JP2015535252A5 - - Google Patents
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- JP2015535252A5 JP2015535252A5 JP2015539755A JP2015539755A JP2015535252A5 JP 2015535252 A5 JP2015535252 A5 JP 2015535252A5 JP 2015539755 A JP2015539755 A JP 2015539755A JP 2015539755 A JP2015539755 A JP 2015539755A JP 2015535252 A5 JP2015535252 A5 JP 2015535252A5
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- JP
- Japan
- Prior art keywords
- indazole
- sulfonamide
- fluoro
- alkyl
- 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.)
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- -1 aralkenyl Chemical group 0.000 claims 47
- 125000000217 alkyl group Chemical group 0.000 claims 36
- 150000003839 salts Chemical class 0.000 claims 17
- 125000000753 cycloalkyl group Chemical group 0.000 claims 16
- 229910052736 halogen Inorganic materials 0.000 claims 15
- 150000002367 halogens Chemical class 0.000 claims 15
- 125000003118 aryl group Chemical group 0.000 claims 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 11
- 125000001072 heteroaryl group Chemical group 0.000 claims 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 11
- 125000001424 substituent group Chemical group 0.000 claims 11
- 125000003710 aryl alkyl group Chemical group 0.000 claims 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 8
- 239000008194 pharmaceutical composition Substances 0.000 claims 8
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 125000002252 acyl group Chemical group 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims 6
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 6
- 125000004414 alkyl thio group Chemical group 0.000 claims 6
- 125000003435 aroyl group Chemical group 0.000 claims 6
- 125000004659 aryl alkyl thio group Chemical group 0.000 claims 6
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims 6
- 125000005135 aryl sulfinyl group Chemical group 0.000 claims 6
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims 6
- 125000005110 aryl thio group Chemical group 0.000 claims 6
- 125000004104 aryloxy group Chemical group 0.000 claims 6
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 6
- 125000005843 halogen group Chemical group 0.000 claims 6
- 125000004475 heteroaralkyl group Chemical group 0.000 claims 6
- 125000005150 heteroarylsulfinyl group Chemical group 0.000 claims 6
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 claims 6
- 125000000623 heterocyclic group Chemical group 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 6
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 6
- 150000001408 amides Chemical class 0.000 claims 5
- 125000005368 heteroarylthio group Chemical group 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 208000035475 disorder Diseases 0.000 claims 4
- 125000005842 heteroatom Chemical group 0.000 claims 4
- 208000004296 neuralgia Diseases 0.000 claims 4
- 208000021722 neuropathic pain Diseases 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims 4
- 125000006413 ring segment Chemical group 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 239000011593 sulfur Substances 0.000 claims 4
- HLIFNQCITGTXJX-DRMXPCRNSA-N 1-[(1r)-1-[2-[2-[(1r,2r)-2-aminocyclohexyl]ethynyl]phenyl]ethyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound C1([C@@H](C)N2C3=CC(F)=C(C=C3C=N2)S(=O)(=O)NC=2N=C(F)C=CC=2)=CC=CC=C1C#C[C@H]1CCCC[C@H]1N HLIFNQCITGTXJX-DRMXPCRNSA-N 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- CAIALQMFYYGXBJ-OAHLLOKOSA-N 1-[(1r)-1-[2-(3-aminopropyl)phenyl]ethyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound C1([C@@H](C)N2C3=CC(F)=C(C=C3C=N2)S(=O)(=O)NC=2N=C(F)C=CC=2)=CC=CC=C1CCCN CAIALQMFYYGXBJ-OAHLLOKOSA-N 0.000 claims 2
- WCWKMFXFWHIFGR-CQSZACIVSA-N 1-[(1r)-1-[2-(azetidin-3-yl)phenyl]ethyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound C1([C@@H](C)N2C3=CC(F)=C(C=C3C=N2)S(=O)(=O)NC=2N=C(F)C=CC=2)=CC=CC=C1C1CNC1 WCWKMFXFWHIFGR-CQSZACIVSA-N 0.000 claims 2
- HLIFNQCITGTXJX-WWEVIYMKSA-N 1-[(1r)-1-[2-[2-[(1s,2s)-2-aminocyclohexyl]ethynyl]phenyl]ethyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound C1([C@@H](C)N2C3=CC(F)=C(C=C3C=N2)S(=O)(=O)NC=2N=C(F)C=CC=2)=CC=CC=C1C#C[C@@H]1CCCC[C@@H]1N HLIFNQCITGTXJX-WWEVIYMKSA-N 0.000 claims 2
- HLIFNQCITGTXJX-UHFFFAOYSA-N 1-[1-[2-[2-(2-aminocyclohexyl)ethynyl]phenyl]ethyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound N1=CC2=CC(S(=O)(=O)NC=3N=C(F)C=CC=3)=C(F)C=C2N1C(C)C1=CC=CC=C1C#CC1CCCCC1N HLIFNQCITGTXJX-UHFFFAOYSA-N 0.000 claims 2
- DBZJNIHBDORRII-OAHLLOKOSA-N 1-[[(7r)-7-amino-5,6,7,8-tetrahydronaphthalen-1-yl]methyl]-6-fluoro-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C([C@H](CC1=2)N)CC1=CC=CC=2CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=NC=NS1 DBZJNIHBDORRII-OAHLLOKOSA-N 0.000 claims 2
- RHZYYEZFTCJSBE-GFCCVEGCSA-N 6-fluoro-1-[(1r)-1-(1,2,3,4-tetrahydroisoquinolin-8-yl)ethyl]-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound FC=1C=C2N([C@@H](C=3C=4CNCCC=4C=CC=3)C)N=CC2=CC=1S(=O)(=O)NC1=NC=NS1 RHZYYEZFTCJSBE-GFCCVEGCSA-N 0.000 claims 2
- YCZYLEYBYBXZRB-CYBMUJFWSA-N 6-fluoro-1-[(1r)-1-(1,2,3,4-tetrahydroisoquinolin-8-yl)ethyl]-n-(1,3-thiazol-2-yl)indazole-5-sulfonamide Chemical compound FC=1C=C2N([C@@H](C=3C=4CNCCC=4C=CC=3)C)N=CC2=CC=1S(=O)(=O)NC1=NC=CS1 YCZYLEYBYBXZRB-CYBMUJFWSA-N 0.000 claims 2
- ZQLOTXCADLUPOP-LLVKDONJSA-N 6-fluoro-1-[(1r)-1-phenylethyl]-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C1([C@@H](C)N2C3=CC(F)=C(C=C3C=N2)S(=O)(=O)NC=2SN=CN=2)=CC=CC=C1 ZQLOTXCADLUPOP-LLVKDONJSA-N 0.000 claims 2
- MTXZEXIUQKVXSK-CQSZACIVSA-N 6-fluoro-n-(5-fluoropyridin-2-yl)-1-[(1r)-1-(1,2,3,4-tetrahydroisoquinolin-8-yl)ethyl]indazole-5-sulfonamide Chemical compound FC=1C=C2N([C@@H](C=3C=4CNCCC=4C=CC=3)C)N=CC2=CC=1S(=O)(=O)NC1=CC=C(F)C=N1 MTXZEXIUQKVXSK-CQSZACIVSA-N 0.000 claims 2
- BDXVDLWUWAYQKL-CQSZACIVSA-N 6-fluoro-n-(6-fluoropyridin-2-yl)-1-[(1r)-1-(1,2,3,4-tetrahydroisoquinolin-8-yl)ethyl]indazole-5-sulfonamide Chemical compound FC=1C=C2N([C@@H](C=3C=4CNCCC=4C=CC=3)C)N=CC2=CC=1S(=O)(=O)NC1=CC=CC(F)=N1 BDXVDLWUWAYQKL-CQSZACIVSA-N 0.000 claims 2
- QMJIVIHONRHYGL-MRXNPFEDSA-N 6-fluoro-n-(6-fluoropyridin-2-yl)-1-[(1r)-1-(2-piperidin-4-ylphenyl)ethyl]indazole-5-sulfonamide Chemical compound C1([C@@H](C)N2C3=CC(F)=C(C=C3C=N2)S(=O)(=O)NC=2N=C(F)C=CC=2)=CC=CC=C1C1CCNCC1 QMJIVIHONRHYGL-MRXNPFEDSA-N 0.000 claims 2
- SRBXSJAKGQJETP-MRXNPFEDSA-N 6-fluoro-n-(6-fluoropyridin-2-yl)-1-[(1r)-1-[2-(1,2,3,6-tetrahydropyridin-4-yl)phenyl]ethyl]indazole-5-sulfonamide Chemical compound C1([C@@H](C)N2C3=CC(F)=C(C=C3C=N2)S(=O)(=O)NC=2N=C(F)C=CC=2)=CC=CC=C1C1=CCNCC1 SRBXSJAKGQJETP-MRXNPFEDSA-N 0.000 claims 2
- 125000005021 aminoalkenyl group Chemical group 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- KVCFFRVMHFWXRQ-GFCCVEGCSA-N n-(5-chloro-1,3-thiazol-2-yl)-6-fluoro-1-[(1r)-1-(1,2,3,4-tetrahydroisoquinolin-8-yl)ethyl]indazole-5-sulfonamide Chemical compound FC=1C=C2N([C@@H](C=3C=4CNCCC=4C=CC=3)C)N=CC2=CC=1S(=O)(=O)NC1=NC=C(Cl)S1 KVCFFRVMHFWXRQ-GFCCVEGCSA-N 0.000 claims 2
- JXVAEAWLORTHQW-GFCCVEGCSA-N n-(5-chloro-1,3-thiazol-2-yl)-6-fluoro-2-[(1r)-1-(1,2,3,4-tetrahydroisoquinolin-8-yl)ethyl]indazole-5-sulfonamide Chemical compound FC1=CC2=NN([C@@H](C=3C=4CNCCC=4C=CC=3)C)C=C2C=C1S(=O)(=O)NC1=NC=C(Cl)S1 JXVAEAWLORTHQW-GFCCVEGCSA-N 0.000 claims 2
- CSCJDGKSKWJIBP-MRXNPFEDSA-N n-(6-fluoropyridin-2-yl)-6-methyl-1-[(1r)-1-(1,2,3,4-tetrahydroisoquinolin-8-yl)ethyl]indazole-5-sulfonamide Chemical compound CC=1C=C2N([C@@H](C=3C=4CNCCC=4C=CC=3)C)N=CC2=CC=1S(=O)(=O)NC1=CC=CC(F)=N1 CSCJDGKSKWJIBP-MRXNPFEDSA-N 0.000 claims 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims 1
- BJAWBFPYZRHYLC-UHFFFAOYSA-N 1-(2,3-dihydro-1h-isoindol-4-ylmethyl)-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound FC1=CC=CC(NS(=O)(=O)C=2C(=CC=3N(CC=4C=5CNCC=5C=CC=4)N=CC=3C=2)F)=N1 BJAWBFPYZRHYLC-UHFFFAOYSA-N 0.000 claims 1
- AYFXUDMBPRBAPJ-UHFFFAOYSA-N 1-[(2-amino-2,3-dihydro-1h-inden-4-yl)methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound C=12CC(N)CC2=CC=CC=1CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=CC=CC(F)=N1 AYFXUDMBPRBAPJ-UHFFFAOYSA-N 0.000 claims 1
- DBZJNIHBDORRII-UHFFFAOYSA-N 1-[(7-amino-5,6,7,8-tetrahydronaphthalen-1-yl)methyl]-6-fluoro-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C=12CC(N)CCC2=CC=CC=1CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=NC=NS1 DBZJNIHBDORRII-UHFFFAOYSA-N 0.000 claims 1
- UKZBXRYSYXZVOR-UHFFFAOYSA-N 1-[(7-amino-5,6,7,8-tetrahydronaphthalen-1-yl)methyl]-6-fluoro-n-(1,3-thiazol-2-yl)indazole-5-sulfonamide Chemical compound C=12CC(N)CCC2=CC=CC=1CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=NC=CS1 UKZBXRYSYXZVOR-UHFFFAOYSA-N 0.000 claims 1
- GQZRFXWUYDBETK-UHFFFAOYSA-N 1-[(7-amino-5,6,7,8-tetrahydronaphthalen-1-yl)methyl]-6-methyl-n-(1,3-thiazol-2-yl)indazole-5-sulfonamide Chemical compound CC1=CC=2N(CC=3C=4CC(N)CCC=4C=CC=3)N=CC=2C=C1S(=O)(=O)NC1=NC=CS1 GQZRFXWUYDBETK-UHFFFAOYSA-N 0.000 claims 1
- PXUKNVBPQYBNED-UHFFFAOYSA-N 1-[(7-amino-5,6,7,8-tetrahydronaphthalen-1-yl)methyl]-n-(5-chloro-1,3-thiazol-2-yl)-6-fluoroindazole-5-sulfonamide Chemical compound C=12CC(N)CCC2=CC=CC=1CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=NC=C(Cl)S1 PXUKNVBPQYBNED-UHFFFAOYSA-N 0.000 claims 1
- CAIALQMFYYGXBJ-UHFFFAOYSA-N 1-[1-[2-(3-aminopropyl)phenyl]ethyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound N1=CC2=CC(S(=O)(=O)NC=3N=C(F)C=CC=3)=C(F)C=C2N1C(C)C1=CC=CC=C1CCCN CAIALQMFYYGXBJ-UHFFFAOYSA-N 0.000 claims 1
- WCWKMFXFWHIFGR-UHFFFAOYSA-N 1-[1-[2-(azetidin-3-yl)phenyl]ethyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound N1=CC2=CC(S(=O)(=O)NC=3N=C(F)C=CC=3)=C(F)C=C2N1C(C)C1=CC=CC=C1C1CNC1 WCWKMFXFWHIFGR-UHFFFAOYSA-N 0.000 claims 1
- UKZBXRYSYXZVOR-MRXNPFEDSA-N 1-[[(7r)-7-amino-5,6,7,8-tetrahydronaphthalen-1-yl]methyl]-6-fluoro-n-(1,3-thiazol-2-yl)indazole-5-sulfonamide Chemical compound C([C@H](CC1=2)N)CC1=CC=CC=2CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=NC=CS1 UKZBXRYSYXZVOR-MRXNPFEDSA-N 0.000 claims 1
- MNUGLDCSCOZYSQ-QGZVFWFLSA-N 1-[[(7r)-7-amino-5,6,7,8-tetrahydronaphthalen-1-yl]methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound C([C@H](CC1=2)N)CC1=CC=CC=2CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=CC=CC(F)=N1 MNUGLDCSCOZYSQ-QGZVFWFLSA-N 0.000 claims 1
- DBZJNIHBDORRII-HNNXBMFYSA-N 1-[[(7s)-7-amino-5,6,7,8-tetrahydronaphthalen-1-yl]methyl]-6-fluoro-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C([C@@H](CC1=2)N)CC1=CC=CC=2CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=NC=NS1 DBZJNIHBDORRII-HNNXBMFYSA-N 0.000 claims 1
- UKZBXRYSYXZVOR-INIZCTEOSA-N 1-[[(7s)-7-amino-5,6,7,8-tetrahydronaphthalen-1-yl]methyl]-6-fluoro-n-(1,3-thiazol-2-yl)indazole-5-sulfonamide Chemical compound C([C@@H](CC1=2)N)CC1=CC=CC=2CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=NC=CS1 UKZBXRYSYXZVOR-INIZCTEOSA-N 0.000 claims 1
- MNUGLDCSCOZYSQ-KRWDZBQOSA-N 1-[[(7s)-7-amino-5,6,7,8-tetrahydronaphthalen-1-yl]methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound C([C@@H](CC1=2)N)CC1=CC=CC=2CN(C1=CC=2F)N=CC1=CC=2S(=O)(=O)NC1=CC=CC(F)=N1 MNUGLDCSCOZYSQ-KRWDZBQOSA-N 0.000 claims 1
- HCYBVAJMNZELNV-UHFFFAOYSA-N 1-[[2-(1,2,3,4-tetrahydroisoquinolin-5-yl)phenyl]methyl]-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C=1C=C2N(CC=3C(=CC=CC=3)C=3C=4CCNCC=4C=CC=3)N=CC2=CC=1S(=O)(=O)NC1=NC=NS1 HCYBVAJMNZELNV-UHFFFAOYSA-N 0.000 claims 1
- KPEIQQYVHAGHIA-UHFFFAOYSA-N 1-[[2-(2,3,4,7-tetrahydro-1h-azepin-5-yl)phenyl]methyl]-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C=1C=C2N(CC=3C(=CC=CC=3)C=3CCCNCC=3)N=CC2=CC=1S(=O)(=O)NC1=NC=NS1 KPEIQQYVHAGHIA-UHFFFAOYSA-N 0.000 claims 1
- IZQQSZDILYAADY-UHFFFAOYSA-N 1-[[2-(2-amino-1-fluoroethyl)phenyl]methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound NCC(F)C1=CC=CC=C1CN1C2=CC(F)=C(S(=O)(=O)NC=3N=C(F)C=CC=3)C=C2C=N1 IZQQSZDILYAADY-UHFFFAOYSA-N 0.000 claims 1
- KJXORRSVLNZSBG-UHFFFAOYSA-N 1-[[2-(2-aminoethyl)phenyl]methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound NCCC1=CC=CC=C1CN1C2=CC(F)=C(S(=O)(=O)NC=3N=C(F)C=CC=3)C=C2C=N1 KJXORRSVLNZSBG-UHFFFAOYSA-N 0.000 claims 1
- DJUDLAQQIDCWFL-UHFFFAOYSA-N 1-[[2-(3-aminoprop-1-ynyl)phenyl]methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound NCC#CC1=CC=CC=C1CN1C2=CC(F)=C(S(=O)(=O)NC=3N=C(F)C=CC=3)C=C2C=N1 DJUDLAQQIDCWFL-UHFFFAOYSA-N 0.000 claims 1
- DTUSTJJVJJTMGW-UHFFFAOYSA-N 1-[[2-(3-aminopropyl)phenyl]methyl]-6-fluoro-n-(1,3-thiazol-2-yl)indazole-5-sulfonamide Chemical compound NCCCC1=CC=CC=C1CN1C2=CC(F)=C(S(=O)(=O)NC=3SC=CN=3)C=C2C=N1 DTUSTJJVJJTMGW-UHFFFAOYSA-N 0.000 claims 1
- IOCLELURYWJHAP-UHFFFAOYSA-N 1-[[2-(3-aminopropyl)phenyl]methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound NCCCC1=CC=CC=C1CN1C2=CC(F)=C(S(=O)(=O)NC=3N=C(F)C=CC=3)C=C2C=N1 IOCLELURYWJHAP-UHFFFAOYSA-N 0.000 claims 1
- CYDWOBCBPTYJCC-UHFFFAOYSA-N 1-[[2-(4-amino-4-methylpent-1-ynyl)phenyl]methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound CC(C)(N)CC#CC1=CC=CC=C1CN1C2=CC(F)=C(S(=O)(=O)NC=3N=C(F)C=CC=3)C=C2C=N1 CYDWOBCBPTYJCC-UHFFFAOYSA-N 0.000 claims 1
- KXFJWALCQLVADP-UHFFFAOYSA-N 1-[[2-(8-azabicyclo[3.2.1]oct-3-en-3-yl)-4-chlorophenyl]methyl]-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C=1C(N2)CCC2CC=1C1=CC(Cl)=CC=C1CN(C1=CC=2)N=CC1=CC=2S(=O)(=O)NC1=NC=NS1 KXFJWALCQLVADP-UHFFFAOYSA-N 0.000 claims 1
- CRZNGZBFLFERPO-UHFFFAOYSA-N 1-[[2-(aminomethyl)phenyl]methyl]-6-fluoro-n-(6-fluoropyridin-2-yl)indazole-5-sulfonamide Chemical compound NCC1=CC=CC=C1CN1C2=CC(F)=C(S(=O)(=O)NC=3N=C(F)C=CC=3)C=C2C=N1 CRZNGZBFLFERPO-UHFFFAOYSA-N 0.000 claims 1
- XCWJYPNQTOFDRK-ZZXKWVIFSA-N 1-[[2-[(e)-3-aminoprop-1-enyl]phenyl]methyl]-6-fluoro-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound NC\C=C\C1=CC=CC=C1CN1C2=CC(F)=C(S(=O)(=O)NC=3SN=CN=3)C=C2C=N1 XCWJYPNQTOFDRK-ZZXKWVIFSA-N 0.000 claims 1
- VMTPZTDENTUFFJ-ZZXKWVIFSA-N 1-[[2-[(e)-3-aminoprop-1-enyl]phenyl]methyl]-7-chloro-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound NC\C=C\C1=CC=CC=C1CN1C2=C(Cl)C=C(S(=O)(=O)NC=3SN=CN=3)C=C2C=N1 VMTPZTDENTUFFJ-ZZXKWVIFSA-N 0.000 claims 1
- KENSZPCZGVMJIS-ZZXKWVIFSA-N 1-[[2-[(e)-3-aminoprop-1-enyl]phenyl]methyl]-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound NC\C=C\C1=CC=CC=C1CN1C2=CC=C(S(=O)(=O)NC=3SN=CN=3)C=C2C=N1 KENSZPCZGVMJIS-ZZXKWVIFSA-N 0.000 claims 1
- WHACZBSIVGAAKF-UHFFFAOYSA-N 1-[[4-chloro-2-(1,2,3,4-tetrahydroisoquinolin-5-yl)phenyl]methyl]-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C=1C=CC=2CNCCC=2C=1C1=CC(Cl)=CC=C1CN(C1=CC=2)N=CC1=CC=2S(=O)(=O)NC1=NC=NS1 WHACZBSIVGAAKF-UHFFFAOYSA-N 0.000 claims 1
- AKCGUMBUZCWBQJ-UHFFFAOYSA-N 1-[[4-chloro-2-(1,2,3,4-tetrahydroisoquinolin-8-yl)phenyl]methyl]-n-(1,2,4-thiadiazol-5-yl)indazole-5-sulfonamide Chemical compound C=1C=CC=2CCNCC=2C=1C1=CC(Cl)=CC=C1CN(C1=CC=2)N=CC1=CC=2S(=O)(=O)NC1=NC=NS1 AKCGUMBUZCWBQJ-UHFFFAOYSA-N 0.000 claims 1
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| CA2874621A1 (en) | 2012-05-22 | 2013-11-28 | Genentech, Inc. | N-substituted benzamides and their use in the treatment of pain |
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| CN106715418A (zh) | 2014-07-07 | 2017-05-24 | 基因泰克公司 | 治疗化合物及其使用方法 |
| US9783527B2 (en) * | 2014-09-16 | 2017-10-10 | Abbvie Inc. | Indazole ureas and method of use |
| JP2018507900A (ja) * | 2015-03-13 | 2018-03-22 | アッヴィ・インコーポレイテッド | （インダゾール−４−イル）ヘキサヒドロピロロピロロン及び使用方法 |
| MA42118A (fr) | 2015-05-22 | 2018-03-28 | Genentech Inc | Benzamides substitués et leurs méthodes d'utilisation |
| WO2017035271A1 (en) | 2015-08-27 | 2017-03-02 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| JP6987746B2 (ja) | 2015-09-28 | 2022-01-05 | ジェネンテック， インコーポレイテッド | 治療用化合物及びその使用方法 |
| US10899732B2 (en) | 2015-11-25 | 2021-01-26 | Genentech, Inc. | Substituted benzamides useful as sodium channel blockers |
| CN108699015A (zh) | 2015-12-18 | 2018-10-23 | 默沙东公司 | 对电压门控性钠通道具有选择性活性的羟基烷基胺-和羟基环烷基胺-取代的二胺-芳基磺胺化合物 |
| US10766858B2 (en) | 2016-03-30 | 2020-09-08 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
| WO2017201468A1 (en) | 2016-05-20 | 2017-11-23 | Xenon Pharmaceuticals Inc. | Benzenesulfonamide compounds and their use as therapeutic agents |
| BR112019007763A2 (pt) | 2016-10-17 | 2019-07-02 | Genentech Inc | composto de fórmula, composição farmacêutica, métodos para tratar uma doença ou condição, para tratar dores, para diminuir o fluxo de íons e para tratar prurido, uso de um composto e invenção |
| EP3551626B1 (en) | 2016-12-09 | 2023-10-25 | Xenon Pharmaceuticals Inc. | Benzenesulfonamide compounds and their use as therapeutic agents |
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| CN107247885B (zh) * | 2017-07-06 | 2020-07-03 | 中国水产科学研究院黄海水产研究所 | 一种电压-门控钠离子通道的结构预测方法 |
| AR114263A1 (es) | 2018-02-26 | 2020-08-12 | Genentech Inc | Compuestos terapéuticos y métodos para utilizarlos |
| WO2019191702A1 (en) | 2018-03-30 | 2019-10-03 | F. Hoffmann-La Roche Ag | Substituted hydro-pyrido-azines as sodium channel inhibitors |
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| AU2019285184B2 (en) | 2018-06-13 | 2023-11-16 | Xenon Pharmaceuticals Inc. | Benzenesulfonamide compounds and their use as therapeutic agents |
| US10981905B2 (en) | 2018-08-31 | 2021-04-20 | Xenon Pharmaceuticals Inc. | Heteroaryl-substituted sulfonamide compounds and their use as therapeutic agents |
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| TW202345811A (zh) * | 2022-03-31 | 2023-12-01 | 大陸商江蘇恆瑞醫藥股份有限公司 | 吲唑類化合物、其製備方法及其在醫藥上的應用 |
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-
2013
- 2013-10-23 AU AU2013334664A patent/AU2013334664A1/en not_active Abandoned
- 2013-10-23 CN CN201380068064.9A patent/CN104869992A/zh active Pending
- 2013-10-23 RU RU2015119640A patent/RU2015119640A/ru not_active Application Discontinuation
- 2013-10-23 WO PCT/US2013/066360 patent/WO2014066491A1/en not_active Ceased
- 2013-10-23 CA CA2891056A patent/CA2891056A1/en not_active Abandoned
- 2013-10-23 JP JP2015539755A patent/JP2015535252A/ja active Pending
- 2013-10-23 KR KR1020157013297A patent/KR20150074123A/ko not_active Withdrawn
- 2013-10-23 US US14/437,142 patent/US9388179B2/en active Active
- 2013-10-23 EP EP13849733.4A patent/EP2911663B1/en active Active
- 2013-10-23 BR BR112015008987A patent/BR112015008987A2/pt not_active IP Right Cessation
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