JP2012525336A5 - - Google Patents
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- JP2012525336A5 JP2012525336A5 JP2012507475A JP2012507475A JP2012525336A5 JP 2012525336 A5 JP2012525336 A5 JP 2012525336A5 JP 2012507475 A JP2012507475 A JP 2012507475A JP 2012507475 A JP2012507475 A JP 2012507475A JP 2012525336 A5 JP2012525336 A5 JP 2012525336A5
- Authority
- JP
- Japan
- Prior art keywords
- dihydro
- inden
- oxo
- dihydropyridine
- carboxamide
- 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.)
- Pending
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- 150000001875 compounds Chemical class 0.000 claims 44
- -1 R 13 Chemical compound 0.000 claims 15
- 150000003839 salts Chemical class 0.000 claims 15
- 239000012453 solvate Substances 0.000 claims 15
- 239000000203 mixture Substances 0.000 claims 11
- 125000003118 aryl group Chemical group 0.000 claims 9
- 125000001072 heteroaryl group Chemical group 0.000 claims 9
- 229910052736 halogen Inorganic materials 0.000 claims 8
- 150000002367 halogens Chemical class 0.000 claims 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 125000006584 (C3-C10) heterocycloalkyl group Chemical group 0.000 claims 7
- 125000004404 heteroalkyl group Chemical group 0.000 claims 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 7
- 102000006495 integrins Human genes 0.000 claims 6
- 108010044426 integrins Proteins 0.000 claims 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 5
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 4
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 230000027455 binding Effects 0.000 claims 4
- 150000003857 carboxamides Chemical class 0.000 claims 4
- 239000003446 ligand Substances 0.000 claims 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 4
- 125000004076 pyridyl group Chemical group 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- MGTSRKSZRYSNRG-UHFFFAOYSA-N 1-(4-bromo-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(Br)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 MGTSRKSZRYSNRG-UHFFFAOYSA-N 0.000 claims 3
- WBJYXSTVRZMYHR-UHFFFAOYSA-N 1-(4-methoxy-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-(4-phenoxyphenyl)pyridine-3-carboxamide Chemical compound C1CC=2C(OC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC(C=C1)=CC=C1OC1=CC=CC=C1 WBJYXSTVRZMYHR-UHFFFAOYSA-N 0.000 claims 3
- DLWITLRKVVCPBW-UHFFFAOYSA-N 1-(4-methoxy-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(OC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 DLWITLRKVVCPBW-UHFFFAOYSA-N 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 238000000099 in vitro assay Methods 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 229930192474 thiophene Natural products 0.000 claims 3
- WFOKKBXIFGWUGP-UHFFFAOYSA-N 1-(4-methoxy-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-(4-phenylphenyl)pyridine-3-carboxamide Chemical compound C1CC=2C(OC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC(C=C1)=CC=C1C1=CC=CC=C1 WFOKKBXIFGWUGP-UHFFFAOYSA-N 0.000 claims 2
- BYQYNXXZYYARKU-UHFFFAOYSA-N 1-(4-morpholin-4-yl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-phenylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)N3CCOCC3)CC2)C(=O)C=1C(=O)NC1=CC=CC=C1 BYQYNXXZYYARKU-UHFFFAOYSA-N 0.000 claims 2
- NOXXXWUZNCFIGU-UHFFFAOYSA-N 1-(6-methoxy-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C12=CC(OC)=CC=C2CCC1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 NOXXXWUZNCFIGU-UHFFFAOYSA-N 0.000 claims 2
- 102000016359 Fibronectins Human genes 0.000 claims 2
- 108010067306 Fibronectins Proteins 0.000 claims 2
- 238000003556 assay Methods 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- 208000027866 inflammatory disease Diseases 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 238000006467 substitution reaction Methods 0.000 claims 2
- CCKYEVWPJBLGSL-UHFFFAOYSA-N 1-(2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=CC=CC=C3CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 CCKYEVWPJBLGSL-UHFFFAOYSA-N 0.000 claims 1
- FHSNQTUPSULWBN-UHFFFAOYSA-N 1-(3-methyl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C12=CC=CC=C2C(C)CC1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 FHSNQTUPSULWBN-UHFFFAOYSA-N 0.000 claims 1
- XFVUNFLEGLIUBD-UHFFFAOYSA-N 1-(4-acetamido-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(NC(=O)C)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 XFVUNFLEGLIUBD-UHFFFAOYSA-N 0.000 claims 1
- GOEROXFHACADLC-UHFFFAOYSA-N 1-(4-amino-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(N)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 GOEROXFHACADLC-UHFFFAOYSA-N 0.000 claims 1
- WOJIKDNMHKTBQP-UHFFFAOYSA-N 1-(4-bromo-2,3-dihydro-1h-inden-1-yl)-n-(4-chlorophenyl)-2-oxopyridine-3-carboxamide Chemical compound C1=CC(Cl)=CC=C1NC(=O)C(C1=O)=CC=CN1C1C(C=CC=C2Br)=C2CC1 WOJIKDNMHKTBQP-UHFFFAOYSA-N 0.000 claims 1
- FNFRZOUOMFBWCP-UHFFFAOYSA-N 1-(4-chloro-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(Cl)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 FNFRZOUOMFBWCP-UHFFFAOYSA-N 0.000 claims 1
- KPWKCFBQCLGQGD-UHFFFAOYSA-N 1-(4-cyano-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)C#N)CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 KPWKCFBQCLGQGD-UHFFFAOYSA-N 0.000 claims 1
- KPLCFCSBJAOAAU-UHFFFAOYSA-N 1-(4-cyclopropyl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)C3CC3)CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 KPLCFCSBJAOAAU-UHFFFAOYSA-N 0.000 claims 1
- PQLTUTXADSMBCD-UHFFFAOYSA-N 1-(4-hydroxy-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-(4-phenylphenyl)pyridine-3-carboxamide Chemical compound C1CC=2C(O)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC(C=C1)=CC=C1C1=CC=CC=C1 PQLTUTXADSMBCD-UHFFFAOYSA-N 0.000 claims 1
- VXPGVFBGQUKIRD-UHFFFAOYSA-N 1-(4-methoxy-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound C1CC=2C(OC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 VXPGVFBGQUKIRD-UHFFFAOYSA-N 0.000 claims 1
- ZWTIJGFALYXVJT-UHFFFAOYSA-N 1-(4-methoxy-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-phenylpyridine-3-carboxamide Chemical compound C1CC=2C(OC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=CC=C1 ZWTIJGFALYXVJT-UHFFFAOYSA-N 0.000 claims 1
- SNCIYGCAKRMIIC-UHFFFAOYSA-N 1-(4-methoxy-2,3-dihydro-1h-inden-1-yl)-n-[4-(2-methoxyphenyl)phenyl]-2-oxopyridine-3-carboxamide Chemical compound C1CC=2C(OC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC(C=C1)=CC=C1C1=CC=CC=C1OC SNCIYGCAKRMIIC-UHFFFAOYSA-N 0.000 claims 1
- MDKSZGHWXVNNHA-UHFFFAOYSA-N 1-(4-methoxy-2,3-dihydro-1h-inden-1-yl)-n-[4-(4-methoxyphenoxy)phenyl]-2-oxopyridine-3-carboxamide Chemical compound C1=CC(OC)=CC=C1OC(C=C1)=CC=C1NC(=O)C(C1=O)=CC=CN1C1C(C=CC=C2OC)=C2CC1 MDKSZGHWXVNNHA-UHFFFAOYSA-N 0.000 claims 1
- JVBDRUXNLPUACH-UHFFFAOYSA-N 1-(4-methoxy-2,3-dihydro-1h-inden-1-yl)-n-[4-(4-methoxyphenyl)phenyl]-2-oxopyridine-3-carboxamide Chemical compound C1=CC(OC)=CC=C1C(C=C1)=CC=C1NC(=O)C(C1=O)=CC=CN1C1C(C=CC=C2OC)=C2CC1 JVBDRUXNLPUACH-UHFFFAOYSA-N 0.000 claims 1
- RBHNCUWUVWCSAY-UHFFFAOYSA-N 1-(4-methyl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(C)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 RBHNCUWUVWCSAY-UHFFFAOYSA-N 0.000 claims 1
- IQQACCNUSCXUCA-UHFFFAOYSA-N 1-(4-methylsulfanyl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(SC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 IQQACCNUSCXUCA-UHFFFAOYSA-N 0.000 claims 1
- MSJRPOFHRHBTEH-UHFFFAOYSA-N 1-(4-methylsulfonyl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(S(=O)(=O)C)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 MSJRPOFHRHBTEH-UHFFFAOYSA-N 0.000 claims 1
- FQGJWZPCMJLUFK-UHFFFAOYSA-N 1-(4-morpholin-4-yl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-(4-phenoxyphenyl)pyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)N3CCOCC3)CC2)C(=O)C=1C(=O)NC(C=C1)=CC=C1OC1=CC=CC=C1 FQGJWZPCMJLUFK-UHFFFAOYSA-N 0.000 claims 1
- OMZUTCXYMPZTTO-UHFFFAOYSA-N 1-(4-morpholin-4-yl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)C(C1=O)=CC=CN1C1C(C=CC=C2N3CCOCC3)=C2CC1 OMZUTCXYMPZTTO-UHFFFAOYSA-N 0.000 claims 1
- OLISEGVDHLJMND-UHFFFAOYSA-N 1-(4-morpholin-4-yl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-[4-(trifluoromethyl)phenyl]pyridine-3-carboxamide Chemical compound C1=CC(C(F)(F)F)=CC=C1NC(=O)C(C1=O)=CC=CN1C1C(C=CC=C2N3CCOCC3)=C2CC1 OLISEGVDHLJMND-UHFFFAOYSA-N 0.000 claims 1
- YCIZPTKCERATII-UHFFFAOYSA-N 1-(4-morpholin-4-yl-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)N3CCOCC3)CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 YCIZPTKCERATII-UHFFFAOYSA-N 0.000 claims 1
- MYVYMEPVMOHNMF-UHFFFAOYSA-N 1-(4-nitro-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C([N+](=O)[O-])=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 MYVYMEPVMOHNMF-UHFFFAOYSA-N 0.000 claims 1
- QIUSZEHWTSLBQF-UHFFFAOYSA-N 1-(6-bromo-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C12=CC(Br)=CC=C2CCC1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 QIUSZEHWTSLBQF-UHFFFAOYSA-N 0.000 claims 1
- BGQSTCMBYRTACM-UHFFFAOYSA-N 1-(6-bromo-2,3-dihydro-1h-inden-1-yl)-n-(4-chlorophenyl)-2-oxopyridine-3-carboxamide Chemical compound C1=CC(Cl)=CC=C1NC(=O)C(C1=O)=CC=CN1C1C2=CC(Br)=CC=C2CC1 BGQSTCMBYRTACM-UHFFFAOYSA-N 0.000 claims 1
- RAWJRBXOODIXOY-UHFFFAOYSA-N 1-(7,8-dihydro-6h-cyclopenta[g][1,3]benzodioxol-6-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C=4OCOC=4C=C3)CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 RAWJRBXOODIXOY-UHFFFAOYSA-N 0.000 claims 1
- UUBVYYFMGGHBAK-UHFFFAOYSA-N 1-(7-methoxy-2,3-dihydro-1h-inden-1-yl)-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1=2C(OC)=CC=CC=2CCC1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 UUBVYYFMGGHBAK-UHFFFAOYSA-N 0.000 claims 1
- CCKYEVWPJBLGSL-GOSISDBHSA-N 1-[(1r)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN([C@H]2C3=CC=CC=C3CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 CCKYEVWPJBLGSL-GOSISDBHSA-N 0.000 claims 1
- WQDDRSUCGRFFEB-ZWKOTPCHSA-N 1-[(1r,2s)-2-hydroxy-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound O=C1N([C@@H]2C3=CC=CC=C3C[C@@H]2O)C=CC=C1C(=O)NC1=CC=NC=C1 WQDDRSUCGRFFEB-ZWKOTPCHSA-N 0.000 claims 1
- CCKYEVWPJBLGSL-SFHVURJKSA-N 1-[(1s)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN([C@@H]2C3=CC=CC=C3CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 CCKYEVWPJBLGSL-SFHVURJKSA-N 0.000 claims 1
- WQDDRSUCGRFFEB-MSOLQXFVSA-N 1-[(1s,2r)-2-hydroxy-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound O=C1N([C@H]2C3=CC=CC=C3C[C@H]2O)C=CC=C1C(=O)NC1=CC=NC=C1 WQDDRSUCGRFFEB-MSOLQXFVSA-N 0.000 claims 1
- QRKJFFQWCLAZIT-UHFFFAOYSA-N 1-[4-(4-acetylpiperazin-1-yl)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CN(C(=O)C)CCN1C1=CC=CC2=C1CCC2N1C(=O)C(C(=O)NC=2C=CN=CC=2)=CC=C1 QRKJFFQWCLAZIT-UHFFFAOYSA-N 0.000 claims 1
- NRVCMCNZPQSNPP-UHFFFAOYSA-N 1-[4-(4-hydroxypiperidin-1-yl)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC(O)CCN1C1=CC=CC2=C1CCC2N1C(=O)C(C(=O)NC=2C=CN=CC=2)=CC=C1 NRVCMCNZPQSNPP-UHFFFAOYSA-N 0.000 claims 1
- ICPVZTPGZXVHTQ-UHFFFAOYSA-N 1-[4-(4-methylpiperazin-1-yl)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CN(C)CCN1C1=CC=CC2=C1CCC2N1C(=O)C(C(=O)NC=2C=CN=CC=2)=CC=C1 ICPVZTPGZXVHTQ-UHFFFAOYSA-N 0.000 claims 1
- XCCQYAUZLYVYON-UHFFFAOYSA-N 1-[4-(cyclopropylamino)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)NC3CC3)CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 XCCQYAUZLYVYON-UHFFFAOYSA-N 0.000 claims 1
- MUZKIXYETQBYFS-UHFFFAOYSA-N 1-[4-(dimethylamino)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(N(C)C)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 MUZKIXYETQBYFS-UHFFFAOYSA-N 0.000 claims 1
- URUJZJKZXLMCCO-UHFFFAOYSA-N 1-[4-(methylamino)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(NC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 URUJZJKZXLMCCO-UHFFFAOYSA-N 0.000 claims 1
- DOVUJQMOXPYQMQ-UHFFFAOYSA-N 1-[4-(methylcarbamoyl)-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(C(=O)NC)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 DOVUJQMOXPYQMQ-UHFFFAOYSA-N 0.000 claims 1
- KKYCOCFTHSEGSX-UHFFFAOYSA-N 1-[4-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]-2,3-dihydro-1h-inden-1-yl]-2-oxo-n-(4-phenylphenyl)pyridine-3-carboxamide Chemical compound C1CC=2C(OCCOCCOCCO)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC(C=C1)=CC=C1C1=CC=CC=C1 KKYCOCFTHSEGSX-UHFFFAOYSA-N 0.000 claims 1
- XUWPENNWWFSKNQ-UHFFFAOYSA-N 1-[4-[4-[2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]acetyl]piperazin-1-yl]-2,3-dihydro-1h-inden-1-yl]-n-(4-chlorophenyl)-2-oxopyridine-3-carboxamide Chemical compound C1CN(C(=O)COCCOCCOCCN)CCN1C1=CC=CC2=C1CCC2N1C(=O)C(C(=O)NC=2C=CC(Cl)=CC=2)=CC=C1 XUWPENNWWFSKNQ-UHFFFAOYSA-N 0.000 claims 1
- TYNSEQWDCJNOFZ-UHFFFAOYSA-N 2-oxo-1-(4-phenyl-2,3-dihydro-1h-inden-1-yl)-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)C=3C=CC=CC=3)CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 TYNSEQWDCJNOFZ-UHFFFAOYSA-N 0.000 claims 1
- DBTUKGQQHXXZRH-UHFFFAOYSA-N 2-oxo-1-(4-piperazin-1-yl-2,3-dihydro-1h-inden-1-yl)-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)N3CCNCC3)CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 DBTUKGQQHXXZRH-UHFFFAOYSA-N 0.000 claims 1
- UPUNKRHTHQKKLY-UHFFFAOYSA-N 2-oxo-1-(4-propan-2-yloxy-2,3-dihydro-1h-inden-1-yl)-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C1CC=2C(OC(C)C)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 UPUNKRHTHQKKLY-UHFFFAOYSA-N 0.000 claims 1
- MMPSZOGBQOYPSL-UHFFFAOYSA-N 2-oxo-n-pyridin-4-yl-1-(4-pyridin-3-yl-2,3-dihydro-1h-inden-1-yl)pyridine-3-carboxamide Chemical compound C=1C=CN(C2C3=C(C(=CC=C3)C=3C=NC=CC=3)CC2)C(=O)C=1C(=O)NC1=CC=NC=C1 MMPSZOGBQOYPSL-UHFFFAOYSA-N 0.000 claims 1
- UKVNNYDWFGPHLQ-UHFFFAOYSA-N 2-oxo-n-pyridin-4-yl-1-[4-(trifluoromethoxy)-2,3-dihydro-1h-inden-1-yl]pyridine-3-carboxamide Chemical compound C1CC=2C(OC(F)(F)F)=CC=CC=2C1N(C1=O)C=CC=C1C(=O)NC1=CC=NC=C1 UKVNNYDWFGPHLQ-UHFFFAOYSA-N 0.000 claims 1
- 206010009900 Colitis ulcerative Diseases 0.000 claims 1
- 208000011231 Crohn disease Diseases 0.000 claims 1
- 102000004264 Osteopontin Human genes 0.000 claims 1
- 108010081689 Osteopontin Proteins 0.000 claims 1
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- 201000006704 Ulcerative Colitis Diseases 0.000 claims 1
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| CA2806341C (en) | 2010-07-29 | 2020-03-24 | Rigel Pharmaceuticals, Inc. | Ampk-activating heterocyclic compounds and methods for using the same |
| KR101317656B1 (ko) * | 2011-06-30 | 2013-10-15 | 연세대학교 산학협력단 | 복제효소 인산화를 조절하는 신규 ｃ형 간염 예방 또는 치료용 조성물 |
| EP2562174A1 (de) * | 2011-08-24 | 2013-02-27 | Bayer Cropscience AG | Herbizid wirksame 6-Oxo-1,6-dihydropyrimidin-5-carboxamide und 2-Oxo-1,2-dihydropyridin-3-carboxamide |
| SG11201404505PA (en) * | 2012-01-31 | 2014-10-30 | Daiichi Sankyo Co Ltd | Pyridone derivative |
| CN104364236B (zh) * | 2012-05-09 | 2018-01-16 | 拜尔农作物科学股份公司 | 5‑卤代吡唑二氢茚基甲酰胺 |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| RU2692485C2 (ru) | 2014-04-02 | 2019-06-25 | Интермьюн, Инк. | Противофиброзные пиридиноны |
| TWI723572B (zh) * | 2014-07-07 | 2021-04-01 | 日商第一三共股份有限公司 | 具有四氫吡喃基甲基之吡啶酮衍生物及其用途 |
| US9840513B2 (en) * | 2015-07-16 | 2017-12-12 | Abbvie S.Á.R.L. | Substituted tricyclics and method of use |
| WO2019200114A1 (en) * | 2018-04-12 | 2019-10-17 | Arbutus Biopharma Corporation | Methods for preparing substituted dihydroindene-4-carboxamide compounds |
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| ES2987796T3 (es) | 2018-10-30 | 2024-11-18 | Gilead Sciences Inc | Derivados de N-benzoil-fenilalanina como inhibidores de la integrina alfa4beta7 para el tratamiento de enfermedades inflamatorias |
| CN112969687B (zh) | 2018-10-30 | 2024-08-23 | 吉利德科学公司 | 作为α4β7整合素抑制剂的喹啉衍生物 |
| CA3114240C (en) | 2018-10-30 | 2023-09-05 | Gilead Sciences, Inc. | Imidazopyridine derivatives as alpha4beta7 integrin inhibitors |
| MX2021010314A (es) * | 2019-02-28 | 2021-11-12 | Kezar Life Sciences | Derivados de tiazol como inhibidores de la secreción de proteínas. |
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-
2010
- 2010-04-27 CA CA2760151A patent/CA2760151A1/en not_active Abandoned
- 2010-04-27 SG SG10201401836RA patent/SG10201401836RA/en unknown
- 2010-04-27 BR BRPI1015259A patent/BRPI1015259A2/pt not_active IP Right Cessation
- 2010-04-27 EP EP10719684A patent/EP2424841A1/en not_active Withdrawn
- 2010-04-27 JP JP2012507475A patent/JP2012525336A/ja active Pending
- 2010-04-27 WO PCT/US2010/032632 patent/WO2010126914A1/en not_active Ceased
- 2010-04-27 MX MX2011011326A patent/MX2011011326A/es active IP Right Grant
- 2010-04-27 US US12/768,680 patent/US8367836B2/en not_active Expired - Fee Related
- 2010-04-27 AU AU2010241742A patent/AU2010241742A1/en not_active Abandoned
- 2010-04-27 CN CN2010800273757A patent/CN102459179A/zh active Pending
- 2010-04-27 SG SG2011078409A patent/SG175355A1/en unknown
-
2011
- 2011-10-26 IL IL215956A patent/IL215956A0/en unknown
-
2012
- 2012-12-28 US US13/730,522 patent/US20130252957A1/en not_active Abandoned
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