JP2013520397A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013520397A5 JP2013520397A5 JP2012538520A JP2012538520A JP2013520397A5 JP 2013520397 A5 JP2013520397 A5 JP 2013520397A5 JP 2012538520 A JP2012538520 A JP 2012538520A JP 2012538520 A JP2012538520 A JP 2012538520A JP 2013520397 A5 JP2013520397 A5 JP 2013520397A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- ethyl
- amino
- carbon atoms
- 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
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims description 135
- 125000000217 alkyl group Chemical group 0.000 claims description 122
- 125000005843 halogen group Chemical group 0.000 claims description 108
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 77
- 125000003545 alkoxy group Chemical group 0.000 claims description 77
- 125000003118 aryl group Chemical group 0.000 claims description 77
- -1 oxopiperidyl group Chemical group 0.000 claims description 70
- 125000002950 monocyclic group Chemical group 0.000 claims description 59
- 125000003277 amino group Chemical group 0.000 claims description 55
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 47
- 150000001875 compounds Chemical class 0.000 claims description 45
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 45
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 44
- 229910052757 nitrogen Inorganic materials 0.000 claims description 42
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 41
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 40
- 125000004434 sulfur atom Chemical group 0.000 claims description 40
- 125000002619 bicyclic group Chemical group 0.000 claims description 36
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 36
- 125000001424 substituent group Chemical group 0.000 claims description 31
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 29
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 29
- 239000004202 carbamide Substances 0.000 claims description 29
- 125000005842 heteroatom Chemical group 0.000 claims description 28
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 27
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 26
- 125000004760 (C1-C4) alkylsulfonylamino group Chemical group 0.000 claims description 25
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 24
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 24
- 125000001072 heteroaryl group Chemical group 0.000 claims description 23
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 23
- 150000003839 salts Chemical class 0.000 claims description 23
- 229910052717 sulfur Inorganic materials 0.000 claims description 23
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 20
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 20
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 18
- 125000003342 alkenyl group Chemical group 0.000 claims description 18
- 125000004414 alkyl thio group Chemical group 0.000 claims description 18
- 125000002947 alkylene group Chemical group 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
- 241001465754 Metazoa Species 0.000 claims description 17
- 241000124008 Mammalia Species 0.000 claims description 15
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical group 0.000 claims description 14
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 12
- 206010020751 Hypersensitivity Diseases 0.000 claims description 12
- 102000013264 Interleukin-23 Human genes 0.000 claims description 12
- 108010065637 Interleukin-23 Proteins 0.000 claims description 12
- 230000007815 allergy Effects 0.000 claims description 12
- 201000010099 disease Diseases 0.000 claims description 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 12
- 208000026278 immune system disease Diseases 0.000 claims description 12
- 230000001404 mediated effect Effects 0.000 claims description 12
- 125000004043 oxo group Chemical group O=* 0.000 claims description 12
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 125000005936 piperidyl group Chemical group 0.000 claims description 11
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 125000005476 oxopyrrolidinyl group Chemical group 0.000 claims description 10
- 230000001225 therapeutic effect Effects 0.000 claims description 10
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 9
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 9
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 9
- 239000005711 Benzoic acid Substances 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 8
- 235000010233 benzoic acid Nutrition 0.000 claims description 8
- 125000001589 carboacyl group Chemical group 0.000 claims description 8
- 239000003814 drug Substances 0.000 claims description 8
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 230000002265 prevention Effects 0.000 claims description 8
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 7
- DOTIWNYTQPDMBR-ZDUSSCGKSA-N 4-[(1s)-1-[[2,5-dimethyl-4-[[4-(trifluoromethyl)phenyl]methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(C)SC(C)=C1CC1=CC=C(C(F)(F)F)C=C1 DOTIWNYTQPDMBR-ZDUSSCGKSA-N 0.000 claims description 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 7
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 6
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 6
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- FKXDPPYCCKCVCW-LBPRGKRZSA-N 4-[(1s)-1-[[5-chloro-2-(3-fluorophenoxy)pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1OC1=CC=CC(F)=C1 FKXDPPYCCKCVCW-LBPRGKRZSA-N 0.000 claims description 5
- JJWCQIGUTYSYQF-ZDUSSCGKSA-N 4-[(1s)-1-[[5-chloro-2-[(3-chlorophenoxy)methyl]pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1COC1=CC=CC(Cl)=C1 JJWCQIGUTYSYQF-ZDUSSCGKSA-N 0.000 claims description 5
- IXDVRRPNWPOPGV-UHFFFAOYSA-N 4-[[4-(5-methoxypyridin-2-yl)phenoxy]methyl]-5-methyl-n-(2-methylphenyl)sulfonylfuran-2-carboxamide Chemical compound N1=CC(OC)=CC=C1C(C=C1)=CC=C1OCC1=C(C)OC(C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C)=C1 IXDVRRPNWPOPGV-UHFFFAOYSA-N 0.000 claims description 5
- 125000000304 alkynyl group Chemical group 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 125000006413 ring segment Chemical group 0.000 claims description 5
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 4
- LRAMPOFRCGKEAQ-AWEZNQCLSA-N 2,5-dimethyl-n-[(1s)-1-[4-(methylsulfonylcarbamoyl)phenyl]ethyl]-4-[[4-(trifluoromethyl)phenyl]methyl]thiophene-3-carboxamide Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(=O)NS(C)(=O)=O)C(=O)C1=C(C)SC(C)=C1CC1=CC=C(C(F)(F)F)C=C1 LRAMPOFRCGKEAQ-AWEZNQCLSA-N 0.000 claims description 4
- CIEAOSWNZSOPSF-UHFFFAOYSA-N 2,5-dimethyl-n-[1-[4-(2h-tetrazol-5-yl)phenyl]cyclopropyl]-4-[[3-(trifluoromethyl)phenyl]methyl]thiophene-3-carboxamide Chemical compound C=1C=CC(C(F)(F)F)=CC=1CC1=C(C)SC(C)=C1C(=O)NC1(C=2C=CC(=CC=2)C2=NNN=N2)CC1 CIEAOSWNZSOPSF-UHFFFAOYSA-N 0.000 claims description 4
- FMLJGBDOSCBJBZ-UHFFFAOYSA-N 2,5-dimethyl-n-[1-[4-(2h-tetrazol-5-yl)phenyl]cyclopropyl]-4-[[4-(trifluoromethyl)phenyl]methyl]thiophene-3-carboxamide Chemical compound C=1C=C(C(F)(F)F)C=CC=1CC1=C(C)SC(C)=C1C(=O)NC1(C=2C=CC(=CC=2)C2=NNN=N2)CC1 FMLJGBDOSCBJBZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 4
- YQUNVWHOTJLOLI-LLVKDONJSA-N 4-[(1r)-1-[[2,5-dichloro-4-[(3-chlorophenyl)methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(Cl)SC(Cl)=C1CC1=CC=CC(Cl)=C1 YQUNVWHOTJLOLI-LLVKDONJSA-N 0.000 claims description 4
- KMCFCSKMVIRYBI-NSHDSACASA-N 4-[(1s)-1-[[2,5-dibromo-4-[(3-chlorophenyl)methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(Br)SC(Br)=C1CC1=CC=CC(Cl)=C1 KMCFCSKMVIRYBI-NSHDSACASA-N 0.000 claims description 4
- WUZXHEDPFNIOGV-JTQLQIEISA-N 4-[(1s)-1-[[2,5-dichloro-4-(3-chlorobenzoyl)thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(Cl)SC(Cl)=C1C(=O)C1=CC=CC(Cl)=C1 WUZXHEDPFNIOGV-JTQLQIEISA-N 0.000 claims description 4
- UUZOSJJYPGRLFD-YGXOJQJDSA-N 4-[(1s)-1-[[2,5-dichloro-4-[(3-chlorophenyl)-(oxan-2-yloxy)methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(Cl)SC(Cl)=C1C(C=1C=C(Cl)C=CC=1)OC1CCCCO1 UUZOSJJYPGRLFD-YGXOJQJDSA-N 0.000 claims description 4
- YJEXRJWDVWQMEX-YOZOHBORSA-N 4-[(1s)-1-[[2,5-dichloro-4-[(3-chlorophenyl)-hydroxymethyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(Cl)SC(Cl)=C1C(O)C1=CC=CC(Cl)=C1 YJEXRJWDVWQMEX-YOZOHBORSA-N 0.000 claims description 4
- YQUNVWHOTJLOLI-NSHDSACASA-N 4-[(1s)-1-[[2,5-dichloro-4-[(3-chlorophenyl)methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(Cl)SC(Cl)=C1CC1=CC=CC(Cl)=C1 YQUNVWHOTJLOLI-NSHDSACASA-N 0.000 claims description 4
- ASHWHAHRKQFQAR-NSHDSACASA-N 4-[(1s)-1-[[2,5-dichloro-4-[[3-(trifluoromethyl)phenyl]methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(Cl)SC(Cl)=C1CC1=CC=CC(C(F)(F)F)=C1 ASHWHAHRKQFQAR-NSHDSACASA-N 0.000 claims description 4
- DLMXCAVYRXOLRT-ZDUSSCGKSA-N 4-[(1s)-1-[[2,5-dimethyl-4-[[3-(trifluoromethyl)phenyl]methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(C)SC(C)=C1CC1=CC=CC(C(F)(F)F)=C1 DLMXCAVYRXOLRT-ZDUSSCGKSA-N 0.000 claims description 4
- YZTUSPHKCBTOSQ-ZDUSSCGKSA-N 4-[(1s)-1-[[4-[(3-chlorophenyl)methyl]-2,5-dimethylthiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(C)SC(C)=C1CC1=CC=CC(Cl)=C1 YZTUSPHKCBTOSQ-ZDUSSCGKSA-N 0.000 claims description 4
- CKYFFWHUNIOYDH-ZDUSSCGKSA-N 4-[(1s)-1-[[4-[(3-chlorophenyl)methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CSC=C1CC1=CC=CC(Cl)=C1 CKYFFWHUNIOYDH-ZDUSSCGKSA-N 0.000 claims description 4
- FADNAZBPTQVMPQ-ZDUSSCGKSA-N 4-[(1s)-1-[[4-[(4-chlorophenyl)methyl]-2,5-dimethylthiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=C(C)SC(C)=C1CC1=CC=C(Cl)C=C1 FADNAZBPTQVMPQ-ZDUSSCGKSA-N 0.000 claims description 4
- RZBIFXATYGZAHD-LBPRGKRZSA-N 4-[(1s)-1-[[5-bromo-4-[(3-chlorophenyl)methyl]thiophene-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CSC(Br)=C1CC1=CC=CC(Cl)=C1 RZBIFXATYGZAHD-LBPRGKRZSA-N 0.000 claims description 4
- FFFKIGGQAODEPS-UHFFFAOYSA-N 4-[1-[[2,5-dimethyl-4-[[3-(trifluoromethyl)phenyl]methyl]thiophene-3-carbonyl]amino]cyclopropyl]benzoic acid Chemical compound C=1C=CC(C(F)(F)F)=CC=1CC1=C(C)SC(C)=C1C(=O)NC1(C=2C=CC(=CC=2)C(O)=O)CC1 FFFKIGGQAODEPS-UHFFFAOYSA-N 0.000 claims description 4
- NCZZPAVJNDIVAY-UHFFFAOYSA-N 4-[1-[[5-chloro-3-[(3-chlorophenyl)methyl]thiophene-2-carbonyl]amino]ethyl]benzoic acid Chemical compound C=1C=C(C(O)=O)C=CC=1C(C)NC(=O)C=1SC(Cl)=CC=1CC1=CC=CC(Cl)=C1 NCZZPAVJNDIVAY-UHFFFAOYSA-N 0.000 claims description 4
- BGASCMMYJZPCSS-UHFFFAOYSA-N 4-[[[2,5-dichloro-4-[(3-chlorophenyl)methyl]thiophene-3-carbonyl]amino]methyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1CNC(=O)C1=C(Cl)SC(Cl)=C1CC1=CC=CC(Cl)=C1 BGASCMMYJZPCSS-UHFFFAOYSA-N 0.000 claims description 4
- PYWZJCKVQWUVPO-UHFFFAOYSA-N 5-chloro-3-[(3-chlorophenyl)methyl]-n-[1-[4-(2h-tetrazol-5-yl)phenyl]ethyl]thiophene-2-carboxamide Chemical compound C=1C=C(C=2NN=NN=2)C=CC=1C(C)NC(=O)C=1SC(Cl)=CC=1CC1=CC=CC(Cl)=C1 PYWZJCKVQWUVPO-UHFFFAOYSA-N 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
- 208000026935 allergic disease Diseases 0.000 claims description 4
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- ZAILXIKGMGZJPJ-SFHVURJKSA-N n-[(1s)-1-[4-(benzenesulfonylcarbamoyl)phenyl]ethyl]-2,5-dimethyl-4-[[4-(trifluoromethyl)phenyl]methyl]thiophene-3-carboxamide Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(=O)NS(=O)(=O)C=1C=CC=CC=1)C(=O)C1=C(C)SC(C)=C1CC1=CC=C(C(F)(F)F)C=C1 ZAILXIKGMGZJPJ-SFHVURJKSA-N 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 208000024891 symptom Diseases 0.000 claims description 4
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 claims description 3
- 125000006591 (C2-C6) alkynylene group Chemical group 0.000 claims description 3
- BTXUOUJHLMYLQA-ZDUSSCGKSA-N 4-[(1s)-1-[[2-[(4-chlorophenoxy)methyl]-5-fluoropyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(F)=CN=C1COC1=CC=C(Cl)C=C1 BTXUOUJHLMYLQA-ZDUSSCGKSA-N 0.000 claims description 3
- ZGFNLKCVKKEJKU-LBPRGKRZSA-N 4-[(1s)-1-[[5-chloro-2-(2,3-difluorophenoxy)benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1OC1=CC=CC(F)=C1F ZGFNLKCVKKEJKU-LBPRGKRZSA-N 0.000 claims description 3
- VKIBSGBBHPHLTP-NSHDSACASA-N 4-[(1s)-1-[[5-chloro-2-(2,3-difluorophenoxy)pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1OC1=CC=CC(F)=C1F VKIBSGBBHPHLTP-NSHDSACASA-N 0.000 claims description 3
- POCXSXWWUUVJIB-NSHDSACASA-N 4-[(1s)-1-[[5-chloro-2-(2-chloro-4-fluorophenoxy)pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1OC1=CC=C(F)C=C1Cl POCXSXWWUUVJIB-NSHDSACASA-N 0.000 claims description 3
- AMOAVOIZVZLGMJ-LBPRGKRZSA-N 4-[(1s)-1-[[5-chloro-2-(3,4-difluorophenoxy)benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1OC1=CC=C(F)C(F)=C1 AMOAVOIZVZLGMJ-LBPRGKRZSA-N 0.000 claims description 3
- NWAARQJHDWAZKA-NSHDSACASA-N 4-[(1s)-1-[[5-chloro-2-(3,4-difluorophenoxy)pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1OC1=CC=C(F)C(F)=C1 NWAARQJHDWAZKA-NSHDSACASA-N 0.000 claims description 3
- JDYZXLWEPUFOQR-NSHDSACASA-N 4-[(1s)-1-[[5-chloro-2-(3-chloro-5-fluorophenoxy)pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1OC1=CC(F)=CC(Cl)=C1 JDYZXLWEPUFOQR-NSHDSACASA-N 0.000 claims description 3
- PSRWNAXGTLCGIF-ZDUSSCGKSA-N 4-[(1s)-1-[[5-chloro-2-(3-chlorophenoxy)benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1OC1=CC=CC(Cl)=C1 PSRWNAXGTLCGIF-ZDUSSCGKSA-N 0.000 claims description 3
- PAASJZUYDQEILO-LBPRGKRZSA-N 4-[(1s)-1-[[5-chloro-2-(3-chlorophenoxy)pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1OC1=CC=CC(Cl)=C1 PAASJZUYDQEILO-LBPRGKRZSA-N 0.000 claims description 3
- QEJPFCHVBBYBQL-ZDUSSCGKSA-N 4-[(1s)-1-[[5-chloro-2-(3-cyanophenoxy)pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1OC1=CC=CC(C#N)=C1 QEJPFCHVBBYBQL-ZDUSSCGKSA-N 0.000 claims description 3
- HXOWIUWRSXNBNJ-ZDUSSCGKSA-N 4-[(1s)-1-[[5-chloro-2-(3-fluorophenoxy)benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1OC1=CC=CC(F)=C1 HXOWIUWRSXNBNJ-ZDUSSCGKSA-N 0.000 claims description 3
- KQRDIJJCEPLGDK-LBPRGKRZSA-N 4-[(1s)-1-[[5-chloro-2-(4-fluorophenoxy)pyridine-3-carbonyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CN=C1OC1=CC=C(F)C=C1 KQRDIJJCEPLGDK-LBPRGKRZSA-N 0.000 claims description 3
- XWIHFKIHPJOELR-INIZCTEOSA-N 4-[(1s)-1-[[5-chloro-2-(cyclohexylmethoxymethyl)benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1COCC1CCCCC1 XWIHFKIHPJOELR-INIZCTEOSA-N 0.000 claims description 3
- ATOZZVAPMQDUSI-ZDUSSCGKSA-N 4-[(1s)-1-[[5-chloro-2-[(2,4-difluorophenoxy)methyl]benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1COC1=CC=C(F)C=C1F ATOZZVAPMQDUSI-ZDUSSCGKSA-N 0.000 claims description 3
- CFRRXXZVKGXOHU-ZDUSSCGKSA-N 4-[(1s)-1-[[5-chloro-2-[(3,5-difluorophenoxy)methyl]benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1COC1=CC(F)=CC(F)=C1 CFRRXXZVKGXOHU-ZDUSSCGKSA-N 0.000 claims description 3
- ATUADYJYXJTVGY-AWEZNQCLSA-N 4-[(1s)-1-[[5-chloro-2-[(3-chlorophenoxy)methyl]benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1COC1=CC=CC(Cl)=C1 ATUADYJYXJTVGY-AWEZNQCLSA-N 0.000 claims description 3
- IJIDEDSKWSQAIX-AWEZNQCLSA-N 4-[(1s)-1-[[5-chloro-2-[(3-fluorophenoxy)methyl]benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1COC1=CC=CC(F)=C1 IJIDEDSKWSQAIX-AWEZNQCLSA-N 0.000 claims description 3
- VXYYNZFXXXAZLQ-AWEZNQCLSA-N 4-[(1s)-1-[[5-chloro-2-[(4-chlorophenoxy)methyl]benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1COC1=CC=C(Cl)C=C1 VXYYNZFXXXAZLQ-AWEZNQCLSA-N 0.000 claims description 3
- RYTPCTBNJWUUHU-AWEZNQCLSA-N 4-[(1s)-1-[[5-chloro-2-[(4-fluorophenoxy)methyl]benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1COC1=CC=C(F)C=C1 RYTPCTBNJWUUHU-AWEZNQCLSA-N 0.000 claims description 3
- MWBNCZHVEXULBD-ZDUSSCGKSA-N Benzoic acid, 4-[(1s)-1-[[5-chloro-2-(4-fluorophenoxy)benzoyl]amino]ethyl]- Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1OC1=CC=C(F)C=C1 MWBNCZHVEXULBD-ZDUSSCGKSA-N 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
- 125000006618 5- to 10-membered aromatic heterocyclic group Chemical group 0.000 claims description 2
- 125000005236 alkanoylamino group Chemical group 0.000 claims description 2
- 125000004450 alkenylene group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000001091 aminosulfinyl group Chemical group [H]N([H])S(*)=O 0.000 claims description 2
- 230000003042 antagnostic effect Effects 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 2
- 125000004428 fluoroalkoxy group Chemical group 0.000 claims description 2
- 125000005114 heteroarylalkoxy group Chemical group 0.000 claims description 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
- 239000000651 prodrug Substances 0.000 claims description 2
- 229940002612 prodrug Drugs 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 1
- 125000005309 thioalkoxy group Chemical group 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 10
- QJZQFVRFJCGDKF-UHFFFAOYSA-N 4-[1-[[2,5-dimethyl-4-[[4-(trifluoromethyl)phenyl]methyl]thiophene-3-carbonyl]amino]cyclopropyl]benzoic acid Chemical compound C=1C=C(C(F)(F)F)C=CC=1CC1=C(C)SC(C)=C1C(=O)NC1(C=2C=CC(=CC=2)C(O)=O)CC1 QJZQFVRFJCGDKF-UHFFFAOYSA-N 0.000 description 2
- 125000001246 bromo group Chemical group Br* 0.000 description 2
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- JNGZXGGOCLZBFB-IVCQMTBJSA-N compound E Chemical compound N([C@@H](C)C(=O)N[C@@H]1C(N(C)C2=CC=CC=C2C(C=2C=CC=CC=2)=N1)=O)C(=O)CC1=CC(F)=CC(F)=C1 JNGZXGGOCLZBFB-IVCQMTBJSA-N 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 2
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- 125000001113 thiadiazolyl group Chemical group 0.000 description 2
- 125000000335 thiazolyl group Chemical group 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 0 **C(NS(*)(=O)=O)=O Chemical compound **C(NS(*)(=O)=O)=O 0.000 description 1
- KYKVWMBQMHXMLJ-ZDUSSCGKSA-N 4-[(1s)-1-[[5-chloro-2-[(3,4-difluorophenoxy)methyl]benzoyl]amino]ethyl]benzoic acid Chemical compound N([C@@H](C)C=1C=CC(=CC=1)C(O)=O)C(=O)C1=CC(Cl)=CC=C1COC1=CC=C(F)C(F)=C1 KYKVWMBQMHXMLJ-ZDUSSCGKSA-N 0.000 description 1
- WKPAOXUEOAHZII-UHFFFAOYSA-N CC(c1nnn[nH]1)S Chemical compound CC(c1nnn[nH]1)S WKPAOXUEOAHZII-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 101150109738 Ptger4 gene Proteins 0.000 description 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28250610P | 2010-02-22 | 2010-02-22 | |
| US61/282,506 | 2010-02-22 | ||
| PCT/JP2011/000994 WO2011102149A1 (en) | 2010-02-22 | 2011-02-22 | Use of ep4 receptor antagonists in the treatment of il-23 mediated diseases |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017013578A Division JP2017095511A (ja) | 2010-02-22 | 2017-01-27 | Ｉｌ−２３媒介疾患を治療するためのｅｐ４受容体拮抗薬の使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013520397A JP2013520397A (ja) | 2013-06-06 |
| JP2013520397A5 true JP2013520397A5 (https=) | 2014-04-10 |
| JP6152643B2 JP6152643B2 (ja) | 2017-06-28 |
Family
ID=44482754
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012538520A Active JP6152643B2 (ja) | 2010-02-22 | 2011-02-22 | Ｉｌ−２３媒介疾患を治療するためのｅｐ４受容体拮抗薬の使用 |
| JP2017013578A Withdrawn JP2017095511A (ja) | 2010-02-22 | 2017-01-27 | Ｉｌ−２３媒介疾患を治療するためのｅｐ４受容体拮抗薬の使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017013578A Withdrawn JP2017095511A (ja) | 2010-02-22 | 2017-01-27 | Ｉｌ−２３媒介疾患を治療するためのｅｐ４受容体拮抗薬の使用 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US9457084B2 (https=) |
| EP (1) | EP2538978B1 (https=) |
| JP (2) | JP6152643B2 (https=) |
| KR (1) | KR101780666B1 (https=) |
| CN (2) | CN107693518A (https=) |
| BR (1) | BR112012020236A2 (https=) |
| CA (2) | CA3009937C (https=) |
| ES (1) | ES2600355T3 (https=) |
| HK (1) | HK1249401A1 (https=) |
| MX (1) | MX341482B (https=) |
| RU (1) | RU2571816C2 (https=) |
| WO (1) | WO2011102149A1 (https=) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO3296B1 (ar) | 2012-06-29 | 2018-09-16 | Lilly Co Eli | مركبات فينوكسي إيثيل بيبريدين |
| UA115576C2 (uk) * | 2012-12-06 | 2017-11-27 | Байєр Фарма Акцієнгезелльшафт | Похідні бензимідазолу як антагоністи ер4 |
| EP2765128A1 (en) | 2013-02-07 | 2014-08-13 | Almirall, S.A. | Substituted benzamides with activity towards EP4 receptors |
| TW201443004A (zh) | 2013-02-15 | 2014-11-16 | Lilly Co Eli | 苯氧基乙氧基化合物 |
| TWI636046B (zh) | 2013-05-17 | 2018-09-21 | 美國禮來大藥廠 | 苯氧基乙基二氫－１ｈ－異喹啉化合物 |
| ME02896B (me) | 2013-12-17 | 2018-04-20 | Lilly Co Eli | Fenoksietilni derivati prstenastog amina i njihova aktivnost kao modulatora receptora ep4 |
| TW201607943A (zh) | 2013-12-19 | 2016-03-01 | 拜耳製藥公司 | 作為ｅｐ４配體之新穎苯并咪唑衍生物 |
| PT3113774T (pt) | 2014-03-06 | 2022-02-28 | Elanco Animal Health Incorporated | Composições de grapiprant e métodos de utilização das mesmas |
| US12109218B2 (en) | 2014-12-09 | 2024-10-08 | Aratana Therapeutics, Inc. | Compositions of grapiprant and methods for using the same |
| BR112018007664B1 (pt) * | 2015-10-16 | 2023-12-19 | Eisai R&D Management Co., Ltd | Compostos antagonistas de ep4, composição compreendendo o composto e uso dos mesmos para tratar câncer |
| US10342785B2 (en) * | 2016-11-04 | 2019-07-09 | Askat Inc. | Use of EP4 receptor antagonists for the treatment of NASH-associated liver cancer |
| CA3047336A1 (en) | 2017-01-23 | 2018-07-26 | Jecure Therapeutics, Inc. | Chemical compounds as inhibitors of interleukin-1 activity |
| CN109836434B (zh) * | 2017-11-27 | 2020-09-25 | 上海宇耀生物科技有限公司 | 噻吩并环类化合物及其合成方法和应用 |
| JP2021522211A (ja) | 2018-04-16 | 2021-08-30 | アリーズ セラピューティクス， インコーポレイテッド | Ｅｐ４阻害剤およびその使用 |
| US10239885B1 (en) | 2018-06-18 | 2019-03-26 | Avista Pharma Solutions, Inc. | Compound 1-[2-[4-(2-ethyl-6,8-dimethylimidazo[1,2-α]pyrazin-3-yl)phenyl]ethyl]-3-(p-tolylsulfonyl)urea as a prostaglandin EP4 receptor antagonist |
| US20210315909A1 (en) | 2018-07-11 | 2021-10-14 | Arrys Therapeutics, Inc. | Polymorphic compounds and uses thereof |
| SG11202012159TA (en) * | 2018-07-20 | 2021-01-28 | Hoffmann La Roche | Sulfonylurea compounds as inhibitors of interleukin-1 activity |
| EP3823974A1 (en) | 2018-07-20 | 2021-05-26 | F. Hoffmann-La Roche AG | Sulfonimidamide compounds as inhibitors of interleukin-1 activity |
| MX2021003904A (es) | 2018-10-05 | 2021-10-26 | Annapurna Bio Inc | Compuestos y composiciones para el tratamiento de afecciones asociadas con la actividad del receptor apj. |
| CA3128024A1 (en) | 2019-01-30 | 2020-08-06 | Avista Pharma Solutions, Inc. | Chemical compounds |
| MX2021009251A (es) | 2019-01-30 | 2021-09-21 | Avista Pharma Solutions Inc | Proceso de sintesis y nuevos compuestos intermedios. |
| CN115697317A (zh) * | 2020-04-08 | 2023-02-03 | 株式会社AskAt | Ep4受体拮抗剂用于治疗肝癌、黑色素瘤、淋巴瘤和白血病的应用 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HN2001000224A (es) * | 2000-10-19 | 2002-06-13 | Pfizer | Compuestos de imidazol condensado con arilo o heteroarilo como agentes anti - inflamatorios y analgesicos. |
| CN100579518C (zh) | 2002-04-12 | 2010-01-13 | 美国辉瑞有限公司 | Ep4受体配体在制备治疗il-6相关疾病的药物中的应用 |
| DE602004013938D1 (de) * | 2003-01-29 | 2008-07-03 | Asterand Uk Ltd | Hemmstoffe des ep4-rezeptors |
| GB0302094D0 (en) | 2003-01-29 | 2003-02-26 | Pharmagene Lab Ltd | EP4 receptor antagonists |
| KR100747401B1 (ko) * | 2003-09-03 | 2007-08-08 | 화이자 인코포레이티드 | 프로스타글란딘 ｅ2 길항제로서의 페닐 또는 피리딜 아미드 화합물 |
| WO2005102389A2 (en) * | 2004-04-20 | 2005-11-03 | Pfizer Products Inc. | Combinations comprising alpha-2-delta ligands and ep4 receptor antagonists |
| MXPA06011555A (es) | 2004-05-04 | 2006-12-15 | Pfizer | Compuestos de metil-aril o heteroaril-amida sustituida. |
| CA2600510C (en) * | 2005-03-11 | 2010-11-02 | Pfizer Inc. | Crystal forms of an imidazole derivative |
| US8969394B2 (en) | 2006-08-11 | 2015-03-03 | Merck Frosst Canada Ltd. | Thiophenecarboxamide derivatives as EP4 receptor ligands |
| EP1886987A1 (en) * | 2006-08-11 | 2008-02-13 | Givaudan S.A. | Process for producing 2,2,3-trimethylcyclopent-3-enecarbaldehyde (campholytic aldehyde) |
-
2011
- 2011-02-22 US US13/580,323 patent/US9457084B2/en active Active
- 2011-02-22 CN CN201711045618.XA patent/CN107693518A/zh active Pending
- 2011-02-22 ES ES11744440.6T patent/ES2600355T3/es active Active
- 2011-02-22 CA CA3009937A patent/CA3009937C/en active Active
- 2011-02-22 MX MX2012009503A patent/MX341482B/es active IP Right Grant
- 2011-02-22 RU RU2012140450/15A patent/RU2571816C2/ru active
- 2011-02-22 KR KR1020127024115A patent/KR101780666B1/ko active Active
- 2011-02-22 CN CN2011800104626A patent/CN102770159A/zh active Pending
- 2011-02-22 WO PCT/JP2011/000994 patent/WO2011102149A1/en not_active Ceased
- 2011-02-22 CA CA2789665A patent/CA2789665C/en active Active
- 2011-02-22 JP JP2012538520A patent/JP6152643B2/ja active Active
- 2011-02-22 BR BR112012020236A patent/BR112012020236A2/pt not_active Application Discontinuation
- 2011-02-22 EP EP11744440.6A patent/EP2538978B1/en active Active
-
2017
- 2017-01-27 JP JP2017013578A patent/JP2017095511A/ja not_active Withdrawn
-
2018
- 2018-06-15 HK HK18107808.7A patent/HK1249401A1/zh unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013520397A5 (https=) | ||
| CA2789665A1 (en) | Use of ep4 receptor antagonists in the treatment of il-23 mediated diseases | |
| RU2015144676A (ru) | Применение рецептора антагониста ер4 для лечения хрящевой болезни | |
| JP6170040B2 (ja) | ピルフェニドン及び選択された患者における抗線維化療法 | |
| JP2023126918A (ja) | 老化細胞を殺し、老化関連疾患および障害を処置するための方法と組成物 | |
| AU2016204638B2 (en) | Compositions and methods of treating pulmonary hypertension | |
| CA2481535A1 (en) | Use of ep4 receptor ligands in the treatment of il-6 involved diseases | |
| JP2014532647A5 (https=) | ||
| JP2016512825A5 (https=) | ||
| JP2012519160A5 (https=) | ||
| BG103803A (bg) | Метод за приложение на инхибитори на циклооксигеназа-2 при предотвратяване на смущения в сърдечно-съдовата система | |
| JP2004517054A5 (https=) | ||
| RU2011147194A (ru) | Селективные антагонисты рецептора ep4 для лечения рака | |
| JP2017528507A5 (https=) | ||
| RU2006137076A (ru) | Комбинации, содержащие лиганды рецептора альфа-2-дельта | |
| MX2014002471A (es) | Combinaciones sinergicas de los inhibidores de p13k y mek. | |
| MX2015017629A (es) | Combinaciones farmaceuticas. | |
| BRPI1014174B8 (pt) | uso de um composto selecionado a partir de 4-((1s)-1-{[5-cloro-2-(4-fluorofenóxi)benzoil]amino}etil)ácido benzóico, 4-[(1s)-1-({[5-cloro-2-(3-fluorofenóxi)piridin-3-il]carbonil}amino)etil]ácido benzóico e 3-[2-(4-{2-etil-4,6-dimetil-1h-imidazo[4,5-c]piridin-1-il}fenil)etil]-1-[(4-metilbenzeno)sulfonil]urea para tratamento de um câncer epitelial relacionado à pge2 | |
| JP2020529995A5 (https=) | ||
| CN102387798A (zh) | 供治疗、预防和控制结核病的pde4调节剂的使用方法及包含其的组合物 | |
| TW202342050A (zh) | 用於治療進行性纖維化間質性肺病之新穎治療組合 | |
| KR20240121251A (ko) | 진행성 섬유화 간질성 폐 질환의 치료를 위한 신규한 경구 약제학적 조성물 및 투여 섭생 | |
| CN118369098A (zh) | 用于治疗进行性纤维化间质性肺病的新颖治疗组合 | |
| HK1177148A (en) | Use of ep4 receptor antagonists in the treatment of il-23 mediated diseases | |
| HK1212211B (zh) | Ep4受体拮抗剂在软骨疾病的治疗中的用途 |