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
- WKWJLMDNSULFGY-UHFFFAOYSA-N 4-[[(8-chloro-1-methyl-4H-chromeno[4,3-c]pyrazole-3-carbonyl)-[(3-methylphenyl)methyl]amino]methyl]benzoic acid Chemical compound Cc1cccc(CN(Cc2ccc(cc2)C(O)=O)C(=O)c2nn(C)c-3c2COc2ccc(Cl)cc-32)c1 WKWJLMDNSULFGY-UHFFFAOYSA-N 0.000 claims description 2
- 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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| EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
| KR102350357B1 (ko) | 2013-11-05 | 2022-01-14 | 노파르티스 아게 | 파르네소이드 x 수용체의 조정을 위한 조성물 및 방법 |
| TWI698430B (zh) | 2015-02-13 | 2020-07-11 | 南北兄弟藥業投資有限公司 | 三環化合物及其在藥物中的應用 |
| CN107531721B (zh) * | 2015-04-30 | 2020-07-17 | 诺华股份有限公司 | 用于调节法尼醇x受体的稠合的三环吡唑衍生物 |
| MX384205B (es) | 2016-02-22 | 2025-03-14 | Novartis Ag | Metodos para usar agonistas de fxr. |
| CA2968836C (en) | 2016-06-13 | 2025-09-02 | Gilead Sciences, Inc. | FXR MODULATING COMPOUNDS (NR1H4) |
| NZ748641A (en) | 2016-06-13 | 2020-04-24 | Gilead Sciences Inc | Fxr (nr1h4) modulating compounds |
| RU2019110780A (ru) * | 2016-09-14 | 2020-10-15 | Новартис Аг | Комбинация агонистов fxr |
| RU2019110779A (ru) * | 2016-09-14 | 2020-10-15 | Новартис Аг | Новые схемы введения агонистов fxr |
| 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 |
| SI4122464T1 (sl) | 2017-03-28 | 2024-07-31 | Gilead Sciences, Inc. | Terapevtske kombinacije za zdravljenje bolezni jeter |
| KR102643558B1 (ko) * | 2017-06-05 | 2024-03-06 | 내셔널 유니버시티 오브 싱가포르 | 인간 트레포일 인자 3을 억제하는데 유용한 화합물 |
| WO2019034693A1 (en) | 2017-08-15 | 2019-02-21 | Inflazome Limited | SULFONYLURATES AND SULFONYLTHIOURES AS INHIBITORS OF NLRP3 |
| MX2020001776A (es) * | 2017-08-15 | 2020-03-24 | Inflazome Ltd | Sulfonilureas y sulfoniltioureas como inhibidores de nlrp3. |
| US11542255B2 (en) | 2017-08-15 | 2023-01-03 | Inflazome Limited | Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors |
| JP2020533339A (ja) * | 2017-09-13 | 2020-11-19 | ノバルティス アーゲー | Ｆｘｒアゴニストを含む組合せ |
| KR20200087759A (ko) | 2017-11-09 | 2020-07-21 | 인플라좀 리미티드 | 신규한 설폰아마이드 카복스아마이드 화합물 |
| US12221434B2 (en) | 2017-11-09 | 2025-02-11 | Inflazome Limited | 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 |
| EP3759077A1 (en) | 2018-03-02 | 2021-01-06 | Inflazome Limited | Novel compounds |
| KR20210038877A (ko) | 2018-07-25 | 2021-04-08 | 노파르티스 아게 | Nlrp3 인플라마좀 억제제 |
| PT3911647T (pt) | 2019-01-15 | 2024-03-04 | Gilead Sciences Inc | Composto de isoxazole como agonista de fxr e composições farmacêuticas que o contenham |
| 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 |
| JP2022519906A (ja) | 2019-02-19 | 2022-03-25 | ギリアード サイエンシーズ， インコーポレイテッド | Ｆｘｒアゴニストの固体形態 |
| AR119731A1 (es) | 2019-05-17 | 2022-01-05 | Novartis Ag | Inhibidores del inflamasoma nlrp3 |
| EP3999101A1 (en) | 2019-07-18 | 2022-05-25 | ENYO Pharma | Method for decreasing adverse-effects of interferon |
| TW202122078A (zh) | 2019-09-06 | 2021-06-16 | 瑞士商諾華公司 | 使用lta4h抑制劑治療肝臟疾病之方法 |
| WO2021144330A1 (en) | 2020-01-15 | 2021-07-22 | INSERM (Institut National de la Santé et de la Recherche Médicale) | 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 |
| KR20230154806A (ko) | 2021-01-14 | 2023-11-09 | 엔요 파마 | Hbv 감염 치료를 위한 fxr 작용제 및 ifn의 상승작용효과 |
| CN117320722A (zh) | 2021-04-28 | 2023-12-29 | 埃尼奥制药公司 | 使用fxr激动剂作为联合治疗强烈增强tlr3激动剂的作用 |
| UY40374A (es) | 2022-08-03 | 2024-02-15 | Novartis Ag | Inhibidores de inflamasoma nlrp3 |
| JP2025527759A (ja) * | 2022-08-26 | 2025-08-22 | セルマティクス インク． | Ｆｓｈｒの新規なモジュレータおよびその使用 |
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| BRPI0712262A2 (pt) * | 2006-05-24 | 2012-07-10 | Lilly Co Eli | agonistas de fxr |
| EP2062365B1 (en) * | 2006-09-15 | 2017-06-07 | Thales Avionics, Inc. | System and method for wirelessly transferring content to and from an aircraft |
| TW200906823A (en) * | 2007-07-16 | 2009-02-16 | Lilly Co Eli | Compounds and methods for modulating FXR |
| CU24152B1 (es) * | 2010-12-20 | 2016-02-29 | Irm Llc | 1,2 oxazol-8-azabiciclo[3,2,1]octano 8 il como moduladores de fxr |
| KR102350357B1 (ko) | 2013-11-05 | 2022-01-14 | 노파르티스 아게 | 파르네소이드 x 수용체의 조정을 위한 조성물 및 방법 |
| CN107531721B (zh) | 2015-04-30 | 2020-07-17 | 诺华股份有限公司 | 用于调节法尼醇x受体的稠合的三环吡唑衍生物 |
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