JP2013501729A5 - - Google Patents
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- Publication number
- JP2013501729A5 JP2013501729A5 JP2012523967A JP2012523967A JP2013501729A5 JP 2013501729 A5 JP2013501729 A5 JP 2013501729A5 JP 2012523967 A JP2012523967 A JP 2012523967A JP 2012523967 A JP2012523967 A JP 2012523967A JP 2013501729 A5 JP2013501729 A5 JP 2013501729A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- oxadiazol
- trifluoromethyl
- hydroxy
- ethyl
- 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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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 108
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 35
- XJLSEXAGTJCILF-RXMQYKEDSA-N (R)-nipecotic acid zwitterion Chemical compound OC(=O)[C@@H]1CCCNC1 XJLSEXAGTJCILF-RXMQYKEDSA-N 0.000 claims 31
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 29
- 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 claims 28
- -1 4-oxazolyl Chemical group 0.000 claims 26
- 125000000217 alkyl group Chemical group 0.000 claims 24
- 150000001875 compounds Chemical class 0.000 claims 15
- 150000003839 salts Chemical class 0.000 claims 15
- 125000001072 heteroaryl group Chemical group 0.000 claims 9
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 9
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000004122 cyclic group Chemical group 0.000 claims 8
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 5
- 239000003814 drug Substances 0.000 claims 5
- 125000005843 halogen group Chemical group 0.000 claims 5
- 125000005842 heteroatom Chemical group 0.000 claims 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 5
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 4
- 125000002950 monocyclic group Chemical group 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 4
- 208000023275 Autoimmune disease Diseases 0.000 claims 3
- 102000004127 Cytokines Human genes 0.000 claims 3
- 108090000695 Cytokines Proteins 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 208000037976 chronic inflammation Diseases 0.000 claims 3
- 208000037893 chronic inflammatory disorder Diseases 0.000 claims 3
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 3
- 125000004438 haloalkoxy group Chemical group 0.000 claims 3
- 125000001188 haloalkyl group Chemical group 0.000 claims 3
- RUWIEFVLBVHOMD-VQCQRNETSA-N (2r)-1-[2-hydroxy-2-[4-[5-(5-phenyl-4-propyl-1,2-oxazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]azetidine-2-carboxylic acid Chemical compound CCCC=1C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2[C@H](CC2)C(O)=O)=NOC=1C1=CC=CC=C1 RUWIEFVLBVHOMD-VQCQRNETSA-N 0.000 claims 2
- VEYWMSKEPZXKDS-MRTLOADZSA-N (2r)-1-[2-hydroxy-2-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidine-2-carboxylic acid Chemical compound C=1C=C(C=2N=C(ON=2)C2=C(C(=NO2)C=2C=CC=CC=2)C(F)(F)F)C=CC=1C(O)CN1CCCC[C@@H]1C(O)=O VEYWMSKEPZXKDS-MRTLOADZSA-N 0.000 claims 2
- FYCRNRZIEVLZDO-BYPYZUCNSA-N (2s)-morpholin-4-ium-2-carboxylate Chemical compound OC(=O)[C@@H]1CNCCO1 FYCRNRZIEVLZDO-BYPYZUCNSA-N 0.000 claims 2
- SJYFMUOMOHKHBR-GHTZIAJQSA-N (3s)-1-[(2s)-2-[4-[5-[1-cyclohexyl-5-(trifluoromethyl)pyrazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]-2-hydroxyethyl]piperidine-3-carboxylic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(N(C2CCCCC2)N=C1)C(F)(F)F)N1CCC[C@H](C(O)=O)C1 SJYFMUOMOHKHBR-GHTZIAJQSA-N 0.000 claims 2
- YECQGGUYVNGSQW-GHTZIAJQSA-N (3s)-1-[(2s)-2-hydroxy-2-[4-[5-[1-phenyl-5-(trifluoromethyl)pyrazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidine-3-carboxylic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(N(N=C1)C=1C=CC=CC=1)C(F)(F)F)N1CCC[C@H](C(O)=O)C1 YECQGGUYVNGSQW-GHTZIAJQSA-N 0.000 claims 2
- KEQLVIFRZVZQOA-RBUKOAKNSA-N (3s)-1-[(2s)-2-hydroxy-2-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidine-3-carboxylic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(C(=NO1)C=1C=CC=CC=1)C(F)(F)F)N1CCC[C@H](C(O)=O)C1 KEQLVIFRZVZQOA-RBUKOAKNSA-N 0.000 claims 2
- NBAJVVQKVFSPLV-YDNXMHBPSA-N (3s)-1-[2-[4-[5-(5-ethyl-1-pyridin-2-ylpyrazol-4-yl)-1,2,4-oxadiazol-3-yl]phenyl]-2-hydroxyethyl]piperidine-3-carboxylic acid Chemical compound CCC1=C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2C[C@H](CCC2)C(O)=O)C=NN1C1=CC=CC=N1 NBAJVVQKVFSPLV-YDNXMHBPSA-N 0.000 claims 2
- AHULNQGXTUEURY-LBOXEOMUSA-N (3s)-1-[2-[4-[5-[3-(2-chlorophenyl)-1h-pyrazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]-2-hydroxyethyl]piperidine-3-carboxylic acid Chemical compound C=1C=C(C=2N=C(ON=2)C=2NN=C(C=2)C=2C(=CC=CC=2)Cl)C=CC=1C(O)CN1CCC[C@H](C(O)=O)C1 AHULNQGXTUEURY-LBOXEOMUSA-N 0.000 claims 2
- IXUPWWKYGWRAAD-HXBUSHRASA-N (3s)-1-[2-[4-[5-[3-(4-chlorophenyl)-1h-pyrazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]-2-hydroxyethyl]piperidine-3-carboxylic acid Chemical compound C=1C=C(C=2N=C(ON=2)C=2NN=C(C=2)C=2C=CC(Cl)=CC=2)C=CC=1C(O)CN1CCC[C@H](C(O)=O)C1 IXUPWWKYGWRAAD-HXBUSHRASA-N 0.000 claims 2
- MOFNVCHJYHWJMD-LROBGIAVSA-N (3s)-1-[2-hydroxy-2-[4-[5-(5-pyridin-2-ylthiophen-2-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidine-3-carboxylic acid Chemical compound C=1C=C(C=2N=C(ON=2)C=2SC(=CC=2)C=2N=CC=CC=2)C=CC=1C(O)CN1CCC[C@H](C(O)=O)C1 MOFNVCHJYHWJMD-LROBGIAVSA-N 0.000 claims 2
- LTIXIGNBOHGXDX-BHWOMJMDSA-N (3s)-1-[2-hydroxy-2-[4-[5-[5-(2-methylpropyl)-4-(trifluoromethyl)-1,2-oxazol-3-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidine-3-carboxylic acid Chemical compound FC(F)(F)C1=C(CC(C)C)ON=C1C1=NC(C=2C=CC(=CC=2)C(O)CN2C[C@H](CCC2)C(O)=O)=NO1 LTIXIGNBOHGXDX-BHWOMJMDSA-N 0.000 claims 2
- WPGIIIKQVNEYLG-UHFFFAOYSA-N 1-[2-hydroxy-2-[4-[5-(5-phenyl-4-propyl-1,2-oxazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]azetidine-3-carboxylic acid Chemical compound CCCC=1C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2CC(C2)C(O)=O)=NOC=1C1=CC=CC=C1 WPGIIIKQVNEYLG-UHFFFAOYSA-N 0.000 claims 2
- QFMFMLVBWMLNIV-UHFFFAOYSA-N 1-[2-hydroxy-2-[4-[5-(5-phenyl-4-propyl-1,2-oxazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-ol Chemical compound CCCC=1C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2CC(O)CCC2)=NOC=1C1=CC=CC=C1 QFMFMLVBWMLNIV-UHFFFAOYSA-N 0.000 claims 2
- SXEARXGUIYUIFF-UHFFFAOYSA-N 1-[2-hydroxy-2-[4-[5-(5-phenyl-4-propyl-1,2-oxazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidine-3-carboxylic acid Chemical compound CCCC=1C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2CC(CCC2)C(O)=O)=NOC=1C1=CC=CC=C1 SXEARXGUIYUIFF-UHFFFAOYSA-N 0.000 claims 2
- JMKXTJZWBTVYGQ-UHFFFAOYSA-N 1-[2-hydroxy-2-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]-3-methylpiperidine-3-carboxylic acid Chemical compound C1C(C)(C(O)=O)CCCN1CC(O)C1=CC=C(C=2N=C(ON=2)C2=C(C(=NO2)C=2C=CC=CC=2)C(F)(F)F)C=C1 JMKXTJZWBTVYGQ-UHFFFAOYSA-N 0.000 claims 2
- HRMZOHUUKHMBOJ-UHFFFAOYSA-N 1-[2-hydroxy-2-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]azetidine-3-carboxylic acid Chemical compound C=1C=C(C=2N=C(ON=2)C2=C(C(=NO2)C=2C=CC=CC=2)C(F)(F)F)C=CC=1C(O)CN1CC(C(O)=O)C1 HRMZOHUUKHMBOJ-UHFFFAOYSA-N 0.000 claims 2
- NYZZVISKNPNJAD-BBQAJUCSSA-N 2-[(2s)-1-[2-hydroxy-2-[4-[5-(5-phenyl-4-propyl-1,2-oxazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]pyrrolidin-2-yl]acetic acid Chemical compound CCCC=1C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2[C@@H](CCC2)CC(O)=O)=NOC=1C1=CC=CC=C1 NYZZVISKNPNJAD-BBQAJUCSSA-N 0.000 claims 2
- ZDBIBQUTMFNXTR-IIBYNOLFSA-N 2-[(3r)-1-[(2s)-2-[4-[5-[1-(4-chlorophenyl)-5-(trifluoromethyl)imidazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]-2-hydroxyethyl]piperidin-3-yl]acetic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(N(C=N1)C=1C=CC(Cl)=CC=1)C(F)(F)F)N1CCC[C@H](CC(O)=O)C1 ZDBIBQUTMFNXTR-IIBYNOLFSA-N 0.000 claims 2
- NPGPDNHISZFRSA-OPAMFIHVSA-N 2-[(3r)-1-[(2s)-2-[4-[5-[1-(4-chlorophenyl)-5-(trifluoromethyl)pyrazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]-2-hydroxyethyl]piperidin-3-yl]acetic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(N(N=C1)C=1C=CC(Cl)=CC=1)C(F)(F)F)N1CCC[C@H](CC(O)=O)C1 NPGPDNHISZFRSA-OPAMFIHVSA-N 0.000 claims 2
- WLSLSTGNQRRUSK-JLTOFOAXSA-N 2-[(3r)-1-[(2s)-2-[4-[5-[1-[5-chloro-3-(trifluoromethyl)pyridin-2-yl]-5-(trifluoromethyl)pyrazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]-2-hydroxyethyl]piperidin-3-yl]acetic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(N(N=C1)C=1C(=CC(Cl)=CN=1)C(F)(F)F)C(F)(F)F)N1CCC[C@H](CC(O)=O)C1 WLSLSTGNQRRUSK-JLTOFOAXSA-N 0.000 claims 2
- QUVDAYCPTOVHAD-FOIQADDNSA-N 2-[(3r)-1-[(2s)-2-[4-[5-[5-(3-chlorophenyl)-4-(trifluoromethyl)-1,2-oxazol-3-yl]-1,2,4-oxadiazol-3-yl]phenyl]-2-hydroxyethyl]piperidin-3-yl]acetic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C=1C(=C(ON=1)C=1C=C(Cl)C=CC=1)C(F)(F)F)N1CCC[C@H](CC(O)=O)C1 QUVDAYCPTOVHAD-FOIQADDNSA-N 0.000 claims 2
- BFBKHGAZEBRFGK-WZONZLPQSA-N 2-[(3r)-1-[(2s)-2-hydroxy-2-[4-[5-[1-(4-methylphenyl)-5-(trifluoromethyl)pyrazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-yl]acetic acid Chemical compound C1=CC(C)=CC=C1N1C(C(F)(F)F)=C(C=2ON=C(N=2)C=2C=CC(=CC=2)[C@H](O)CN2C[C@@H](CC(O)=O)CCC2)C=N1 BFBKHGAZEBRFGK-WZONZLPQSA-N 0.000 claims 2
- BWIJAIFJJYVYQA-IIBYNOLFSA-N 2-[(3r)-1-[(2s)-2-hydroxy-2-[4-[5-[1-(oxan-4-yl)-5-(trifluoromethyl)pyrazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-yl]acetic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(N(C2CCOCC2)N=C1)C(F)(F)F)N1CCC[C@H](CC(O)=O)C1 BWIJAIFJJYVYQA-IIBYNOLFSA-N 0.000 claims 2
- KUQLVOCPMLBBBL-VQIMIIECSA-N 2-[(3r)-1-[(2s)-2-hydroxy-2-[4-[5-[1-pyridin-2-yl-5-(trifluoromethyl)imidazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-yl]acetic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(N(C=N1)C=1N=CC=CC=1)C(F)(F)F)N1CCC[C@H](CC(O)=O)C1 KUQLVOCPMLBBBL-VQIMIIECSA-N 0.000 claims 2
- AAMQECSNTHSBOY-OPAMFIHVSA-N 2-[(3r)-1-[(2s)-2-hydroxy-2-[4-[5-[5-(trifluoromethyl)-1-[4-(trifluoromethyl)phenyl]pyrazol-4-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-yl]acetic acid Chemical compound C([C@@H](O)C=1C=CC(=CC=1)C=1N=C(ON=1)C1=C(N(N=C1)C=1C=CC(=CC=1)C(F)(F)F)C(F)(F)F)N1CCC[C@H](CC(O)=O)C1 AAMQECSNTHSBOY-OPAMFIHVSA-N 0.000 claims 2
- YNXRXFSUFSBGFK-PHSANKKPSA-N 2-[(3r)-1-[2-hydroxy-2-[4-[5-(5-phenyl-4-propyl-1,2-oxazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-yl]acetic acid Chemical compound CCCC=1C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2C[C@@H](CC(O)=O)CCC2)=NOC=1C1=CC=CC=C1 YNXRXFSUFSBGFK-PHSANKKPSA-N 0.000 claims 2
- HLZSDCGIRNHZFD-QRIPLOBPSA-N 2-[(3r)-1-[2-hydroxy-2-[4-[5-[5-phenyl-4-(trifluoromethyl)-1,2-oxazol-3-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-yl]acetic acid Chemical compound C=1C=C(C=2N=C(ON=2)C=2C(=C(ON=2)C=2C=CC=CC=2)C(F)(F)F)C=CC=1C(O)CN1CCC[C@H](CC(O)=O)C1 HLZSDCGIRNHZFD-QRIPLOBPSA-N 0.000 claims 2
- YNXRXFSUFSBGFK-XGLRFROISA-N 2-[(3s)-1-[2-hydroxy-2-[4-[5-(5-phenyl-4-propyl-1,2-oxazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-yl]acetic acid Chemical compound CCCC=1C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2C[C@H](CC(O)=O)CCC2)=NOC=1C1=CC=CC=C1 YNXRXFSUFSBGFK-XGLRFROISA-N 0.000 claims 2
- FOLYEQMBFAIKNS-UHFFFAOYSA-N 2-[3-(2-hydroxyethyl)piperidin-1-yl]-1-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethanol Chemical compound C1C(CCO)CCCN1CC(O)C1=CC=C(C=2N=C(ON=2)C2=C(C(=NO2)C=2C=CC=CC=2)C(F)(F)F)C=C1 FOLYEQMBFAIKNS-UHFFFAOYSA-N 0.000 claims 2
- PYANEAOOIPMWGW-UHFFFAOYSA-N 2-[3-(hydroxymethyl)piperidin-1-yl]-1-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethanol Chemical compound C1C(CO)CCCN1CC(O)C1=CC=C(C=2N=C(ON=2)C2=C(C(=NO2)C=2C=CC=CC=2)C(F)(F)F)C=C1 PYANEAOOIPMWGW-UHFFFAOYSA-N 0.000 claims 2
- KIWRFMLROJOCPY-UHFFFAOYSA-N 3-[1-[2-hydroxy-2-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidin-3-yl]propanoic acid Chemical compound C=1C=C(C=2N=C(ON=2)C2=C(C(=NO2)C=2C=CC=CC=2)C(F)(F)F)C=CC=1C(O)CN1CCCC(CCC(O)=O)C1 KIWRFMLROJOCPY-UHFFFAOYSA-N 0.000 claims 2
- LHTVETFHXOGXNI-UHFFFAOYSA-N 3-hydroxy-1-[2-hydroxy-2-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidine-3-carboxylic acid Chemical compound C=1C=C(C=2N=C(ON=2)C2=C(C(=NO2)C=2C=CC=CC=2)C(F)(F)F)C=CC=1C(O)CN1CCCC(O)(C(O)=O)C1 LHTVETFHXOGXNI-UHFFFAOYSA-N 0.000 claims 2
- CXNANLOOTYJTIE-UHFFFAOYSA-N 4-[2-hydroxy-2-[4-[5-(5-phenyl-4-propyl-1,2-oxazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]ethyl]morpholine-2-carboxylic acid Chemical compound CCCC=1C(C=2ON=C(N=2)C=2C=CC(=CC=2)C(O)CN2CC(OCC2)C(O)=O)=NOC=1C1=CC=CC=C1 CXNANLOOTYJTIE-UHFFFAOYSA-N 0.000 claims 2
- ZDFKJCZJWMALGB-UHFFFAOYSA-N 5-hydroxy-1-[2-hydroxy-2-[4-[5-[3-phenyl-4-(trifluoromethyl)-1,2-oxazol-5-yl]-1,2,4-oxadiazol-3-yl]phenyl]ethyl]piperidine-3-carboxylic acid Chemical compound C=1C=C(C=2N=C(ON=2)C2=C(C(=NO2)C=2C=CC=CC=2)C(F)(F)F)C=CC=1C(O)CN1CC(O)CC(C(O)=O)C1 ZDFKJCZJWMALGB-UHFFFAOYSA-N 0.000 claims 2
- CWDWFSXUQODZGW-UHFFFAOYSA-N 5-thiazolyl Chemical group [C]1=CN=CS1 CWDWFSXUQODZGW-UHFFFAOYSA-N 0.000 claims 2
- XWNYRQCNTYBSGA-UHFFFAOYSA-N CN1N=C(C=2C=CC=CC=2)C=C1C(ON=1)=NC=1C(C=C1)=CC=C1C(O)CN1CCCC(C(O)=O)C1 Chemical compound CN1N=C(C=2C=CC=CC=2)C=C1C(ON=1)=NC=1C(C=C1)=CC=C1C(O)CN1CCCC(C(O)=O)C1 XWNYRQCNTYBSGA-UHFFFAOYSA-N 0.000 claims 2
- 210000004027 cell Anatomy 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 102000037865 fusion proteins Human genes 0.000 claims 2
- 108020001507 fusion proteins Proteins 0.000 claims 2
- 239000003102 growth factor Substances 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 239000003112 inhibitor Substances 0.000 claims 2
- 125000001786 isothiazolyl group Chemical group 0.000 claims 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims 2
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 claims 2
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 claims 2
- HXEACLLIILLPRG-UHFFFAOYSA-N pipecolic acid Chemical compound OC(=O)C1CCCCN1 HXEACLLIILLPRG-UHFFFAOYSA-N 0.000 claims 2
- JSSXHAMIXJGYCS-UHFFFAOYSA-N piperazin-4-ium-2-carboxylate Chemical compound OC(=O)C1CNCCN1 JSSXHAMIXJGYCS-UHFFFAOYSA-N 0.000 claims 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims 2
- JAEIBKXSIXOLOL-UHFFFAOYSA-N pyrrolidin-1-ium-3-carboxylate Chemical compound OC(=O)C1CCNC1 JAEIBKXSIXOLOL-UHFFFAOYSA-N 0.000 claims 2
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical class CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- LJRDOKAZOAKLDU-UDXJMMFXSA-N (2s,3s,4r,5r,6r)-5-amino-2-(aminomethyl)-6-[(2r,3s,4r,5s)-5-[(1r,2r,3s,5r,6s)-3,5-diamino-2-[(2s,3r,4r,5s,6r)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxycyclohexyl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxyoxane-3,4-diol;sulfuric ac Chemical compound OS(O)(=O)=O.N[C@@H]1[C@@H](O)[C@H](O)[C@H](CN)O[C@@H]1O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](N)C[C@@H](N)[C@@H]2O)O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)N)O[C@@H]1CO LJRDOKAZOAKLDU-UDXJMMFXSA-N 0.000 claims 1
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| US9115054B2 (en) | 2013-02-21 | 2015-08-25 | Bristol-Myers Squibb Company | Tetrahydronaphthalenyl compounds useful as sipi agonists |
| AR101591A1 (es) | 2014-08-20 | 2016-12-28 | Bristol Myers Squibb Co | Compuestos bicíclicos sustituidos |
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2010
- 2010-08-05 US US12/850,892 patent/US8399451B2/en active Active
- 2010-08-06 KR KR1020127005901A patent/KR20120108963A/ko not_active Withdrawn
- 2010-08-06 CA CA2770194A patent/CA2770194A1/en not_active Abandoned
- 2010-08-06 AU AU2010279354A patent/AU2010279354A1/en not_active Abandoned
- 2010-08-06 TW TW099126390A patent/TW201109323A/zh unknown
- 2010-08-06 AR ARP100102904A patent/AR077819A1/es not_active Application Discontinuation
- 2010-08-06 CN CN2010800453726A patent/CN102548989A/zh active Pending
- 2010-08-06 WO PCT/US2010/044627 patent/WO2011017578A1/en not_active Ceased
- 2010-08-06 ES ES10742067.1T patent/ES2533095T3/es active Active
- 2010-08-06 BR BR112012002824A patent/BR112012002824A2/pt not_active IP Right Cessation
- 2010-08-06 EP EP10742067.1A patent/EP2462139B1/en not_active Not-in-force
- 2010-08-06 EA EA201270266A patent/EA201270266A1/ru unknown
- 2010-08-06 MX MX2012001160A patent/MX2012001160A/es not_active Application Discontinuation
- 2010-08-06 JP JP2012523967A patent/JP5602230B2/ja not_active Expired - Fee Related
- 2010-08-06 PE PE2012000174A patent/PE20120732A1/es not_active Application Discontinuation
- 2010-08-06 SG SG2012003430A patent/SG177691A1/en unknown
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2012
- 2012-01-24 ZA ZA2012/00641A patent/ZA201200641B/en unknown
- 2012-02-07 CL CL2012000326A patent/CL2012000326A1/es unknown
- 2012-02-16 CO CO12027713A patent/CO6430439A2/es not_active Application Discontinuation