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NZ764190B2 - Pladienolide pyridine compounds and methods of use - Google Patents

Pladienolide pyridine compounds and methods of use Download PDF

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Publication number
NZ764190B2
NZ764190B2 NZ764190A NZ76419015A NZ764190B2 NZ 764190 B2 NZ764190 B2 NZ 764190B2 NZ 764190 A NZ764190 A NZ 764190A NZ 76419015 A NZ76419015 A NZ 76419015A NZ 764190 B2 NZ764190 B2 NZ 764190B2
Authority
NZ
New Zealand
Prior art keywords
compound
use according
formula
pharmaceutically acceptable
splicing factor
Prior art date
Application number
NZ764190A
Other versions
NZ764190A (en
Inventor
Kenzo Arai
Silvia Buonamici
Betty Chan
Nicholas C Gearhart
Baudouin Gerard
Sonobe Regina Kanada
Gregg F Keaney
Kazunobu Kira
Yoshihiko Kotake
Kian Huat Lim
Original Assignee
Eisai R&D Management Co Ltd
Filing date
Publication date
Application filed by Eisai R&D Management Co Ltd filed Critical Eisai R&D Management Co Ltd
Publication of NZ764190A publication Critical patent/NZ764190A/en
Publication of NZ764190B2 publication Critical patent/NZ764190B2/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Abstract

The present invention provides novel pladienolide pyridine compounds, pharmaceutical compositions containing such compounds, and methods for using the compounds as therapeutic agents. These compounds may be useful in the treatment of cancer, particularly cancers in which agents that target the spliceosome and mutations therein are known to be useful.

Claims (14)

What is claimed is:
1. Use of a compound selected from a compound of formula 1: N O OH a compound of formula 2: N O OH a compound of formula 3: a compound of formula 4: and pharmaceutically acceptable salts thereof, in the manufacture of a medicament for the therapeutic treatment of cancer that is positive for one or more mutations in a spliceosome gene or protein.
2. The use according to claim 1, wherein said spliceosome gene or protein is selected from splicing factor 3B subunit 1 (SF3B1), U2 small nuclear RNA auxiliary factor 1 (U2AF1), serine/arginine-rich splicing factor 2 (SRSF2), zinc finger (CCCH type) RNA-binding motif and serine/arginine rich 2 (ZRSR2), premRNA-processing-splicing factor 8 (PRPF8), U2 small nuclear RNA auxiliary factor 2 (U2AF2), splicing factor 1 (SF1), splicing factor 3a subunit 1 (SF3A1), PRP40 pre-mRNA processing factor 40 homolog B (PRPF40B), RNA binding motif protein 10 (RBM10), poly(rC) binding protein 1 (PCBP1), crooked neck pre-mRNA splicing factor 1 (CRNKL1), DEAH (Asp-Glu-Ala-His) box helicase 9 (DHX9), peptidyl-prolyl cis-trans isomerase-like 2 (PPIL2), RNA binding motif protein 22 (RBM22), small nuclear ribonucleoprotein Sm D3 (SNRPD3), probable ATP-dependent RNA helicase DDX5 (DDX5), pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 (DHX15), and polyadenylate- binding protein 1 (PABPC1).
3. The use according to claim 1, wherein said spliceosome gene or protein is splicing factor 3B subunit 1.
4. The use according to claim 1 wherein the compound is the compound of formula 1: N O OH , or a pharmaceutically acceptable salt thereof.
5. The use according to claim 1 wherein the compound is the compound of formula 2: or a pharmaceutically acceptable salt thereof.
6. The use according to claim 5 wherein the compound is the compound of formula 2: N O OH
7. The use according to claim 1 wherein the compound is the compound of formula 3: or a pharmaceutically acceptable salt thereof.
8. The use according to claim 1 wherein the compound is the compound of formula 4: or a pharmaceutically acceptable salt thereof.
9. The use according to any one of claims 1-8, wherein said compound comprises greater than about 80% by weight of one stereoisomer of the compound and less than about 20% by weight of the other stereoisomers of the compound, or a pharmaceutically acceptable salt thereof.
10. The use according to any one of claims 1-9, wherein said compound comprises greater than about 97% by weight of one stereoisomer of the compound and less than about 3% by weight of the other stereoisomers of the compound, or a pharmaceutically acceptable salt thereof.
11. The use according to any one of claims 1-10, wherein the cancer is myelodysplastic syndrome (MDS), acute myeloid leukemia (AML), chronic myelomonocytic leukemia (CMML), lung adenocarcinoma (LUAD), uterine corpus endometrial carcinoma (UCEC), progressive massive fibrosis (PMF), prostate adenocarcinoma (PRAD, colon adenocarcinoma (COAD), ovarian serous cystadenocarcinoma (OV), skin cutaneous melanoma (SKCM), lung squamous cell carcinoma (LUSC), stomach adenocarcinoma (STAD), glioblastoma multiforme (GBM), brain lower grade glioma (LGG), or diffuse large B-cell lymphoma (DLBCL).
12. The use according to any one of claims 1 to 11, wherein said medicament is to be administered by intravenous, oral, subcutaneous, or intramuscular administration.
13. The use according to claim 12, wherein said medicament is to be administered by oral administration.
14. The use according to claim 1, substantially as herein described with reference to any one of the examples and/or
NZ764190A 2015-05-13 Pladienolide pyridine compounds and methods of use NZ764190B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201461993423P 2014-05-15 2014-05-15
NZ725603A NZ725603B2 (en) 2015-05-13 Pladienolide pyridine compounds and methods of use

Publications (2)

Publication Number Publication Date
NZ764190A NZ764190A (en) 2023-11-24
NZ764190B2 true NZ764190B2 (en) 2024-02-27

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