JP2016535784A5 - - Google Patents
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- Publication number
- JP2016535784A5 JP2016535784A5 JP2016552453A JP2016552453A JP2016535784A5 JP 2016535784 A5 JP2016535784 A5 JP 2016535784A5 JP 2016552453 A JP2016552453 A JP 2016552453A JP 2016552453 A JP2016552453 A JP 2016552453A JP 2016535784 A5 JP2016535784 A5 JP 2016535784A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- pyrazole
- dihydrochromeno
- carboxamido
- fluorobenzyl
- 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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- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 63
- 150000001875 compounds Chemical class 0.000 claims description 61
- 239000002253 acid Substances 0.000 claims description 42
- 125000000217 alkyl group Chemical group 0.000 claims description 33
- 239000005711 Benzoic acid Substances 0.000 claims description 31
- 235000010233 benzoic acid Nutrition 0.000 claims description 31
- 150000003839 salts Chemical class 0.000 claims description 23
- 125000001424 substituent group Chemical group 0.000 claims description 20
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- 239000003814 drug Substances 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- 125000005843 halogen group Chemical group 0.000 claims description 16
- 208000008338 non-alcoholic fatty liver disease Diseases 0.000 claims description 16
- 102100038495 Bile acid receptor Human genes 0.000 claims description 12
- 101000603876 Homo sapiens Bile acid receptor Proteins 0.000 claims description 12
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 12
- 125000005842 heteroatom Chemical group 0.000 claims description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 230000001404 mediated effect Effects 0.000 claims description 11
- 206010008635 Cholestasis Diseases 0.000 claims description 10
- -1 N- (2-fluorobenzyl) -1-methyl-1,4-dihydrochromeno [4,3-c] pyrazole-3-carboxamido Chemical group 0.000 claims description 10
- 230000007870 cholestasis Effects 0.000 claims description 10
- 231100000359 cholestasis Toxicity 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 10
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 9
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 206010053219 non-alcoholic steatohepatitis Diseases 0.000 claims description 8
- 125000004076 pyridyl group Chemical group 0.000 claims description 8
- 125000006413 ring segment Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 7
- 208000019423 liver disease Diseases 0.000 claims description 7
- 229940124597 therapeutic agent Drugs 0.000 claims description 6
- FWXWRVYLLDLGNU-UHFFFAOYSA-N 8-fluoro-N-[(2-fluorophenyl)methyl]-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carboxamide Chemical compound FC1=CC2=C(C=C1)OCC1=C2N(N=C1C(=O)NCC1=C(C=CC=C1)F)C FWXWRVYLLDLGNU-UHFFFAOYSA-N 0.000 claims description 5
- JYTIXGYXBIBOMN-UHFFFAOYSA-N nidufexor Chemical compound Cn1nc(C(=O)N(Cc2ccccc2)Cc2ccc(cc2)C(O)=O)c2COc3ccc(Cl)cc3-c12 JYTIXGYXBIBOMN-UHFFFAOYSA-N 0.000 claims description 5
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 claims description 4
- 208000008439 Biliary Liver Cirrhosis Diseases 0.000 claims description 4
- 208000033222 Biliary cirrhosis primary Diseases 0.000 claims description 4
- 206010012735 Diarrhoea Diseases 0.000 claims description 4
- 208000012654 Primary biliary cholangitis Diseases 0.000 claims description 4
- 239000003613 bile acid Substances 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 125000001041 indolyl group Chemical group 0.000 claims description 4
- 235000016236 parenteral nutrition Nutrition 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- FSJRFMYCVARFJU-UHFFFAOYSA-N 3-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]ethoxy]benzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2cccc(c2)C(O)=O)Cc2ccccc2F)c2COc3ccc(Cl)cc3-c12 FSJRFMYCVARFJU-UHFFFAOYSA-N 0.000 claims description 3
- LYVMCHZYDPLRTR-UHFFFAOYSA-N 3-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]ethylamino]benzoic acid Chemical compound Cn1nc(C(=O)N(CCNc2cccc(c2)C(O)=O)Cc2ccccc2F)c2COc3ccc(Cl)cc3-c12 LYVMCHZYDPLRTR-UHFFFAOYSA-N 0.000 claims description 3
- LRPVFIZBQAZGFZ-UHFFFAOYSA-N 3-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluorophenyl)methyl]amino]ethylamino]-4-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCNc2cc(ccc2F)C(O)=O)Cc2cccc(F)c2)c2COc3ccc(Cl)cc3-c12 LRPVFIZBQAZGFZ-UHFFFAOYSA-N 0.000 claims description 3
- IQIHHXCDAAIRAM-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]methyl]benzoic acid Chemical compound Cn1nc(C(=O)N(Cc2ccc(cc2)C(O)=O)Cc2ccccc2F)c2COc3ccc(Cl)cc3-c12 IQIHHXCDAAIRAM-UHFFFAOYSA-N 0.000 claims description 3
- AUCJHDHYRSXPGJ-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluorophenyl)methyl]amino]methyl]benzoic acid Chemical compound Cn1nc(C(=O)N(Cc2ccc(cc2)C(O)=O)Cc2cccc(F)c2)c2COc3ccc(Cl)cc3-c12 AUCJHDHYRSXPGJ-UHFFFAOYSA-N 0.000 claims description 3
- YMOMNUUERLHSSV-UHFFFAOYSA-N 4-fluoro-3-[2-[(8-fluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluorophenyl)methyl]amino]ethylamino]benzoic acid Chemical compound Cn1nc(C(=O)N(CCNc2cc(ccc2F)C(O)=O)Cc2cccc(F)c2)c2COc3ccc(F)cc3-c12 YMOMNUUERLHSSV-UHFFFAOYSA-N 0.000 claims description 3
- WUTSLVYMBGNFGH-UHFFFAOYSA-N 8-fluoro-N-[(3-fluorophenyl)methyl]-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carboxamide Chemical compound FC1=CC2=C(C=C1)OCC1=C2N(N=C1C(=O)NCC1=CC(=CC=C1)F)C WUTSLVYMBGNFGH-UHFFFAOYSA-N 0.000 claims description 3
- 208000018522 Gastrointestinal disease Diseases 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- IMDAWGZBLRKXIE-UHFFFAOYSA-N 1-[[[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]acetyl]amino]methyl]cyclopropane-1-carboxylic acid Chemical compound ClC1=CC2=C(C=C1)OCC1=C2N(N=C1C(=O)N(CC1=C(C=CC=C1)F)CC(=O)NCC1(CC1)C(=O)O)C IMDAWGZBLRKXIE-UHFFFAOYSA-N 0.000 claims description 2
- AONSLHFVFSDBGZ-UHFFFAOYSA-N 3-[2-[(7,8-difluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluorophenyl)methyl]amino]ethylamino]-4-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCNc2cc(ccc2F)C(O)=O)Cc2cccc(F)c2)c2COc3cc(F)c(F)cc3-c12 AONSLHFVFSDBGZ-UHFFFAOYSA-N 0.000 claims description 2
- OUAXPCFXYLDFRI-UHFFFAOYSA-N 3-[2-[(7,8-difluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-methylphenyl)methyl]amino]ethylamino]-4-fluorobenzoic acid Chemical compound Cc1cccc(CN(CCNc2cc(ccc2F)C(O)=O)C(=O)c2nn(C)c-3c2COc2cc(F)c(F)cc-32)c1 OUAXPCFXYLDFRI-UHFFFAOYSA-N 0.000 claims description 2
- PDRYWSXZQFRPQR-UHFFFAOYSA-N 3-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]ethoxy]-4-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2cc(ccc2F)C(O)=O)Cc2ccccc2F)c2COc3ccc(Cl)cc3-c12 PDRYWSXZQFRPQR-UHFFFAOYSA-N 0.000 claims description 2
- VKWOWOMXUPXAMP-UHFFFAOYSA-N 3-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-methylphenyl)methyl]amino]ethylamino]-4-fluorobenzoic acid Chemical compound Cc1cccc(CN(CCNc2cc(ccc2F)C(O)=O)C(=O)c2nn(C)c-3c2COc2ccc(Cl)cc-32)c1 VKWOWOMXUPXAMP-UHFFFAOYSA-N 0.000 claims description 2
- HIYVXBLCLCKENU-UHFFFAOYSA-N 3-[2-[benzyl-(7,8-difluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]ethylamino]-4-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCNc2cc(ccc2F)C(O)=O)Cc2ccccc2)c2COc3cc(F)c(F)cc3-c12 HIYVXBLCLCKENU-UHFFFAOYSA-N 0.000 claims description 2
- NYZPDZBXJAVCNO-UHFFFAOYSA-N 3-[2-[benzyl-(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]ethylamino]-4-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCNc2cc(ccc2F)C(O)=O)Cc2ccccc2)c2COc3ccc(Cl)cc3-c12 NYZPDZBXJAVCNO-UHFFFAOYSA-N 0.000 claims description 2
- FFTIMDOOUCFJRA-UHFFFAOYSA-N 3-[2-[benzyl-(8-fluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]ethylamino]-4-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCNc2cc(ccc2F)C(O)=O)Cc2ccccc2)c2COc3ccc(F)cc3-c12 FFTIMDOOUCFJRA-UHFFFAOYSA-N 0.000 claims description 2
- DKTKXEQFYHWHHL-UHFFFAOYSA-N 3-[[2-[(1,8-dimethyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]acetyl]amino]benzoic acid Chemical compound Cc1ccc2OCc3c(nn(C)c3-c2c1)C(=O)N(CC(=O)Nc1cccc(c1)C(O)=O)Cc1ccccc1F DKTKXEQFYHWHHL-UHFFFAOYSA-N 0.000 claims description 2
- BNDBVALGKOEGJJ-UHFFFAOYSA-N 3-fluoro-4-[[(8-fluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]methyl]benzoic acid Chemical compound FC=1C=C(C(=O)O)C=CC1CN(C(=O)C=1C2=C(N(N1)C)C=1C=C(C=CC1OC2)F)CC2=C(C=CC=C2)F BNDBVALGKOEGJJ-UHFFFAOYSA-N 0.000 claims description 2
- JPDGNBLMRHRLTN-UHFFFAOYSA-N 3-fluoro-4-[[(8-fluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-methylphenyl)methyl]amino]methyl]benzoic acid Chemical compound Cc1cccc(CN(Cc2ccc(cc2F)C(O)=O)C(=O)c2nn(C)c-3c2COc2ccc(F)cc-32)c1 JPDGNBLMRHRLTN-UHFFFAOYSA-N 0.000 claims description 2
- AZQSCICKUHOZOX-UHFFFAOYSA-N 4-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-(cyclopentylmethyl)amino]ethoxy]-3,5-dimethylbenzoic acid Chemical compound Cc1cc(cc(C)c1OCCN(CC1CCCC1)C(=O)c1nn(C)c-2c1COc1ccc(Cl)cc-21)C(O)=O AZQSCICKUHOZOX-UHFFFAOYSA-N 0.000 claims description 2
- XIDJZZCPABSJCW-UHFFFAOYSA-N 4-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]ethoxy]-3,5-difluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2c(F)cc(cc2F)C(O)=O)Cc2ccccc2F)c2COc3ccc(Cl)cc3-c12 XIDJZZCPABSJCW-UHFFFAOYSA-N 0.000 claims description 2
- BYGKMYHAYBMJMM-UHFFFAOYSA-N 4-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]ethoxy]-3,5-dimethylbenzoic acid Chemical compound Cc1cc(cc(C)c1OCCN(Cc1ccccc1F)C(=O)c1nn(C)c-2c1COc1ccc(Cl)cc-21)C(O)=O BYGKMYHAYBMJMM-UHFFFAOYSA-N 0.000 claims description 2
- XFQFNZQSKREHRE-UHFFFAOYSA-N 4-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]ethoxy]-3-(trifluoromethyl)benzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2ccc(cc2C(F)(F)F)C(O)=O)Cc2ccccc2F)c2COc3ccc(Cl)cc3-c12 XFQFNZQSKREHRE-UHFFFAOYSA-N 0.000 claims description 2
- YPNFQWNWBXQXPH-UHFFFAOYSA-N 4-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]ethoxy]-3-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2ccc(cc2F)C(O)=O)Cc2ccccc2F)c2COc3ccc(Cl)cc3-c12 YPNFQWNWBXQXPH-UHFFFAOYSA-N 0.000 claims description 2
- BOOUDOVTRORLGS-UHFFFAOYSA-N 4-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]ethoxy]benzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2ccc(cc2)C(O)=O)Cc2ccccc2F)c2COc3ccc(Cl)cc3-c12 BOOUDOVTRORLGS-UHFFFAOYSA-N 0.000 claims description 2
- SMJHCJJTEVTFLW-UHFFFAOYSA-N 4-[2-[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluorophenyl)methyl]amino]ethoxy]-3-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2ccc(cc2F)C(O)=O)Cc2cccc(F)c2)c2COc3ccc(Cl)cc3-c12 SMJHCJJTEVTFLW-UHFFFAOYSA-N 0.000 claims description 2
- ZVYKQLMAEOESRQ-UHFFFAOYSA-N 4-[2-[benzyl-(7,8-difluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]ethoxy]-3-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2ccc(cc2F)C(O)=O)Cc2ccccc2)c2COc3cc(F)c(F)cc3-c12 ZVYKQLMAEOESRQ-UHFFFAOYSA-N 0.000 claims description 2
- OQNSPIUYFRIRCH-UHFFFAOYSA-N 4-[2-[benzyl-(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]ethoxy]-3,5-difluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2c(F)cc(cc2F)C(O)=O)Cc2ccccc2)c2COc3ccc(Cl)cc3-c12 OQNSPIUYFRIRCH-UHFFFAOYSA-N 0.000 claims description 2
- JZCFSXBSTOWTKD-UHFFFAOYSA-N 4-[2-[benzyl-(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]ethoxy]-3-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2ccc(cc2F)C(O)=O)Cc2ccccc2)c2COc3ccc(Cl)cc3-c12 JZCFSXBSTOWTKD-UHFFFAOYSA-N 0.000 claims description 2
- ULAMPKYWOCISHL-UHFFFAOYSA-N 4-[2-[benzyl-(8-fluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]ethoxy]-3,5-difluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2c(F)cc(cc2F)C(O)=O)Cc2ccccc2)c2COc3ccc(F)cc3-c12 ULAMPKYWOCISHL-UHFFFAOYSA-N 0.000 claims description 2
- RQLKTWUCUCJISI-UHFFFAOYSA-N 4-[2-[benzyl-(8-fluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]ethoxy]-3-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(CCOc2ccc(cc2F)C(O)=O)Cc2ccccc2)c2COc3ccc(F)cc3-c12 RQLKTWUCUCJISI-UHFFFAOYSA-N 0.000 claims description 2
- QNHJQIUNQURVID-UHFFFAOYSA-N 4-[[(3,5-difluorophenyl)methyl-(8-fluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)amino]methyl]benzoic acid Chemical compound Cn1nc(C(=O)N(Cc2ccc(cc2)C(O)=O)Cc2cc(F)cc(F)c2)c2COc3ccc(F)cc3-c12 QNHJQIUNQURVID-UHFFFAOYSA-N 0.000 claims description 2
- PWAIFGUTQDTORG-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-(1H-indol-5-ylmethyl)amino]methyl]benzoic acid Chemical compound N1C=CC2=CC(=CC=C12)CN(C(=O)C=1C2=C(N(N1)C)C=1C=C(C=CC1OC2)Cl)CC2=CC=C(C(=O)O)C=C2 PWAIFGUTQDTORG-UHFFFAOYSA-N 0.000 claims description 2
- ASAGXPHLRIABEH-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2,3-difluorophenyl)methyl]amino]methyl]benzoic acid Chemical compound ClC1=CC2=C(C=C1)OCC1=C2N(N=C1C(=O)N(CC1=C(C(=CC=C1)F)F)CC1=CC=C(C(=O)O)C=C1)C ASAGXPHLRIABEH-UHFFFAOYSA-N 0.000 claims description 2
- AIKMRRXUJZVITP-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]methyl]-2-fluorobenzoic acid Chemical compound ClC1=CC2=C(C=C1)OCC1=C2N(N=C1C(=O)N(CC1=C(C=CC=C1)F)CC1=CC(=C(C(=O)O)C=C1)F)C AIKMRRXUJZVITP-UHFFFAOYSA-N 0.000 claims description 2
- LIBJDTRMQPEPNY-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(2-fluorophenyl)methyl]amino]methyl]-3-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(Cc2ccccc2F)Cc2ccc(cc2F)C(O)=O)c2COc3ccc(Cl)cc3-c12 LIBJDTRMQPEPNY-UHFFFAOYSA-N 0.000 claims description 2
- UQQMPQAPKULNGX-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3,5-difluorophenyl)methyl]amino]methyl]benzoic acid Chemical compound Cn1nc(C(=O)N(Cc2ccc(cc2)C(O)=O)Cc2cc(F)cc(F)c2)c2COc3ccc(Cl)cc3-c12 UQQMPQAPKULNGX-UHFFFAOYSA-N 0.000 claims description 2
- RXVZGZPKRSNTGR-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluoro-5-methylphenyl)methyl]amino]methyl]benzoic acid Chemical compound Cc1cc(F)cc(CN(Cc2ccc(cc2)C(O)=O)C(=O)c2nn(C)c-3c2COc2ccc(Cl)cc-32)c1 RXVZGZPKRSNTGR-UHFFFAOYSA-N 0.000 claims description 2
- KRWBWJRLLXSGJQ-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluorophenyl)methyl]amino]methyl]-2-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(Cc2cccc(F)c2)Cc2ccc(C(O)=O)c(F)c2)c2COc3ccc(Cl)cc3-c12 KRWBWJRLLXSGJQ-UHFFFAOYSA-N 0.000 claims description 2
- WGTXKQXGMOALMS-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluorophenyl)methyl]amino]methyl]-3-fluorobenzoic acid Chemical compound Cn1nc(C(=O)N(Cc2cccc(F)c2)Cc2ccc(cc2F)C(O)=O)c2COc3ccc(Cl)cc3-c12 WGTXKQXGMOALMS-UHFFFAOYSA-N 0.000 claims description 2
- OISCITBTBYYNPZ-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-methylphenyl)methyl]amino]methyl]-3-fluorobenzoic acid Chemical compound Cc1cccc(CN(Cc2ccc(cc2F)C(O)=O)C(=O)c2nn(C)c-3c2COc2ccc(Cl)cc-32)c1 OISCITBTBYYNPZ-UHFFFAOYSA-N 0.000 claims description 2
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- CIRYTQMPVZUZPH-UHFFFAOYSA-N 4-[[(8-fluoro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-fluorophenyl)methyl]amino]methyl]benzoic acid Chemical compound Cn1nc(C(=O)N(Cc2ccc(cc2)C(O)=O)Cc2cccc(F)c2)c2COc3ccc(F)cc3-c12 CIRYTQMPVZUZPH-UHFFFAOYSA-N 0.000 claims description 2
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| MX384205B (es) | 2016-02-22 | 2025-03-14 | Novartis Ag | Metodos para usar agonistas de fxr. |
| CA3252823A1 (en) | 2016-06-13 | 2025-02-25 | Gilead Sciences, Inc. | Substituted tert-butyl-3-(2-chloro-phenyl)-3-hydroxyazetidine-1-carboxylate compounds |
| MX385718B (es) | 2016-06-13 | 2025-03-18 | Gilead Sciences Inc | Compuestos moduladores de fxr (nr1h4). |
| RU2019110779A (ru) * | 2016-09-14 | 2020-10-15 | Новартис Аг | Новые схемы введения агонистов fxr |
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| RU2019113150A (ru) * | 2016-10-05 | 2020-11-06 | Новартис Аг | Комбинация композиций, содержащих агонисты fxr, предназначенная для лечения или предупреждения фиброзирующего, цирротического заболевания или нарушения |
| CN107973790A (zh) * | 2016-10-22 | 2018-05-01 | 合帕吉恩治疗公司 | 杂环fxr调节剂 |
| PT3600309T (pt) | 2017-03-28 | 2022-10-03 | Gilead Sciences Inc | Combinações terapêuticas para o tratamento de doenças hepáticas |
| KR102643558B1 (ko) * | 2017-06-05 | 2024-03-06 | 내셔널 유니버시티 오브 싱가포르 | 인간 트레포일 인자 3을 억제하는데 유용한 화합물 |
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| MA49903A (fr) * | 2017-08-15 | 2020-06-24 | Inflazome Ltd | Sulfonylureés et sulfonylthioureés en tant qu'inhibiteurs de nlrp3 |
| UY37848A (es) | 2017-08-15 | 2019-03-29 | Inflazome Ltd | Sulfonilureas y sulfoniltioureas útiles como inhibidores de nlrp3 |
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| CN111315733A (zh) | 2017-11-09 | 2020-06-19 | 英夫拉索姆有限公司 | 新颖磺酰胺甲酰胺化合物 |
| WO2019092171A1 (en) | 2017-11-09 | 2019-05-16 | Inflazome Limited | Novel sulfonamide carboxamide compounds |
| CN110128432B (zh) * | 2018-02-02 | 2021-03-02 | 广东东阳光药业有限公司 | 含氮三环化合物及其在药物中的应用 |
| US11905252B2 (en) | 2018-03-02 | 2024-02-20 | Inflazome Limited | Compounds |
| MA53388A (fr) | 2018-07-25 | 2021-06-02 | Novartis Ag | Inhibiteurs d'inflammasome nlrp3 |
| EP3911647B1 (en) | 2019-01-15 | 2023-12-13 | Gilead Sciences, Inc. | Isoxazole compound as fxr agonist and pharmaceutical compositions comprising same |
| US10610280B1 (en) | 2019-02-02 | 2020-04-07 | Ayad K. M. Agha | Surgical method and apparatus for destruction and removal of intraperitoneal, visceral, and subcutaneous fat |
| CA3233305A1 (en) | 2019-02-19 | 2020-08-27 | Gilead Sciences, Inc. | Solid forms of fxr agonists |
| UY38687A (es) | 2019-05-17 | 2023-05-15 | Novartis Ag | Inhibidores del inflamasoma nlrp3, composiciones, combinaciones de los mismos y métodos para su uso |
| KR20220035365A (ko) | 2019-07-18 | 2022-03-22 | 엔요 파마 | 인터페론의 부작용을 감소시키는 방법 |
| WO2021044351A1 (en) | 2019-09-06 | 2021-03-11 | Novartis Ag | Methods of treating liver disease using lta4h inhibitors |
| IL293892A (en) | 2020-01-15 | 2022-08-01 | Inserm Institut National De La Sant? Et De La Rech M?Dicale | Use of fxr agonists for treating an infection by hepatitis d virus |
| CN113387828A (zh) * | 2020-03-14 | 2021-09-14 | 江巨东 | 一种阿利克仑中间体的制备方法 |
| WO2022037663A1 (zh) * | 2020-08-21 | 2022-02-24 | 苏州晶云药物科技股份有限公司 | 苯甲酸衍生物的新晶型及其制备方法 |
| JP2024502673A (ja) | 2021-01-14 | 2024-01-22 | ウエヌイグレックオ・ファーマ | Ｈｂｖ感染の処置のためのｆｘｒアゴニストとｉｆｎの相乗効果 |
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| TW200906823A (en) * | 2007-07-16 | 2009-02-16 | Lilly Co Eli | Compounds and methods for modulating FXR |
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- 2014-11-04 TW TW103138253A patent/TWI662027B/zh not_active IP Right Cessation
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- 2014-11-04 CA CA2927705A patent/CA2927705C/en not_active Expired - Fee Related
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- 2014-11-04 WO PCT/US2014/063948 patent/WO2015069666A1/en not_active Ceased
- 2014-11-04 UY UY0001035818A patent/UY35818A/es not_active Application Discontinuation
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