JP2015526441A5 - - Google Patents
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- Publication number
- JP2015526441A5 JP2015526441A5 JP2015527566A JP2015527566A JP2015526441A5 JP 2015526441 A5 JP2015526441 A5 JP 2015526441A5 JP 2015527566 A JP2015527566 A JP 2015527566A JP 2015527566 A JP2015527566 A JP 2015527566A JP 2015526441 A5 JP2015526441 A5 JP 2015526441A5
- Authority
- JP
- Japan
- Prior art keywords
- chloro
- trifluoromethyl
- indazol
- benzoyl
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims 59
- -1 nitro, hydroxy Chemical group 0.000 claims 34
- 125000003545 alkoxy group Chemical group 0.000 claims 31
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 31
- 229910052736 halogen Inorganic materials 0.000 claims 31
- 150000002367 halogens Chemical class 0.000 claims 31
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 25
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 18
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims 13
- 125000004043 oxo group Chemical group O=* 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 12
- 239000012453 solvate Substances 0.000 claims 12
- 125000003282 alkyl amino group Chemical group 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
- 239000005711 Benzoic acid Substances 0.000 claims 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims 3
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 235000010233 benzoic acid Nutrition 0.000 claims 3
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 3
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 claims 3
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 2
- FOCBRZYNWUYTNP-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(morpholine-4-carbonyl)indazol-3-yl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(C1=CC=C(C=C11)C(=O)N2CCOCC2)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F FOCBRZYNWUYTNP-UHFFFAOYSA-N 0.000 claims 2
- 102000001691 Member 3 Group F Nuclear Receptor Subfamily 1 Human genes 0.000 claims 2
- 108010029279 Member 3 Group F Nuclear Receptor Subfamily 1 Proteins 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 230000001404 mediated effect Effects 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 125000004760 (C1-C4) alkylsulfonylamino group Chemical group 0.000 claims 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 1
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 1
- CUJAFWQPUBJJEJ-UHFFFAOYSA-N 2-acetamido-4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]indazol-3-yl]benzoic acid Chemical compound C1=C(C(O)=O)C(NC(=O)C)=CC(C=2C3=CC=CC=C3N(C(=O)C=3C(=CC=CC=3Cl)C(F)(F)F)N=2)=C1 CUJAFWQPUBJJEJ-UHFFFAOYSA-N 0.000 claims 1
- RQBDVVCZSCAYQL-UHFFFAOYSA-N 3-(4-carboxyphenyl)-1-[2-chloro-6-(trifluoromethyl)benzoyl]indazole-6-carboxylic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(C1=CC=C(C=C11)C(O)=O)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F RQBDVVCZSCAYQL-UHFFFAOYSA-N 0.000 claims 1
- FGSXFZVLHMWUDU-UHFFFAOYSA-N 3-fluoro-4-[1-(1-methylindole-2-carbonyl)indazol-3-yl]benzoic acid Chemical compound C=1C2=CC=CC=C2N(C)C=1C(=O)N(C1=CC=CC=C11)N=C1C1=CC=C(C(O)=O)C=C1F FGSXFZVLHMWUDU-UHFFFAOYSA-N 0.000 claims 1
- BPPONUKAAREGJL-UHFFFAOYSA-N 3-fluoro-4-[1-(2-methoxyacetyl)indazol-3-yl]benzoic acid Chemical compound C12=CC=CC=C2N(C(=O)COC)N=C1C1=CC=C(C(O)=O)C=C1F BPPONUKAAREGJL-UHFFFAOYSA-N 0.000 claims 1
- VWAYLDITYUHKSI-UHFFFAOYSA-N 3-fluoro-4-[1-(2-phenylpropanoyl)indazol-3-yl]benzoic acid Chemical compound C=1C=CC=CC=1C(C)C(=O)N(C1=CC=CC=C11)N=C1C1=CC=C(C(O)=O)C=C1F VWAYLDITYUHKSI-UHFFFAOYSA-N 0.000 claims 1
- URJOBDIUNWPXTR-UHFFFAOYSA-N 3-fluoro-4-[1-(naphthalene-1-carbonyl)indazol-3-yl]benzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)C1=CC=CC2=CC=CC=C12 URJOBDIUNWPXTR-UHFFFAOYSA-N 0.000 claims 1
- RQLYGRRZWKTFLU-UHFFFAOYSA-N 3-fluoro-4-[1-(oxolane-2-carbonyl)indazol-3-yl]benzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)C1OCCC1 RQLYGRRZWKTFLU-UHFFFAOYSA-N 0.000 claims 1
- AHXGVYIRKMKSAV-UHFFFAOYSA-N 3-fluoro-4-[1-(pyridine-3-carbonyl)indazol-3-yl]benzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)C1=CC=CN=C1 AHXGVYIRKMKSAV-UHFFFAOYSA-N 0.000 claims 1
- FEMMZTXFLFEFMF-UHFFFAOYSA-N 3-fluoro-4-[1-[2-(2-oxopyrrolidin-1-yl)acetyl]indazol-3-yl]benzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)CN1C(=O)CCC1 FEMMZTXFLFEFMF-UHFFFAOYSA-N 0.000 claims 1
- UFMFURBJBPRJFN-UHFFFAOYSA-N 3-fluoro-4-[1-[3-[(2-methylpropan-2-yl)oxycarbonyl]-3-azabicyclo[3.1.0]hexane-6-carbonyl]indazol-3-yl]benzoic acid Chemical compound C1N(C(=O)OC(C)(C)C)CC2C1C2C(=O)N(C1=CC=CC=C11)N=C1C1=CC=C(C(O)=O)C=C1F UFMFURBJBPRJFN-UHFFFAOYSA-N 0.000 claims 1
- MYRZEDFAAXWOCE-UHFFFAOYSA-N 4-[1-(1-benzofuran-7-carbonyl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)C1=CC=CC2=C1OC=C2 MYRZEDFAAXWOCE-UHFFFAOYSA-N 0.000 claims 1
- HLQBLHMEGINUEZ-UHFFFAOYSA-N 4-[1-(2,3-dihydro-1-benzofuran-7-carbonyl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)C1=CC=CC2=C1OCC2 HLQBLHMEGINUEZ-UHFFFAOYSA-N 0.000 claims 1
- ZQSOJGWWQMLPEG-UHFFFAOYSA-N 4-[1-(2,3-dihydro-1h-indene-4-carbonyl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)C1=CC=CC2=C1CCC2 ZQSOJGWWQMLPEG-UHFFFAOYSA-N 0.000 claims 1
- KNXIOXOXYSMFDK-UHFFFAOYSA-N 4-[1-(2-bromo-3-chlorobenzoyl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)C1=CC=CC(Cl)=C1Br KNXIOXOXYSMFDK-UHFFFAOYSA-N 0.000 claims 1
- VQYAVXSWJIEBDY-UHFFFAOYSA-N 4-[1-(2-bromo-3-methylbenzoyl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound CC1=CC=CC(C(=O)N2C3=CC=CC=C3C(C=3C(=CC(=CC=3)C(O)=O)F)=N2)=C1Br VQYAVXSWJIEBDY-UHFFFAOYSA-N 0.000 claims 1
- BCDKQBWCSBECKY-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclobutylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3,5-difluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC(F)=C1C(C1=NC=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C1CCC1 BCDKQBWCSBECKY-UHFFFAOYSA-N 0.000 claims 1
- CKFNTMBCGYATAC-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclobutylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=NC=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C1CCC1 CKFNTMBCGYATAC-UHFFFAOYSA-N 0.000 claims 1
- RDQQWHRZYWLWJC-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclopentylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=NC=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C1CCCC1 RDQQWHRZYWLWJC-UHFFFAOYSA-N 0.000 claims 1
- RUPATPKYIMISQN-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclopropylbenzoyl)-4-fluoroindazol-3-yl]-3,5-difluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC(F)=C1C(C1=C(F)C=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C1CC1 RUPATPKYIMISQN-UHFFFAOYSA-N 0.000 claims 1
- ITAJZCHZGRGIEJ-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclopropylbenzoyl)-4-fluoroindazol-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=C(F)C=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C1CC1 ITAJZCHZGRGIEJ-UHFFFAOYSA-N 0.000 claims 1
- AAADBGOEWPPOQQ-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclopropylbenzoyl)indazol-3-yl]-3,5-difluorobenzoic acid Chemical compound ClC1=C(C(=O)N2N=C(C3=CC=CC=C23)C2=C(C=C(C(=O)O)C=C2F)F)C(=CC=C1)C1CC1 AAADBGOEWPPOQQ-UHFFFAOYSA-N 0.000 claims 1
- CSTNVZNXJBJIAB-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclopropylbenzoyl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C1CC1 CSTNVZNXJBJIAB-UHFFFAOYSA-N 0.000 claims 1
- AMQKIZZEIKBRFO-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclopropylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3,5-difluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC(F)=C1C(C1=NC=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C1CC1 AMQKIZZEIKBRFO-UHFFFAOYSA-N 0.000 claims 1
- LMIWUTKCGKCAPR-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclopropylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=NC=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C1CC1 LMIWUTKCGKCAPR-UHFFFAOYSA-N 0.000 claims 1
- NAJJOZBHQMYRCQ-UHFFFAOYSA-N 4-[1-(2-chloro-6-cyclopropylbenzoyl)pyrrolo[3,2-b]pyridin-3-yl]-3,5-difluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC(F)=C1C(C1=NC=CC=C11)=CN1C(=O)C1=C(Cl)C=CC=C1C1CC1 NAJJOZBHQMYRCQ-UHFFFAOYSA-N 0.000 claims 1
- XQLORDGAAKKHJV-UHFFFAOYSA-N 4-[1-(2-chloro-6-methyl-4-morpholin-4-ylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound CC1=CC(N2CCOCC2)=CC(Cl)=C1C(=O)N(C1=CC=CN=C11)N=C1C1=CC=C(C(O)=O)C=C1F XQLORDGAAKKHJV-UHFFFAOYSA-N 0.000 claims 1
- MRUIGUAOGXKSOD-UHFFFAOYSA-N 4-[1-(2-chloro-6-morpholin-4-ylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=NC=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1N1CCOCC1 MRUIGUAOGXKSOD-UHFFFAOYSA-N 0.000 claims 1
- STTDKBXVHRDKSV-UHFFFAOYSA-N 4-[1-(2-chloro-6-prop-1-en-2-ylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound CC(=C)C1=CC=CC(Cl)=C1C(=O)N1C2=CC=CN=C2C(C=2C(=CC(=CC=2)C(O)=O)F)=N1 STTDKBXVHRDKSV-UHFFFAOYSA-N 0.000 claims 1
- SZTKTFVKDORSMX-UHFFFAOYSA-N 4-[1-(4-amino-2-chloro-6-methylbenzoyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound CC1=CC(N)=CC(Cl)=C1C(=O)N1C2=CC=CN=C2C(C=2C(=CC(=CC=2)C(O)=O)F)=N1 SZTKTFVKDORSMX-UHFFFAOYSA-N 0.000 claims 1
- ULGRACMCPGVEEK-UHFFFAOYSA-N 4-[1-(6-chloro-2,3-dihydro-1,4-benzodioxine-5-carbonyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=NC=CC=C11)=NN1C(=O)C1=C(Cl)C=CC2=C1OCCO2 ULGRACMCPGVEEK-UHFFFAOYSA-N 0.000 claims 1
- ULWLHAACQVHNPR-UHFFFAOYSA-N 4-[1-[2-(dimethylamino)-6-methylbenzoyl]pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound CN(C)C1=CC=CC(C)=C1C(=O)N1C2=CC=CN=C2C(C=2C(=CC(=CC=2)C(O)=O)F)=N1 ULWLHAACQVHNPR-UHFFFAOYSA-N 0.000 claims 1
- OEJKIMIEMMNCSZ-UHFFFAOYSA-N 4-[1-[2-chloro-4-(2-methoxyethoxy)-6-methylbenzoyl]pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound ClC1=CC(OCCOC)=CC(C)=C1C(=O)N1C2=CC=CN=C2C(C=2C(=CC(=CC=2)C(O)=O)F)=N1 OEJKIMIEMMNCSZ-UHFFFAOYSA-N 0.000 claims 1
- BIUDEVDBTBYDTN-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-2-methylindol-3-yl]-3-fluorobenzoic acid Chemical compound C12=CC=CC=C2N(C(=O)C=2C(=CC=CC=2Cl)C(F)(F)F)C(C)=C1C1=CC=C(C(O)=O)C=C1F BIUDEVDBTBYDTN-UHFFFAOYSA-N 0.000 claims 1
- IIYPHUTYQFNHTA-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-4-formylindazol-3-yl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(C1=C(C=O)C=CC=C11)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F IIYPHUTYQFNHTA-UHFFFAOYSA-N 0.000 claims 1
- LDWYFJQKADHORK-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-5-(methylamino)pyrrolo[2,3-c]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound C1=2C=NC(NC)=CC=2C(C=2C(=CC(=CC=2)C(O)=O)F)=CN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F LDWYFJQKADHORK-UHFFFAOYSA-N 0.000 claims 1
- ZAFJKTHLHAQPER-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-5-[(2-methylpropan-2-yl)oxycarbonylamino]pyrrolo[2,3-c]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound C1=2C=NC(NC(=O)OC(C)(C)C)=CC=2C(C=2C(=CC(=CC=2)C(O)=O)F)=CN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F ZAFJKTHLHAQPER-UHFFFAOYSA-N 0.000 claims 1
- VWLWIRYLQWWKSU-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1,3-oxazinane-3-carbonyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=NC=C(C=C11)C(=O)N2COCCC2)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F VWLWIRYLQWWKSU-UHFFFAOYSA-N 0.000 claims 1
- MUIQMFMWWHLGBL-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1,3-oxazol-2-yl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=C(C=C11)C=2OC=CN=2)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F MUIQMFMWWHLGBL-UHFFFAOYSA-N 0.000 claims 1
- NTVUUWMYIXCQPR-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1,3-oxazole-2-carbonyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=NC=C(C=C11)C(=O)C=2OC=CN=2)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F NTVUUWMYIXCQPR-UHFFFAOYSA-N 0.000 claims 1
- ZXYDLCCOBGDIMX-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1,3-oxazolidine-3-carbonyl)pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=NC=C(C=C11)C(=O)N2COCC2)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F ZXYDLCCOBGDIMX-UHFFFAOYSA-N 0.000 claims 1
- SOLIBFAOUSRRQU-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1,3-thiazol-4-yl)indazol-3-yl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(C1=CC=C(C=C11)C=2N=CSC=2)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F SOLIBFAOUSRRQU-UHFFFAOYSA-N 0.000 claims 1
- JJOYOICIYBODAK-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1,3-thiazol-5-yl)indazol-3-yl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(C1=CC=C(C=C11)C=2SC=NC=2)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F JJOYOICIYBODAK-UHFFFAOYSA-N 0.000 claims 1
- NACDHOZIQUKVIW-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1-methylimidazol-2-yl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound CN1C=CN=C1C1=CC=C(C(=NN2C(=O)C=3C(=CC=CC=3Cl)C(F)(F)F)C=3C(=CC(=CC=3)C(O)=O)F)C2=C1 NACDHOZIQUKVIW-UHFFFAOYSA-N 0.000 claims 1
- FLOCZDVOIMRSCY-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1-methylimidazol-4-yl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound CN1C=NC(C=2C=C3N(C(=O)C=4C(=CC=CC=4Cl)C(F)(F)F)N=C(C3=CC=2)C=2C(=CC(=CC=2)C(O)=O)F)=C1 FLOCZDVOIMRSCY-UHFFFAOYSA-N 0.000 claims 1
- AOMVCSGXIXOKEM-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(1-methylimidazol-4-yl)indazol-3-yl]benzoic acid Chemical compound CN1C=NC(C=2C=C3N(C(=O)C=4C(=CC=CC=4Cl)C(F)(F)F)N=C(C3=CC=2)C=2C=CC(=CC=2)C(O)=O)=C1 AOMVCSGXIXOKEM-UHFFFAOYSA-N 0.000 claims 1
- YNUXZWMHLUWWNJ-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(2,5-dioxoimidazolidin-4-yl)indazol-3-yl]-3-fluorobenzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C(C1=CC=C(C=C11)C2C(NC(=O)N2)=O)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F YNUXZWMHLUWWNJ-UHFFFAOYSA-N 0.000 claims 1
- DAEJUPFLIPARNN-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-(2-cyanophenyl)indazol-3-yl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(C1=CC=C(C=C11)C=2C(=CC=CC=2)C#N)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F DAEJUPFLIPARNN-UHFFFAOYSA-N 0.000 claims 1
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- WHGQARDUXBSUDH-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[(2-methylpropan-2-yl)oxycarbonylamino]pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound C12=CC(NC(=O)OC(C)(C)C)=CN=C2C(C=2C(=CC(=CC=2)C(O)=O)F)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F WHGQARDUXBSUDH-UHFFFAOYSA-N 0.000 claims 1
- FYCDYBZKAVRDMF-GASCZTMLSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[(2r,6s)-2,6-dimethylmorpholine-4-carbonyl]indazol-3-yl]-3-fluorobenzoic acid Chemical compound C1[C@@H](C)O[C@@H](C)CN1C(=O)C1=CC=C(C(=NN2C(=O)C=3C(=CC=CC=3Cl)C(F)(F)F)C=3C(=CC(=CC=3)C(O)=O)F)C2=C1 FYCDYBZKAVRDMF-GASCZTMLSA-N 0.000 claims 1
- IAHCCNRIJKPZTM-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[2-(dimethylamino)-2-oxoethyl]pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound C12=CC(CC(=O)N(C)C)=CN=C2C(C=2C(=CC(=CC=2)C(O)=O)F)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F IAHCCNRIJKPZTM-UHFFFAOYSA-N 0.000 claims 1
- FBVPAOCGDMHZAL-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[2-(methylamino)-2-oxoethyl]pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound C12=CC(CC(=O)NC)=CN=C2C(C=2C(=CC(=CC=2)C(O)=O)F)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F FBVPAOCGDMHZAL-UHFFFAOYSA-N 0.000 claims 1
- DBLOLXXKJOBMTA-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[5-(hydroxymethyl)-1,3-oxazol-2-yl]indazol-3-yl]-3-fluorobenzoic acid Chemical compound O1C(CO)=CN=C1C1=CC=C(C(=NN2C(=O)C=3C(=CC=CC=3Cl)C(F)(F)F)C=3C(=CC(=CC=3)C(O)=O)F)C2=C1 DBLOLXXKJOBMTA-UHFFFAOYSA-N 0.000 claims 1
- MHRAJUWMBYVALM-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[cyclopropyl(hydroxy)methyl]pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound C=1N=C2C(C=3C(=CC(=CC=3)C(O)=O)F)=NN(C(=O)C=3C(=CC=CC=3Cl)C(F)(F)F)C2=CC=1C(O)C1CC1 MHRAJUWMBYVALM-UHFFFAOYSA-N 0.000 claims 1
- KPPSRVSRXSXIEN-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[cyclopropyl(methyl)carbamoyl]pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound C=1N=C2C(C=3C(=CC(=CC=3)C(O)=O)F)=NN(C(=O)C=3C(=CC=CC=3Cl)C(F)(F)F)C2=CC=1C(=O)N(C)C1CC1 KPPSRVSRXSXIEN-UHFFFAOYSA-N 0.000 claims 1
- WDPHOVASCHHXHY-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[hydroxy(1,3-oxazol-2-yl)methyl]pyrazolo[4,3-b]pyridin-3-yl]-3-fluorobenzoic acid Chemical compound C=1N=C2C(C=3C(=CC(=CC=3)C(O)=O)F)=NN(C(=O)C=3C(=CC=CC=3Cl)C(F)(F)F)C2=CC=1C(O)C1=NC=CO1 WDPHOVASCHHXHY-UHFFFAOYSA-N 0.000 claims 1
- PLUSZQBSIICZOQ-UHFFFAOYSA-N 4-[1-[2-chloro-6-(trifluoromethyl)benzoyl]-6-[methyl(methylcarbamoyl)amino]indazol-3-yl]-3-fluorobenzoic acid Chemical compound C12=CC(N(C)C(=O)NC)=CC=C2C(C=2C(=CC(=CC=2)C(O)=O)F)=NN1C(=O)C1=C(Cl)C=CC=C1C(F)(F)F PLUSZQBSIICZOQ-UHFFFAOYSA-N 0.000 claims 1
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| KR102408261B1 (ko) | 2014-02-03 | 2022-06-10 | 비타이 파마슈티컬즈, 엘엘씨 | Ror-감마의 디하이드로피롤로피리딘 저해제 |
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| GB201419015D0 (en) | 2014-10-24 | 2014-12-10 | Orca Pharmaceuticals Ltd | Compounds |
| US9845308B2 (en) | 2014-11-05 | 2017-12-19 | Vitae Pharmaceuticals, Inc. | Isoindoline inhibitors of ROR-gamma |
| US9663515B2 (en) | 2014-11-05 | 2017-05-30 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| MA41179A (fr) | 2014-12-19 | 2017-10-24 | Cancer Research Tech Ltd | Composés inhibiteurs de parg |
| EP3242878B1 (en) * | 2015-01-08 | 2020-10-14 | Impetis Biosciences Ltd. | Bicyclic compounds, compositions and medicinal applications thereof |
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| CN107614062A (zh) | 2015-03-12 | 2018-01-19 | 加利福尼亚大学董事会 | 用RORγ抑制剂治疗癌症的方法 |
| AU2016257997A1 (en) | 2015-05-05 | 2017-11-09 | Lycera Corporation | Dihydro-2H-benzo[b][1,4]oxazine sulfonamide and related compounds for use as agonists of RORy and the treatment of disease |
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| US10301261B2 (en) | 2015-08-05 | 2019-05-28 | Vitae Pharmaceuticals, Llc | Substituted indoles as modulators of ROR-gamma |
| CA3129180A1 (en) * | 2015-09-21 | 2017-03-30 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| EP3368535B1 (en) * | 2015-10-27 | 2020-12-02 | Merck Sharp & Dohme Corp. | Heteroaryl substituted benzoic acids as rorgammat inhibitors and uses thereof |
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| EP3868750A1 (en) | 2015-11-20 | 2021-08-25 | Vitae Pharmaceuticals, LLC | Modulators of ror-gamma |
| EA201891626A1 (ru) * | 2016-01-21 | 2019-04-30 | Зибо Биополар Чангшенг Фармасьютикал Ко. Лтд. | Ингибиторы тирозинкиназы брутона |
| TWI757266B (zh) | 2016-01-29 | 2022-03-11 | 美商維它藥物有限責任公司 | ＲＯＲ－γ調節劑 |
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| JP6985388B2 (ja) * | 2016-07-29 | 2021-12-22 | ラプト・セラピューティクス・インコーポレイテッド | ケモカイン受容体調節剤及びそれの使用 |
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| CN117043162A (zh) * | 2021-05-19 | 2023-11-10 | 迈巴制药(南京)有限公司 | Tyk2选择性抑制剂及其用途 |
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-
2012
- 2012-08-15 WO PCT/CN2012/080131 patent/WO2014026327A1/en not_active Ceased
-
2013
- 2013-08-14 KR KR1020157006322A patent/KR20150042266A/ko not_active Withdrawn
- 2013-08-14 CA CA2881688A patent/CA2881688A1/en not_active Abandoned
- 2013-08-14 WO PCT/US2013/054887 patent/WO2014028589A2/en not_active Ceased
- 2013-08-14 RU RU2015108894A patent/RU2015108894A/ru unknown
- 2013-08-14 AU AU2013302725A patent/AU2013302725A1/en not_active Abandoned
- 2013-08-14 EP EP13829282.6A patent/EP2884981B1/en active Active
- 2013-08-14 MX MX2015001941A patent/MX2015001941A/es unknown
- 2013-08-14 JP JP2015527566A patent/JP6422438B2/ja not_active Expired - Fee Related
- 2013-08-14 US US14/421,048 patent/US9745265B2/en active Active
- 2013-08-14 BR BR112015003188A patent/BR112015003188A2/pt not_active IP Right Cessation
-
2015
- 2015-02-12 IN IN1156DEN2015 patent/IN2015DN01156A/en unknown
-
2017
- 2017-07-12 US US15/647,437 patent/US10196354B2/en active Active
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