AR109974A2 - Agentes inductores de apoptosis para el tratamiento de cáncer y enfermedades inmunes y autoinmunes - Google Patents
Agentes inductores de apoptosis para el tratamiento de cáncer y enfermedades inmunes y autoinmunesInfo
- Publication number
- AR109974A2 AR109974A2 ARP170102895A ARP170102895A AR109974A2 AR 109974 A2 AR109974 A2 AR 109974A2 AR P170102895 A ARP170102895 A AR P170102895A AR P170102895 A ARP170102895 A AR P170102895A AR 109974 A2 AR109974 A2 AR 109974A2
- Authority
- AR
- Argentina
- Prior art keywords
- nhc
- fused
- nhr1
- heterocycloalkene
- heterocycloalkane
- Prior art date
Links
- 208000023275 Autoimmune disease Diseases 0.000 title 1
- 206010028980 Neoplasm Diseases 0.000 title 1
- 230000006907 apoptotic process Effects 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 208000026278 immune system disease Diseases 0.000 title 1
- 230000001939 inductive effect Effects 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 114
- 101150009274 nhr-1 gene Proteins 0.000 abstract 40
- 150000001925 cycloalkenes Chemical class 0.000 abstract 39
- 150000002390 heteroarenes Chemical class 0.000 abstract 38
- 150000001924 cycloalkanes Chemical class 0.000 abstract 36
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 abstract 32
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 abstract 32
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 20
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 18
- 125000000565 sulfonamide group Chemical group 0.000 abstract 18
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 14
- 229910052799 carbon Inorganic materials 0.000 abstract 13
- 125000000217 alkyl group Chemical group 0.000 abstract 12
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 12
- 125000001072 heteroaryl group Chemical group 0.000 abstract 12
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 abstract 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 12
- -1 C (O) N (R1) 2 Proteins 0.000 abstract 11
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 11
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 11
- 229910052739 hydrogen Inorganic materials 0.000 abstract 11
- 125000003342 alkenyl group Chemical group 0.000 abstract 10
- 125000000304 alkynyl group Chemical group 0.000 abstract 10
- 125000001424 substituent group Chemical group 0.000 abstract 10
- OTXBWGUYZNKPMG-UHFFFAOYSA-N isofulminic acid Chemical compound O[N+]#[C-] OTXBWGUYZNKPMG-UHFFFAOYSA-N 0.000 abstract 9
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 9
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 8
- 101100240518 Caenorhabditis elegans nhr-12 gene Proteins 0.000 abstract 5
- 101100240527 Caenorhabditis elegans nhr-22 gene Proteins 0.000 abstract 5
- 101100294108 Caenorhabditis elegans nhr-41 gene Proteins 0.000 abstract 5
- 101100294121 Caenorhabditis elegans nhr-57 gene Proteins 0.000 abstract 5
- 101100516557 Caenorhabditis elegans nhr-62 gene Proteins 0.000 abstract 5
- 101100516560 Caenorhabditis elegans nhr-67 gene Proteins 0.000 abstract 5
- 101100516561 Caenorhabditis elegans nhr-68 gene Proteins 0.000 abstract 5
- 101100516568 Caenorhabditis elegans nhr-7 gene Proteins 0.000 abstract 4
- 102220492355 2'-5'-oligoadenylate synthase 3_R30A_mutation Human genes 0.000 abstract 3
- 102220544041 60S ribosomal protein L27_R10A_mutation Human genes 0.000 abstract 3
- 102220542311 60S ribosomal protein L27_R19A_mutation Human genes 0.000 abstract 3
- 102220473072 Chemerin-like receptor 2_R14Q_mutation Human genes 0.000 abstract 3
- 102220586234 Chemerin-like receptor 2_R18A_mutation Human genes 0.000 abstract 3
- 102220503849 Cortexin-1_R40A_mutation Human genes 0.000 abstract 3
- 102220598877 DNA-directed RNA polymerases I, II, and III subunit RPABC4_R15A_mutation Human genes 0.000 abstract 3
- 102220516986 Double homeobox protein 4_R23A_mutation Human genes 0.000 abstract 3
- 102220503968 Endogenous retrovirus group K member 6 Rec protein_R20A_mutation Human genes 0.000 abstract 3
- 102220555063 Holliday junction recognition protein_R25A_mutation Human genes 0.000 abstract 3
- 102220507264 Rab11 family-interacting protein 1_R29A_mutation Human genes 0.000 abstract 3
- 102220507254 Rab11 family-interacting protein 1_R38K_mutation Human genes 0.000 abstract 3
- 102220507255 Rab11 family-interacting protein 1_R39K_mutation Human genes 0.000 abstract 3
- 102220494498 Receptor of activated protein C kinase 1_R57A_mutation Human genes 0.000 abstract 3
- 102220470414 Thymosin beta-10_R26A_mutation Human genes 0.000 abstract 3
- 102220470367 Thymosin beta-10_R28A_mutation Human genes 0.000 abstract 3
- 102220475496 Vacuolar protein sorting-associated protein 33A_R13A_mutation Human genes 0.000 abstract 3
- 102220475445 Vacuolar protein sorting-associated protein 33A_R24A_mutation Human genes 0.000 abstract 3
- 125000004957 naphthylene group Chemical group 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 102220497337 14-3-3 protein zeta/delta_R59A_mutation Human genes 0.000 abstract 2
- 102220598618 5-hydroxytryptamine receptor 1E_R43A_mutation Human genes 0.000 abstract 2
- 102220518322 Casein kinase I isoform gamma-2_R60A_mutation Human genes 0.000 abstract 2
- 102220586235 Chemerin-like receptor 2_R63A_mutation Human genes 0.000 abstract 2
- 102220586050 Chemerin-like receptor 2_R64A_mutation Human genes 0.000 abstract 2
- 102220586191 Chemerin-like receptor 2_R65A_mutation Human genes 0.000 abstract 2
- 102220474817 Chemerin-like receptor 2_R69A_mutation Human genes 0.000 abstract 2
- 102220586055 Chemerin-like receptor 2_R70A_mutation Human genes 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- 102220521126 Ribosome biogenesis protein NSA2 homolog_R58A_mutation Human genes 0.000 abstract 2
- 102220521661 Ribosome biogenesis protein NSA2 homolog_R71A_mutation Human genes 0.000 abstract 2
- 102220599428 Serum amyloid A-1 protein_R37A_mutation Human genes 0.000 abstract 2
- 102220475443 Vacuolar protein sorting-associated protein 33A_R27A_mutation Human genes 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000005549 heteroarylene group Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 2
- 102200140336 rs786204767 Human genes 0.000 abstract 2
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 108091008648 NR7C Proteins 0.000 abstract 1
- 101100212791 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) YBL068W-A gene Proteins 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 abstract 1
- 125000004266 aziridin-1-yl group Chemical group [H]C1([H])N(*)C1([H])[H] 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000005724 cycloalkenylene group Chemical group 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 125000006588 heterocycloalkylene group Chemical group 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/4353—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Health & Medical Sciences (AREA)
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- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- Hematology (AREA)
- AIDS & HIV (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
- Peptides Or Proteins (AREA)
Abstract
Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1), o una sal terapéuticamente aceptable del mismo, en donde A¹ es N o C(A²); A² es H, R¹, OR¹, SR¹, S(O)R¹, SO₂R¹, C(O)R¹, C(O)OR¹, OC(O)R¹, NHR¹, N(R¹)₂, C(O)NHR¹, C(O)N(R¹)₂, NHC(O)R¹, NR¹C(O)R¹, NHC(O)OR¹, NR¹C(O)OR¹, NHC(O)NH₂, NHC(O)NHR¹, NHC(O)N(R¹)₂, NR¹C(O)NHR¹, NR¹C(O)N(R¹)₂, SO₂NH₂, SO₂NHR¹, SO₂N(R¹)₂, NHSO₂R¹, NR¹SO₂R¹, NHSO₂NHR¹, NHSO₂N(R¹)₂, NR¹SO₂NHR¹, NR¹SO₂N(R¹)₂, C(O)NHNOH, C(O)NHNOR¹, C(O)NHSO₂R¹, C(NH)NH₂, C(NH)NHR¹, C(NH)N(R¹)₂, NHSO₂NHR¹, NHSO₂N(CH₃)R¹, N(CH₃)SO₂N(CH₃)R¹, F, Cl, Br, I, CN, NO₂, N₃, OH, C(O)H, CHNOH, CH(NOCH₃), CF₃, C(O)OH, C(O)NH₂ o C(O)OR¹A; B¹ es H, R¹, OR¹, SR¹, S(O)R¹, SO₂R¹, C(O)R¹, C(O)OR¹, OC(O)R¹, NHR¹, N(R¹)₂, C(O)NHR¹, C(O)N(R¹)₂, NHC(O)R¹, NR¹C(O)R¹, NHC(O)OR¹, NR¹C(O)OR¹, NHC(O)NH₂, NHC(O)NHR¹, NHC(O)N(R¹)₂, NR¹C(O)NHR¹, NR¹C(O)N(R¹)₂, SO₂NH₂, SO₂NHR¹, SO₂N(R¹)₂, NHSO₂R¹, NR¹SO₂R¹, NHSO₂NHR¹, NHSO₂N(R¹)₂, NR¹SO₂NHR¹, NR¹SO₂N(R¹)₂, C(O)NHNOH, C(O)NHNOR¹, C(O)NHSO₂R¹, C(NH)NH₂, C(NH)NHR¹, C(NH)N(R¹)₂, NHSO₂NHR¹, NHSO₂N(CH₃)R¹, N(CH₃)SO₂N(CH₃)R¹, F, Cl, Br, I, CN, NO₂, N₃, OH, C(O)H, CHNOH, CH(NOCH₃), CF₃, C(O)OH, C(O)NH₂ o C(O)OR¹A; D¹ es H, R¹, OR¹, SR¹, S(O)R¹, SO₂R¹, C(O)R¹, C(O)OR¹, OC(O)R¹, NHR¹, N(R¹)₂, C(O)NHR¹, C(O)N(R¹)₂, NHC(O)R¹, NR¹C(O)R¹, NHC(O)OR¹, NR¹C(O)OR¹, NHC(O)NH₂, NHC(O)NHR¹, NHC(O)N(R¹)₂, NR¹C(O)NHR¹, NR¹C(O)N(R¹)₂, SO₂NH₂, SO₂NHR¹, SO₂N(R¹)₂, NHSO₂R¹, NR¹SO₂R¹, NHSO₂NHR¹, NHSO₂N(R¹)₂, NR¹SO₂NHR¹, NR¹SO₂N(R¹)₂, C(O)NHNOH, C(O)NHNOR¹, C(O)NHSO₂R¹, C(NH)NH₂, C(NH)NHR¹, C(NH)N(R¹)₂, NHSO₂NHR¹, NHSO₂N(CH₃)R¹, N(CH₃)SO₂N(CH₃)R¹, F, Cl, Br, I, CN, NO₂, N₃, OH, C(O)H, CHNOH, CH(NOCH₃), CF₃, C(O)OH, C(O)NH₂ o C(O)OR¹A; E¹ es H, R¹, OR¹, SR¹, S(O)R¹, SO₂R¹, C(O)R¹, C(O)OR¹, OC(O)R¹, NHR¹, N(R¹)₂, C(O)NHR¹, C(O)N(R¹)₂, NHC(O)R¹, NR¹C(O)R¹, NHC(O)OR¹, NR¹C(O)OR¹, NHC(O)NH₂, NHC(O)NHR¹, NHC(O)N(R¹)₂, NR¹C(O)NHR¹, NR¹C(O)N(R¹)₂, SO₂NH₂, SO₂NHR¹, SO₂N(R¹)₂, NHSO₂R¹, NR¹SO₂R¹, NHSO₂NHR¹, NHSO₂N(R¹)₂, NR¹SO₂NHR¹, NR¹SO₂N(R¹)₂, C(O)NHNOH, C(O)NHNOR¹, C(O)NHSO₂R¹, C(NH)NH₂, C(NH)NHR¹, C(NH)N(R¹)₂, NHSO₂NHR¹, NHSO₂N(CH₃)R¹, N(CH₃)SO₂N(CH₃)R¹, F, Cl, Br, I, CN, NO₂, N₃, OH, C(O)H, CHNOH, CH(NOCH₃), CF₃, C(O)OH, C(O)NH₂ o C(O)OR¹A; e Y¹ es H, CN, NO₂, C(O)OH, F, Cl, Br, I, CF₃, OCF₃, CF₂CF₃, OCF₂CF₃, R¹⁷, OR¹⁷, C(O)R¹⁷, C(O)OR¹⁷, SR¹⁷, SO₂R¹⁷, NH₂, NHR¹⁷, N(R¹⁷)₂, NHC(O)R¹⁷, C(O)NH₂, C(O)NHR¹⁷, C(O)N(R¹⁷)₂, NHS(O)R¹⁷ o NHSO₂R¹⁷; o E¹ e Y¹, junto con los átomos a los cuales están unidos, son benceno, naftileno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; y A², B¹, y D¹ se seleccionan en forma independiente entre H, R¹, OR¹, SR¹, S(O)R¹, SO₂R¹, C(O)R¹, C(O)OR¹, OC(O)R¹, NHR¹, N(R¹)₂, C(O)NHR¹, C(O)N(R¹)₂, NHC(O)R¹, NR¹C(O)R¹, NHC(O)OR¹, NR¹C(O)OR¹, NHC(O)NH₂, NHC(O)NHR¹, NHC(O)N(R¹)₂, NR¹C(O)NHR¹, NR¹C(O)N(R¹)₂, SO₂NH₂, SO₂NHR¹, SO₂N(R¹)₂, NHSO₂R¹, NR¹SO₂R¹, NHSO₂NHR¹, NHSO₂N(R¹)₂, NR¹SO₂NHR¹, NR¹SO₂N(R¹)₂, C(O)NHNOH, C(O)NHNOR¹, C(O)NHSO₂R¹, C(NH)NH₂, C(NH)NHR¹, C(NH)N(R¹)₂, NHSO₂NHR¹, NHSO₂N(CH₃)R¹, N(CH₃)SO₂N(CH₃)R¹, F, Cl, Br, I, CN, NO₂, N₃, OH, C(O)H, CHNOH, CH(NOCH₃), CF₃, C(O)OH, C(O)NH₂ o C(O)OR¹A; o Y¹ y B1, junto con los átomos a los cuales están unidos, son benceno, naftileno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; y A², D¹, y E¹ se seleccionan en forma independiente entre H, R¹, OR¹, SR¹, S(O)R¹, SO₂R¹, C(O)R¹, C(O)OR¹, OC(O)R¹, NHR¹, N(R¹)₂, C(O)NHR¹, C(O)N(R¹)₂, NHC(O)R¹, NR¹C(O)R¹, NHC(O)OR¹, NR¹C(O)OR¹, NHC(O)NH₂, NHC(O)NHR¹, NHC(O)N(R¹)₂, NR¹C(O)NHR¹, NR¹C(O)N(R¹)₂, SO₂NH₂, SO₂NHR¹, SO₂N(R¹)₂, NHSO₂R¹, NR¹SO₂R¹, NHSO₂NHR¹, NHSO₂N(R¹)₂, NR¹SO₂NHR¹, NR¹SO₂N(R¹)₂, C(O)NHNOH, C(O)NHNOR¹, C(O)NHSO₂R¹, C(NH)NH₂, C(NH)NHR¹, C(NH)N(R¹)₂, NHSO₂NHR¹, NHSO₂N(CH₃)R¹, N(CH₃)SO₂N(CH₃)R¹, F, Cl, Br, I, CN, NO₂, N₃, OH, C(O)H, CHNOH, CH(NOCH₃), CF₃, C(O)OH, C(O)NH₂ o C(O)OR¹A; o A² y B¹, junto con los átomos a los cuales están unidos, son benceno, naftileno, heteroareno cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; y D¹, E¹, e Y¹ se seleccionan en forma independiente entre H, R¹, OR¹, SR¹, S(O)R¹, SO₂R¹, C(O)R¹, C(O)OR¹, OC(O)R¹, NHR¹, N(R¹)₂, C(O)NHR¹, C(O)N(R¹)₂, NHC(O)R¹, NR¹C(O)R¹, NHC(O)OR¹, NR¹C(O)OR¹, NHC(O)NH₂, NHC(O)NHR¹, NHC(O)N(R¹)₂, NR¹C(O)NHR¹, NR¹C(O)N(R¹)₂, SO₂NH₂, SO₂NHR¹, SO₂N(R¹)₂, NHSO₂R¹, NR¹SO₂R¹, NHSO₂NHR¹, NHSO₂N(R¹)₂, NR¹SO₂NHR¹, NR¹SO₂N(R¹)₂, C(O)NHNOH, C(O)NHNOR¹, C(O)NHSO₂R¹, C(NH)NH₂, C(NH)NHR¹, C(NH)N(R¹)₂, NHSO₂NHR¹, NHSO₂N(CH₃)R¹, N(CH₃)SO₂N(CH₃)R¹, F, Cl, Br, I, CN, NO₂, N₃, OH, C(O)H, CHNOH, CH(NOCH₃), CF₃, C(O)OH, C(O)NH₂ o C(O)OR¹A; o A² y D¹, junto con los átomos a los cuales están unidos, son benceno, naftaleno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; y B¹, E¹, e Y¹ se seleccionan en forma independiente entre H, R¹, OR¹, SR¹, S(O)R¹, SO₂R¹, C(O)R¹, C(O)OR¹, OC(O)R¹, NHR¹, N(R¹)₂, C(O)NHR¹, C(O)N(R¹)₂, NHC(O)R¹, NR¹C(O)R¹, NHC(O)OR¹, NR¹C(O)OR¹, NHC(O)NH₂, NHC(O)NHR¹, NHC(O)N(R¹)₂, NR¹C(O)NHR¹, NR¹C(O)N(R¹)₂, SO₂NH₂, SO₂NHR¹, SO₂N(R¹)₂, NHSO₂R¹, NR¹SO₂R¹, NHSO₂NHR¹, NHSO₂N(R¹)₂, NR¹SO₂NHR¹, NR¹SO₂N(R¹)₂, C(O)NHNOH, C(O)NHNOR¹, C(O)NHSO₂R¹, C(NH)NH₂, C(NH)NHR¹, C(NH)N(R¹)₂, NHSO₂NHR¹, NHSO₂N(CH₃)R¹, N(CH₃)SO₂N(CH₃)R¹, F, Cl, Br, I, CN, NO₂, N₃, OH, C(O)H, CHNOH, CH(NOCH₃), CF₃, C(O)OH, C(O)NH₂ o C(O)OR¹A; G¹ es H, o C(O)O; R es alquilo; R¹ es R², R³, R⁴ o R⁵; R¹A es cicloalquilo, cicloalquenilo o cicloalquinilo; R² es fenilo, que no está fusionado o está fusionado con R²A; R²A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R³ es heteroarilo, que no está fusionado o está fusionado con R³A; R³A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁴ es cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo, cada uno de los cuales no está fusionado o está fusionado con R⁴A; R⁴A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁵ es alquilo, alquenilo o alquinilo, cada uno de los cuales no está sustituido o está sustituido con uno o dos o tres sustituyentes seleccionados en forma independiente entre R⁶, NC(R⁶A)(R⁶B), R⁷, OR⁷, SR⁷, S(O)R⁷, SO₂R⁷, NHR⁷, N(R⁷)₂, C(O)R⁷, C(O)NH₂, C(O)NHR⁷, C(O)N(R⁷)₂, NHC(O)R⁷, NR⁷C(O)R⁷, NHSO₂R⁷, NHC(O)OR⁷, SO₂NH₂, SO₂NHR⁷, SO₂N(R⁷)₂, NHC(O)NH₂, NHC(O)NHR⁷, NHC(O)CH(CH₃)NHC(O)CH(CH₃)NH₂, NHC(O)CH(CH₃)NHC(O)CH(CH₃)NHR⁷, OH, (O), C(O)OH, N₃, CN, NH₂, CF₃, CF₂CF₃, F, Cl, Br o I; R⁶ es C₂₋₅-espiroalquilo, cada uno de los cuales no está sustituido o está sustituido con OH, (O), N₃, CN, CF₃, CF₂CF₃, F, Cl, Br, I, NH₂, NH(CH₃) o N(CH₃)₂; R⁶A y R⁶B se seleccionan en forma independiente entre alquilo o, junto con el N al cual están unidos, R⁶C; R⁶C es aziridin-1-ilo, azetidin-1-ilo, pirrolidin-1-ilo o piperidin-1-ilo, donde cada uno tiene una unidad CH₂ no reemplazada o reemplazada con O, C(O), CNOH, CNOCH₃, S, S(O), SO₂ o NH; R⁷ es R⁸, R⁹, R¹⁰ o R¹¹; R⁸ es fenilo, que no está fusionado o está fusionado con R⁸A; R⁸A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁹ es heteroarilo, que no está fusionado o está fusionado con R⁹A; R⁹A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R¹⁰ es cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo, cada uno de los cuales no está fusionado o está fusionado con R¹⁰A; R¹⁰A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R¹¹ es alquilo, alquenilo o alquinilo, cada uno de los cuales no está sustituido o está sustituido con uno o dos o tres sustituyentes seleccionados en forma independiente entre R¹², OR¹², SR¹², S(O)R¹², SO₂R¹², C(O)R¹², CO(O)R¹², OC(O)R¹², OC(O)OR¹², NH₂, NHR¹², N(R¹²)₂, NHC(O)R¹², NR¹²C(O)R¹², NHS(O)₂R¹², NR¹²S(O)₂R¹², NHC(O)OR¹², NR¹²C(O)OR¹², NHC(O)NH₂, NHC(O)NHR¹², NHC(O)N(R¹²)₂, NR¹²C(O)NHR¹², NR¹²C(O)N(R¹²)₂, C(O)NH₂, C(O)NHR¹², C(O)N(R¹²)₂, C(O)NHOH, C(O)NHOR¹², C(O)NHSO₂R¹², C(O)NR¹²SO₂R¹², SO₂NH₂, SO₂NHR¹², SO₂N(R¹²)₂, C(O)H, C(O)OH, C(N)NH₂, C(N)NHR¹², C(N)N(R¹²)₂, CNOH, CNOCH₃, OH, (O), CN, N₃, NO₂, CF₃, CF₂CF₃, OCF₃, OCF₂CF₃, F, Cl, Br o I; R¹² es R¹³, R¹⁴, R¹⁵ o R¹⁶; R¹³ es fenilo, que no está fusionado o está fusionado con R¹³A; R¹³A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R¹⁴ es heteroarilo, que no está fusionado o está fusionado con R¹⁴A; R¹⁴A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R¹⁵ es cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno, cada uno de los cuales no está fusionado o está fusionado con R¹⁵A; R¹⁵A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R¹⁶ es alquilo, alquenilo o alquinilo; R¹⁷ es R¹⁸, R¹⁹, R²⁰ o R²¹; R¹⁸ es fenilo, que no está fusionado o está fusionado con R¹⁸A; R¹⁸A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R¹⁹ es heteroarilo, que no está fusionado o está fusionado con R¹⁹A; R¹⁹A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R²⁰ es cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo cada uno de los cuales no está fusionado o está fusionado con R²⁰A; R²⁰A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R²¹ es alquilo, alquenilo o alquinilo, cada uno de los cuales no está sustituido o está sustituido con uno o dos o tres sustituyentes seleccionados en forma independiente entre R²², OR²², SR²², S(O)R²², SO₂R²², C(O)R²², CO(O)R²², OC(O)R²², OC(O)OR²², NH₂, NHR²², N(R²²)₂, NHC(O)R²², NR²²C(O)R²², NHS(O)₂R²², NR²²S(O)₂R²², NHC(O)OR²², NR²²C(O)OR²², NHC(O)NH₂, NHC(O)NHR²², NHC(O)N(R²²)₂, NR²²C(O)NHR²², NR²²C(O)N(R²²)₂, C(O)NH₂, C(O)NHR²², C(O)N(R²²)₂, C(O)NHOH, C(O)NHOR²², C(O)NHSO₂R²², C(O)NR²²SO₂R²², SO₂NH₂, SO₂NHR²², SO₂N(R²²)₂, C(O)H, C(O)OH, C(N)NH₂, C(N)NHR²², C(N)N(R²²)₂, CNOH, CNOCH₃, OH, (O), CN, N₃, NO₂, CF₃, CF₂CF₃, OCF₃, OCF₂CF₃, F, Cl, Br o I; R²² es R²³, R²⁴ o R²⁵; R²³ es fenilo, que no está fusionado o está fusionado con R²³A; R²³A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R²⁴ es heteroareno, que no está fusionado o está fusionado con R²⁴A; R²⁴A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R²⁵ es cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo, cada uno de los cuales no está fusionado o está fusionado con R²⁵A; R²⁵A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; Z¹ es R²⁶ o R²⁷; Z² es R²⁸, R²⁹ o R³⁰; Z¹A y Z²A están ambos ausentes o se toman juntos para formar CH₂, CH₂CH₂ o Z¹²A; Z¹²A es C₂₋₆-alquileno que tienen una o dos unidades CH₂ reemplazadas por NH, N(CH₃), S, S(O) o SO₂; L¹ es un R³⁷, OR³⁷, SR³⁷, S(O)R³⁷, SO₂R³⁷, C(O)R³⁷, CO(O)R³⁷, OC(O)R³⁷, OC(O)OR³⁷, NHR³⁷, C(O)NH, C(O)NR³⁷, C(O)NHOR³⁷, C(O)NHSO₂R³⁷, SO₂NH, SO₂NHR³⁷, C(N)NH, C(N)NHR³⁷; R²⁶ es fenileno, que no está fusionado o está fusionado con R²⁶A; R²⁶A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R²⁷ es heteroarileno, que no está fusionado o está fusionado con R²⁷A; R²⁷A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R²⁸ es fenileno, que no está fusionado o está fusionado con R²⁸A; R²⁸A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R²⁹ es heteroarileno, que no está fusionado o está fusionado con R²⁹A; R²⁹A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R³⁰ es cicloalquileno, cicloalquenileno, heterocicloalquileno o heterocicloalquenileno, cada uno de los cuales no está fusionado o está fusionado con R³⁰A; R³⁰A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R³⁷ es una unión o R³⁷A; R³⁷A es alquileno, alquenileno, o alquinileno, cada uno de los cuales no está sustituido o está sustituido con uno o dos o tres sustituyentes seleccionados en forma independiente entre R³⁷B, OR³⁷B, SR³⁷B, S(O)R³⁷B, SO₂R³⁷B, C(O)R³⁷B, CO(O)R³⁷B, OC(O)R³⁷B, OC(O)OR³⁷B, NH₂, NHR³⁷B, N(R³⁷B)₂, NHC(O)R³⁷B, NR³⁷BC(O)R³⁷B, NHS(O)₂R³⁷B, NR³⁷BS(O)₂R³⁷B, NHC(O)OR³⁷B, NR³⁷BC(O)OR³⁷B, NHC(O)NH₂, NHC(O)NHR³⁷B, NHC(O)N(R³⁷B)₂, NR³⁷BC(O)NHR³⁷B, NR³⁷BC(O)N(R³⁷B)₂, C(O)NH₂, C(O)NHR³⁷B, C(O)N(R³⁷B)₂, C(O)NHOH, C(O)NHOR³⁷B, C(O)NHSO₂R³⁷B, C(O)NR³⁷BSO₂R³⁷B, SO₂NH₂, SO₂NHR³⁷B, SO₂N(R³⁷B)₂, C(O)H, C(O)OH, C(N)NH₂, C(N)NHR³⁷B, C(N)N(R³⁷B)₂, CNOH, CNOCH₃, OH, (O), CN, N₃, NO₂, CF₃, CF₂CF₃, OCF₃, OCF₂CF₃, F, Cl, Br y I; R³⁷B es alquilo, alquenilo, alquinilo, o R³⁷C; R³⁷C es fenilo, heteroarilo, cicloalquilo, cicloalquenilo, heterocicloalquilo, o heterocicloalquenilo; Z³ es R³⁸, R³⁹ o R⁴⁰; R³⁸ es fenilo, que no está fusionado o está fusionado con R³⁸A; R³⁸A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R³⁹ es heteroarilo, que no está fusionado o está fusionado con R³⁹A; R³⁹A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁴⁰ es cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo, cada uno de los cuales no está fusionado o está fusionado con R⁴⁰A; R⁴⁰A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; en donde las unidades representadas por R²⁶ y R²⁷ están sustituidas (es decir, si Z¹A y Z²A están ausentes) o adicionalmente sustituidas (es decir, si Z¹A y Z²A están presentes) con R⁴¹, OR⁴¹, SR⁴¹, S(O)R⁴¹, SO₂R⁴¹, C(O)R⁴¹, CO(O)R⁴¹, OC(O)R⁴¹, OC(O)OR⁴¹, NHR⁴¹, N(R⁴¹)₂, NHC(O)R⁴¹, NR⁴¹C(O)R⁴¹, NHS(O)₂R⁴¹, NR⁴¹S(O)₂R⁴¹, NHC(O)OR⁴¹, NR⁴¹C(O)OR⁴¹, NHC(O)NHR⁴¹, NHC(O)N(R⁴¹)₂, NR⁴¹C(O)NHR⁴¹, NR⁴¹C(O)N(R⁴¹)₂, C(O)NHR⁴¹, C(O)N(R⁴¹)₂, C(O)NHOR⁴¹, C(O)NHSO₂R⁴¹, C(O)NR⁴¹SO₂R⁴¹, SO₂NHR⁴¹, SO₂N(R⁴¹)₂, C(N)NHR⁴¹, o C(N)N(R⁴¹)₂; R⁴¹ es heteroarilo, que está fusionado con R⁴³A; R⁴³A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; que no está fusionado o está fusionado con benceno, heteroareno o R⁴³B; R⁴³B es cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; en donde las porciones cíclicas representadas por E¹ e Y¹ juntos, Y¹ y B¹ juntos, A² y B¹ juntos, A² y D¹ juntos, R¹A, R², R²A, R³, R³A, R⁴, R⁴A, R⁶, R⁶C, R⁸, R⁸A, R⁹, R⁹A, R¹⁰, R¹⁰A, R¹³, R¹³A, R¹⁴, R¹⁴A, R¹⁵, R¹⁵A, R¹⁸, R¹⁸A, R¹⁹, R¹⁹A, R²⁰, R²⁰A, R²³, R²³A, R²⁴, R²⁴A, R²⁵, R²⁵A, R²⁶, R²⁶A, R²⁷, R²⁷A, R²⁸, R²⁸A, R²⁹, R²⁹A, R³⁰, R³⁰A, R³⁷B, R³⁸, R³⁸A, R³⁹, R³⁹A, R⁴⁰, y R⁴⁰A están no sustituidas, no sustituidas adicionalmente, sustituidas o sustituidas adicionalmente en forma independiente con uno o dos o tres o cuatro o cinco sustituyentes seleccionados en forma independiente entre R⁵⁷A, R⁵⁷, OR⁵⁷, SR⁵⁷, S(O)R⁵⁷, SO₂R⁵⁷, C(O)R⁵⁷, CO(O)R⁵⁷, OC(O)R⁵⁷, OC(O)OR⁵⁷, NH₂, NHR⁵⁷, N(R⁵⁷)₂, NHC(O)R⁵⁷, NR⁵⁷C(O)R⁵⁷, NHS(O)₂R⁵⁷, NR⁵⁷S(O)₂R⁵⁷, NHC(O)OR⁵⁷, NR⁵⁷C(O)OR⁵⁷, NHC(O)NH₂, NHC(O)NHR⁵⁷, NHC(O)N(R⁵⁷)₂, NR⁵⁷C(O)NHR⁵⁷, NR⁵⁷C(O)N(R⁵⁷)₂, C(O)NH₂, C(O)NHR⁵⁷, C(O)N(R⁵⁷)₂, C(O)NHOH, C(O)NHOR⁵⁷, C(O)NHSO₂R⁵⁷, C(O)NR⁵⁷SO₂R⁵⁷, SO₂NH₂, SO₂NHR⁵⁷, SO₂N(R⁵⁷)₂, C(O)H, C(O)OH, C(N)NH₂, C(N)NHR⁵⁷, C(N)N(R⁵⁷)₂, CNOH, CNOCH₃, OH, (O), CN, N₃, NO₂, CF₃, CF₂CF₃, OCF₃, OCF₂CF₃, F, Cl, Br o I; R⁵⁷A es espiroalquilo, o espiroheteroalquilo; R⁵⁷ es R⁵⁸, R⁵⁹, R⁶⁰ o R⁶¹; R⁵⁸ es fenilo, que no está fusionado o está fusionado con R⁵⁸A; R⁵⁸A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁵⁹ es heteroarilo, que no está fusionado o está fusionado con R⁵⁹A; R⁵⁹A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁶⁰ es cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo, cada uno de los cuales no está fusionado o está fusionado con R⁶⁰A; R⁶⁰A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁶¹ es alquilo, alquenilo o alquinilo, cada uno de los cuales no está sustituido o está sustituido con uno o dos o tres sustituyentes seleccionados en forma independiente entre R⁶², OR⁶², SR⁶², S(O)R⁶², SO₂R⁶², C(O)R⁶², CO(O)R⁶², OC(O)R⁶², OC(O)OR⁶², NH₂, NHR⁶², N(R⁶²)₂, NHC(O)R⁶², NR⁶²C(O)R⁶², NHS(O)₂R⁶², NR⁶²S(O)₂R⁶², NHC(O)OR⁶², NR⁶²C(O)OR⁶², NHC(O)NH₂, NHC(O)NHR⁶², NHC(O)N(R⁶²)₂, NR⁶²C(O)NHR⁶², NR⁶²C(O)N(R⁶²)₂, C(O)NH₂, C(O)NHR⁶², C(O)N(R⁶²)₂, C(O)NHOH, C(O)NHOR⁶², C(O)NHSO₂R⁶², C(O)NR⁶²SO₂R⁶², SO₂NH₂, SO₂NHR⁶², SO₂N(R⁶²)₂, C(O)H, C(O)OH, C(N)NH₂, C(N)NHR⁶², C(N)N(R⁶²)₂, CNOH, CNOCH₃, OH, (O), CN, N₃, NO₂, CF₃, CF₂CF₃, OCF₃, OCF₂CF₃, F, Cl, Br o I; R⁶² es R⁶³, R⁶⁴, R⁶⁵ o R⁶⁶; R⁶³ es fenilo, que no está fusionado o está fusionado con R⁶³A; R⁶³A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁶⁴ es heteroarilo, que no está fusionado o está fusionado con R⁶⁴A; R⁶⁴A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁶⁵ es cicloalquilo, cicloalquenilo, heterocicloalquilo, o heterocicloalquenilo, cada uno de los cuales no está fusionado o está fusionado con R⁶⁵A; R⁶⁵A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁶⁶ es alquilo, alquenilo o alquinilo, cada uno de los cuales no está sustituido o está sustituido con uno o dos o tres sustituyentes seleccionados en forma independiente entre R⁶⁷, OR⁶⁷, SR⁶⁷, S(O)R⁶⁷, SO₂R⁶⁷, C(O)R⁶⁷, CO(O)R⁶⁷, OC(O)R⁶⁷, OC(O)OR⁶⁷, NH₂, NHR⁶⁷, N(R⁶⁷)₂, NHC(O)R⁶⁷, NR⁶⁷C(O)R⁶⁷, NHS(O)₂R⁶⁷, NR⁶⁷S(O)₂R⁶⁷, NHC(O)OR⁶⁷, NR⁶⁷C(O)OR⁶⁷, NHC(O)NH₂, NHC(O)NHR⁶⁷, NHC(O)N(R⁶⁷)₂, NR⁶⁷C(O)NHR⁶⁷, NR⁶⁷C(O)N(R⁶⁷)₂, C(O)NH₂, C(O)NHR⁶⁷, C(O)N(R⁶⁷)₂, C(O)NHOH, C(O)NHOR⁶⁷, C(O)NHSO₂R⁶⁷, C(O)NR⁶⁷SO₂R⁶⁷, SO₂NH₂, SO₂NHR⁶⁷, SO₂N(R⁶⁷)₂, C(O)H, C(O)OH, C(N)NH₂, C(N)NHR⁶⁷, C(N)N(R⁶⁷)₂, CNOH, CNOCH₃, OH, (O), CN, N₃, NO₂, CF₃, CF₂CF₃, OCF₃, OCF₂CF₃, F, Cl, Br o I; R⁶⁷ es alquilo, alquenilo, alquinilo, fenilo, heteroarilo, cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo; en donde las porciones cíclicas representadas por R⁵⁷A, R⁵⁸, R⁵⁹, R⁶⁰, R⁶³, R⁶⁴, R⁶⁵, y R⁶⁷ no están sustituidas o están sustituidas con uno o dos o tres o cuatro sustituyentes seleccionados en forma independiente entre R⁶⁸, OR⁶⁸, SR⁶⁸, S(O)R⁶⁸, SO₂R⁶⁸, C(O)R⁶⁸, CO(O)R⁶⁸, OC(O)R⁶⁸, OC(O)OR⁶⁸, NH₂, NHR⁶⁸, N(R⁶⁸)₂, NHC(O)R⁶⁸, NR⁶⁸C(O)R⁶⁸, NHS(O)₂R⁶⁸, NR⁶⁸S(O)₂R⁶⁸, NHC(O)OR⁶⁸, NR⁶⁸C(O)OR⁶⁸, NHC(O)NH₂, NHC(O)NHR⁶⁸, NHC(O)N(R⁶⁸)₂, NR⁶⁸C(O)NHR⁶⁸, NR⁶⁸C(O)N(R⁶⁸)₂, C(O)NH₂, C(O)NHR⁶⁸, C(O)N(R⁶⁸)₂, C(O)NHOH, C(O)NHOR⁶⁸, C(O)NHSO₂R⁶⁸, C(O)NR⁶⁸SO₂R⁶⁸, SO₂NH₂, SO₂NHR⁶⁸, SO₂N(R⁶⁸)₂, C(O)H, C(O)OH, C(N)NH₂, C(N)NHR⁶⁸, C(N)N(R⁶⁸)₂, CNOH, CNOCH₃, OH, (O), CN, N₃, NO₂, CF₃, CF₂CF₃, OCF₃, OCF₂CF₃, F, Cl, Br o I; R⁶⁸ es R⁶⁹, R⁷⁰, R⁷¹ o R⁷²; R⁶⁹ es fenilo, que no está fusionado o está fusionado con R⁶⁹A; R⁶⁹A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁷⁰ es heteroarilo, que no está fusionado o está fusionado con R⁷⁰A; R⁷⁰A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁷¹ es cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo, cada uno de los cuales no está fusionado o está fusionado con R⁷¹A; R⁷¹A es benceno, heteroareno, cicloalcano, cicloalqueno, heterocicloalcano o heterocicloalqueno; R⁷² es alquilo, alquenilo o alquinilo, cada uno de los cuales no está sustituido o está sustituido con uno o dos o tres sustituyentes seleccionados en forma independiente entre R⁷³, OR⁷³, SR⁷³, S(O)R⁷³, SO₂R⁷³, C(O)R⁷³, CO(O)R⁷³, OC(O)R⁷³, OC(O)OR⁷³, NH₂, NHR⁷³, N(R⁷³)₂, NHC(O)R⁷³, NR⁷³C(O)R⁷³, NHS(O)₂R⁷³, NR⁷³S(O)₂R⁷³, NHC(O)OR⁷³, NR⁷³C(O)OR⁷³, NHC(O)NH₂, NHC(O)NHR⁷³, NHC(O)N(R⁷³)₂, NR⁷³C(O)NHR⁷³, NR⁷³C(O)N(R⁷³)₂, C(O)NH₂, C(O)NHR⁷³, C(O)N(R⁷³)₂, C(O)NHOH, C(O)NHOR⁷³, C(O)NHSO₂R⁷³, C(O)NR⁷³SO₂R⁷³, SO₂NH₂, SO₂NHR⁷³, SO₂N(R⁷³)₂, C(O)H, C(O)OH, C(N)NH₂, C(N)NHR⁷³, C(N)N(R⁷³)₂, CNOH, CNOCH₃, OH, (O), CN, N₃, NO₂, CF₃, CF₂CF₃, OCF₃, OCF₂CF₃, F, Cl, Br o I; R⁷³ es alquilo, alquenilo, alquinilo, fenilo, heteroarilo, cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo; y en donde las unidades representadas por R⁶⁹, R⁷⁰, y R⁷¹ no están sustituidas o están sustituidas con uno o dos o tres o cuatro sustituyentes seleccionados en forma independiente entre NH₂, C(O)NH₂, C(O)NHOH, SO₂NH₂, CF₃, CF₂CF₃, C(O)H, C(O)OH, C(N)NH₂, OH, (O), CN
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| AU2010204555B2 (en) | 2009-01-19 | 2013-03-07 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| US8546399B2 (en) | 2009-05-26 | 2013-10-01 | Abbvie Inc. | Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases |
| UA106079C2 (uk) * | 2009-05-26 | 2014-07-25 | Еббві Бахамаз Лтд. | Індукуючі апоптоз засоби для лікування злоякісної пухлини і імунних і аутоімунних захворювань |
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