JP2004534755A5 - - Google Patents
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- Publication number
- JP2004534755A5 JP2004534755A5 JP2002589470A JP2002589470A JP2004534755A5 JP 2004534755 A5 JP2004534755 A5 JP 2004534755A5 JP 2002589470 A JP2002589470 A JP 2002589470A JP 2002589470 A JP2002589470 A JP 2002589470A JP 2004534755 A5 JP2004534755 A5 JP 2004534755A5
- Authority
- JP
- Japan
- Prior art keywords
- amino
- phenyl
- diazepan
- hydrochloride
- benzenesulfonamide
- 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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- 150000001875 compounds Chemical class 0.000 claims 25
- -1 Cinnamoyl Chemical group 0.000 claims 12
- 208000008589 Obesity Diseases 0.000 claims 10
- 235000020824 obesity Nutrition 0.000 claims 10
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 10
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 230000002265 prevention Effects 0.000 claims 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- 125000000623 heterocyclic group Chemical group 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 4
- 241000124008 Mammalia Species 0.000 claims 4
- 239000004480 active ingredient Substances 0.000 claims 4
- 150000001412 amines Chemical class 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 239000000825 pharmaceutical preparation Substances 0.000 claims 4
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 150000001350 alkyl halides Chemical class 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 229910052717 sulfur Chemical group 0.000 claims 3
- 239000011593 sulfur Chemical group 0.000 claims 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 2
- FQUYSHZXSKYCSY-UHFFFAOYSA-N 1,4-diazepane Chemical compound C1CNCCNC1 FQUYSHZXSKYCSY-UHFFFAOYSA-N 0.000 claims 2
- FXHRAKUEZPSMLJ-UHFFFAOYSA-N 1-methyl-1,4-diazepane Chemical compound CN1CCCNCC1 FXHRAKUEZPSMLJ-UHFFFAOYSA-N 0.000 claims 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000002619 bicyclic group Chemical group 0.000 claims 2
- 125000003636 chemical group Chemical group 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- YBVFGIVGPAJLHK-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-n-methylbenzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)N(C)C(C(=C1)NS(C)(=O)=O)=CC=C1N1CCCNCC1 YBVFGIVGPAJLHK-UHFFFAOYSA-N 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 102000005962 receptors Human genes 0.000 claims 2
- 108020003175 receptors Proteins 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 1
- UFVNNBAKIVCCJV-UHFFFAOYSA-N 2-(1,4-diazepan-1-yl)-5-(3,4-dihydro-1h-isoquinolin-2-ylsulfonyl)aniline;dihydrochloride Chemical compound Cl.Cl.NC1=CC(S(=O)(=O)N2CC3=CC=CC=C3CC2)=CC=C1N1CCCNCC1 UFVNNBAKIVCCJV-UHFFFAOYSA-N 0.000 claims 1
- OXPGVPJGNUTOIJ-UHFFFAOYSA-N 2-(1,4-diazepan-1-yl)-5-(3,4-dihydro-2h-quinolin-1-ylsulfonyl)aniline;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F.NC1=CC(S(=O)(=O)N2C3=CC=CC=C3CCC2)=CC=C1N1CCCNCC1 OXPGVPJGNUTOIJ-UHFFFAOYSA-N 0.000 claims 1
- IAVOMOLJEUUEJJ-UHFFFAOYSA-N 2-(1,4-diazepan-1-yl)-5-morpholin-4-ylsulfonylaniline;hydrochloride Chemical compound Cl.NC1=CC(S(=O)(=O)N2CCOCC2)=CC=C1N1CCCNCC1 IAVOMOLJEUUEJJ-UHFFFAOYSA-N 0.000 claims 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
- JRABVEPQBHTNEB-UHFFFAOYSA-N 3-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)-n-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=C(N2CCNCCC2)C(NS(=O)(=O)C=2C=CC=CC=2)=CC=1S(=O)(=O)NC1=CC=CC=C1 JRABVEPQBHTNEB-UHFFFAOYSA-N 0.000 claims 1
- BQJGPBTZYNGMTH-UHFFFAOYSA-N 3-amino-2-chloro-n-naphthalen-1-yl-4-piperazin-1-ylbenzenesulfonamide Chemical compound NC1=C(Cl)C(S(=O)(=O)NC=2C3=CC=CC=C3C=CC=2)=CC=C1N1CCNCC1 BQJGPBTZYNGMTH-UHFFFAOYSA-N 0.000 claims 1
- FYGYVBUXDONVKW-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-(2,5-dimethylphenyl)benzenesulfonamide Chemical compound CC1=CC=C(C)C(NS(=O)(=O)C=2C=C(N)C(N3CCNCCC3)=CC=2)=C1 FYGYVBUXDONVKW-UHFFFAOYSA-N 0.000 claims 1
- YIEMYULZHPOHDR-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-(2-methoxyphenyl)benzenesulfonamide Chemical compound COC1=CC=CC=C1NS(=O)(=O)C(C=C1N)=CC=C1N1CCNCCC1 YIEMYULZHPOHDR-UHFFFAOYSA-N 0.000 claims 1
- JJDPZXRUIVQMDK-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-(3-fluoro-2-methoxyphenyl)benzenesulfonamide;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F.COC1=C(F)C=CC=C1NS(=O)(=O)C(C=C1N)=CC=C1N1CCNCCC1 JJDPZXRUIVQMDK-UHFFFAOYSA-N 0.000 claims 1
- SAUZITPHYKKGRB-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-(3-fluorophenyl)benzenesulfonamide Chemical compound NC1=CC(S(=O)(=O)NC=2C=C(F)C=CC=2)=CC=C1N1CCCNCC1 SAUZITPHYKKGRB-UHFFFAOYSA-N 0.000 claims 1
- XLKMIAYZWUNVHK-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-(3-methoxyphenyl)benzenesulfonamide Chemical compound COC1=CC=CC(NS(=O)(=O)C=2C=C(N)C(N3CCNCCC3)=CC=2)=C1 XLKMIAYZWUNVHK-UHFFFAOYSA-N 0.000 claims 1
- QRMJOOKTGVZCJI-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-(4-methoxyphenyl)benzenesulfonamide Chemical compound C1=CC(OC)=CC=C1NS(=O)(=O)C(C=C1N)=CC=C1N1CCNCCC1 QRMJOOKTGVZCJI-UHFFFAOYSA-N 0.000 claims 1
- GRCSUIIMHXGBJI-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-(4-methylphenyl)benzenesulfonamide Chemical compound C1=CC(C)=CC=C1NS(=O)(=O)C(C=C1N)=CC=C1N1CCNCCC1 GRCSUIIMHXGBJI-UHFFFAOYSA-N 0.000 claims 1
- DEHKDJZMLDFXCM-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-methyl-n-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=C(N2CCNCCC2)C(N)=CC=1S(=O)(=O)N(C)C1=CC=CC=C1 DEHKDJZMLDFXCM-UHFFFAOYSA-N 0.000 claims 1
- XWTGZLBSOQBINS-UHFFFAOYSA-N 3-amino-4-(1,4-diazepan-1-yl)-n-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.NC1=CC(S(=O)(=O)NC=2C=CC=CC=2)=CC=C1N1CCCNCC1 XWTGZLBSOQBINS-UHFFFAOYSA-N 0.000 claims 1
- IHYHRJXVPAXBLE-UHFFFAOYSA-N 3-amino-4-(3-methylpiperazin-1-yl)-n-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.C1CNC(C)CN1C1=CC=C(S(=O)(=O)NC=2C=CC=CC=2)C=C1N IHYHRJXVPAXBLE-UHFFFAOYSA-N 0.000 claims 1
- NUEOVOLDSBQFFU-UHFFFAOYSA-N 3-amino-4-(4-ethylpiperazin-1-yl)-n-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.C1CN(CC)CCN1C1=CC=C(S(=O)(=O)NC=2C=CC=CC=2)C=C1N NUEOVOLDSBQFFU-UHFFFAOYSA-N 0.000 claims 1
- GVSUDVZBAQYBOA-UHFFFAOYSA-N 3-amino-4-(4-methyl-1,4-diazepan-1-yl)-n-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.C1CN(C)CCCN1C1=CC=C(S(=O)(=O)NC=2C=CC=CC=2)C=C1N GVSUDVZBAQYBOA-UHFFFAOYSA-N 0.000 claims 1
- JLMXYYCQKXBTGS-UHFFFAOYSA-N 3-amino-n-(2-chlorophenyl)-4-(1,4-diazepan-1-yl)benzenesulfonamide Chemical compound NC1=CC(S(=O)(=O)NC=2C(=CC=CC=2)Cl)=CC=C1N1CCCNCC1 JLMXYYCQKXBTGS-UHFFFAOYSA-N 0.000 claims 1
- FHPZBWWLSCRQPJ-UHFFFAOYSA-N 3-amino-n-(3-chlorophenyl)-4-(1,4-diazepan-1-yl)benzenesulfonamide Chemical compound NC1=CC(S(=O)(=O)NC=2C=C(Cl)C=CC=2)=CC=C1N1CCCNCC1 FHPZBWWLSCRQPJ-UHFFFAOYSA-N 0.000 claims 1
- BUNZFNATZFRHOM-UHFFFAOYSA-N 3-amino-n-phenyl-4-piperazin-1-ylbenzenesulfonamide;hydrochloride Chemical compound Cl.NC1=CC(S(=O)(=O)NC=2C=CC=CC=2)=CC=C1N1CCNCC1 BUNZFNATZFRHOM-UHFFFAOYSA-N 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- CVCBYAPWYGLGSN-UHFFFAOYSA-N 4-(1,4-diazepan-1-yl)-3-(methanesulfonamido)-n-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)NC1=CC(S(=O)(=O)NC=2C=CC=CC=2)=CC=C1N1CCCNCC1 CVCBYAPWYGLGSN-UHFFFAOYSA-N 0.000 claims 1
- CJMASYSSFWANNC-UHFFFAOYSA-N 4-(3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl)-3-amino-n-(2-methoxyphenyl)benzenesulfonamide;hydrochloride Chemical compound Cl.COC1=CC=CC=C1NS(=O)(=O)C(C=C1N)=CC=C1N1CC2CCCN2CC1 CJMASYSSFWANNC-UHFFFAOYSA-N 0.000 claims 1
- XMCXZCACDJSZGQ-UHFFFAOYSA-N 4-(3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl)-3-amino-n-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=C(N2CC3CCCN3CC2)C(N)=CC=1S(=O)(=O)NC1=CC=CC=C1 XMCXZCACDJSZGQ-UHFFFAOYSA-N 0.000 claims 1
- XGKGXIWSMCPQQW-UHFFFAOYSA-N 4-chloro-n-[5-(4-methyl-1,4-diazepan-1-yl)-2-nitrophenyl]benzenesulfonamide Chemical compound C1CN(C)CCCN1C1=CC=C([N+]([O-])=O)C(NS(=O)(=O)C=2C=CC(Cl)=CC=2)=C1 XGKGXIWSMCPQQW-UHFFFAOYSA-N 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- QECVIPBZOPUTRD-UHFFFAOYSA-N N=S(=O)=O Chemical group N=S(=O)=O QECVIPBZOPUTRD-UHFFFAOYSA-N 0.000 claims 1
- RFEWGXFJJSWGGZ-UHFFFAOYSA-N acetic acid;2-[3-amino-4-(1,4-diazepan-1-yl)phenyl]sulfonylbenzamide Chemical compound CC(O)=O.CC(O)=O.NC(=O)C1=CC=CC=C1S(=O)(=O)C(C=C1N)=CC=C1N1CCNCCC1 RFEWGXFJJSWGGZ-UHFFFAOYSA-N 0.000 claims 1
- 230000029936 alkylation Effects 0.000 claims 1
- 238000005804 alkylation reaction Methods 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- ODVBYGKHVGIJOU-UHFFFAOYSA-N n-(2-amino-4-piperazin-1-ylphenyl)-3-fluorobenzenesulfonamide Chemical compound NC1=CC(N2CCNCC2)=CC=C1NS(=O)(=O)C1=CC=CC(F)=C1 ODVBYGKHVGIJOU-UHFFFAOYSA-N 0.000 claims 1
- PZQNRGJRFSLRNK-UHFFFAOYSA-N n-(4-amino-3-piperazin-1-ylphenyl)benzenesulfonamide Chemical compound C1=C(N2CCNCC2)C(N)=CC=C1NS(=O)(=O)C1=CC=CC=C1 PZQNRGJRFSLRNK-UHFFFAOYSA-N 0.000 claims 1
- XANFNWPZLJAOCV-UHFFFAOYSA-N n-(4-nitro-3-piperazin-1-ylphenyl)benzenesulfonamide Chemical compound C1=C(N2CCNCC2)C([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=CC=C1 XANFNWPZLJAOCV-UHFFFAOYSA-N 0.000 claims 1
- YDYABFVXSAOHTL-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-2,1,3-benzoxadiazole-4-sulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)NC(C(=CC=1)NS(=O)(=O)C=2C3=NON=C3C=CC=2)=CC=1N1CCCNCC1 YDYABFVXSAOHTL-UHFFFAOYSA-N 0.000 claims 1
- IPWXILJLPMFMRF-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-2,4,6-trimethylbenzenesulfonamide;hydrochloride Chemical compound Cl.CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 IPWXILJLPMFMRF-UHFFFAOYSA-N 0.000 claims 1
- NPUAYJWTUOGONW-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-2,5-dimethoxybenzenesulfonamide;hydrochloride Chemical compound Cl.COC1=CC=C(OC)C(S(=O)(=O)NC=2C(=CC(=CC=2)N2CCNCCC2)NS(=O)(=O)C=2C=CC=CC=2)=C1 NPUAYJWTUOGONW-UHFFFAOYSA-N 0.000 claims 1
- XADLAHNCVSFSCC-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-3,5-dimethyl-1,2-oxazole-4-sulfonamide;hydrochloride Chemical compound Cl.CC1=NOC(C)=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 XADLAHNCVSFSCC-UHFFFAOYSA-N 0.000 claims 1
- WPROYZRPQCTUSR-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-4-butoxybenzenesulfonamide;hydrochloride Chemical compound Cl.C1=CC(OCCCC)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 WPROYZRPQCTUSR-UHFFFAOYSA-N 0.000 claims 1
- NUBFAPLYMNVBKK-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-4-methylbenzenesulfonamide;hydrochloride Chemical compound Cl.C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 NUBFAPLYMNVBKK-UHFFFAOYSA-N 0.000 claims 1
- XSUPQKCOFZZPIF-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-4-methylsulfonylbenzenesulfonamide;hydrochloride Chemical compound Cl.C1=CC(S(=O)(=O)C)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 XSUPQKCOFZZPIF-UHFFFAOYSA-N 0.000 claims 1
- GKUGYOYYBBFMHV-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-4-phenylbenzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=C(C=2C=CC=CC=2)C=CC=1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 GKUGYOYYBBFMHV-UHFFFAOYSA-N 0.000 claims 1
- ZPHHDOAAXLFOFN-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-5-(dimethylamino)naphthalene-1-sulfonamide;hydrochloride Chemical compound Cl.C1=CC=C2C(N(C)C)=CC=CC2=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 ZPHHDOAAXLFOFN-UHFFFAOYSA-N 0.000 claims 1
- VEOHAQSHRONNRY-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]-5-fluoro-2-methylbenzenesulfonamide;hydrochloride Chemical compound Cl.CC1=CC=C(F)C=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 VEOHAQSHRONNRY-UHFFFAOYSA-N 0.000 claims 1
- SQKWYZRAQFWPAE-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]benzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 SQKWYZRAQFWPAE-UHFFFAOYSA-N 0.000 claims 1
- XKQQZDWFFNBRPR-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]naphthalene-1-sulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)NC(C(=CC=1)NS(=O)(=O)C=2C3=CC=CC=C3C=CC=2)=CC=1N1CCCNCC1 XKQQZDWFFNBRPR-UHFFFAOYSA-N 0.000 claims 1
- HIWYWMDAICBRTA-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]naphthalene-2-sulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)NC(C(=CC=1)NS(=O)(=O)C=2C=C3C=CC=CC3=CC=2)=CC=1N1CCCNCC1 HIWYWMDAICBRTA-UHFFFAOYSA-N 0.000 claims 1
- MHWJWMJSUDQQBI-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-(1,4-diazepan-1-yl)phenyl]quinoline-8-sulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)NC(C(=CC=1)NS(=O)(=O)C=2C3=NC=CC=C3C=CC=2)=CC=1N1CCCNCC1 MHWJWMJSUDQQBI-UHFFFAOYSA-N 0.000 claims 1
- FKHLEGQCZVSWCG-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-2,4,6-trimethylbenzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 FKHLEGQCZVSWCG-UHFFFAOYSA-N 0.000 claims 1
- AWQGTSVAHFRBDI-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-2,4-difluorobenzenesulfonamide Chemical compound FC1=CC(F)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 AWQGTSVAHFRBDI-UHFFFAOYSA-N 0.000 claims 1
- YHJZADCUNJRKAR-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-2,5-dimethoxybenzenesulfonamide Chemical compound COC1=CC=C(OC)C(S(=O)(=O)NC=2C(=CC(=CC=2)N2CCNCC2)NS(=O)(=O)C=2C=CC=CC=2)=C1 YHJZADCUNJRKAR-UHFFFAOYSA-N 0.000 claims 1
- YKUZGTKBSULKAA-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-2-methoxy-4-methylbenzenesulfonamide Chemical compound COC1=CC(C)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 YKUZGTKBSULKAA-UHFFFAOYSA-N 0.000 claims 1
- LNQLZGMOFVYNDA-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-2-methylbenzenesulfonamide Chemical compound CC1=CC=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 LNQLZGMOFVYNDA-UHFFFAOYSA-N 0.000 claims 1
- YMABHSWGVLONQV-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-2-methylsulfonylbenzenesulfonamide Chemical compound CS(=O)(=O)C1=CC=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 YMABHSWGVLONQV-UHFFFAOYSA-N 0.000 claims 1
- FHNWRSGDPHETAK-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-3,5-dimethyl-1,2-oxazole-4-sulfonamide Chemical compound CC1=NOC(C)=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 FHNWRSGDPHETAK-UHFFFAOYSA-N 0.000 claims 1
- WBQDCETZDTVJDX-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-4-butoxybenzenesulfonamide Chemical compound C1=CC(OCCCC)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 WBQDCETZDTVJDX-UHFFFAOYSA-N 0.000 claims 1
- PCAXUKBJYSESNW-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-4-methoxy-2-methylbenzenesulfonamide Chemical compound CC1=CC(OC)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 PCAXUKBJYSESNW-UHFFFAOYSA-N 0.000 claims 1
- ZQHAHDQGZFTEMW-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 ZQHAHDQGZFTEMW-UHFFFAOYSA-N 0.000 claims 1
- BKSYGSPXBRAATP-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-4-methylsulfonylbenzenesulfonamide Chemical compound C1=CC(S(=O)(=O)C)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 BKSYGSPXBRAATP-UHFFFAOYSA-N 0.000 claims 1
- JPEZHTHWWWHEQU-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-5-(dimethylamino)naphthalene-1-sulfonamide Chemical compound C1=CC=C2C(N(C)C)=CC=CC2=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 JPEZHTHWWWHEQU-UHFFFAOYSA-N 0.000 claims 1
- JSCDSQDNRVXDNZ-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]-5-fluoro-2-methylbenzenesulfonamide Chemical compound CC1=CC=C(F)C=C1S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 JSCDSQDNRVXDNZ-UHFFFAOYSA-N 0.000 claims 1
- BOIKEIGQIBCDGM-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]naphthalene-1-sulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C(=CC=1)NS(=O)(=O)C=2C3=CC=CC=C3C=CC=2)=CC=1N1CCNCC1 BOIKEIGQIBCDGM-UHFFFAOYSA-N 0.000 claims 1
- BVIBTQYYWPYZKT-UHFFFAOYSA-N n-[2-(benzenesulfonamido)-4-piperazin-1-ylphenyl]quinoline-8-sulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C(=CC=1)NS(=O)(=O)C=2C3=NC=CC=C3C=CC=2)=CC=1N1CCNCC1 BVIBTQYYWPYZKT-UHFFFAOYSA-N 0.000 claims 1
- QPUFHIPBJRUGOU-UHFFFAOYSA-N n-[2-(ethylamino)-4-piperazin-1-ylphenyl]-3-fluorobenzenesulfonamide Chemical compound CCNC1=CC(N2CCNCC2)=CC=C1NS(=O)(=O)C1=CC=CC(F)=C1 QPUFHIPBJRUGOU-UHFFFAOYSA-N 0.000 claims 1
- IJZHBOUVMUVKPN-QGOAFFKASA-N n-[2-[[(e)-2-phenylethenyl]sulfonylamino]-5-piperazin-1-ylphenyl]benzenesulfonamide Chemical compound C=1C=CC=CC=1/C=C/S(=O)(=O)NC1=CC=C(N2CCNCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 IJZHBOUVMUVKPN-QGOAFFKASA-N 0.000 claims 1
- RQSXWTIKILELLD-UHFFFAOYSA-N n-[2-[benzenesulfonyl(ethyl)amino]-4-(1,4-diazepan-1-yl)phenyl]benzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)N(CC)C1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=CC=C1 RQSXWTIKILELLD-UHFFFAOYSA-N 0.000 claims 1
- HCLQSFNUFYGOPJ-UHFFFAOYSA-N n-[2-[benzenesulfonyl(ethyl)amino]-4-(4-methylpiperazin-1-yl)phenyl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)N(CC)C1=CC(N2CCN(C)CC2)=CC=C1NS(=O)(=O)C1=CC=CC=C1 HCLQSFNUFYGOPJ-UHFFFAOYSA-N 0.000 claims 1
- JQSROWAMCOAXKN-UHFFFAOYSA-N n-[2-[benzenesulfonyl(methyl)amino]-4-(1,4-diazepan-1-yl)phenyl]benzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)N(C)C1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=CC=C1 JQSROWAMCOAXKN-UHFFFAOYSA-N 0.000 claims 1
- YTEYXRVZHOKRQR-UHFFFAOYSA-N n-[2-[benzenesulfonyl(methyl)amino]-5-(1,4-diazepan-1-yl)phenyl]-4-methylbenzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1S(=O)(=O)N(C)C1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=C(C)C=C1 YTEYXRVZHOKRQR-UHFFFAOYSA-N 0.000 claims 1
- HTIDWAKPMVVSJG-UHFFFAOYSA-N n-[2-[ethyl-(3-fluorophenyl)sulfonylamino]-4-(4-methylpiperazin-1-yl)phenyl]-3-fluorobenzenesulfonamide Chemical compound C=1C=CC(F)=CC=1S(=O)(=O)N(CC)C1=CC(N2CCN(C)CC2)=CC=C1NS(=O)(=O)C1=CC=CC(F)=C1 HTIDWAKPMVVSJG-UHFFFAOYSA-N 0.000 claims 1
- DDQIYTCVKDBHTQ-UHFFFAOYSA-N n-[2-amino-5-(1,4-diazepan-1-yl)phenyl]benzenesulfonamide Chemical compound NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 DDQIYTCVKDBHTQ-UHFFFAOYSA-N 0.000 claims 1
- PTNYOQRNLMUNCP-UHFFFAOYSA-N n-[2-amino-5-(4-methyl-1,4-diazepan-1-yl)phenyl]benzenesulfonamide Chemical compound C1CN(C)CCCN1C1=CC=C(N)C(NS(=O)(=O)C=2C=CC=CC=2)=C1 PTNYOQRNLMUNCP-UHFFFAOYSA-N 0.000 claims 1
- BXWFCFGBYXGFBJ-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-2-methylbenzenesulfonamide;hydrochloride Chemical compound Cl.CC1=CC=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(C)(=O)=O BXWFCFGBYXGFBJ-UHFFFAOYSA-N 0.000 claims 1
- DSKVIVKXGMWLPW-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-3,5-dimethyl-1,2-oxazole-4-sulfonamide;hydrochloride Chemical compound Cl.CC1=NOC(C)=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(C)(=O)=O DSKVIVKXGMWLPW-UHFFFAOYSA-N 0.000 claims 1
- QUBISYLUMIHISN-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-3-(trifluoromethyl)benzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)NC1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=CC(C(F)(F)F)=C1 QUBISYLUMIHISN-UHFFFAOYSA-N 0.000 claims 1
- GPZADXDSUWFZAJ-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-3-methoxybenzenesulfonamide;hydrochloride Chemical compound Cl.COC1=CC=CC(S(=O)(=O)NC=2C(=CC(=CC=2)N2CCNCCC2)NS(C)(=O)=O)=C1 GPZADXDSUWFZAJ-UHFFFAOYSA-N 0.000 claims 1
- DWNIJQDAHACGQF-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-4-(trifluoromethoxy)benzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)NC1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=C(OC(F)(F)F)C=C1 DWNIJQDAHACGQF-UHFFFAOYSA-N 0.000 claims 1
- IZJDSXPYJIGXSC-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-4-fluorobenzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)NC1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=C(F)C=C1 IZJDSXPYJIGXSC-UHFFFAOYSA-N 0.000 claims 1
- YZKZNXKEILWBSH-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-4-methylbenzenesulfonamide;hydrochloride Chemical compound Cl.C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(C)(=O)=O YZKZNXKEILWBSH-UHFFFAOYSA-N 0.000 claims 1
- MHDNIIFIXQMKSV-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]-4-nitrobenzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)NC1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=C([N+]([O-])=O)C=C1 MHDNIIFIXQMKSV-UHFFFAOYSA-N 0.000 claims 1
- PFZSHSDQRXQRMX-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]benzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)NC1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=CC=C1 PFZSHSDQRXQRMX-UHFFFAOYSA-N 0.000 claims 1
- VBMQIWFDKQQRLF-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]naphthalene-1-sulfonamide;hydrochloride Chemical compound Cl.C=1C=C(NS(=O)(=O)C=2C3=CC=CC=C3C=CC=2)C(NS(=O)(=O)C)=CC=1N1CCCNCC1 VBMQIWFDKQQRLF-UHFFFAOYSA-N 0.000 claims 1
- CNOXKMJLZGWSAF-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]naphthalene-2-sulfonamide;hydrochloride Chemical compound Cl.C=1C=C(NS(=O)(=O)C=2C=C3C=CC=CC3=CC=2)C(NS(=O)(=O)C)=CC=1N1CCCNCC1 CNOXKMJLZGWSAF-UHFFFAOYSA-N 0.000 claims 1
- RHLRJEOCEVHSSL-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-[(3-fluorophenyl)sulfonylamino]phenyl]-3-fluorobenzenesulfonamide;hydrochloride Chemical compound Cl.FC1=CC=CC(S(=O)(=O)NC=2C(=CC(=CC=2)N2CCNCCC2)NS(=O)(=O)C=2C=C(F)C=CC=2)=C1 RHLRJEOCEVHSSL-UHFFFAOYSA-N 0.000 claims 1
- HPSHQVBPGMTJFS-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-[ethyl(methylsulfonyl)amino]phenyl]-3,4-dimethoxybenzenesulfonamide;hydrochloride Chemical compound Cl.CCN(S(C)(=O)=O)C1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=C(OC)C(OC)=C1 HPSHQVBPGMTJFS-UHFFFAOYSA-N 0.000 claims 1
- GOOBZFVEEZKGKZ-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-[ethyl(methylsulfonyl)amino]phenyl]-4-methylbenzenesulfonamide;hydrochloride Chemical compound Cl.CCN(S(C)(=O)=O)C1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=C(C)C=C1 GOOBZFVEEZKGKZ-UHFFFAOYSA-N 0.000 claims 1
- NUVGANLKRZGKKD-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-[ethyl(methylsulfonyl)amino]phenyl]quinoline-7-sulfonamide;hydrochloride Chemical compound Cl.C=1C=C(NS(=O)(=O)C=2C=C3N=CC=CC3=CC=2)C(N(CC)S(C)(=O)=O)=CC=1N1CCCNCC1 NUVGANLKRZGKKD-UHFFFAOYSA-N 0.000 claims 1
- YCPANVLPEOYUNL-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-[methyl(methylsulfonyl)amino]phenyl]-4-methylbenzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)N(C)C1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=C(C)C=C1 YCPANVLPEOYUNL-UHFFFAOYSA-N 0.000 claims 1
- YVWKKDYBLDOCQN-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-[methyl(methylsulfonyl)amino]phenyl]-5-pyridin-2-ylthiophene-2-sulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)N(C)C1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C(S1)=CC=C1C1=CC=CC=N1 YVWKKDYBLDOCQN-UHFFFAOYSA-N 0.000 claims 1
- ZEUYNSOKZSGTJU-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-[methyl(methylsulfonyl)amino]phenyl]benzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)N(C)C1=CC(N2CCNCCC2)=CC=C1NS(=O)(=O)C1=CC=CC=C1 ZEUYNSOKZSGTJU-UHFFFAOYSA-N 0.000 claims 1
- OWIYCPKRHAFIGE-UHFFFAOYSA-N n-[4-(1,4-diazepan-1-yl)-2-[methyl(methylsulfonyl)amino]phenyl]naphthalene-1-sulfonamide;hydrochloride Chemical compound Cl.C=1C=C(NS(=O)(=O)C=2C3=CC=CC=C3C=CC=2)C(N(C)S(C)(=O)=O)=CC=1N1CCCNCC1 OWIYCPKRHAFIGE-UHFFFAOYSA-N 0.000 claims 1
- DHBNBIHGOOLDDS-UHFFFAOYSA-N n-[4-(4-methylpiperazin-1-yl)-2-(quinolin-7-ylsulfonylamino)phenyl]quinoline-8-sulfonamide Chemical compound C1CN(C)CCN1C(C=C1NS(=O)(=O)C=2C=C3N=CC=CC3=CC=2)=CC=C1NS(=O)(=O)C1=CC=CC2=CC=CN=C12 DHBNBIHGOOLDDS-UHFFFAOYSA-N 0.000 claims 1
- HPWAWHCBDKJWMS-UHFFFAOYSA-N n-[4-[[2-(benzenesulfonamido)-4-(4-methylpiperazin-1-yl)phenyl]sulfamoyl]-2-chlorophenyl]acetamide Chemical compound C1CN(C)CCN1C(C=C1NS(=O)(=O)C=2C=CC=CC=2)=CC=C1NS(=O)(=O)C1=CC=C(NC(C)=O)C(Cl)=C1 HPWAWHCBDKJWMS-UHFFFAOYSA-N 0.000 claims 1
- SWNOCPKUGYCXBV-UHFFFAOYSA-N n-[5-(1,4-diazepan-1-yl)-2-(methanesulfonamido)phenyl]benzenesulfonamide;hydrochloride Chemical compound Cl.CS(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 SWNOCPKUGYCXBV-UHFFFAOYSA-N 0.000 claims 1
- KPFUAXHHXMLTLY-UGAWPWHASA-N n-[5-(1,4-diazepan-1-yl)-2-[[(e)-2-phenylethenyl]sulfonylamino]phenyl]benzenesulfonamide;hydrochloride Chemical compound Cl.C=1C=CC=CC=1/C=C/S(=O)(=O)NC1=CC=C(N2CCNCCC2)C=C1NS(=O)(=O)C1=CC=CC=C1 KPFUAXHHXMLTLY-UGAWPWHASA-N 0.000 claims 1
- 238000010534 nucleophilic substitution reaction Methods 0.000 claims 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims 1
- 230000006103 sulfonylation Effects 0.000 claims 1
- 238000005694 sulfonylation reaction Methods 0.000 claims 1
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| US29410201P | 2001-05-29 | 2001-05-29 | |
| SE0101958A SE0101958D0 (sv) | 2001-06-05 | 2001-06-05 | New compounds |
| PCT/SE2002/000906 WO2002092585A1 (en) | 2001-05-11 | 2002-05-08 | Novel, arylsusfonamide compounds for the treatment of obesity, type ii diabetes and cns-disorders |
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| EP1406884A1 (en) * | 2001-05-11 | 2004-04-14 | Biovitrum Ab | Arylsusfonamide compounds for the treatment of obesity, type ii diabetes and cns-disorders |
| US7718650B2 (en) * | 2001-05-11 | 2010-05-18 | Biovitrum Ab | Aryl sulfonamide compounds for treating obesity |
| US20020197228A1 (en) * | 2001-05-29 | 2002-12-26 | Lasala William Kater | Skin care kit |
| CN1800185A (zh) | 2001-06-11 | 2006-07-12 | 比奥维特罗姆股份公司 | 取代的磺酰胺化合物、其制备方法及其作为治疗cns疾病、肥胖和ii型糖尿病的药物的应用 |
| US7354923B2 (en) * | 2001-08-10 | 2008-04-08 | Palatin Technologies, Inc. | Piperazine melanocortin-specific compounds |
| US7655658B2 (en) | 2001-08-10 | 2010-02-02 | Palatin Technologies, Inc. | Thieno [2,3-D]pyrimidine-2,4-dione melanocortin-specific compounds |
| US7456184B2 (en) | 2003-05-01 | 2008-11-25 | Palatin Technologies Inc. | Melanocortin receptor-specific compounds |
| US7732451B2 (en) | 2001-08-10 | 2010-06-08 | Palatin Technologies, Inc. | Naphthalene-containing melanocortin receptor-specific small molecule |
| AU2002331064B2 (en) | 2001-08-10 | 2007-08-23 | Palatin Technologies, Inc. | Peptidomimetics of biologically active metallopeptides |
| US7718802B2 (en) | 2001-08-10 | 2010-05-18 | Palatin Technologies, Inc. | Substituted melanocortin receptor-specific piperazine compounds |
| EP1534284B1 (en) * | 2002-02-28 | 2011-07-27 | Temple University - Of The Commonwealth System of Higher Education | Amino-substituted sulfonanilides and derivatives thereof for treating proliferative disorders |
| WO2004000828A1 (en) * | 2002-06-20 | 2003-12-31 | Biovitrum Ab | New compounds useful for the treatment of obesity, type ii diabetes and cns disorders |
| JP4754821B2 (ja) | 2002-06-20 | 2011-08-24 | プロキシマゲン・リミテッド | 肥満症、ｉｉ型糖尿病およびｃｎｓ障害の治療に有用な新規化合物 |
| GB0224830D0 (en) | 2002-10-24 | 2002-12-04 | Sterix Ltd | Compound |
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-
2002
- 2002-05-08 EP EP02769640A patent/EP1406884A1/en not_active Withdrawn
- 2002-05-08 AU AU2002303061A patent/AU2002303061B2/en not_active Ceased
- 2002-05-08 JP JP2002589470A patent/JP4597480B2/ja not_active Expired - Fee Related
- 2002-05-08 PL PL02366619A patent/PL366619A1/xx not_active Application Discontinuation
- 2002-05-08 BR BR0209558-0A patent/BR0209558A/pt not_active IP Right Cessation
- 2002-05-08 CA CA002443724A patent/CA2443724C/en not_active Expired - Fee Related
- 2002-05-08 MX MXPA03010232A patent/MXPA03010232A/es not_active Application Discontinuation
- 2002-05-08 CN CNB028096142A patent/CN1329382C/zh not_active Expired - Fee Related
- 2002-05-08 EA EA200301232A patent/EA009647B1/ru not_active IP Right Cessation
- 2002-05-08 IL IL15859302A patent/IL158593A0/xx unknown
- 2002-05-08 WO PCT/SE2002/000906 patent/WO2002092585A1/en not_active Ceased
- 2002-05-08 NZ NZ528450A patent/NZ528450A/en unknown
- 2002-05-08 KR KR1020097014381A patent/KR20090092832A/ko not_active Ceased
- 2002-05-10 US US10/143,335 patent/US7173035B2/en not_active Expired - Fee Related
- 2002-05-13 US US10/144,677 patent/US6969710B2/en not_active Expired - Fee Related
-
2003
- 2003-10-23 IL IL158593A patent/IL158593A/en not_active IP Right Cessation
- 2003-11-10 NO NO20034996A patent/NO326690B1/no not_active IP Right Cessation
-
2005
- 2005-08-30 US US11/214,523 patent/US7319097B2/en not_active Expired - Fee Related
- 2005-08-30 US US11/215,173 patent/US7566715B2/en not_active Expired - Fee Related
-
2008
- 2008-10-27 IL IL194950A patent/IL194950A0/en unknown
-
2010
- 2010-07-12 JP JP2010157953A patent/JP2011016801A/ja not_active Withdrawn
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