitor in the small intestine. In at least some embodiments, a pharmaceutical composition is provided which comprises a peptide inhibitor of the present invention and a protease inhibitor, such as aprotinin, in a delayed release pharmaceutical formulation. In some instances, pharmaceutical compositions of the instant invention comprise an enteric coat that is soluble in gastric juice at a pH of about 5.0 or higher. In at least one embodiment, a pharmaceutical composition is provided comprising an enteric coating comprising a polymer having dissociable carboxylic groups, such as derivatives of cellulose, including hydroxypropylmethyl cellulose phthalate, cellulose acetate phthalate and cellulose acetate trimellitate and similar derivatives of cellulose and other carbohydrate polymers.
1006371In one embodiment, a pharmaceutical composition comprising a peptide inhibitor of the present invention is provided in an enteric coating, the enteric coating being designed to protect and release the pharmaceutical composition in a controlled manner within the subject's lower gastrointestinal system, and to avoid systemic side effects. In addition to enteric coatings, the peptide inhibitors of the instant invention may be encapsulated, coated, engaged or otherwise associated within any compatible oral drug delivery system or component. For example, in some embodiments a peptide inhibitor of the present invention is provided in a lipid carrier system comprising at least one of polymeric hydrogels, nanoparticles, microspheres, micelles, and other lipid systems.
[00638] To overcome peptide degradation in the small intestine, some embodiments of the present invention comprise a hydrogel polymer carrier system in which a peptide inhibitor of the present invention is contained, whereby the hydrogel polymer protects the peptide inhibitor from proteolysis in the small intestine and/or colon. The peptide inhibitors of the present invention may further be formulated for compatible use with a carrier system that is designed to increase the dissolution kinetics and enhance intestinal absorption of the peptide.
These methods include the use of liposomes, micelles and nanoparticles to increase GI tract permeation of peptides.
[00639] Various bioresponsive systems may also be combined with one or more peptide inhibitor of the present invention to provide a pharmaceutical agent for oral delivery.
In some embodiments, a peptide inhibitor of the instant invention is used in combination with a bioresponsive system, such as hydrogels and mucoadhesive polymers with hydrogen bonding groups (e.g., PEG, poly(methacrylic) acid [PMAA], cellulose, Eudragit , chitosan and alginate) to provide a therapeutic agent for oral administration. Other embodiments include a method for optimizing or prolonging drug residence time for a peptide inhibitor disclosed herein, wherein the surface of the peptide inhibitor surface is modified to comprise mucoadhesive properties through hydrogen bonds, polymers with linked mucins or/and hydrophobic interactions. These modified peptide molecules may demonstrate increase drug residence time within the subject, in accordance with a desired feature of the invention. Moreover, targeted mucoadhesive systems may specifically bind to receptors at the enterocytes and M-cell surfaces, thereby further increasing the uptake of particles containing the peptide inhibitor.
1006401 Other embodiments comprise a method for oral delivery of a peptide inhibitor of the present invention, wherein the peptide inhibitor is provided to a subject in combination with permeation enhancers that promote the transport of the peptides across the intestinal mucosa by increasing paracellular or transcellular permeation. Various permeation enhancers and methods for the oral delivery of therapeutic agents is described in Brayden, D.J., Mrsny, R.J., 2011. Oral peptide delivery: prioritizing the leading technologies. Ther. Delivery 2 (12), 1567-1573.
1006411In certain embodiments, pharmaceutical compositions and formulations of the present invention comprises a peptide inhibitor of the present invention and one or more permeation enhancer. Examples of absorption enhancers may include Bile salts, fatty acids, surfactants (anionic, cationic, and nonanionic) chelators, Zonular OT, esters, cyclodextrin, dextran sulfate, azone, crown ethers, EDTA, sucrose esters, and phosphotidyl choline, for example. Although absorption enhancers are not typically carriers by themselves, they are also widely associated with other carriers to improve oral bioavailability by transporting of peptides and proteins across the intestinal mucosa. Such substances can be added to the formulation as excipients or incorporated to form non specific interactions with the intended peptide inhibitor.
[00642]Dietary components and/or other naturally occurring substances affirmed as enhancing tight junction permeation and as Generally Recognized As Safe (GRAS) include, e.g., asglycerides, acylcarnitines, bile salts, and medium chain fatty acids. Sodium salts of medium chain fatty acids (MCFAS) were also suggested to be permeation enhancers. The most extensively studied MCFAS is sodium caprate, a salt of capric acid, which comprises 2-3% of the fatty acids in the milk fat fraction. To date, sodium caprate is mainly used as an excipient in a suppository formulation (DoktacillinTM) for improving rectal ampicillin absorption. The permeation properties of another dietary MCFAS, sodium caprylate (8-carbon), were shown in vitro to be lower when compared to sodium caprate. Sodium caprylate and a peptidic drug were formulated in an admixture with other excipients in oil to generate an oily suspension (OS) that enhanced permeability (Tuvia, S. et al., Pharmaceutical Research, Vol. 31, No.
8, pp. 2010-2021 (2014).
[00643]For example, in one embodiment, a permeation enhancer is combined with a peptide inhibitor, wherein the permeation enhancer comprises at least one of a medium-chain fatty acid, a long-chain fatty acid, a bile salt, an amphiphilic surfactant, and a chelating agent. In certain embodiments, medium-chain fatty acid salts promote absorption by increasing paracellular permeability of the intestinal epithelium. In one embodiment, a permeation enhancer comprising sodium N4hydroxybenzoyl)amino] caprylate is used to form a weak noncovalent association with the peptide inhibitor of the instant invention, wherein the permeation enhancer favors membrane transport and further dissociation once reaching the blood circulation. In another embodiment, a peptide inhibitor of the present invention is conjugated to oligoarginine, thereby increasing cellular penetration of the peptide into various cell types.
Further, in at least one embodiment a noncovalent bond is provided between a peptide inhibibitor of the present invention and a permeation enhancer selected from the group consisting of a cyclodextrin (CD) and a dendrimers, wherein the permeation enhancer reduces peptide aggregation and increasing stability and solubility for the peptide inhibitor molecule.
1006441In certain embodiments, a pharmaceutical composition or formulation comprises a peptide inhibitor of the present invention and a transient permeability enhancers (TPEs).
Permeation enhancers and TPEs may be used to increase orally bioavailability or the peptide inhibitor. One example of a TPE that may be used is an oily suspension formulation that disperses a powder containing sodioum caprylate and a therapeutic agent (Tuvia, S. et al., Pharmaceutical Research, Vol. 31, No. 8, pp. 2010-2021 (2014).

1006451In certain embodiments, pharmaceutical composition and formulations may include a peptide inhibitor of the present invention and one or more absorption enhancers, enzyme inhibitors, or mucoso adhesive polymers.
1006461In particular embodiments, peptide inhibors of the present invention are formulated in a formulation vehicle, such as, e.g., emulsions, liposomes, microsphere or nanoparticles.
[00647] Other embodiments of the invention provide a method for treating a subject with a peptide inhibitor of the present invention having an increased half-life. In one aspect, the present invention provides a peptide inhibitor having a half-life of at least several hours to one day in vitro or in vivo (e.g., when administered to a human subject) sufficient for daily (q.d.) or twice daily (b.i.d.) dosing of a therapeutically effective amount. In another embodiment, the peptide inhibitor has a half-life of three days or longer sufficient for weekly (q.w.) dosing of a therapeutically effective amount. Further, in another embodiment, the peptide inhibitor has a half-life of eight days or longer sufficient for bi-weekly (b.i.w.) or monthly dosing of a therapeutically effective amount. In another embodiment, the peptide inhibitor is derivatized or modified such that is has a longer half-life as compared to the underivatized or unmodified peptide inhibitor. In another embodiment, the peptide inhibitor contains one or more chemical modifications to increase serum half-life.
[00648] When used in at least one of the treatments or delivery systems described herein, a peptide inhibitor of the present invention may be employed in pure form or, where such forms exist, in pharmaceutically acceptable salt form.
[00649] The total daily usage of the peptide inhibitors and compositions of the present invention can be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular subject will depend upon a variety of factors including: a) the disorder being treated and the severity of the disorder; b) activity of the specific compound employed; c) the specific composition employed, the age, body weight, general health, sex and diet of the patient; d) the time of administration, route of administration, and rate of excretion of the specific peptide inhibitor employed; e) the duration of the treatment;
f) drugs used in combination or coincidental with the specific peptide inhibitor employed, and like factors well known in the medical arts.

1006501 In particlar embodiments, the total daily dose of the peptide inhibitors of the invention to be administered to a human or other mammal host in single or divided doses may be in amounts, for example, from 0.0001 to 300 mg/kg body weight daily or 1 to 300 mg/kg body weight daily.
Non-invasive Detection of Intestinal Inflammation 1006511The peptide inhibitors of the invention may be used for detection, assessment and diagnosis of intestinal inflammation by microPET imaging, wherein the peptide inhibitor is labeled with a chelating group or a detectable label, as part of a a non-invasive diagnostic procedure. In one embodiment, a peptide inhibitor is conjugated with a bifunctional chelator. In another embodiment, a peptide inhibitor is radiolabeled. The labeled peptide inhibitor is then administered to a subject orally or rectally. In one embodiment, the labeled peptide inhibitor is included in drinking water. Following uptake of the peptide inhibitor, microPET imaging may be used to visualize inflammation throughout the subject's bowels and digestive track.
Identification of Peptide Inhibitors that Inhibit IL-23 Signalling 1006521 As described herein, in certain embodiments, peptide inhibitors of the present invention preferentially bind to human IL-23R and/or rat IL-23R as compared to mouse IL-23R. Mouse IL-23R contains additional amino acids as compared to human IL-23R or rat IL-23R in the region corresponding to about amino acid residue 315 to about amino acid residue 340 of the mouse IL23R protein, e.g., amino acid region NVVQPWSSPFVHQTSQETGKR (see, e.g., Figure 4). In particular embodiments, the peptide inhibitors bind to a region of human IL-23R from about amino acid 230 to about amino acid residue 370.
1006531 The present invention provides a new method to identify an inhibitor (e.g., a peptide inhibitor) of IL-23R, based on identifying an agent (e.g., a peptide) that preferentially binds to human IL-23R or rat IL-23R as compared to mouse IL-23R. In certain embodiments, the method comprises: (a) determining an amount of binding of a candidate agent to a human IL-23R polypeptide or a rat IL-23R polypeptide; (b) determining an amount of binding of the candidate agent to the mouse IL-23R polypeptide; and (c) comparing the determined amount of binding to the human IL-23R polypeptide or the rat IL-23R polypeptide to the determined amount of binding to the mouse IL-23R polypeptide, wherein if the determined amount of binding to the human IL-23R polypeptide or the rat IL-23R polypeptide is greater than the amount of binding to the mouse IL-23R polypeptide, the candidate compound is an inhibitor of IL-23R. In particular embodiments, the candidate compound is identified as an inhibitor of IL-23R if the determined amount of binding to the human IL-23R polypeptide or the rat IL-23R
polypeptide is at least 1.5-fold, at least 2-fold, at least 3-fold, at least 4-fold, at least 5-fold, at least 10-fold, at least 20-fold, at least 30-fold, at least 40-fold, at least 50-fold, at least 100-fold, at least 200-fold, at least 500-fold, or at least 100-fold the determined amount of binding to the mouse IL-23R polypeptide. In particular embodiments, the candidate compound is a peptide. In particular embodiments, the peptide is a peptide of one of the formulas described herein. In particular embodiments, the human IL-23 polypeptide or rat IL-23R polypeptide comprises or consists of the full length human IL-23R or rat IL-23R protein, respectively.
In other embodiments, the human IL-23R polypeptide is a fragment of the full length human IL-23R
protein, comprising 8 or more amino acid residues within the region of human IL-23R from about amino acid residue 230 to about amino acid residue 370. In other embodiments, the rat IL-23R polypeptide is a fragment of the full length rat IL-23R protein, comprising 8 or more amino acid residues within the region of rat IL-23R from about amino acid residue 245 to about amino acid residue 385.
1006541In another embodiment, the present invention provides a new method to identify an inhibitor (e.g., a peptide inhibitor) of IL-23R, based on identifying an agent that binds to a region of human IL-23R or rat IL-23 that is disrupted in mouse IL-23R by the presence of additional amino acids from about amino acid residues 315 to about amino acid residue 340 of the mouse IL23R protein, e.g., amino acid region NWQPWSSPFVHQTSQETGKR (see, e.g., Figure 4). In certain embodiments, the method comprises: (a) determining an amount of binding of a candidate agent to a fragment of human IL-23R polypeptide that falls within about amino acid residue 230 to about amino acid residue 370, or to a fragment of rat IL-23R
polypeptide that falls within about amino acid residue 245 to about amino acid residue 385; (b) determining an amount of binding of the candidate agent to a negative control (e.g., a negative control peptide unrelated to human IL-23R or rat-IL-23R); and (c) comparing the determined amount of binding to the fragment of human IL-23R polypeptide or the fragment of rat IL-23R polypeptide to the determined amount of binding to the negative control, wherein if the determined amount of binding to the human IL-23R polypeptide fragment or the rat IL-23R polypeptide fragment is greater than the amount of binding to the negative control, the candidate compound is an inhibitor of IL-23R. In particular embodiments, the candidate compound is identified as an inhibitor of IL-23R if the determined amount of binding to the human IL-23R
polypeptide fragment or the rat IL-23R polypeptide fragment is at least 1.5-fold, at least 2-fold, at least 3-fold, at least 4-fold, at least 5-fold, at least 10-fold, at least 20-fold, at least 30-fold, at least 40-fold, at least 50-fold, at least 100-fold, at least 200-fold, at least 500-fold, or at least 100-fold the determined amount of binding to the negative control. In particular embodiments, the candidate compound is a peptide. In particular embodiments, the peptide is a peptide of one of the formulas described herein. In particular embodiments, the fragment of human IL-23R includes at least 8, at least 12, at least 20, at least 50, or at least 100, or all amino acid residues within the region of human IL-23R from about amino acid residue 230 to about amino acid residue 370. In other embodiments, the fragment of rat IL-23R polypeptide includes at least 8, at least 12, at least 20, at least 50, or at least 100, or all amino acid residues within the region of rat IL-23R
from about amino acid residue 245 to about amino acid residue 385.
1006551 Methods of determining binding of a candidate compound to an IL-23 polypeptide are known in the art and include but are not limited to in vitro and cell-based binding assays, including those described herein. For example, a labeled candidate compound may be incubated with a recombinantly produced IL-23R polypeptide or negative control bound to a solid support under conditions and for a time sufficient to allow binding, and then binding determined by measuring the amount of label associated with the bound IL-23R polypeptide.
Non-invasive Detection of Intestinal Inflammation 1006561 The peptide inhibitors of the invention may be used for detection, assessment and diagnosis of intestinal inflammation by microPET imaging, wherein the peptide inhibitor is labeled with a chelating group or a detectable label, as part of a a non-invasive diagnostic procedure. In one embodiment, a peptide inhibitor is conjugated with a bifunctional chelator. In another embodiment, a peptide inhibitor is radiolabeled. The labeled peptide inhibitor is then administered to a subject orally or rectally. In one embodiment, the labeled peptide inhibitor is included in drinking water. Following uptake of the peptide inhibitor, microPET imaging may be used to visualize inflammation throughout the subject's bowels and digestive track.

Animal Models of IBD
[00657] The present invention includes models of animal disease, including inflammatory diseases and disorders, such as inflammatory bowel diseases, e.g., Crohn's disease and colitis.
As described in the accompanying Examples, several animal models of inflammatory diseases and disorders were developed.
1006581In one embodiment, the present invention includes a method of assessing the ability of a candidate compound to inhibit or reduce an inflammatory disease disorder, comprising:
1006591(a) providing to a rat an amount of dextran sulfate sodium (DSS) sufficient to induce IBD;
1006601(b) providing to the rat an amount of a candidate compound; and 1006611(c) measuring an amount of IBD symptoms present in the rat after being provided with the DSS and the candidate compound;
[00662] wherein if the amount of IBD symptoms measured in (c) are significantly lower than the amount measured in a control rat provided with the amount of DSS and either an amount of a control compound or no peptide (e.g., vehicle control), the candidate compound inhibits or reduces the inflammatory disease or disorder.
[00663] In certain embodiments, the rat is provided with DSS for about 5 to 12 days, e.g., about 9 days. In particular embodiments, the rat is provided with DSS by providing to the rat ad lib exposure to drinking water containing DSS, e.g., about 1% to about 10% DSS, about 2% to about 5% DSS, or about 3% DSS. In particular embodiments, the rat is provided with the test compound at about 5 mg/kg to about 100 mg/kg, or about 10 mg/kg to about 50 mg/kg, or about 20 mg/kg or about 30 mg/kg. In particular embodiments, the rat is provided with test compound orally, e.g., in drinking water. In certain embodiments, the DSS assay is performed as described in the accompanying Examples.
1006641In another embodiment, the present invention includes a method of assessing the ability of a candidate compound to inhibit or reduce an inflammatory disease disorder, comprising:

1006651(a) providing to a rat an amount of 2,4,6-Trinitrobenzenesu1fonic acid (TNBS) sufficient to induce IBD;
1006661(b) providing to the rat an amount of a candidate compound; and 1006671(c) measuring an amount of IBD symptoms present in the rat after being provided with the TNBS and the candidate compound;
[00668] wherein if the amount of IBD symptoms measured in (c) are significantly lower than the amount measured in a control rat provided with the amount of TNBS and either an amount of a control compound or no peptide (e.g., vehicle control), the candidate compound inhibits or reduces the inflammatory disease or disorder.
1006691In certain embodiments, the animals are provided with about 10mg/kg to about 200 mg/kg TNBS, e.g., about 10 mg/kg, about 20 mg/kg, about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, about 60 mg/kg, about 70 mg/kg, about 80 mg/kg, about 90 mg/kg, about 100 mg/kg, about 120 mg/kg, about 150 mg/kg or about 200 mg/kg of TNBS. In certain embodiemnts, the TNBS is in alcohol, e.g., in 45%-50% ethanol. In particular embodiments, the TNBS is administered intrarectally. In particular embodiments, the rat is provided with the test compound at about 5 mg/kg to about 100 mg/kg, or about 10 mg/kg to about 50 mg/kg, or about 20 mg/kg or about 30 mg/kg. In particular embodiments, the rat is provided with the test compound orally, e.g., in drinking water. In certain embodiments, the TNBS assay is performed as described in the accompanying Examples.
[00670] In particular embodiments IBD symptoms are measured immediately following provision of the DSS or TNBS and candidate compound (or test compound or no compound), or later, e.g., at about 3 days, 5 days, or 9 days following initial provision of DSS or TNBS
and candidate compound (or test compound or no compound). In particular embodiments, the IBD
symptoms measured include one or more of percent body weight loss, stool consistency, a quantitative hemoccult score, and ratio of colon weight:colon length. In certain embodiments, the IBD
symptoms are measured using a disease activity index (DAI) score and/or ratio of colon weight: colon length, wherein the DAI score consists of ratings from three parameters, including percent body weight loss, stool consistency, and a quantitative hemoccult score, and can achieve a maximum of three units.
[00671]In certain embodiments, a neutralizing anti-IL-23p19 antibody is used as a comparator or positive control.
1006721In certain embodiments, to assess the extent of the inflammatory response, animals are observed, e.g., daily, for clinical signs which included percent body weight loss and signs of loose stools or diarrhea. Following a time period after inoculation of with DSS or TNBS (e.g., 5 days, 6, days, or seven days), rats are sacrificed and their entire colon length and colon weight from cecum to rectum recorded. The severity of colitis may be evaluated by a pathologist blinded to the identity of treatments. In addition to the colon wall thickness, the gross colon damage may be assessed based on a 0-4 scale according to Table 19 below, and histopathological scores were determined based on below parameters (Tables 20 and 21).
1006731 In certain embodiments, IBD symptoms are measured in three groups of rats, each with at least 3 animals, e.g., six animals each, wherein the three groups include:
vehicle, DSS or TNBS, and DSS or TNBS with a positive control (e.g., sulfasalazine administered at 100 mg/kg PO, QD).
EXAMPLES

SYNTHESIS OF PEPTIDE MONOMERS
1006741Peptide monomers of the present invention were synthesized using the Merrifield solid phase synthesis techniques on Protein Technology's Symphony multiple channel synthesizer.
The peptides were assembled using EIBTU (0-Benzotriazole-N,N,N',N'-tetramethyl-uronium-hexafluoro-phosphate), Diisopropylethylamine(DIEA) coupling conditions. For some amino acid couplings PyA0P(7-Azabenzotriazo1-1-y1oxy)tripyrro1idinophosponium hexafiuorophosphate) and DIEA conditions were used. Rink Amide 1\41311A resin (100-200 mesh, 0.57 mmol/a) was used for peptide with C-tenninal amides and pre-loaded Wang Resin with N-a-Frnoc protected amino acid was used for peptide with C-terminal acids. The coupling reagents (I-IBTU and DIEA premixed) were prepared at 100mmol concentration. Similarly amino acids solutions were prepared at 100 mmol concentration. Peptide inhibitors of the present invention were identified based on medical chemistry optimization and/or phage display and screened to identify those having superior binding and/or inhibitory properties.
Assembly [00675] The peptides were assembled using standard Symphony protocols. The peptide sequences were assembled as follows: Resin (250 mg, 0.14 mmol) in each reaction vial was washed twice with 4m1 of DMF followed by treatment with 2.5ml of 20% 4-methyl piperidine (Fmoc de-protection) for 10min. The resin was then filtered and washed two times with DMF (4m1) and re-treated with N-methyl piperifine for additional 30 minute. The resin was again washed three times with DMF (4 ml) followed by addition 2.5ml of amino acid and 2.5ml of HBTU-DIEA
mixture. After 45min of frequent agitations, the resin was filtered and washed three timed with DMF (4 ml each). For a typical peptide of the present invention, double couplings were performed. After completing the coupling reaction, the resin was washed three times with DMF
(4 ml each) before proceeding to the next amino acid coupling.
Ring Closing Metathesis to form Olefins [00676] The resin (100 umol) was washed with 2 ml of DCM (3 x 1 min) and then with 2 ml of DCE (3 x 1 min) before being treated with a solution of 2 ml of a 6 mM
solution of Grubbs' first-generation catalyst in DCE (4.94 mg m1-1; 20 mol% with regard to the resin substitution). The solution was refluxed overnight (12 h) under nitrogenbefore being drained. The resin was washed three times with DMF (4 ml each); DCM (4 ml) before being dried and cleavaed.
Cleavage [00677] Following completion of the peptide assembly, the peptide was cleaved from the resin by treatment with cleavage reagent, such as reagent K (82.5% trigluoroacetic acid, 5% water, 5%
thioanisole, 5% phenol, 2.5% 1,2-ethanedithiol). The cleavage reagent was able to successfully cleave the peptide from the resin, as well as all remaining side chain protecting groups.
[00678] The cleaved peptides were precipitated in cold diethyl ether followed by two washings with ethyl ether. The filtrate was poured off and a second aliquot of cold ether was added, and the procedure repeated. The crude peptide was dissolved in a solution of acetonitrile:water (7:3 with 1% TFA) and filtered. The quality of linear peptide was then verified using electrospray ionization mass spectrometry (ESI-MS) (Micromass/Waters ZQ) before being purified.
Disulfide Bond Formation via Oxidation [00679] The peptide containing the free thiol (for example diPen) was assembled on a Rink Amide-MBHA resin following general Fmoc-SPPS procedure. The peptide was cleaved from the resin by treatment with cleavage reagent 90% trifluoroacetic acid, 5% water, 2.5% 1,2-ethanedithiol, 2.5% tri-isopropylsilane). The cleaved peptides were precipitated in cold diethyl ether followed by two washings with ethyl ether. The filtrate was poured off and a second aliquot of cold ether was added, and the procedure repeated. The crude peptide was dissolved in a solution of acetonitrile:water (7:3 with 1% TFA) and filtered giving the wanted unoxidized peptide crude peptide [00680] The crude, cleaved peptide with X4 and X9 possessing either Cys, Pen, hCys, (D)Pen, (D)Cys or (D)hCys, was dissolved in 20m1 of water: acetonitrile. Saturated Iodine in acetic acid was then added drop wise with stirring until yellow color persisted. The solution was stirred for 15 minutes, and the reaction was monitored with analytic HPLC and LCMS. When the reaction was completed, solid ascorbic acid was added until the solution became clear.
The solvent mixture was then purified by first being diluted with water and then loaded onto a reverse phase HPLC machine (Luna C18 support, 10u, 100A, Mobile phase A: water containing 0.1% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA, gradient began with 5%
B, and changed to 50% B over 60 minutes at a flow rate of 15m1/min). Fractions containing pure product were then freeze-dried on a lyophilyzer.
Lactam Bond Formation [00681] 100mg of crude, cleaved peptide (approx. 0.12mmol) is dissolved in 100m1 of anhydrous dichloromethane. HOBt (1-Hydroxybenzotriazole hydrate) (0.24mmol, 2 equivalents) is added followed by DIEA (N,N-Diisopropylethylamine) (1.2mmol, 10equivalents) and TBTU
(0-(Benzotriazol-1-y1)-N,N,N',N' -tetramethyluronium tetrafluoroborate)(0.24 mmol, 2 equivalents).
The mixture is stirred overnight and followed the reaction by HPLC. When the reaction is completed, dichloromethane is evaporated and diluted with water and Acetonitrile and then loaded onto a reverse phase HPLC machine (Luna C18 support, 10u, 100A, Mobile phase A:

water containing 0.1% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1%
TFA, gradient begins with 5% B, and is changed to 50% B over 60 minutes at a flow rate of 15m1/min).
Fractions containing pure product are then freeze-dried on a lyophilyzer.
Triazole bond formation [00682] The purified peptide containing the relevant amino acids alkyne and azide was stirred at room temperature in a phosphate / Me0H (2 :1) at pH 7.4 (1 mg per 2 ml). CuSO4 .5 H20 (10 equiv.), and sodium ascorbate (10 equiv.) was added and the mixture was agitated in at room temperature for 36 h. Me0H was removed and the solution was acidified to pH 3 with 1%TFA
water mix. The solution was then filtered before being loaded onto EIPLC for peptide purification.
Thioether Bond Formation [00683] The peptide containing the free thiol (eg Cys) and hSer(OTBDMS) was assembled on a Rink Amide-MBHA resin following general Fmoc-SPPS procedure. Chlorination was carried out by treating the resin with PPh3 (10 equiv.) and C13CCN (10 equiv.) in DCM
for 2 h. The peptide was cleaved from the resin by treatment with cleavage reagent 90%
trifluoroacetic acid, 5% water, 2.5% 1,2-ethanedithiol, 2.5% tri-isopropylsilane). The cleaved peptides were precipitated in cold diethyl ether followed by two washings with ethyl ether.
The filtrate was poured off and a second aliquot of cold ether was added, and the procedure repeated. The crude peptide was dissolved in a solution of acetonitrile:water (7:3 with 1% TFA) and filtered giving the wanted uncyclized crude peptide [00684] The crude peptide possessing a free thiol (eg, Cys, Pen, hCys, (D)Pen, (D)Cys or (D)hCys) and the alkyl halide (hSer(C1)) at either the X4 and X9 position or X9 and X4 position was dissolved in 0.1 M TRIS buffer pH 8.5. Cyclization was allowed to take place overnight at RT. The solvent mixture was then purified by first being diluted two-fold with water and then loaded onto a reverse phase EIPLC machine (Luna C18 support, 10u, 100A, Mobile phase A:
water containing 0.1% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1%
TFA, gradient began with 5% B, and changed to 50% B over 60 minutes at a flow rate of 15m1/min). Fractions containing pure product were then freeze-dried on a lyophilyzer.
S elenoether Bond Formation [00685] Crude peptide containing the thiol protected -Selenium amino acid and the alkyl halide at X4 and X9 was dissolved in 0.1 M sodium phosphate buffer pH 5.5 containing DTT
(40 equ.).
Cyclization was allowed to take place over 24 h at RT. The solution was then diluted two-fold with water, and the final cyclized peptide was purified using RP-HPLC, affording the selenoether.
Diselenide Bond Formation 1006861Diselenide precursor was dissolved in a solution of 0.1 M phosphate buffer pH 6.0 and isopropanolcontaining DTT (40 equiv), and the reaction mixture was incubated at 37 C. After 20h, additional DTT (10 equiv) was added to the reaction. After a total of 32h, the cyclization reaction was then diluted with twofold water, and the final cyclized peptide was purified using RP-HPLC, affording the diselenide.
Purification [00687] Analytical reverse-phase, high performance liquid chromatography (HPLC) was performed on a Gemini C18 column (4.6 mm x 250 mm) (Phenomenex). Semi-Preparative reverse phase HPLC was performed on a Gemini 10 pm C18 column (22 mm x 250 mm) (Phenomenex) or Jupiter 10 pm, 300 A C18 column (21.2 mm x 250 mm) (Phenomenex).
Separations were achieved using linear gradients of buffer B in A (Mobile phase A: water containing 0.15% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA), at a flow rate of 1 mL/min (analytical) and 15 mL/min (preparative). Separations were achieved using linear gradients of buffer B in A (Mobile phase A: water containing 0.15% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA), at a flow rate of 1 mL/min (analytical) and 15mL/min (preparative).
Linker Activation and Dimerization 1006881Peptid monomer subunits were linked to form peptide dimer inhibitors as described below.
[00689] Small Scale DIG Linker Activation Procedure: 5mL of NMP was added to a glass vial containing IDA diacid (304.2 mg, 1 mmol), N-hydroxysuccinimide (NHS, 253.2 mg, 2.2 eq.
2.2mmol) and a stirring bar. The mixture was stirred at room temperature to completely dissolve the solid starting materials. N, N'-Dicyclohexylcarbodiimide (DCC, 453.9mg, 2.2 eq., 2.2 mmol) was then added to the mixture. Precipitation appeared within 10 min and the reaction mixture was further stirred at room temperature overnight. The reaction mixture was then filtered to remove the precipitated dicyclohexylurea (DCU). The activated linker was kept in a closed vial prior to use for dimerization. The nominal concentration of the activated linker was approximately 0.20 M.
[00690]For dimerization using PEG linkers, there is no pre-activation step involved.
Commercially available pre-activated bi-functional PEG linkers were used.
[00691]Dimerization Procedure: 2mL of anhydrous DMF was added to a vial containing peptide monomer (0.1 mmol). The pH of the peptide was the adjusted to 8-9 with DIEA.
Activated linker (IDA or PEG13, PEG 25) (0.48eq relative to monomer, 0.048 mmol) was then added to the monomer solution. The reaction mixture was stirred at room temperature for one hour.
Completion of the dimerization reaction was monitored using analytical HPLC.
The time for completion of dimerization reaction varied depending upon the linker. After completion of reaction, the peptide was precipitated in cold ether and centrifuged. The supernatant ether layer was discarded. The precipitation step was repeated twice. The crude dimer was then purified using reverse phase HPLC (Luna C18 support, 10u, 100A, Mobile phase A: water containing 0.1% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA, gradient of 15%B and change to 45%B over 60min, flow rate 15m1/min). Fractions containing pure product were then freeze-dried on a lyophilyzer.

1006921 Peptide optimization was performed to identify peptide inhibitors of IL-23 signalling that were active at low concentrations (e.g., IC50 <10 nM) while exhibiting gastrointestinal (GI) stability. Certain peptides were tested to identify peptides that inhibit the binding of IL-23 to human IL-23R and inhibit IL-23/IL-23R functional activity, as described below.
Peptides tested included peptides containing a variety of different cyclization chemistries, including, e.g., cyclic amides (side chain cyclizations), peptides containing a disulfide linkage, e.g., between two Pen residues, and peptides containing a thioether linkage. Peptide inhibitors of the present invention include but are not limited to peptides having any of the structures depicted herein. In addition, peptide inhibitors of the present invention include those having the same amino acid sequence of the peptides or structures described herein, without being required to have the same or any N- or C-terminal "capping" groups, such as, e.g., Ac or NH2.
[00693] Assays performed to determine peptide activity are described below, and the results of these assays is provided in Tables E3A-E3H, E4A and E4B, E5A-E5C, E6, E7, and E8. Human ELISA indicates the 1L23-IL23R competitive binding assay described below, Rat ELISA
indicates the rat IL-23R competitive binding ELISA assay described below, and pStat3HTRF
indicates the DB cells IL-23R pSTAT3 cell assay described below. The peptides depicted in Tables E3B-E3E are cyclized via a disulfide bridge formed between two cysteine residues in these peptides. The peptides depicted in Table E3F are dimerized via a linker moiety or through internal cysteine moieties, as indicated. The peptides depicted in Tables E4A
and E4B are cyclized via the two Pen residues present in each of these peptides. The peptides depicted in Table E5A are cyclized via a thioether bond between the indicated amino acid residues. Table E5B provides an illustrative structure depicting thioether cyclization, which is indicated in the table by the term "Cyclo," with the cyclic region bracketed immediately following. The monomer subunits of the peptide dimers shown in Table E5C are cyclized as indicated by the term "Cyclo" and linked to each other via the indicated linker. The peptides shown in Table E6 are cyclized via ring closing metathesis of the indicated residues. Table E7 provides two illustrative structures depicting side chain cyclizations via cyclic amides, and the peptides in this table are cyclized as indicated following the term "Cyclo." Table E8 depicts peptides cyclized via a cysteine residue and a Pen residue.
[00694] Peptide inhibitors of the present invention include both the cyclized form of the peptides shown herein, as well as the non-cyclized forms. For certain peptides, the residue Abu is present where indicated, whereas in other embodiments related to the non-cyclized form, the Abu may be referred to as a hSer(C1) or homoSer residue.
1L23-IL23R Competitive Binding ELISA
[00695] An Immulon 4I-113X plate was coated with 50 ng/well of IL23R huFC
and incubated overnight at 4 C. The wells were washed four times with PBST, blocked with PBS

containing 3% Skim Milk for 1 hour at room temperature, and washed again four times with PBS T. Serial dilutions of test peptides and IL-23 at a final concentration of 2 nIVI diluted in Assay Buffer (PBS containing 1% Skim Milk) were added to each well, and incubated for 2 hours at room temperature. After the wells were washed, bound IL-23 was detected by incubation with 50 ng/well of goat anti-p40 polyclonal antibodies (R&D Systems #AF309) diluted in Assay Buffer for 1 hour at room temperature. The wells were again washed four times with PBST. The secondary antibodies, EIRP conjugated donkey anti-goat IgG
(Jackson ImmunoResearch Laboratories #705-035-147) diluted 1:5000 in Assay Buffer was then added, and incubated for 30 minutes at room temperature. The plate was finally washed as above.
Signals were visualized with TMB One Component EIRP Membrane Substrate, quenched with 2 M sulfuric acid and read spectrophotometrically at 450 nm. IC50 values for various test peptides determined from these data are shown in Tables E3A-E3H, E4A and 4EB, ESA-ESC, E6, E7, and E8.
Rat IL-23R Competitive Binding ELISA
100696] An assay plate was coated with 300 ng/well of Rat IL-23R huFC and incubated overnight at 4 C. The wells were washed, blocked, and washed again. Serial dilutions of test peptides and IL-23 at a final concentration of 7 nIVI were added to each well, and incubated for 2 hours at room temperature. After the wells were washed, bound IL-23 was detected with goat anti-p40 polyclonal antibodies, followed by an EIRP conjugated donkey anti-goat IgG. Signals were visualized with TMB One Component EIRP Membrane Substrate and quenched with 2 M
sulfuric acid. IC50 values for various test peptides determined from these data are shown in Tables E3G, E3H, E4A, E4B, E5B, ESC and E8.
DB Cells IL23R pSTAT3 Cell Assay 1006971 IL-23 plays a central role in supporting and maintaining Th17 differentiation in vivo.
This process is thought to mediated primarily through the Signal Transducer and Activator of Transcription 3 (STAT3), with phosphorylation of STAT3 (to yield pSTAT3) leading to upregulation of RORC and pro-inflammatory IL-17. This cell assay examines the levels of pSTAT3 in IL-23R-expressing DB cells when stimulated with IL-23 in the presence of test compounds. DB cells (ATCC #CRL-2289), cultured in RPMI-1640 medium (ATCC #30-2001) supplemented with 10% FBS and 1% Glutamine, were seeded at 5 X 10E5 cells/well in a 96 well tissue culture plate. Serial dilutions of test peptides and IL-23 at a final concentration of 0.5 nIVI
were added to each well, and incubated for 30 minutes at 37 C in a 5% CO2 humidified incubator. Changes in phospho-STAT3 levels in the cell lysates were detected using the Cisbio HTRF pSTAT3 Cellular Assay Kit, according to manufacturer's Two Plate Assay protocol. IC50 values determined from these data are shown in Tables E3E, E3G, E3H, E4A, E4B, E5B, ESC, and E8 as absolute values or within ranges. Where not shown, data was not determined.
Table E3A. Illustrative Non-cyclic Peptides and Activities ELBA
=.
=

NO Sequenceii

11,23 .
in ii Moles =(11050) ........
1 Ac-[Ailp] - [Ail3FTWQDYVVLY4AibFR-NEI. 2 >100,000 2 Ac-CAMTWQDYVVLYGRC-NH2 7200 3 Ac-[Aib]-[Aib]-TWQDYVVLYGR-NH2 >100,000 4 Ac-AMTWQDYVVLYGRK-NH2 4100 Ac-CAMTWQDYVVLYGRCK-NH2 8500 6 Ac-KAMTWQDYWLYGR-NH2 5600 7 Ac-KCAMTWQDYWLYGRC-NH2 10600 8 Ac-AMTWAibDYVVLYGR-NH2 >37,500 9 Ac-AMTWQDYVVLYGR-NH2 6100 Cyclo-[AMTWQDYVVLYGR] Not active 11 Hy-AATWQDYWLYGR-OH 7785

12 Hy-AMAWQDYVVLYGR-OH 24225

13 Hy-AMTAQDYVVLYGR-OH N/A

14 Hy-AMTWADYVVLYGR-OH 6248 Hy-AMTWQAYVVLYGR-OH 9589 Table E3B. Illustrative Peptides Containing the C)000(C Motif with IC50 >1 uM
in IL23-IL23R Competitive Binding ELISA
SEQ
ID NO. Sequence =
87 Hy-CSDWECYVVHIFG-NH2 88 Hy-CETWECYVVHSFS-NH2 89 Hy-CQSWECYVVHYYG-NH2 90 Hy-CSDWRCYWHVFG-NH2 91 Hy-CHTWVCYVVEIEFS-NH2 92 Hy-CTDWVCYVVEIEYS-NH2 93 Hy-CQTWVCYVVHTYG-NH2 SEQ.
ID NO. õ Sequence 94 Hy-CGNVVECYVVHVYG-NH2 95 Hy-CKDWKCYVVHIYG-NH2 96 Hy-CRTWVCYVVHVFG-NH2 97 Hy-CAD-[1-Nal]-VCYVVHTFG-NH2 98 Hy-CAD-[2-Nall-VCYVVHTFG-NH2 99 Hy-CAD-[1-BIP]-VCYVVHTFG-NH2 100 Hy-CAD-[Tic]-VCYVVHTFG-NH2 101 Hy-CAD-[[3hW]-VCYVVHTFG-NH2 102 Hy-CADWVCY-[1-BIP]-HTFG-NH2 103 Hy-CADWVCY-[Tic]-HTFG-NH2 104 Hy-CADWVCY-[f3hW]-HTFG-NH2 105 Hy-CADWVCYAHTFG-NH2 106 Hy-ACDWVCYVVHTFG-NH2 107 Hy-ACDWCCYVVCTFG-NH2 108 Hy-AADWCAYVVCTFG-NH2 109 Hy-CADWCCYVVCTFG-NH2 110 Hy-CADWCCYVVCTFG-NH2 111 Hy-CADWCCYVVCTFG-NH2 112 Hy-CADWVCYVVHTF-NH2 113 Hy-CADWVCYVVHT-NH2 114 Hy-CADWVCYVV-NH2 115 Hy-[(3-Ala]-SCADWVCYVVHTFG-OH
116 Ac-[(D)Lys]-SCADWVCYVVHTFG-OH
117 Ac-[(D)Lys]-[(3-Ala]-CADWVCYVVHTFG-OH
118 Hy-[AEA]-CADWVCYVVHTFG-OH
119 Ac-[(D)Lys]-CADWVCYVVHTFG-OH
120 Ac-CKDWVCYVVHTFG-OH
121 Ac-CADWKCYVVHTFG-OH
122 Ac-CADWVCYVVKTFG-OH
123 Ac-CADWVCYVVEIKFG-OH
124 Ac-CADWVCYVVHTKG-OH
125 Ac-CADWVCYWHTF-[(D)Lys]-0H
126 Ac-CADWVCYVVHTFG-NH2 127 Hy-CADWVCY-[1-Nal]-HTF-OH
128 Hy-CADWVCY-[1-Nall-HT-[N-Me-Phe]-NH2 129 Hy-CADWVCY-[1-Nal]-H-[Sarc]-F-OH
130 Hy-CADWVCY-[1-Nall-[N-Me-His]-TF-OH
131 Hy-CADWVCYVVHTFGK-OH
132 Hy-C-[Sarc]-DWVCY-[1-Nall-HTF-OH
133 Hy-CAD-[N-Me-Trp]-VCY-[1-Nal]-HTF-OH
134 Hy-CADW-[Sarc]-CY-[1-Nal]-HTF-OH
135 Hy-CADWVCY-[1-Nal]-HT-[(D)Phe]-0H
136 Hy-CADWVCY-[1-Nal]-HTF-[Sarc]-0H

SEQ.
ID NO. Sequence 137 Ac-CATWVCYWHTFG-NH2 138 Ac-CADWECYWHTFG-NH2 139 Ac-CADWVCYVVEIRCGWWGC-NH2 140 Ac-CADWVCY-[1-Nall-H-RD)AlaFFG-NH2 141 Ac-CADWVCY-[1-Nall-H-[Aib]-FG-NH2 142 Ac-CADWVCY-[1-Nall-H-[b-Ala]-FG-NH2 143 Ac-CADWVCY-[1-Nall-FTFG-NH2 144 Ac-CADWVCY-[1-Nall-RD)Ala]-TFG-NH2 145 Ac-CADWVCY-[1-Nall-H-[Aib]-[(D)Phe]-G-NH2 146 Ac-CADWVCY-[1-Nall-HTF-[Aib]-NH2 147 Ac-CADWVCY41-Nall4N-Me-HisH(D)AlaFF-[Aib]-NH2 148 Ac-CADWVCY-[1-Nall-H-[AEP]-G-NH2 149 Ac-CADWVCYVV-[N-MeHis]-TFG-[AEA]-[(D)Lys]-NH2 150 Ac-CADWVCY-[Aic]-HTFG-[AEA]-[(D)Lys]-NH2 151 Ac-CADWVCY-[Bip]-HTFG-[AEA]-[(D)Lys]-NH2 152 Ac-CQTWQCYVV-[N-MeArg]-ENG-[AEA]- [(D)-Lys] -NH2 153 Ac-CQTWQCYWR-[N-MeArg]-NG-[AEA]- [(D)-Lys] -NH2 154 Ac-CQTWQCYVVR-[N-MeLys]-NG-[AEA1-[(D)-Lys] -NH2 155 Ac-CQTWQCYVVR-[Sarc]-NG-[AEA]- [(D)-Lys]-NH2 156 Ac-CQTWQCYVVR-RD)Glu]-NG-[AEA]-[(D)-Lys]-NH2 157 Ac-CQTWQCYVV- [(D)Arg]-ENG-[AEA]-[(D)-Lys]-NH2 158 Ac-CQTWQCYVV-RD)Arg]-[(D)Glu]-NG-[AEA]-[(D)Lys]-NH2 159 Ac-CQTWQCYW-[N-MeGlu]-NG-[AEA]-[(D)-Lys]
160 Ac-CADWVC-NH2 161 Ac-CRDWQCYVV -[N-MeArg]-KFG-[AEP]-[(D)-Lys] -NH2 162 Ac-CRDWQCYVVR-RD)Lys]-FG-[AEP]-[(D)-Lys] -NH2 163 Ac-CRDWQCYVV-RD)Arg]-KFG-[AEP]-[(D)-Lys] -NH2 164 Ac-CRDWQCYVV-RD)Arg]-[(D)Lys]-FG-[AEPH(D)-Lys] -NH2 165 Ac-CQTWQCYVV-[N-MeArg]-ENG-[AEA]-[(D)-Lys] -NH2 Table E3C. Illustrative Peptides Containing the C)000(C Motif with IC50 of 500nM to 1000nM in 1L23-IL23R Competitive Binding ELISA
SEQ
ID NO. Sequence 166 Hy-CTDWKCYVVHEFG-NH2 167 Hy-CRTWTCYVVHVYG-NH2 168 Hy-CPNVVECYVVEIRFG-NH2 169 Hy-CADWVCYVVHTFG-NH2 170 Hy-CADWIVICYVVHEYG-NH2 171 Hy-CTTWKCYVVHQYG-NH2 172 Hy-CSNVVECYVVEIHYG-NH2 173 Hy-CSDWVCYVVHVYG-NH2 174 Hy-CDTWKCYVVEIRQS-NH2 175 Hy-CADWVCY-[1-Nal]-HTFG-NH2 176 Hy-CADWVCY-[2-Nal]-HTFG-NH2 177 Hy-CADWVCYVVHTFG-NH2 178 Ac-CADWVCYVVHTFG-[(D)Lys]-0H
179 Ac-CADWVCYVVHTFGAP-[(D)Lys]-0H
180 Ac-CTDWKCYVVHTFG-NH2 181 Ac-CRDWVCYWHTFG-NH2 182 Ac-CADWVCYVVEIEFG-NH2 183 Ac-CADWVCYVVEIFHQLRDA-NH, 184 Ac-CADWVCYVVEIEHSERVG-NH2 185 Ac-CADWVCYVVHNHSEGSG-NH2 186 Ac-CADWVCYVVEIRSTGGQH-NH2 187 Ac- [(D)Ly s] -CRDWQ CY- [1 -Na!] -HTH- [ S arc]- [AEP] - [(D)Arg] -188 Ac-TQFDCRTWECYVVHTFG-NH2 189 Ac-GGVECNDWQCYVVHTFG-NH2 190 Ac-REGTCSTWKCYVVHTFG-NH2 191 Ac-DTPRCRTWECYVVHTFG-NH2 192 Ac-GGGECENVVECYVVHTFG-NH2 193 Ac-GDHKCSSWECYVVHTFG-NH2 194 Ac-GSVHCMTWECYWHTFG-NH2 195 Ac-CADWVCY-[1-Nal]-VTFG-NH2 196 Ac-CADWVCYVV-[(D)His]-TFG-[AEA]-[(D)Lys]-NH2 Table E3D. Illustrative Peptides Containing the C)000(C Motif with IC50 <500nM
in IL23-IL23R Competitive Binding ELISA
SEQ
Sequence ID NO.
"
197 Hy-CRDWQCYVVEIKFG-NH2 198 Hy-CSNVVVCYVVHTYG-NH2 199 Ac-CADWVCYVVHTFG-[(3-Ala]-[(D)Lys]-0H
200 Ac-CADWVCYVVHTFG-[AEA]-[(D)Lys]-0H
201 Ac-CADWVCYVVHTFG-OH
202 Ac-CADWVCYVVHTFG-[AEP]-(D)Arg]-0H
203 Ac-CADWVCYWHTFG-[AEP]-K-OH
204 Ac-CADWVCYVVHTFG-[Gaba]-[(D)Lys]-0H
205 Ac-CADWVCYWHTFG-[Hexanoic]-[(D)Lys]-0H
206 Ac-CADWVCYVVHTFG-[(PEG)2-[(D)-Lys]-0H
207 Ac-CADWVCYWHTFGP-[(D)Lys]-0H
208 Ac-CADWVCYWHTFG-[Azt]-[(D)-Lys]-0H
209 Ac-CADWVCYVVHTFGA-[(D)Lys]-0H
210 Ac-CADWVCYVVHTFGAP-[(D)Lys]-0H
211 Ac-CADWVCYVVHTFGA[Azt]-[(D)Lys]-0H
212 Ac-CADWVCYWHTFGAA[(D)Lys]-0H
213 Ac-CRDWQCYVVEIKFG-[AEP]-[(D)Lys]-0H

SEQ.
ID NO. Sequence 214 Ac-CATWQCYVVEIEYG-NH2 215 Ac-CKTWTCYVVEIEFG-NH2 216 Ac-CTTWTCYWHQYG-NH2 217 Ac-CRTWECYVVEIEFG-NH2 218 Ac-CRTWQCYWHEYG-NH2 219 Ac-CQTWQCYVVRENG-NH2 220 Ac-CRTWECYVVEIEYG-NH2 221 Ac-CTTWECYVVEIEYG-NH2 222 Ac-CRTWECYVVEIEQS-NH2 223 Ac-CTTWECYWHQFG-NH2 224 Ac-CTTWECYVVEIEFG-NH2 225 Ac-CQTWECYVVEILYG-NH2 226 Ac-CEDWKCYVVEIKYG-NH2 227 Ac-CTDWVCYWHTFG-NH2 228 Ac-CADWVCYVVHTYG-NH2 229 Ac-CADWVCYVVEIRHADRVK-NH2 230 Ac-CADWVCYVVHTFGER-NH2 231 Ac-CADWVCYVVHTHGER-NH2 232 Ac-DTPRCRTWECYWHTFG-NH2 233 Ac-CQTWVCYVVRENG- [AEA]- [(D)-Lys] -NH2 234 Ac-CQTWQCYVVRENG-[AEA]-[(D)-Lys]-NH2 235 Ac-CQTWQCYVVRTNG- [AEA]- [(D)-Lys] -NH2 236 Ac-CQTWQCYVVRKNG-[AEA]- [(D)-Lys] -NH2 237 Ac-CQTWQCYVVRRNG-[AEA] [(D)-Lys] -NH2 238 Ac-CQTWQCYVVR-[Dapa]-NG- [AEA]- [(D)-Lys] -NH2 239 Ac-CQTWQCYWR-[Orn]-NG- [AEA]- [(D)-Lys] -NH2 240 Ac-CRTWQCYVVRKFG-[AEA] [(D)-Lys] -NH2 241 Ac-CQTWQCYVVRENG-[AEA]-[(D)Arg]-NH2 242 Ac-CQTWQCYVVRENG-[AEA]-[(D)-Lys]-NH2 243 Ac-CQDWQCYVVRENG-[AEA]- [(D)-Lys] -NH2 244 Ac-CQTWQCYVVRENG-[AEA]-[(D)-Lys]-NH2 245 Ac-CQTWQCYVVRTNG-[AEA]-[(D)-Lys]-NH2 246 Ac-CQTWVCYVVRENG-[AEA]-[(D)-Lys]-NH2 247 Ac-CQTWQCYWRKNG- [AEA]- [(D)-Lys]-NH2 248 Ac-CQTWQCYW-[Cav]-ENG-NH2 249 Ac-CQTWQCYW-[Cpa]-ENG-NH2 250 Ac-CQTWQCYVVLENG-NH2 251 Ac-CQTWQCYVV[-hLeu]-ENG-NH2 252 Ac-CQTWQCYWR-[K-Ac]-NG-NH2 253 Hy-CRTWQCYVVRKFG-NH2 Table E3E. IC50 of Illustrative Peptides Containing the C)000(C Motif with Activities ELISA
ii SEQ ,. pStat3 I-ITRF in ii ii ID NO. quencoi 1L23 in00 n Moles i .:
= n NI
169 Hy-CADWVCYWHTFG-NH2 ****
****
178 Ac-CADWVCYVVHTFG-[(D)Lys]-0H **** ****
210 Ac-CADWVCYVVHTFGAP-[(D)Lys]-0H **** ND
211 Ac-CADWVCYWHTFGA[Azt]-[(D)Lys]-0H **** ND
180 Ac-CTDWKCYWHTFG-NH2 **** ****
Ac-CADWVCYW-RD)His]-TFG-[AEA]-[(D)Lys]-196 **** ****

281 DIG dimererisation through N-termina Lysine ***** *****
(Ac-KMTWQDYVVLYGR-NH2)2 284 DIG dimererisation through C-terminal Lysine *****
*****
(Ac-AMTWQDYVVLYGK-NH2)2 *=<10nIVI; **=10-25 nM *** = 25-100 nM, **** = 100-1000 nM, *****=1000-10,000 nM.
Table E3F. IC50 of Illustrative Peptide Dimers Human SEQ ID 'iii ::::::
......
: :: ..
.. ii ii IL23R/IL23 itinlier NI oictSti ::::::
:: : Seci u en cOii NO. ::iii : ::
:.:.:.
...... E LISA
== =
oxidized dimer through 277 (Hy-FPTWEWYWCNRD-NH2)2 *****
the cysteine oxidized dimer through 278 (Hy-ALTWEFYWLCRE-NH2)2 >10,000 the cysteine 291 DIG through Lysine (Hy-113A1a1SCADWVCYWHTFG-OH)2DIG
>10,000 (Ac-RD)Lys] -SCADWVCYWHTFG-OH) 292 DIG through Lysine >10,000 (Ac-(D)Lys-H3Alal -CADWVCYWHTFG-293 DIG through Lysine >10,000 OH)2DIG
294 DIG through Lysine (Hy-AEA-CADWVCYWHTFG-OH)2DIG
>10,000 (Ac-RD)Lys] -CADWVCYWHTFG-OH) 295 DIG through Lysine >10,000 296 DIG through Lysine (Ac-CKDWVCYWHTFG-OH)2DIG
>10,000 297 DIG through Lysine (Ac-CADWKCYWHTFG-OH)2DIG
>10,000 298 DIG through Lysine (Ac-CADWVCYWKTFG-OH)2DIG
299 DIG through Lysine (Ac-CADWVCYWHKFG-OH)2DIG
>10,000 300 DIG through Lysine (Ac-CADWVCYWHTKG-OH)2DIG *****
301 DIG through Lysine (Ac-CADWVCYWHTFDK-OH)2DIG
>10,000 302 DIG through Lysine (Ac-CADWVCYWHTFGDK)2DIG *****
303 DIG through Lysine (Ac-CADWVCYWHTFG- H3-Alal - RD)Lys] -304 DIG through Lysine ***
OH)2DIG
(Ac-CADWVCYWHTF G- [AEA] - [(D)Ly s] -***
OH)2DIG
DIG through C terminal 305 (Hy-CADWVCYWHTFGK-OH)2DIG *****
Lysine 306 PEG25 through Lysine (Hy- 113Alal-SCADWVCYWHTFG-OH) Humaii SEQ ID :: ... iiii i)l_,er ink Moietf iiiiii iiiSequenc0ii NO. g :.ELISA

307 PEG25 through Lysine (Ac-RD)Lys1-SCADWVCYWHTFG-OH)2 308 PEG25 through Lysine (Ac-(D)Lys)-H3A1a1-CADWVCYWHTFG-OH)2 309 PEG25 through Lysine (Hy-{AEA1-CADWVCYWHTFG-OH)2 310 PEG25 through Lysine (Ac-[(D)Lys1-CADWVCYWHTFG-OH)2 311 PEG25 through Lysine (Ac-CKDWVCYWHTFG-OH)2 312 PEG25 through Lysine (Ac-CADWKCYWHTFG-OH)2 313 PEG25 through Lysine (Ac-CADWVCYWKTFG-OH)2 314 PEG25 through Lysine (Ac-CADWVCYWHKFG-OH)2 315 PEG25 through Lysine (Ac-CADWVCYWHTKG-OH)2 316 PEG25 through Lysine (Ac-CADWVCYWHTF-RD)Lys1-0H)2 317 PEG25 through Lysine (Ac-CADWVCYWHTFG-[(D)Lys1-0H)2 (Ac-CADWVCYWHTFG-[bAla1-[(D)Lys1-318 PEG25 through Lysine OH)2 319 PEG25 through Lysine (Ac-CADWVCYWHTFG4AEA1-[(D)Lys1-OH)2 PEG25 through C-320 (Hy-CADWVCYWHTFGK-OH)2 terminal Lysine *=<10nIVI; **=10-25 nM *** = 25-100 nIVI, **** = 100-1000 nIVI, *****=1000-10,000 nIVI.
Table E3G. IC50 of Illustrative Peptides Containing the 00(WX0000(X-[(D)Lys]
Motif _ : Human .::
Rat :" pStat3 :
.....
:H ELISA .E.L.I.SA
HTRE
ill SEQ I
ID NO Sequence ii:: IL23/ :.. IL23/ (nNI) . .:iii ii IL23R IL23R
=
.:
... .....
.. ...
16 Ac-CQDWQCYWR-[Cha]-FG-[AEA1-[(D)Lys1-NH2 113 17 Ac-CQTWQCYWR-[0g11-FG-[AEA1-[(D)Lys1-NH2 206 18 Ac-CQTWQCYWK4Dap1-FG-[AEA1-[(D)Lys1-NH2 32 19 Ac-CQTWQCYWH4Dap1-FG-[AEA1-[(D)Lys1-NH2 49 59 20 Ac-CQTWQCYWRLFG-[AEA1-[(D)Lys1-NH2 51 47 21 Ac-CQTWQCYW-[hArg]-[Dap1-FG-[AEA1-[(D)Lys1-NH2 56 22 Ac-CQTWQCYW-[Cit]-[Dap]-FG-[AEA1-[(D)Lys1-NH2 25 23 Ac-CQTWQCYWRVFG-[AEA1-[(D)Lys1-NH2 39 62 14 24 Ac-CQTWQCYWR-[Dap]-[Tic]-G-[AEA1-[(D)Lys1-NH2 892 65 12 25 Ac-CQTWQCY4Tic14Orn1-KFG4AEA14(D)Lys1-NH2 >30000 26 Ac-CQTWQCYWR-[Dab]-FG-[AEA1-[(D)Lys1-NH2 37 27 Ac-CQTWQCYW-[Orn1-{Dap1-FG-[AEA1-[(D)Lysl-NH2 79 276 37 28 Ac-CQTWQCYWHENGA-[(D)Lys1-NH2 220 29 Ac-CRTWQCYWRENGA4(D)Lys1-NH2 102 86 17 30 Ac-CRTWQCYWREYGA4(D)Lys1-NH2 78 80 8 31 Ac-C-[N-MeAla1-DWVCYWHTFG-[AEA1-[(D)Lys1-NH2 183 Human Rat 1. pStat3 ELISA ELISA HTRF
SEQ
ID NO Sequence IL23/ IL23/ (nNI) ..,iii (nNI) (n111) 32 Ac-CADWVCYWRKFG- [13Alal- [(D)Ly s] -NH2 57 33(1) 13 33 Ac-CADWVCYW- [(D)Lys] -NH2 52 29 34 Ac-CADWVCYW-[Cit]-[Tlel-FG-H3-Alal-RD)Lysl-NH2 518 35 Ac-CADWVCYW- [Cit]- [Tba] -FG- [13-A1al - [(D)Lys] -NH2 153 36 Ac-CADWVCYW-[Cit]-[Chal-FG-[(3-Alal-RD)LYs1-NH2 223 37 Ac-CADWVCY41-Na1l - [Cit] -VFG- [13-Alal - [(D)Lys] -NH2 79 38 Ac-CADWVCYW- [(D)Lys] -NH2 124 39 Ac-CADWVCYW- [Cit]- [Chg] -FG- [13-A1al - [(D)Lys] -NH2 >30000 40 Ac-CADWVCYW- [Cit] - [13A1al -FG- [(D)Lys] -NH2 2584 41 Ac-CADWVCYW- [Tle] - [Tle] -FG- [13-A1al - [(D)Lys] -NH2 ¨30000 42 Ac-CADWVCYW- [Tle] -KFG- [13-A1al - [(D)Lys] -NH2 199 43 Ac-CQTWQCYW- [(D)Ala] -VFG- [AEA] - [(D)Lys] -NH2 232 44 Ac-CQTWQCYW- [13Alal -VFG- [AEAl- [(D)Lys] -NH2 2207 45 Ac-CQTWQCYW- [(D)Leu] -VFG- [AEAH(D)Lys] -NH2 188 46 Ac-CQTWQCYW-RD)Phel -VFG- [AEAl- [(D)Lys] -NH2 848 47 Ac-CQTWQCYW- [(D)Asn] -VFG-[AEA] - [(D)Lys] -NH2 61 48 Ac-CQTWQCYW-RD)Thr] -VFG-[AEA] -[(D)Lys] -NH2 3662 49 Ac-CQTWQCYW- [(D)Asp] -VFG-[AEA] - [(D)Lys] -NH2 129 50 Ac-CQTWQCYW- [Cit] - [(D)Leu] -FG- [AEA] - [(D)Lys] -NH2 709 51 Ac-CQTWQCYW- [Cit] - [(D)Phel -FG- [AEAH(D)Lys] -NH2 1304 52 Ac-CQTWQCYW- [Citl- [(D)Asn] -FG-[AEAl- [(D)Lys] -NH2 269 53 Ac-CQTWQCYW- [Citl- [(D)Thr] -FG- [AEAl- [(D)Lys] -NH2 1214 54 Ac-CQTWQCYW- [Agp] -VNG-[AEA] -[(D)Lys] -NH2 241 55 Ac-CQTWQCY- [cc-MeTrp] -RVNG- [AEA] - [(D)Lys] -NH2 ¨6000 56 Ac-CQTWQCY- [cc¨MeTrp] - [Cit]- [hLeul -NG- [AEA] -¨6000 [(D)Lys] -NH2 57 Ac-CQTWQCYW- [Cit]-VNG- [AEAl- [(D)Lys] -NH2 73 58 Ac-CQTWQCYW- [Agp]- [Dap] -NG- [AEA] - [(D)Lys]-NH2 38 59 Ac-CQTWQCYW-[Cit] -VF- [(D)Ala] - [AEAH(D)Lys] -NH2 397 60 Ac-CQ TWQCYW-[Cit] -VF- [(D)Leu] -[AEA] -[(D)Ly s] -NH2 444 61 Ac-CQTWQCYW-[Cit] -VF- [(D)Phel- [AEA] - [(D)Lys] -NH2 784 62 Ac-CQTWQCYW- [Cit] -VF- [(D)Asn]- [AEA] - [(D)Lys] -NH2 93 63 Ac-CQTWQCYW-[Cit] -VF- [(D)Thr] - [AEAH(D)Lys] -NH2 518 64 Ac-CQTWQCYW- [Cit] -VF- [(D)Asp] - [AEAH(D)Lys] -NH2 551 65 Ac-C- [N-MeArg] -TWQCYWRVFG-[AEA] - [(D)Lys] -NH2 149 66 Ac-C- [N-MeQ1n] -TWQCYWRVFG-[AEA] - [(D)Lys] -NH2 69 85 67 Ac-C- [Cit]-TWQCYWRVFG- [AEA] -[(D)Ly sl-NH2 50 76 68 Ac-CADWVCYW- [Ornl- [Dap]-FG- [AEA] - [(D)Lysl-NH2 382 69 Ac-CADWVCY41 -Nal] -[Ornl- [Dal:11-FG- [AEAl- [(D)Lys] -70 Ac-CADWVCY- [(D)Trp] -[Orn] -[Dap] -FG- [AEA] - >30000 Human Rat 1. pStat3 ELISA ELISA HTRF
SEQ
ID NO Sequence IL23/ IL23/ (nNI) .

(nNI) (n111) RD)Lys] -NH2 71 Ac-CADWVCY- [hPhel- [Ornl- [Dap] -FG- [AEA]- [(D)Lys]-72 Ac-CADWVCY- [Bipl- [Ornl- [Dap] -FG- [AEA] -[(D)Lys] ->30000 73 Ac-CADWVCY- [Phe(3,5-F2)]- [Orn]-[Dap]-FG- [AEA] -¨6000 [(D)Lys] -NH2 74 Ac-CADWVCY- [Phe(CONH2)]- [Orn] - [Dap]-FG- [AEA] -¨6000 [(D)Lys] -NH2 75 Ac-CADWVCY- [Phe(4-CF3)]- [Orn] - [Dal:11-FG- [AEA] ->1000 [(D)Lys] -NH2 76 Ac-CADWVCY- [Phe(2,4-Me2)]- [Orn] - [Dap] -FG- [AEA] -[(D)Lys] -NH2 77 Ac-CMTWQCYWLYGR- [AEAl- [(D)Lys] -NH2 398 77 Hy-CMTWQCYWLYGR- [AEA] - [(D)Lysl-NH2 >30000 78 Ac-CADWVCY- [13hTrp] - [Oral- [Dap]-FG- [AEA] - [(D)Lys]-79 Ac-CADWVCYW- [Orn] - [c(-MeLeul -FG- [AEA] -[(D)Ly s] -¨6000 80 Ac-CADWVCYW- [Orn] - [13-spira1-pip] -FG-[AEA] -[(D)Lys] -NH2 81 Ac-CADWVCY44-Pheny1cy1cohexy1a1aninel- [Orn] - [Dap] ->3000 FG- [AEAH(D)Lys] -NH2 82 Ac-CADWVCYW-[Orn]-[Aib] -FG- [AEAH(D)Lys] -NH2 1085 83 Ac-CADWVCYW-[Orn]-[DiethylGlyl-FG- [AEA] -¨6000 [(D)Lys] -NH2 84 Ac-CADWVCY- [c(-MePhe(4-F)l- [Ornl- [Dap] -FG-[AEA] ->30000 [(D)Lys] -NH2 85 Ac-CQTWQCY- [13hPhel -RVNG- [AEA] - [(D)Lys] -NH2 >30000 86 Ac-CQTWQCY- [13(1-Nal)] -RVNG-[AEA] -[(D)Lys] -NH2 >30000 321 Ac-CQTWQCY- [13hTyrl-RVNG- [AEA] - [(D)Lysl-NH2 >30000 322 Ac-CQTWQCY-H3hPhe(4-F) -RVNG-[AEAH(D)Lysl-NH2 >30000 323 Ac-CQTWQCY-H3Nya(5-Pheny1)]-RVNG-[AEAl->30000 [(D)Lys] -NH2 324 Ac-CQTWQCY- [Phe(3,4-C12)l-RVNG- [AEA] - [(D)Lys] ->30000 325 Ac-CQTWQCY- [Tqal-RVNG- [AEA] - [(D)Ly s] -NH2 >30000 326 Ac-CQTWQCYWR-H3hLeul -NG- [AEA] - [(D)Lys] -NH2 224 327 Ac-CQTWQCYWR- [Aib] -NG- [AEA] - [(D)Lys] -NH2 1065 328 Ac-CQTWQCYWR-H3hAlal -NG- [AEA] -[(D)Lys] -NH2 457 329 Ac-CQTWQCYWR-H3hVall -NG- [AEA] -[(D)Lys] -NH2 328 330 Ac-CQTWQCYWR-H3-spira1-pip] -NG- [AEA] - [(D)Lysl-Human ' Rat 1. pStat3 ELISA ELISA HTRF
ID NO Sequence iii. IL23/ :. IL23/
(nNI) . .,iii IL23R IL23R i ..........................................iiii...... (nNI) ......p........ (n111) ......
............................................ii 331 Ac-CQTWQCYWR-[13Glul-NG-[AEA1-[(D)Lysl-NH2 250 332 Ac-CQTWQCYW-[13hLeul-VNG-[AEA1-[(D)Lysl-NH2 311 333 Ac-CQTWQCYW-H3Aibl-VNG-[AEA1-[(D)Lysl-NH2 2903 334 Ac-CQTWQCYW-H3hAlal-VNG-[AEA1-[(D)Lysl-NH2 355 335 Ac-CQTWQCYW-H3hVall-VNG-[AEAl-RD)Lysl-NH2 501 336 Ac-CQTWQCYW-H3-spiral-pipl-VNG-[AEA1-[(D)Lysl->6000 337 Ac-CQTWQCYW-H3hArgl-VNG-[AEA1-[(D)Lysl-NH2 922 338 Ac-MRTWQ-[MeCysl-YWRKFG-[AEA1-[(D)Lysl-NH2 4251 339 Ac-ACDWVCYWRKFG-[AEA1-[(D)Lysl-NH2 630 340 Ac-SRTWQSYWRKFG-{AEA1-[(D)Lysl-NH2 2816 341 Ac-CDWVCYWRKFG-[AEA1-[(D)Lysl-NH2 664 342 Ac-ARTWQ-[MeCysl-YWRKFG-[AEA1-[(D)Lysl-NH2 7571 343 Ac-ARTWQAYWRKFG-[AEA1-[(D)Lysl-NH2 3194 344 Ac-CQTWQCYW-[hLeul-EN-[AEAl-RD)Lysl-NH2 132 345 Ac-CQTWQCYWOLcul-ENG-[AEA1-[(D)Lysl-NH2 222 346 Ac-CSTWECYWRVYG-[AEAl-RD)Lysl-NH2 47 347 Ac-C4Ornl-TWQCYWRVFG4AEA1-[(D)Lysl-NH2 22 69 95 348 Ac-CQTWQCYW-[Orn1-[Dapl-FG-[AEA1-[(D)Lysl-NH2 96 349 Ac-C-[N-MeAsnl-TWQCYWRVFG-[AEAl-RD)Lysl-NH2 148 350 Ac-C-[N-MeLysl-TWQCYWRVFG-[AEA1-[(D)Lysl-NH2 80 351 Ac-C4Dabl-TWQCYWRVFG-[AEAl-RD)Lysl-NH2 23 51 99 352 Ac-CQTWQCYY4Orn14Dapl-FG4AEA14(D)Lysl-NH2 710 353 Ac-CSTWQCYW4Orn14Dapl-YG4AEA1-[(D)Lysl-NH2 371 354 Ac-CSTWECYW-[Cit]-[Dap]-YG-[AEA1-[(D)Lysl-NH2 74 355 Ac-CQTWQCFF-[Orn1-{Dapl-FG-[AEA1-[(D)Lysl-NH2 4274 356 Ac-CPTWQCYWRVFG-[AEA1-[(D)Lysl-NH2 422 347 Ac-CSTWECYW4Orn14Dabl-YG4AEA1-[(D)Lysl-NH2 338 358 Ac-CSTWECYWRVFG-[AEA1-[(D)Lysl-NH2 48 359 Ac-CLTWQCYWRVFG-[AEA1-[(D)Lysl-NH2 134 360 Ac-CQTWQCYF-[Orn1-{Dapl-FG-[AEA1-[(D)Lysl-NH2 1885 461 Ac-CNTWQCYWRVFG-[AEA14(D)Lysl-NH2 21 79 96 362 Ac-C-[Dapl-TWQCYWRVFG-[AEAl-RD)Lysl-NH2 31 363 Ac-C-[N-Me-Alal-TWQCYWRVFG-[AEAl-RD)Lysl-NH2 139 364 Ac-CKTWQCYWRVFG-[AEA1-[(D)Lysl-NH2 40 365 Ac-CQDWQCYWR-[Cha]-FG-[AEAl-RD)Lysl-NH2 113 366 Ac-CQTWQCYWR-[0g11-FG-[AEA1-[(D)Lysl-NH2 206 367 Ac-CQTWQCYWK4Dapl-FG-[AEA1-[(D)Lysl-NH2 32 368 Ac-CQTWQCYWH4Dapl-FG4AEA1-[(D)Lysl-NH2 49 59 369 Ac-CQTWQCYWRLFG-[AEA1-[(D)Lysl-NH2 51 47 370 Ac-CQTWQCYW-[hArg]-[Dap]-FG-[AEA1-[(D)Lysl-NH2 56 Table E3H. IC50 of Illustrative Peptides Containing the 00(WX0000( Motif Human .iii Rat A pStat3 SE ID 11,23/ iii I L23/
HTRF
Q iiiii Sequence iiii IL23R iii 11,23R (nM) ELISA iii ELISA
...............................................................................
.......................................................................iiii....
.. (nM) ...... iii...... (nM) ......iii ............................................iii 371 Ac-CSTWECYWRTFG-NH2 252 372 Ac-CDSWECYWRTYG-NH2 366 373 Ac-CSTWECYWHTYG-NH2 181 286 97 374 Ac-CKTWTCYWHTYG-NH2 381 375 Ac-CRTWECYWHEYS-NH2 416 376 Ac-CRTWTCYWHEYG-NH2 434 377 Ac-CFTWQCYWHEYS-NH2 515 378 Ac-CQTWQCYW43-Pall-ENG-NH2 56 20 379 Ac-CQTWQC-NH2 >30000 380 Ac-CRTWQC-NH2 >30000 381 Ac-CADWVCY-NH2 >30000 382 Ac-CADWVCYW-NH2 >30000 383 Ac-CADWVCYWH-NH2 ¨30000 384 Ac-CADWVCYWHT-NH2 4795 385 Ac-CADWVCYWHTF-NH2 3277 386 Ac-CMTWQCYWLYGR-NH2 613 387 Ac-CRTWQCYWHEFG-NH2 388 Ac-CRTWECYWHTFG-NH2 389 Ac-CQTWQCYWHEFG-NH2 390 Ac-CRTWQCYWQQFGGE-NH2 81 391 Ac-CRSWQCYWLNFGPD-NH2 101 392 Ac-CRTWQCYWLKMGDS-NH2 39 393 Ac-CQTWQCYWIKRDQG-NH2 67 394 Ac-CSTWQCYWLKHGGE-NH2 19 24 2 395 Ac-CSTWECYWSQRADQ-NH2 240 396 Ac-CQTWECYWRTFGPS-NH2 58 397 Ac-CRTWQCYWQEKGTD-NH2 118 398 Ac-CQTWQCYWLDSLGD-NH2 93 399 Ac-CRTWQCYWTKFGSEP-NH2 87 57 340 Ac-CRSWQCYWNKFGADD-NH2 142 341 Ac-CHTWQCYWLNFGDEE-NH2 323 342 Ac-CRTWQCYWLNFGNEQ-NH2 127 343 Ac-CRTWQCYWSEFGTGE-NH2 180 778 344 Ac-CRTWQCYWLRLGDEG-NH2 352 483 345 Ac-CHTWQCYWSTLGPEA-NH2 222 346 Ac-CSTWQCYWSKQSGGS-NH2 133 204 89 347 Ac-CHTWQCYWLNNGTSQ-NH2 113 348 Ac-CHTWQCYWRANDGRD-NH2 210 349 Ac-SGCRTWQCYWHEFG-NH2 390 350 Ac-NKCRTWQCYWHEYG-NH2 112 V Human Rat pStat3 NO Sequence IL23R 11,23R (nM) .
ELISA ELISA
(nM) (nM) 351 Ac-SGCRTWECYWHEYG-NH2 257 352 Ac-DACRTWECYWHKFG-NH2 165 353 Ac-PECRTWECYWHKFG-NH2 197 354 Ac-QVCQTWECYWREFG-NH2 145 355 Ac-DRCVTWECYWREFG-NH2 217 356 Ac-ADQCRTWQCYWHEFG-NH2 228 357 Ac-KENCRTWECYWREFG-NH2 148 358 Ac-VQECSTWQCYWRTFG-NH2 138 359 Ac-GEECSTWQCYWRKFG-NH2 53 24 360 Ac-DGSCRTWQCYWHQFG-NH2 240 361 Ac-NADCHSWECYWREFG-NH2 872 362 Ac-ERNCSTWECYWRAFG-NH2 855 363 Ac-RVGCSTWECYWREFG-NH2 417 364 Ac-KANCRTWQCYWRKFE-NH2 412 365 Ac-YEDCRTWQCYWENFG-NH2 280 366 Ac-CQTWQCYWRNFGDS-NH2 367 Ac-CQTWQCYWRNFESG-NH2 368 Ac-CQDWQCYWREFGPG-NH2 369 Ac-CQDWQCYWRSFGPQ-NH2 370 Ac-CQTWQCYWRTLGPS-NH2 371 Ac-CRTWQCYWQNFG-NH2 235 372 Ac-CGTWQCYWRTFGPS-NH2 76 373 Ac-CSTWQCYWHKFGNE-NH2 182 374 Ac-CRTWECYWRTYGPS-NH2 116 375 Ac-CRTWQCYWWENSQM-NH2 99 376 Ac-CQTWQCYWREFGGG-NH2 165 377 Ac-CQTWQCYWRTHGDR-NH2 83 378 Ac-CRDWQCYWLSRP-NH2 330 379 Ac-CQTWQCYW-[K(Palm)l-ENG-NH2 4880 380 Ac-CQTWQCYW4K(PEG8)1-ENG-NH2 153 381 Ac-CQTWQCYW4hLetil-EQG-NH2 128 382 Ac-CQTWQABUC-RD)Tyr1-WOLeul-ENG-NH2 >30000 383 Ac-CQTWQC-[(N-MeTyil-W-[hLeul-ENG-NH2 >30000 384 Ac-CQTWQC-[Tic-OH1-W4hLeul-ENG-NH2 >30000 385 Ac-CQTWQCEW-[hLeul-ENG-NH2 >30000 386 Ac-CQTWQCTW-[hLeul-ENG-NH2 >30000 387 Ac-CQTWQC4Chal-W4hLetil-ENG-NH2 ¨6000 388 Ac-CQTWQCYW-[cc-MeLeul-ENG-NH2 22 27 5 389 Ac-CQTWQCYW-RD)Leul-ENG-NH2 319 390 Ac-CQTWQCYW4hLeul-ENG-[(D)Lysl-NH2 121 391 Ac-CQTWQCYW-[hLeul-ENG-OH 317 392 Ac-CQTWQCYW4hLetil-ENE-NH2 222 1002 393 Ac-CQTWQCYWOLeul-ENR-NH2 93 Human .ii Rat A pStat3 SEQ ID I L23/ iii IL23/ HTRF
iiiii NO Sequence iiii IL23R
iii 11,23R (nM) . iiiii ELISA ELISA
...............................................................................
.......................................iiii...... (nM) ...... iii......
(nM) ....iii ............................................iii 394 Ac-CQTWQCYW4hLeul-ENF-NH2 82 182 69 395 Ac-CQTWQCYW4hLeul-ENP-NH2 253 114 31 396 Ac-CQTWQCYW-[hLeul-ENQ-NH2 347 397 Ac-CQTWQCYW-[hLeul-ENL-NH2 45 398 Ac-CQTWQCYW4hLeul-EEG-NH2 135 53 16 399 Ac-CQTWQCYW-[hLeul-ERG-NH2 647 400 Ac-CQTWQCYW4hLeul-EPG-NH2 108 140 27 401 Ac-CQTWQCYW-[hLeul-ELG-NH2 158 402 Ac-CQTWQCYW-[hLeul-ETG-NH2 818 403 Ac-CQTWQCYW4hLeul-FNG-NH2 395 404 Ac-CQTWQCYW4hLeul-PNG-NH2 4828 405 Ac-CQTWQCYW4hLeul-NNG-NH2 89 26 406 Ac-CQTWQCYW4hLeul-LNG-NH2 78 407 Ac-CQTWQCYW4hLeul-TNG-NH2 109 408 Ac-CQTWQCYWFENG-NH2 185 409 Ac-CQTWQCYWPENG-NH2 >30000 410 Ac-CQTWQCYWQENG-NH2 173 411 Ac-CQTWQCYWTENG-NH2 114 412 Ac-CQTWQCYWEENG-NH2 147 413 Ac-CQTWFCYW4hLeul-ENG-NH2 1412 414 Ac-CQTWPCYW-[hLeul-ENG-NH2 2735 415 Ac-CQTWNCYW-[hLeul-ENG-NH2 1849 416 Ac-CQTWRCYW-[hLeul-ENG-NH2 278 417 Ac-CQTWTCYW4hLeul-ENG-NH2 114 418 Ac-CQTWECYW-[hLeul-ENG-NH2 164 419 Ac-CQTGQCYW4hLeul-ENG-NH2 >10,000 420 Ac-CQTPQCYWOLeul-ENG-NH2 >10,000 421 Ac-CQTNQCYW4hLeul-ENG-NH2 >10,000 422 Ac-CQTRQCYW4hLeul-ENG-NH2 >10,000 423 Ac-CQTTQCYW4hLeul-ENG-NH2 >10,000 424 Ac-CQTEQCYW4hLeul-ENG-NH2 >10,000 425 Ac-CQFWQCYW4hLeul-ENG-NH2 1152 426 Ac-CQPWQCYW4hLeul-ENG-NH2 >10,000 427 Ac-CQNWQCYW-[hLeul-ENG-NH2 336 428 Ac-CQRWQCYW-[hLeul-ENG-NH2 469 429 Ac-CQEWQCYW-[hLeul-ENG-NH2 773 450 Ac-CFTWQCYWOLeul-ENG-NH2 205 451 Ac-CPTWQCYWOLeul-ENG-NH2 27412 452 Ac-CNTWQCYW4hLeul-ENG-NH2 61 453 Ac-CGTWQCYW4hLeul-ENG-NH2 167 454 Ac-CTTWQCYW4hLeul-ENG-NH2 59 28 10 455 Ac-CETWQCYW-[hLeul-ENG-NH2 101 456 Ac-CQTWQCYW-[N-MeLeul-ENG-NH2 >6000 ============'=================
==================t-n p Human Rat ,:. pStat3 SEQ ID I L23/ iii IL23/
HTRF
iiiii NO Sequence iiii IL23R iii 11,23R (nM) . iiiii ELISA iii ELISA
...............................................................................
.....................iiii........ (nM) ...... iii...... (nM) ......iii ............................................iii 457 Ac-CQTWQCYW- [cc-MeOrn] -ENG-NH2 46 64 12 458 Ac-CQTWQCYW- [cc-MeOrn] -ENG-NH2 28 31 7 459 Ac-CQTWQC-[cc-MePhel-W-[hLeul-ENG-NH2 ¨30000 460 Ac-CQTWQCYW4Aibl-ENG-NH2 31 34 12 461 Ac-CQTWQC-[hTyr]-W-[hLeul-ENG-NH2 ¨6000 462 Ac-CQTWQC-[Bipl-W-[hLeul-ENG-NH2 237 463 Ac-CQTWQCYW40g11-ENG-NH2 66 163 76 464 Ac-CQTWQCYW- [hLeul - [Lys(Ac) ] -NG-NH2 19 32 3 465 Ac-CQTWQCYW4hLeul-ENGG-NH2 61 140 24 466 Ac-CQTWQCYW-[hLeul-ENGP-NH2 97 467 Ac-CQTWQCYW-[hLeul-ENGE-NH2 180 468 Ac-CQTWQCYWOLeul-ENG-(D)Glu-NH2 183 469 Ac-CQTWQCY-[cc-MePhel-[hLeul-ENG-NH2 ¨30000 470 Ac-CQTWQCYW-[hLeul-ENGP-NH2 239 471 Ac-CQTWQCYW-[hLeul-ENGG-NH2 362 472 Ac-CQTWQCYW- [hLeul -ENGL -NH2 174 473 Ac-CQTWQCYW4hLeul-ENGF-NH2 131 474 Ac-CQTWQCYW-[hLeul-ENGE-NH2 129 475 Ac-CQTWQCYW-[hLeul-ENGN-NH2 66 23 476 Ac-CQTWQCYW- [hLeul -ENGT -NH2 160 477 Ac-CQTWQCYW4hLeul-ENGR-NH2 >10,000 >1000 478 Ac-PCQTWQCYW-[hLeul-ENG-NH2 97 479 Ac-LCQTWQCYW4hLeul-ENG-NH2 61 26 21 480 Ac-FCQTWQCYW4hLeul-ENG-NH2 56 25 16 481 Ac-ECQTWQCYW4hLeul-ENG-NH2 482 Ac-NCQTWQCYW4hLeul-ENG-NH2 483 Ac-RCQTWQCYW4hLeul-ENG-NH2 484 Ac-CQTWQCY- [2-Na1l - [hLeul -ENG-NH2 485 Ac-CQTWQCY41-Nall4hLeul-ENG-NH2 18 37 6 486 Ac-CQTWQC42-Nall-W4hLeul-ENG-NH2 48 73 11 487 Ac-CQ TWQC- [1 -Nal] - [2-Nall -[hLetil -ENG-NH2 78 125 17 488 Ac-CQ TWQC- [2-Nall - [1-Nall -[hLetil -ENG-NH2 117 489 Ac-CQTWQC-[Aic]-W-[hLeul-ENG-NH2 126 490 Ac-CQTWQCHW-[hLeul-ENG-NH2 ¨6000 491 Ac-CQTWQCYH- [hL eh] -ENG-NH2 398 492 Ac-CQ TWQC- [Tyr(OMe)] -W- [hLeul -ENG-NH2 ¨30000 493 Ac-CQTWQCY-[134:11-[hLeul-ENG-NH2 42 51 11 494 Ac-CQTWQCY- [Tyr(OMe)] - [hLeul -ENG-NH2 998 495 Ac-CQTWQCHH- [hL eh] -ENG-NH2 148 496 Ac-CQTWQCY- [cc¨MeTrp] - [hLeul -EQG-NH2 >30000 497 Ac-CQTW-RK(PEG8)1-CYWLENG-NH2 212 498 Ac-CQTWQCYWZ-LNG-NH2 800 499 Ac-CQTW- [K(PEG8)] CYW- [K(PEG8)1-ENG-NH2 753 : Human Rat ::. pStat3 ... .....
...
i SE ID 11,23/ ii IL23/
HTRF
Q iiiii :::
Sequence iii IL23R iii 11,23R :: (nM) ELISA iii ELISA
..
.==
.....
::
..
.==
:: ...
= ::
500 Ac-CQTW- [K(Palm)1-CYWLENG-NH2 ¨30000 501 Ac-CQTWQCYW-[Orn1-[K(Palm)1-NG-NH2 >6000 502 Ac-Gly-[(D)Asn]-(D)Glu-(D)Leu-(D)Trp-(D)Tyr-(D)Cys->30000 (D)G1n-(D)Trp-(D)Thr-(D)G1n-(D)Cys-NH2 503 Ac-CQTWQCYW-[(Orn)14K(Peg8)1-NG-NH2 169 504 Ac-CRTWQCYWHEFG-NH2 166 505 Ac-CRTWECYWHTFG-NH2 333 506 Ac-CQTWQCYWHEFG-NH2 169 507 Ac-CQTWQCYWRNFGDS-NH2 96 508 Ac-CQTWQCYWRNFESG-NH2 315 509 Ac-CQDWQCYWREFGPG-NH2 82 510 Ac-CQDWQCYWRSFGPQ-NH2 117 511 Ac-CQTWQCYWRTLGPSNH2 66 512 Ac-CQTWQCYW-[(D)Prol-ENG-NH2 >30000 513 Ac-CQTWQCYWELNG-NH2 79 514 Ac-CQTWECYWELNG-NH2 154 515 Ac-CQTWQCYR1-Nall-[cc-MeLeul-ENG-NH2 22 67 13 516 Ac-CQTWQCY41-Nall4RDAsnl-ENG-NH2 145 98 517 Ac-CQTWQCYWLE-[K(Palm)I-G-NH2 >6000 518 Ac-CQTWQCYWLEN-[K(Palm)1-NH2 2800 519 Ac-CSTWECYWRTFG-NH2 252 520 Ac-CDSWECYWRTYG-NH2 366 521 Ac-CSTWECYWHTYG-NH2 181 286 97 Table E4A. IC50 of Illustrative examples of dimers of Peptides Containing the Ac-[Pen]-)0(WX-[Pen]-X)00( Motif and analogues SEQ ID =
Human Rat 1)St8t3 NO SequencOi ELISA ELISA HTRF
. .
[Ac- [Penl-QTWQ-[Pen]-[Phe(4-0Me)]-[2-Nall -[cc-MeLys]-522 ** *

[Ac- [Penl-QTWQ- [Pei+ [Phe(4-0Me)1- [2-Nall - [ec-MeLysl-523 * **

[Ac- [Penl-QTWQ- [Penl- [Phe [4-(2-aminoethoxy)142-Nall - [ec-524 ** **
Me-Leul-QNN-NH212 DIG
[Ac- [Penl-QTWQ- [Penl- [Phe [4-(2-aminoethoxy)142-Nall - [ec-525 * **
Me-Leul-QNN-NH212 PEG25 [Ac- [Penl-QTWQ- [Penl- [Phe [4-(2-aminoethoxy)1- [2-Nall -526 *** ***
[Aibl4Lys(Ac)1-NQ-NH212 DIG
[Ac- [Penl-QTWQ- [Penl- [Phe [4-(2-aminoethoxy)1- [2-Nall -527 ** ***
[Aibl4Lys(Ac)1-NQ-NH212 PEG25 H um:tit-1¨ Rat¨ p Stat3.-SEQ ID
Sequ en c0 ELISA ELISA HTRF
NO.
(n M) (n M) (n M) 528 [Ac-[Pen]-QTWQ-[Pen1-[Phe(4-0Me)]-[2-Nal]-[a-MeVall-[Lys(Ac)1-NN4D)Lys112 DIG
529 [Ac- [Penl-QTWQ [Pei+ [Phe P-(2-acety1aminoethoxy)1- [2-Nall- [cc-MeVa1l-[Lys(Ac)1-NN4D)Lys112 DIG
[Ac- [Penl-QTWQ [Pei+ [Phe P-(2-acetylaminoethoxy)1-530 **
Nailcc-MeVall-KNN-NH212 DIG
531 [Ac- [Pen] -QTWQ [Pei+ [Phe [4 -(2 -acetylaminoethoxy)] - [2- ***
Nall-K-[Lys(Ac)1-NN-NH212DIG
532 [Ac- Wen] -QTWQ- [Pei+ [Phe (4-0Me)] - [2-Nall - [cc-MeLys] - **
[Lys(Ac)1-NN-NH212 DIG
533 [Ac- [cc-MeLysl-Wenl-QTWQ- [Pei+ [Phe(4-CONH2)1- 2-Nail - ****
[cc-MeVall-[Lys(Ac)1-NN-NH212 DIG
534 [Ac-[Penl-QTWQ-[Pen1-[Phe(4-CONH2)1-P-Nail-k-MeLysl- **
[Lys(Ac)1-NN-NH212 DIG
535 [Ac-[Penl-NTWQ-[Pen1-[Phe(4-CONH2)1-P-Nail-[Aibl-KNN-**

536 [Ac-[Penl-NTWQ-[Pen1-[Phe(4-CONH2)1-P-Nail-P-amino-4-carboxy-tetrahydropyranl-KNN-NH212 DIG
537 [Ac-IPenl-NTWQ-[Pen1-[Phe(4-CONH2)1-P-Nall-[Achcl-538[Pen] -NTWQ- [Pen] - [Phe(4-CONH2)1- -Nail - [Acvc] - **

539 [Ac-[Penl-NTWQ-[Pen1-[Phe(4-CONH2)1-P-Nail-k-MeLeul-540 [Ac- [Penl-NTWQ- [Penl- [Phe(4-0Me)1- [2-Nall- [Aibl-KNN-541 [Ac- [Penl-NTWQ- [Penl- [Phe(4-0Me)1- [2-Nall- 4-amino-4-carboxy-tetrahydropyranl-KNN-NH212DIG
542 [Ac- [Penl-NTWQ- [Penl- [Phe(4-0Me)1- [2-Nall- [Achcl-KNN-543 [Ac-[Penl-NTWQ-[Pen1-[Phe(4-0Me)]-[2-Nall-[Acycl-KNN-[Ac- [Penl-NTWQ- [Pei+ [Phe(4-0Me)1- [2-Nall - [cc-MeLet+

545 [Ac-[Penl-QTWQ-[Pen1-[Phe(4-CONH2)1-P-Nail-k-MeLysl-[Lys(Ac)1-NN-NH212 IDA
546 [Ac-[Penl-QTWQ-[Pen1-[Phe(4-CONH2)1-P-Nail-k-MeLys1-[Lys(Ac)1-NN-NH212 [IDA-13Alal *=<10nIVI; **=10-25 nM*** = 25-100 nJVI,**** = 100-1000 nIVI, *****=1000-10,000 Table E4B. IC50 of Illustrative Peptides Containing the Ac-[Pen]-X(WX-[Pen]-)000( Motif and Analogues ...............................................................................
.............................................................i.
SE" D Human.¨ Rat ......
i)Stat.3.:

I ., SequencOi ELISA ELISA HTRF
NO.
...............................................................................
...............................................................................
...............................................................................
...............................................................................
.........................................t..... -- (nM) -- ......õõ.... --(nM) -- (nM)....
547 Ac-[Pen] -RTWQ- [Pen] -YWRKFG- [AEAl- RD)-Lys] -NH2 **** ****
***
548 Ac-A- [Pen] -DWV- [Pen] -YWRKF G- [AEA] - [(D)-Lysl-NH2 >30000 549 Ac- [[Pen] -QTWQ- [Pen] -YW-[hLetil -ENG-NH2 ****
550 Ac- [Pen] -QTWQ- [Pen] -YW [N-MeArg] -ENG-NH2 >30000 551 Ac- [Pen] -QTWQ- [Penl-YW- [hLeul -ENG-NH2 ****
552 Ac- [Pen] -QTWQ- [Penl-YW- [N-MeArg] -ENG-NH2 >30000 Ac-A- [Pen] -DWV- [Pen] -YW- [Ornl- [Dap] -F G- [AEA] - RD)-Lys] ->30000 554 Ac- [Pen] -QTWQ- [Pen] -YW- [cc-MeLeul -ENG-NH2 *** **** **
555 Ac- [Pen] -QTWQ- [Penl-YW- [(D)Asn] -ENG-NH2 *****
556 Ac- [Pen] -QTWQ- [Pen] -Y- [2-Nall - [cc-MeLy s] -ENG-NH2 ***
**** *
Ac- [Pen]-QTWQ- [Penl- [Phe(4-0Me)] 42-Nall - [cc-MeLys] -ENG- ***
557 **** **

558 Ac- [Pen] -OTWQ- [Pen] -12-Na11-12-Nall - [cc-MeLy s] -ENG-NH2 ****
**** **
559 Ac- [Pen] -OTWO- [Pen] -Y42-Nall - [cc-MeOrn] -ENG-NH2 *** ****
**
560 Ac- [Pen] -OTWO- [Penl-YW- [oc-MeOrn] -ENG-NH2 **** **** ***
561 Ac- [Pen] -OTWO- [Pen] -Y41-Nall - [cc-MeOrn] -ENG-NH2 **** ****
***
Ac- [Pen] -QTWQ- [Penl- [Phe(4-0Me)] 42-Nall - [cc-MeOrn] -562 **** ***
[Lys(Ac) ] -NG-NH2 563 Ac- [Pen] -QTWQ- [Pen] -YW- [cc-MeLys] - [Lys(Ac) ] -NG-NH2 ****
***
Ac- [Pen] -QTWQ- [Penl- [Phe-(4-0Me)]-W- [cc-MeLy s] -564 *** *** **
[Lys(Ac) ] -NG-NH2 Ac- [Pen] -QTWQ- [Penl- [Phe(4-0Me)] 42-Nall - [cc-MeLys] -565 *** *** *
[Lys(Ac) ] -NG-NH2 Hurnan...''... Rat pStat.3.' SEQ ID
SequencOi ELISA ELISA HTRF
NO.
(nM) (nM) Ac-[Pen]-QTWQ-[Pen]-[Phe(4-0Me)]-[1-Nal]-[ct-MeLysl-566 *** **** ***
[Lys(Ac)l-NG-NH2 Ac-[Penl-QTWQ-[Pen1-[BIP1-[2-Nall-[ec-MeLysl-[Lys(Ac)]-567 >10,000 Ac-[Penl-QTWQ-[Penl-Phe(3,4-C12)42-Nall-[ec-MeLysl-568 ****
[Lys(Ac)l-NG-NH2 Ac-[Penl-QTWQ-[Pen1-[Phe(3,5-F2)]-[2-Nall-[ec-MeLysl-569 ****
[Lys(Ac)l-NG-NH2 Ac-[Penl-QTWQ-[Pen1-[Phe(4-NH2)142-Nall-[ec-MeLysl-570 ****
[Lys(Ac)l-NG-NH2 571 Ac-[Penl-QTWQ-[Pen1-[2-Nall-[cc-MeLys1-[Lys(Ac)]-NG-NH2 >10000 572 Ac-[Penl-QTWQ[Pen1-[Phe(3,4-C12)]-[2-Nall-[cc-MeOrnl-ENG- ****

Ac-[Penl-QTWQ[Pen1-[Phe(4-CN)142-Nall-k-MeOrnl-ENG-573 ****

Ac-[Penl-QTWQ[Pen1-[Phe(3,5-F2)]-[2-Nall-[ec-MeOrnl-ENG-574 ****

Ac-[Penl-QTWQ[Pen1-[Phe(4-CH2CO2M-P-Nall-[cc-MeOrnl-576 Ac-[Penl-QTWQ[Pen1-[Phe(4-CH2C0E12)1-P-Nall-[cc-MeOrnl-Ac-[Penl-QTWQ[Pen1-[Phe(penta-F)]-[2-Nall-[cc-MeOrnl-ENG-Ac-[Penl-QTWQ[Pen1-[Phe(4-CF3)]-[2-Nall-k-MeLysl-ENG-Ac-[Penl-QTWQ[Pen1-[Phe[4-(2-aminoethoxy)]-[2-Nall-[ec-MeLysl-ENG-NH2 580 Ac-[Penl-QTWQ[Pen1-[Phe[4-(2-aminoethoxy)]-[2-Nall-[ec-MeLysl-ENG-NH2 Ac-[Penl-QTWQ-[Pen1-[Phe(4-0Me)142-Nall-k-MeLysl-581 ****
K(iyDde)-NG-NH2 succinic acid-[Penl-QTWQ[Pen1-[Phe(4-0Me)]-[2-Nall-k-582 *** ***
MeLys1-[Lys(Ac)]-NG-NH2 glutaric acid-[Penl-QTWQ[Pen1-[Phe(4-0Me)142-Nall-[ec-583 *** *** **
MeLys1-[Lys(Ac)]-NG-NH2 4-methylmorpholine-2,6-dione-[Penl-QTWQ[Pen1-[Phe(4-584 *** *** **
OMe)l-p-Nall-k-MeLys1-[Lys(Ac)]-NG-NH2 pyroglutamic acid-[Penl-QTWQ[Pen1-[Phe(4-0Me)142-Nall-[ec- ***
585 ***
MeLys1-[Lys(Ac)]-NG-NH2 Human¨ Rat pStat.3.' SEQ ID
SequencOi ELISA ELISA HTRF
NO.
(nNI) (01) isovaleric acid-[Pen[-QTWQ[Pen]-[Phe(4-0Me)142-Nall-ret-586 *** ***
**
MeLysl-[Lys(Ac)l-NG-NH2 587 gallic acid-[Penl-QTWQ[Pen]-[Phe(4-0Me)]-[2-Nall-[cc- *****
MeLysl-[Lys(Ac)l-NG-NH2 octanoic acid-[Penl-QTWQ[Pen]-[Phe(4-0Me)]-[2-Nall-[cc-588 ****
MeLysl--[Lys(Ac)l-NG-NH2 589 4-Biphenylacetic acid-[Penl-QTWQ[Pen]-[Phe(4-0Me)l-[2-Nall- ****
-[cc-MeLysl-[Lys(Ac)l-NG-NH2 4-fluorophenylacetic acid-[Penl-QTWQ-[Pen]-[Phe(4-0Me)]-[2- ***
590 ****
Nall-[cc-MeLysl-[Lys(Ac)l-NG-NH2 591 Hy-[Penl-ADWV-[Penl-YWHTFG-NH2 >6000 Ac-[Penl-GTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-592 **
MeLysl-ENG-NH2 Ac-[Penl-TTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-593 **
MeLysl-ENG-NH2 Ac-[Penl-STWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-594 **
MeLysl-ENG-NH2 Ac-[Pen]-[Dapl-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-595 ***
11cc-MeLysl-ENG-NH2 Ac- [Pen] - [cc-MeOrn] -TWQ [Pen] - [Phe [4-(2-amino ethoxy)] -112-596 ****
Nall-[cc-MeLysl-ENG-NH2 Ac-[Penl-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-MeLysl-ENG-NH2 Ac-[Penl-QTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-598 ***
MeLysl-[Lys(Ac)l-NG-NH2 Ac-[Penl-QTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall4a-599 **
MeLysl-[Lys(Ac)l-NN-NH2 Ac-[Penl-QTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-600 **
MeLysl-ENG-NH2 Ac-[Penl-QTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-601 ***
MeLysl-ENA-NH2 602 Ac-[Penl-QTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-MeLeul-[Lys(Ac)l-NN-NH2 603 Ac-[Penl-QTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[cc-MeLeul-QNN-NH2 604 Ac-[Penl-QTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[Aibl-605 Ac-[Penl-QTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-Aib-11Lys(Ac)l-NN-NH2 Hum Rat pStat.3.' SEQ ID
Sequel] cOi ELISA ELISA HTRF
NO.
(n NI) (n M) 606 Ac- [Pert] -QTWQ-[Pen] -[Phe [4-(2-aminocthoxy)] -[Aibl -[Ly s(Ac)] -NQ-NH2 Ac- [Pert] -Dap (Ac)TWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)] -607 **
[2-Na1l- [c(-MeLys(Ac)] -ENG-NH2 Ac- [Pen] - [c(-MeOrn(Ac)l-TWQ- [Pen] - [Phe [4-(2-608 ****
acetylaminoethoxY)1-12-Nall- [c(-MeLy s(Ac)] -ENG-NH2 609 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acety1aminoethoxy)]
[c(-MeLy s(Ac)] - [Ly s(Ac)l-NG-NH2 610 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acety1aminoethoxy)]
[c(-MeLy s(Ac)] - [Ly s(Ac)l-NN-NH2 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)]
611 **
[cc-MeLy s(Ac)] -ENG-NH2 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)]
612 **
[c(-MeLy s(Ac)] -ENA-NH2 613 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)]
[c(-MeLeul-[Lys(Ac)]-NN-NH2 614 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)]
[c(-MeLeul-QNN-NH2 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)]
615 **
[Aibl-ENN-NH2 616 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)]
[Aibl - [Ly s(Ac)] -NN-NH2 617 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)]
[Aibl - [Ly s(Ac)] -NQ-NH2 618 Ac- [Pen] -QTWQ- [Penl- [Phe(4-0Me)142-Nall-[Aibl-ENN-NH2 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-aminoethoxy)] -619 **
[hLeul-ENA-NH2 620 Ac- [Pen] -TTWQ- [Pen] -[Phc [4-(2-aminoethoxy)] - [2-Nall- [Aib] -[Ly s(Ac)] -NN-NH2 621 Ac- [Pen] -QTWQ- [Pen] - [Phe(4-0Me)] - [2-Nall - [Aib] - [Lys(Ac)l-622 Ac- [Pen] -TTWQ- [Pen] -[Phc [4-(2-aminoethoxy)] - [2-Nall- [Aib] -[Ly s(Ac)] -NQ-NH2 623 Ac- [Pen] -QTWQ- [Pen] - [Phe(4-0Me)] - [2-Nall - [Aib] - [Lys(Ac)l-624 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-aminoethoxy)] - [2-Nall -[Aibl -[Ly s(Ac)] -NA-NH2 625 Ac- [Pen] -QTWQ- [Pen] - [Phe(4-0Me)] - [2-Nall - [Aib] - [Lys(Ac)l-Hum Rat pStat.3.' SEQ ID
Sequel] cOi ELISA ELISA HTRF
NO.
(n NI) (n M) 626 Ac- [Pen] -QTWQ-[Pen] -[Phe [4-(2-aminoethoxy)] -[2-Nall -RILeul 4Lys(Ac)1-N-H3Alal -NH2 627 Ac- [Pen] -QTWQ- [Pen] - [Phe (4 -0Me)1- [2-Nall - [hLeu] -[Lys(Ac)1-N-H3Alal -NH2 628 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-am ino ethoxy)] - [2-Nall -[Aib] -[Lys(Ac)1-N-H3Alal -NH2 629 Ac- [Pen] -QTWQ- [Pen] - [Phe (4-0Me)] - [2-Nall - [Aib] - [Lys(Ac)l-N-13Alal -NH2 630 Ac- [Pen] -NTWQ- [Pen]- [Phe(4-0Me)142-Nall- [Aib] -ENN-NH2 631 Ac- [Pen] -NTWQ- [Pen] - [Phe [4-(2-aminoethoxy)] -RiLeul -ENA-NH2 632 Ac- [Pen] -NTWQ- [Pen] - [Phe [4-(2-am ino ethoxy)] - [2-Nall -[Aib] -[Ly s (Ac)] -NN-NH2 633 Ac- [Pen] -NTWQ- [Pen] - [Phe (4-0Me)] - [2-Nall - [Aib] - [Lys(Ac)l-N-H3Ala] -NH2 634 Ac- [Pen] -NTWQ- [Pen] - [Phe [4-(2-am ino ethoxy)] - [2-Nall -[Aib] -[Ly s (Ac)] -NQ -NH2 635 Ac- [Pen] -NTWQ- [Pen] - [Phe (4-0Me)] - [2-Nall - [Aib] - [Lys(Ac)l-636 Ac- [Pen] -NTWQ- [Pen] - [Phe [4-(2-am ino ethoxy)] - [2-Nall -[Aib] -[Ly s (Ac)] -NA-NH2 637 Ac- [Pen] -NTWQ- [Pen] - [Phe (4-0Me)] - [2-Nall - [Aib] - [Lys(Ac)l-638 Ac- [Pen] -NTWQ- [Pen] - [Phe (4-0Me)] - [2-Nall - [Aib] - [Lys(Ac)l-Ac- [Pen] -NTWQ- [Pen] - [Phe [4-(2-am ino ethoxy)] - [2-Nall -[Aib] -639 **
[Lys(Ac)1-N-H3Alal -NH2 640 Ac- [Pen] -NTWQ- [Pen] - [Phe (4 -0Me)1- [2-Nall - [hLeu] -[Lys(Ac)1-N-H3Alal -NH2 641 Ac- [Pen] -NTWQ- [Pen] - [Phe [4-(2-aminoethoxy)] -RiLeul4Lys(Ac)1-N- H3Ala] -NH2 642 Ac-E- [Pen] -QTWQ- [Penl- [Phe [4-(2-aminoethoxy)1- [2 -Nal] -[Aib] - [Ly s (Ac)] -NN-NH2 643 Ac-(D)Asp- [Pen] -QTWQ - [Pen] - [Phe [4 -(2 -am ino ethoxy)] -[2-Nall- [Aibl-[Lys(Ac)1-NN-NH2 644 Ac-R- [Pen] -Q TWQ -Wen] -[Phe [4 -(2 -am ino ethoxy)] - [2-Nall -[Aib] - [Ly s (Ac)] -NN-NH2 645 Ac-(D)Arg -Wen] -QTWQ- [Pen]- [Phe [4-(2-aminoethoxy)] - [2 -Nall- [Aibl-[Lys(Ac)1-NN-NH2 Hu man¨ Rat i)Stat3.:
SEQ ID
Sequel) cOi ELISA ELISA HTRF
NO.
(n M) (n (n M ) 646 Ac-Phe-[Perd -QTWQ- [Pen1-[Phe [4-(2-aminoethoxy)] 42-Nail -[Aib] - [Ly s (Ac)] -NN-NH2 647 Ac-(D)Phe- [Pen] -Q TWQ- [Pen] - [Phe [4-(2-am inoethoxy)] -112-Nail - [Aib] - [Ly s (Ac)] -NN-Nt12 648 Ac- 112-N al] - [Pen] -QTWQ- [Pen]- [Phe [4-(2-aminoethoxy)1- 112-Nail - [Aib] - [Ly s (Ac)] -NN-Nt12 649 Ac-T- [Pen] -QTWQ- [Penl- [Phe [4-(2-am inoethoxy)1- 112-Nail-[Aib] - [Ly s (Ac)] -NN-NH2 650 Ac-L- [Pen] -QTWQ- [Penl- [Phe [4-(2-am inoethoxy)1- 112-Nail-[Aib] - [Ly s (Ac)] -NN-NH2 Ac-(D)G1n- [Pen] -Q TWQ- [Pen] - [Phe [4-(2-am inoethoxy)] -112-Nail - [Aib] - [Ly s (Ac)] -NN-Nt12 Ac- [(D)Asn] -[Pen] -QTWQ- [Pen] - [Phe [4-(2-aminoethoxy)] -112-Nail - [Aib] - [Ly s (Ac)] -NN-NH2 653 Ac- [Pen] -QTWQ- [Pen]- [Phe(4-0Me)] -[c(-MeVall -[Ly s (Ac)] -NN- [(D)Lys] -NH2 654 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)] -[c(-MeV al] -KNN-Nt12 Ac- [Pen] -QTWQ- [Pen] - [Phe [4-(2-acetylaminoethoxy)] -655 ** *
K- [Ly s (Ac)] -NN-NH2 666 Ac- [Pen] -QTWQ- [Pen]- [Phe(4-0Me)] - [c(-MeLys] -[Ly s (Ac)] -NN-NH2 Ac- [(D)Ly s] - [Pen] -QTWQ- [Pen] - [Phe(4-C ONH2)] - [cc-667 *****
MeVal] - [Lys (Ac)] -NN-Nt12 Ac- [Pen] -QTWQ- [Pen] - [Phe (4-C ONH2)] - [c(-MeLy s] -668 * **
[Ly s (Ac)] -NN-NH2 Ac- [Pen] -QTWQ- [Pen] - [Phe (4-C ONH2)] -[c(-MeVall -669 **
[Ly s (Ac)] -NN-NH2 Ac- [Pen] -QTWQ [Per+ [Phe (4-C ONH2)1-1Phe (3,4-0Me2)14c(-670 **
MeVal] - [Lys (Ac)] -NN-Nt12 Ac-RD)Phe] -[Pen] -NTWQ [Pen] -[Phe [4-(2-aminoethoxy)] -112-Nail - [Aib] - [Ly s (Ac)] -NN-Nt12 Ac- [(D)Phe] - [Pen] -NTWQ - [Pen]- [Phe [4-(2-aminoethoxy)] 42-Nail - [4-amino-4-c arboxy-tetrahydropyran] -[Ly s (Ac)] -NN-Nt12 Ac-RD)Phe] -[Pen] -NTWQ [Pen] -[Phe [4-(2-aminoethoxy)] -112-Nail- [Ache] - [Ly s (Ac)] -NN-Nt12 Ac- [(D)Phe] - [Pen] -NTWQ - [Pen]- [Phe [4-(2-aminoethoxy)] -112-Nail - [4-amino-4-c arboxy-tetrahydropyran] - [Cit] -NN-Nt12 Ac- [(D)Phe] - [Pen] -NTWQ - [Pen]- [Phe [4-(2-aminoethoxy)] -112-Nail - [Ache] - [Cit] -NN-NH2 SEQ ID
SequencOi ELISA ELISA HTRF
NO.

Ac-[(D)Phe]-[Penl-NTWQ-[Pen1-[Phe[4-(2-aminoethoxy)]-[2-Nall- [Aib] -{Lys(Ac) ] -N- H3A1a] -NH2 Ac- RD)Phe] -{Pen] -NTWQ- [Pen] - [Phe(4-0Me)] - [2-Na1l -114-am ino-4-c arb oxy-tetrahydropyran] - [Lys (Ac)] -NN-NH2 678 Ac- RD)Phe] -{Pen] -NTWQ- [Pen] - 11Phe(4-0Me)1- 112-Nall- [Achc] -[Lys(Ac) ] -NN-NH2 Ac- RD)Phe] -{Pen] -NTWQ- [Pen] - 11Phe(4-0Me)1- 112-Nall -114-am ino-4-c arb oxy-tetrahydropyran] - rit] -NN-NH2 680 Ac- RD)Phe] -{Pen] -NTWQ- [Pen] - 11Phe(4-0Me)1- 112-Nall- [Achc] -rit] -NN-NH2 681 Ac- RD)Phe] -{Pen] -NTWQ- [Pen] - 11Phe(4-0Me)1- 112-Nall- [Achc] -682 Ac- [Pen] -NTWQ Wei+ [Phe (4-C ONH2)1- 112-Nall - [Aib] -[Ly s (Ac)] -NN-NH2 Ac- [Pen] -NTWQ Wei+ [Phe (4-C ONH2)1- 112-Nall- 114-amino-4-carboxy-tetrahydropyran] -Ly s (Ac)] -NN-NH2 684 Ac- [Pen] -NTWQ Wei+ [Phe (4-C ONH2)1- 112-Nall- [Achc] -[Ly s (Ac)] -NN-NH2 685 Ac- [Pen] -NTWQ Wei+ [Phe (4-C ONH2)1- 112-Nall- [Acpc] -[Ly s (Ac)] -NN-NH2 Ac- [Pen] -NTWQ Wei+ [Phe (4-C ONH2)1- 112-Nall - [cc-MeL eu] -[Ly s (Ac)] -NN-NH2 687 Ac- [Pen] -NTWQ [Pen] 4Phe (4-0Me)l- [2-Nall- [Aib] -[Ly s (Ac)] -Ac- [Pen] -NTWQ [Pen] 4Phe (4-0Me)] - [2-Nall- [4-am ino-4-carboxy-tetrahydropyran] - [Ly s (AO] -NN-NH2 689 Ac- [Pen] -NTWQ [Pen] 4Phe (4-0Me)l- [2-Nall- [Achc] -[Ly s (Ac)] -670 Ac- [Pen] -NTWQ [Pen] 4Phe (4-0Me)l- [2-Nall- [Acpc] -[Ly s (Ac)] -671 Ac- [Pen] -NTWQ [Pen] 4Phe(4-0Me)] - [2-Nall- [cc-MeLeu] -[Ly s (Ac)] -NN-NH2 *=<10nIVI; **=10-25 nM*** = 25-100 nJVI,**** = 100-1000 nIVI, *****=1000-10,000 Table E5A. IC50 of Illustrative Peptide Inhibitors (Thioethers) SEQ Human ID iii$equence/StructurC ELISA
NO. (nNI) [N-MeAla]-DWVCYWHTF G-[AEA]-[(D)Lys] -NH2 ¨6000 .SEQ Human ID iiiSeq en ce/Stru ctu reiii HASA ..
NO. .

[N-MeAla]-DWV-[Pen]-YWHTFG-[AEA]-[(D)Lys] -NH2 >30000 [N-MeAla]-DWV-(D)Pen]-YWHTFG-[AEA]-[(D)Lys] -NH2 >30000 [N-MeAlal-DWV-[hCysl-YWHTFG-[AEA1-[(D)Lys] -NH2 ¨6000 ADWVCYWHTFG-[AEA]-[(D)Lys] -NH2 ¨3000 ADWV_-_[PYWHTFG-[AEA1-[(D)Lys] -NH2 >30000 ADWV-[(D)Pen]-YWHTFG-[AEA1-[(D)Lys] -NH2 >30000 ADWV-[hCys]-YWHTFG-[AEA]-[(D)Lys] -NH2 100 ¨6000 680 tj....?DWQCYWRENG-[AEA](D)Lys] -NH2 >6000 681 <1¨ QDWQCYWRENG-[AEA]-[(D)Lys] -NH2 ¨30000 682 QDWQCYWRENG-[AEA]-[(D)Lys] -NH2 ¨6000 QDWQCYWRENG-[AEA]-[(D)Lys] -NH2 ¨6000 QDWQCYWRENG-[AEA]-[(D)Lys] -NH2 ¨30000 SEQ = Human ID iiiSequence/Structureiii ELISA
NO. . ( iNI) QDWQCYWRENG- [AEA]-[(D)Lys] -NH2 >6000 686 QDWQ-[hCys]-YWRENG-[AEA]-[(D)Lys] -NH2 >6000 687 QDWQ-[hCys]-YWRENG- [AEA] -[(D)Lys] -NH2 >6000 QDWQ- [hCys]-YWRENG-[AEA]-[(D)Lys] -NH2 S >6000 QDWQ- [hCys]-YWRENG- [AEA]- [(D)Lys] -NH2 S ¨30000 QDWQCYWRENG-[AEA]-[(D)Lys] -NH, s >30000 QDWQ-[hCysl-CYWRENG-[AEA]-[(D)Lys] -NH2 >30000 s¨j Table E5B. IC50 of Illustrative Peptide Inhibitors (Thioethers) Ac, N----[Phe(4-0Me)]-[2-Nal]-XXXX-NH 2 Ac-Cyc10-[[Abui-XXWXCHPhe(4-0Mc)]42-Na1]-XXX-NH 2 SEQ Human = Rat pStat3."
ID Sequence ELISA .ELISA H.TRF
NO ,4 Ac-Cyclo-[[Abu]RTWQC]-YVVRKFG-*** **** ***
[AEA]-[(D)Lys]-NH2 SEQ Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
N.Q. (nm) .... .(1m) Ac-Cyclo-[CRTWQ-[Abu]]-YVVRKFG- **** **** ***
[AEA]-[(D)Lys]- NH2 Ac-Cyclo-[[Abu]-QTWQC]-YVVRENG- **** **** ***
[AEA]-[(D)Lys]- NH2 Ac-Cyclo-[[Abu]-RTWQ-[Pen]]-695 *****
YVVRKFG-[AEA]-[(D)Lys]- NH2 Ac- Cyclo-[[Pen]-RTWQ-[Abu]]-696 ****
YVVRKFG-[AEA]-[(D) Lys]-NH2 Ac-Cyclo-[[(D)Cys]-RTWQ- [Abu]]-697 ****
YVVRKFG-[AEA]-[(D)-Lys]- NH2 698 Ac-Cyclo-[[Abu]-QTWQC]-YVV-[Orn]- ****
[Dap]-NG-[AEA]-[(D) Lys]- NH2 Ac-Cyclo-[[Abu]-QTWQC]-YW-[hLeu]- ***
699 **

700 Ac-Cyclo-[Abu]-QTWQ-(D)Cys]]-YVV- *****
[hLeu]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQ- [Pen]]-YVV-701 *****
[hLeu]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-*** ****
OMe)]-[2-Nall-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCFYVV- [a-703 ** ***
MeLeu]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCFY-[2-Nal]-704 ** **
[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-705 ** **
OMe)]-[2-Nall-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-706 ** ***
OMe)]-[2-Nall-[a-MeOrn]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-*** ***
OMe)]-W-[a-MeOrn]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-708 ** ***
OMe)]-[2-Nall-[a-MeLys]-ENG-NH2 SEQ" Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO.
Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-709 ** ** **
OMe)]-W-[a-MeLys]- [Ly s(Ac)] -NG-NH2 Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-710 ** * ** **
OMe)]-W-[a-MeLys]-ENG-NH2 Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-711 OMe)] - [1 -Nal] - [a-MeLys] - [Lys(Ac)]- ** * * ** **

Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-712 OMe)] - [2-Nal] - [a-MeLys] - [Lys(Ac)]- **

Ac-Cyclo-[[Abu]-QTWQCFYVV- [a-713 ** * * ** **
MeOrn]- [Ly s(Ac)] -NG-NH2 Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-714 OMe)] - [2-Nal] - [(D)Asn] - [Lys(Ac)] -NG- *** **** ***

Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-715 Phenoxy)]- [2-Nail- [a-MeLysHLys(Ac)]- ****

Ac-Cyclo- [ [Abu] -QTWQC] - [hPhe(3 ,4-716 dirnethoxy)] - [2-Nail- [a-MeLys]- *****
[Lys(Ac)]-NG-NH2 717 Ac-Cyclo- [ [Abu] -Q TWQC] - [DMT] - [2- * * * * *
Nail - [a-MeLy s] - [Lys(Ac)]-NG-NH2 Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-718 CONH2)]-[2-Nal[a-MeLys]- * **
[Lys(Ac)]NG-NH2 Ac-Cyclo- [ [Abu] -Q TWQC] -Phe(3 ,4-719 C12) [2-Nal]-[a-MeLysHLys(Ac)]NG- **** ***

720 Ac-Cyclo- [ [Abu] -QTWQ- [Pen]] - [Phe(4- * * * * * * * * *
* *
OMe)] - [2-Nall -[a-MeLys]-ENG-NH2 Ac-Cyclo- [ [Abu] -QTWQ- [Pen]] - [Phe(4-721 OMe)]-[2-Nal[a-MeLys]- [Lys(Ac)]NG- *** **** ***

Ac-Cy cl o- [ [Pen] -Q TWQ- [Abu] ] - [Phe(4-722 OMe)] - [2-Nall -[a-MeLys]- [Ly s(Ac)]NG-Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-723 >10,000 OMe)] - [Trp(2,5,7-tri-tert-B utyl)] - [cc-SEQ Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO.
MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-724 OMe)]- [Phe(4-0ally1)] - [a-MeLysFENG- ****

Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-725 OMe)]-[Tyr(3-tBu)]-[a-MeLys]-ENG- *** **** **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-726 OMe)]-[Phe(4-tBu)]-[a-MeLys]-ENG- *****

Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-727 OMe)]-[Phe(4-guanidino)]-[a-MeLys]- ****

Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-728 ****
OMe)]-[Phe(Bz1)]-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCHTyr(3-tBu)]-729 >10,000 W-[a-MeLys]-ENG-NH2 780 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-tBu)]- *****
W-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-781 *** *** ***
guanidino)]-W-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-782 ** **
aminoethoxy)1-W-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-783 ****
CO2H)]-W-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-784 *** *** **
phenoxy)1-W-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe(4-CNA *** -785 ***
W-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe(4-BrA *** -786 *** ***
W-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-*** ***
NH2)]-W-[a-MeLys]-ENG-NH2 SEQ" Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO.
Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-788 ****
OMe)]-Phe(4-Me)-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-789 *** *** **
OMe)]-[1-Nall-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-790 OMe)]-[2-Nal]-[a-MeOrn]-[Lys(Ac)]- ** **

Ac-Cyclo-[[Abu]-QTWQC]-[2-Nall-[2-791 *** ****
Nall-[a-MeOrn]-[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Bip]-[2-792 ****
Nall-[a-MeLys]-[Lys(Ac)l-NG-NH2 793 Ac-Cyclo-[[Abu]-QTWQC]-Cha-[2-Nall- *****
[a-MeLys]-[Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[2-Nall-[2-794 *** *** **
Nall-[a-MeLys]-[Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[4-795 Pyridylalanine]-[2-NalHa-MeLys]- ****
[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[(3-796 homoTyr1[2-Nail[a-MeLys]-[Lys(Ac)]- ¨10000 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-797 CONH2)]-[2-Nall-[a-MeLys]-[Lys(Ac)]- ** **

Ac-Cyclo-[[Abu]-QTWQC]-[2-Nall-[2-798 *** ***
Nall-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT42-Nall-QC]-799 [Phe(4-0Me)]-[2-Nall-[a-MeLys]- ****
[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QT-[1-Nall-QC]-800 [Phe(4-0Me)]-[2-Nall-[a-MeLys]- ****
[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTYQCHPhe(4-801 OMe)]-[2-Nall-[a-MeLys]-[Lys(Ac)]- ¨10000 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-802 OMe)]-[2-Nall-[a-MeLys]-[Lys(Ac)]-SEQ" Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO.
Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-803 OMe)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]- ***

Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-804 OMe)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]-Ac-Cyclo-[[Abu]-STWQC]-[Phe(4-805 OMe)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]-Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-806 OMe)]-W-[a-MeLys]-[Lys(Ac)]-NGGE-Ac-Cyclo-[[Abu]-QTWQC]-Y-[2-Nal]-[a-MeLys]-[Lys(Ac)]-NGGE-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-808 OMe)]-[2-Nal[a-MeLys]-[Lys(Ac)]-NS- ** **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-809 OMe)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]- **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-810 ** ***
OMe)]-[2-Nall-[Aib]-[Lys(A0]-NG-NH2 811 Ac-Cyclo-[[Abu]-QTWQC]-[Phe-4-N3]- *** *** **
[2-Nall-[a-MeLys]-[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-812 OMe)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]- *** ***

Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-813 OMe)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]-[Cit]-G-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-814 *** ***
OMe)]-[2-Nall-[a-MeLys]-VNG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-815 ****
OMe)]-[2-Na1]-[Orti]-[Lys(A0]-NG- NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-816 ****
OMe)]-[2-Nall-[0m]-[Dap]-NG-NH2 Ac-Cyclo-[[Abu]-NTWQC]-[Phe(4-817 OMe)]-[2-Nal]-[a-MeLys]-[Lys(Ac)]- ** ***

ir-SEQ Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-RAbu]-QT- [Bip]-QC]- [Phe(4-818 OMe)] - [2-Nal] - [a-MeLys] - [Lys(Ac)]- ¨10000 Ac-Cy clo- [ [Abu] -Q TWQC] - [Phe(4-819 *** ***
OMe)] - [2-Nall - [Cha] - [Lys(Ac)] -NG-NH2 Ac-Cy clo- [ [Abu] -Q TWQC] - [Phe(4-820 ***
OMe)] - [2-Nall - [Chg]- [Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QT-[Octgly]-QC]-821 [Phe(4-OMe)] - [2-Nal] - [a-MeLy s]- >10000 [Lys(Ac)] -NG-NH2 Ac-Cyclo-[[Abu]-QTWQCHOctgly]- [2-822 ¨10000 Nail - [a-MeLy s] - [Lys(Ac)]-NG-NH2 Ac-Cy clo- [ [Abu] -Q TWQC] - [Phe(4-823 OMe)]-[Octgly]- [a-MeLys]-[Lys(Ac)]- ¨10000 Ac-Cy clo- [ [Abu] -Q TWQC] - [Phe(4-824 OMe)] - [2-Nal] - [a-MeLys] - [Lys(Ac)]- *** ***

Ac-Cy clo- [ [Abu] -Q TWQC] - [Phe(4-825 OMe)] - [2-Nal] - [a-MeLys] - [Lys(Ac)]- **

Ac-Cy clo- [ [Abu] -S TWQC] - [Phe(4-826 OMe)] - [2-Nal] - [a-MeLys] - [Lys(Ac)]- *** *** ***

Ac-Cy clo- [ [Abu] -Q TWQC] - [Phe(4-827 OMe)]-W-[a-MeLys]- [Lys(Ac)]-NGE- ****

Ac-Cyclo-[[Abu]-QTWQCFY- [2-Nall-828 ***
[a-MeLy s] - [Lys(Ac)] -NGE-NH2 Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-829 aminoethoxy)]]-[2-Nal[a-MeLysFENG- *

Ac-Cyclo- [[Abu]-Q TQQC]- [Phe[4-(2-830 aminoethoxy)]]- [2-Nall 4a-MeLysFENG- >3000 Ac-Cyclo- [[Abu]-Q THQC]- [Phe[4-(2-831 aminoethoxy)]]- [2-Nall 4a-MeLysFENG- >3000 SEQ" Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-[[Abu]-QT-[hPhe]-QCHPhet4-832 (2-aminoethoxy)]]-[2-Nall-[a-MeLys]- >3000 Ac-Cyclo-[[Abu]-QT-[Glu(Bz1)]-QC]-833 [Phe[4-(2-aminoethoxy)]]-[2-NalHa- >3000 MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Bip]-QC]-[Phe[4-834 (2-aminoethoxy)]]-[2-Nall-[a-MeLys]- >3000 Ac-Cyclo-[[Abu]-QT-[Tic]-QC]-[Phe[4-835 (2-aminoethoxy)]]-[2-Nall-[a-MeLys]- >3000 Ac-Cyclo-[[Abu]-QT-[Phe[4-(2-aminoethoxy)]]-QC]-[Phe[4-(2-836 >3000 aminoethoxy)]]-[2-NalHa-MeLysFENG-Ac-Cyclo-[[Abu]-QT-[Phe(3,4-C12)]-837 QCF[Phe[4-(2-aminoethoxy)]]-[2-Nall- >3000 [a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Phe(4-0Me)]-QC]-838 [Phe[4-(2-aminoethoxy)]]-[2-Nall-[a- >3000 MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Orn(Benzyl)]-QC]-839 [Phe[4-(2-aminoethoxy)]]-[2-Nall-[a- >3000 MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Orn(Benzaldehyde)]-QC]-[Phe[4-(2-aminoethoxy)]]-[2-NalHa-MeLysFENG-Ac-Cyclo-[[Abu]-QTWQC]-841 [PheOCH2CH2NHAc]-[2-Nall-[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-842 aminoethoxy)]]-[2-NalHa-MeLeuFENG-Ac-Cyclo-[[Abu]-QT-[5-hydroxyTrp]-843 QCF[Phe[4-(2-aminoethoxy)]]-[2-Nall- ¨3000 [a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[6-chloroTrp]-QC]-844 [Phe[4-(2-aminoethoxy)]]-[2-Nail[a- ** **
MeLys]-ENG-NH2 SEQ Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-[[Abu]-QT-[N-MeTrp]-0q-845 [Phe[4-(2-aminoethoxy)]]-[2-Nall-[a- >3000 MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[1,2,3,4-tetrahydro-norharman]-QC]-[Phe[4-(2-846 ****
aminoethoxy)]]-[2-Nall4a-MeLysFENG-Ac-Cyclo-[[Abu]-QT-[Phe(4-CO2H)]-847 QCF[Phe[4-(2-aminoethoxy)]]-[2-Nall- >3000 [a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Ph(4-CONH2)]-848 QCF[Phe[4-(2-aminoethoxy)]]-[2-Nall- >3000 [a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Ph(4-CONH2)]-849 QCF[Phe[4-(2-aminoethoxy)]]-[2-Nall- >3000 [a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Phe(3,4-0Me)]-850 QCF[Phe[4-(2-aminoethoxy)]]-[2-Nall- ¨3000 [a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT4a-MePhe]-QC]-851 [Phe[4-(2-aminoethoxy)]]-[2-Nail[a- ****
MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Phe(4-CF3)]-QC]-852 [Phe[4-(2-aminoethoxy)]]-[2-Naila- ¨3000 MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Phe(4-tBu)]-QC]-853 [Phe[4-(2-aminoethoxy)]]-[2-NalHa- >3000 MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QT-[Phe(2,4-Me2)]-854 QCF[Phe[4-(2-aminoethoxy)]]-[2-Nall- ****
[a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-855 aminoethoxy)]]-[2-Nail[a-MeLys]- **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-856 aminoethoxy)]]-[2-Nall4a-MeLys]-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-857 aminoethoxy)]]-[2-Nall4a-MeLys]-[Lys(Benzoic acid)]-NG-NH2 SEQ" Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-[[Abu]-QTWOC]-[Phe[4.-(2-858 aminoethoxy)]]-[2-Nal[a-MeLys]- **
[Lys(succinic acid)]-NG-NE12 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-NalHa-MeLys]-[Lys(glutaric acid)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-NalHa-MeLys]-[Lys(pyroglutamic acid)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal[a-MeLys]- **
[Lys(isovaleric acid)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-862 aminoethoxy)]]-[2-Nal] - [a-MeLys]- -- ¨3000 [Lys(Palm)]-NG-NE12 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-863 aminoethoxy)]]-[2-Nal] - [a-MeLys]-Lys [(PEG1)]-NG-NE12 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-864 aminoethoxy)]]-[2-Nal] - [a-MeLys]-[Lys(PEG2)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-865 aminoethoxy)]]-[2-Nal] - [a-MeLys]-[Dap(Benzoic acid)]-NG-NE12 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-866 aminoethoxy)]]-[2-Nal] - [a-MeLys]-[Dap(succinic acid)]-NG-NE12 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-867 aminoethoxy)]]-[2-Nal] - [a-MeLys]-[Dap(glutaric acid)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-868 aminoethoxy)]]-[2-Nal] - [a-MeLys]- **
[Dap(pyroglutamic acid)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-869 aminoethoxy)]]-[2-Nal] - [a-MeLys]-Dap(IVA)NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-870 aminoethoxy)]]-[2-Nal] - [a-MeLys]-[Dap(PEG1)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-871 aminoethoxy)]]-[2-Nal] - [a-MeLys]-[Dap(PEG2)]-NG-NH2 SEQ" Hamad' Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-872 aminoethoxy)]]-[2-Nal] - [a-MeLys]- ** **
[Dap(PEG2-Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-873 aminoethoxy)]]42-Nall4a-MeLys]-[Lys(Ac)]--NG-[AEA]-[(D)Lys]-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-874 aminoethoxy)]]42-Nall4a-MeLys]-[Lys(A0]-NG-RD)14s1-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-875 aminoethoxy)]]42-Nall4a-MeLys]-[Lys(Ac)]-NG-[AEA]-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-876 aminoethoxy)]]42-Nall4AibHLys(Ac)]- **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-877 **
aminoethoxY)]]-[2-Nall-[Aib]-QNG-NH2 878 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxY)]]-[2-Nall-[AibFENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-879 aminoethoxy)]]-1-Nal[Aib]-[Lys(Ac)]- *** **
NG-NH
Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-880 aminoethoxy)]]42-Nall4AibHLys(Ac)]- **
NA-NH
881 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxY)]]-[2-Nall-[Aib]-KNG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-882 aminoethoxy)]]4Phe(4-CO2H)14a- ****
MeLys]-[Lys(A0]-NG-NH2 Ac-Cyclo-[[Abu]-[Dap]-TWQC]-[Phe[4-883 (2-aminoethoxy)]]-[Phe(4-Phenoxy)]-[cc- ****
MeLys]-[Lys(A0]-NG-NH2 Ac-Cyclo-[[Abu]-DapTWQC]-[Phe[4-(2-aminoethoxy)]]-[Phe[4-(2-884 ****
aminoethoxy)]]-[a-MeLys]-[Lys(Ac)]-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-885 aminoethoxy)]Ha-MeLysHLys(Ac)]- >3000 NG-NH

SEQ" Hamad' Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-[[Abu]-DabTWQC]-[Phe[4-(2-886 aminoethoxy)]]-[hPhe] - [a-MeLys]- >1000 [Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-DapTWQC]-[Phe[4-(2-887 aminoethoxy)]]-[Glu(Bz1)] - [a-MeLys]- >3000 [Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-888 aminoethoxy)]]-W-[a-Me-Orn]-ENG- **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-889 aminoethoxy)]]-W-[a-MeLys]-[Lys(Ac)]- *

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-890 aminoethoxy)]]-W-[a-Me-Orn]- ** **
[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-891 aminoethoxy)]]-[2-Nall4a-Me-Orn]-[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-892 aminoethoxy)]]-[2-Nal]-[a-MeLys]-[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-893 aminoethoxy)]]-[2-Nal]- [OrnHLys(Ac)]- ** **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-894 ***
aminoethoxY)]i-W-[Orn]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-895 ****
aminoethoxy)]]-W-[Orn]-[Dap]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-896 aminoethoxy)]]-W-[Orn]-[Dap(Ac)]-NG- ****

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-897 aminoethoxy)]]-[2-Nal]- [Orn]-[Dap]-NG- *** ***

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-898 aminoethoxy)]]-[2-Nall-[Orn]-[Dap(Ac)]- ***

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-899 **
aminoethoxY)]i-W-[hLeu]-ENG-NH2 SEQ" Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[442:-900 (acetyl-aminoethoxy)] ] - [2-Nal] - [a-MeLys(Ac)] - [Lys(Ac)] -NG-NH2 Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-901 aminoethoxy)] ] -W- [a-Me-Leu] -ENG-Succicinyl-Cyclo- [[Abu]-QTWQC]-902 [Phe[4-(2-aminoethoxy)]]-[2-Nall4a-MeLys] - [Lys(Ac)] -NG-NH2 Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-903 aminoethoxy)]]-W- [a-MeLys]- [Lys(Ac)]- *****
[Dap] -G-NH2 Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-904 aminoethoxy)]]-W- [a-MeLys]- [Lys(Ac)]- ***
[6-amino-1,4-diazepane-2,5-dione] -NH2 Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-905 aminoethoxy)] ] -W-Chg- [Lys(Ac)] -NG- ***

Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-906 (acetyl-aminoethoxy)] ] - [2-Nall - [a-MeLys(Ac)]-ENG-NH2 Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-907 aminoethoxy)]]- [Phe(4-CONH2)]-[a- ****
MeLys] - [Lys(Ac)] -NG-NH2 Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-908 aminoethoxy)] ] - [Phe(3,4-0Me2] - [a- ** ***
MeLys] - [Lys(Ac)] -NG-NH2 Ac-Cyclo- [[Abu]- [Dap]-TWQC]- [Phe[4-909 (2-aminoethoxy)]]-[Tic]-[a-MeLys]- >3000 [Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-DapTWQC]- [Phe[4-(2-910 aminoethoxy)]]- [Phe(3,4-C12)]- [a- ***
MeLys] [Lys(Ac)] -NG-NH2 Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-911 aminoethoxy)]]-[2-Nal]- [a-MeLys]-ENQ- *

Ac-Cyclo- [[Abu]-Q TWQC]- [Phe[4-(2-912 aminoethoxy)]]- [2-Nall 4a-MeLysFENN- *

Ac-Cyclo- [[Abu]-TTWQC]- [Phe[4-(2-913 aminoethoxy)]]- [2-Nall 4a-MeLysFENG- *

SEQ" Hamad' Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-[[Abu]-QTWOCHPhe[4-(2-914 aminoethoxy)]]-[2-NalHa-Me-Gly(Ethyl)] Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTWOCHPhe[4-(2-915 aminoethoxy)]]-[2-NalHa-MeVal]-[Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTWOCHPhe[4-(2-916 aminoethoxy)]]-[2-NalHa-MeSer]-[Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTDapQC]-[Phe[4-(2-917 aminoethoxy)]]-[2-NalHa-MeLys]- >3000 [Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTWOCHPhe[4-(2-918 aminoethoxy)]]-[Dap[a-MeLys]- >3000 [Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTRQC]-[Phe[4-(2-919 aminoethoxy)]]-[2-NalHa-MeLys]- >3000 [Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTWOCHPhe[4-(2-920 aminoethoxy)fi-R4a-MeLysHLys(Ac)]- >3000 Ac-Cyclo-[[Abu]-QTDapQC]-[Phe[4-(2-921 aminoethoxy)]]-[Dap]-[a-MeLys]- >3000 [Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTDOCHPhe[4-(2-922 aminoethoxy)]]-[2-NalHa-MeLys]- >3000 [Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTWOCHPhe[4-(2-923 aminoethoxy)fi-D4a-MeLysHLys(Ac)]- >3000 Ac-Cyclo-[[Abu]-QTDOCHPhe[4-(2-924 aminoethoxy)fi-D4a-MeLysHLys(Ac)]- >3000 Ac-(D)Lys-[Cyclo-[[Abu]-QTWQQ-925 [Phe(4-0Me)]-[2-Nall-[a-MeLeu]-ENG- **

Ac-Cyclo-[[Abu]-QTWOCHPhe[4-(2-926 aminoethoxy)]]-[2-Nall-[a-MeLysFRNG- **

Ac-Cyclo-[[Abu]-QTWOCHPhe[4-(2-927 aminoethoxy)]]-[2-NalHa-MeLys]-[Orn]-NG-NH2 SEQ" Hamad' Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-928 arninoethoxy)]]-[2-NalHa-MeLys]-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-929 arninoethoxy)]]-[2-NalHa-MeLys]-hRNG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-930 arninoethoxy)]]-[2-Nall-[hLeu]-[Lys(Ac)]-N-[f3Ala]-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-931 arninoethoxy)]]-[2-Nall-[CitHDap]-NG- **

Ac-Cyclo-[[Abu]-[a-Me-Orn]-TWQC]-932 [Phe[4-(2-aminoethoxy)]]-[2-Nail[a- *** **
MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-933 arninoethoxy)]]-[2-NalHa-MeLys]-Ac-Cyclo-[[Abu]-STWQC]-[Phe[4-(2-934 arninoethoxy)]]-[2-NalHa-MeLys]- ****

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-935 (acetyl-arninoethoxy)]]-[2-Nall-[a-MeLys(A01-ENQ-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-936 (acetyl-aminoethoxy)]]-[2-Nall-[cc-MeLys(Ac)]-ENN-NH2 Ac-Cyclo-[[Abu]-TWQC]-[Phe[4-(2-937 aminoethoxy)]]-[2-NalHa-MeLysFENG-938 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-Me)]- *
[2-Nall-[a-MeLys]-[Lys(A01-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(3-Me)]- **

[2-Nall-[a-MeLys]-[Lys(A01-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[hTyr]-[2-940 *****
Nall-[a-MeLys]-[Lys(Ac)l-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-941 arninoethoxy)]Ha-MeTrpHa-MeLys]- ¨3000 [Lys(Ac)]-NG-NH2 SEQ" Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-Cyclo-RAbul-ra-MeSed-TWQ6-942 [Phe[4-(2-aminoethoxy)]]-[2-Nal]-[a- *** **
MeLys]-[Lys(A0]-NG-NH2 Ac-Cyclo-[[Abu]-Q4a-MeSed-WQC]-943 [Phe[4-(2-aminoethoxy)]]-[2-Nall-[a- >3000 MeLys]-[Lys(A0]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-944 aminoethoxy)]]-[a-MePhe]- [a-MeLys]- >3000 [Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-945 **
aminoethoxY)]i-W-[AiN-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-946 aminoethoxy)]]-[2-Nall-[AiN4Lys(Ac)]-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-947 aminoethoxy)]]-[2-Nall-[AiN-E- **
[Dap(Ac)]-G-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-948 aminoethoxy)]]-[2-Nal]-[AiN-E-[Dab(Ac)]-G-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-949 aminoethoxy)]]-[2-Nall-[AiN-E- **
[Lys(A0]-G-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-950 **
aminoethoxY)]I-W-[AiN-ENN-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-951 aminoethoxy)]]-[2-Nal]-[a-MeLeu]-ENN- *

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-952 aminoethoxy)]]-[Phe(3,4-0Me2)]-[AiN- *** **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-953 aminoethoxy)]]-[Phe(3,4-C12)]-[AiN- ***

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-954 aminoethoxy)]]-[2-NalHa-MeLeu)-[Cit]- *

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-955 aminoethoxy)]]-[2-Nal]-[a-MeLeu]-[Lys(Ac)]-NN-NH2 SEQ Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO.
I
956 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-Me)]- **
[2-Nall-[AiN-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(3,4-957 *** **
F2)1-[2-NalHAN-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe(3-958 ****
CONH2)]-[2-Nall-[AiN-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCF[Phe(2,4-959 ****
C12)]-[2-Nall-[AilA-ENG-NH2 960 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(3-Me)]- **
[2-Nall-[AiN-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe(4-C1)]-961 **
[2-Nall-[AiN-ENG-NH2 962 Ac-Cyclo-[[Abu]-QTWQCHPhe(4-F)l- ****
[2-Nall-[AiN-ENG-NH2 963 Ac-Cyclo-[[Abtil-QTWQCF[Phe(2,4-C12, *****
4-0Bz)]-[2-Nall-[AiN-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-964 OMe)]-[2-Nall-[a-MeLeu]-ENG- *** **
[(D)Lys] -NH2 Ac-E-Cyclo-[[Abti]-QTWQC]-[Phe[4-(2-965 aminoethoxy)]]-[2-Nail[a-MeLysFENN- *

Ac-(D)Glu-[Cyclo-[[Abu]-QTWQC]-966 [Phe[4-(2-aminoethoxy)]]-[2-NalHa-MeLys]-ENN-NH2 Ac-Arg-Cyclo-[[Abu]-QTWQC]-[Phe[4-967 (2-aminoethoxy)]]-[2-Nall-[a-MeLys]-Ac-RD)Arg]-Cyclo-[[Abu]-QTWQC]-968 [Phe[4-(2-aminoethoxy)]]-[2-NalHa-MeLys]-ENN-NH2 Ac-F-Cyclo-[[Abu]-QTWQC]]-[Phe[4-(2-969 aminoethoxy)]]-[2-Nail[a-MeLysFENN- *

Ac-[(D)Phe]-Cyclo-[[Abti]-QTWQC]-970 [Phe[4-(2-aminoethoxy)]]-[2-NalHa-MeLys]-ENN-NH2 SEQ" Hamad Rat pStat..3.4 ID Sequence ELISA ELISA HTRF
NO. .1 Ac-[2-Nal]-Cyclo-RAbuFQTWQC. ]-971 [Phe[4-(2-anainoethoxy)]]-[2-Nail[a- **
MeLys]-ENN-NH2 Ac-T-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-972 aminoethoxy)]]-[2-Nall[a-MeLysFENN- *

Ac-Leu-Cyclo-[[Abu]-QTWQC]-[Phe[4-973 (2-anainoethoxy)]]-[2-Nall-[a-MeLys]-Ac-[(D)Gln]-Cyclo-[[Abu]-QTWQC]-974 [Phe[4-(2-anainoethoxy)]]-[2-NalHa-MeLys]-ENN-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-975 anainoethoxy)]]-[2-Nall-[AcpcFENN- **

Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-976 aminoethoxy)]]-[2-Nall-[AcbcFENN-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-977 aminoethoxy)]]-[2-Nall-[Achc]- ENN-978 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxY)]]-[2-Nall-[Acvc]-ENN-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-979 aminoethoxy)]]-[2-Nall44-amino-4-carboxy-piperidineFENN-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-980 aminoethoxy)]]-[2-Nall44-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-981 aminoethoxy)]]-[2-Nall-[a-MeLeu]-[Lys(Ac)]-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-982 aminoethoxy)]]-[2-Nall4a-MeLeuFENG-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-983 aminoethoxy)]]-[2-Nall-[a-MeLeu]-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-984 aminoethoxy)]]-[2-Nall-[a-MeLeuFQN-[f3Ala]-NH2 SEQ Human Rat pStat3 ID Sequence ELISA ELISA HTRF
NO. == (nNI
Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-***
985 aminoethoxy)]]-[2-Nal]-[a-MeLeu]-Ac-Cyclo-[[Abu]-QTWQC]-****
986 cycloaPhe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeLeu]-QD]-G-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-987 aminoethoxy)]]-[2-Nall-[Aib] -QN-[j3Ala]-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-988 aminoethoxy)]]-[1,2,3,4-tetrahydro¨
norharman]-[A113]-QNG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2- **
989 aminoethoxy)]]-[5-hydroxyTrp]-[Aib]-Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-990 aminoethoxy)]]-[2-Nal] -[a-MeLys]- ***
[Lys(Ac)]-[Asn(isobutyl)]-G-N-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeLys]-991 ***
[Lys(Ac)]-[Asp(1,4-diaminoethane)]-G-Ac-(D)Phe-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-Ac-[(D)Arg]-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-*=<10nIVI; **=10-25 nM *** = 25-100 nJVI,**** = 100-1000 nM, *****=>1000 Table ESC. IC50 of Illustrative Thioether Peptide Dimers Synthesized Rat SEQ= = Human pStat3ID ' Linker ELIS
Moiety Sequenceii [LISA HTRF
== A
NO. (iiM) (nM) [Ac-[(D)Lys]-Cyclo-[[Abu]-DIG through QTWQC]-[Phe(4-0Me)]- [2-***

(D)Lys Nal]-[a-MeLeu]-ENG-NH2]2 DIG
DIG through [Ac-Cyclo-[[Abu]-QTWQC]-Phe[4-(2-995 [Phe[4-(2-aminoethoxy)]]- [2- *** **
aminoethox [Aib]-QNG-NH2]2 DIG
[Ac-Cyclo-[[Abu]-QTWQC]-DIG through 996 [Phe(4-0Me)]-[2-Nal]- [a- **
a-MeLys MeLys]-ENG-NH2]2 DIG
[Ac-[(D)Lys]-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]- [2- **
997 through a-Nall4a-MeLysFENG-NH2]2 MeLys [Ac-Cyclo-[[Abu]-QTWQC]-DIG through 998 [Phe(4-0Bz1)]-W-[a-MeLys]-(D)Lys ENG-NH2]2 DIG
PEG25 [Ac-Cyclo-[[Abu]-QTWQC]-999 through Y(Bz1)-W-[a-MeLys]-ENG-(D)Lys NH2]2PEG25 Alexa488-[D-Arg]-Cyclo-[[Abu]-QTWQC]-[Phe(4-2ae)]-[2-through [D-Nail -Arg]
*=<10nIVI; **=10-25 nM *** = 25-100 nJVI,**** = 100-1000 nM, *****=>1000 Table E5D. Illustrative Thioether Peptides SEQ ID Human NO. IL23R /
Sequence IL23 ELISA
(nM) 993 Ac-[D-Arg]- Cyclo-[[Abu]-QTWQC]-[Phe(4-2ae)]-[2-Nall-[THP1-ENN-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-QTWQC]-[Phe(4-2ae)]-[2-**
Nall-[THP1]-END-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-QTWQC]-[Phe(4-2ae)]-[2-***
Nall-[THP1-EDN-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-QTWEC]-[Phe(4-2ae)]-[2-**
Nall-[THP]-ENN-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-ETWQC]-[Phe(4-2ae)]-[2-**
Nall-[THP]-ENN-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-QTWQC]-[Phe(4-2ae)]-[2-***
Nall-[THP1-EDD-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-QTWEC]-[Phe(4-2ae)]-[2-**
Nall-[THP1-END-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-ETWQC]-[Phe(4-2ae)]-[2-**
NaI]-[Tetrahydropyran-A]-END-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-QTWEC]-[Phe(4-2ae)]-[2-***
Nall-[THP1-EDN-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-ETWQC1-[Phe(4-2ae)1-[2-***
Nall-[THP1-EDN-NH2 Ac-[D-Arg]- Cyclo-[Abu-ETWEC1-[Phe(4-2ae)]-[2-Nal]-**
[THP]-ENN-NH2 Ac-[D-Arg]- Cyclo-[[Abu]-QTWQC1-[Phe(4-2ae)1-[2-**
Nall-[THP1-ENN-OH
Ac-[D-Arg]- Cyclo-[[Abu]-QTWQC1-[Phe(4-2ae)1-[2-***
Nall-[THP1-END-OH
Ac-[D-Arg]- Cyclo-[[Abu]-QTWQC1-[Phe(4-2ae)1-[2-***
Nall-[THP]-EDN-OH
Ac-[D-Arg]- Cyclo-[[Abu]-QTWEC1-[Phe(4-2ae)1-[2-**
Nall-[THP1-ENN-OH
Ac-[D-Arg]- Cyclo-[[Abu1ETWQC1-[Phe(4-2ae)1-[2-**
Nall-[THP]-ENN-OH
* =< 1 nIVI; ** = 1 nM - 10 nM; *** = 10 nM¨ 100 nM
Table E6. IC50 of Peptide Inhibitors (Ring Closing Metathesis) Human SE'' ID
NO ii5eq u en ce/Stru ctu rgi EL I SA
.
(ii M) 1000 NH2 --))L YWHTFG-NH2 ¨

Ac-NH 0 1001 ,ADWV YWHTFG-NH2 ¨30000 Ac-NH 0 H
RTWQ N
1002 YWRKFG-[AEA1-[(D)Lys] -NH2 *****
2 ¨ 3 Ac-NH
1003 'õ..R_TWQ-- NO)L
YWRKFG-[AEA]-[(D)Lys] -NH2 *****
( ) 3 _ O ()))LH0 Ac-NH
Q
RTW ' N
1004 YWRKFG-[AEA]-[(D)Lys] -NH2 *****

Ac-NH
1005 RTWQ --.))L YWRKFG-[AEA]-[(D)Lys] -NH2 ****
( 3 _ Ac-NH 0 H
1006 .....RTWQ;NO)L YWRKFG-[AEA]-[(D)Lys] -NH2 ****
( ) O H
Ac-NH
1007 RTWQ "...) YWRKFG- [AEA] -[(D)Lys] -NH2 ****
( O H
Ac-NH
1008 - RTWQ ' N YWRKF G- [AEA] -[(D)Lys] -NH2 ****
)2 *=<10nIVI; **=10-25 nM *** = 25-100 nIVI, **** = 100-1000 nIVI, *****=1000-10,000 nIVI.
Table E7. IC50 of Illustrative Peptides Containing Cyclic amides (side chain cyclizations) o H
( t 4....i._ 1 1 -Y7.2 ) 1.2 1 I 1.2 NThrYWXXXX-AEA-(D)Lys-N H2 Ac......Ni XXWX , N ,y(WXXXX-AEA-(D)Lys-' SE' ID
Uhlman :
NO Sequence . õii ...............................................................................
..............................................................................t .. ELnIS'I;(..;
(N
1009 Ac-Cyclo-[[Dap]-QTWQE]-YWRENG-[AEA]-[(D)Lys]-NH2 ¨6000 1010 Ac-Cyclo-[EQTWQ-[Dab]]-YVVRENG-[AEA]-[(D)Lys]-NH2 >6000 1011 Ac-Cyclo-[EQTWQ-[Dap]]-YVVRENG-[AEA]-[(D)Lys]-NH2 ¨6000 1012 Ac-Cyclo-[[Dab]QTWQE]-YVVRENG-[AEA]-[(D)Lys]-NH2 ¨30000 1013 Ac-Cyclo-[[Dap]-QTWQ-[(D)Asp]-YVVRENG-[AEA]-[(D)Lys]-NH2 >30000 1014 Ac-Cyclo-[[Dap]-QTWQD]-YVVRENG-[AEA]-[(D)Lys]-NH2 >30000 1015 Ac-Cyclo-[[DQTWQ-[Dab]]-YWRENG-[AEA]-[(D)Lys]-NH2 ¨6000 1016 Ac-Cyclo-[[Dab]QTWQD]-YVVRENG-[AEA]-[(D)Lys]-NH2 >6000 1017 Ac-Cyclo-[[(D)Dab]-QTWQ-[(D)Asp]]-YVVRENG-[AEA]-[(D)Lys]-1018 Ac-Cy cl o- [ [(D)Asp]-Q TWQ- [(D)D ab] ] -YVVRENG- [AEA] - [(D)Ly s] - _1400 1019 Ac-Cyclo-[[(D)Asp]-QTWQ-[(D)Dap]]-YVVRENG-[AEA]-[(D)Lys]-Table E8. IC50 of Illustrative Peptides Containing the Ac-[Pen]-XXWX)0000( Motif and Ac-)00(WX-[Pen]-)000( analogues SEQ Human........Rat pStat.31 ID SetittenM ELISA ELISA HTRF
NO.

( nM) ( nM) (nM) ................
1020 Ac-[Penl-ADWVCYWHTFG-NH2 *****
1021 Ac-CADWV-[Penl-YWHTFG-NH2 *****
1022 Ac4(D)Penl-ADWVCYWHTFG4AEAl-RD)-Lysl-NH2 **** ***** ****
1023 Ac-CADWV4(D)Penl-YWHTFG4AEA]-[(D)-Lysl-NH2 >30000 ***** ****
1024 Ac-{Penl-RTWQCYWRKFG-{AEAI-RD)-Lysl-NH2 **** **** ****
1025 Ac-ACDWV-[Penl-YWRKFG-[AEAl-RD)-Lysl-NH2 *****
1026 Ac-A-[Penl-DWVCYWRKFG-[AEAl-RD)-Lysl-NH2 ****
1027 Ac-A-[hCys]-DWV-[Penl-YWRKFG-[AEAl-RD)-Lysl-NH2 ¨30000 1028 Ac-CQTWQ-[Penl-YW-[cc-MeLeul-ENG-NH2 **** ****
1029 Ac-CQTWQ-[Penl-YW-RD)Asnl-ENG-NH2 *****
*=<10nIVI; **=10-25 nM *** = 25-100 nJVI,**** = 100-1000 nIVI, *****=1000-10,000 [00698] SAR analysis of the activities of the peptide inhibitors tested indicated that the C)000(C
disulphide is associated with high activity. The two Trp residues and the Phe residue are also associated with high activity, but it is recognized that these amino acids can be readily exchanged with similar homologs (e.g., 1-Nal substitued for Trp and/or Phe substituted for Tyr).
In addition, the data suggested that the presence of one or more basic residues at the C-terminus is associated with high activity. Also, His-9 can be replaced by Arg or another homolog and maintain or improve activity. The schematic below provides one illustrative consensus sequence showing certain residues associated with high activity.

Cys-Xxx-Xxx-Trp-Xxx-Cys-Tyr-Trp-His-Xxx-Phe-Xxx-Xxx-(D)Lys-OH

STABILITY OF PEPTIDE INHIBITORS IN SIMULATED INTESTINAL FLUID (SIF), SIMULATED
GASTRIC
FLUID (SGF) AND REDOX CONDITIONS
[00699] Studies were carried out in simulated intestinal fluid (SIF) and simulated gastric fluid (SGF) to evaluate gastric stability of the peptide inhibitors of the present invention. In addition, studies were carried out to assess redox stability of the peptide inhibiotrs of the present invention.
1007001SIF was prepared by adding 6.8 g of monobasic potassium phosphate and 10.0 g of pancreatin to 1.0 L of water. After dissolution, the pH was adjusted to 6.8 using NaOH. DMSO
stocks (2 mM) were first prepared for the test compounds. Aliquots of the DMSO
solutions were dosed into 6 individual tubes, each containing 0.5 mL of SIF, which is pre-warmed to 37 C. The final test compound concentration was 20 p.M. The vials were kept in a benchtop Thermomixer for the duration of the experiment. At each timepoint (0, 5, 10, 20, 40, 60, or 360 minutes or 24 hours), 1.0 mL of acetonitrile containing 1% formic acid was added to one vial to terminate the reaction. Samples were stored at 4 C until the end of the experiment. After the final timepoint is sampled, the tubes were mixed and then centrifuged at 3,000 rpm for 10 minutes. Aliquots of the supernatant were removed, diluted 1:1 into distilled water containing internal standard, and analyzed by LCMSNIS. Percent remaining at each timepoint was calculated based on the peak area response ratio of test to compound to internal standard. Time 0 was set to 100%, and all later timepoints were calculated relative to time 0. Half-lives were calculated by fitting to a first-order exponential decay equation using Graphpad. Stablity in SIF assays is shown in Tables E9 and E10.

[00701] SGF was prepared by adding 20 mg NaC1, 32 mg porcine pepsin (MP
Biochemicals, catalog 02102599), and 70p1 HC1 to 10m1 water (final pH=2). Aliquots of SGF
(0.5ml each) were pre-warmed at 37 C. To start the reaction, 1 1 of peptide stock solution (10mM in DMSO) was added to 0.5ml SGF and thoroughly mixed such that the final peptide concentration was 20p.M. The reactions were incubated at 37 C with gentle shaking. At each time point (0, 15, 30, 60 min) 500 aliquots were removed and added to 200 ul acetonitrile containing 0.1% formic acid to quench the reaction. Samples are stored at 4 C until the end of the experiment and centrifuged at 10,000 rpm for 5 minutes. Aliquots of the supernatant were removed, diluted 1:1 into distilled water containing internal standard, and analyzed by LCMSNIS.
Percent remaining at each timepoint was calculated based on the peak area response ratio of test to compound to internal standard. Time 0 was set to 100%, and all later timepoints were calculated relative to time 0. Half-lives were calculated by fitting to a first-order exponential decay equation using GraphPad. Stability in SGF assays in shown in Tables E9 and El O.
Table E9. Stability of Illustrative Peptides containing the Ac-[Pen]-)0(WX-[Pen]-)000( Motif and Analogues in Simulated Intestinal Fluid (SIF) and Simulated Gastric Fluid (SGF) SEQ SGF' S
IF
ID NO: t I /2 t iiiSeAl nen*
=
=== ( m in ) (ruin ) .=
549 Ac- [[Pen] -QTWQ- [Pen] -YW- [hLeul -ENG-NH2 *****
1030 Ac- [Pen] -QTWQ- [Pen] -YWN-Me-RENG-NH2 ****
551 Ac- [Pen] -QTWQ- [Pen] -YW- [hL eu] -ENG-NH2 *****
552 Ac- [Pen] -QTWQ- [Pen] -YW- [N-MeArg] -ENG-NH2 ***
554 Ac- [Pen] -QTWQ-[Pen] -YW- [cc-MeLeul-ENG-NH2 **
1028 Ac-CQ TWQ- [Pen] -YW- [cc-MeL eu] -ENG-NH2 *****
555 Ac- [Pen] -QTWQ- [Pen] -YW- [(D)Asn] -ENG-NH2 **
1029 Ac-CQTWQ-[Penl-YW-RD)Asnl-ENG-NH2 *****
556 Ac- [Pen] -QTWQ- [Pen] -[cc-MeLy s] -ENG-NH2 **
557 Ac- [Pen] -QTWQ- [Pen] - [Phe(4-0M01- [2-Na11- [cc-MeLy s] -ENG-NH2 *** **
558 Ac- [Pen] -QTWQ- [Peril -12-Nall -12-Nall - [cc-MeLy s] -ENG-NH2 **

SEQ '" SG F' S
IF
ID NO: ti!' ti/' i e(luenlif =
(min) (min) 559 Ac413enl-QTWQ-1Penl-Y-12-Nall-1cc-MeOrn1-ENG-NH2 **
560 Ac-113enl-QTWQ-1Penl-YW-10t-MeOrn1-ENG-NH2 **
561 Ac-113enl-QTWQ-1Penl-Y-11-Nall-1cc-MeOrn1-ENG-NH2 **
1031 Ac-113en] -QTWQ-1Pen1-11Phe(4 -OW)] (OW)] -12-Nal] -1cc-MeOrn1-11Lys(Ac)1-NG-NH2 563 Ac-113enl-QTWQ-1Penl-YW-1cc-MeLys1-1Lys(Ac)1-NG-NH2 1032 Ac-113enl-QTWQ-1Penl- 11Phe(4-0Me)1-W-1cc-MeLys1-1Lys(Ac)1-NG-NH2 565 Ac-113enl-QTWQ-1Pen1-1Phe(4-0Me)]-12-Nall-1cc-MeLys1-1Lys(Ac)1-NG-566 Ac-113enl-QTWQ-1Pen1-1Phe(4-0Me)]-11-Nall-1cc-MeLys1-1Lys(Ac)1-NG-1033 succinic anhydride- [Pen] -Q TWQ [Pen] - [Phe (4-0Me)] -12-Nall - [cc-MeLys] - **
11Lys(Ac)1-NG-NH2 585 pyroglutamic acid-113enl-QTWQ[Pen1-1Phe(4-0Me)]-12-Nall-1cc-MeLysl-**
11Lys(Ac)1-NG-NH2 1034 Ac-113enl-QTWQ-1Pen1-1Phe14-(2-aminoethoxy)]-12-Nall-1cc-MeLysl-[Lys(Ac)1-NN-NH2 601 Ac-113enl-QTWQ-1Pen1-1Phe14-(2-aminoethoxy)]-12-Nall-1cc-MeLysl-602 Ac-113enl-QTWQ-1Pen1-1Phe14-(2-aminoethoxy)]-12-Nall-1cc-MeLeul- **
***
11Lys(Ac)1-NN-NH2 603 Ac-113enl-QTWQ-1Pen1-1Phe14-(2-aminoethoxy)]-12-Nall-1cc-MeLeul-604 Ac-113enl-QTWQ-1Pen1-1Phe14-(2-aminoethoxy)]-12.-Nall-1Aibl-ENN-605 Ac-113enl-QTWQ-1Pen1-1Phe14-(2-aminoethoxy)]-12-Nall-Aib-1Lys(Ac)l-** ***

606 Ac-113enl-QTWQ-1Pen1-1Phe14-(2-aminoethoxy)]-12-Nall-1Aibl-[Lys(Ac)1-NQ-NH2 607 Ac-113enl-Dap(Ac)TWQ-1Pen1-1Phe14-(2-acetylaminoethoxy)]-12-Nall-1cc-SEQ " SG F' S I F
ID NO: t1/2 t1/2 i equenlif MeLys(Ac)1-ENG-NH2 608 Ac-[Pen1-[cc-MeOrn(Ac)1-TWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)1-p-**
****
Nall-[cc-MeLys(Ac)-ENG-NH2 609 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[cc-MeLys(Ac)-[Lys(Ac)-NG-NH2 610 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[cc-MeLys(Ac)-[Lys(Ac)1-NN-NH2 611 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[cc- **
MeLys(Ac)1-ENG-NH2 612 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[cc-MeLys(Ac)1-ENA-NH2 613 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[cc-MeLeul-[Lys(Ac)l-NN-NH2 614 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[cc-MeLeul-QNN-NH2 615 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[Aibl-616 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[Aibl-[Lys(Ac)1-NN-NH2 617 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-acetylaminoethoxy)]-[2-Nall-[Aibl-[Lys(Ac)1-NQ-NH2 522 11Ac-[Penl-QTWQ-11Pen1-11Phe(4-0Me)]-112-Nan-11cc-MeLysl-ENG-Nt1212 ****
DIG
618 Ac-[Penl-QTWQ-[Pen1-[Phe(4-0Me)]-[2-Nall-[Aibl-ENN-NH2 ***
619 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-aminoethoxy)]-[2-Nall-[hLeul-ENA-***** *****

620 Ac-[Penl-TTWQ-[Pen1-[Phe[4-(2-aminoethoxy)]-[2-Nall-[Aibl-[Lys(Ac)1-NN-NH2 625 Ac-[Penl-QTWQ-[Pen1-[Phe(4-0Me)]-[2-Nan-[Aibl-[Lys(Ac)l-NN-NH2 **
628 Ac-[Penl-QTWQ-[Pen1-[Phe[4-(2-aminoethoxy)]-[2-Nall-[Aibl-[Lys(Ac)1-N-H3Alal-NH2 SEQ SG F' S
I F
ID NO: t1/2 t1/2 i e(luenlif 630 Ac- [Pen] -NTWQ-Pen] - [Phe(4-0Me)] - [2-Na1l -[Aibl-ENN-NH2 ***
631 Ac- [Pen] -NTWQ- [Pen] - [Phe [4-(2-aminoethoxy)] - [2-Nall -[hLeul -ENA-***** ****

632 Ac- [Pen] -NTWQ- [Pen] -[Phe [4-(2-am inoethoxy)] - [2-Na1l -[Aibl -[Ly s (Ac)] -NN-NH2 633 Ac- [Pen] -NTWQ-[Pen] - [Phe(4-0Me)] - [2-Na1l - [Aib] - [Lys(Ac) ] -**

634 Ac- [Pen] -NTWQ- [Pen] -[Phe [4-(2-am inoethoxy)] - [2-Na1l -[Aibl -[Lys(Ac)] -NQ-Nt12 636 Ac- [Pen] -NTWQ- [Pen] -[Phe [4-(2-am inoethoxy)] - [2-Na1l -[Aibl -[Ly s (Ac)] -NA-NH2 637 Ac- [Pen] -NTWQ-[Pen] - [Phe(4-0Me)] - [2-Na1] - [Aib]- [Ly s(Ac)l-NN-Nt12 638 Ac- [Pen] -NTWQ-[Pen] - [Phe(4-0Me)] - [2-Na1] - [Aib]- [Ly s(Ac)l-NQ-Nt12 639 Ac- [Pen] -NTWQ- [Pen] -[Phe [4-(2-am inoethoxy)] - [2-Na1l -[Aibl -[Lys(Ac) ] -N- [PAW -NH2 640 Ac- [Pen] -NTWQ-[Pen] - [Phe(4-0Me)] -[hLeul - [Lys (Ac)] -N-***** *****
[13A1al -NH2 641 Ac- [Pen] -NTWQ- [Pen] -[Phe [4-(2-am inoethoxy)] - [2-Nall -[hLeul -***** *****
[Lys(Ac) ] -N- [PAW -NH2 669 Ac- [Pen] -QTWQ- [Penl- [Phe(4-CONH2)] - [2-Na1l -[cc-MeV al] -[Lys(Ac) ] - **

534 [Ac-[Pen] -QTWQ- [Penl- [Phe(4-CONH2)] - [2-Nall- [cc-MeLy sl- [Lys (Ac)] - **

1035 Ac-[(D)Phel - [Pen] -NTWQ- [Pen] - [Phe [4-(2-aminoethoxy)] [Aib]-[Ly s (Ac)] -NN-NH2 676 Ac-[(D)Phel - [Pen] -NTWQ- [Pen] - [Phe [4-(2-aminoethoxy)] -[Aib]-**
[Lys(Ac) ] -N- [PAla] -NH2 682 Ac- [Pen] -NTWQ [Pen] - [Phe(4-CONH2)] - [2-Na1l - [AIN- [Lys(Ac) ] -NN-** ****

683 Ac- [Pen] -NTWQ [Pen] - [Phe(4-CONH2)] - [2-N al] 44-am ino-4-c arboxy-**
tetrahydropyranl-Ly s(Ac)] -NN-NH2 ii SEQ '" iii "
SG F' iii SIF
ii ID NO: .:: iii il t1/2 iii t1/2 iietluen114ii .:..:
(m in ) 1::: (m in ) ..
684 Ac-[Penl-NTWQ[Pen]-[Phe(4-CONH2)]-[2-Nall-[Achc]- [Lys(Ac)[-NN- *
*

1036 Ac-[Penl-NTWQ[Pen]-[Phe(4-CONH2)]-[2-Nall-[Acycl- [Lys(Ac)]-NN- *
*

686 Ac-[Penl-NTWQ[Pen]-[Phe(4-CONH2)]-[2-Nall-k-MeLeul-[Lys(Ac)]- *
*

688 Ac-[Penl-NTWQ[Pen]-[Phe(4-0Me)]-[2-Nall-[4-amino-4-carboxy- *
*
tetrahydropyranl-[Lys(Ac)l-NN-Nt12 689 Ac-[Penl-NTWQ[Pen]-[Phe(4-0Me)]-[2-Nall-[Achc]-[Lys(Ac)i-NN-Nt12 *
**
1037 Ac-[Penl-NTWQ[Pen]-[Phe(4-0Me)]-[2-Nall-[Acycl-[Lys(Ac)l-NN-Nt12 **
*
671 Ac-[Penl-NTWQ[Pen]-[Phe(4-0Me)]-[2-Nall-[a-MeLeul-[Lys(Ac)]-NN- *
*

535 [Ac4Penl-NTWQ-[Pen]-[Phe(4-CONH2)1-12-Nall-[Aibl-KNN-NH2l2DIG **
**
536 [Ac4Penl-NTWQ4Pen]4Phe(4-CONH2)]42-Nall44-amino-4-carboxy- *
*
tetrahydropyranl-KNN-NH2l2 DIG
537 [Ac4Penl-NTWQ-[Pen]-[Phe(4-CONH2)142-Nall4Achcl-KNN-NH2l2 **
***
DIG
539 [Ac-[Penl-NTWQ-[Pen]-[Phe(4-CONH2)]-[2-Nall-k-MeLeul-KNN-** **
NH2l2 DIG
the matrix used is 100 fold dilution of standard SIF concentration *=>360min; **=180-360minn; ***=120-180min; ****=<60-120min; *****=<60min Table E10. Stability of Illustrative Peptides Containing Thioethers Motif and Analogues Within Simulated Intestinal Fluid (SIF) and Simulated Gastric Fluid (SGF) ir SEQ ID SIP

...:. ...
ii 4NO;:: iiiii iiequen0iii iii ii 11/2 iii 11/2 -(min) (min) .= .....
...
692 Ac-Cyclo-r[Abu]RTWQC1-YWRKFG-[AEA]-[(D)Lys]-NH2 *****
694 Ac-Cyclo-[[Abu]-QTWQC]-YVVRENG-[AEA]-[(D)Lys]- NH2 *****
699 Ac-Cyclo-[[Abu]-QTWQC]-YW-[hLeu]-ENG- NH2 ***** ND
700 Ac-Cyclo-[Abu]-QTWQ-(D)Cys]]-YW-[hLeu]-ENG-NH2 ****

ipS'EQifl SIP"ninSGPri NO Siqutnce 11/2 11/2 (min) (min) 701 Ac-Cy cl o- [ [Abu]- Q TWQ - [Pen] ] -YW- [hLeu] -ENG-NH2 *****
703 Ac-Cyclo-[[Abu]-QTWQC]-YW- [a-MeLeu]-ENG-NH2 *****
704 Ac-Cyclo- [[Abu]-QTWQC]-Y- [2-Na!]- a-MeLysFENG-NH2 *****
702 Ac-Cyclo- [[Abu]-QTWQC]-[Phe(4-0Me)]- [2-Nal]-[a-*** *****
MeLys]-ENG-NH2 706 Ac-Cyclo- [[Abu]-QTWQC]-[Phe(4-0Me)]- [2-Nal]-[a-*** *****
MeOrnFENG-NH2 707 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-W-[a-MeOrn]- **
*****

702 Ac-Cyclo- [[Abu]-QTWQC]-[Phe(4-0Me)]- [2-Na!]-[a- **
*****
MeLys]-ENG-NH2 709 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-W-[a-MeLys]-*****
[Lys(Ac)]-NG-NH2 710 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-W-[a-MeLys]-*****

711 Ac-Cyclo- [[Abu]-QTWQC]-[Phe(4-0Me)]- [1-Nal]-[a-*****
MeLys]-[Lys(Ac)]-NG-NH2 712 Ac-Cyclo- [[Abu]-QTWQC]-[Phe(4-0Me)]- [2-Nal]-[a-** *****
MeLy s] - [Ly s(Ac)] -NG-NH2 713 Ac-Cyclo-[[Abu]-QTWQC]-YVV- [a-MeOrn]-[Lys(Ac)]-NG-**

714 Ac-Cy cl o- [ [Abu] -Q TWQ C] - [Phe(4-0Me)] - [2-Na!]- [(D)Asn]-[Lys(Ac)]-NG-NH2 715 Ac-Cyclo- [ [Abu] -QTWQC]- [Phe(4-Phenoxy)]-[2-Nal] - [a-MeLy s] - [Ly s(Ac)] -NG-NH2 716 Ac-Cyclo- [[Abu]-QTWQC]-[hPhe(3,4-dimethoxy)]- [2-Na!] - [a-MeLys]-[Lys(Ac)]-NG-NH2 717 Ac-Cyclo- [ [Abu] -QTWQC]-[DMT]-[2-NalHa-MeLys]-[Lys(Ac)]-NG-NH2 718 Ac-Cyclo- [[Abu]-QTWQC]-[Phe(4-CONH2)]- [2-Nal]-[a-*** *****
MeLys]-[Lys(A0]NG-NH2 719 Ac-Cyclo- [ [Abu] - QTWQC] -Phe(3,4-C12) [2-Na!]- [a-MeLys]- ***
[Lys(Ac)]NG-NH2 720 Ac-Cyclo- [ [Abu]- QTWQ - [Pen]] - [Phe(4-0Me)] - [2-Nal]-[a- **
***
MeLys]-ENG-NH2 721 Ac-Cyclo- [ [Abu]- QTWQ - [Pen]] - [Phe(4-0Me)] - [2-Nal]-[a- **
***
MeLys]-[Lys(Ac)]NG-NH2 782 Ac-Cyclo- [ [Abu] -Q TWQC] - [Phe[4-(2-aminoethoxy)] -W- [a-***
MeLys]-ENG-NH2 NO Siqutnce 11/2 11/2 (min) (min) 790 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[2-Nal]-[a-*** *****
MeOrn]-[Lys(A0]-NG-NH2 791 Ac-Cyclo-[[Abu]-QTWQC]-[2-Nal]-[2-Nal]-[a-MeOrn]- *** ND
[Lys(Ac)]-NG-NH2 794 Ac-Cyclo-[[Abu]-QTWQC]-[2-Nal]-[2-Nal]-[a-MeLys]- ** ND
[Lys(Ac)]-NG-NH2 797 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-CONH2)]-[2-Nal]-[a- **** *****
MeLys]-[Lys(A0]-NG-NH2 798 Ac-Cyclo-[[Abu]-QTWQC]-[2-Nall-[2-NalHa-MeLysFENG- .
ND

810 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[2-Nall-[Aib]-[Lys(Ac)]-NG-NH2 815 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[2-Nall-[Orn]-[Lys(Ac)]-NG- NH2 820 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[2-Nall-[Chg]-***
[Lys(Ac)]-NG-NH2 822 Ac-Cyclo-[[Abu]-QTWQC]-[Octgly]-[2-Nal]-[a-MeLys]- *****
[Lys(Ac)]-NG-NH2 823 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[Octgly]-[a- ****
MeLys]-[Lys(A01-NG-NH2 823 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[Octgly]-[a- *****
MeLys]-[Lys(A0]-NG-NH2 829 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- *
[a-MeLys]-ENG-NH2 857 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- .
[a-MeLys]-[Lys(Benzoic acid)]NG-NH2 861 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- *
[a-MeLys]-[Lys(isovaleric acid)]-NG-NH2 876 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- *.
*****
[Aib]-[Lys(A0]-QG-NH2 877 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- *.
**
[Aib]-QNG-NH2 878 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- ***.
***
[Aib]-ENG-NH2 879 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-1-Nal[Aib]-[Lys(Ac)]-NG-NH2 880 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- ****
*****
[Aib]-[Lys(Ac)]-NA-NH2 891 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- .
**
[a-Me-Orn]-[Lys(A01-NG-NH2 892 Ac-Cyclo-[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]]-[2-Nall- *

NO Siqutnce 11/2 11/2 (min) (min).
[a-MeLys]-[Lys(Ac)]-NG-M-12 893 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- ***.
[Orn]-[Lys(Ac)]-NG-NH2 894 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-W-*****
[Orn]-ENG-NH2 895 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-W-*****
[Orn]-[Dap]-NG-NH2 896 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-W-*****
[Orn]-[Dap(Ac)]-NG-NH2 897 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- *****
[Orn]-[Dap]-NG-NH2 898 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- *****
[Orn]-[Dap(Ac)]-NG-NH2 899 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-W-***** *****
[hLeu]-ENG-NH2 900 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-(acetyl-aminoethoxy)]]-** *****
[2-Nall-[a-MeLys(Ac)]-[Lys(Ac)]-NG-NH2 901 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-W-[a- **
Me-Leu]-ENG-NH2 902 Succicinyl-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]- **
[2-Nall-[a-MeLys]-[Lys(Ac)]-NG-NH2 906 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-(acetyl-aminoethoxy)]]- ****
*****
[2-Nall-[a-MeLys(Ac)]-ENG-NH2 820 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[2-Nall-[Chg]- **
[Lys(Ac)]-NG-NH2 911 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- .
**
[a-MeLys]-ENQ-NH2 912 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- .
**
[a-MeLys]-ENN-NH2 913 Ac-Cyclo-[[Abu]-TTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- .
**
[a-MeLys]-ENG-NH2 914 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- ****
*****
[a-Me-Gly(Ethyl)] Lys(Ac)l-NG-NH2 915 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- ***
****
[a-MeVa1]-[Lys(A0]-NG-NH2 916 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]- *****
***
[a-MeSer]-[Lys(Ac)]-NG-NH2 925 Ac-(D)Lys-[Cyclo-[[Abu]-QTWQC]]-[Phe(4-0Me)]-[2-Nal]-**** *****
[a-MeLeu]-ENG-NH2 1039 [Ac-[(D)Lys]-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[2-Nall- ****
*****
[a-MeLeu]-ENG-NH2]2 DIG: dimerization through (D)Lys NO Siqutnce 11/2 11/2 (min) (min) 930 Ac-Cyclo-r[AbuFQTWQC]-[Phe[4-(2-aminoethoxy)]142-Nall- *****
ND
[hLeu]-[Lys(Ac)]-N-[f3Ala]-NH2 933 Ac-Cyclo-[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall- .
**
[a-MeLys]-NNG-NH2 946 Ac-Cyclo-[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall- ****
****
[Aib]-[Lys(Ac)]-NG-NH2 955 Ac-Cyclo-[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall- ***
*****
[a-MeLeu]-[Lys(A01-NN-NH2 1040 [Ac-Cyclo-[[Abu]-QTWQCFY(Bz1)-W4a-MeLysFENG-** *****
NH212;PEG25 through [a-MeLys]
965 Ac-E-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2- ***
Nall-[a-MeLys]-ENN-NH2 966 Ac-(D)Glu-[Cyclo-[[Abu]-QTWQC]-[Phe[4-(2- ****
aminoethoxY)lF[2-Nall-[a-MeLys]-ENN-NH2 967 Ac-Arg-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2- *****
***
Nall-[a-MeLys]-ENN-NH2 1041 Ac-[(D)Arg-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2- **
aminoethoxy)]]-[2-Nall-[a-MeLys]-ENN-NH2 969 Ac-F-Cyclo-[[Abu]-QTWQC]]-[Phe[4-(2-aminoethoxy)]]-[2-**** ***
Nall-[a-MeLys]-ENN-NH2 970 Ac-[(D)Phe]-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-** ***
aminoethoxy)]]-[2-Nall-[a-MeLys]-ENN-NH2 972 Ac-T-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2- ***
Nall-[a-MeLys]-ENN-NH2 973 Ac-Leu-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-***
Nall-[a-MeLys]-ENN-NH2 1042 Ac-RD)Q1n]-Cyclo-[[Abu]-QTWQCHPhe[4-(2- ***
aminoethoxy)]]-[2-Nall-[a-MeLys]-ENN-NH2 975 Ac-Cyclo-[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall- *****
[Acpc]-ENN-NH2 976 Ac-Cyclo-[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall- ***** ****
[Acbc]-ENN-NH2 1043 Ac-Cyclo-[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall- .
[Acpc]- ENN-NH2 978 Ac-Cyclo-[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall- *.
[Acyc]-ENN-NH2 979 Ac-Cyclo-[[AbuFQTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall- *
[4-amino-4-carboxy-piperidineFENN-NH2 972 Ac-T-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeLys]-ENN-NH2 the matrix used is 100 fold dilution of standard SIF concentration *=>360min; **=180-360minn; ***=120-180min; ****=<60-120min; *****=<60min [00702] For each peptide tested, the DTT stability assay was conducted by adding 5p1 of a 10mM
peptide stock solution in DMSO to lml of 100mM Tris-C1, pH 7.5 (final peptide concentration is 50pM). At time 0 min, Sul of a freshly thawed 100mM DTT solution was added to the incubation tube containing the peptide, such that the final DTT concentration was 0.5mM. The reactions were incubated at room temperature. At different time points up to 120 minutes (20 min, 40 min, 80 min, 120 min), 500 aliquots were removed, and the reaction was quenched by adding 10p1 of 5M acetic acid. To measure disappearance of the parent peptide, the quenched samples (300) were analyzed by reverse phase EIPLC and UV absorbance at 220nm.
The fraction oxidized remaining was graphed versus time, and half-lives were calculated by fitting to a first-order exponential decay equation using Excel. The results of these studies are shown in Table El 1. The peptides having half-life >120 min are all considered stable.
Table El 1. Stability of Illustrative Peptides in DTT Assay DTT
Sequence Stability (min) Ac-CRTWECYWHEFG-NH2 <10 Ac-CQTWQCYW-[hLeu]-ENG-NH2 Ac-CADWVWCYVVHTFGA-[Azt]-[(D)Lys]-NH2 Ac-Cyclo-[[Abu]-RTWQC]-YVVRKFG-[AEA]-[(D)Lys]-NH2 >120 Ac-Pen] -QTWQ- [Pen] -YW- [hLetil -ENG-Nt12 >120 Ac-{Pen] -QTWQ- [Pen] -YW- [c(-MeLeul -ENG-Nt12 >120 Ac-Cyclo- [ [Abu] -Q TWQ - [Phe(4-0Me)]- [2-Nal]- [a-MeLys]->120 Ac-{Pen] -QTWQ- [Phe(4 -Ome)142-Nall - [cc-MeLysl-ENG-Nt12 >120 Ac-Cyclo- [ [Abu] -QTWQ C] - [Phe [4-(2-aminoethoxy)] -W- [a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]]-[2-Nal]-[4->120 amino-4-carboxy-tetrahydropyran]-ENN-NH2 [Ac-[Pen] -QTWQ- [Phe(4-CONH2)] - -Nall- [c(-MeLy s] - [Lys(Ac) ] ->120 *=10-120 min CROSS-REACTIVITY OF PEPTIDE INHIBITORS
1007031 The amino acids of the extracellular domain of the human IL-23R are 95%, 77% and 70% identical to the cyno IL-23R, rat IL-23R and mouse IL-23R, respectively.
Interestingly, the mouse receptor contains an insertion of 21 residues that are absent in human, mouse, chimp, dog and cow receptor. These additional amino acids are located in a region where human IL-23R is thought to bind to IL-23.
[00704] To identify peptide inhibitors that cross-reacted with species other than human IL-23R, the ability of certain peptide inhibitors to inhibit human IL-23R, cyno IL-23R, rat IL-23R and mouse IL-23R by ELISA assay. In line with the observation regarding the sequence differences between human IL-23R and mouse IL-23R, the peptide antagonists tested showed a lack of or very weak inhibitory activities in the mouse IL-23R ELISA (see Table E12). In contrast, the antagonists tested to date displayed comparable potency towards the rat receptor and slightly less activity towards the cyno receptor.
[00705] Various bioassays performed to determine the potency, cross reactivity and the selectivity of IL-23R antagonists are described below.
Assays for Selectivity of specific IL-23R Antagonists Human IL-12Rf31 ELI SA
[00706] An assay plate was coated with 100 ng/well of human IL-12Rf31 huFC and incubated overnight at 4 C. The wells were washed, blocked, and washed again. Serial dilutions of test peptides and IL-23 at a final concentration of 2.5 nIVI were added to each well, and incubated for 2 hours at room temperature. After the wells were washed, bound IL-23 was detected with goat anti-p40 polyclonal antibodies, followed by an EIRP conjugated donkey anti-goat IgG. Signals were visualized with TMB One Component EIRP Membrane Substrate and quenched with 2 M
sulfuric acid.
Mouse IL-23R Competitive Binding ELISA
[00707] An assay plate was coated with 50 ng/well of Mouse IL-23R huFC and incubated overnight at 4 C. The wells were washed, blocked, and washed again. Serial dilutions of test peptides and IL-23 at a final concentration of 4 nM were added to each well, and incubated for 2 hours at room temperature. After the wells were washed, bound IL-23 was detected with goat anti-p40 polyclonal antibodies, followed by an HIRP conjugated donkey anti-goat IgG. Signals were visualized with TMB One Component HIRP Membrane Substrate and quenched with 2 M
sulfuric acid.
Rat IL-23R Competitive Binding ELISA
[00708]An assay plate was coated with 300 ng/well of Rat IL-23R huFC and incubated overnight at 4 C. The wells were washed, blocked, and washed again. Serial dilutions of test peptides and IL-23 at a final concentration of 7 nM were added to each well, and incubated for 2 hours at room temperature. After the wells were washed, bound IL-23 was detected with goat anti-p40 polyclonal antibodies, followed by an HIRP conjugated donkey anti-goat IgG. Signals were visualized with TMB One Component HIRP Membrane Substrate and quenched with 2 M
sulfuric acid.
Cyno IL-23R Competitive Binding ELISA
1007091 An assay plate was coated with 50 ng/well of Cyno IL-23R huFC and incubated overnight at 4 C. The wells were washed, blocked, and washed again. Serial dilutions of test peptides and IL-23 at a final concentration of 2 nM were added to each well, and incubated for 2 hours at room temperature. After the wells were washed, bound IL-23 was detected with goat anti-p40 polyclonal antibodies, followed by an HIRP conjugated donkey anti-goat IgG. Signals were visualized with TMB One Component HIRP Membrane Substrate and quenched with 2 M
sulfuric acid.
Table E12. Cross-Reactivity of Illustrative Peptide Inhibitors Human IL-23R Rodent and Cyno IL-23R
Cross Activity (nM) Reactivity (nM) Cmpd.
ELISA ELISA ELISA
Number Cell Assay ELISA cyno hulL23R mouse IL23R rat IL23R

pSTAT3 HTRF IL23 IL23 IL23R IL23 197 ++ ND ++ ND
169 ++ ++ ++

198 +++ +++ ND +++ +++
213 +++ +++ ND +++ ND
219 +++ +++ ND +++ ND
230 +++ +++ ND +++ ND
+++ indicates 0-250 nIVI
++ indicates 251-1000 nIVI
+ indicates 1001-10,000 nM
- indicates > 25,000 nIVI

NK CELL ASSAY
1007101Natural killer (NK) cells, purified from human peripheral blood of healthy donors by negative selection (Miltenyi Biotech, Cat # 130-092-657), were cultured in complete media (RPMI 1640 containing 10% FBS, L-glutamine and penicillin-streptomycin) in the presence of IL-2 (RnD, Cat # 202-IL-010/CF) at 25 ng/mL. After 7 days, cells were centrifuged, and resuspended in complete media at 1E6 cells/mL. Recombinant IL-23 at predetermined EC50 to EC75 and IL-18 (RnD, Cat # B003-5) at 10 ng/mL were mixed with varying concentrations of peptides, and added to NK cells seeded at 1E5 cells per well. After 20 to 24 hours, IFNy in the supernatant was quantified using Quantikine ELISA (RnD, Cat # DIF50).
Table E13. IC50 of Illustrative Peptide Inhibitors in Primary Cell Line (NK
Cell Assay) NK cell assay Sequence (nM) Ac-Cyclo-[[Abu]-QTWQC]-Y42-NalHa-MeLysFENG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[2-Nal]-[a-MeLys]-Ac-Cyclo-[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]-W4a-MeLys]-ENG-NH2 Ac-Cyclo-[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]]-[2-Nal]-[a-MeLys]-[Lys(isovaleric acid)]-NG-NE12 Ac-Cyclo-[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]]-[2-Nal]-[Ai13]-QNG-NE12 Ac-Cyclo-[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]]-[2-Nal]-[Aib]-[Lys(Ac)]-NA-NH2 Ac-Cyclo- [[Abu]-QTWQC]-[Phe[4-(2-(acetyl-aminoethoxy)]]-[2-Nall-[a-MeLys(Ac)]-[Lys(Ac)1-NG-NH2 Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[Phe(3,4-OMe21-[a-MeLys]-[Lys(Ac)1-NG-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeLys]-ENQ-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeLys]-ENN-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeVal]-[Lys(Ac)1-NG-NH2 [Ac-Cyclo-[[Abu]-QTWQC]-[Phe(4-0Me)]-[2-Nall-[a-MeLys]-ENG-NH2]2; DIG through a-MeLys Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeLeu)-[Cit]-NN-NH2 Ac-[(D)Phe]-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]- [a-MeLys]-ENN-NH2 Ac-T-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeLysFENN-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[Acbc]-ENN-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[Acpc]- ENN-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[AchcFENN-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-Cyclo-[[Abu]-QTWQCHPhe[4-(2-aminoethoxy)]]-[2-Nall-[a-MeLeu]-QN-[f3Ala]-NH2 Ac-(D)Phe-Cyclo-[ [Abu]-QTWQC]- [Phe[4-(2-aminoethoxy)]]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-[(D)Arg]-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nall- [4-amino-4-carboxy-tetrahydropyran]-*=<25nIVI
Table 14. IC50 of Illustrative Peptides Containing the Ac-[Pen]-XXWX-[Pen]-)000( Motif and analogues (NK cell assay) NK Cell Sequence assay (nM) Ac-[Pen] -QTWQ- [Pen] -[Phe [4-(2-am ino ethoxy)] - [2-Nall - [cc-MeLeul -[Lys(Ac) ] -NN-NH2 Ac-[Pen] -NTWQ- [Pen] -[Phe [4-(2-amino ethoxy)] - [2-Nall - [Aib]- [Lys(Ac)]-Ac-[Pen] -NTWQ- [Pen] -[Phe [4-(2-amino ethoxy)] - [2-Nall - [Aib]- [Lys(Ac)]-N- [13Alal -NH2 Ac-[Pen] -QTWQ- [Pen] -[Phe(4-0Me)] - [cc-MeLy s] - [Lys (Ac)] -NN-Ac- [Pen] -QTWQ- [Pen] -[Phe(4-CONH2)] - [2-Nall -[cc-MeLysl- [Lys(Ac)]-Ac- [Pen] -QTWQ- [Pen] -[Phe(4-CONH2)] - [2-Nall -[cc-MeV al] -[Lys(Ac)] -**

[Ac- [Pen] -QTWQ [Pen] - [Phe [4-(2-acetylamino ethoxy)] - [2-Nall - [cc-MeVal] -KNN-NH212 DIG
[Ac- [Pen] -QTWQ [Pen] - [Phe[4-(2-acetylaminoethoxy)l- 112-Nall -K-[Lys(Ac)] -NN-NH212 DIG
[Ac- [Pen] -QTWQ- [Pen] - [Phe(4-0Me)] - [2-Nall- [cc-MeLy s] - [Lys(Ac)]-NN-11Ac-11Pen1-01W0-11Pen1-11Phe(4-CONH2)1-I2-Nall-kx-MeLysl-[Lys(Ac)l-Ac- [(D)Phel -[Pen] -NTWQ [Pen] - [Phe(4-0Me)] - 112-Nall - [4-amino-4-carboxy-tetrahydropyran] - [Cit] -NN-Nt12 Ac- [(D)Phel -[Pen] -NTWQ [Pen] - [Phe(4-0Me)] - - 11Achcl-ENN-Nt12 Ac-[Pen] -NTWQ [Pen] - [Phe(CONH2)] - 112-Nail -[Aibl - 11Lys(Ac)l-NN-NH2 [Ac- [Pen] -NTWQ- [Pei+ 11Phe(4-CONH2)1- 11Aibl-KNN-NH212 DIG
*=<10nIVI; **=10-25nM

BIOASSAY CHARACTERIZATION OF PEPTIDE INHIBITORS
[00711] The potency, cross reactivity, and selectivity of certain peptide inhibitors was determined using various bioassays developed for this purpose and described below.
Rat Splenocyte Assay [00712] A new assay developed was the rat splenocyte assay. This assay examined the levels of IL-17A in activated rat splenocytes following stimulation with IL-23 in the presence of test compound.
[00713] Briefly, splenocytes freshly isolated from rat were seeded in 96-well tissue culture plates in complete medium containing IL-1 ft Serial dilutions of test compounds were distributed to each well along with rat IL-23 at a final concentration that is between EC50 to EC80 values;
plates then were incubated for 3 days at 37 C in a 5% CO2 humidified incubator. Changes in IL-17A levels in the supernatants were detected using an ELISA.
Rat Colitis Model: 9 Days of 3% DSS-Containing Drinking Water [00714] There is a body of evidence in the literature supporting the pathogenic role of IL-23/IL-23R signaling in animal models of colitis. For the IL-23 ligand, this requirement has been shown in multiple models, including an IL-104- spontaneous colitis model, a Helicobacter hepaticus-driven colitis model, the anti-CD40 innate colitis model, and the chronic CD45RBh1gh CD4+ T-cell transfer model. For the IL-23 receptor, the requirement for colitis development has been shown in the acute models of colitis induced by DSS or by anti-CD40, as well as the chronic CD45RBhigh CD4+ T-cell transfer model. Since certain peptide inhibitors of the present invention do not cross react with the IL-23 receptor from mouse but do recognize that from the rat, a rat model of IBD relevant to the IL-23 pathway was developed.
1007151In this model, colitis was induced in SD rats by 9 days of ad lib exposure to drinking water containing 3% DSS. The disease activity index (DAI) score and ratio of colon weight: colon length were compared between three study groups (n=6 rats/group): vehicle, 3%
DSS, and 3% DSS with positive control (sulfasalazine administered at 100 mg/kg PO, QD). The DAI score consisted of ratings from three parameters, including percent body weight loss, stool consistency, and a quantitative hemoccult score, and could achieve a maximum value of 3 units.
DSS-exposed animals displayed significantly elevated DAI score (compared to vehicle control) from Day 4 onward, with DAI values peaking at approximately 2.5 by the end of the study (Day 9). Treatment of the DSS-exposed rats with the positive control (sulfasalazine) attenuated the disease score (compared to DSS alone) from Day 5. The differences observed in the terminal ratio of colon weight:colon length also were significant for DSS-induced disease animals with and without sulfasalazine treatment.
Ex Vivo Activity and Stability [00716] Two peptides (Compound A and Compound B) were selected for use in further biological studies (shown below). One contained a thioether linkage and the other contained a Pen-Pen disulfide bond. The activity, selectivity and ex vivo stability profiles of the two compounds are provided herein.
100717] Assays for selectivity of peptide inhibitors included a human IL-12Rb 1 ELISA and measurement of the production of IL-12 in PHA activated human PBMC, which are described briefly below.
Human IL-12Rf31 ELIS A
[00718] An assay plate was coated with 100 ng/well of human IL-12Rbl huFC and incubated overnight at 4 C. The wells were washed, blocked, and washed again. Serial dilutions of test peptides and IL-23 at a final concentration of 2.5 nIVI were added to each well, and incubated for 2 hours at room temperature. After the wells were washed, bound IL-23 was detected with goat anti-p40 polyclonal antibodies, followed by an EIRP conjugated donkey anti-goat IgG. Signals were visualized with TMB One Component EIRP Membrane Substrate and quenched with 2 M
sulfuric acid. Data from these assays is provided herein.
Production of IFNy by IL-12 in PHA Activated Human PBMC
[00719] This assay examined the ability of IL-23R antagonists to neutralize production of IFNy proteins in IL-12-stimulated human PBMCs. IL-23R peptide inhibitors specific to the IL-23/IL-23R pathway are not expected to alter the levels of IFNy produced. Compound A
and Compound B were tested in this assay, and a graph showing that they do not alter the levels of IFNy produced at most concentrations tested is provided in Figure 2.

is 0 0 ______________________ ANQ T W Q-N))1 N __ N __ N EN G-NH2 104.
Compound A

NQ
0 _________ T W N N ____ N ____ EN G-NH2 104.
Compound B
In Vivo Activity [00720] Acute colitis was induced by feeding female Sprague Dawley rats with 3% (wt/vol) DSS
dissolved in drinking water. For nine days starting at the same day as DSS, Compounds A or B
was administered orally three times per day at 20 mg/kg or 30 mg/kg. Compounds A was also administered intraperitoneally three times per day at 30 mg/kg. A neutralizing anti-IL-23p19 antibody was used as a comparator, and was administered intraperitoneally at 4 mg/kg on the same day and fifth day after starting DSS. To quantify colitis with clinical activity, disease activity index (DAI) was determined daily for each animal as an average of three parameters:
body weight change (scale 0-3), stool consistency (scale 0-3) and hemoccult blood (scale 0-3), as shown in Table E15. At necropsy, the entire colon was removed from the cecum to the rectum.
The colon was measured for length, flushed with PBS to remove feces, weighed, and opened longitudinally to determine macroscopic score. The visible damage of the colon was scored on a scale from 0-3, as shown in Table E16.
100721] Table E17 shows that at Day 7, treatment with Compound A and B
significantly improved DAI scores compared to vehicle treated group. FIG. 1 shows results for DAI values from Day 7. In addition, a significant reduction was also observed in the colon weight to colon length ratios, and colon macroscopic scores (FIG. 3). The reduction in inflammation observed with orally delivered peptides was similar to the effects observed from neutralizing anti-IL23p19 monoclonal antibody. Statistical analysis for significance was compared to the vehicle treated group and was determined using Student's T-test (GraphPad Prism). Differences were noted as signficant *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.
Table El 5. Scoring of the Disease Activity Index Score Percent Body Weight Change Stool Consistency Hemoccult Score 0 None Normal Normal 1 1 to 7 Semi solid Guaiac+
2 8 to 15 Loose Bleeding+
3 > 15 Diarrhea Bleeding++
Table E16. Scoring of Gross Morphologic Damage of the Colon Score Gross morphology 0 Normal 1 Erythemia 2 Erythemia, slight edema, small erosions 3 Two are more bleeding ulcers, inflammation, moderate adhesions 4 Severe ulceration, stenosis with dilations, severe adhesions Table E17. Disease activity index scores and the individual parameters scores at Day 7, colon weight to length ratios and colon macroscopic scores at Day 9.
Day 7 Day 9 Necropsy Colon Colon Percent Body Weight Stool Hemoccult Weight/Length Macrosopic Change Consistency Score DAI (g/cm) Score Group Mean SD Mean SD Mean SD Mean SD Mean SD
Mean SD
No DSS 11.00 2.08**** 0 0**** 0 0**** 0 0**** 75.51 7.03***
ND ND
3% DSS, 2.00 0.58 1.50 0.50 1.72 0.45 124.36 17.11 1.00 1.00 Vehicle -6.39 1.11 Anti-1.00 0.58* 0.50 0.5* 0.67 0.43** 99.96 16.19* 0.00 0**
IL23p19 mAb -0.05 1.92****
Compound 1.17 0.90 0.50 0.5* 0.56 0.46** 98.38 6.91*
0.00 0**
A, PO 3.18 2.09****
Compound 0.83 0.69* 0.67 0.47* 0.61 0.3*** 97.36 9.32*
0.00 0**
B, PO 0.13 1.24****
Compound 1.17 0.69 0.83 0.69 0.83 0.54* 104.32 12.45 0.33 0.47 A, IP -0.50 1.88***

IN VITRO ASSAYS AND SURFACE PLASMON RESONANCE (SPR) ANALYSIS
1007221 In vitro assays and SPR were performed to further characterize an illustrative compound, Compound C:

Q T W Q-N N NJ

____________________________________________________ N ____ EN G-NH2 Ac-Cyclo-[[Abti]-QTWQC]-[Phe[4-(2-aminoethoxy)]-W-[a-MeLys]-ENG-NI-12 Compound C.

[00723] Assays described in previous examples were performed to demonstrate that Compound C
is a potent, selective and competitive inhibitor of IL-23R, showing potent inhibition of IL-23-dependent upregulation of phosphor-STAT3 (pSTAT3) in human DB cells and IFNy production in human peripheral blood natural killer (PB NK) cells. In adition, Compound C
was selective, showing little inhibition in a cell free ELISA for human IL6R, or in IL-12-dependent production of IFNg in PBMC. Data is shown below in Table El 8A. Compound C also cross-reacted with cynomolgus IL-23R (IC50 7 nM) and rat IL-23R (IC50 17 nM), and inhibited IL-23-dependent IL-17A production in rat splenocytes (IC50 130 nM) (data not shown).
Table El 8A. In vitro Characterization of Compound C

pSTAT3 IFNy/PB NK IFNy/IL-12 IL-Primary Cell PBMC Cell 12Rf31 Cell ELISA Surface Assay Assay Surface Assay Compound 4 nM 27nM >100 uM >100 uM 2.4nM None [00724] Compound C exposure was also restricted to the GI following oral administration to rats does PO at 20 mg/kg, with AUC values of 355 ug.h/g for small intestine mucosa;
77 ug.h/g for colon mucosa; and 0.3 ug.h/mL for plasma, with a 40% recovery in feces.
[00725] Compound C was also stable in a variety of GI fluids and reducing environment, having a SIF half-life of > 24 h; a SGF half-life of > 24 h; a human intestinal fluid half-life of > 24 h, and a half-life of > 2 h in a DTT assay.
[00726] SPR experiments were carried out using a Biacore 2000 instrument and T100 optical biosensors equipped with Biacore CM4 and Xantec HC1500m sensor chips.
Recombinant human IL-23R huFC (RnD), or recombinant human IL-12Rf31 huFC (RnD) or a mixture of the two receptor subunits were captured on an anti-human IgG surface. Recombinant human IL-23 (Humanzyme) or Compound C was used as the analyte. SPR sensorgrams were fitted to a one to one interaction model, giving rise to a rough estimate of the association rate constant (km), dissociation rate constant (koff) and dissociation constant (KD) of the complexes, as shown in Table El 1. The data show that Compound C does not bind to IL-12Rf31, and binds to IL-23R
and the mixed surface of IL-12Rf31 and IL-23R with similar potency, at 2.42nM
and 2.56nM, respectively. This affinity for IL-23R is comparable to that from IL-23. In contrast, the affinity of IL-23 to the mixed surface is approximately 14x faster than that from Compound C.
Table E18B. Binding characteristics of IL-23 and Compound C for IL-12Rf31, IL-23R or mixed IL-12Rf31 and IL-23R as determined by SPR.
IL-23 Compound C
Surface ka(M1 sec-1) kd (sec-i) KD (um) ka(M1 sec1) kd (sec-i) KD (nM) IL-12Rbl huFC 5.01E+05 4.38E-04 0.87 does not bind up to 16.7 uM
IL-23R huFC 7.82E+05 0.00132 1.69 1.37E+07 0.033 2.42 IL-12Rbl huFC/IL-23R huFC 6.31E+05 1.15E-04 0.18 1.59E+07 0.041 2.56 1007271To further evaluate the efficacy of IL-23R antagonists in an animal model of disease, acute colitis was induced by providing 7-week-old female Sprague-Dawley rats with 60 mg/kg 2,4, 6-Trin itro benzenes Mfonic acid (TNBS) in 45%-50% ethanol (TNBS/ethanol) administered intrarectally at Day 0. Compound C (described in Example 7) was administered orally three times a day at 20 mg/kg or 6.7 mg/kg and was provided in drinking water at 0.6 mg/mL or 0.2 mg/mL, respectively, for 8 days starting approximately 24 hours (Day -1) prior TNBS
inoculation. A neutralizing anti-IL-23p19 antibody was used as a comparator, and was administered intraperioneally at 4 mg/kg on Day -1 and again on Day 3. All animals received orally PBS (pH 7.4) vehicle which was used to formulate Compound C. The study design in shown in Figure 5.
1007281 To assess the extent of the inflammatory response, animals were observed daily for clinical signs which included percent body weight loss and signs of loose stools or diarrhea. Six days after inoculation of TNBS, rats were sacrificed and the entire colon length and colon weight from cecum to rectum from each animal were recorded. The severity of colitis was evaluated by a pathologist blinded to the identity of treatments. In addition to the colon wall thickness, the gross colon damage was scored on a 0-4 scale according to Table E19 below, and histopathological scores were determined based on below parameters (Tables E20 and E21).
Table El 9. Definitions for colon macroscopic scores Score Colon Gross Morphology 0 Normal 1 Erythema 2 Erythema, slight edema, small erosions 3 Two or more bleeding ulcers, inflammation, moderate adhesions 4 Severe ulceration, stenosis with dilations, severe adhesions Table E20. Definitions for histopathology Parameter Definition Extent and severity of inflammatory cells infiltration, localized and/or diffuse involving full thickness of the colon section (transmural). Inflammatory cells include polymorpho-nuclear leukocytes (neutrophils), mononuclear cells Inflammation (macrophages + lymphopcytes), fibroplasia and neovascularization.
Necrosis in the mucosa with loss of surface epithelium, hemorrhage and cellular Mucosal debris; measured as the length of the lesion on the total length of the colon Necrosis section to determine % area affected Gland Loss % crypt epithelial degeneration with or without superficial mucosal erosion Colon the average thickness of the colon measured transmurally (full thickness) from Thickness the mucosal surface to the serosa Table E21. Scoring criteria Score Inflammation 0 Normal tissue, no inflammation Very minimal localized infiltrates in the superficial mucosa affecting <2% of the 0.5 colon section Minimal degree of multifocal infiltrates in the mucosa affecting approximately 1 - 10% of the colon section Mild degree of multifocal infiltrates in the mucosa, submucosa, outer muscle 2 band, and serosa affecting approximately 11 - 25% of the colon section Moderate degree of multifocal infiltrates in the mucosa submucosa, outer 3 muscle band and serosa affecting approximately 26 - 50% of the colon section Marked degree of multifocal to diffuse infiltrates in the mucosa submucosa, 4 outer muscle band and serosa affecting approximately 51- 75% of the colon section Sever degree of multifocal to diffuse infiltrates in the mucosa submucosa, outer muscle band and serosa affecting approximately >75% of the colon section Score Mucosal Necrosis 0 No Necrosis 0.5 Very minimal and localized region affecting <2% of the total colon section 1 Minimal focal to multifocal regions affecting 2 - 10% of the total colon section 2 Mild focal to multifocal regions affecting 11 - 25% of the total colon section Moderate focal to multifocal regions affecting 26 - 50% of the total colon 3 section 4 Marked focal to multifocal regions affecting 51 - 75% of the total colon section 5 Severe focal to multifocal regions affecting >75% of the total colon section Score Gland Loss 0 No loss, normal crypt epithelium and mucosa 0.5 Very minimal loss not exceeding 1 - 2 regions of mucosa/gland affected 1 Minima1,1-10% regions of mucosa/gland affected 2 Mild, 11-25% regions of mucosa/gland affected 3 Moderate, 26-50% regions of mucosa/gland affected 4 Marked, 51-75% regions of mucosa/gland affected 5 Severe, >75% regions of mucosa/gland affected Score Colon Thickness 0 Normal = <350 microns or less 0.5 Very Minimal = 351-400 microns 1 Minimal = 400- 500 microns 2 Mild = 501 - 600 microns 3 Moderate = 601 - 700 microns 4 Marked = 701 - 800 microns 5 Severe = >801 microns 1007291 Compared to the sham group, rats challenged with TNBS suffered acute weight loss, displayed increased incidence of loose stools, and increased colon weight to length ratio. These data were confirmed by the macroscopic examination of colon which revealed mild colonic injury characterized by erythema, edema and small erosions. Treatment with Compound C
attenuated these changes as compared to the TNBS colitis group. At the high dose, Compound C
was significantly effective in reducing the colon weight to length ratio, diminishing the thickness of the colon walls, and more importantly, improving the colon gross pathology scores to normal in 70% of the animals. Statistical significances were observed at the low dose in all above indications except colon wall thickness although a trend was evident. The reduction in inflammation observed with orally delivered Compound C was similar to the effect observed from the neutralizing anti-IL-23p19 monoclonal antibody (Figure 6).
[00730] Histological examination of H&E stained distal colons show that the majority of the lesions observed from the vehicle group are transmural, characterized by necrosis with inflammatory cells transversing the entire thickness of the colon, presence of necrotic tissue debris on the lumen surface, and mucosa devoid of crypts. The animals treated with Compound C generally showed localized lesions limited in the mucosa and submucosa regions, with colon tissues showed potential signs of healing at sites of necrosis. Specifically, the animals treated with 160 mg/kg/d Compound C showed a significant reduction in inflammation, mucosal necrosis and colon wall thickness leading to a significant reduction in the overall histological score, comparable to that from the anti-IL-23p19 antibody control (FIG. 7).
[00731] Concentration analysis of samples collected 1 hour post the last PO
dose show that the plasma concentrations of Compound C detected from all animals are <=2X below the IC75 of the compounds as determined in the rat splenocyte/IL-17A cell based assay or the rat IL-23R
ELISA, suggesting that the efficacies observed from oral treatment are most likely due to its local activity at the colon (see FIG. 8). Collectively, these data highlights the protective effect of an IL-23R antagonist in the development of TNBS colitis.
[00732] These studies demonstrate that peptides of the present invention are potent, selective and orally efficacious IL-23R peptide antagonists that are promising therapeutics for the treatment of IBD and other disorders. As shown herein, the present invention provides petpides that are:
potent blockers of IL-23/IL-23R signaling in a human cell line and in human primary cells;
selective for IL-23R, and do not inhibit binding to IL-6R or signaling through IL-12R; cross-reactive towards rat and cynomolgus but not mouse homologs, enabling in vivo studies in these species; resistant to proteolytic and reducing environments of the GI, resulting in high drug levels in the intestinal tissues and limited drug concentrations in the circulation, offering potential safety advantages over systemically delivered therapeutics; and effective and comparable to an anti-IL23p19 monoclonal antibody in attenuating colitis in a TNBS-induced rat colitis model, most like through GI-restricted activities.

[00733] To evaluate the properties of efficacy the IL-23R peptide antagonist of SEQ ID NOS:
980 (Peptide 980), 993 (Peptide 993), and 1185 (Peptide 1185) experiments to determine potency, selectivity, and stability of the peptides were performed as described above. The IC50 values of the peptides as measured by quantitative ELISA for IL-23/IL-23R
competitive binding assays (performed as described above in Example 2) for human (Hu), cynomolgus monkey (Cyno), and rat (Rat) IL-23 and IL-23R binding are shown in Table E22. The potencies of the peptides were also evaluated by IL-23R activity assays as described above. The IC50 values of the peptides as determined by the reduction of phospho-STAT3 (pSTAT3) levels in human DB
cells exposed to IL-23 (Hu DB Cell (pSTAT3); performed as described above in Example 2); by the reduction of IFNy produced by human NK cells exposed to IL-23 (Hu NK cell;
performed as described above n Example 5); and by the reduction of IL-17A produced by activated splenocytes exposed to IL-23 (Rat(spleen); performed as described above in Example 6).
Selectivity was evaluated by measuring the IC50 of the peptides for inhibiting human IL-23/IL-12R betal interactions (see Example 4) or human IL-6/IL-6R interactions (see Example 6). The stabilities of the peptides were determined by measuring the half-life of the peptides exposed to simulated intestinal fluid (SIF), simulated gastric fluid (SGF), or human intestinal fluid (SIF).
Table E22. Properties of illustrative IL-23R antagonists Peptide :=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=.:1::=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:
=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:11.:::=:=:=:=:=:=:=:=:=:=:=:=:=:=:=
:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:
=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=*=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=
:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=p:=:=:=:=:=:=
:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:=:
=. EL1SA all ass* Seleen% it). Stabilil .
.
.
.
.
.
.
.
.
.
.
.
.
(n.1\1) 011\4) (EL ISA, 111\1) 0 1 2. hr) =
=.
.
.................................... .............. ............
.......... ........
Hu DB Cell Hu NK Rat IL-23/ IL-6/
iL
Peptide Hu C' to Rat , SIF SGF HIP (pSTAT.1) cell (Spleen) IL-12R11 IL-6R
..
' ' I === ===
I I
Peptide 2.0 2.0 2.0 0.6 2.2 18.3 >100,000 >100,000 12 6 24 Peptide 1 1.3 3 0.6 2.8 11.5 >100,000 >100,000 11 10 Peptide 2 3 3 2 3.9 35 >100,000 >100,000 33 12 24 The structure of Peptide 993 is shown below:
kit*
et e.' Ci=--9.
Ni=4 .,:ei ,...: , e, N. =-1 N.. e 0 L
0 I ''' q 1 I . 0 1 0 0 _,.11õ , N ii, A. I, it.õ xii JJ. ,:. A, 3 ,Il 1,, , .,," 4õ. - lc ,,,....,,, .y, N. , .<.= .
14... .. N.,...,,,,,, 4NN:z.
1: N 4 14 i I
' 41 ..-,:f: . .e I 1%, I. N
0.*-= N'r'''' y t¨

is. .i.:
re-- .
: .
...,..

, .
ligit 0 hir HztisrAs'W
Ac-[(D)-Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-N1-12 (SEQ ID NO: 993) The structure of Peptide 1185 is shown below:

f r ,,lot, 41. ,,,,.:9-, tõ,,--0 mt., .,..,1 .=., õA' i'-'7 $7.ff=
tt.tti Akb Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]- [2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 (SEQ ID NO: 1185) The structure of Peptide 980 is shown below:
r r ..),,..õ
I.....'.. NH ,.,..,t,N.y,40 14.1 . , .1 D
" - 1 I
tit i4 õ..., 9 .0 0 gi i ( Iii . ,....1,,, a=C .N. , N.,,Arte .--N-,,,õ"4,1r4- x-R---,-õ,,,k, ,--e-N--,..A"
...¨ci,.
,,.
,sp .-s=
$

111:1*, N ).. fik#1' NN'ee' . hill I lia- 0 L?) i Ac-Cyclo-[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 (SEQ ID NO: 980) [00734] The results summarized in Table E22 indicate that the peptides potently and selectively inhibit IL-23/IL-23R binding as compared to IL-23/IL-12R betal or IL-6/IL-6R
interactions.
This inhibition was confirmed with cell culture assays that measure the IL-23R-dependent such as STAT3 phosphorylation, IFNy production, and IL-17A production. The peptides were also determined to have a high degree of stability when exposed to simulated intestinal fluid, simulated gastric fluid, or human intestinal fluid.
1007351 Data from the Human DB Cell (pSTAT3) experiment were used for S child analysis (see FIG. 17). For Schild analysis, concentrations of 0.3nM, 1nM, 3nM, 1 OnM, 30nM, 100nM of Peptide 993 were tested. The Schild slope was determined to be 1.068, indicating that Peptide 993 behaves as a simple competitive antagonist. S child analysis was also performed on a peptide with the structure of SEQ ID NO: 1169, which is highly similar to the stuctures of Peptide 1185.
The Schild slope was determined to be 0.91, indicating that peptides with similar structure, including Petide 1185, are likely behave as a simple competitive antagonist.
Schild analysis was also performed on the peptide of SEQ ID NO: 1211, which has a structure similar to to Peptide 980. The Schild slope was determined to be 0.76. However, when the slop was fixed to 1, the R2 value was 0.975. These data suggest that peptides with similar structure, including Petide 1185, could behave as a simple competitive antagonist.

[00736] Pharmacokinetic properties of example peptides were measured in vivo.
Sprague Dawley rats were administered Peptide 993 at 10 mg/kg P.O.
1007371A single oral dose of Peptide 933 was administered to normal female Sprague-Dawley rats (N=3 rats per time point) either with or without a drinking water dose that was provided ad libitum (see FIG. 11). Following the oral dose, the exposure of Peptide 993 was determined in the plasma at 0.25, 0.5, 1, 3, 6, 8, and 24 hours post-dose. The levels of Peptide 993 were also determined in small intestine, colon, small intestine mucosa, colon mucosa, small intestine mucus, Peyer's patch and Mesenteric Lymph Node (MLN) at 1, 3, 6, 8 and 24 hours post-dose.
Urine and feces were collected at 6 and 24 hours to determine the excretion of Peptide 993.
Plasma, feces, and tissue samples were stored at ¨80 10 C prior to analysis. For plasma, 50 [IL of the sample was used to extract compound by means of protein precipitation using a quench solution (MeOH:ACN w/ 0.1% formic acid, 50:50 volume) with internal standard.
For feces, samples were homogenized with 0.1% Formic acid in water (water:feces ratio of 4:1) prior to extraction. 50 [IL of fecal homogenate was used to extract compound by means of protein precipitation using a quench solution (MeOH:ACN w/ 0.1% formic acid, 50:50 volume) with internal standard. For tissues such as colon or small intestine, samples were homogenized with 0.1% Formic acid in water (water:tissue ratio of 3:1) prior to extraction. For tissue such as Peyer's Patch and Mesenteric Lymph Nodes, samples were homogenized with 0.1%
Formic acid in water (water:tissue ratio of 20:1) prior to extraction. 50 [IL of tissue homogenate was used to extract compound by means of protein precipitation using a quench solution (MeOH:ACN w/
0.1% formic acid, 50:50 volume) with internal standard. The precipitated protein was removed by filter plate and the collected supernatant was dried and reconstituted.
Processed samples were analyzed on an AB/MDS Sciex API 4000 mass spectrometer. Positive ions were monitored in the multiple reaction-monitoring (MRM) mode. Quantitation was by peak area ratio.
[00738] No detectable levels of Peptide 993 were observed in rat plasma between 0 and 24 hours following administration (see FIG. 11A). In contrast, detectable levels of Peptide 993 were present in the Peyer's Patch and small intestine for at least six hours (see FIGS. 11B and 11C), and for at least 8 hours in the colon post-dose administration (see FIG 11D).
Levels greater than 5% of the total administered dose of Peptide 993 were detected in the rat feces at 24 hours following administration, further indicating that Peptide 993 has a high degree of oral stability.
Taken together, these results demonstrate that Peptide 993 is an orally stabile GI restricted peptide, that demonstrates a high GI content and limited systemic distribution following oral administration.
[00739] Sprague Dawley rats were administered Peptide 1185 at 10 mg/kg P.O. A
single oral dose of Peptide 1185 was administered to normal female Sprague-Dawley rats (N=3 rats per time point). Following the oral dose, the exposure of Peptide 1185 was determined in the plasma in samples taken up to 8 hours post-dose. Urine and feces were collected to hours to determine the excretion of Peptide 1185 (FIG 18).
[00740] Sprague Dawley rats were administered Peptide 980 at 10 mg/kg P.O. A
single oral dose of Peptide 980 was administered to normal female Sprague-Dawley rats (N=3 rats per time point). Following the oral dose, the exposure of Peptide 980 was determined in the plasma in samples taken up to 8 hours post-dose. Urine and feces were collected to hours to determine the excretion of Peptide 980 (FIG 19).

1007411 Saftey profiles of illustrative peptide inhibitors were characterized.
Peptide 993 and Peptide 1185 were evaluated in a safety panel examining binding to a panel of 44 targets. The targets included G protein coupled receptors (GPCRs), transporters, e.g., dopamine transporter (DAT), and ion channels. For all targets, these peptides displayed no activity, as defined by a change (inhibitory or stimulatory) in the target's activity of greater than 25%. The targets tested in the safety panel are listed in Table E24. For each target, Peptide 993 and Peptide 1185 was determined to be inactive at concentrations of up to 10 M. The safety profile of Peptide 980 was evaluated by testing compounds selected from Table E24. For all compounds tested, Peptide 980 showed only moderate activity in the acetylcholinesterase assay (33%), and otherwise did not display any activity, as defined by by a change in the target's activity of greater than 25%.
Table E24. Peptide 993 and Peptide 1185 are Inactive in a Safety Panel Panel of 44 targets 2+
alphaiA delta2 (DOP) Ca channel (L, dihydropyridine site) alpha2A kappa (KOP) hERG (membrane preparation) beta mu (MOP) K channel beta2 5-HT1A Na channel (site 2) CCK (CCKA) 5-HT

2B Lck kinase Via COX

D2S dopamine transporter (DAT) COX2 norepinephrine transporter ETA (NET) acetylcholinesterase Panel of 44 targets 5-HT transporter (SERT) MAO-A
H2 BZD (central) PDE3A

N neuronal a4132 EFFECTS OF AN ILLUSTRATIVE PEPTIDE INHIBITOR IN A RAT MODEL OF ACUTE COLITIS
[00742] To evaluate the efficacy of the illustrative peptide inhibitor Peptide 1185 in an animal model of disease, acute colitis was induced by providing 7-week-old female Sprague-Dawley rats with 64 mg/kg TNBS in 50% ethanol administered intrarectally at Day 0.
Peptide 1185 was administered orally 37mg/kg/day (combined PO and in drinking water), PO BID, day -1 to day 7.
A sham group that was not exposed to TNBS and a TNBS treated group that received treatment with vehicle were used as control groups. For comparators, neutralizing anti-IL-23p19 antibody was administered intraperioneally at 4 mg/kg on Day -1 and again on Day 3, and prednisolone was administered at 10 mg/day P.O. All animals received orally water as the vehicle which was used to formulate Peptide 993.
[00743] As described above, animals were observed daily for clinical signs which included percent body weight loss and signs of loose stools or diarrhea. Six days after inoculation of TNBS, rats were sacrificed and the entire colon length and colon weight from each animal were recorded. The severity of colitis was evaluated by a pathologist. In addition to the colon wall thickness, the gross colon damage was scored on a 0-5 scale according to Table E29, and histopathological scores were determined based on the parameters listed in Table E30.
[00744] Treatment with Peptide 1185 significantly reduced some of the disease parameters that were observed in the TNBS rat model of acute colitis. While rats in the sham group continued to gain weight over the course of the study, rats exposed to TNBS and treated with vehicle experienced weight loss. Oral treatment with prednisolone or systemic treatment with anti-IL-23p19 prevented the weight loss in TNBS exposed rats. Treatment with orally administered Peptide 1185 did not significantly prevent the weight loss in TNBS challenged rats (see FIG. 13).
A significant reduction was also observed in the colon weight to colon length ratios following treatment with prednisolone or anti-IL-23p19 as compared to treatment with vehicle. Oral administration of Peptide1185 resulted in similar reductions of colon weight to colon length ratios and colon macroscopic scores in TNBS exposed rats. Higher colon macroscopic scores indicated a higher degree of colon pathology. The colon macroscopic score was determined by adding the scores for adhesion, strictures, ulcer, and colon wall thickness, all of which were significantly reduced by treatment with prednisolone, anti-IL-23p19, or Peptide 1185, as compared to vehicle treated controls. These data demonstrate that oral administration of Peptide 1185 has comparable efficacy to systemic administration of anti-IL-23p19 monoclonal antibody.
1007451 The pathological features of tissue sections from colon taken from rats in the sham, vehicle, anti-IL-23p19, and Peptide 1185 groups were examined. Mucosal inflammation, transmural inflammation, gland loss, and erosion were scored according to the criteria listed in Table E29 For all of these features, treatment with anti-IL-23p19 or Prednisolone reduced the histopathology scores associated with TNBS exposure. Treatment with Peptide 1185 did not significantly reduce the histopathology scores.

EFFECTS OF AN ILLUSTRATIVE PEPTIDE INHIBITOR IN A RAT MODEL OF ACUTE COLITIS
1007461 To evaluate the efficacy of the illustrative IL-23R peptide inhibitor Peptide 993 in an animal model of disease, acute colitis was induced by providing 7-week-old female Sprague-Dawley rats with 64 mg/kg TNBS in 50% ethanol administered intrarectally at Day 0. Peptide 993 was administered orally two times a day at 10 mg/kg, for a total of 42 mg/kg per day, for 8 days starting approximately 24 hours (Day -1) prior TNBS inoculation. A sham group that was not exposed to TNBS and a TNBS treated group that received treatment with vehicle were used as control groups. All animals received orally water as the vehicle which was used to formulate Peptide 993.
1007471 As described above, animals were observed daily for clinical signs which included percent body weight loss and signs of loose stools or diarrhea. Six days after inoculation of TNBS, rats were sacrificed and the entire colon length and colon weight from each animal were recorded. The severity of colitis was evaluated by a pathologist. In addition to the colon wall thickness, the gross colon damage was scored on a 0-5 scale according to Table E29, and histopathological scores were determined based on the parameters listed in Table E30.
1007481 Treatment with Peptide 993 significantly reduced all disease parameters that were observed in the TNBS rat model of acute colitis. While rats in the sham group continued to gain weight over the course of the study, rats exposed to TNBS and treated with vehicle experienced weight loss. Treatment with orally administered Peptide 993 also prevented the weight loss in TNBS challenged rats (see FIG. 12). In addition, a significant reduction was also observed in the colon weight to colon length ratios following treatment with oral administration of Peptide 993.
Higher colon macroscopic scores indicated a higher degree of colon pathology and was significantly reduced by treatment with Peptide 993, as compared to vehicle treated controls.
Oral administration of Peptide 993 has comparable efficacy to systemic administration of anti-IL-23p19 monoclonal antibody, which served as a positive control.
Histopathological scores were significantly reduced in colons from Peptide 993 treated rats as compared to vehicle group.

EFFECTS OF AN ILLUSTRATIVE PEPTIDE INHIBITOR IN A RAT MODEL OF ACUTE COLITIS
1007491 To evaluate the efficacy of the illustrative IL-23R peptide inhibitor Peptide 980 in an animal model of disease, acute colitis was induced by providing 7-week-old female Sprague-Dawley rats with 64 mg/kg Ti\TBS in 50% ethanol administered intrarectally at Day 0. Peptide 980 was administered orally 37mg/kg/day (combined PO and in drinking water), PO BID, day -1 to day 7. A sham group that was not exposed to TNBS and a TNBS treated group that received treatment with vehicle were used as control groups. All animals received orally PBS as the vehicle which was used to formulate Peptide 980.
1007501 As described above, animals were observed daily for clinical signs which included percent body weight loss and signs of loose stools or diarrhea. Six days after inoculation of TNBS, rats were sacrificed and the entire colon length and colon weight from each animal were recorded. The severity of colitis was evaluated by a pathologist. In addition to the colon wall thickness, the gross colon damage was scored on a 0-5 scale according to Table E29, and histopathological scores were determined based on the parameters listed in Table E30.
Treatment with Peptide 980 significantly reduced all disease parameters that were observed in the TNBS rat model of acute colitis.
1007511Treatment with orally administered Peptide 980 prevented the weight loss in TNBS
challenged rats (see FIG. 14). In addition, a significant reduction was also observed in the colon weight to colon length ratios following treatment with oral administration of Peptide 980.
Higher colon macroscopic score indicates a higher degree of colon pathology, and was significantly reduced by treatment with Peptide 980, as compared to vehicle treated controls (see FIG. 14).
1007521Pathological features of tissue sections from colon taken from rats in the sham, vehicle, and Peptide 980 treated groups were examined.
Mucosal inflammation, transmural inflammation, gland loss, and erosion (see FIG. 14D) were scored according to the criteria listed in Table E30. The sum of the histopathology score was significantly reduced by Peptide 980 treatment as compared to vehicle.

LEVELS OF BIOMARKERS FOLLOWING TREATMENT WITH PEPTIDE INHIBITORS IN
A RAT MODEL OF ACUTE COLITIS
1007531 Levels of inflammatory markers were examined in the colons. The distal colon tissue samples, designated for protein expression analysis, were flash frozen after collection. For protein extraction, the samples were thawed, weighed and homogenized in the extraction buffer (PBS pH 7.2 supplemented with Protease Inhibitors, 3x volume:weight). The homogenates were centrifuged at 13krpm at 4 C for 15 minutes, a total of two times to remove the debris. The supernatants were saved in multiple aliquots in -80 C and subsequently used for protein expression analysis on ELISA. The total protein in each sample was quantified using BCA assay.
MPO, IL-1(3, IL-6, IL-17A and IL-22 protein expression in the distal colon samples were analyzed using commercially available rat ELISA kits.
[00754] Treatment with Peptide 993 reduced levels of inflammatory markers present in the colon.
The disease defining (MPO, IL-6 and IL- 1 beta) and IL-23 directed biomarkers (IL-22, and IL-17A) were reduced by treatment with Peptide 993 as compared to vehicle treated controls (see FIG. 15). These data demonstrate that administration of Peptide 993 in amounts that can reduce pathology in vivo also decrease levels of biomarkers present in the colon that are associated with IL-23R activity. Treatment with Peptide 980 reduced levels MPO and IL-22 as compared to vehicle treated controls (see FIG. 16). Treatment with Peptide 1185 at the dose tested did not significantly reduce levels of MPO, IL-22, or IL-17A.
Table E29. Colon Macroscopic Score Colonic Score Parameter r¨ihe alues for each amma was surnmed to obtain the colonic,:scoreltnaxinium...value..T7 Adhesions:
none =0 minimal = 1 involving several bowel loops = 2 Strictures:
none =0 minimal = 1 mild = 2 severe, proximal dilatation = 3 Ulcers:
none focal hyperemia, no ulcers = 1 ulcer without significant inflammation (hyperemia and bowel wall thickening = 2 ulceration of 1- <3 cm = 3 ulceration 3- <6 cm = 4 ulceration > 6 cm = 5 Wall thickness:
Wall thickness:
less than 1 mm = 0 1-3 mm= 1 > 3 mm = 2 Table E30a. Histopathology - Mucosal/Submucosal Inflammation Score Mucosal/Submucosal Inflammation Score The extent of macrophage, lymphocyte, neutrophil and other inflammatory infiltrateswas assigned severity scores according to the following criteria:
0= Normal 1=Minimal, larger focal area with MNIC and neutrophils or minimal diffuse,no separation of glands, may be mostly in areas of submucosal edema or mesentery 2=Mild, diffuse mild, or multifocal affecting 11-25% of mucosa with minor focal ormultifocal gland separation, no separation in most areas 3=Moderate, 26-50% of mucosa affected with minimal to mild focal ormultifocal separation of glands by inflammatory cell infiltrate, milder in remaining areasof mucosa with some areas having no gland separation by inflammation 4=Marked, 51-75% of mucosa affected with mild to moderate separation of glandsby inflammatory cell infiltrate, minimal to mild in remaining areas of mucosa but allglands have some separation by infiltrate 5=Severe, 76-100% of mucosa affected with moderate to marked areas of gland separation by inflammatory cell infiltrate, mild to moderate in remaining areas of mucosa Table E30b.
Mucosa! Thickness Score Mucosal thickness was scored in the colon in a non-tangential area of the section that best represented the overall mucosa!
thickness. This parameter is indicative of gland elongation and mucosa! hyperplasia. A hyperplasia score was determined as follows.
- =No mucosa present 0= Normal 1= Minimal, 5-10% thicker than control mucosa 2=Mild, 11-25% thicker than control mucosa 3=Moderate, 26-50% thicker than control mucosa 4=Marked, 51-75% thicker than control mucosa Table E30c.
Transmural Inflammation Presence of inflammatory cell infiltrates within the tunica muscularis mucosa and increased fibroblasts/fibrocytes with perpendicularly arranged blood vessels (granulation tissue), possibly extending to the serosa.
0= Normal 1=Minimal, 5-10% infiltration 2=Mild, 11-25% infiltration 3=Moderate, 26-50% infiltration 4=Marked, 51-75% infiltration 5=Severe, infiltrates reach the serosa and mesentery Table E30d.
Gland Loss Score Crypt epithelial and remaining gland epithelial loss was scored based on the approximate percent of the mucosa that was affected as follows:
0=None 1=Minimal, 1-10% of the mucosa affected 2=Mild, 11-25% of the mucosa affected 3=Moderate, 26-50% of the mucosa affected 4= Marked, 51-75% of the mucosa affected 5=Severe, 76-100% of the mucosa affected Table E30e.
Erosion Score The loss of surface epithelium was scored based on the approximate percent of the mucosa thatwas affected as follows.
0=None 1=Minimal, 1-10% of the mucosa affected 2=Mild, 11-25% of the mucosa affected 3=Moderate, 26-50% of the mucosa affected 4= Marked, 51-75% of the mucosa affected 5=Severe, 76-100% of the mucosa affected Table E3 Of.
Histopathology Sum A sum of inflammation, gland loss, erosion, and transmural inflammation scores was calculated.

1007551 Peptide optimization was performed to identify additional peptide inhibitors of IL-23 signalling that were active at low concentrations (e.g., IC50 <10 nM) while exhibiting gastrointestinal (GI) stability. Certain peptides were tested to identify peptides that inhibit the binding of IL-23 to human IL-23R and inhibit IL-23/IL-23R functional activity, as described below. Peptides tested included peptides containing a variety of different cyclization chemistries, including, e.g., peptides containing a disulfide linkage, e.g., between two Pen residues, and peptides containing a thioether linkage. Peptide inhibitors of the present invention include but are not limited to peptides having any of the structures depicted herein. In addition, peptide inhibitors of the present invention include those having the same amino acid sequence of the peptides or structures described herein, without being required to have the same or any N- or C-terminal "capping" groups, such as, e.g., Ac or NH2.
[00756] Assays performed to determine peptide activity were performed as described in Example 2 above. Human ELISA indicates the 1L23-IL23R competitive binding assay, Rat ELISA
indicates the rat IL-23R competitive binding ELISA assay, and pStat3HTRF
indicates the DB
cells IL-23R pSTAT3 cell assay. The peptides depicted in Table E31 are cyclized via a disulfide bridge formed between two residues in these peptides. The peptides depicted in Table E32 are cyclized via a thioether bond between the indicated amino acid residues. Table E32 provides an illustrative structure depicting thioether cyclization, which may also be indicated in the table by the term "Cyclo," with the cyclic region bracketed immediately following.
Table E31. Illustrative Peptides Containing the Ac-[Pen]-)0(WX-[Pen]-)000( Motif and Analogues SE Q Human Rat pStat3 ID Sequence ELISA ELISA HTRF
NO:
(nM) (nM) (nM) [PalmHisoGluHPEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-1115 **
[2-Nall-[Aib]-[Lys(Ac)]-NN-NFI2 1116 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-[Lys(PEG4-isoGlu-Palm)]-NN-NH2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-NalHa-MeLys(Acil-1117 **
[Lys(Ac)]-NN-N H2 [OctanylHlsoGluHPEG4HPerd-NTWQ-[PenHPhe[4-(2-1118 **
arninoethoxy)]-[2-NalHAibHLys(Ac)]-NN-NH2 [Octany1HPEG4HPerd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-1119 **
NalHAilDHLys(Ac)]-NN-N H2 [PalmHPEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-1120 *
[AilD]-[Lys(Ac)l-NN-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1121 ** *
[Lys(PEG4-OctanyI)]-NN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1122 *
[Lys(PEG4-Palm)]-NN-NH2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-Palm)]-[2-1123 ***
Nal]-[Aibl-[Lys(Ac)]NN-NFI2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-Laury1)]-[2-1124 **
Nal]-[Aib]-[Lys(Ac)]-NN-N H2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-NalHa-[a-Palm)-1125 *
[Lys(Ac)]-NN-N H2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-NalHa-[a-1126 *
LauryI)]-[Lys(Ac)]-NN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-IsoGlu-1127 ***
Palm)]-[2-Nal]-[Aibl-[Lys(Ac)]-NN-NFI2 Ac-[Pen]-NTWQ-[Pen]- [Phe[4-(2-aminoethoxy)-(PEG4-lsoGLu-***
Laury1)]-[2-Nal]-[AibHLys(Ac)]-NN-N H2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-NalHa-[a-1129 ** *
IsoGlu-Palm)]-[Lys(Ac)]-NN-N H2 Ac-[Per]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-a-Me-K(PEG4-IsoGlu-1130 *
LauryI)]-[Lys(Ac)]-NN-NH2 Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-NalHa-[a-1131 ** *
[Lys(Ac)]-NN-N H2 Ac-[Per]-QTWQ-[Pen]-phe(4-CONH2)-[2-NalHa-MeLys(Biotinil-1132 * ** *
[Lys(Ac)]-NN-N H2 Ac-[Pen]-QTWQ-[Pen]-phe(4-CONH2)-[2-NalHa-MeLys(Octanylil-1133 ** *
[Lys(Ac)]-NN-N H2 Ac-[Pen]-[Lys(IVA)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-1134 ** *
[AilD]-[Lys(Ac)l-NN-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1135 *
[Lys(Ac)]-[Lys(IVA)]-N-NFI2 Ac-[PenHLys(Biotin)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-1136 ** *
[AilD]-[Lys(Ac)l-NN-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1137 **
[Lys(Ac)]-[Lys(Biotin)]-N-NH2 Ac-[Pen]-TWQ-[PenHPhe[4-(2-aminoethoxy)]-[2-1138 **
Nal]-[Aib]-[Lys(Ac)]-NN-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1139 **
[Lys(AO]-[Lys(octany1)1-N-N H2 Ac-[PenHLys(Palm)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--1140 >1000 [AilD]-[Lys(Ac)l-NN-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1141 >1000 [Lys(Ac)]-Lys(Palm)l-N-NH2 Ac-[PenHLys(PEG8)1-TWQ-[Per]-[Phe[4-(2-arninoethoxy)H2-Nall--1142 **
[AilD]-[Lys(Ac)]-NN-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall--[Aib]-1143 **
[Lys(Ac)]-[Lys(PEG8)1-N-NFI2 Ac-[Per]-K(Peg11-Palm)TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-1144 **
NalHAilDHLys(Ac)]-NN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall--[Aib]-1145 **
[Lys(Ac)]-[Lys(Peg11-palm)]-N-N H2 Ac-[Pen]-TW-[CitHPenHPhe[4-(2-[Pen]-Nall--1146 * *
[AilD]-[Lys(Ac)]-NN-NFI2 Ac-[Pen]-[Lys(Ac)]-TW-[Cit]-[Perd-[Phe[4-(2-aminoethoxy)]-[2-Nall-1147 ** *
[AilD]-[Lys(Ac)]-NN-NFI2 Ac-[Per]-NT-[Phe(3,4-0CF13)2]-Q-[PenHPhe[4-(2-aminoethoxy)H2-1148 ¨1000 NalHAilDHLys(Ac)]-NN-N H2 Ac-[Pen]-NT-[Phe(2,4-CF13)2]-Q-[Pen]-(2-aminoethoxy)H2-1149 ***
NalHAilDHLys(Ac)]-NN-N H2 Ac-[Per]-NT-[Phe(3-CH3)]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall--***
[AilD]-[Lys(Ac)]-NN-NFI2 Ac-[Per]-NT-[Phe(4-CH3)]-Q-[PenHPhe[4-(2-aminoethoxy)H2-Nall-1151 ***
[AilD]-[Lys(Ac)]-NN-NFI2 Ac[(D)Arg]-[Perd-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall--1152 * * *
[AilD]-[Lys(Ac)]-N-[13Ala]-NH2 Ac-[(D)Tyr]-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-1153 * * *
[AilD]-[Lys(Ac)]-N-[13Ala]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1154 *
[Lys(Ac)]-QN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1155 *
[Lys(Ac)]-[Lys(Ac)]-N-NE12 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1156 *
[Lys(Ac)]-N-[Lys(Ac)]-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1157 ** *
[Lys(Ac)]-QQ-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1158 ** *
[Lys(A0]-Q-[PAIa]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1159 *
[Lys(Ac)]-N-[Cit]-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1160 ** *
[Lys(Ac)]-[Cit]-NNFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1161 *
[Lys(Ac)]-[ati-Q-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1162 **
[Lys(Ac)]-[Cit]-[Lys(Ac)]-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1163 **
[Lys(Ac)]-[Lys(Ac)]-[Cit]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-QN-1164 * * *
[13Ala]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-E-[Cit]-1165 *

Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1166 * *
CitNCitNH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibHCitl-1167 *
Q-[Cit]-NH2 Ac-[PenHCitl-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1168 * *
[Lys(Ac)]-NN-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-[Lys(Ac)]-NN-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-QNN-1170 * *

Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-ENQ-1171 ** *

Ac-[Per]-GPWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1172 >1000 [Lys(Ac)]-NN-N H2 Ac-[Per]-PGWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-[Lys(Ac)]-NN-N H2 Ac-[Per]-NTWN-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1174 **
[Lys(Ac)]-NN-N H2 Ac-[Per]-NSWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1175 *
[Lys(Ac)]-NN-N H2 Ac-[Per]-N-[Aib]-WQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1176 >1000 [Lys(Ac)]-NN-N H2 Ac-[Per]-NTW-[Aib]-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1177 **
[Lys(Ac)]N-[Aib]-NH2 Ac-[Per]-QTW-[Lys(Ac)]-[Pen]-[Phe[4-(2-aminoethoxy)H2-Nall-1178 * *
[AilD]-[Lys(Ac)l-NN-NH2 Ac-[Pen]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-Nall--1179 *
[AilD]- [Lys(Ac)]NNNH2 Ac-[Per]-QVWQ-[PenHPhe[4-(2-aminoethoxy)H2-NalHAibl-1180 *
[Lys(Ac)]-NN-N H2 Ac-[Per]-NT-[2-Nal]-Q-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1181 **
[Lys(Ac)]-NN-N H2 Ac-[Per]-NT-[1-Nal]-Q-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHAibl-1182 **
[Lys(Ac)]-NN-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-NalHa-MeLeul-1183 * * *
[Lys(Ac)]-NN-N H2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)H2-[2-MeLys]-[a 1184 * * *
[Lys(Ac)]-NN-N H2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-1185 * * *
carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHa-MeLeul-1186 * * *
[Lys(Ac)]-N-[13Ala]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHa-MeLysl-1187 * * *
[Lys(Ac)]-N-[13Ala]-NH2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-1188 * * *
carboxy-tetrahydropyran]-[Lys(Ac)]-N-U3Alal-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1189 *
[Lys(Ac)]-LN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1190 *
[Lys(Ac)]-GN-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1191 ** *
[Lys(Ac)]-SN-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1192 *
[Lys(Ac)]-[Aib]-N-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1193 *
[Lys(Ac)]-FN-N H2 Ac-[Per]-NTW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1194 * * *
[Lys(Ac)]-NN-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1195 ***
[Lys(Ac)]-[Tic]PAlal-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1196 *
[Lys(Ac)]-[nLeu]-[13Ala]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1197 *
[Lys(Ac)]-G-[13Ala]-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1198 *
[Lys(Ac)]-R-[13Ala]-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-1199 **
[Lys(Ac)]-W-U3Alal-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-1200 *
[Lys(Ac)]-5-[13Ala]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-1201 *
[Lys(Ac)]-L-[13Ala]-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-1202 *
[Lys(Ac)[AIBHI3Alal-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-1203 ***
[Lys(Ac)]-[N-MeAla]-U3Alal-NH2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1204 ** *
[Lys(Ac)][2-NapHPAlal-N H2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1205 ** *
[Lys(Ac)]-F-[13Ala]-NH2 Ac-[(D)Arg]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[ 4-1206 *
amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]NN-NH2 Table E32. IC50 of Illustrative Peptide Inhibitors (Thioethers) ......õ-- S--õ..,...
Ac, r....XXWX,N
N '\i[Phe(4-0Me)]-[2-Nal]-XXXX-NH2 Ac-Cyclo- [[Abu]-XXWXC]4Phe(4-0Me)]- [2-Nal]-XXX-1\TH 2 SEQ Human Rat pStat3 ID Sequence ELISA ELISA HTRF
NO: (nM) (nM) (nM) Biotin-[PEG4]-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-1207 TBC * *
[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)H2-NalH4-amino-1208 TBC * *
4-carboxy-tetrahydropyranHLys(Ac)l-NN-NH2 Ac-[(D)Ard-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-1209 TBC * *
[4-arnino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-[(D)Ard-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-1210 * * *
[4-arnino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 Ac-E-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-[(D)Asp]-[(D)Argl-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyrard-ENN-NH2 Ac-R-[(D)Arg]-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-1213 * * *
[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-[(D)ArgH(D)Argl-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)]-1214 TBC * *
[2-Nal]-[4-amino-4-carboxy-tetrahydropyrard-ENN-NH2 Ac-F-[(D)Arg]-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-1215 *
[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-[(D)Phe]-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyrard-ENN-NH2 Ac-[2-Nal]-[(D)Arg]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-1217 *
[2-Nal]-[4-amino-4-carboxy-tetrahydropyrard-ENN-NH2 Ac-T-[(D)Arg]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-1218 *
[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-L-[(D)Arg]-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-1219 *
[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac-[(D)G1n]-[(D)Arg]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-1220 TBC * *
[2-Nal]-[4-amino-4-carboxy-tetrahydropyrard-ENN-NH2 Ac-[(D)Asn]-[(D)Arg]-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)]-1221 * *
[2-Nal]-[4-amino-4-carboxy-tetrahydropyrard-ENN-NH2 1222 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)-(PEG4-A1exa488)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyrard-ENN-NH2 1223 [A1exa488]-[PEG41-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]--[2-Nal]-[4-amino-4-carboxy-tetrahydropyrard-ENN-NH2 [Alexa647HPEG41-cyclo[[Abu]-QTWOCHPhe [4-(2-aminoethoxy)H2-[2 NalH4-amino-4-carboxy-tetrahydropyranl-ENN-NH2 [Alexa-647]-[PEG4H(D)Argl-cycloRAbul-QTWOCHPhe[4-(2-1225 aminoethoxy)]-[2-NalH4-amino-4-carboxy-tetrahydropyrard-[Lys(Ac)]-NN-NFI2 [A1exa647]-[PEG121-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-1226 aminoethoxy)]-[2-NalH4-amino-4-carboxy-tetrahydropyrard-[Lys(Ac)]-NN-NFI2 [A1exa488]-[PEG4H(D)Argl-cycloRAbul-QTWOCHPhe [4-(2-1227 aminoethoxy)]-[2-NalH4-amino-4-carboxy-tetrahydropyrard-[Lys(Ac)]-NN-NFI2 * < 1 0 nIVI; ** > 10 and < 100 nM; *** > 100 and < 1,000 nIVI

STABILITY OF ADDITIONAL PEPTIDE INHIBITORS IN SIMULATED INTESTINAL FLUID
(SIF), SIMULATED GASTRIC FLUID (SGF) AND REDOX CONDITIONS
[00757] Studies were carried out in simulated intestinal fluid (SIF) and simulated gastric fluid (SGF) to evaluate gastric stability of additional peptide inhibitors of the present invention. In addition, studies were carried out to assess redox stability of the additional peptide inhibitors of the present invention.
Table E33. Thioethers and Dipens SIF SGF
SEQ ID t1/2 t1/2 Sequence NO:
(min) (min) Biotin-[PEE1]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-[4-1228 >90 >180 a mino-4-carboxy-tetra hydropyranl-ENN-NH2 Ac-cyclo[[Abu]-QTWOCH Phe[4-(2-aminoethoxy)H2-NalH4-amino-4-1229 >180 >180 carboxy-tetrahydropyranHLys(Ac)]-NN-N H2 Ac-[(D)Arg]-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)H2-Nall-[4-1230 >180 <180 a mino-4-carboxy-tetra hydropyran]-[Lys(Ac)]-NN-N H2 1231 Ac-[(D)Arg]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-Nall-[4->180, >180 a mino-4-carboxy-tetra hydropyran]-[Lys(Ac)]-NN-N H2 >180 >180 [Octany1]-[PEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-1232 >180 >180 [AilD]-[Lys(Ac)1-NN-NFI2 [PalmHPEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nall-1233 >180 >10 [AilD]-[Lys(Ac)1-NN-NFI2 Ac-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)-(PEG4-Alexa488)]-[2-1234 >180 >90 Nal]-[4-amino-4-carboxy-tetrahydropyranl-ENN-NH2 [Alexa488]-[PEG4]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)] [2 1235 > 180 > 180 Nal]-[4-amino-4-carboxy-tetrahydropyranl-ENN-NH2 [A1exa647]-[PEG4]-cyclo[[Abu]-QTWOC]-[Phe[4-(2-aminoethoxy)]-[2-1236 >180 >180 Nal]-[4-amino-4-carboxy-tetrahydropyranl-ENN-NH2 Ac[(D)Arg]-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-1237 >180 >180 [Lys(Ac)]-N-[13Alal-NFI2 Ac-[(D)Tyr]-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-1238 >180 >180 [Lys(Ac)]-N-[13Alal-NFI2 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aibl-QN-WAlal-1239 Stable >180 >180 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[a-MeLeul- >180, 1240 >180 [Lys(Ac)]-NN-N H2 >180 >180, Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4- >180, 1241 >180 carboxy-tetrahydropyran]-[Lys(AcH-NN-NH2 >180 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[a-MeLeul- Stable 1242 >180 [Lys(Ac)]-N-[13Alal-NFI2 Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4- >180 >180 carboxy-tetrahydropyran]-[Lys(Ac)]-N-[Ala]-NFI2 Ac-[Pen]-NTW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aibl- >180 >180 [Lys(Ac)]-NN-N H2 Ac-[(D)Arg]-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4- > 180 > 180 AMINO-4-CARBOXY-TETRAHYDROPYRAN]-[Lys(Ac)]NNNH2 [A1exa488]-[PEG4]-[(D)Arg]-cycloRAbul-QTWOCHPhe[4-(2-> 180 >180 1246 arninoethoxy)]-[2-Nall-[4-arnino-4-carboxy-tetrahydropyran]-[Lys(AcH->90 = less than or equal to 180 min and greater than 90 min; >45 min = less than or equal to 90 min and greater than 45 min; >10 = less than or equal to 45 min and greater than 10 min; <10 =
less than 10 min.

NK CELL AS SAY
1007581 Natural killer (NK) cells, purified from human peripheral blood of healthy donors by negative selection (Miltenyi Biotech, Cat # 130-092-657), were cultured in complete media (RPMI 1640 containing 10% FBS, L-glutamine and penicillin-streptomycin) in the presence of IL-2 (RnD, Cat # 202-IL-010/CF) at 25 ng/mL. After 7 days, cells were centrifuged, and resuspended in complete media at 1E6 cells/mL. Recombinant IL-23 at predetermined EC50 to EC75 and IL-18 (RnD, Cat # B003-5) at 10 ng/mL were mixed with varying concentrations of peptides, and added to NK cells seeded at 1E5 cells per well. After 20 to 24 hours, IFNy in the supernatant was quantified using Quantikine ELISA (RnD, Cat # DIF50). Results are shown in Table E34. Multiple results shown for a single peptide are from separate assays.
Table E34. Primary Cell Assay (Thioethers and Dipens) SEQ ID NK cell NO: Sequence Assay (nM) Ac-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-1247 * * *
tetrahydropyran]-[Lys(Ac)]-NN-NH2 1248 Ac-[(D)Arg]-cycloRAbul-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4- * ** **
carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 [Alexa647]-[PEG4]-cyclo[[Abu]-QTWOCHPhe[4-(2-aminoethoxy)]-[2-Nal]-[4-1249 **, *
amino-4-carboxy-tetrahydropyran]-ENN-NH2 Ac[(D)Arg]-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-1250 **
[Lys(Ac)]-N-[13Ala]-NH2 1251 Ac-[Per]-NTVVQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aibl-QN-[13Ala]-N H2 **
Ac-[Per]-QTW-[Lys(Ac)]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-NalHAibl-[Lys(Ac)]-1252 **

1253 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[a-MeLeuHLys(Ac)]-1254 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2 1255 Ac-[Per]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-N-U3Alal-NH2 1256 Ac-[Per]-NTW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aibl-[Lys(Ac)]-NN-1007591A11 of the above U.S. patents, U.S. patent application publications, U.S. patent applications, foreign patents, foreign patent applications and non-patent publications referred to in this specification and/or listed in the Application Data Sheet, are incorporated herein by reference, in their entirety.

1007611From the foregoing it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention.
Accordingly, the invention is not limited except as by the appended claims.

Claims

What is claimed is:

1. A peptide inhibitor of an interleukin-23 receptor, or a pharmaceutically acceptable salt or solvate thereof, wherein the peptide inhibitor comprises an amino acid sequence of Formula (Xa):
X1-X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-X13-X14-X15-X16-X17-X18-X19-X20 (Xa) wherein X1 is any amino acid or absent;
X2 is any amino acid or absent;
X3 is any amino acid or absent;
X4 is any amino acid or chemical moiety capable of forming a bond with X9;
X5 is any amino acid;
X6 is any amino acid;
X7 is any amino acid;
X8 is any amino acid;
X9 is any amino acid or chemical moiety capable of forming a bond with X4;
X10 is any amino acid;
X11 is any amino acid;
X12 is any amino acid;
X13 is any amino acid;
X14 is any amino acid;
X15 is any amino acid, X16 is any amino acid or absent;
X17 is any amino acid or absent;
X18 is any amino acid or absent;
X19 is any amino acid or absent; and X20 is any amino acid or absent, wherein the peptide inhibitor is cyclized via a bond between X4 and X9, and wherein the peptide inhibitor inhibits the binding of an interleukin-23 (IL-23) to an IL-23 receptor.

2. The peptide inhibitor of claim 1, wherein the bond between X4 and X9, is a disulfide bond, a thioether bond, a lactam bond, a triazole ring, a selenoether bond, a diselenide bond, or an olefin bond.

3. The peptide inhibitor of claim 1, wherein X4 is Cys and X9 is Cys, and the bond is a disulfide bond.

4. The peptide inhibitor of claim 1, wherein X4 is Pen and X9 is Pen, and the bond is a disulfide bond.

5. The peptide inhibitor of claim 1, wherein the peptide inhibitor comprises an amino acid sequence of any one of SEQ ID NOS: 365-370, 857-1029.

6. The peptide inhibitor of claim 1, wherein the peptide inhibitor comprises an amino acid sequence set forth in any of Formulas (Va), (Vb), (Vc), (Vd), (Ve), (Vf), (Vg) and (Vh).

7. The peptide inhibitor of claim 1, wherein the peptide inhibitor comprises any of the following amino acid sequences:
[Palm]-[isoGlu]-[PEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NNNH2 ;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(PEG4-isoGlu-Palm)]-NN-NH2;
Ac-[Pen]-QTWO-[Pen]-Phe(4-CONH2)-[2-Nal]-[.alpha.-MeLys(Ac)]-[Lys(Ac)]-NN-NH2;

[Octanyl]-[IsoGlu]-[PEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
[Octanyl]-[PEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;

[Palm]-[PEG4]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(PEG4-Octanyl)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(PEG4-Palm)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-Palm)]-[2-Nal]-[Aib]-[Lys(Ac)]NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-Lauryl)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[.alpha.-MeLys(PEG4-Palm)-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[.alpha.-MeLys(PEG4-Lauryl)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)-(PEG4-IsoGlu-Palm)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]- [Phe[4-(2-aminoethoxy)-(PEG4-IsoGLu-Lauryl)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[.alpha.-MeLys(PEG4-IsoGlu-Palm)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[.alpha.-MeLys(PEG4-IsoGlu-Lauryl)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[.alpha.-MeLys(IVA)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[.alpha.-MeLys(Biotin)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-QTWQ-[Pen]-Phe(4-CONH2)-[2-Nal]-[.alpha.-MeLys(Octanyl)]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-[Lys(IVA)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(IVA)]-N-NH2;
Ac-[Pen]-[Lys(Biotin)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(Biotin)]-N-NH2;
Ac-[Pen]-[Lys(Octanyl)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(octanyl)]-N-NH2;
Ac-[Pen]-[Lys(Palm)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[A113]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-Lys(Palm)]-N-NH2;
Ac-[Pen]-[Lys(PEG8)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(PEG8)]-N-NH2;
Ac-[Pen]-K(Peg11-Palm)TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-[Lys(Peg11-palm)]-N-NH2;
Ac-[Pen]-[Cit]-TW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-[Lys(Ac)]-TW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[Phe(3,4-OCH3)2]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[Phe(2,4-CH3)2]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[Phe(3-CH3)]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[Phe(4-CH3)]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac[(D)Arg]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal] - [Aib]-[Lys(Ac)]-N-[.beta.Ala]-NH2;
Ac-[(D)Tyr]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-N-[f.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-QN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(Ac)]-N-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-N-[Lys(Ac)]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-QQ-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-Q-[.beta.Ala]-NH2;

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-N-[Cit]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Cit]-NNH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Cit]-Q-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Cit]-[Lys(Ac)]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Lys(Ac)]-[Cit]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-QN-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-E-[Cit]-Q-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Cit]-N-[Cit]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)] - [2-Nal]-[Aib]-[Cit]-Q-[Cit]-NH2;

Ac-[Pen]-[Cit]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-QNN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-ENQ-NH2;
Ac-[Pen]-GPWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-PGWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWN-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NSWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-N-[Aib]-WQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTW-[Aib]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]N-[Aib]-NH2;
Ac-[Pen]-QTW- [Lys(Ac)]- [Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-[Lys(Ac)]-TWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]NNNH2 ;
Ac-[Pen]-QVWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[2-Nal]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NT-[1-Nal]-Q-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[.alpha.-MeLeu]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[.alpha.-MeLys]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[.alpha.-MeLeu]-[Lys(Ac)]-N-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[.alpha.-MeLys]-[Lys(Ac)]-N-[.beta.Ala]-NH2;

Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-N-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-LN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-GN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-SN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Aib]-N-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-FN-NH2;
Ac-[Pen]-NTW-[Cit]-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-NN-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[Tic]-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[nLeu]-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-G-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-R-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-W-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-S-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-L-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-[AIB]-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]--[Aib]-[Lys(Ac)]-[N-MeAla]-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-[2-Nap]-[.beta.Ala]-NH2;
Ac-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[Aib]-[Lys(Ac)]-F-[.beta.Ala]-NH2;
Ac-[(D)Arg]-[Pen]-NTWQ-[Pen]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[ 4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]NNNH2;
Biotin-[PEG4]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2;
Ac-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2;
Ac-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Nal]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2;

Ac-E-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-[(D)Asp]-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-R-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
inoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-F-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-[(D)Phe]-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-[2-Na1]-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-T-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-L-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-[(D)Gln]-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-[(D)Asn]-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-ENN-NH2;
Ac-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)-(PEG4-Alexa488)]-[2-Na1]-[4-amino-carboxy-tetrahydropyran]-ENN-NH2;
[Alexa488]-[PEG4]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]--[2-Na1]-[4-amino-carboxy-tetrahydropyran]-ENN-NH2;
[Alexa647]-[PEG4]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-carboxy-tetrahydropyran]-ENN-NH2;
[Alexa-647]-[PEG4]-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyrab]-[Lys(Ac)]-NN-NH2;

[Alexa647]-[PEG12]-[(D)Arg]-cyclo[[Abu]-QTWQC] - [Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2; and [Alexa488]-[PEG4]-[(D)Arg]-cyclo[[Abu]-QTWQC]-[Phe[4-(2-aminoethoxy)]-[2-Na1]-[4-amino-4-carboxy-tetrahydropyran]-[Lys(Ac)]-NN-NH2, wherein the peptide inhibitor is cyclized via a disulfide bond between two Pen residues or by a thioether bond between Abu and a Cys residue, and wherein the peptide inhibitor inhibits the binding of an interleukin-23 (IL-23) to an IL-23 receptor.

8. The peptide inhibitor of any one of claims 1-7, further comprising one or more half-life extension moiety and/or one or more linker moiety conjugated to the peptide inhibitor.

9. The peptide inhibitor of claim 8, wherein the half-life extension moiety is conjugated to the peptide inhibitor via one or more linker moieties.

10. The peptide inhibitor of any one of claims 1-9, wherein the peptide inhibitor comprises the structure of Formula I:
R1-X-R2 (I) or a pharmaceutically acceptable salt or solvate thereof, wherein R1 is a bond, hydrogen, a C1-C6 alkyl, a C6-C12 aryl, a C6-C12 aryl, a C1-C6 alkyl, a C1-C20 alkanoyl, and including PEGylated versions alone or as spacers of any of the foregoing; X is the amino acid sequence; and R2 is OH or NH2.

11. A peptide dimer inhibitor of an interleukin-23 receptor, wherein the peptide dimer inhibitor comprises two peptide monomer subunits connected via one or more linker moieties, wherein each peptide monomer subunit has a sequence or structure set forth in any one of claims 1-10.

12. The peptide dimer inhibitor of claim 11, wherein one or both peptide monomer subunit is cyclized via an intramolecular bond between X4 and X9.

13. The peptide dimer inhibitor of claim12, wherein one or both intramolecular bond is a disulfide bond, a thioether bond, a lactam bond, a selenoether, diselenide, or an olefin bond.

14. The peptide dimer inhibitor of any one of claims 11-13, wherein the linker moiety is a diethylene glycol linker, an iminodiacetic acid (IDA) linker, a .beta.-Ala-iminodiaceticacid (.beta.-Ala-IDA) linker, or a PEG linker.

15. The peptide dimer inhibitor of any one of claims 11-14, wherein the N-terminus of each peptide monomer subunit is connected by the linker moiety or wherein the C-terminus of each peptide monomer subunit is connected by the linker moiety.

16. The peptide inhibitor of any one of claims 1-10 or the peptide dimer of any of claims 11-15 further comprising a conjugated chemical substituent.

17. The peptide inhibitor or the peptide dimer of claim 16, wherein the conjugated chemical substituent is a lipophilic substituent or a polymeric moiety.

18. The peptide inhibitor or the peptide dimer of claim 16, wherein the conjugated chemical substituent is Ac, Palm, gamaGlu-Palm, isoGlu-Palm, PEG2-Ac, PEG4-isoGlu-Palm, (PEG)5-Palm, succinic acid, glutaric acid, pyroglutaric acid, benzoic acid, IVA, octanoic acid, 1,4 diaminobutane, isobutyl, or biotin.

19. The peptide inhibitor or the peptide dimer of claim 16, wherein the conjugated chemical substituent is a polyethylene glycol with a molecular mass of 400 Da to 40,000 Da.

20. A polynucleotide comprising a sequence encoding the peptide inhibitor of any one of claims 1-10 or one or both peptide monomer subunit of the peptide dimer inhibitor of any one of claims 11-15.

21. A vector comprising the polynucleotide of claim 20.

22. A pharmaceutical composition comprising the peptide inhibitor or the peptide dimer inhibitor of any one of claims 1-19, and a pharmaceutically acceptable carrier, excipient, or diluent.

23. The pharmaceutical composition of claim 22, further comprising an enteric coating.

24. The pharmaceutical composition of claim 23, wherein the enteric coating protects and releases the pharmaceutical composition within a subject's lower gastrointestinal system.

25. A method for treating an Inflammatory Bowel Disease (IBD), ulcerative colitis, Crohn's disease, Celiac disease (nontropical Sprue), enteropathy associated with seronegative arthropathies, microscopic colitis, collagenous colitis, eosinophilic gastroenteritis, colitis associated with radio- or chemo-therapy, colitis associated with disorders of innate immunity as in leukocyte adhesion deficiency-1, chronic granulomatous disease, glycogen storage disease type 1 b, Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, and Wiskott-Aldrich Syndrome, pouchitis resulting after proctocolectomy and ileoanal anastomosis, gastrointestinal cancer, pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, pericholangitis, chronic bronchitis, chronic sinusitis, asthma, psoriasis, psoriatic arthritis, or graft versus host disease in a subject, comprising providing to the subject an effective amount of the peptide inhibitor or peptide dimer inhibitor of any one of claims 1-19, or the pharmaceutical composition of any one of claims 22-24.

26. The method of claim 25, wherein the pharmaceutical composition is provided to the subject by an oral, parenteral, intravenous, peritoneal, intradermal, subcutaneous, intramuscular, intrathecal, inhalation, vaporization, nebulization, sublingual, buccal, parenteral, rectal, intraocular, inhalation, topically, vaginal, or topical route of administration.

27. The method of claim 25 for treating Inflammatory Bowel Disease (IBD), ulcerative colitis, Crohn's disease, wherein the pharmaceutical composition is provided to the subject orally.

28. The method of claim 25 for treating psoriasis, wherein the pharmaceutical composition is provided to the subject orally, topically, parenterally, intravenously, subcutaneously, peritonealy, or intravenously.

29. The method of any one claims 25-28, wherein the peptide inhibitor or the peptide dimer inhibitor inhibits binding of an interleukin-23 (IL-23) to the interleukin-23 receptor (IL-23R).