CN113874361A - 具有抗癌活性的新型化合物及其制备方法 - Google Patents
具有抗癌活性的新型化合物及其制备方法 Download PDFInfo
- Publication number
- CN113874361A CN113874361A CN202080039308.0A CN202080039308A CN113874361A CN 113874361 A CN113874361 A CN 113874361A CN 202080039308 A CN202080039308 A CN 202080039308A CN 113874361 A CN113874361 A CN 113874361A
- Authority
- CN
- China
- Prior art keywords
- indol
- methyl
- methylphenylsulfonamido
- morpholinophenyl
- propionamide
- 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
- 150000001875 compounds Chemical class 0.000 title claims abstract description 77
- 230000001093 anti-cancer Effects 0.000 title abstract description 9
- 238000002360 preparation method Methods 0.000 title description 5
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 32
- 201000011510 cancer Diseases 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims abstract description 22
- 201000010099 disease Diseases 0.000 claims abstract description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 9
- -1 hydroxy, hydroxycarbonyl Chemical group 0.000 claims description 535
- 125000000814 indol-3-yl group Chemical group [H]C1=C([H])C([H])=C2N([H])C([H])=C([*])C2=C1[H] 0.000 claims description 181
- 150000003839 salts Chemical class 0.000 claims description 41
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 239000008194 pharmaceutical composition Substances 0.000 claims description 23
- 239000004480 active ingredient Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 20
- 208000027866 inflammatory disease Diseases 0.000 claims description 19
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
- 239000003814 drug Substances 0.000 claims description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 9
- 206010003246 arthritis Diseases 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000011282 treatment Methods 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 7
- UZECCNDOASGYNH-UHFFFAOYSA-N 4-cyanobenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=C(C#N)C=C1 UZECCNDOASGYNH-UHFFFAOYSA-N 0.000 claims description 6
- PBCNJEIZXZYCST-DEOSSOPVSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NNC(C1=CC=C(C=C1)OC)=O)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NNC(C1=CC=C(C=C1)OC)=O)NS(=O)(=O)C1=CC=C(C=C1)C PBCNJEIZXZYCST-DEOSSOPVSA-N 0.000 claims description 6
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 6
- 125000005605 benzo group Chemical group 0.000 claims description 6
- WYZSTJGYPZJPAC-FQEVSTJZSA-N benzyl (2S)-2-[3-(benzenesulfonyl)propanoylamino]-4-methylpentanoate Chemical compound CC(C[C@@H](C(=O)OCC1=CC=CC=C1)NC(CCS(=O)(=O)C1=CC=CC=C1)=O)C WYZSTJGYPZJPAC-FQEVSTJZSA-N 0.000 claims description 6
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 6
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 claims description 6
- 125000006301 indolyl methyl group Chemical group 0.000 claims description 6
- RUZLIIJDZBWWSA-INIZCTEOSA-N methyl 2-[[(1s)-1-(7-methyl-2-morpholin-4-yl-4-oxopyrido[1,2-a]pyrimidin-9-yl)ethyl]amino]benzoate Chemical group COC(=O)C1=CC=CC=C1N[C@@H](C)C1=CC(C)=CN2C(=O)C=C(N3CCOCC3)N=C12 RUZLIIJDZBWWSA-INIZCTEOSA-N 0.000 claims description 6
- 150000002825 nitriles Chemical group 0.000 claims description 6
- SFDGJDBLYNJMFI-UHFFFAOYSA-N 3,1-benzoxazin-4-one Chemical compound C1=CC=C2C(=O)OC=NC2=C1 SFDGJDBLYNJMFI-UHFFFAOYSA-N 0.000 claims description 5
- IOXKXVZSNIJLOI-VWLOTQADSA-N CC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)CC1=CC=CC=C1 Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)CC1=CC=CC=C1 IOXKXVZSNIJLOI-VWLOTQADSA-N 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 5
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims description 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 4
- 208000036487 Arthropathies Diseases 0.000 claims description 4
- 206010006448 Bronchiolitis Diseases 0.000 claims description 4
- 208000004575 Infectious Arthritis Diseases 0.000 claims description 4
- 206010061218 Inflammation Diseases 0.000 claims description 4
- 208000012659 Joint disease Diseases 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 4
- 206010006451 bronchitis Diseases 0.000 claims description 4
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 4
- 230000004054 inflammatory process Effects 0.000 claims description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
- 208000002574 reactive arthritis Diseases 0.000 claims description 4
- BFYSIYWEMZAFCB-INIZCTEOSA-N (2s)-2-[(4-bromophenyl)sulfonylamino]-3-(1h-indol-3-yl)propanoic acid Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)O)S(=O)(=O)C1=CC=C(Br)C=C1 BFYSIYWEMZAFCB-INIZCTEOSA-N 0.000 claims description 3
- LFRLEBFHLCJPDU-KRWDZBQOSA-N (2s)-3-(1h-indol-3-yl)-2-[(4-methylphenyl)sulfonylamino]propanoic acid Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N[C@H](C(O)=O)CC1=CNC2=CC=CC=C12 LFRLEBFHLCJPDU-KRWDZBQOSA-N 0.000 claims description 3
- RPFCNKLHUMNOGF-UHFFFAOYSA-N 3-[3-ethoxy-2-[(4-methylphenyl)sulfonylamino]-3-oxopropyl]-1H-indole-5-carboxylic acid Chemical compound C(C)OC(C(CC1=CNC2=CC=C(C=C12)C(=O)O)NS(=O)(=O)C1=CC=C(C=C1)C)=O RPFCNKLHUMNOGF-UHFFFAOYSA-N 0.000 claims description 3
- XLASGKFUJTXPMR-SANMLTNESA-N 4-[[(2S)-3-(1H-indol-3-yl)-1-(4-morpholin-4-ylanilino)-1-oxopropan-2-yl]sulfamoyl]benzoic acid Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)NS(=O)(=O)C1=CC=C(C(=O)O)C=C1 XLASGKFUJTXPMR-SANMLTNESA-N 0.000 claims description 3
- GTSYOGFRMHGOMG-IBGZPJMESA-N 4-[[(2S)-4-methyl-1-oxo-1-(1,4,7-trioxa-10-azacyclododec-10-yl)pentan-2-yl]sulfamoyl]benzoic acid Chemical compound CC(C[C@@H](C(N1CCOCCOCCOCC1)=O)NS(=O)(=O)C1=CC=C(C(=O)O)C=C1)C GTSYOGFRMHGOMG-IBGZPJMESA-N 0.000 claims description 3
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 3
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims description 3
- WXADTGRCXHGCRG-IBGZPJMESA-N BrC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NC(C)C)CC1=CNC2=CC=CC=C12 Chemical compound BrC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NC(C)C)CC1=CNC2=CC=CC=C12 WXADTGRCXHGCRG-IBGZPJMESA-N 0.000 claims description 3
- ZUVFBCWHEXSSIR-QFIPXVFZSA-N BrC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NC1=CC=CC=C1)CC1=CNC2=CC=CC=C12 Chemical compound BrC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NC1=CC=CC=C1)CC1=CNC2=CC=CC=C12 ZUVFBCWHEXSSIR-QFIPXVFZSA-N 0.000 claims description 3
- SOQWRTZYWOHJCX-HNNXBMFYSA-N CC(C)C[C@H](NC(=O)Nc1ccccc1)C(=O)N1CCOCC1 Chemical compound CC(C)C[C@H](NC(=O)Nc1ccccc1)C(=O)N1CCOCC1 SOQWRTZYWOHJCX-HNNXBMFYSA-N 0.000 claims description 3
- YDWRQUJPWQWLSG-HNNXBMFYSA-N CC(C)C[C@H](NS(=O)(=O)c1cccc(c1)[N+]([O-])=O)C(=O)N1CCOCC1 Chemical compound CC(C)C[C@H](NS(=O)(=O)c1cccc(c1)[N+]([O-])=O)C(=O)N1CCOCC1 YDWRQUJPWQWLSG-HNNXBMFYSA-N 0.000 claims description 3
- LYZXDRHSRJEYGZ-KRWDZBQOSA-N CC(C[C@@H](C(=O)N1CCOCC1)NS(=O)(=O)C=1C=C(C=CC=1)NC(C)=O)C Chemical compound CC(C[C@@H](C(=O)N1CCOCC1)NS(=O)(=O)C=1C=C(C=CC=1)NC(C)=O)C LYZXDRHSRJEYGZ-KRWDZBQOSA-N 0.000 claims description 3
- PFUYRXPQCPTVDO-IBGZPJMESA-N CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CC(=O)O)C(=O)NC1=CC=C(C=C1)N1CCOCC1 Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CC(=O)O)C(=O)NC1=CC=C(C=C1)N1CCOCC1 PFUYRXPQCPTVDO-IBGZPJMESA-N 0.000 claims description 3
- CHZZCZDDDQXKNH-FQEVSTJZSA-N CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CCC(=O)O)C(=O)NC1=CC=C(C=C1)N1CCOCC1 Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CCC(=O)O)C(=O)NC1=CC=C(C=C1)N1CCOCC1 CHZZCZDDDQXKNH-FQEVSTJZSA-N 0.000 claims description 3
- OYPAMCABJSVCIO-DEOSSOPVSA-N CC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)CCC(=O)N1CCOCC1 Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)CCC(=O)N1CCOCC1 OYPAMCABJSVCIO-DEOSSOPVSA-N 0.000 claims description 3
- XNEOFVUJRNLZHD-NRFANRHFSA-N COC1=CC=C(C=C1)C=1N=C(SC=1)NC([C@H](CNC(=O)C=1C=NC=NC=1)NS(=O)(=O)C1=CC=C(C=C1)C)=O Chemical compound COC1=CC=C(C=C1)C=1N=C(SC=1)NC([C@H](CNC(=O)C=1C=NC=NC=1)NS(=O)(=O)C1=CC=C(C=C1)C)=O XNEOFVUJRNLZHD-NRFANRHFSA-N 0.000 claims description 3
- HTWJUEZJOSNYIE-QHCPKHFHSA-N COC1=CC=C(C=C1)C=1N=C(SC=1)NC([C@H](CNC(C1=CC=CC=C1)=O)NS(=O)(=O)C1=CC=C(C=C1)C)=O Chemical compound COC1=CC=C(C=C1)C=1N=C(SC=1)NC([C@H](CNC(C1=CC=CC=C1)=O)NS(=O)(=O)C1=CC=C(C=C1)C)=O HTWJUEZJOSNYIE-QHCPKHFHSA-N 0.000 claims description 3
- QLMYMMDTDLVRMI-QFIPXVFZSA-N COC1=CC=C(C=C1)C=1N=C(SC=1)NC([C@H](CNC(C1=CN=CC=C1)=O)NS(=O)(=O)C1=CC=C(C=C1)C)=O Chemical compound COC1=CC=C(C=C1)C=1N=C(SC=1)NC([C@H](CNC(C1=CN=CC=C1)=O)NS(=O)(=O)C1=CC=C(C=C1)C)=O QLMYMMDTDLVRMI-QFIPXVFZSA-N 0.000 claims description 3
- 208000031814 IgA Vasculitis Diseases 0.000 claims description 3
- DUDJNYRIVVEPFB-VWLOTQADSA-N N-[(2S)-3-(1H-indol-3-yl)-1-oxo-1-(1,4,7-trioxa-10-azacyclododec-10-yl)propan-2-yl]-4-methylbenzenesulfonamide Chemical compound Cc1ccc(cc1)S(=O)(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCOCCOCCOCC1 DUDJNYRIVVEPFB-VWLOTQADSA-N 0.000 claims description 3
- MOAQCJSAUZAALZ-ZDUSSCGKSA-N N-[(2S)-3-hydroxy-1-morpholin-4-yl-1-oxopropan-2-yl]-4-methylbenzenesulfonamide Chemical compound OC[C@@H](C(=O)N1CCOCC1)NS(=O)(=O)C1=CC=C(C=C1)C MOAQCJSAUZAALZ-ZDUSSCGKSA-N 0.000 claims description 3
- YGMVFEIZUVBRIF-MHZLTWQESA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)N1CCN(CC1)C1=CC=C(C=C1)OC)NS(=O)(=O)C1=CC=C(C=C1)Br Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)N1CCN(CC1)C1=CC=C(C=C1)OC)NS(=O)(=O)C1=CC=C(C=C1)Br YGMVFEIZUVBRIF-MHZLTWQESA-N 0.000 claims description 3
- YEELFHWTLIQOAU-NRFANRHFSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)N1CCOCC1)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)N1CCOCC1)NS(=O)(=O)C1=CC=C(C=C1)C YEELFHWTLIQOAU-NRFANRHFSA-N 0.000 claims description 3
- IEBBOMVOVWWIHA-QBHOUYDASA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC(C(=O)O)CC1=CNC2=CC=CC=C12)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC(C(=O)O)CC1=CNC2=CC=CC=C12)NS(=O)(=O)C1=CC=C(C=C1)C IEBBOMVOVWWIHA-QBHOUYDASA-N 0.000 claims description 3
- KDHUUNSOBUEDIO-MHZLTWQESA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)NC(C1=CC=C(C=C1)C)=O Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)NC(C1=CC=C(C=C1)C)=O KDHUUNSOBUEDIO-MHZLTWQESA-N 0.000 claims description 3
- WVCRLMDVFILJGL-MHZLTWQESA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)NS(=O)(=O)C1=CC=C(C(=O)NC)C=C1 Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)NS(=O)(=O)C1=CC=C(C(=O)NC)C=C1 WVCRLMDVFILJGL-MHZLTWQESA-N 0.000 claims description 3
- BTAFZIAKUBCCAD-QHCPKHFHSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=CC=C1)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=CC=C1)NS(=O)(=O)C1=CC=C(C=C1)C BTAFZIAKUBCCAD-QHCPKHFHSA-N 0.000 claims description 3
- ZNMCIBRLAPIZMT-DEOSSOPVSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C(=O)O)C=C1)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C(=O)O)C=C1)NS(=O)(=O)C1=CC=C(C=C1)C ZNMCIBRLAPIZMT-DEOSSOPVSA-N 0.000 claims description 3
- IKKKEMIATXSEDX-VWLOTQADSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C=C1)OC)NC(C1=CC=C(C=C1)C)=O Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C=C1)OC)NC(C1=CC=C(C=C1)C)=O IKKKEMIATXSEDX-VWLOTQADSA-N 0.000 claims description 3
- YIWNUXXSPLZEMA-VWLOTQADSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NCCC1=CC=C(C(=O)O)C=C1)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NCCC1=CC=C(C(=O)O)C=C1)NS(=O)(=O)C1=CC=C(C=C1)C YIWNUXXSPLZEMA-VWLOTQADSA-N 0.000 claims description 3
- HHAGSXAQZRCDGT-MHZLTWQESA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NNC(C1=CC=C(C=C1)N1CCOCC1)=O)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NNC(C1=CC=C(C=C1)N1CCOCC1)=O)NS(=O)(=O)C1=CC=C(C=C1)C HHAGSXAQZRCDGT-MHZLTWQESA-N 0.000 claims description 3
- UQEUZSTYFUHBGT-VWLOTQADSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(N1N=C(C=C1)C1=CC=CC=C1)=O)NS(=O)(=O)C1=CC=C(C=C1)Br Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(N1N=C(C=C1)C1=CC=CC=C1)=O)NS(=O)(=O)C1=CC=C(C=C1)Br UQEUZSTYFUHBGT-VWLOTQADSA-N 0.000 claims description 3
- KKPSGLUUBKUHLX-FQEVSTJZSA-N O=C(N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCOCC1)Nc1ccccc1 Chemical compound O=C(N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCOCC1)Nc1ccccc1 KKPSGLUUBKUHLX-FQEVSTJZSA-N 0.000 claims description 3
- JNBRDPBSBFDDPH-WBVHZDCISA-N OC[C@@H]1N(CCC1)C([C@H](CC(C)C)NS(=O)(=O)C1=CC=C(C=C1)C)=O Chemical compound OC[C@@H]1N(CCC1)C([C@H](CC(C)C)NS(=O)(=O)C1=CC=C(C=C1)C)=O JNBRDPBSBFDDPH-WBVHZDCISA-N 0.000 claims description 3
- ZYZNGQKFHRFWAR-ZDUSSCGKSA-N SC[C@@H](C(=O)N1CCOCC1)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound SC[C@@H](C(=O)N1CCOCC1)NS(=O)(=O)C1=CC=C(C=C1)C ZYZNGQKFHRFWAR-ZDUSSCGKSA-N 0.000 claims description 3
- GVQQZRSGSGSDQE-SFHVURJKSA-N benzyl (2S)-4-methyl-2-(phenylcarbamoylamino)pentanoate Chemical compound N([C@@H](CC(C)C)C(=O)OCC=1C=CC=CC=1)C(=O)NC1=CC=CC=C1 GVQQZRSGSGSDQE-SFHVURJKSA-N 0.000 claims description 3
- ZADJXRQMRDERDG-IBGZPJMESA-N benzyl (2S)-4-methyl-2-[(4-methylbenzoyl)amino]pentanoate Chemical compound CC(C[C@@H](C(=O)OCC1=CC=CC=C1)NC(C1=CC=C(C=C1)C)=O)C ZADJXRQMRDERDG-IBGZPJMESA-N 0.000 claims description 3
- VBSWRBJOWZTPPP-IBGZPJMESA-N benzyl (2S)-4-methyl-2-[(4-methylphenyl)sulfonylamino]pentanoate Chemical compound CC(C[C@@H](C(=O)OCC1=CC=CC=C1)NS(=O)(=O)C1=CC=C(C=C1)C)C VBSWRBJOWZTPPP-IBGZPJMESA-N 0.000 claims description 3
- JPKKBZUYDOJFCV-NRFANRHFSA-N benzyl (2S)-4-methyl-2-[[4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoyl]amino]pentanoate Chemical compound C(C)(C)(C)OC(=O)NC1=CC=C(C(=O)N[C@H](C(=O)OCC2=CC=CC=C2)CC(C)C)C=C1 JPKKBZUYDOJFCV-NRFANRHFSA-N 0.000 claims description 3
- VVVISZUIDHNICS-SANMLTNESA-N benzyl (3S)-3-[(4-methylphenyl)sulfonylamino]-4-(4-morpholin-4-ylanilino)-4-oxobutanoate Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CC(=O)OCC1=CC=CC=C1)C(=O)NC1=CC=C(C=C1)N1CCOCC1 VVVISZUIDHNICS-SANMLTNESA-N 0.000 claims description 3
- OPJZMJWMIVLWGN-MHZLTWQESA-N benzyl (4S)-4-[(4-methylphenyl)sulfonylamino]-5-(4-morpholin-4-ylanilino)-5-oxopentanoate Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CCC(=O)OCC1=CC=CC=C1)C(=O)NC1=CC=C(C=C1)N1CCOCC1 OPJZMJWMIVLWGN-MHZLTWQESA-N 0.000 claims description 3
- FURUCDZCROATNG-LJAQVGFWSA-N benzyl N-[(5S)-5-[(4-methylphenyl)sulfonylamino]-6-(4-morpholin-4-ylanilino)-6-oxohexyl]carbamate Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CCCCNC(OCC1=CC=CC=C1)=O)C(=O)NC1=CC=C(C=C1)N1CCOCC1 FURUCDZCROATNG-LJAQVGFWSA-N 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 claims description 3
- 125000002249 indol-2-yl group Chemical group [H]C1=C([H])C([H])=C2N([H])C([*])=C([H])C2=C1[H] 0.000 claims description 3
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 3
- KAGZPZAHOMVEAF-UHFFFAOYSA-N n'-phenylpentanediamide Chemical class NC(=O)CCCC(=O)NC1=CC=CC=C1 KAGZPZAHOMVEAF-UHFFFAOYSA-N 0.000 claims description 3
- 201000006292 polyarteritis nodosa Diseases 0.000 claims description 3
- 230000002265 prevention Effects 0.000 claims description 3
- KJXFBYDZWHGDIA-INIZCTEOSA-N tert-butyl (3S)-3-[(4-methylphenyl)sulfonylamino]-4-morpholin-4-yl-4-oxobutanoate Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CC(=O)OC(C)(C)C)C(=O)N1CCOCC1 KJXFBYDZWHGDIA-INIZCTEOSA-N 0.000 claims description 3
- ODMZSEPBLOKOOI-PMERELPUSA-N tert-butyl 4-[4-[[(2S)-3-(1H-indol-3-yl)-2-[(4-methylphenyl)sulfonylamino]propanoyl]amino]-3-methoxyphenyl]piperazine-1-carboxylate Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=C(C=C(C=C1)N1CCN(CC1)C(=O)OC(C)(C)C)OC)NS(=O)(=O)C1=CC=C(C=C1)C ODMZSEPBLOKOOI-PMERELPUSA-N 0.000 claims description 3
- HYMAPQFDZGZPBR-PMERELPUSA-N tert-butyl 4-[4-[[(2S)-3-(1H-indol-3-yl)-2-[(4-methylphenyl)sulfonylamino]propanoyl]amino]phenyl]piperazine-1-carboxylate Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCN(CC1)C(=O)OC(C)(C)C)NS(=O)(=O)C1=CC=C(C=C1)C HYMAPQFDZGZPBR-PMERELPUSA-N 0.000 claims description 3
- OEITZNWOKPXTGA-QHCPKHFHSA-N tert-butyl N-[(2S)-3-(1H-indol-3-yl)-1-(4-morpholin-4-ylanilino)-1-oxopropan-2-yl]carbamate Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)NC(OC(C)(C)C)=O OEITZNWOKPXTGA-QHCPKHFHSA-N 0.000 claims description 3
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 claims description 3
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims description 2
- 208000008190 Agammaglobulinemia Diseases 0.000 claims description 2
- 206010002556 Ankylosing Spondylitis Diseases 0.000 claims description 2
- 206010003256 Arthritis gonococcal Diseases 0.000 claims description 2
- 206010003267 Arthritis reactive Diseases 0.000 claims description 2
- 206010003274 Arthritis viral Diseases 0.000 claims description 2
- KQEQTCNZFDAIJA-DEOSSOPVSA-N BrC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NCCC1=CC=CC=C1)CC1=CNC2=CC=CC=C12 Chemical compound BrC1=CC=C(C=C1)S(=O)(=O)N[C@H](C(=O)NCCC1=CC=CC=C1)CC1=CNC2=CC=CC=C12 KQEQTCNZFDAIJA-DEOSSOPVSA-N 0.000 claims description 2
- 206010006187 Breast cancer Diseases 0.000 claims description 2
- 208000026310 Breast neoplasm Diseases 0.000 claims description 2
- 206010006458 Bronchitis chronic Diseases 0.000 claims description 2
- 206010006811 Bursitis Diseases 0.000 claims description 2
- XVIOEXPUKZJIEB-QHCPKHFHSA-N CC(C[C@@H](C(=O)NC=1C=CC(=NC=1)N1CCN(CC1)C(=O)OC(C)(C)C)NS(=O)(=O)C1=CC=C(C=C1)C)C Chemical compound CC(C[C@@H](C(=O)NC=1C=CC(=NC=1)N1CCN(CC1)C(=O)OC(C)(C)C)NS(=O)(=O)C1=CC=C(C=C1)C)C XVIOEXPUKZJIEB-QHCPKHFHSA-N 0.000 claims description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- 206010007882 Cellulitis Diseases 0.000 claims description 2
- 206010008690 Chondrocalcinosis pyrophosphate Diseases 0.000 claims description 2
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 2
- 206010009900 Colitis ulcerative Diseases 0.000 claims description 2
- 208000011231 Crohn disease Diseases 0.000 claims description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical group C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 2
- 201000003883 Cystic fibrosis Diseases 0.000 claims description 2
- 201000004624 Dermatitis Diseases 0.000 claims description 2
- 201000011275 Epicondylitis Diseases 0.000 claims description 2
- 201000005569 Gout Diseases 0.000 claims description 2
- 208000018565 Hemochromatosis Diseases 0.000 claims description 2
- 201000004331 Henoch-Schoenlein purpura Diseases 0.000 claims description 2
- 206010019617 Henoch-Schonlein purpura Diseases 0.000 claims description 2
- 206010020740 Hyperproteinaemia Diseases 0.000 claims description 2
- 206010020877 Hypertrophic osteoarthropathy Diseases 0.000 claims description 2
- 206010020983 Hypogammaglobulinaemia Diseases 0.000 claims description 2
- 208000008839 Kidney Neoplasms Diseases 0.000 claims description 2
- 208000032514 Leukocytoclastic vasculitis Diseases 0.000 claims description 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 2
- 208000016604 Lyme disease Diseases 0.000 claims description 2
- 201000009906 Meningitis Diseases 0.000 claims description 2
- 208000010718 Multiple Organ Failure Diseases 0.000 claims description 2
- 208000005268 Neurogenic Arthropathy Diseases 0.000 claims description 2
- 206010031252 Osteomyelitis Diseases 0.000 claims description 2
- 206010033645 Pancreatitis Diseases 0.000 claims description 2
- 208000007048 Polymyalgia Rheumatica Diseases 0.000 claims description 2
- 201000004681 Psoriasis Diseases 0.000 claims description 2
- 208000036824 Psoriatic arthropathy Diseases 0.000 claims description 2
- 208000033464 Reiter syndrome Diseases 0.000 claims description 2
- 206010038389 Renal cancer Diseases 0.000 claims description 2
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims description 2
- 206010039085 Rhinitis allergic Diseases 0.000 claims description 2
- 206010040047 Sepsis Diseases 0.000 claims description 2
- 206010040070 Septic Shock Diseases 0.000 claims description 2
- 208000000453 Skin Neoplasms Diseases 0.000 claims description 2
- 208000006045 Spondylarthropathies Diseases 0.000 claims description 2
- 208000006011 Stroke Diseases 0.000 claims description 2
- 208000000491 Tendinopathy Diseases 0.000 claims description 2
- 206010043255 Tendonitis Diseases 0.000 claims description 2
- 208000002240 Tennis Elbow Diseases 0.000 claims description 2
- 208000002903 Thalassemia Diseases 0.000 claims description 2
- 206010044541 Traumatic shock Diseases 0.000 claims description 2
- 201000006704 Ulcerative Colitis Diseases 0.000 claims description 2
- 206010047115 Vasculitis Diseases 0.000 claims description 2
- 208000021240 acute bronchiolitis Diseases 0.000 claims description 2
- 206010069351 acute lung injury Diseases 0.000 claims description 2
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims description 2
- 201000010105 allergic rhinitis Diseases 0.000 claims description 2
- 206010003230 arteritis Diseases 0.000 claims description 2
- 208000006673 asthma Diseases 0.000 claims description 2
- 206010006475 bronchopulmonary dysplasia Diseases 0.000 claims description 2
- 239000011575 calcium Substances 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 208000002849 chondrocalcinosis Diseases 0.000 claims description 2
- 208000007451 chronic bronchitis Diseases 0.000 claims description 2
- 230000001684 chronic effect Effects 0.000 claims description 2
- 239000013078 crystal Substances 0.000 claims description 2
- 230000008021 deposition Effects 0.000 claims description 2
- 206010014599 encephalitis Diseases 0.000 claims description 2
- 230000002538 fungal effect Effects 0.000 claims description 2
- 208000002085 hemarthrosis Diseases 0.000 claims description 2
- 208000034737 hemoglobinopathy Diseases 0.000 claims description 2
- 208000015446 immunoglobulin a vasculitis Diseases 0.000 claims description 2
- 208000030603 inherited susceptibility to asthma Diseases 0.000 claims description 2
- 201000004990 juvenile ankylosing spondylitis Diseases 0.000 claims description 2
- 230000000366 juvenile effect Effects 0.000 claims description 2
- 201000010982 kidney cancer Diseases 0.000 claims description 2
- 201000007270 liver cancer Diseases 0.000 claims description 2
- 208000014018 liver neoplasm Diseases 0.000 claims description 2
- 201000005202 lung cancer Diseases 0.000 claims description 2
- 208000020816 lung neoplasm Diseases 0.000 claims description 2
- 208000029744 multiple organ dysfunction syndrome Diseases 0.000 claims description 2
- 201000006417 multiple sclerosis Diseases 0.000 claims description 2
- 201000008482 osteoarthritis Diseases 0.000 claims description 2
- 206010034674 peritonitis Diseases 0.000 claims description 2
- 208000007865 relapsing fever Diseases 0.000 claims description 2
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 2
- 201000001223 septic arthritis Diseases 0.000 claims description 2
- 230000036303 septic shock Effects 0.000 claims description 2
- 208000007056 sickle cell anemia Diseases 0.000 claims description 2
- 201000000849 skin cancer Diseases 0.000 claims description 2
- 201000005671 spondyloarthropathy Diseases 0.000 claims description 2
- 208000011580 syndromic disease Diseases 0.000 claims description 2
- 201000000596 systemic lupus erythematosus Diseases 0.000 claims description 2
- 201000004415 tendinitis Diseases 0.000 claims description 2
- 206010009944 Colon cancer Diseases 0.000 claims 2
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims 2
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 1
- 206010005003 Bladder cancer Diseases 0.000 claims 1
- 208000003174 Brain Neoplasms Diseases 0.000 claims 1
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims 1
- 208000000461 Esophageal Neoplasms Diseases 0.000 claims 1
- 208000022072 Gallbladder Neoplasms Diseases 0.000 claims 1
- 206010025323 Lymphomas Diseases 0.000 claims 1
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 claims 1
- 206010029326 Neuropathic arthropathy Diseases 0.000 claims 1
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims 1
- 206010033128 Ovarian cancer Diseases 0.000 claims 1
- 206010061535 Ovarian neoplasm Diseases 0.000 claims 1
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims 1
- 206010060862 Prostate cancer Diseases 0.000 claims 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 1
- 201000002661 Spondylitis Diseases 0.000 claims 1
- 208000005718 Stomach Neoplasms Diseases 0.000 claims 1
- 208000024770 Thyroid neoplasm Diseases 0.000 claims 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 1
- 208000002495 Uterine Neoplasms Diseases 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 208000029742 colonic neoplasm Diseases 0.000 claims 1
- 201000004101 esophageal cancer Diseases 0.000 claims 1
- 201000010175 gallbladder cancer Diseases 0.000 claims 1
- 206010017758 gastric cancer Diseases 0.000 claims 1
- 201000010536 head and neck cancer Diseases 0.000 claims 1
- 208000014829 head and neck neoplasm Diseases 0.000 claims 1
- 230000000968 intestinal effect Effects 0.000 claims 1
- 208000032839 leukemia Diseases 0.000 claims 1
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 208000037819 metastatic cancer Diseases 0.000 claims 1
- 208000011575 metastatic malignant neoplasm Diseases 0.000 claims 1
- 201000002528 pancreatic cancer Diseases 0.000 claims 1
- 208000008443 pancreatic carcinoma Diseases 0.000 claims 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 201000011549 stomach cancer Diseases 0.000 claims 1
- 201000002510 thyroid cancer Diseases 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 1
- 206010046766 uterine cancer Diseases 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 abstract description 21
- 238000011161 development Methods 0.000 abstract description 4
- 230000001747 exhibiting effect Effects 0.000 abstract description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 254
- 238000005160 1H NMR spectroscopy Methods 0.000 description 232
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 174
- OKKJLVBELUTLKV-MZCSYVLQSA-N Deuterated methanol Chemical compound [2H]OC([2H])([2H])[2H] OKKJLVBELUTLKV-MZCSYVLQSA-N 0.000 description 22
- 230000000694 effects Effects 0.000 description 16
- QOVYHDHLFPKQQG-NDEPHWFRSA-N N[C@@H](CCC(=O)N1CCC(CC1)NC1=C2C=CC=CC2=NC(NCC2=CN(CCCNCCCNC3CCCCC3)N=N2)=N1)C(O)=O Chemical compound N[C@@H](CCC(=O)N1CCC(CC1)NC1=C2C=CC=CC2=NC(NCC2=CN(CCCNCCCNC3CCCCC3)N=N2)=N1)C(O)=O QOVYHDHLFPKQQG-NDEPHWFRSA-N 0.000 description 14
- 102100022417 Aminoacyl tRNA synthase complex-interacting multifunctional protein 2 Human genes 0.000 description 10
- 101000755758 Homo sapiens Aminoacyl tRNA synthase complex-interacting multifunctional protein 2 Proteins 0.000 description 10
- 241001465754 Metazoa Species 0.000 description 8
- OKKJLVBELUTLKV-VMNATFBRSA-N methanol-d1 Chemical compound [2H]OC OKKJLVBELUTLKV-VMNATFBRSA-N 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000037396 body weight Effects 0.000 description 6
- 230000005764 inhibitory process Effects 0.000 description 6
- WYFCZWSWFGJODV-MIANJLSGSA-N 4-[[(1s)-2-[(e)-3-[3-chloro-2-fluoro-6-(tetrazol-1-yl)phenyl]prop-2-enoyl]-5-(4-methyl-2-oxopiperazin-1-yl)-3,4-dihydro-1h-isoquinoline-1-carbonyl]amino]benzoic acid Chemical compound O=C1CN(C)CCN1C1=CC=CC2=C1CCN(C(=O)\C=C\C=1C(=CC=C(Cl)C=1F)N1N=NN=C1)[C@@H]2C(=O)NC1=CC=C(C(O)=O)C=C1 WYFCZWSWFGJODV-MIANJLSGSA-N 0.000 description 5
- 101710163595 Chaperone protein DnaK Proteins 0.000 description 5
- 101710178376 Heat shock 70 kDa protein Proteins 0.000 description 5
- 101710152018 Heat shock cognate 70 kDa protein Proteins 0.000 description 5
- 230000005907 cancer growth Effects 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000001727 in vivo Methods 0.000 description 4
- 238000007911 parenteral administration Methods 0.000 description 4
- 235000018102 proteins Nutrition 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 108090000623 proteins and genes Proteins 0.000 description 4
- 125000003396 thiol group Chemical class [H]S* 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 102000052866 Amino Acyl-tRNA Synthetases Human genes 0.000 description 3
- 108700028939 Amino Acyl-tRNA Synthetases Proteins 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 229920002472 Starch Chemical class 0.000 description 3
- 229920002678 cellulose Chemical class 0.000 description 3
- 235000010980 cellulose Nutrition 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000003937 drug carrier Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 108700043045 nanoluc Proteins 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229940124597 therapeutic agent Drugs 0.000 description 3
- 230000004614 tumor growth Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- VRDSMDGZAAKTJY-NRFANRHFSA-N CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CCC(=O)OC)C(=O)NC1=CC=C(C=C1)N1CCOCC1 Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N[C@@H](CCC(=O)OC)C(=O)NC1=CC=C(C=C1)N1CCOCC1 VRDSMDGZAAKTJY-NRFANRHFSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- 101000839464 Leishmania braziliensis Heat shock 70 kDa protein Proteins 0.000 description 2
- 108060001084 Luciferase Proteins 0.000 description 2
- 239000005089 Luciferase Substances 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
- OACSVMHTLOMZGN-NDEPHWFRSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)N1CCN(CC1)C1=CC=C(C=C1)OC)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)N1CCN(CC1)C1=CC=C(C=C1)OC)NS(=O)(=O)C1=CC=C(C=C1)C OACSVMHTLOMZGN-NDEPHWFRSA-N 0.000 description 2
- 229930012538 Paclitaxel Natural products 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 102100038280 Prostaglandin G/H synthase 2 Human genes 0.000 description 2
- 108050003267 Prostaglandin G/H synthase 2 Proteins 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- WLGNXNWOSAHJOZ-DEOSSOPVSA-N benzyl (2S)-3-(1H-indol-3-yl)-2-[(4-methylbenzoyl)amino]propanoate Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)OCC1=CC=CC=C1)NC(C1=CC=C(C=C1)C)=O WLGNXNWOSAHJOZ-DEOSSOPVSA-N 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 230000003833 cell viability Effects 0.000 description 2
- 239000001913 cellulose Chemical class 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- OSASVXMJTNOKOY-UHFFFAOYSA-N chlorobutanol Chemical compound CC(C)(O)C(Cl)(Cl)Cl OSASVXMJTNOKOY-UHFFFAOYSA-N 0.000 description 2
- 230000003013 cytotoxicity Effects 0.000 description 2
- 231100000135 cytotoxicity Toxicity 0.000 description 2
- 239000008121 dextrose Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000008298 dragée Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 238000003670 luciferase enzyme activity assay Methods 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L magnesium sulphate Substances [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- XQJHNJHNOBEFLO-VWLOTQADSA-N methyl 4-[2-[[(2S)-3-(1H-indol-3-yl)-2-[(4-methylphenyl)sulfonylamino]propanoyl]amino]-1,3-thiazol-4-yl]benzoate Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C(=O)OC)C=C1)NS(=O)(=O)C1=CC=C(C=C1)C XQJHNJHNOBEFLO-VWLOTQADSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 229960001592 paclitaxel Drugs 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000013612 plasmid Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 238000010379 pull-down assay Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 230000011664 signaling Effects 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- HUSYTLMIRXITQS-UHFFFAOYSA-N 1,3-benzodioxole-5-carboxamide Chemical compound NC(=O)C1=CC=C2OCOC2=C1 HUSYTLMIRXITQS-UHFFFAOYSA-N 0.000 description 1
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 1
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- NHBKXEKEPDILRR-UHFFFAOYSA-N 2,3-bis(butanoylsulfanyl)propyl butanoate Chemical compound CCCC(=O)OCC(SC(=O)CCC)CSC(=O)CCC NHBKXEKEPDILRR-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- GOZMBJCYMQQACI-UHFFFAOYSA-N 6,7-dimethyl-3-[[methyl-[2-[methyl-[[1-[3-(trifluoromethyl)phenyl]indol-3-yl]methyl]amino]ethyl]amino]methyl]chromen-4-one;dihydrochloride Chemical compound Cl.Cl.C=1OC2=CC(C)=C(C)C=C2C(=O)C=1CN(C)CCN(C)CC(C1=CC=CC=C11)=CN1C1=CC=CC(C(F)(F)F)=C1 GOZMBJCYMQQACI-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- XASOHFCUIQARJT-UHFFFAOYSA-N 8-methoxy-6-[7-(2-morpholin-4-ylethoxy)imidazo[1,2-a]pyridin-3-yl]-2-(2,2,2-trifluoroethyl)-3,4-dihydroisoquinolin-1-one Chemical compound C(N1C(=O)C2=C(OC)C=C(C=3N4C(=NC=3)C=C(C=C4)OCCN3CCOCC3)C=C2CC1)C(F)(F)F XASOHFCUIQARJT-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- SESFRYSPDFLNCH-UHFFFAOYSA-N Benzyl benzoate Natural products C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- QJHQUHMEFAHHBH-FQEVSTJZSA-N CC(C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C(=O)OC)C=C1)NS(=O)(=O)C1=CC=C(C=C1)C)C Chemical compound CC(C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C(=O)OC)C=C1)NS(=O)(=O)C1=CC=C(C=C1)C)C QJHQUHMEFAHHBH-FQEVSTJZSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- 102100025751 Mothers against decapentaplegic homolog 2 Human genes 0.000 description 1
- 101710143123 Mothers against decapentaplegic homolog 2 Proteins 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 101710135898 Myc proto-oncogene protein Proteins 0.000 description 1
- 102100038895 Myc proto-oncogene protein Human genes 0.000 description 1
- HSHXDCVZWHOWCS-UHFFFAOYSA-N N'-hexadecylthiophene-2-carbohydrazide Chemical compound CCCCCCCCCCCCCCCCNNC(=O)c1cccs1 HSHXDCVZWHOWCS-UHFFFAOYSA-N 0.000 description 1
- 150000001204 N-oxides Chemical class 0.000 description 1
- HVMGKUAQWHNMMZ-XLTVJXRZSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC(C(=O)OCC)CC1=CNC2=CC=CC=C12)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC(C(=O)OCC)CC1=CNC2=CC=CC=C12)NS(=O)(=O)C1=CC=C(C=C1)C HVMGKUAQWHNMMZ-XLTVJXRZSA-N 0.000 description 1
- VLPGAOXBMXGNGM-VWLOTQADSA-N N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C=C1)OC)NS(=O)(=O)C1=CC=C(C=C1)C Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC=1SC=C(N=1)C1=CC=C(C=C1)OC)NS(=O)(=O)C1=CC=C(C=C1)C VLPGAOXBMXGNGM-VWLOTQADSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 201000001263 Psoriatic Arthritis Diseases 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 206010039710 Scleroderma Diseases 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 108090000925 TNF receptor-associated factor 2 Proteins 0.000 description 1
- 102100034779 TRAF family member-associated NF-kappa-B activator Human genes 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 101710150448 Transcriptional regulator Myc Proteins 0.000 description 1
- 102000001742 Tumor Suppressor Proteins Human genes 0.000 description 1
- 108010040002 Tumor Suppressor Proteins Proteins 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 229940023476 agar Drugs 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000005262 alkoxyamine group Chemical group 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001409 amidines Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 230000002744 anti-aggregatory effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 230000001640 apoptogenic effect Effects 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 229960004926 chlorobutanol Drugs 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 150000001913 cyanates Chemical class 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000009266 disease activity Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000009509 drug development Methods 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002081 enamines Chemical class 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- GHKTXLWPQFDSBM-NDEPHWFRSA-N ethyl 4-[[(2S)-3-(1H-indol-3-yl)-1-(4-morpholin-4-ylanilino)-1-oxopropan-2-yl]sulfamoyl]benzoate Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)NS(=O)(=O)C1=CC=C(C(=O)OCC)C=C1 GHKTXLWPQFDSBM-NDEPHWFRSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 150000007857 hydrazones Chemical class 0.000 description 1
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 125000002140 imidazol-4-yl group Chemical group [H]N1C([H])=NC([*])=C1[H] 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000001361 intraarterial administration Methods 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 238000007913 intrathecal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002540 isothiocyanates Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- CDEDFXPPFAEHRM-MHZLTWQESA-N methyl 4-[[(2S)-3-(1H-indol-3-yl)-1-(4-morpholin-4-ylanilino)-1-oxopropan-2-yl]sulfamoyl]benzoate Chemical compound N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC1=CC=C(C=C1)N1CCOCC1)NS(=O)(=O)C1=CC=C(C(=O)OC)C=C1 CDEDFXPPFAEHRM-MHZLTWQESA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical compound COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 238000010172 mouse model Methods 0.000 description 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 description 1
- 229940100661 nasal inhalant Drugs 0.000 description 1
- 230000004770 neurodegeneration Effects 0.000 description 1
- 208000015122 neurodegenerative disease Diseases 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 201000008968 osteosarcoma Diseases 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N p-hydroxybenzoic acid methyl ester Natural products COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- RCCYSVYHULFYHE-UHFFFAOYSA-N pentanediamide Chemical compound NC(=O)CCCC(N)=O RCCYSVYHULFYHE-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 229940116317 potato starch Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 238000001243 protein synthesis Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000012439 solid excipient Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000008107 starch Chemical class 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/357—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
- A61K31/36—Compounds containing methylenedioxyphenyl groups, e.g. sesamin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4168—1,3-Diazoles having a nitrogen attached in position 2, e.g. clonidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4453—Non condensed piperidines, e.g. piperocaine only substituted in position 1, e.g. propipocaine, diperodon
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/81—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/82—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/83—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
- C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
- C07C311/19—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
- C07C317/46—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/10—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
- C07D211/14—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
- C07D241/44—Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/01—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having one nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/40—Unsubstituted amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/135—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
- C07D317/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/34—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
Abstract
本发明涉及具有抗癌活性的新型化合物及其制备方法,更具体地,涉及通过抑制AIMP2‑DX2的表达而表现出优异抗癌活性的新型化合物及其制备方法。本发明的由化学式1表示的化合物对于抑制AIMP2‑DX2的表达高度有效,因此可非常有益地用于治疗多种疾病(特别是由AIMP2‑DX2导致的癌症)的药剂的开发。
Description
技术领域
本申请要求于2019年3月29日提交的韩国专利申请第10-2019-0037271号的优先权,其整个说明书通过援引以其整体加入本文。
本发明涉及具有抗癌活性的新型化合物及其制备方法,更具体地,涉及通过抑制AIMP2-DX2的表达而表现出优异抗癌活性的新型化合物及其制备方法。
发明背景
氨酰tRNA合成酶复合物相互作用多功能蛋白(aminoacyl-tRNA synthetasecomplex-interacting multifunctional protein 2,AIMP2)是参与氨酰tRNA合成酶(ARS)复合物形成的蛋白质之一。已知AIMP2除了其在蛋白质合成中的原始功能外,还具有通过与作为新型肿瘤抑制因子的Smad2/3直接相互作用而增强TGF-β信号传导的功能。
正如由本发明人的韩国专利第10-0762995号中所知,观察到一种缺失AIMP2外显子2的突变体AIMP2-DX2在多种癌细胞系(例如肺癌、肝癌、皮肤癌、乳腺癌、肾癌、骨肉瘤)和组织中过表达。另一方面,当正常细胞转化为过表达AIMP2-DX2时,野生型(WT)AIMP2的水平大大降低,并且AIMP2的活性受到抑制(如阻断AIMP2向细胞核转移),c-myc表达增加,并且已证明它会导致TGF-β信号传导功能障碍(例如促进细胞生长)。这说明AIMP2-DX2与癌症的发生和发展有着密切的关系。
此外,在本发明人的另一项韩国专利第10-1067816号中,AIMP2通过与TRAF2相互作用介导TNF-α的凋亡活性,并首次表明该活性受AIMP2-DX2的调控。此外,已证实AIMP2-DX2还影响炎症标志物COX-2的表达,并表明通过抑制AIMP2-DX2的活性,可以产生对炎症性疾病的治疗作用。已提出它可以通过抑制AIMP2-DX2的活性对炎症性疾病产生治疗作用。
由于发现AIMP2-DX2蛋白参与多种疾病的诱导和进展,AIMP2-DX2正在成为药物开发的新靶点。
发明详述
技术问题
因此,本发明人经过反复深入研究,开发出能够抑制与多种疾病密切相关的AIMP2-DX2表达的新型化合物。发现本说明书中由式1表示的化合物抑制AIMP2-DX2的表达而表现出优异的抗癌活性,从而完成了本发明。
因此,本发明的一个目的是提供由下式1表示的化合物或其药学上可接受的盐:
<式1>
在式1中,
R1是氢;被一个或多个选自羟基、取代或未取代的苯基、巯基和C1~C5烷硫基的取代基取代或未取代的C1~C5直链或支链烷基;未取代的或被一个或多个选自C1~C5烷基、羟基、羟基羰基和甲酰基的取代基取代的吲哚基甲基;C1~C5羧甲基;C7~C10羟基苯基烷基;取代或未取代的C3~C8环烷基;取代或未取代的C1~C5氨基烷基;
R2是氢;未取代的或被一个或多个选自C1~C5直链或支链烷基、硝基、胺基、卤素、-CF3、C1~C5烷基羰基氨基、-COOH、C1~C5烷氧基、苯基、-OCH2Ph、羟基、-COOCH2Ph、C1~C5烷氧基羰基、-CONHCH3和腈的取代基取代的苯磺酰基;萘磺酰基;苄基磺酰基;未取代的或被一个或多个选自C1~C5直链或支链烷基和C1~C5直链或支链烷基胺基的取代基取代的苯甲酰基;噻吩磺酰基;C1~C5烷氧基羰基;或苯基氨基羰基;
本发明的另一个目的是提供用于预防或治疗癌症的药物组合物,其包含式1的化合物或其药学上可接受的盐作为活性成分。
本发明的另一个目的是提供用于预防或治疗癌症的药物组合物,其由作为活性成分的式1的化合物或其药学上可接受的盐组成。
本发明的另一个目的是提供用于预防或治疗癌症的药物组合物,其基本上由作为活性成分的式1的化合物或其药学上可接受的盐组成。
本发明的另一目的是提供式1的化合物或其药学上可接受的盐在制备用于预防或治疗癌症的药剂中的用途。
本发明的另一个目的是提供治疗癌症的方法,其包括向需要其的个体给药有效量的包含式1的化合物或其药学上可接受的盐作为活性成分的组合物。
本发明的另一目的是提供式1的化合物或其药学上可接受的盐在制备用于预防或治疗炎症性疾病的药剂中的用途。
本发明的另一个目的是提供治疗炎症性疾病的方法,其包括向需要其的个体给药有效量的包含式1的化合物或其药学上可接受的盐作为活性成分的组合物。
技术方案
为实现本发明的上述目的,本发明提供由下式1表示的化合物或其药学上可接受的盐:
[式1]
在式1中,
R1是氢;被一个或多个选自羟基、取代或未取代的苯基、巯基和C1~C5烷硫基的取代基取代或未取代的C1~C5直链或支链烷基;未取代的或被一个或多个选自C1~C5烷基、羟基、羟基羰基和甲酰基的取代基取代的吲哚基甲基;C1~C5羧甲基;C7~C10羟基苯基烷基;取代或未取代的C3~C8环烷基;取代或未取代的C1~C5氨基烷基;
R2是氢;未取代的或被一个或多个选自C1~C5直链或支链烷基、硝基、胺基、卤素、-CF3、C1~C5烷基羰基氨基、-COOH、C1~C5烷氧基、苯基、-OCH2Ph、羟基、-COOCH2Ph、C1~C5烷氧基羰基、-CONHCH3和腈的取代基取代的苯磺酰基;萘磺酰基;苄基磺酰基;未取代的或被一个或多个选自C1~C5直链或支链烷基和C1~C5直链或支链烷基胺基的取代基取代的苯甲酰基;噻吩磺酰基;C1~C5烷氧基羰基;或苯基氨基羰基;
为实现本发明的另一目的,本发明提供药物组合物,其包含式1的化合物或其药学上可接受的盐作为活性成分。
为实现本发明的另一目的,本发明提供药物组合物,其由作为活性成分的式1的化合物或其药学上可接受的盐组成。
为实现本发明的另一个目的,本发明提供药物组合物,其基本上由作为活性成分的式1的化合物或其药学上可接受的盐组成。
为实现本发明的另一目的,本发明提供式1的化合物或其药学上可接受的盐在制备用于预防或治疗癌症的药剂中的用途。
为实现本发明的另一个目的,本发明提供治疗癌症的方法,其包括向需要其的个体给药有效量的包含式1的化合物或其药学上可接受的盐作为活性成分的组合物。
为实现本发明的另一目的,本发明提供式1的化合物或其药学上可接受的盐在制备用于预防或治疗炎症性疾病的药剂中的用途。
为实现本发明的另一个目的,本发明提供治疗炎症性疾病的方法,其包括向需要其的个体给药有效量的包含式1的化合物或其药学上可接受的盐作为活性成分的组合物。
下文会详细描述本发明。
本发明提供由下式1表示的化合物或其药学上可接受的盐:
[式1]
在式1中,
R1是氢;被一个或多个选自羟基、取代或未取代的苯基、巯基和C1~C5烷硫基的取代基取代或未取代的C1~C5直链或支链烷基;未取代的或被一个或多个选自C1~C5烷基、羟基、羟基羰基和甲酰基的取代基取代的吲哚基甲基;C1~C5羧甲基;C7~C10羟基苯基烷基;取代或未取代的C3~C8环烷基;取代或未取代的C1~C5氨基烷基;
R2是氢;未取代的或被一个或多个选自C1~C5直链或支链烷基、硝基、胺基、卤素、-CF3、C1~C5烷基羰基氨基、-COOH、C1~C5烷氧基、苯基、-OCH2Ph、羟基、-COOCH2Ph、C1~C5烷氧基羰基、-CONHCH3和腈的取代基取代的苯磺酰基;萘磺酰基;苄基磺酰基;未取代的或被一个或多个选自C1~C5直链或支链烷基和C1~C5直链或支链烷基胺基的取代基取代的苯甲酰基;噻吩磺酰基;C1~C5烷氧基羰基;或苯基氨基羰基;
在本发明中,术语“烷基”是指链中含有1至5个碳原子的可以是直链或支链的脂族烃基。优选的烷基基团链中含有1至3个碳原子。更优选的烷基基团链中含有约1、2或3个碳原子。支链是指一个或多个低级烷基(如甲基、乙基或丙基)连接到线性烷基链上。“低级烷基”是指链中具有1至5个碳原子的可以是直链或支链的基团。“烷基”可以是未取代的或任选地被一个或多个可以相同或不同的取代基取代。
在本发明中,“卤代”或“卤素”是指氟原子、氯原子、溴原子或碘原子。
当本文中公开的基团表示为“取代”时,这些基团可以被任何合适的一个或多个取代基取代。取代基的说明性实例包括在本文中公开的示例性化合物和实施方案中可见的那些,以及卤素(氯、碘、溴或氟基团)、烷基、羟基、烷氧基、烷氧基烷基、氨基、烷基氨基、羧基、硝基、氨基(ano)、硫醇、硫醚、亚胺、酰亚胺、脒、胍、烯胺、氨基羰基、酰氨基、膦酰基、膦、硫代羰基、磺酰基、砜、磺酰胺、酮、醛、酯、脲、氨基甲酸酯、肟、羟胺、烷氧基胺、芳烷氧基胺、N-氧化物、肼、酰肼、腙、叠氮化物、异氰酸酯、异硫氰酸酯、氰酸酯、硫氰酸酯等。
在本发明的一个实施方案中,其中R1为未取代的或被一个或多个选自以下的取代基取代的吲哚基甲基:羟基、取代或未取代的苯基、巯基和被一个或多个选自C1~C5烷硫基的取代基取代或未取代的直链或支链烷基;或烷基、羟基、羟基羰基和甲酰基,
其中R2是未取代的或被一个或多个选自C1~C5直链或支链烷基、硝基、胺基、卤素、-CF3、C1~C5烷基羰基氨基、-COOH、C1~C5烷氧基、苯基、-OCH2Ph、羟基、-COOCH2Ph、C1~C5烷氧基羰基、-CONHCH3和腈的取代基取代的苯磺酰基,
优选地,其中R1为未取代的C1~C5直链或支链烷基;或未取代的吲哚基甲基,
在本发明的一个实施方案中,其中R1可以优选为氢或环己烷、
在本发明的另一个实施方案中,其中R1可以最优选为
在本发明的另一个实施方案中,其中R2可以优选是氢、
此外,在本发明中,其中所述式1的化合物可为:
(S)-4-甲基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺,
(R)-4-甲基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺,
(S)-4-甲基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺,
(R)-4-甲基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)-戊-2-基)苯磺酰胺,
(S)-N-(1-(1,1-二氧化硫代吗啉代)-4-甲基-1-氧代戊-2-基)-4-甲基苯磺酰胺,
(N-((S)-1-((R)-2-(羟甲基)吡咯烷-1-基)-4-甲基-1-氧代戊-2-基)-4-甲基苯磺酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(哌啶-1-基)苯基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-甲基哌啶-1-基)苯基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-(4-甲基哌啶-1-基)吡啶-3-基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-(4-甲基哌啶-1-基)嘧啶-4-基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-吗啉代吡啶-3-基)戊酰胺,
(S)-N-(6-((2S,6R)-2,6-二甲基吗啉代)吡啶-3-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(3-氟-4-吗啉代苯基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(4-(1,1-二氧化硫代吗啉代)苯基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-(5-(4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺基)吡啶-2-基)哌嗪-1-甲酸叔丁基酯,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(吡咯烷-1-基)苯基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(2-吗啉代乙基)戊酰胺,
(S)-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-硝基苯磺酰胺,
(S)-3-氨基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺,
(S)-2-(4-氟苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-2-(4-溴苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(4-(三氟甲基)苯基磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(3-硝基苯基磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(萘-1-磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(萘-2-磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(苯基磺酰胺基)戊酰胺,
(S)-4-甲基-2-(3-(苯基磺酰基)丙酰胺基)戊酸苄酯,
(S)-2-(4-甲氧基苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(噻吩-2-磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(4-硝基苯基磺酰胺基)戊酰胺,
(S)-2-(4-异丙基苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-2-(联苯-4-基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-4-(苄基氧基)-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺,
(S)-4-羟基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺,
(S)-4-(N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)氨磺酰基)苯甲酸苄酯,
(S)-3-(4-甲基苯基磺酰胺基)-4-吗啉代-4-氧代丁酸叔丁酯,
(S)-4-甲基-N-(1-吗啉代-1-氧代-3-苯基丙-2-基)苯磺酰胺,
(S)-N-(3-羟基-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-4-甲基-N-(3-甲基-1-吗啉代-1-氧代丁-2-基)苯磺酰胺,
(R)-N-(3-巯基-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(2S,3S)-3-羟基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丁酰胺,
(2S,3S)-3-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)戊酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-4-(甲硫基)-N-(4-吗啉代苯基)丁酰胺,
(S)-3-(1H-吲哚-2-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1-甲基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-苯基丙酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酸苄酯,
(S)-4-甲基-2-(4-甲基苯甲酰胺基)戊酸苄酯,
(S)-2-(4-叔丁基苯甲酰胺基)-4-甲基戊酸苄酯,
(S)-2-(苯并[d][1,3]二氧杂环戊烯-5-甲酰胺基)-4-甲基戊酸苄酯,
(S)-2-(4-(叔丁氧基羰基氨基)苯甲酰胺基)-4-甲基戊酸苄酯,
(S)-4-甲基-2-(3-(苯基磺酰基)丙酰胺基)戊酸苄酯,
(S)-N-(4-(4-甲氧基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-1-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-苯基脲,
(S)-4-叔丁基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯甲酰胺,
(S)-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-(苯基磺酰基)丙酰胺,
(S)-4-叔丁基-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯甲酰胺,
(S)-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯并[d][1,3]二氧杂环戊烯-5-甲酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(3-(苯基磺酰基)丙酰胺基)戊酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(2-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(3-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-2-(3,5-二甲基苯基磺酰胺基)-3-(1H-吲哚-3-基)N-(4吗啉代苯基)丙酰胺,
(S)-2-(4-氟苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(4-(三氟甲基)苯基磺酰胺基)丙酰胺,
(S)-3-(5-羟基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(5-吗啉代噻唑-2-基)丙酰胺,
(S)-2-(2,4-二甲基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
3-(3-乙氧基-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)-1H-吲哚-5-羧酸,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-(1-甲苯磺酰基-1H-咪唑-4-基)丙酰胺,
(S)-N-(6-((2S,6R)-2,6-二甲基吗啉代)吡啶-3-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙烯酰胺,
(R)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-N-(3-氟-4-吗啉代苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(4-硝基苯基磺酰胺基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲氧基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-异丙基苯基磺酰胺基)-N-(4吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-异丙基苯基磺酰胺基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙烯酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-甲基噻唑-2-基)丙酰胺,
(S)-N-(苯并[d]噻唑-2-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酸,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(5-吗啉代噻唑-2-基)戊酰胺,
(S)-N-(5-(4-甲氧基苯基)-1,3,4-噻二唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(5-(4-甲氧基苯基)异噁唑-3-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(3-(4-甲氧基苯基)异噁唑-5-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)戊酰胺,
(S)-N-(4-(3,4-二甲氧基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(4-(2-溴-4-氟苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-(2-氨基噻唑-4-基)苯基-4-甲基-2-(4-甲基苯基磺酰胺基)戊酸酯,
(S)-N-(4-(4-氟苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲氧基)苯基)噻唑-2-基)戊酰胺,
(S)-N-(4-(4-羟基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-对甲苯基噻唑-2-基)戊酰胺,
(S)-N-(4-(4-((S)-1-甲氧基丙-2-基氧基)苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-吗啉代苯基)噻唑-2-基)戊酰胺,
(S)-甲基-4-(2-(4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺基)噻唑-4-基)苯甲酸酯,
(S)-4-(2-(4-甲基苯基磺酰胺基)-3-(4-吗啉代苯基氨基)-3-氧代丙基)苯基4-甲基苯磺酸酯,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-咪唑-4-基)N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-N-甲氧基-N,4-二甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-3-(1H-吲哚-3-基)-N-甲氧基-N-甲基-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)丙-2-基)-4-甲基苯磺酰胺,
(S)-2-(4-叔丁基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(2-氯苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(2,4-二甲氧基苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(噻唑-2-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(5-甲基噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-甲基噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(5-甲基噻唑-2-基)丙酰胺,
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸甲酯,
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸乙酯,
(S)-3-(4-苯甲酰基苯基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)-N-甲基苯甲酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-(萘-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基氨基甲酸叔丁酯,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酸,
(S)-4-(4-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-甲氧基苯基)哌嗪-1-甲酸叔丁酯,
(S)-3-(1H-吲哚-3-基)-N-(2-甲氧基-4-(哌嗪-1-基)苯基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-4-(4-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)苯基)哌嗪-1-甲酸叔丁酯,
(S)-3-(1H-吲哚-3-基)-N-(2-甲氧基-4-吗啉代苯基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(哌嗪-1-基)苯基)丙酰胺,
(S)-3-(1-甲酰基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(3-(4-甲氧基苯基)异噁唑-5-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酸苄酯,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯甲酰胺基)丙酸苄酯,
(S)-N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)-4-甲基苯甲酰胺,
(S)-3-羟基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丁酰胺,
(S)-1-(3-(1H-吲哚-3-基)-1-吗啉代-1-氧代丙-2-基)-3-苯基脲,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(6-吗啉代吡啶-3-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(2-吗啉代嘧啶-5-基)丙酰胺,
(S)-2-(4-氰基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(6-(三氟甲基)吡啶-3-磺酰胺基)丙酰胺,
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸甲酯,
(S)-3-(1H-苯并[d]咪唑-1-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(R)-3-(2,3-二氧代-3,4-二氢喹喔啉-1(2H)-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-N-(5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基)-5-(三氟甲基)吡啶甲酰胺,
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸苄酯,
(S)-3-(4-甲基苯基磺酰胺基)-4-(4-吗啉代苯基氨基)-4-氧代丁酸苄酯,
(S)-4-甲基-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯甲酰胺,
2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)乙酰胺,
(S)-3-(4-甲基苯基磺酰胺基)-4-(4-吗啉代苯基氨基)-4-氧代丁酸,
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-苯基丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-苯基丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-苯基丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(噻吩-2-基甲基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(噻吩-2-基甲基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(2-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-N-(3-(N-(4-甲基-1-吗啉代-1-氧代戊-2-基)氨磺酰基)苯基)乙酰胺,
(S)-4-甲基-2-(3-苯基脲基)戊酸苄酯,
4-甲基-N-(2-吗啉代-2-氧代乙基)苯磺酰胺,
4-甲基-N-(1-(吗啉-4-羰基)环己基)苯磺酰胺,
(S)-4-(N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)氨磺酰基)苯甲酸,
(S)-2-(4-羟基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙烯酰胺,
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸,
(S)-2-氨基-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙烯酰胺,
(S)-N-(4-(4-乙酰基哌嗪-1-基)-2-甲氧基苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙烯酰胺,
(S)-N-(4-(4-乙酰基哌嗪-1-基)苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙烯酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-吗啉代苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(4-吗啉代苯基)噻唑-2-基)丙酰胺,
(S)-甲基-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸酯,
(S)-3-(1H-吲哚-3-基)-2-(6-(三氟甲基)吡啶-3-磺酰胺基)丙酸苄酯,
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-(4-硝基苯基)戊二酰胺,
(S)-5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基氨基甲酸苄酯,
(S)-6-氨基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)己酰胺,
(S)-3,5-二甲氧基-N-(5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基)苯甲酰胺,
(S)-N5-(4-甲氧基苄基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-苯基戊二酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-5-吗啉代-N-(4-吗啉代苯基)-5-氧代戊酰胺,
S)-N5-(4-氟苯基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺,
(S)-N5-(4-叔丁基苯基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-(4-(三氟甲基)苯基)戊二酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N4-(4-硝基苯基)琥珀酰胺,
(S)-N-(呋喃-2-基甲基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(呋喃-2-基甲基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-异丙基-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-异丙基丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-甲氧基苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰基)-N-(4-甲氧基苯基)肼甲酰胺,
(S)-4-溴-N-(1-(3,5-二甲基-1H-吡唑-1-基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-氧代-1-(3-苯基-1H-吡唑-1-基)丙-2-基)-4-溴苯磺酰胺,
N-((S)-1-(2-((3S,5S,7S)-金刚烷-1-羰基)肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(对甲苯基)噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-苯乙基丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-氟苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-硝基苯基)噻唑-2-基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-甲氧基苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-氰基苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)丙酰胺,
(S)-4-溴-N-(1-(2-十二酰基肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺,
(S)-4-溴-N-(1-(2-癸酰基肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-苯乙基丙酰胺,
N-((S)-1-(2-((3S,5S,7S)-金刚烷-1-羰基)肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)-4-溴苯磺酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-氟苯乙基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-甲氧基苯乙基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(3-苯基丙基)丙酰胺,
(S)-N-((3R,5R,7R)-金刚烷-1-基)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(4-(4-甲氧基苯基)哌嗪-1-基)-1-氧代丙-2-基)-4-溴苯磺酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(4-(4-甲氧基苯基)哌嗪-1-基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-N-((3R,5R,7R)-金刚烷-1-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-甲氧基苯乙基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(3-苯基丙基)丙酰胺,
(S)-N-(4-氟苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)丙酰胺,
(S)-N-(2-(1H-吲哚-3-基)乙基)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-1-氧代丙-2-基)-4-甲基苯甲酰胺,
(S)-2-(4-氯苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-(三氟甲基)苯基磺酰胺基)丙酰胺,
(S)-2-(4-氟苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-((1r,3R,5S,7S)-3,5-二甲基金刚烷-1-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-氰基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯甲酰胺基)丙酸苄酯,
(S)-2-(4-溴苯基磺酰胺基)-3-(5-羟基-1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-3-(5-甲基-1H-吲哚-3-基)丙烯酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(5-氟-1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)乙基)苯甲酸,
(S)-N-(4-溴苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-N-(2-(1H-吲哚-3-基)乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙烯酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-甲基苯乙基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
2-((S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-(1H-吲哚-3-基)丙酸乙酯,
(S)-N-(4-氯苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
2-((S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-(1H-吲哚-3-基)丙酸,
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸甲酯,
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸,
(S)-3-(苯并[d]噁唑-2-基氨基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)苯甲酰胺,
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)烟酰胺,或者
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)嘧啶-5-甲酰胺。
上文所列化合物的结构式、这些化合物对AIMP2-DX2表达的抑制效果以及对癌细胞的细胞毒性如下表1中所示。
表1
本发明的式1的化合物可以药学上可接受的盐的形式使用。作为盐,可以使用与多种药学或生理学上可接受的有机或无机酸形成的酸加成盐。作为合适的有机酸,可以采用例如羧酸、膦酸、磺酸、乙酸、丙酸、辛酸、癸酸、乙醇酸、乳酸、富马酸、琥珀酸、己二酸、苹果酸、酒石酸、柠檬酸、谷氨酸、天冬氨酸、马来酸、苯甲酸、水杨酸、邻苯二甲酸、苯乙酸、苯磺酸、2-萘磺酸、甲基硫酸、乙基硫酸、十二烷基硫酸等等,并且作为合适的无机酸,可以采用例如盐酸、硫酸或磷酸。
本发明的式1的化合物可以包括所有可通过常规方法制备的盐、水合物和溶剂合物、外消旋物或立体异构体以及药学上可接受的盐。
根据本发明的实施方案,证实所述化合物表现出抑制AIMP2-DX2表达的活性。具体而言,通过抑制与有助于AIMP2-DX2蛋白稳定化的HSP70的结合,证实了该活性。
因此,本发明提供的化合物的特征可以在于它们表现出抑制AIMP2-DX2表达的活性。
本发明还提供制备权利要求1的化合物或其药学上可接受的盐的方法,所述化合物通过以下反应式制备:
[反应式1]
在反应式1中,
R1、R2和R3如上文所定义。
另一方面,根据本发明的一实施方案,证实式1的化合物或其药学上可接受的盐通过抑制AIMP2-DX2的表达而对癌细胞表现出优异的细胞毒性,并且在体内肿瘤模型中,抑制肿瘤生长的作用也非常优异。
因此,本发明提供用于预防或治疗癌症的药物组合物,其包含式1的化合物或其药学上可接受的盐作为活性成分。
另一方面,根据之前的报道,已经证实,当AIMP2-DX2的表达被抑制时,COX-2的表达受到抑制,且炎症反应得到缓解(韩国专利第1067816号)。因此,本发明的抑制AIMP2-DX2表达的化合物可表现出优异的抗炎症性疾病活性。
因此,本发明提供用于预防或治疗炎症性疾病的药物组合物,其包含式1的化合物或其药学上可接受的盐作为活性成分。
在本发明中,所述炎症性疾病可以选自炎症性皮肤病、克罗恩病、溃疡性结肠炎、腹膜炎、骨髓炎、蜂窝织炎、脑膜炎、脑炎、胰腺炎、创伤性休克、支气管哮喘、变应性鼻炎、囊性纤维化、中风、急性支气管炎、慢性支气管炎、急性细支气管炎、慢性细支气管炎、骨关节炎、痛风、脊椎关节病、强直性脊柱炎、莱特尔氏综合征、牛皮癣性关节病、肠脊椎炎、青少年关节病、青少年强直性脊柱炎、反应性关节病、感染性关节炎、感染后关节炎、淋球菌性关节炎、结核性关节炎、病毒性关节炎、真菌性关节炎、梅毒性关节炎、莱姆病、与“血管炎综合征”相关的关节炎、结节性多动脉炎、过敏性血管炎、卢伽雷(Lou Gehrig′s)肉芽肿病、风湿性多肌痛、关节细胞动脉炎、钙结晶沉积性关节病、假性痛风、非关节风湿病、滑囊炎、肌腱炎、上髁炎(网球肘)、神经性关节病(夏科氏关节(charco and joint))、关节积血、过敏性紫癜(Henoch-purpura)、肥大性骨关节病、多中心网状细胞瘤、腹股沟炎(surcoilosis)、血色素沉着病、镰刀形细胞病和其他血红蛋白病、高蛋白血症、低丙球蛋白血症、家族性地中海贫血、Behat′s病、系统性红斑狼疮、回归热、银屑病、多发性硬化症、败血症、感染性休克、多器官功能障碍综合征、急性呼吸窘迫综合征、慢性阻塞性肺病、类风湿性关节炎、急性肺损伤和支气管肺发育不良,但不限于此。
根据本发明的药物组合物可以单独包含式1的化合物或其药学上可接受的盐,或者可另外包含一种或多种药学上可接受的载体、赋形剂或稀释剂。
所述药学上可接受的载体可以进一步包括例如用于口服给药的载体或用于肠胃外给药的载体。用于口服给药的载体可以包括乳糖、淀粉、纤维素衍生物、硬脂酸镁、硬脂酸等。此外,肠胃外给药的载体可以包括水、合适的油、盐水、葡萄糖水溶液和乙二醇等,并且可以进一步包括稳定剂和防腐剂。合适的稳定剂包括抗氧化剂,例如亚硫酸氢钠、亚硫酸钠或抗坏血酸。合适的防腐剂包括苯扎氯铵、对羟基苯甲酸甲酯或丙酯以及氯丁醇。其他药学上可接受的载体可参考本领域已知的那些。
本发明的药物组合物可以通过任意方法向包括人的哺乳动物给药。例如,它可以口服或肠胃外给药。肠胃外给药方法不限于此,可以是静脉内、肌肉内、动脉内、髓内、鞘内、心内、经皮、皮下、腹膜内、鼻内、肠内、局部、舌下或直肠给药。例如,本发明的药物组合物可以制备为可注射形式并通过用30号细注射针轻轻刺入皮肤给药,或通过将其直接施用于皮肤。
根据上述给药途径,本发明的药物组合物可以配制成用于口服给药或肠胃外给药的药剂。
在用于口服给药的药剂的情况下,本发明的组合物可以使用本领域已知的方法配制成散剂、颗粒剂、片剂、丸剂、糖衣丸、胶囊剂、液体剂、凝胶剂、糖浆剂、浆剂、混悬剂等。例如,口服制剂可以通过将活性成分与固体赋形剂混合,研磨,加入合适的辅料,并加工成颗粒混合物,以得到片剂或糖衣丸。合适的赋形剂的实例可以包括糖类(包括乳糖、右旋糖、蔗糖、山梨糖醇、甘露糖醇、木糖醇、赤藓糖醇和麦芽糖醇等),淀粉类(包括玉米淀粉、小麦淀粉、大米淀粉和马铃薯淀粉等),纤维素类(包括纤维素、甲基纤维素、羧甲基纤维素钠和羟丙基甲基纤维素等),以及诸如明胶、聚乙烯吡咯烷酮等的填充剂。另外,如果需要,可以加入交联聚乙烯吡咯烷酮、琼脂、海藻酸或海藻酸钠作为崩解剂。此外,本发明的药物组合物还可包含抗聚集剂、润滑剂、润湿剂、调味剂、乳化剂和防腐剂。
肠胃外给药的药剂可以通过本领域已知的方法配制成注射剂或乳膏剂、洗剂、外用软膏剂、油剂、保湿剂、凝胶剂、气雾剂和鼻吸入剂的形式。这些制剂在所有药物化学中公知的处方集中都有描述。
本发明的药物组合物的总有效量可以作为单剂量形式向患者给药,并且可以通过长时间给药多剂量的分次治疗方案给药。本发明的药物组合物可根据疾病的严重程度改变活性成分的含量。优选地,本发明的药物组合物的总剂量可为每天每1kg患者体重约0.01ug至1,000mg,最优选0.1ug至100mg。然而,由于本发明的药物组合物的剂量是考虑到患者的年龄、体重、健康状况、性别、疾病严重程度、饮食和排泄率等多种因素以及给药途径和治疗次数来确定的,并且确定对患者的有效剂量,考虑到这一点,本领域普通技术人员能够根据本发明药物组合物作为神经退行性疾病的治疗剂的具体用途确定合适的有效剂量。根据本发明的药物组合物在其配方、给药途径和给药方法方面没有特别限制,只要表现出本发明的效果即可。
在本发明中,“治疗”是指全面改善癌症或炎症性疾病的症状,这可以优选地包括治愈、基本上预防或改善癌症或炎性疾病的病况,包括但不限于减轻、治愈或预防由癌症或炎症性疾病引起的一种或大部分症状。
本发明提供式1的化合物或其药学上可接受的盐在制备用于预防或治疗癌症的药剂中的用途。
本发明提供了治疗癌症的方法,其包括向需要其的个体给药有效量的包含式1的化合物或其药学上可接受的盐作为活性成分的组合物。
本发明提供式1的化合物或其药学上可接受的盐在制备用于预防或治疗炎症性疾病的药剂中的用途。
本发明提供治疗炎症性疾病的方法,其包括向需要其的个体给药有效量的包含式1的化合物或其药学上可接受的盐作为活性成分的组合物。
本发明的“有效量”是指当向个体给药时显示改善、治疗、预防、检测、诊断癌症或炎症性疾病,或者抑制或减轻癌症或炎性疾病的效果的量,所述“个体”可以是动物,优选包括哺乳动物的动物,特别是人,并且可以是源自动物的细胞、组织、器官等。所述个体可以是需要所述效果的患者。
如本文所用,术语“包含”与“包括”或“特征在于”同义使用,在根据本发明的组合物或方法中,不排除未具体提及的方法的其他组分或步骤。此外,术语“由...组成”是指排除未具体描述的附加要素、步骤或成分。术语“基本上由...组成”是指,在组合物或方法的范围内,除了所描述的物质或步骤之外,它还可以包括基本上不影响其基本性质的物质或步骤。
有益效果
本发明托由式1表示的化合物在抑制AIMP2-DX2的表达方面非常有效,因此可以非常有用地在AIMP2-DX2引起的各种疾病的发展中使用,特别地用作癌症的治疗剂。
附图简要说明
图1是用本发明的化合物63在各个浓度处理表达NanoLuc萤光素酶-DX2或-AIMP2的A549细胞4小时后通过测量荧光来计算AIMP2-DX2和AIMP2的IC50的结果。
图2是通过体外拉下试验证实本发明的化合物63抑制AIMP2-DX2和HPS70结合的结果。将纯化的AIMP2-DX2-His6和HSP70蛋白混合并用各个浓度的化合物63处理4小时后,AIMP2-DX2用Ni-IDA树脂沉淀,用AIMP2-DX2沉淀的HSP70通过SDS-PAGE和考马斯染色显示。
图3a至3d是对移植了H460细胞的小鼠每两天腹膜内给药化合物63(50mg/kg)共15天时观察肿瘤生长的结果。(图3a:给药结束后每只小鼠和肿瘤的宏观观察,图3b:肿瘤随时间的生长曲线,图3c:给药结束时获得的每个肿瘤的重量,图3d:给药期间动物的体重变化)。
图4为根据本发明的式1的化合物中化合物55和化合物89对癌细胞生长抑制作用及药物在H460异种移植动物模型中的肿瘤分布测试结果。紫杉醇用作阳性对照。
具体实施方式
下文中会详细描述本发明。
然而,以下实施例仅用于说明本发明,本发明的内容不限于以下实施例。
实施例1:化合物的制备
在本发明中,式1的化合物按照以下反应式1制备:
[反应式1]
在反应式中,R1、R2和R3如上所定义。
具体地,采用以下原料:酸(1)(1.0当量)、2M NaOH溶液(1.0当量)。将混合物在0℃搅拌数分钟直至形成澄清溶液。向上述溶液中加入磺酰氯(1.05当量)、DIPEA(1.1当量)和丙酮。将混合物在0℃下搅拌10分钟,然后在室温下搅拌12小时。反应完成后,将混合物用乙醚洗涤以除去有机杂质。将合并的有机层再次用2M NaOH洗涤。在0℃下向水层中加入2NHCl,直至pH值为2。然后用乙酸乙酯、水和盐水萃取整个含水混合物。有机溶剂用MgSO4干燥并真空蒸发以获得化合物(2)。
向15mL的DMF或DCM∶THF=1∶1中加入上述化合物(2)(2当量)、胺(1.1当量)、EDCI(1.1当量)和HOBt(1.1当量)。将混合物在室温下搅拌过夜,然后用乙酸乙酯、水和盐水萃取。将有机层用MgSO4干燥并真空蒸发以得到化合物(3)的粗产物,将其通过柱色谱法纯化得到纯的化合物(3)。
根据上述方法制备的式1的化合物的具体实例、结构和NMR分析结果如下详细所示。
(S)-4-甲基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.70(d,J=8.40Hz,2H),7.29(d,J=8.00Hz,2H),5.74(d,J=9.60Hz,1H),4.06-4.01(m,1H),3.61-3.51(m,2H),3.41-3.36(m,1H),3.31-3.14(m,5H),2.42(s,3H),2.00-1.93(m,1H),1.50-1.43(m,1H),1.17-1.11(m,1H),0.95(d,J=6.80Hz,3H),0.92(d,J=6.80Hz,3H)
(R)-4-甲基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.70(d,J=8.80Hz,2H),7.29(d,J=8.40Hz,2H),5.78(d,J=9.60Hz,1H),4.08-4.02(m,1H),3.59-3.42(m,2H),3.41-3.32(m,1H),3.31-3.15(m,5H),2.41(s,3H),1.99-1.92(m,1H),1.50-1.42(m,1H),1.19-1.12(m,1H),0.95(d,J=6.80Hz,3H),0.92(d,J=6.80Hz,3H)
(S)-4-甲基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.71(d,J=8.00Hz,2H),7.27(d,J=8.00Hz,2H),5.59(d,J=10.0Hz,1H),4.25-4.19(m,1H),3.78-3.71(m,2H),3.69-3.37(m,11H),3.22-3.12(m,3H),2.40(s,3H),1.98-1.91(m,1H),1.49-1.33(m,2H),0.91(t,J=6.00Hz,6H)
(R)-4-甲基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)-戊-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.71(d,J=8.00Hz,2H),7.27(d,J=8.40Hz,2H),5.66(d,J=9.60Hz,1H),4.26-4.20(m,1H),3.79-3.67(m,2H),3.66-3.38(m,11H),3.23-3.12(m,3H),2.40(s,3H),1.97-1.90(m,1H),1.49-1.33(m,2H),0.92(d,J=4.20Hz,3H),0.89(d,J=5.60Hz,3H)
(S)-N-(1-(1,1-二氧化硫代吗啉代)-4-甲基-1-氧代戊-2-基)-4-甲基苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.73(d,J=7.60Hz,2H),7.34(d,J=7.60Hz,2H),5.59(d,J=9.60Hz,1H),4.40(d,J=14.0Hz,1H),4.05-3.99(m,1H),3.81(d,J=14.8Hz,1H),3.66(t,J=12.6Hz,1H),3.32(t,J=12.2Hz,1H),2.88(t,J=11.2Hz,2H),2.61-2.56(m,1H),2.50-2.40(m,4H),1.97-1.92(m,1H),1.52-1.46(m,1H),1.22-1.16(m,1H),0.93(d,J=6.40Hz,3H),0.85(d,J=6.40Hz,3H)
N-((S)-1-((R)-2-(羟甲基)吡咯烷-1-基)-4-甲基-1-氧代戊-2-基)-4-甲基苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.70(d,J=8.20Hz,2H),7.28(d,J=7.60Hz,2H),5.60(d,J=9.60Hz,1H),4.05(dd,J=3.00,7.40Hz,1H),3.97-3.91(m,1H),4.06-4.03(m,1H),3.97-3.91(m,1H),3.63-3.61(m,1H),3.52-3.49(m,1H),3.29-3.25(m,2H),2.42(s,3H),1.94-1.85(m,2H),1.77-1.68(m,2H),1.56-1.47(m,2H),1.25-1.19(m,1H),0.94(d,J=3.20Hz,3H),0.93(d,J=4.00Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(哌啶-1-基)苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.85(s,1H),7.76(d,J=8.00Hz,2H),7.22-7.12(m,4H),6.82-6.78(m,2H),5.48(s,1H),3.84-3.82(m,1H),3.07(t,J=5.60Hz,4H),2.32(s,3H),1.71-1.46(m,8H),0.85(d,J=6.00Hz,3H),0.72(d,J=5.60Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-甲基哌啶-1-基)苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.97(s,1H),7.76(d,J=8.00Hz,2H),7.21-7.12(m,4H),6.81-6.77(m,2H),5.66(d,J=7.60Hz,1H),3.88-3.83(m,1H),3.56-3.53(m,2H),2.65-2.58(m,2H),2.31(s,3H),1.73-1.70(m,2H),1.62-1.56(m,2H),1.50-1.45(m,2H),1.37-1.25(m,2H),0.97(d,J=6.40Hz,3H),0.84(d,J=6.00Hz,3H),0.71(d,J=5.60Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-(4-甲基哌啶-1-基)吡啶-3-基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.21(s,1H),7.98(d,J=2.80Hz,1H),7.76(d,J=8.40Hz,2H),7.48(dd,J=2.80,8.80Hz,1H),7.22(d,J=8.00Hz,2H),6.52(d,J=8.80Hz,1H),5.85(d,J=8.00Hz,1H),4.16-4.11(m,2H),3.91-3.86(m,1H),2.78-2.72(m,2H),2.32(s,3H),1.69-1.47(m,6H),1.23-1.13(m,2H),0.95(d,J=6.00Hz,3H),0.83(d,J=6.40Hz,3H),0.68(d,J=6.40Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-(4-甲基哌啶-1-基)嘧啶-4-基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.76(s,1H),8.31(s,1H),7.75(d,J=8.40Hz,2H),7.22(d,J=8.40Hz,3H),6.21(s,2H),4.37(s,2H),3.85(s,1H),2.90-2.84(m,2H),2.31(s,3H),1.80-1.60(m,4H),1.53-1.1.47(m,2H),1.19-1.09(m,2H),0.97(d,J=6.80Hz,3H),0.82(d,J=6.80Hz,3H),0.70(d,J=6.40Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.95(s,1H),7.76(d,J=8.00Hz,2H),7.28-7.16(m,4H),6.84-6.71(m,2H),5.49(d,J=7.60Hz,1H),3.84(t,J=4.80Hz,4H),3.08(t,J=4.80Hz,4H),2.33(s,3H),1.60-1.58(m,2H),1.50-1.46(m,1H),0.84(d,J=6.00Hz,3H),0.70(d,J=5.60Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-吗啉代吡啶-3-基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.29(s,1H),8.04(d,J=2.40Hz,1H),7.77(d,J=8.40Hz,2H),7.59(dd,J=2.80,9.20Hz,1H),7.23(d,J=8.40Hz,2H),6.52(d,J=8.80Hz,1H),5.90(d,J=8.00Hz,1H),3.92-3.86(m,1H),3.80(t,J=5.00Hz,4H),3.42(t,J=4.60Hz,4H),2.34(s,3H),1.60-1.48(m,3H),0.83(d,J=6.00Hz,3H),0.67(d,J=6.00Hz,3H)
(S)-N-(6-((2S,6R)-2,6-二甲基吗啉代)吡啶-3-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.03(d,J=2.40Hz,2H),8.00(s,1H),7.77(d,J=8.40Hz,2H),7.61(dd,J=2.80,9.20Hz,1H),7.26(d,J=8.00Hz,2H),6.53(d,J=9.20Hz,1H),5.48(d,J=7.60Hz,1H),4.13(q,J=7.20Hz,1H),3.95(dd,J=2.00,12.8Hz,2H),3.87-3.82(m,1H),3.72-3.68(m,2H),2.49-2.44(m,2H),2.35(s,3H),1.63-1.58(m,2H),1.52-1.47(m,1H),1.25(d,J=8.00Hz,6H),0.85(d,J=6.00Hz,3H),0.69(d,J=6.40Hz,3H)
(S)-N-(3-氟-4-吗啉代苯基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.81(s,1H),7.76(d,J=8.00Hz,2H),7.29(d,J=8.00Hz,2H),7.26-7.21(m,1H),6.98(d,J=6.00Hz,1H),6.85(t,J=9.00Hz,1H),4.90(d,J=7.20Hz,1H),3.86(t,J=4.60Hz,4H),3.77-3.72(m,1H),3.04(t,J=4.40Hz,4H),2.38(s,3H),1.67-1.43(m,3H),0.86(d,J=6.40Hz,3H),0.68(d,J=6.40Hz,3H)
(S)-N-(4-(1,1-二氧化硫代吗啉代)苯基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.07(s,1H),7.78(d,J=8.40Hz,2H),7.33(d,J=9.20Hz,2H),7.28(d,J=8.40Hz,2H),6.84(d,J=8.40Hz,2H),5.31(d,J=7.20Hz,1H),3.82-3.76(m,5H),3.10(t,J=5.20Hz,4H),2.37(s,3H),1.67-1.45(m,3H),0.84(d,J=6.40Hz,3H),0.65(d,J=6.40Hz,3H)
(S)-4-(5-(4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺基)吡啶-2-基)哌嗪-1-甲酸叔丁酯
1H-NMR(400MHz,CDCl3)δ8.15(s,1H),8.02(d,J=2.80Hz,1H),7.77(d,J=8.40Hz,2H),7.6(dd,J=2.80,9.20Hz,1H),7.25(d,J=8.40Hz,2H),6.55(d,J=9.20Hz,2H),5.58(d,J=8.00Hz,1H),3.89-3.84(m,1H),3.53-3.43(m,8H),2.33(s,3H),1.62-1.59(m,2H),1.52-1.48(m,10H),0.85(d,J=5.60Hz,3H),0.69(d,J=6.00Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(吡咯烷-1-基)苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.76(d,J=8.00Hz,2H),7.71(s,1H),7.23(d,J=8.00Hz,2H),7.08-7.04(m,2H),6.43-6.39(m,2H),5.47(d,J=7.60Hz,1H),3.85-3.79(m,1H),3.22(t,J=6.40Hz,4H),2.43(s,3H),2.03-1.96(m,4H),1.64-1.47(m,3H),0.86(d,J=6.40Hz,3H),0.74(d,J=6.40Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(2-吗啉代乙基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.76-7.73(m,2H),7.29(d,J=8.00Hz,2H),6.65(t,J=4.80Hz,1H),5.50(d,J=7.20Hz,1H),3.71-3.63(m,5H),3.29-3.23(m,1H),3.18-3.11(m,1H),2.46-2.37(m,9H),1.57-1.50(m,2H),1.44-1.39(m,1H),0.83(d,J=6.40Hz,3H),0.67(d,J=6.00Hz,3H)
(S)-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-硝基苯磺酰胺
1H-NMR(400MHz,CDCl3)δ8.62(t,J=2.00Hz,1H),8.43-8.40(m,1H),8.17-8.14(m,1H),7.73(t,J=8.00Hz,1H),5.82(d,J=10.0Hz,1H),4.28-4.22(m,1H),3.66-3.58(m,1H),3.57-3.51(m,2H),3.39-3.21(m,5H),1.97-1.90(m,1H),1.53-1.45(m,1H),1.25-1.18(m,1H),0.98(d,J=6.80Hz,3H),0.94(d,J=6.40Hz,3H)
(S)-3-氨基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.23(t,J=7.80Hz,1H),7.14-7.09(m,2H),6.80(dd,J=1.40,7.80Hz,1H),4.11-4.02(m,3H),3.61-3.53(m,2H),3.44-3.35(m,3H),3.29-3.20(m,3H),1.97-1.93(m,1H),1.51-1.41(m,1H),1.19-1.13(m,1H),0.95(d,J=6.00Hz,3H),0.91(d,J=6.80Hz,3H)
(S)-2-(4-氟苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.98(s,1H),7.91-7.87(m,2H),7.22-7.19(m,2H),7.12-7.07(m,2H),6.80(dd,J=2.20,6.60Hz,2H),5.74(d,J=7.60Hz,1H),3.85(t,J=5.00Hz,4H),3.09(t,J=4.80Hz,4H),1.63-1.57(m,2H),1.53-1.48(m,1H),0.86(d,J=6.40Hz,3H),0.73(d,J=6.00Hz,3H)
(S)-2-(4-溴苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.72(d,J=8.40Hz,2H),7.59(d,J=8.40Hz,2H),7.45(s,1H),7.18(d,J=9.20Hz,2H),6.85(d,J=8.80Hz,2H),5.19(d,J=8.00Hz,1H),3.86(t,J=4.60Hz,4H),3.82-3.77(m,1H),3.12(t,J=5.00Hz,4H),2.04-1.50(m,3H),0.90(d,J=6.40Hz,3H),0.8(d,J=5.60Hz,3H)
(S)-4-甲基-N-(4-吗啉代苯基)-2-(4-(三氟甲基)苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.99(d,J=8.00Hz,2H),7.68(s,1H),7.66(d,J=4.00Hz,2H),7.10(d,J=12.4Hz,2H),6.79(d,J=12.0Hz,2H),5.70(d,J=8.40Hz,1H),3.92-3.98(m,1H),3.85(t,J=4.80Hz,4H),3.09(t,J=4.80Hz,4H),1.67-1.54(m,3H),0.89(d,J=6.00Hz,3H),0.79(d,J=6.40Hz,3H)
(S)-4-甲基-N-(4-吗啉代苯基)-2-(3-硝基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.70(s,1H),8.26(d,J=8.00Hz,1H),8.0(d,J=8.20Hz,1H),7.95(s,1H),7.61(t,J=8.00Hz,1H),7.12(d,J=8.80Hz,2H),6.73(d,J=9.20Hz,2H)),6.15(d,J=8.80Hz,1H),4.07-4.03(m,1H),3.85(t,J=4.60Hz,4H),3.08(t,J=4.60Hz,4H),1.72-1.67(m,1H),1.60-1.56(m,2H),0.90(d,J=6.40Hz,3H),0.84(d,J=6.40Hz,3H)
(S)-4-甲基-N-(4-吗啉代苯基)-2-(萘-1-磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.82(d,J=8.40Hz,1H),8.38(dd,J=0.80,7.60Hz,1H),8.13(s,1H),8.09(d,J=8.00Hz,1H),7.99(d,J=8.00Hz,1H),7.76-7.65(m,2H),7.55(t,J=7.80Hz,1H),7.09-7.06(m,2H),6.79-6.76(m,2H),6.07(d,J=7.20Hz,1H),3.95-3.90(m,5H),3.13(t,J=4.60Hz,4H),1.65-1.61(m,1H),1.51-1.44(m,2H),0.76(d,J=6.00Hz,3H),0.50(d,J=6.80Hz,3H)
(S)-4-甲基-N-(4-吗啉代苯基)-2-(萘-2-磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.47(s,1H),7.96(s,1H),7.80-7.81(m,4H),7.62-7.52(m,2H),7.08-7.05(m,2H),6.68-6.64(m,2H),5.70(d,J=7.60Hz,1H),3.97-3.91(m,1H),3.83(t,J=4.80Hz,4H),3.04(t,J=4.80Hz,4H),1.63-1.48(m,3H),0.81(d,J=6.40Hz,3H),0.63(d,J=5.60Hz,3H)
(S)-4-甲基-N-(4-吗啉代苯基)-2-(苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.89(d,J=7.20Hz,2H),7.75(s,1H),7.56(t,J=7.40Hz,1H),7.49(t,J=7.40Hz,2H),7.24(d,J=9.20Hz,2H),6.82(d,J=9.20Hz,2H),5.20(d,J=7.20Hz,2H)),3.85(t,J=4.80Hz,4H),3.81-3.77(m,1H),3.10(t,J=4.80Hz,4H),1.66-1.46(m,3H),0.85(d,J=6.00Hz,3H),0.69(d,J=6.00Hz,3H)
(S)-4-甲基-2-(3-(苯基磺酰基)丙酰胺基)戊酸苄酯
1H-NMR(400MHz,CDCl3)δ7.50(s,1H),7.42-7.31(m,7H),6.88-6.84(m,2H),5.01(d,J=8.000Hz,1H),4.27(d,J=3.20Hz,2H),3.86-3.81(m,5H),3.12(t,J=4.80Hz,4H),1.74-1.60(m,2H),1.54-1.47(m,1H),0.93(d,J=6.40Hz,3H),0.90(d,J=6.40Hz,3H)
(S)-2-(4-甲氧基苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.10(s,1H),7.83-7.79(m,2H),7.26-7.22(m,2H),6.89-6.86(m,2H),6.80-6.76(m,2H),5.60(d,J=7.60Hz,1H),3.87-3.81(m,5H),3.76(s,3H),3.08(t,J=5.40Hz,4H),1.63-1.58(m,2H),1.51-1.47(m,1H),0.85(d,J=6.00Hz,3H),0.70(d,J=5.60Hz,3H)
(S)-4-甲基-N-(4-吗啉代苯基)-2-(噻吩-2-磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.73(s,1H),7.65(dd,J=1.20,4.00Hz,1H),7.58(dd,J=1.20,4.80Hz,1H),7.30-7.27(m,2H),7.05(dd,J=3.60,5.20Hz,1H),6.85-6.81(m,2H),5.34(s,1H),3.91-3.84(m,5H),3.11(t,J=5.00Hz,4H),1.72-1.51(m,3H),0.89(d,J=6.00Hz,3H),0.79(d,J=6.00Hz,3H)
(S)-4-甲基-N-(4-吗啉代苯基)-2-(4-硝基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.23-8.21(m,2H),8.03-8.00(m,2H),7.12(d,J=8.80Hz,2H),6.79(d,J=9.20Hz,2H),5.49(d,J=8.80Hz,1H),3.91-3.84(m,5H),3.10(t,J=4.80Hz,4H),1.76-1.70(m,1H),1.61-1.58(m,3H),0.93(d,J=6.80Hz,3H),0.87(d,J=6.80Hz,3H)
(S)-2-(4-异丙基苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.81-7.78(m,3H),7.31(d,J=8.40Hz,2H),7.26-7.21(m,2H),6.82-6.78(m,2H),5.17(d,J=6.40Hz,1H),3.85(t,J=4.00Hz,4H),3.79-3.77(m,1H),3.09(t,J=4.80Hz,4H),2.94-2.87(m,1H),1.68-1.44(m,3H),1.19(d,J=6.80Hz,6H),0.85(d,J=6.00Hz,3H),0.67(d,J=6.00Hz,3H)
(S)-2-(联苯-4-基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.94(d,J=8.20Hz,2H),7.87(brs,1H),7.59-7.64(m,2H),7.37-7.49(m,5H),7.15-7.20(m,2H),6.72(d,J=9.00Hz,2H),5.48-5.60(m,1H),3.87-3.95(m,1H),3.79-3.85(m,4H),2.98-3.05(m,4H),1.62-1.69(m,2H),1.51-1.60(m,1H),0.88(d,J=5.80Hz,3H),0.76(d,J=5.80Hz,3H)
(S)-4-(苄基氧基)-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.76-7.73(m,2H),7.41-7.32(m,5H),7.03-6.99(m,2H),5.55(d,J=10.0Hz,1H),5.11(s,2H),4.22-4.17(m,1H),3.78-3.39(m,13H),3.22-3.06(m,3H),1.97-1.90(m,1H),1.48-1.33(m,2H),0.92(d,J=4.00Hz,3H),0.89(d,J=4.80Hz,3H)
(S)-4-羟基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ8.20(s,1H),7.65(d,J=8.80Hz,2H),6.83(d,J=8.80Hz,2H),5.65(d,J=9.60Hz,1H),4.31-4.26(m,1H),3.84-3.19(m,16H),1.99-1.93(m,1H),1.53-1.52(m,2H),0.93(t,J=6.20Hz,6H)
(S)-4-(N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)氨磺酰基)苯甲酸苄酯
1H-NMR(400MHz,CDCl3)δ8.19-8.16(m,2H),7.92-7.89(m,2H),7.45-7.34(m,5H),5.76(d,J=9.20Hz,1H),5.37(s,2H),4.34-4.28(m,1H),3.82-3.76(m,1H),3.68-3.63(m,1H),3.58-3.07(m,14H),1.97-1.90(m,1H),1.50-1.34(m,2H),0.94(d,J=6.40Hz,3H),0.91(d,J=6.80Hz,3H)
(S)-3-(4-甲基苯基磺酰胺基)-4-吗啉代-4-氧代丁酸叔丁酯
1H-NMR(400MHz,CDCl3)δ7.72(d,J=8.40Hz,2H),7.31(d,J=7.60Hz,2H),5.89(d,J=9.60Hz,1H),4.55-4.498(m,1H),3.62-3.28(m,8H),2.55-2.40(m,4H),1.41(m,9H)
(S)-4-甲基-N-(1-吗啉代-1-氧代-3-苯基丙-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.68(d,J=4.80Hz,2H),7.23-7.29(m,5H),7.11-7.16(m,2H),5.88(d,J=9.60Hz,1H),4.29-4.35(m,1H),3.22-3.34(m,3H),3.05-3.14(m,2H),2.90-2.98(m,2H),2.74-2.81(m,1H),2.55-2.61(m,2H),2.40(s,3H)
(S)-N-(3-羟基-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.74(d,J=8.40Hz,2H),7.32(d,J=8.4Hz,2H),6.00(d,J=8.80Hz,1H),4.19-4.24(m,1H),3.52-3.68(m,4H),3.34-3.49(m,6H),2.82(q,J=4.30Hz,1H),2.44(s,3H)
(S)-4-甲基-N-(3-甲基-1-吗啉代-1-氧代丁-2-基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.69(d,J=8.40Hz,2H),7.29(d,J=8.40Hz,2H),5.66(d,J=9.20Hz,1H),3.81(q,J=4.80Hz,1H),3.51-3.58(m,2H),3.24-3.35(m,5H),3.10-3.17(m,1H),2.42(s,3H),1.76-1.84(m,1H),1.02(d,J=6.80Hz,3H),0.88(d,J=6.80Hz,3H)
(R)-N-(3-巯基-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.76(d,J=8.00Hz,2H),7.33(d,J=8.00Hz,2H),5.95(d,J=9.60Hz,1H),4.48-4.53(m,1H),3.54-3.63(m,2H),3.30-3.45(m,6H),2.95(dd,J=7.00,13.8Hz,1H),2.84(dd,J=6.20,14.2Hz,1H),2.44(s,3H)
(2S,3S)-3-羟基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丁酰胺
1H-NMR(400MHz,DMSO-d6)δ8.44(s,1H),7.77(d,J=7.20Hz,2H),7.28-7.30(m,3H),6.82(d,J=8.80Hz,2H),5.95(d,J=7.20Hz,1H),4.38-4.40(m,1H),3.84(t,J=4.60Hz,4H),3.77(dd,J=2.20,6.60Hz,1H),3.08-3.10(m,5H),2.39(s,3H),0.96(d,J=6.40Hz,3H)
(2S,3S)-3-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.57(s,1H),7.84(d,J=7.60Hz,1H),7.61(d,J=8.40Hz,2H),7.18(d,J=8.00Hz,2H),7.11(d,J=9.20Hz,2H),6.80(d,J=8.80Hz,2H),3.71(t,J=4.80Hz,4H),3.57(t,J=7.60Hz,1H),3.00(t,J=4.60Hz,4H),2.20(s,3H),1.50-1.63(m,2H),1.08-1.12(m,1H),0.76-0.79(m,6H)
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ9.63(s,1H),8.00(s,1H)7.66(d,J=7.60Hz,2H),7.23-7.29(m,4H),6.84(d,J=8.80Hz,2H),3.87(q,J=6.80Hz,1H),3.71(t,J=4.60Hz,4H),3.01(t,J=4.40Hz,4H),2.29(s,3H),1.12(d,J=7.20Hz,3H)
(S)-2-(4-甲基苯基磺酰胺基)-4-(甲硫基)-N-(4-吗啉代苯基)丁酰胺
1H-NMR(400MHz,DMSO-d6)δ10.06(s,1H),8.42(s,1H),8.03(d,J=8.00Hz,2H),7.63(d,J=8.40Hz,2H),7.59(d,J=9.20Hz,2H),7.21(d,J=8.80Hz,2H),4.26-4.29(m,1H),4.09(t,J=4.40Hz,4H),3.76(s,3H),3.39(t,J=4.60Hz,4H),2.74-2.87(m,2H),2.33(s,3H),2.05-2.25(m,2H)
(S)-3-(1H-吲哚-2-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.75(s,1H),9.64(s,1H),8.05(s,1H),7.50(d,J=8.00Hz,2H),7.39(d,J=7.60Hz,1H),7.27(d,J=8.40Hz,1H),7.18(d,J=9.20Hz,2H),7.09(d,J=8.40Hz,2H),7.06(d,J=2.00Hz,1H),7.02(t,J=7.40Hz,1H),6.91(t,J=7.20Hz,1H),6.81(d,J=8.80Hz,2H),3.99-4.06(m,1H),3.71(t,J=4.80Hz,4H),2.99-3.05(m,5H),2.79-2.85(m,1H),2.18(s,3H)
(S)-3-(1-甲基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.04(s,1H),7.48(d,J=8.20Hz,2H),7.17-7.31(m,5H),7.06(d,J=8.20Hz,2H),7.00(dt,J=1.10,7.20Hz,1H),6.82(d,J=9.00Hz,2H),6.76(s,1H),5.17(d,J=6.20Hz,1H),4.01(q,J=6.20Hz,1H),3.82-3.87(m,3H),3.67(s,2H),3.17(dd,J=2.93,6.46Hz,1H),3.07-3.12(m,2H),2.34(s,3H)
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-苯基丙酰胺
1H-NMR(400MHz,DMSO-d6)δ9.64(s,1H),8.11(s,1H),7.48(d,J=7.60Hz,2H),7.12-7.20(m,9H),6.81(d,J=8.40Hz,2H),4.03-4.05(m,1H),3.71(t,J=4.40Hz,4H),3.01(t,J=4.40Hz,4H),2.85-2.90(m,1H),2.70-2.73(m,1H),2.24(s,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酸苄酯
1H-NMR(400MHz,CDCl3)δ7.66-7.73(m,2H),7.30-7.38(m,3H),7.15-7.24(m,4H),5.20(d,J=10.1Hz,1H),4.79-4.89(m,2H),3.98(ddd,J=6.20,8.30,10.0Hz,1H),2.39(s,3H),1.72-1.85(m,1H),1.43-1.55(m,2H),0.87(dd,J=6.60,7.80Hz,6H)
(S)-4-甲基-2-(4-甲基苯甲酰胺基)戊酸苄酯
1H-NMR(400MHz,CDCl3)δ7.69(d,J=8.00Hz,2H),7.39-7.32(m,5H),7.24(d,J=8.40Hz,2H),6.48(d,J=7.60Hz,1H),5.20(d,J=1.20Hz,2H),4.93-4.87(m,1H),2.40(s,3H),1.80-1.62(m,3H),0.97(d,J=6.00Hz,3H),0.95(d,J=6.00Hz,3H)
(S)-2-(4-叔丁基苯甲酰胺基)-4-甲基戊酸苄酯
1H-NMR(400MHz,CDCl3)δ7.74-7.72(m,2H),7.52-7.44(m,2H),7.37-7.31(m,5H),6.49(d,J=8.40Hz,1H),5.19(s,2H),4.94-4.88(m,1H),1.78-1.63(m,3H),1.33(s,9H),0.97(d,J=6.00Hz,3H),0.94(d,J=5.60Hz,3H)
(S)-2-(苯并[d][1,3]二氧杂环戊烯-5-甲酰胺基)-4-甲基戊酸苄酯
1H-NMR(400MHz,CDCl3)δ7.71(dd,J=2.00,8.00Hz,1H),7.51(d,J=2.00Hz,1H),7.38-7.33(m,5H),6.86(d,J=8.40Hz,1H),6.06(s,2H),5.16(d,J=1.20Hz,2H),3.56-3.52(m,1H),1.78-1.73(m,1H),1.63-1.56(m,1H),1.48-1.41(m,1H),0.93(d,J=6.40Hz,3H),0.91(d,J=6.80Hz,3H)
(S)-2-(4-(叔丁氧基羰基氨基)苯甲酰胺基)-4-甲基戊酸苄酯
1H-NMR(400MHz,CDCl3)δ7.75-7.72(m,2H),7.43(d,J=8.40Hz,2H),7.39-7.31(m,5H),6.61(s,1H),6.43(d,J=8.40Hz,1H),5.19(d,J=2.00Hz,2H),4.92-4.86(m,1H),1.78-1.62(m,3H),0.97(d,J=6.00Hz,3H),0.95(d,J=6.40Hz,3H)
(S)-4-甲基-2-(3-(苯基磺酰基)丙酰胺基)戊酸苄酯
1H-NMR(400MHz,CDCl3)δ7.91-7.89(m,2H),7.68-7.54(m,3H),7.38-7.31(m,5H),5.97(d,J=8.00Hz,1H),5.14(s,2H),4.61-4.56(m,1H),3.46-3.40(m,2H),2.71-2.66(m,2H),1.64-1.50(m,3H),0.90(d,J=5.60Hz,6H)
(S)-N-(4-(4-甲氧基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.54(brs,1H),7.75(t,J=7.60Hz,4H),7.26(d,J=8.20Hz,2H),6.99(d,J=0.70Hz,1H),6.95(d,J=8.20Hz,2H),5.19(d,J=7.00Hz,1H),3.91(d,J=5.00Hz,1H),3.84(d,J=0.70Hz,3H),2.32(s,3H),1.53-1.63(m,2H),1.43-1.51(m,1H),0.84(d,J=5.80Hz,3H),0.68(d,J=5.80Hz,3H)
(S)-1-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-苯基脲
1H-NMR(400MHz,CDCl3)δ7.80(s,1H),7.26-7.17(m,4H),6.94-6.90(m,1H),6.72(d,J=8.80Hz,1H),5.03-4.97(m,1H),3.81-3.57(m,8H),1.84-1.77(m,1H),1.61-1.43(m,2H),0.90(d,J=3.60Hz,3H),0.87(d,J=7.20Hz,3H)
(S)-4-叔丁基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯甲酰胺
1H-NMR(400MHz,DMSO-d6)δ8.40(s,1H),7.81(d,J=8.00Hz,2H),7.45(d,J=8.80Hz,2H),4.82-4.73(m,1H),3.53-3.42(m,8H),1.74-1.50(m,3H),1.28(s,9H),0.89(d,J=6.80Hz,6H)
(S)-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-(苯基磺酰基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ8.30(d,J=8.80Hz,1H),7.88-7.86(m,2H),7.75(t,J=8.00Hz,1H),7.65(d,J=8.00Hz,2H),4.66-4.61(m,1H),3.52-3.25(m,10H),2.46-2.42(m,2H),1.52-1.46(m,1H),1.38-1.33(m,2H),0.82(d,J=6.60Hz,6H)
(S)-4-叔丁基-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯甲酰胺
1H-NMR(400MHz,MeOD)δ7.81(d,J=8.00Hz,2H),7.51(t,J=8.80Hz,2H),7.45(d,J=8.80Hz,2H),6.94(d,J=8.80Hz,2H),4.85-4.81(m,1H),3.82(t,J=5.00Hz,3H),3.10(t,J=4.80Hz,3H),1.82-1.62(m,3H),1.28(s,9H),1.03(d,J=6.60Hz,6H)
(S)-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯并[d][1,3]二氧杂环戊烯-5-甲酰胺
1H-NMR(400MHz,DMSO-d6)δ9.84(s,1H),8.35(d,J=7.60Hz,1H),7.52-7.44(m,4H),6.97(d,J=8.40Hz,1H),6.87(d,J=9.20Hz,2H),6.08(d,J=2.40Hz,2H),4.60-4.54(m,1H),3.71(d,J=4.80Hz,4H),3.02(t,J=4.80Hz,4H),1.74-1.50(m,3H),0.92(d,J=6.80Hz,3H),0.89(d,J=6.40Hz,3H)
(S)-4-甲基-N-(4-吗啉代苯基)-2-(3-(苯基磺酰基)丙酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.69-8.63(m,1H),7.87(d,J=7.20Hz,2H),7.71-7.32(m,5H),7.18-6.60(m,3H),4.59-4.55(m,1H),3.82(t,J=5.00Hz,3H),3.54-3.48(m,2H),3.06(t,J=4.80Hz,3H),2.75-2.73(m,2H),1.85-1.56(m,3H),0.89(d,J=6.2Hz,6H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.44(s,1H),10.78(s,1H),8.51(brs,1H),7.82-7.80(d,J=8.50Hz,2H),7.47-7.37(m,6H),7.28-7.26(d,J=8.00Hz),7.08-6.90(m,5H),4.32(brs,1H),3.79(s,3H),3.33(s,2H),3.11-3.07(dd,J=14.5,6.00Hz,1H),2.90-2.85(dd,J=14.0,8.50Hz,1H)
(S)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.3(s,1H),10.7(s,1H),8.24-8.22(d,J=8.50Hz,1H),7.95-7.93(d,J=8.50Hz,1H),7.50-7.48(d,J=8.50Hz,2H),7.15-7.09(m,4H),6.97-6.95(d,J=8.00Hz,1H),6.74-6.58(m,6H),4.01-3.96(q,J=7.50Hz,1H),3.47(s,3H),2.79-2.74(dd,J=14.2,7.00Hz,1H),2.56-2.51(dd,J=14.5,8.00Hz,1H),1.86(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(2-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.27(s,1H),7.86-7.83(m,2H),7.33-7.29(m,3H),7.20-7.14(m,4H),7.01-6.95(m,2H),6.91(d,J=2.40Hz,4H),6.80-6.78(m,2H),5.38(d,J=5.60Hz,1H),4.00-3.95(m,1H),3.83(t,J=4.60Hz,4H),3.27-3.14(m,2H),3.07(t,J=5.00Hz,4H),2.23(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(3-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.76(s,1H),9.70(s,1H),8.11(s,1H),7.45-7.39(m,3H),7.28-7.19(m,5H),7.06-7.00(m,2H),6.93-6.89(m,1H),6.81(d,J=8.80Hz,2H),4.09-4.07(m,1H),3.71(t,J=4.80Hz,4H),3.05-2.99(m,5H),2.85-2.79(m,1H),2.14(s,3H)
(S)-2-(3,5-二甲基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.77(s,1H),9.71(s,1H),8.04(s,1H),7.42(d,J=8.00Hz,1H),7.28-7.22(m,5H),7.07-7.00(m,3H),6.92(t,J=7.40Hz,1H),6.82(d,J=9.20Hz,2H),4.11-4.07(m,1H),3.71(t,J=4.80Hz,4H),3.05-2.99(m,5H),2.85-2.80(m,1H),2.12(s,6H)
(S)-2-(4-氟苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.77(d,J=2.00Hz,1H),9.75(s,1H),8.26(s,1H),7.62-7.59(m,2H),7.46(d,J=8.00Hz,1H),7.28-7.22(m,3H),7.09-7.01(m,4H),6.93(t,J=7.40Hz,1H),6.85-6.81(m,2H),4.10(s,1H),3.72(t,J=4.80Hz,4H),3.07-3.01(m,5H),2.89-2.83(m,1H)
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(4-(三氟甲基)苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.77(d,J=1.60Hz,1H),9.79(s,1H),8.55(s,1H),7.72(d,J=8.80Hz,2H),7.57(d,J=8.40Hz,2H),4.47(d,J=8.00Hz,1H),7.25(d,J=7.60Hz,1H),7.19(d,J=9.20Hz,2H),7.11(d,J=2.40Hz,1H),7.02(t,J=7.60Hz,1H),6.92(t,J=7.40Hz,1H),6.81(d,J=9.20Hz,2H),4.14(s,1H),3.72(t,J=4.60Hz,4H),3.08-2.99(m,5H),2.92-2.86(m,1H)
(S)-3-(5-羟基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.45(d,J=2.00Hz,1H),9.63(s,1H),8.54(s,1H),8.02(s,1H),7.53(d,J=8.00Hz,2H),7.18(d,J=9.20Hz,2H),7.11(d,J=8.20Hz,2H),7.07(d,J=8.40Hz,1H),6.97(d,J=2.40Hz,1H),6.81(d,J=8.00Hz,2H),6.77(d,J=2.00Hz,1H),6.57(dd,J=2.00,8.40Hz,1H),4.09-4.06(s,1H),3.72(t,J=4.80Hz,4H),3.01(t,J=5.00Hz,4H),2.96-2.91(m,1H),2.76-2.70(m,1H),2.23(s,3H)
(S)-N-(3-(1H-吲哚-3-基)-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺
1H-NMR(400MHz,CDCl3)δ8.19(brs,1H),7.67-7.71(m,2H),7.48(d,J=7.83Hz,1H),7.34(d,J=8.22Hz,1H),7.25(d,J=7.83Hz,2H),7.18(dt,J=1.17,7.63Hz,1H),7.07-7.12(m,1H),7.06(d,J=1.96Hz,1H),5.92(d,J=9.78Hz,1H),4.42(dt,J=5.28,9.88Hz,1H),3.19-3.34(m,4H),3.08-3.15(m,1H),2.86-2.98(m,2H),2.75(m,1H),2.62-2.70(m,1H),2.50-2.56(m,1H),2.39(s,3H),2.19(m,1H).
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(5-吗啉代噻唑-2-基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.20-8.24(m,1H),7.54(d,J=8.22Hz,2H),7.20(d,J=8.22Hz,2H),7.01-7.10(m,3H),6.91(t,J=7.43Hz,1H),6.86(d,J=2.35Hz,1H),6.48(s,1H),6.17-6.23(m,1H),4.27(d,J=6.65Hz,1H),3.78(t,J=4.70Hz,4H),3.16(d,J=6.65Hz,2H),2.87-2.99(m,4H),2.25(s,3H)
(S)-2-(2,4-二甲基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.75(s,1H),9.58(s,1H),7.98(s,1H),7.54(d,J=8.00Hz,1H),7.38(d,J=8.00Hz,1H),7.28(d,J=8.40Hz,1H),7.19(d,J=9.20Hz,2H),7.08(d,J=2.40Hz,1H),7.02(t,J=7.40Hz,1H),6.90-6.81(m,5H),4.05-4.03(m,1H),3.72(t,J=4.60Hz,4H),3.04-3.00(m,5H),2.90-2.85(m,1H),2.39(s,3H),2.15(s,3H)
3-(3-乙氧基-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)-1H-吲哚-5-羧酸
1H-NMR(400MHz,CDCl3)δ12.37(s,1H),11.17(s,1H),8.37(d,J=8.40Hz,1H),8.01(s,1H),7.68(dd,J=1.40,8.60Hz,1H),7.48(d,J=8.00Hz,1H),7.35(d,J=8.40Hz,1H),7.20-7.08(m,3H),3.96-3.90(m,1H),3.08-3.06(m,1H),2.94-2.88(m,1H),2.31(s,1H),0.86(t,J=6.60Hz,3H)
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-(1-甲苯磺酰基-1H-咪唑-4-基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.62(s,1H),7.84(s,1H),7.71(t,J=8.40Hz,4H),7.29-7.23(m,6H),6.98(s,1H),6.89(d,J=6.40Hz,1H),6.83(dt,J=8.80Hz,2H),3.99-3.97(m,1H),3.85(t,J=4.80Hz,4H),3.10(t,J=4.80Hz,4H),3.01(dd,J=5.60,15.2Hz,1H),2.61(dd,J=4.80,14.8Hz,1H),2.40(d,J=8.40Hz,6H)
(S)-N-(6-((2S,6R)-2,6-二甲基吗啉代)吡啶-3-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.14(brs,1H),8.00(d,J=2.35Hz,1H),7.86(s,1H),7.62(dd,J=2.74,9.00Hz,1H),7.49-7.53(m,2H),7.33(dd,J=3.91,7.83Hz,2H),7.20(t,J=7.63Hz,1H),7.08-7.12(m,2H),7.02(t,J=7.63Hz,1H),6.96(d,J=1.96Hz,1H),6.57(d,J=9.00Hz,1H),5.11(d,J=6.26Hz,1H),4.05(q,J=6.52Hz,1H),3.97(d,J=11.35Hz,2H),3.67-3.77(m,2H),3.12-3.28(m,2H),2.45-2.53(m,2H),2.36(s,3H),1.27(d,J=6.26Hz,6H)
(R)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.80(brs,1H),8.27(s,1H),7.97(s,2H),7.45-7.48(m,2H),7.32(d,J=7.83Hz,1H),7.29(d,J=3.52Hz,1H),7.22(s,1H),7.13(t,J=7.43Hz,1H),7.00(d,J=8.22Hz,2H),6.94(s,1H),6.78-6.81(m,J=9.00Hz,2H),5.57(d,J=6.65Hz,1H),4.05(d,J=6.65Hz,1H),3.80-3.86(m,4H),3.19(dd,J=6.46,13.50Hz,2H),3.05-3.10(m,4H),2.28(s,3H)
(S)-N-(3-氟-4-吗啉代苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.78(s,1H),9.90(s,1H),8.16(brs,1H),7.51(d,J=8.22Hz,2H),7.40(d,J=7.83Hz,1H),7.29(d,J=7.83Hz,1H),7.22(dd,J=2.15,15.1Hz,1H),7.09(d,J=8.61Hz,3H),7.04(t,J=7.63Hz,1H),6.89-6.99(m,3H),4.06(brs,1H),3.70-3.74(m,4H),3.04(dd,J=6.85,14.3Hz,1H),2.90-2.94(m,4H),2.85(dd,J=7.40,14.4Hz,1H),2.21(s,3H)
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(4-硝基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.71(brs,1H),9.90(s,1H),8.66(brs,1H),7.84-7.90(m,2H),7.56-7.61(m,2H),7.48(d,J=7.83Hz,1H),7.29-7.35(m,J=9.00Hz,2H),7.12(d,J=7.83Hz,1H),7.05-7.08(m,1H),6.87-6.96(m,2H),6.81-6.86(m,2H),4.13(dd,J=5.28,9.19Hz,1H),3.70-3.75(m,4H),2.98-3.05(m,5H),2.88(dd,J=9.78,14.5Hz,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.77(brs,1H),9.77(s,1H),8.35(brs,1H),7.40-7.48(m,5H),7.28(d,J=8.22Hz,1H),7.19-7.24(m,2H),7.07-7.11(m,1H),7.04(t,J=7.43Hz,1H),6.91-6.96(m,1H),6.81-6.86(m,2H),4.10(t,J=7.24Hz,1H),3.69-3.75(m,4H),3.00-3.08(m,5H),2.86(dd,J=8.41,14.28Hz,1H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲氧基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.78(brs,1H),9.67(s,1H),7.99(brs,1H),7.54(d,J=8.61Hz,2H),7.41(d,J=7.83Hz,1H),7.28(d,J=8.22Hz,1H),7.22(d,J=9.00Hz,2H),7.07-7.10(m,1H),7.03(t,J=7.63Hz,1H),6.90-6.95(m,1H),6.81(t,J=9.59Hz,4H),4.06(brs,1H),3.70-3.74(m,4H),3.69(s,3H),2.98-3.07(m,5H),2.80-2.90(m,1H)
(S)-3-(1H-吲哚-3-基)-2-(4-异丙基苯基磺酰胺基)-N-(4吗啉代苯基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.09(brs,1H),8.03(s,1H),7.81(s,1H),7.58-7.62(m,2H),7.33-7.38(m,2H),7.18-7.25(m,5H),7.05(t,J=7.43Hz,1H),6.97(d,J=2.35Hz,1H),6.80-6.85(m,J=9.00Hz,2H),5.11(d,J=6.26Hz,1H),4.08(d,J=6.26Hz,1H),3.83-3.89(m,4H),3.34(dd,J=6.06,14.28Hz,1H),3.09-3.16(m,5H),1.25(dd,J=2.35,7.04Hz,6H)
(S)-3-(1H-吲哚-3-基)-2-(4-异丙基苯基磺酰胺基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(400MHz,CDCl3)δ7.74(d,J=8.40Hz,2H),7.67(d,J=7.60Hz,2H),7.21(t,J=6.80Hz,4H),7.04(s,1H),3.98-3.95(m,1H),2.37(s,1H),2.26(m,3H),1.64-1.49(m,3H),0.85(d,J=6.40Hz,3H),0.72(d,J=6.40Hz,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-甲基噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.13(s,1H),10.83(s,1H),8.26-8.24(d,J=8.50Hz,1H),7.45-7.44(d,J=8.00Hz,2H),7.39-7.38(d,J=7.50Hz,1H),7.29-7.27(d,J=8.00Hz,1H),7.06-7.02(m,4H),6.91-6.89(m,1H),6.72(s,1H),4.27-4.22(m,1H),3.07-3.03(dd,J=14.2,7.50Hz,1H),2.86-2.81(dd,J=14.2,8.00Hz,1H),2.24(s,3H),2.22(s,3H)
(S)-N-(苯并[d]噻唑-2-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.4(s,1H),10.8(s,1H),8.32(m,1H),7.91(m,1H),7.72(m,1H),7.47-7.44(m,6H),7.03-6.91(m,5H),4.34(brs,1H),3.11(m,1H),2.91(m,1H),2.08(s,3H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酸
1H-NMR(500MHz,DMSO-d6)δ12.73(brs,1H),10.80(s,1H),8.41-8.39(d,J=8.50Hz,1H),7.51-7.49(d,J=8.50Hz,2H),7.42-7.40(d,J=8.00Hz,2H),7.32-7.29(t,J=8.00Hz,2H),7.08-7.03(m,2H),6.94-6.91(t,J=7.50Hz,1H),3.94-3.89(m,1H),3.10-3.08(dd,J=14.5,6.00Hz,1H),2.89-2.84(dd,J=14.0,8.50Hz,1H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(5-吗啉代噻唑-2-基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.71(d,J=8.00Hz,2H),7.16(d,J=8.00Hz,2H),6.95(s,1H),6.35(d,J=10.0Hz,1H),4.14-4.06(m,1H),3.86(t,J=4.80Hz,4H),3.13-3.07(m,4H),2.29(s,3H),1.75-1.70(m,1H),1.60-1.53(m,1H),1.46-1.41(m,1H),0.81(d,J=6.80Hz,6H)
(S)-N-(5-(4-甲氧基苯基)-1,3,4-噻二唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ13.52(s,1H),8.14(d,J=8.80Hz,1H),7.92-7.88(m,2H),7.68(d,J=8.40Hz,2H),7.18(d,J=8.40Hz,2H),7.07-7.04(m,2H),4.36-4.29(m,1H),3.91(s,3H),2.21(s,3H),1.84-1.79(m,1H),1.72-1.64(m,1H),1.59-1.54(m,1H),0.89(d,J=6.40Hz,3H),0.86(d,J=6.80Hz,1H)
(S)-N-(5-(4-甲氧基苯基)异噁唑-3-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ10.55(s,1H),7.80-7.76(m,4H),7.19-7.15(m,3H),6.99(d,J=9.20Hz,2H),6.43(d,J=9.20Hz,1H),4.22-4.16(m,1H),3.86(s,3H),2.21(s,3H),1.88-1.83(m,1H),1.72-1.59(m,2H),0.91(d,J=6.80Hz,3H),0.88(d,J=6.40Hz,3H).
(S)-N-(3-(4-甲氧基苯基)异噁唑-5-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.22(s,1H),7.78(d,J=8.40Hz,2H),7.74-7.71(m,2H),7.30(d,J=8.00Hz,2H),6.98-6.94(m,2H),6.56(s,1H),5.40(d,J=7.20Hz,1H),3.97-3.92(m,1H),3.85(s,3H),2.35(s,3H),1.64-1.47(m,3H),0.83(d,J=6.40Hz,3H),0.66(d,J=5.60Hz,1H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.69(s,1H),7.91(d,J=8.40Hz,2H),7.79(d,J=8.40Hz,2H),7.65(d,J=8.40Hz,2H),7.29-7.26(m,2H),7.23(s,1H),5.26(d,J=6.80Hz,1H),3.97-3.92(m,1H),2.33(s,3H),1.67-1.45(m,3H),0.83(d,J=6.40Hz,3H),0.65(d,J=6.40Hz,3H)
(S)-N-(4-(3,4-二甲氧基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.74(s,1H),7.76(d,J=7.60Hz,2H),7.38-7.34(m,2H),7.26(d,J=6.80Hz,2H),7.01(s,1H),6.90(d,J=8.00Hz,1H),5.40(d,J=6.80Hz,1H),4.19-4.10(m,1H),3.95(s,3H),3.90(s,3H),2.32(s,3H),1.60-1.42(m,3H),0.80(d,J=6.00Hz,3H),0.63(d,J=5.60Hz,3H)
(S)-N-(4-(2-溴-4-氟苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.62(s,1H),7.78-7.75(m,4H),7.26(s,1H),7.10-7.05(m,3H),5.31(d,J=7.60Hz,1H),3.95-3.92(m,1H),2.32(s,3H),1.64-1.46(m,3H),0.82(d,J=6.40Hz,3H),0.66(d,J=6.00Hz,3H).
(S)-4-(2-氨基噻唑-4-基)苯基4-甲基-2-(4-甲基苯基磺酰胺基)戊酸酯
1H-NMR(400MHz,CDCl3)δ7.79(d,J=7.60Hz,2H),7.67(d,J=7.60Hz,2H),7.29(d,J=7.20Hz,2H),6.68(d,J=7.60Hz,2H),6.65(s,1H),5.53(d,J=9.20Hz,1H),5.27(s,2H),4.16-4.11(m,1H),2.41(m,3H),1.90-1.87(m,1H),1.63-1.60(m,1H),1.27-1.24(m,1H),0.94(s,6H)
(S)-N-(4-(4-氟苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.58(s,1H),7.79-7.76(m,3H),7.28-7.26(m,2H),7.11-7.06(m,2H),5.20(d,J=6.80Hz,2H),5.27(s,2H),3.93-3.91(m,1H),2.41(m,3H),1.66-1.46(m,3H),0.83(d,J=6.40Hz,3H),0.65(d,J=6.40Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲氧基)苯基)噻唑-2-基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.60(s,1H),7.83(d,J=8.80Hz,2H),7.79(d,J=8.00Hz,2H),7.29-7.23(m,4H),7.13(s,1H),5.21(d,J=6.80Hz,1H),3.93(s,1H),2.33(m,3H),1.65-1.48(m,3H),0.83(d,J=6.40Hz,3H),0.64(d,J=6.00Hz,3H)
(S)-N-(4-(4-羟基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.72(d,J=8.00Hz,2H),7.64(d,J=8.80Hz,2H),7.20(d,J=8.00Hz,2H),6.93(s,1H),6.88(d,J=8.40Hz,2H),3.97-3.93(m,1H),2.25(s,3H),1.65-1.51(m,3H),0.88(d,J=6.40Hz,3H),0.75(d,J=6.00Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-对甲苯基噻唑-2-基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.74(d,J=8.40Hz,2H),7.67(d,J=7.60Hz,2H),7.21(t,J=6.80Hz,4H),7.04(s,1H),3.98-3.95(m,1H),2.37(s,1H),2.26(m,3H),1.64-1.49(m,3H),0.85(d,J=6.40Hz,3H),0.72(d,J=6.40Hz,3H)
(S)-N-(4-(4-((S)-1-甲氧基丙-2-基氧基)苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ9.97(s,1H),7.74(d,J=8.40Hz,2H),7.69(d,J=8.80Hz,2H),7.23(d,J=8.00Hz,2H),6.97(s,1H),6.95(d,J=9.20Hz,2H),5.71(d,J=7.60Hz,1H),4.58-4.54(m,1H),4.00-3.94(m,1H),3.60-3.46(m,2H),3.40(s,3H),2.28(s,3H),1.56-1.40(m,3H),1.31(d,J=6.00Hz,3H),0.78(d,J=6.00Hz,3H),0.66(d,J=5.60Hz,3H)
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-吗啉代苯基)噻唑-2-基)戊酰胺
1H-NMR(400MHz,CDCl3)δ8.28(dd,J=9.00,11.4Hz,4H),7.19(d,J=8.40Hz,2H),6.95(t,J=4.60Hz,3H),4.13-3.95(m,1H),3.89(t,J=4.80Hz,3H),3.21(t,J=5.00Hz,3H),2.25(s,3H),1.67-1.64(m,1H),1.55-1.51(m,2H),0.88(d,J=6.80Hz,3H),0.75(d,J=6.40Hz,3H)
(S)-4-(2-(4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺基)噻唑-4-基)苯甲酸甲酯
1H-NMR(400MHz,CDCl3)δ10.05(s,1H),8.18(d,J=8.00Hz,2H),7.93(d,J=8.40Hz,2H),7.76(d,J=8.00Hz,2H),7.26(s,1H),7.20(d,J=8.00Hz,2H),5.63(d,J=8.00Hz,1H),4.12-4.09(m,1H),3.99(s,3H),2.24(s,3H),1.65-1.52(m,1H),0.86(d,J=5.60Hz,3H),0.74(d,J=5.60Hz,3H)
(S)-4-(2-(4-甲基苯基磺酰胺基)-3-(4-吗啉代苯基氨基)-3-氧代丙基)苯基4-甲基苯磺酸酯
1H-NMR(400MHz,DMSO-d6)δ9.62(s,1H),9.18(s,1H),8.05(s,1H),7.49(d,J=8.00Hz,2H),7.15(d,J=8.40Hz,4H),6.93(d,J=8.40Hz,2H),6.83(d,J=9.20Hz,2H),6.58(d,J=8.00Hz,2H),3.95(m,1H),3.72(t,J=4.60Hz,4H),3.02(t,J=4.60Hz,4H),2.78-2.58(m,2H),2.25(s,3H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-咪唑-4-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)7.80-7.71(d,J=9.00Hz,2H),7.59(s,4H),7.45-7.41(d,J=15.0Hz 2H),6.98-6.96(d,J=11.5Hz,2H),6.75(brs,1H),4.31-4.28(t,J=7.50Hz,1H),3.77(s,3H),2.92-2.90(dd,J1=14.0,7.00Hz,1H),2.77-2.73(dd,J=14.0,7.50Hz,1H)
(S)-N-甲氧基-N,4-二甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
1H-NMR(400MHz,CDCl3)δ7.72(d,J=8.00Hz,2H),7.27(d,J=8.40Hz,2H),5.40(d,J=10.4Hz,1H),4.28(t,J=10.4Hz,1H),3.56(s,3H),2.92(s,3H),2.40(m,3H),1.92-1.89(m,1H),1.45-1.39(m,3H),1.31-1.24(m,1H),0.91(d,J=6.40Hz,6H)
(S)-3-(1H-吲哚-3-基)-N-甲氧基-N-甲基-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.00(s,1H),7.54(d,J=8.40Hz,2H),7.44(d,J=7.60Hz,1H),7.31(d,J=8.00Hz,1H),7.16(t,J=7.40Hz,1H),7.11-7.03(m,4H),5.46(d,J=9.60Hz,1H),4.61-4.55(m,1H),3.45(s,3H),3.17-3.12(m,1H),3.05-3.00(m,1H),2.95(s,3H),2.34(m,3H)
(S)-N-(3-(1H-吲哚-3-基)-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)丙-2-基)-4-甲基苯磺酰胺
1H-NMR(400MHz,CDCl3)δ8.25(s,1H),7.60(d,J=8.40Hz,2H),7.47(d,J=8.00Hz,1H),7.29-7.26(m,1H),7.14-7.02(m,5H),5.86(d,J=9.60Hz,1H),4.66-4.60(m,1H),3.67-3.63(m,1H),3.58-3.36(m,13H),3.25-2.97(m,4H)
(S)-2-(4-叔丁基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,CD3OD)δ7.94(s,1H),7.58-7.62(m,2H),7.39(d,J=7.83Hz,1H),7.30-7.34(m,2H),7.25(d,J=7.83Hz,1H),6.99-7.04(m,4H),6.90(s,1H),6.77(d,J=9.00Hz,2H),4.06(s,1H),3.75-3.79(m,4H),3.12-3.20(m,1H),2.98-3.05(m,5H),1.18(s,9H)
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(2-氯苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.89-2.93(dd,J=14.67,8.80Hz,1H),3.10-3.14(dd,J=14.18,6.35Hz,1H),4.34(brs,1H),6.91-6.94(t,J=7.33Hz,1H),7.04-7.07(t,J=7.82Hz,1H),7.11(s,1H),7.28-7.30(d,J=8.31Hz,1H),7.37-7.45(m,6H),7.47-7.49(d,J=7.82Hz,1H),7.55-7.57(d,J=7.82Hz,1H),7.60(s,1H),7.81-7.83(m,1H),8.55(brs,1H),10.80(brs,1H),12.53(brs,1H)
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(2,4-二甲氧基苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.85-2.90(dd,J=14.18,8.80Hz,1H),3.08-3.12(dd,J=14.67,6.35Hz,1H),3.80(s,3H),3.90(s,3H),4.32-4.34(d,J=6.35Hz,1H),6.61-6.63(d,J=8.80Hz,1H),6.66(s,1H),6.90-6.93(t,J=7.33Hz,1H),7.03-7.06(t,J=7.33Hz,1H),7.08(s,1H),7.26-7.28(d,J=7.82Hz,1H),7.36-7.40(m,4H),7.47-7.48(m,2H),7.96-7.98(d,J=8.80Hz,1H),8.51-8.52(d,J=6.84Hz,1H),10.78(s,1H),12.39(s,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.34(s,1H),10.80(s,1H),8.53(s,1H),7.48-7.45(m,2H),7.40-7.36(m,4H),7.30-7.27(m,1H),7.23-7.20(m,1H),7.10-7.02(m,2H),6.95-6.90(m,1H),4.33(brs,1H),3.12-3.07(m,1H),2.92-2.86(m,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(5-甲基噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.10(s,1H),10.80(s,1H),8.50-8.45(d,J=8.00Hz,1H),7.46-7.45(d,J=7.50Hz,1H),7.41-7.36(m,4H),7.29-7.27(d,J=8.00Hz,1H),7.11-7.03(m,3H),6.93-6.90(t,J=7.00Hz,1H),4.32-4.27(m,1H),3.08-3.04(dd,J=14.20,6.50Hz,1H),2.89-2.85(dd,J=14.20,8.50Hz,1H),2.52(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-甲基噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.2(s,1H),10.8(s,1H),8.53-8.52(d,J=8.50Hz,1H),7.45-7.44(d,J=8.00Hz,1H),7.39(m,4H),7.28-7.27(d,J=8.00Hz,1H),7.07-7.02(m,2H),6.92-6.90(t,J=7.00Hz,1H),6.75(s,1H),4.29-4.25(m,1H),3.09-3.05(dd,J=14.2,6.00Hz,1H),2.89-2.85(dd,J=14.7,8.00Hz,1H),2.52(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(5-甲基噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.01(s,1H),10.79(s,1H),8.25(d,J=8.00Hz,1H),7.46-7.44(m,2H),7.40-7.39(d,J=7.50Hz,1H),7.29-7.27(d,J=8.00Hz,1H),7.10-7.02(m,5H),6.93-6.90(m,1H),4.28-4.26(m,1H),3.04-3.03(dd,J=14.2,7.00Hz,1H),2.86-2.84(dd,J=14.2,7.00Hz,1H),2.32(s,3H),2.22(s,3H)
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸甲酯
1H-NMR(400MHz,DMSO-d6)δ10.74(s,1H),9.77(s,1H),8.44(s,1H),7.74(d,J=8.40Hz,2H),7.62(d,J=8.00Hz,2H),7.44(d,J=7.20Hz,1H),7.22(t,J=8.40Hz,3H),7.08(d,J=2.00Hz,1H),6.99(d,J=7.40Hz,1H),6.90(t,J=7.20Hz,1H),6.81(d,J=9.20Hz,2H),4.13-4.09(m,1H),3.72(t,J=4.60Hz,4H),3.05-3.00(m,5H),2.89-2.83(m,1H)
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸乙酯
1H-NMR(400MHz,DMSO-d6)δ10.74(s,1H),9.76(s,1H),7.73(d,J=8.80Hz,2H),7.62(d,J=8.40Hz,2H),7.44(d,J=7.60Hz,1H),7.23-7.20(m,3H),7.09(d,J=2.40Hz,1H),7.00-6.81(m,2H),6.81(d,J=9.20Hz,2H),4.31(d,J=7.10Hz,2H),4.12-4.09(m,1H),3.72(t,J=4.60Hz,4H),3.05-3.00(m,5H),2.89-2.83(m,1H),1.34(t,J=7.00Hz,3H)
(S)-3-(4-苯甲酰基苯基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ9.75(s,1H),7.68(d,J=7.20Hz,3H),7.57(t,J=5.80Hz,4H),7.47(d,J=8.00Hz,2H),7.33(d,J=8.00Hz,2H),7.20(d,J=8.80Hz,2H),7.12(d,J=7.60Hz,2H),6.85(d,J=8.80Hz,2H),4.31(d,J=7.10Hz,2H),4.12-4.09(m,1H),3.72(t,J=4.40Hz,4H),3.04-2.95(m,5H),2.20(s,3H)
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)-N-甲基苯甲酰胺
1H-NMR(400MHz,DMSO-d6)δ10.75(s,1H),9.72(s,1H),8.44(d,J=4.00Hz,1H),8.22(s,1H),7.75(d,J=8.40Hz,2H),7.67(d,J=8.00Hz,2H),7.42(d,J=7.60Hz,1H),7.26(d,J=8.00Hz,1H),7.18(d,J=9.20Hz,2H),7.07(d,J=1.60Hz,1H),7.01(t,J=7.60Hz,1H),6.92(t,J=7.60Hz,1H),6.79(d,J=8.80Hz,2H),4.15-4.11(m,1H),3.72(t,J=4.80Hz,4H),3.08-2.99(m,5H),2.88-2.82(m,3H),2.78(d,J=4.40Hz,3H)
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-(萘-2-基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ9.64(s,1H),8.27(s,1H),7.89-7.84(m,2H),7.75(t,J=4.60Hz,1H),7.50-7.46(m,4H),7.33(d,J=4.20Hz,2H),7.17(d,J=8.80Hz,2H),7.09(d,J=8.40Hz,2H),7.82(d,J=9.20Hz,2H),4.17-4.14(m,1H),3.72(t,J=4.60Hz,4H),3.40-3.34(m,1H),3.18-3.13(m,1H),3.02(t,J=5.00Hz,4H),2.24(s,3H)
(S)-3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基氨基甲酸叔丁酯
1H-NMR(400MHz,DMSO-d6)δ10.80(s,1H),9.80(s,1H),7.64(d,J=8.00Hz,1H),7.45(d,J=9.20Hz,2H),7.32(d,J=8.40Hz,1H),7.15(s,1H),7.05(t,J=7.40Hz,1H),6.97(t,J=7.20Hz,2H),6.90-6.84(m,3H),4.34-4.33(m,1H),3.73(t,J=4.80Hz,4H),3.13-2.95(m,6H),1.32(s,9H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酸
1H-NMR(400MHz,DMSO-d6)δ10.77(s,1H),8.12(d,J=8.00Hz,1H),7.45(d,J=4.00Hz,2H),7.25(t,J=12.00Hz,2H),7.12(d,J=16.40Hz,2H),6.96-7.01(m,2H),6.88(t,J=11.80Hz,1H),3.86(m,1H),3.03(m,1H),2.83(m,1H),2.30(s,3H)
(S)-4-(4-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-甲氧基苯基)哌嗪-1-甲酸叔丁酯
1H-NMR(400MHz,CDCl3)δ8.42(s,1H),8.36(s,1H),8.11(d,J=8.80Hz,1H),7.48(d,J=8.00Hz,2H),7.33(d,J=8.00Hz,1H),7.28(d,J=8.40Hz,1H),7.14(t,J=7.60Hz,1H),7.02-6.96(m,2H),6.92(d,J=2.40Hz,1H),6.45(dd,J=2.40,9.20Hz,1H),6.41(d,J=2.40Hz,1H),5.25(d,J=6.40Hz,1H),4.14-4.05(m,1H),3.57(t,J=5.20Hz,4H),3.20(d,J=6.80Hz,2H),3.05(t,J=4.80Hz,4H),2.28(s,6H),1.48(s,9H)
(S)-3-(1H-吲哚-3-基)-N-(2-甲氧基-4-(哌嗪-1-基)苯基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.69(s,1H),8.97(s,1H),7.50(d,J=9.20Hz,1H),7.40(d,J=7.60Hz,2H),7.35(d,J=8.00Hz,1H),7.26(d,J=7.60Hz,1H),7.08(d,J=2.00Hz,1H),7.03-7.00(m,3H),6.90(d,J=7.40Hz,1H),6.56(d,J=2.40Hz,1H),6.38(dd,J=2.60,8.60Hz,1H),4.12-4.09(m,2H),3.77(s,3H),3.10-3.05(m,1H),3.01(t,J=4.80Hz,4H),2.85-2.79(m,5H),2.24(s,3H)
(S)-4-(4-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)苯基)哌嗪-1-甲酸叔丁酯
1H-NMR(400MHz,CDCl3)δ8.28(s,1H),8.02(s,1H),7.46(d,J=8.40Hz,2H),7.30(d,J=8.80Hz,2H),7.24(d,J=7.20Hz,2H),7.16(t,J=7.20Hz,1H),7.04(d,J=8.00Hz,2H),6.98(t,J=7.40Hz,1H),6.93(d,J=2.40Hz,1H),6.82(d,J=9.20Hz,2H),5.19(d,J=5.60Hz,1H),4.01-4.00(m,1H),3.56(t,J=5.20Hz,4H),3.18(d,J=6.00Hz,2H),3.05(t,J=4.80Hz,4H),2.31(s,3H),1.48(s,9H)
(S)-3-(1H-吲哚-3-基)-N-(2-甲氧基-4-吗啉代苯基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.37(s,1H),8.13(d,J=8.80Hz,1H),8.02(s,1H),7.53(d,J=8.00Hz,2H),7.36(d,J=8.00Hz,1H),7.32(d,J=8.40Hz,1H),7.18(t,J=7.60Hz,1H),7.08(d,J=8.40Hz,2H),7.02(t,J=7.00Hz,1H),6.96(d,J=2.40Hz,1H),6.47(dd,J=2.40,8.80Hz,1H),6.41(d,J=2.40Hz,1H),5.08(d,J=6.40Hz,1H),4.14-4.05(m,1H),3.86(t,J=4.60Hz,4H),3.73(s,3H),3.29-3.14(m,2H),3.11(t,J=4.80Hz,4H),2.32(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(哌嗪-1-基)苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.76(s,1H),9.63(s,1H),7.51(d,J=8.40Hz,2H),7.40(d,J=7.60Hz,1H),7.28(d,J=8.40Hz,1H),7.17(d,J=8.80Hz,2H),7.10-7.01(m,4H),6.92(t,J=7.20Hz,1H),6.79(d,J=9.20Hz,2H),4.08-4.05(m,2H),3.05-3.00(m,1H),2.95(t,J=4.80Hz,4H),2.85-2.79(m,5H),2.23(s,3H)
(S)-3-(1-甲酰基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ9.86(s,1H),9.14(s,1H),8.23(s,1H),8.15(s,1H),7.60-7.43(m,2H),7.37-7.28(m,6H),6.95(d,J=8.00Hz,2H),6.88(d,J=8.40Hz,2H),4.13(m,2H),3.73(t,J=4.60Hz,3H),3.05-2.96(m,5H),2.89-2.83(m,1H),2.20(s,3H)
(S)-3-(1H-吲哚-3-基)-N-(3-(4-甲氧基苯基)异噁唑-5-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,CDCl3)δ9.42(s,1H),8.28(d,J=1.60Hz,1H),7.73-7.70(m,2H),7.42(d,J=8.40Hz,2H),7.22(t,J=7.60Hz,1H),7.12(t,J=7.60Hz,1H),6.97-6.90(m,6H),6.65(s,1H),5.39(d,J=6.00Hz,1H),4.15-4.09(m,1H),3.83(s,3H),3.26-3.08(m,2H),2.25(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酸苄酯
1H-NMR(400MHz,CDCl3)δ8.06(brs,1H),7.57(d,J=8.20Hz,2H),7.42(d,J=8.20Hz,1H),7.25-7.33(m,4H),7.08-7.18(m,3H),6.99-7.07(m,3H),6.84(d,J=2.30Hz,1H),5.24(d,J=9.00Hz,1H),4.74-4.83(m,2H),4.29(td,J=5.60,9.00Hz,1H),3.17-3.27(m,2H),2.34(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯甲酰胺基)丙酸苄酯
1H-NMR(400MHz,CDCl3)δ7.95(brs,1H),7.52-7.60(m,3H),7.33-7.38(m,3H),7.27-7.32(m,2H),7.16-7.21(m,3H),7.06(t,J=7.43Hz,1H),6.75(d,J=2.35Hz,1H),6.64(d,J=7.83Hz,1H),5.17-5.23(m,1H),5.14(d,J=7.04Hz,2H),3.44(d,J=5.09Hz,2H),2.37(s,3H)
(S)-N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)-4-甲基苯甲酰胺
1H-NMR(400MHz,CDCl3)δ8.10(brs,1H),7.84(d,J=7.83Hz,1H),7.64(d,J=8.22Hz,2H),7.38(d,J=8.22Hz,1H),7.15-7.24(m,5H),7.14(d,J=2.35Hz,1H),7.03(d,J=7.43Hz,1H),6.78-6.82(m,2H),5.06(dt,J=5.09,7.83Hz,1H),3.82-3.86(m,4H),3.57(dd,J=5.09,14.48,4H)
(S)-3-羟基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.39(s,1H),7.79(d,J=8.40Hz,2H),7.33-7.38(m,4H),6.87(d,J=9.20Hz,2H),5.69(s,1H),4.11(d,J=10.40Hz,1H),3.85-3.87(m,5H),3.49-3.50(m,1H),3.36-3.39(m,1H),3.12(t,J=5.00Hz,4H),2.43(s,3H),2.30(s,1H)
(S)-3-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丁酰胺
1H-NMR(400MHz,DMSO-d6)δ9.56(s,1H),7.81(s,1H),7.62(d,J=8.00Hz,2H),7.20(d,J=8.40Hz,2H),7.13(d,J=8.80Hz,2H),6.81(d,J=8.80Hz,2H),3.71(t,J=4.80Hz,4H),3.53(d,J=7.60Hz,1H),3.00(t,J=4.60Hz,4H),1.81-1.86(m,1H),0.82(q,J=6.10Hz,6H)
(S)-1-(3-(1H-吲哚-3-基)-1-吗啉代-1-氧代丙-2-基)-3-苯基脲
1H-NMR(400MHz,DMSO-d6)δ10.90(s,1H),8.72(s,1H),7.53(d,J=7.60Hz,1H),7.36(t,J=8.20Hz,3H),7.22-7.17(m,3H),7.06(d,J=3.40Hz,1H),7.00-6.89(m,2H),6.59(d,J=8.00Hz,1H),4.96(d,J=6.00Hz,1H),3.45-3.42(m,2H),3.26-3.04(m,8H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(6-吗啉代吡啶-3-基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.78(s,1H),9.71(s,1H),8.12(s,1H),8.00(d,J=2.40Hz,1H),7.53(d,J=8.00Hz,2H),7.45(dd,J=2.40,9.20Hz,1H),7.40(d,J=8.00Hz,1H),7.29(d,J=7.60Hz,1H),7.12(d,J=7.60Hz,2H),7.08(d,J=2.00Hz,1H),7.04(t,J=7.40Hz,1H),6.92(t,J=7.40Hz,1H),6.74(d,J=9.20Hz,1H),4.06(s,1H),3.68(t,J=4.80Hz,4H),3.34-3.33(m,4H),3.07-3.01(m,1H),2.88-2.82(m,1H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(2-吗啉代嘧啶-5-基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.80(s,1H),9.75(s,1H),8.19(s,1H),8.15(s,2H),7.54(d,J=8.40Hz,2H),7.40(d,J=8.00Hz,1H),7.30(d,J=8.00Hz,1H),7.15(d,J=8.40Hz,1H),7.09(s,1H),7.04(t,J=7.40Hz,1H),6.93(t,J=7.40Hz,1H),4.04(m,1H),3.62-3.61(m,8H),3.08-3.02(m,1H),2.91-2.85(m,1H),2.23(s,3H)
(S)-2-(4-氰基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.72(s,1H),9.85(s,1H),8.57(s,1H),7.57(s,4H),7.48(d,J=7.60Hz,1H),7.29-7.23(m,3H),7.07-7.01(m,2H),6.93(t,J=7.20Hz,1H),6.86(d,J=8.80Hz,2H),4.12(s,1H),3.73(s,4H),3.04-3.00(m,3H),2.90-2.84(m,1H)
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(6-(三氟甲基)吡啶-3磺酰胺基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.76(s,1H),9.92(s,1H),8.87(s,1H),8.81(s,1H),8.0(d,J=8.40Hz,1H),7.60(d,J=8.00Hz,1H),7.52(d,J=7.60Hz,1H),7.22-7.19(m,3H),7.12(d,J=1.60Hz,1H),7.01(d,J=7.40Hz,1H),6.92(d,J=7.40Hz,1H),6.82(d,J=9.20Hz,2H),4.21(m,1H),3.73(t,J=4.40Hz,4H),3.08-2.90(m,6H)
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸甲酯
1H-NMR(400MHz,CDCl3)δ8.16(s,1H),7.74(d,J=8.40Hz,2H),7.27-7.25(m,4H),6.83(d,J=8.80Hz,2H),6.21(d,J=7.20Hz,1H),3.9-3.84(m,5H),3.69(s,3H),3.10(t,J=4.60Hz,4H),2.58-2.50(m,1H),2.36(s,3H),2.32-2.25(m,1H),2.05-1.93(m,2H)
(S)-3-(1H-苯并[d]咪唑-1-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.97(s,1H),7.68(s,1H),7.57(d,J=7.60Hz,2H),7.38(d,J=8.00Hz,1H),7.27(d,J=8.00Hz,1H),7.12-7.00(m,6H),6.72(d,J=8.80Hz,2H),4.49(s,2H),4.44-4.43(m,1H),3.80(t,J=4.60Hz,4H),3.03(t,J=4.60Hz,4H),2.24(s,3H)
(R)-3-(2,3-二氧代-3,4-二氢喹喔啉-1(2H)-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,CDCl3)δ7.48(d,J=8.80Hz,2H),7.43(d,J=7.60Hz,2H),7.37(d,J=8.00Hz,1H),7.32(s,1H),7.27-7.20(m,2H),7.07(d,J=7.20Hz,1H),6.91(t,J=6.60Hz,4H),4.75-4.68(m,1H),4.32(d,J=12.4Hz,2H),3.87(s,4H),3.14(s,4H),2.26(s,3H)
(S)-N-(5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基)-5-(三氟甲基)吡啶甲酰胺
1H-NMR(400MHz,CDCl3)δ8.82(s,1H),8.35(d,J=8.00Hz,1H),8.22(s,1H),8.13(d,J=8.00Hz,1H),7.71(d,J=8.00Hz,2H),7.28-7.25(m,2H),7.19(d,J=8.40Hz,2H),6.81(d,J=8.80Hz,2H),3.85(t,J=4.80Hz,4H),3.80-3.76(m,1H),3.45-3.39(m,2H),3.09(t,J=4.60Hz,4H),2.31(s,3H),1.87-1.73(m,2H),1.60-1.55(m,2H),1.33-1.30(m,2H)
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸苄酯
1H-NMR(400MHz,CDCl3)δ8.25(s,1H),7.71(d,J=8.00Hz,2H),7.36-7.30(m,5H),7.21(d,J=8.80Hz,2H),7.16(d,J=8.00Hz,2H),6.77(d,J=8.80Hz,2H),6.30(d,J=7.60Hz,1H),5.12-5.04(m,2H),3.95-3.90(m,1H),3.83(t,J=4.60Hz,4H),3.06(t,J=4.80Hz,4H),2.55-2.48(m,1H),2.36-2.30(m,1H),2.28(s,3H),2.06-2.03(m,1H),1.96-1.93(m,1H)
(S)-3-(4-甲基苯基磺酰胺基)-4-(4-吗啉代苯基氨基)-4-氧代丁酸苄酯
1H-NMR(400MHz,CDCl3)δ8.39(s,1H),7.75(d,J=8.00Hz,2H),7.33-7.23(m,9H),6.81(d,J=8.80Hz,2H),6.25(d,J=8.80Hz,1H),5.09-5.00(m,2H),4.22-4.21(m,1H),3.84(t,J=4.80Hz,4H),3.08(t,J=4.80Hz,4H),3.03(dd,J=4.00,17.2Hz,1H),2.41(dd,J=6.20,17.4Hz,1H),2.36(s,3H)
(S)-4-甲基-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯甲酰胺
1H-NMR(400MHz,CDCl3)δ8.73(s,1H),7.69(d,J=8.00Hz,2H),7.42(d,J=8.00Hz,2H),7.22(d,J=8.80Hz,2H),6.84-6.80(m,3H)4.90-4.86(m,1H),3.84(t,J=4.80Hz,4H),3.08(t,J=4.80Hz,4H),2.39(s,3H),1.90-1.88(m,1H),1.86-1.71(m,2H),0.97(d,J=6.40Hz,3H),0.90(d,J=6.40Hz,3H)
2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)乙酰胺
1H-NMR(400MHz,CDCl3)δ7.96(s,1H),7.76(d,J=8.40Hz,2H),7.35-7.32(m,4H),6.85(d,J=8.80Hz,2H),5.31(t,J=6.80Hz,1H),3.85(t,J=4.80Hz,4H),3.69(d,J=6.40Hz,2H),3.11(t,J=4.80Hz,4H),2.42(s,3H)
(S)-3-(4-甲基苯基磺酰胺基)-4-(4-吗啉代苯基氨基)-4-氧代丁酸
1H-NMR(400MHz,DMSO-d6)δ9.77(s,1H),7.65-7.20(m,4H),7.21(d,J=4.00Hz,2H),6.82(d,J=8.80Hz,2H),4.17(t,J=7.00Hz,1H),3.72(t,J=4.40Hz,4H),3.02(t,J=4.60Hz,4H),2.57(dd,J=16.2,6.60Hz,1H),2.35(dd,J=16.0,7.60Hz,1H),2.25(s,3H)
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸
1H-NMR(400MHz,DMSO-d6)δ9.67(s,1H),7.65(d,J=8.40Hz,2H),7.25(d,J=7.60Hz,2H),7.19(d,J=8.80Hz,2H),6.84(d,J=8.40Hz,2H),3.83-3.79(m,1H),3.72(t,J=4.60Hz,4H),3.02(t,J=4.80Hz,4H),2.26(s,3H),2.20-2.11(m,2H),1.80-1.70(m,2H)
(s)-3-(4-羟基苯基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ9.61(s,1H),9.18(s,1H),8.05(s,1H),7.49(d,J=8.00Hz,2H),7.15(d,J=8.40Hz,4H),6.93(d,J=7.60Hz,2H),6.82(d,J=9.20Hz,2H),6.57(d,J=8.80Hz,2H),3.98-3.85(m,1H),3.72(t,J=4.60Hz,4H),3.01(t,J=4.60Hz,4H),2.78-2.73(m,1H),2.67-2.59(m,1H),2.33(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-苯基丙酰胺
1H-NMR(400MHz,CDCl3)δ8.14(s,1H),8.10(s,1H),7.45(d,J=8.40Hz,2H),7.34(d,J=7.60Hz,2H),7.30-7.24(m,4H),7.17-7.11(m,2H),7.09-6.92(m,3H),6.91(s,1H),5.19(d,J=5.60Hz,1H),4.05-4.01(m,1H),3.20-3.17(m,2H),2.29(s,3H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-苯基丙酰胺)
1H NMR(400MHz,DMSO-d6)δ10.78(s,1H),9.98(s,1H),8.40(s,1H),7.40-7.39(m,5H),7.36(d,J=8.40Hz,2H),7.30-7.23(m,3H),7.10(s,1H),7.06-7.01(m,2H),6.93(t,J=7.20Hz,1H),4.16-4.13(m,1H),3.05(dd,J=14.2,6.00Hz,1H),2.87(dd,J=14.7,8.00Hz,1H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(噻吩-2-基甲基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.20(s,1H),7.41(d,J=8.40Hz,2H),7.28-7.24(m,2H),7.16-7.11(m,2H),7.01-6.88(m,3H),6.87(s,1H),6.81(s,1H),6.74(s,1H),5.13(d,J=6.00Hz,1H),4.48-4.45(m,2H),3.94-3.91(m,1H),3.11-3.09(m,2H),2.31(s,3H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(噻吩-2-基甲基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.73(s,1H),8.62(t,J=6.00Hz,1H),8.22(s,1H),7.42-7.33(m,6H),7.27(d,J=8.40Hz,1H),7.05-7.01(m,2H),6.94-6.88(m,2H),6.86(d,J=2.40Hz,1H),4.30-4.26(m,2H),3.99-3.95(m,1H),2.99(dd,J=14.2,6.00Hz,1H),2.80(dd,J=14.7,8.00Hz,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(2-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ12.39(s,1H),10.76(s,1H),8.48(s,1H),7.64(s,1H),7.47(d,J=7.60Hz,1H),7.41-7.11(m,6H),7.08-7.01(m,5H),6.91(t,J=7.60Hz,1H),4.34-4.30(m,1H),3.91(s,3H),3.12-3.07(m,1H),2.91-2.85(m,1H)
(S)-N-(3-(N-(4-甲基-1-吗啉代-1-氧代戊-2-基)氨磺酰基)苯基)乙酰胺
1H-NMR(400MHz,CDCl3)δ8.47(s,1H),8.25(d,J=8.80Hz,1H),7.76(t,J=1.80Hz,1H),7.54(d,J=7.60Hz,1H),7.45(t,J=8.00Hz,1H),6.69(d,J=9.60Hz,1H),4.15-4.08(m,1H),3.59-3.49(m,2H),3.42-3.18(m,6H),2.16(s,3H),1.99-1.94(m,1H),1.52-1.45(m,1H),1.18-1.11(m,1H),0.95(d,J=6.80Hz,3H),0.91(d,J=6.80Hz,3H)
(S)-4-甲基-2-(3-苯基脲基)戊酸苄酯
1H-NMR(400MHz,CDCl3)δ7.38(s,1H),7.34-7.01(m,8H),6.99-6.97(m,1H),5.83(d,J=8.00Hz,1H),5.19-5.07(m,2H),4.65-4.60(m,1H),1.71-1.57(m,2H),1.51-1.46(m,1H),0.91(d,J=6.40Hz,3H),0.88(d,J=6.40Hz,3H)
4-甲基-N-(2-吗啉代-2-氧代乙基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.76(d,J=8.00Hz,2H),7.30(d,J=8.00Hz,2H),6.20(t,J=4.60Hz,1H),3.79(d,J=4.80Hz,2H),3.58-3.62(m,4H),3.51(t,J=4.40Hz,2H),3.32(t,J=4.60Hz,2H),2.4(s,3H)
4-甲基-N-(1-(吗啉-4-羰基)环己基)苯磺酰胺
1H-NMR(400MHz,CDCl3)δ7.79(d,J=8.00Hz,2H),7.29(d,J=8.00Hz,2H),5.33(s,1H),3.74-3.78(m,8H),2.43(s,3H),1.74-1.91(m,4H),1.17-1.40(m,6H).
(S)-4-(N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)氨磺酰基)苯甲酸
1H-NMR(400MHz,CDCl3)δ8.20(d,J=8.40Hz,2H),7.94(d,J=8.40Hz,2H),6.49(d,J=9.20Hz,1H),4.46-4.41(m,1H),3.84-3.78(m,2H),3.65-3.25(m,14H),1.93-1.89(m,1H),1.56-1.36(m,2H),0.91(t,J=7.00Hz,6H)
(S)-2-(4-羟基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ10.78(s,1H),10.18(s,1H),9.64(s,1H),7.84(d,J=8.40Hz,1H),7.50(d,J=8.80Hz,2H),7.39(d,J=7.60Hz,1H),7.29(d,J=7.60Hz,1H),7.22(d,J=9.20Hz,2H),7.06(d,J=2.40Hz,1H),7.03(d,J=7.20Hz,1H),6.93(t,J=7.40Hz,1H),6.82(d,J=9.20Hz,2H),6.70(d,J=8.40Hz,2H),4.08-4.02(m,1H),3.72(t,J=4.80Hz,4H),3.07-3.00(m,5H),2.84-2.79(m,1H)
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸
1H-NMR(400MHz,DMSO-d6)δ10.77(s,1H),9.83(s,1H),8.43(d,J=9.20Hz,1H),7.76(d,J=8.00Hz,2H),7.63(d,J=8.40Hz,2H),7.44(d,J=7.60Hz,1H),7.26-7.22(m,3H),7.09(d,J=2.04Hz,1H),7.00(t,J=7.20Hz,1H),6.91(t,J=7.60Hz,3H),4.14-4.12(m,1H),3.76(t,J=4.60Hz,4H),3.07-3.03(m,5H),2.90-2.86(m,1H)
(S)-2-氨基-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺
1H-NMR(400MHz,CDCl3)δ9.27(s,1H),8.21(s,1H),7.70(d,J=8.00Hz,1H),7.51-7.47(m,2H),7.37(d,J=8.40Hz,1H),7.22-7.11(m,2H),7.08(d,J=2.40Hz,1H),6.89-6.86(m,2H),3.86-3.82(m,5H),3.49-3.45(m,1H),3.11(t,J=4.80Hz,4H),3.04-2.99(m,1H),1.81(s,2H)
(S)-N-(4-(4-乙酰基哌嗪-1-基)-2-甲氧基苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.54(s,1H),8.49(s,1H),8.12(d,J=8.40Hz,1H),7.46(d,J=8.40Hz,2H),7.32-7.26(m,2H),7.13(t,J=7.60Hz,1H),7.00-6.95(m,3H),6.92(d,J=2.40Hz,1H),6.45-6.40(m,2H),5.37(d,J=5.60Hz,1H),4.09-4.05(m,1H),3.75(t,J=5.40Hz,2H),3.71(s,3H),3.59(t,J=5.00Hz,2H),3.21-3.04(m,6H),2.28(s,3H),2.13(s,3H)
(S)-N-(4-(4-乙酰基哌嗪-1-基)苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(400MHz,CDCl3)δ8.31(s,1H),8.11(s,1H),8.47(d,J=8.40Hz,2H),7.31-7.25(m,5H),7.16(t,J=7.60Hz,1H),7.04(d,J=8.40Hz,2H),6.99(t,J=7.60Hz,1H),6.94(d,J=2.40Hz,1H),6.82(d,J=9.20Hz,2H),5.22(d,J=6.00Hz,1H),4.02-4.00(m,1H),3.74(t,J=5.00Hz,2H),3.59(t,J=5.00Hz,2H),3.18(d,J=6.40Hz,2H),3.10(t,J=5.00Hz,2H),3.05(t,J=5.00Hz,2H),2.31(s,3H),2.12(s,3H)
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-吗啉代苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺
1H-NMR(400MHz,DMSO-d6)δ10.71(s,1H),10.17(s,2H),7.99(s,1H),7.82(d,J=8.80Hz,2H),7.37(d,J=8.00Hz,1H),7.33(d,J=8.40Hz,2H),7.26(d,J=7.26Hz,1H),7.14(s,1H),7.04-6.98(m,5H),6.90(t,J=7.40Hz,1H),4.07(s,1H),3.74(t,J=4.40Hz,4H),3.24(t,J=4.80Hz,4H),3.11-3.06(m,1H),2.80-2.74(m,1H),2.21(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(4-吗啉代苯基)噻唑-2-基)丙酰胺
1H-NMR(400MHz,DMSO-d6)δ12.24(s,1H),10.76(s,1H),8.21(s,1H),7.73(d,J=8.80Hz,2H),7.46(d,J=8.00Hz,2H),7.41(d,J=8.00Hz,1H),7.35(s,1H),7.27(d,J=8.40Hz,1H),7.05-6.97(m,6H),6.91(t,J=7.60Hz,1H),4.29(s,1H),3.74(t,J=4.60Hz,4H),3.15(t,J=4.60Hz,4H),3.10-3.05(m,1H),2.88-2.82(m,1H),2.18(s,3H)
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸甲酯
1H-NMR(400MHz,DMSO-d6)δ12.39(s,1H),10.77(s,1H),8.25(d,J=8.00Hz,1H),8.02(s,4H),7.81(s,1H),7.46(d,J=8.40Hz,2H),7.42(d,J=8.00Hz,1H),7.27(d,J=8.40Hz,1H),7.06-7.01(m,4H),6.91(t,J=7.60Hz,1H),4.32-4.30(s,1H),3.86(s,3H),3.12-3.06(m,1H),2.90-2.84(m,1H),2.17(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(6-(三氟甲基)吡啶-3-磺酰胺基)丙酸苄酯
1H-NMR(400MHz,CDCl3)δ8.85(d,J=1.60Hz,1H),7.91(s,1H),7.83(dd,J=1.60,8.40Hz,1H),7.42(d,J=8.40Hz,1H),7.36-7.33(m,4H),7.26-7.15(m,5H),7.08-7.04(m,1H),6.84(d,J=2.40Hz,1H),5.40(d,J=8.80Hz,1H),5.03(s,2H),4.43-4.38(m,1H),3.33-3.28(m,1H),3.16-3.10(m,1H)
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-(4-硝基苯基)戊二酰胺
1H-NMR(400MHz,DMSO-d6)δ10.57(s,1H),9.71(s,1H),8.21(d,J=8.80Hz,2H),8.08(s,1H),7.81(d,J=9.20Hz,2H),7.65(d,J=8.40Hz,2H),7.22-7.18(m,4H),6.84(d,J=8.80Hz,2H),3.86(t,J=6.80Hz,1H),3.72(t,J=4.60Hz,4H),3.02(t,J=4.80Hz,4H),2.46-2.37(m,2H),2.21(s,3H),1.93-1.79(m,2H)
(S)-5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基氨基甲酸苄酯
1H-NMR(400MHz,CD3OD)δ7.71(d,J=8.00Hz,2H),7.32-7.25(m,5H),7.22(d,J=8.40Hz,2H),7.15(d,J=8.40Hz,2H),6.86(d,J=9.20Hz,2H),5.06(s,2H),3.82-3.78(m,5H),3.07-3.03(m,6H),2.26(s,3H),1.69-1.59(m,2H),1.48-1.28(m,4H)
(S)-6-氨基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)己酰胺
1H-NMR(400MHz,DMSO-d6)δ9.65(s,1H),7.65(d,J=8.40Hz,2H),7.25-7.19(m,4H),6.83(d,J=8.80Hz,2H),3.77-3.71(m,5H),3.02(t,J=4.80Hz,4H),2.42(t,J=6.40Hz,2H),2.26(s,3H),1.52-1.44(m,2H),1.24-1.12(m,4H)
(S)-3,5-二甲氧基-N-(5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基)苯甲酰胺
1H-NMR(400MHz,CDCl3)δ8.60(s,1H),7.68(d,J=8.00Hz,2H),7.25(d,J=8.80Hz,2H),7.14(d,J=8.40Hz,2H),6.98(d,J=2.40Hz,2H),6.77(d,J=9.20Hz,2H),6.86(t,J=6.00Hz,1H),6.58(s,1H),6.35(d,J=7.20Hz,1H),3.83(t,J=4.60Hz,4H),3.78-3.75(m,7H),3.39-3.32(m,2H),3.06(t,J=4.80Hz,4H),2.26(s,3H),1.85-1.71(m,2H),1.52-1.47(m,2H),1.30-1.23(m,2H)
(S)-N5-(4-甲氧基苄基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺
1H-NMR(400MHz,DMSO-d6)δ9.60(s,1H),8.25(t,J=5.80Hz,1H),7.95(s,1H),7.64(d,J=8.40Hz,2H),7.23(d,J=8.40Hz,2H),7.19(d,J=9.20Hz,2H),7.14(d,J=8.80Hz,2H),6.84(t,J=8.80Hz,4H),4.15(d,J=6.00Hz,2H),3.82-3.71(m,8H),3.02(t,J=4.80Hz,4H),2.26(s,3H),2.17-2.05(m,2H),1.82-1.75(m,2H)
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-苯基戊二酰胺
1H-NMR(400MHz,DMSO-d6)δ9.89(s,1H),9.64(s,1H),7.98(s,1H),7.66(d,J=8.00Hz,2H),7.56(d,J=8.40Hz,2H),7.28-7.19(m,6H),7.01(t,J=7.40Hz,1H),6.84(d,J=8.80Hz,2H),3.86(t,J=6.80Hz,1H),3.72(t,J=4.60Hz,4H),3.02(t,J=4.60Hz,4H),2.41-2.26(m,2H),2.23(s,3H),1.94-1.80(m,2H)
(S)-2-(4-甲基苯基磺酰胺基)-5-吗啉代-N-(4-吗啉代苯基)-5-氧代戊酰胺
1H-NMR(400MHz,CDCl3)δ8.75(s,1H),7.74(d,J=8.40Hz,2H),7.34(d,J=8.80Hz,2H),7.28(d,J=8.00Hz,2H),7.11(d,J=6.00Hz,1H),8.65(d,J=8.80Hz,2H),3.86(t,J=4.60Hz,1H),3.78-3.65(m,6H),3.59-3.55(m,1H),3.45-3.33(m,2H),3.10(t,J=5.00Hz,4H),2.64-2.63(m,2H),2.38(s,3H),2.23-2.18(m,2H),2.07-2.02(m,2H)
(S)-N5-(4-氟苯基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺
1H-NMR(400MHz,DMSO-d6)δ9.99(s,1H),9.68(s,1H),8.04(s,1H),7.65(d,J=8.00Hz,2H),7.58-7.55(m,2H),7.21(t,J=8.00Hz,4H),7.12(t,J=8.80Hz,2H),6.84(d,J=8.80Hz,2H),3.85(s,1H),3.72(s,4H),3.02(s,4H),2.38-2.26(m,2H),2.22(s,3H),1.89-1.81(m,2H)
(S)-N5-(4-叔丁基苯基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺
1H-NMR(400MHz,DMSO-d6)δ9.86(s,1H),9.69(s,1H),8.05(s,1H),7.65(d,J=8.40Hz,2H),7.47(d,J=8.80Hz,2H),7.29(d,J=8.80Hz,2H),7.22-7.19(m,4H),6.84(d,J=8.80Hz,2H),3.84(t,J=6.80Hz,1H),3.73(t,J=4.60Hz,4H),3.02(t,J=4.80Hz,4H),2.40-2.25(m,2H),2.22(s,3H),1.92-1.77(m,2H),1.24(s,9H)
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-(4-(三氟甲基)苯基)戊二酰胺
1H-NMR(400MHz,DMSO-d6)δ10.30(s,1H),9.69(s,1H),8.05(s,1H),7.77(d,J=8.80Hz,2H),7.65(d,J=8.00Hz,4H),7.22-7.19(m,4H),6.84(d,J=8.80Hz,2H),3.86(s,1H),3.72(s,4H),3.02(s,4H),2.44-2.33(m,2H),2.21(s,3H),1.93-1.82(m,2H)
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N4-(4-硝基苯基)琥珀酰胺
1H-NMR(400MHz,DMSO-d6)δ10.55(s,1H),9.80(s,1H),8.21(d,J=8.80Hz,2H),8.18(s,1H),7.75(d,J=9.20Hz,2H),7.65(d,J=8.40Hz,2H),7.25(d,J=8.80Hz,2H),7.18(d,J=8.40Hz,2H),6.84(d,J=8.80Hz,2H),4.35(t,J=6.80Hz,1H),3.72(t,J=4.60Hz,4H),3.02(t,J=4.80Hz,4H),2.78(dd,J=6.60,15.40Hz,1H),2.62(dd,J=7.80,15.40Hz,1H),2.21(s,3H)
(S)-N-(呋喃-2-基甲基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,CDCl3)δ8.10(s,1H),7.45-7.43(d,J=10.00Hz,2H),7.32(s,1H),7.31-7.30(d,J=5.00Hz,1H),7.26-7.25(d,J=5.00Hz,1H),7.18-7.15(t,J=7.50Hz,1H),7.06-7.05(d,J=5.00Hz,2H),7.01-6.98(t,J=7.50Hz,1H),6.83(s,1H),6.67(s,1H),6.30(s,1H),6.15(s,1H),4.97-4.96(d,J=0.94Hz,1H),4.40-4.31(m,2H),3.93-3.90(m,1H),3.15-3.07(m,2H),2.34(s,3H)
(S)-2-(4-溴苯基磺酰胺基)-N-(呋喃-2-基甲基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,CDCl3)δ8.64(s,1H),7.98(s,3H),7.32-7.22(m,6H),7.18-7.15(t,J=7.50Hz,1H),6.88(s,1H),6.29(s,1H),6.15(s,1H),5.69(s,1H),4.33(m,2H),3.95-3.91(m,1H),3.28-3.24(m,1H),3.05-3.00(m,1H)
(S)-3-(1H-吲哚-3-基)-N-异丙基-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,CDCl3)δ8.27(s,1H),7.47-7.45(d,J=10.00Hz,2H),7.33-7.31(d,J=10.00Hz,2H),7.19-7.16(t,J=7.50Hz,1H),7.07-7.05(d,J=10.00Hz,2H),7.02-6.99(t,J=7.50Hz,1H),6.92(s,1H),6.02-6.00(d,J=10.00Hz,1H),5.09-5.07(d,J=10.00Hz,1H),3.97-3.90(m,1H),3.86-3.82(m,1H),3.15-3.07(m,2H),2.33(s,3H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-异丙基丙酰胺
1H-NMR(500MHz,MeOD)δ10.23(s,1H),7.97-7.95(d,J=5.00Hz,1H),7.50-7.48(d,J=10.00Hz,2H),7.42-7.41(d,J=5.00Hz,1H),7.27-7.25(d,J=10.00Hz,1H),7.06-7.02(m,4H),6.94-6.90(m,2H),6.86-6.84(d,J=10.00Hz,1H),6.80-6.76(t,J=10.00Hz,1H),4.66(s,1H),4.15-4.12(t,J=7.50Hz,1H),3.22-3.18(m,1H),3.03-2.99(m,1H),2.11(s,3H)
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-甲氧基苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺
1H-NMR(500MHz,CDCl3)δ7.86-7.64(d,J=8.50Hz,2H),7.31-7.26(m,4H),7.11-7.08(t,J=7.50Hz,1H),7.04(s,1H),6.95-6.91(m,3H),6.89-6.87(d,J=8.00Hz,2H),4.10-4.07(m,1H),3.85(s,3H),3.35-3.31(m,1H),3.04-3.00(m,1H),2.26(s,3H)
(S)-2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰基)-N-(4-甲氧基苯基)肼甲酰胺
1H-NMR(500MHz,MeOD)δ7.39-7.36(t,J=7.00Hz,4H),7.28-7.26(d,J=8.00Hz,1H),7.22-7.20(d,J=7.50Hz,1H),7.08-7.05(t,J=7.50Hz,1H),7.01(s,1H),6.98(s,1H),6.97(s,1H),6.89-6.84(m,3H),3.89-3.86(m,1H),3.76(s,3H),3.25-3.21(m,1H),2.93-2.89(m,1H),2.30(s,3H)
(S)-4-溴-N-(1-(3,5-二甲基-1H-吡唑-1-基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺
1H-NMR(500MHz,DMSO-d6)δ10.76(s,1H),8.65(s,1H),7.66-7.65(d,J=9.50Hz,1H),7.30-7.27(t,J=7.50Hz,3H),7.16-7.15(d,J=8.00Hz,2H),7.10(s,1H),7.07-7.04(t,J=7.50Hz,1H),6.96-6.93(t,J=7.50Hz,1H),6.24(s,2H),5.39-5.37(d,J=8.50Hz,1H),3.20-3.16(d,J=14.00,3.00Hz,1H),2.89-2.84(d,J=14.00,10.50Hz,1H),2.92(s,3H),2.27(s,3H)
(S)-N-(3-(1H-吲哚-3-基)-1-氧代-1-(3-苯基-1H-吡唑-1-基)丙-2-基)-4-溴苯磺酰胺
1H-NMR(500MHz,DMSO-d6)δ10.77(s,1H),8.86(s,1H),8.48(s,1H),8.00-7.98(d,J=7.50Hz,2H),7.69-7.68(d,J=7.50Hz,1H),7.58-7.55(t,J=7.00Hz,2H),7.52-7.49(t,J=7.50Hz,1H),7.29-7.23(m,4H),7.17(s,1H),7.15(s,1H),7.11-7.04(m,2H),6.98-6.92(m,1H),5.50-5.49(d,J=7.00Hz,1H),3.28-3.25(d,J=14.00,4.00Hz,1H),2.97-2.92(d,J=14.00,10.00Hz,1H)
N-((S)-1-(2-((3S,5S,7S)-金刚烷-1-羰基)肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)-4-甲基苯磺酰胺
1H-NMR(500MHz,MeOD)δ7.33-7.32(d,J=8.00Hz,1H),7.25-7.20(t,J=7.50Hz,3H),7.06-7.03(t,J=7.50Hz,1H),7.00(s,1H),6.91-6.88(t,J=8.00Hz,1H),6.85-6.83(d,J=8.00Hz,2H),4.04-4.01(d,J=9.50,4.50Hz,1H),3.29-3.25(d,J=15.00,5.00Hz,1H),2.94-2.89(d,J=15.00,10.00Hz,1H),2.24(s,3H),2.02-2.01(d,J=6.00Hz,3H),1.95(s,6H),1.80-1.74(t,J=12.50Hz,6H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(对甲苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ12.47(s,1H),10.79(s,1H),8.53-8.52(d,J=7.50Hz,1H),7.78-7.77(d,J=8.00Hz,2H),7.55(s,1H),7.48-7.47(d,J=7.50Hz,1H),7.44-7.37(m,4H),7.29-7.27(d,J=8.00Hz,1H),7.25-7.23(d,J=8.50Hz,2H),7.09(d,J=2.50Hz,1H),7.06-7.03(t,J=7.50Hz,1H),6.94-6.91(t,J=7.50Hz,1H),4.35-4.31(m,1H),3.12-3.08(d,J=14.50,6.50Hz,1H),2.91-2.86(d,J=15.00,10.00Hz,1H),2.33(s,3H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-苯乙基丙酰胺
1H-NMR(500MHz,CDCl3)δ8.27(s,1H),8.02(s,1H),7.47-7.46(d,J=10.00Hz,2H),7.32-7.31(d,J=5.00Hz,2H),7.28-7.25(d,J=7.50Hz,2H),7.23-7.22(d,J=5.00Hz,1H),7.20-7.17(t,J=7.50Hz,1H),7.08-7.01(m,5H),6.84(s,1H),6.37-6.35(t,J=5.00Hz,1H),5.08-5.07(d,J=5.00Hz,1H),3.43-3.35(m,2H),3.10-3.07(t,J=7.50Hz,2H),2.70-2.59(m,2H),2.35(s,3H)
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-氟苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,MeOD)δ7.91-7.88(m,2H),7.45-7.42(m,3H),7.32(s,1H),7.30-7.27(m,3H),7.14-7.10(t,J=10.00Hz,2H),7.09-7.06(t,J=7.50Hz,1H),7.02(s,1H),6.97-6.94(t,J=7.50Hz,1H),4.31-4.28(m,1H),3.28-3.24(m,1H),3.08-3.03(m,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-硝基苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,MeOD)δ8.28-8.26(d,J=10.00Hz,2H),8.12-8.10(d,J=10.00Hz,2H),7.68(s,1H),7.47-7.44(m,3H),7.31-7.27(m,3H),7.09-7.06(t,J=7.50Hz,1H),6.97-6.94(t,J=7.50Hz,1H),4.31-4.28(m,1H),3.29-3.25(m,1H),3.10-3.05(m,1H)
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-甲氧基苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺
1H-NMR(500MHz,MeOD)δ7.89-7.88(d,J=8.50Hz,2H),7.43-7.41(d,J=8.80Hz,1H),7.28-7.26(d,J=8.00Hz,1H),7.22-7.21(d,J=8.50Hz,2H),7.16-7.14(d,J=8.00Hz,2H),7.10-7.07(t,J=7.00Hz,1H),7.03-7.01(d,J=11.00Hz,3H),6.96-6.93(t,J=7.00Hz,1H),4.18-4.15(d,J=10.00,5.00Hz,1H),3.87(s,3H),3.35-3.32(m,1H),3.00-2.95(d,J=10.50,4.00Hz,1H)
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-氰基苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.88-2.93(dd,J=14.18,8.80Hz,1H),3.09-3.13(dd,J=14.18,6.35Hz,1H),4.34-4.35(d,J=6.35Hz,1H),6.91-6.94(t,J=7.33Hz,1H),7.02-7.05(t,J=7.82Hz,1H),7.09-7.10(d,J=1.95Hz,1H),7.27-7.28(d,J=8.31Hz,1H),7.37-7.42(m,4H),7.47-7.48(d,J=7.82Hz,1H),7.88-7.91(m,3H),8.05-8.06(d,J=8.31Hz,2H),8.55-8.57(d,J=7.33Hz,1H),10.80(s,1H),12.55(brs,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2-88-2.92(dd,J=14.18,8.80Hz,1H),3.09-3.13(dd,J=14.18,6.35Hz,1H),4.33-4.35(m,1H),6.90-6.93(t,J=7.33Hz,1H),7.02-7.05(t,J=7.33Hz,1H),7.09(d,J=1.95Hz,1H),7.27-7.28(d,J=8.31Hz,1H),7.37-7.42(q,J=8.31,8.80,7.82Hz,4H),7.47-7.48(d,J=7.82Hz,1H),7.78-7.80(d,J=8.31Hz,2H),7.85(s,1H),8.08-8.10(d,J=8.31Hz,2H),8.52-8.54(d,J=7.33Hz,1H),10.78(s,1H),12.54(brs,1H).
(S)-4-溴-N-(1-(2-十二酰基肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺
1H-NMR(500MHz,CDCl3)δ0.86-0.89(t,J=6.84Hz,3H),1.26(s,16H),1.51-1.54(t,J=6.35Hz,2H),2.30-2.37(m,2H),3.13-3.17(dd,J=14.67,7.82Hz,1H),3.22-3.26(dd,J=14.67,5.86Hz,1H),4.36-4.38(t,J=6.84Hz,1H),7.02(s,1H),7.06-7.09(t,J=7.33Hz,1H),7.18-7.21(t,J=7.33Hz,1H),7.32-7.34(d,J=8.31Hz,1H),7.38-7.39(d,J=8.31Hz,2H),7.42-7.44(d,J=7.82Hz,1H),7.47-7.48(d,J=8.31Hz,2H),8.34(brs,1H)
(S)-4-溴-N-(1-(2-癸酰基肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺
1H-NMR(500MHz,CDCl3)δ0.87-0.89(t,J=6.35Hz,3H),1.28(s,12H),1.50-1.54(m,2H),2.28-2.39(m,2H),3.13-3.23(dd,J=14.67,7.33Hz,1H),3.23-3.27(dd,J=14.67,5.38Hz,1H),4.36-4.39(t,J=6.84Hz,1H),7.02(s,1H),7.06-7.09(t,J=7.82Hz,1H),7.19-7.22(t,J=7.33Hz,1H),7.33-7.34(d,J=8.31Hz,1H),7.39-7.40(d,J=8.31Hz,2H),7.42-7.44(d,J=7.82Hz,1H),7.47-7.48(d,J=8.31Hz,2H),8.33(brs.1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-苯乙基丙酰胺
1H-NMR(500MHz,CDCl3)δ2.60-2.73(m,2H),2.93-2.98(dd,J=14.18,7.82Hz,1H),3.17-3.21(dd,J=14.67,5.38Hz,1H),3.33-3.40(dq,J=13.69,6.84x3Hz,1H),3.43-3.49(dq,J=13.20,6.84x2,6.35Hz,1H),3.83-3.87(q,J=6.35x2,6.84Hz,1H),5.26-5.27(d,J=6.35Hz,1H),6.36-6.38(t,J=5.38Hz,1H),6.82(s,1H),7.00-7.03(t,J=7.33Hz,1H),7.06-7.08(d,J=7.82Hz,2H),7.19-7.31(m,10H),8.16(brs,1H)
N-((S)-1-(2-((3S,5S,7S)-金刚烷-1-羰基)肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)-4-溴苯磺酰胺
1H-NMR(500MHz,CDCl3)δ1.66-1.75(m,6H),1.89(s,6H),2.03(s,3H),3.03-3.07(dd,J=14.67,9.29Hz,1H),3.26-3.30(dd,J=15.16,4.89Hz,1H),4.27(brs,1H),6.54(brs,1H),6.96-7.01(m,2H),7.13-7.18(m,3H),7.24-7.32(m,4H),8.32(brs,1H),8.49(brs,1H),9.66(brs,1H)
(S)-2-(4-溴苯基磺酰胺基)-N-(4-氟苯乙基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,CDCl3)δ2.59-2.71(m,2H),2.92-3.00(m,1H),3.18-3.22(dd,J=14.67,5.86Hz,1H),3.31-3.37(m,1H),3.43-3.49(m,1H),3.83-3.87(m,1H),5.19-5.22(m,1H),6.41-6.43(m,1H),6.86-7.04(m,5H),7.20-7.35(m,7H),8.17-7.20(m,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-甲氧基苯乙基)丙酰胺
1H-NMR(500MHz,CDCl3)δ2.55-2.67(m,2H),2.95-3.00(m,1H),3.17-3.21(m,1H),3.32-3.35(m,1H),3.41-3.45(m,1H),3.77-3.78(d,J=4.40Hz,3H),3.86(m,1H),5.21-5.23(t,J=4.40Hz,1H),6.34-6.35(d,J=4.40Hz,1H),6.80-6.82(m,3H),6.98-7.05(m,3H),7.20-7.33(m,7H),8.17(brs,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(3-苯基丙基)丙酰胺
1H-NMR(500MHz,CDCl3)δ1.69-1.74(m,2H),2.53-2.56(t,6.84Hz,2H),2.95-2.99(dd,J=14.67,6.84Hz,1H),3.13-3.19(m,1H),3.22-3.26(dd,J=13.20,5.86Hz,2H),3.83-3.86(m,1H),5.20-5.21(d,J=3.91Hz,1H),6.37(brs,1H),6.90(s,1H),7.00-7.03(m,1H),7.11-7.12(d,J=7.33Hz,2H),7.17-7.31(m,10H),8.15(brs,1H)
(S)-N-((3R,5R,7R)-金刚烷-1-基)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,CDCl3)δ1.58-1.64(m,6H),1.74-1.80(m,6H),2.01(s,3H),3.05-3.09(dd,J=14.67,7.33Hz,1H),3.15-3.20(dd,J=14.67,6.84Hz,1H),3.77-3.81(q,J=7.33,6.84,6.35Hz,1H),5.35-5.36(d,J=6.35Hz,1H),5.65(s,1H),6.96(d,J=1.95Hz,1H),7.04-7.07(t,J=7.82Hz,1H),7.20-7.23(t,J=7.82Hz,1H),7.33-7.39(m,6H),8.21(brs,1H)
(S)-N-(3-(1H-吲哚-3-基)-1-(4-(4-甲氧基苯基)哌嗪-1-基)-1-氧代丙-2-基)-4-溴苯磺酰胺
1H-NMR(500MHz,CDCl3)δ1.77-1.80(t,J=8.31Hz,1H),2.34-2.41(m,2H),2.62-2.66(m,1H),2.78-2.81(m,1H),2.92-2.97(m,1H),3.10-3.16(m,2H),3.19-3.23(m,1H),3.38-3.42(m,1H),3.76(s,3H),4.48-4.53(m,1H),6.02-6.04(d,J=9.78Hz,1H),6.68-6.66(m,2H),6.77-6.80(m,2H),7.04(d,J=2.44Hz,1H),7.11-7.14(t,J=7.82Hz,1H),7.17-7.20(t,J=7.33Hz,1H),7.30-7.31(d,J=8.31Hz,1H),7.50-7.54(m,3H),7.62-7.64(d,J=8.31Hz,2H),8.11(brs,1H)
(S)-N-(3-(1H-吲哚-3-基)-1-(4-(4-甲氧基苯基)哌嗪-1-基)-1-氧代丙-2-基)-4-甲基苯磺酰胺
1H-NMR(500MHz,CDCl3)δ1.65-1.69(m,1H),2.21-2.24(m,1H),2.28-2.37(m,4H),2.53-2.56(m,1H),2.66-2.69(m,1H),2.81-2.84(m,1H),3.04-3.15(m,2H),3.21-3.25(dd,J=13.69,4.89Hz,1H),3.32-3.35(m,1H),3.75(s,3H),4.45-4.50(td,J=5.38x2,4.40Hz,1H),5.91-5.93(d,J=9.78Hz,1H),6.59-6.61(d,J=9.29Hz,2H),6.77-6.79(d,J=9.29Hz,2H),7.05-7.06(d,J=2.44Hz,1H),7.10-7.13(t,J=7.82Hz,1H),7.16-7.19(t,J=7.33Hz,1H),7.20-7.22(d,J=8.31Hz,2H),7.29-7.31(d,J=7.82Hz,1H),7.51-7.53(d,J=7.82Hz,1H),7.68-7.70(d,J=8.31Hz,2H,8.14(brs,1H)
(S)-N-((3R,5R,7R)-金刚烷-1-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,CDCl3)δ1.57-1.64(m,6H),1.74-1.80(m,6H),2.00(brs,3H),2.34(s,3H),3.04-3.08(m,1H),3.12-3.16(m,1H),3.78-3.82(q,J=6.84,6.35x2Hz,1H),5.13-5.14(d,J=6.35Hz,1H),5.75(s,1H),6.94-6.95(d,J=1.46Hz,1H),7.01-7.04(t,J=7.33Hz,1H),7.08-7.09(d,J=7.82Hz,2H),7.15-7.19(m,1H),7.32-7.36(t,J=8.80Hz,2H),7.48-7.50(d,J=8.31Hz,2H),8.27(brs,1H)
(S)-3-(1H-吲哚-3-基)-N-(4-甲氧基苯乙基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,CDCl3)δ2.33(s,3H),2.50-2.63(m,2H),3.01-3.10(m,2H),3.30-3.40(m,2H),3.77(s,3H),3.85-3.89(q,J=6.35Hz,1H),5.03-5.04(d,J=5.86Hz,1H),6.36-6.38(t,5.38Hz,1H),6.77-6.81(m,3H),6.93-6.95(d,J=8.80Hz,2H),6.98-7.01(t,J=7.33Hz,1H),7.04-7.06(d,J=7.82Hz,2H),7.15-7.18(t,J=7.82Hz,1H),7.26-7.31(m,2H),7.43-7.45(d,J=8.31Hz,2H),8.22(brs,1H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(3-苯基丙基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ1.40-1.46(m,2H),2.23(s,3H),2.34-2.37(t,J=7.33Hz,2H),2.75-2.83(m,3H),2.94-2.99(dd,J=14.18,6.84Hz,1H),3.89-3.92(t,J=6.84Hz,1H),6.90-6.93(t,J=7.33Hz,1H),7.01-7.04(t,J=7.33Hz,1H),7.07-7.17(m,6H),7.24-7.28(m,3H),7.34-7.36(d,J=7.82Hz,1H),7.48-7.49(d,J=7.82Hz,2H),7.85-7.87(t,J=5.38Hz,1H),7.93(brs,1H),10.77(s,1H)
(S)-N-(4-氟苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,CD3OD)δ2.28(s,3H),2.49-2.54(m,2H),2.80-2.84(dd,J=14.18,7.82Hz,1H),3.07-3.14(m,2H),3.23-3.27(m,1H),3.86-3.89(t,J=7.82Hz,1H),6.92-7.06(m,9H),7.26-7.27(d,J=7.82Hz,1H),7.31-7.33(d,J=7.82Hz,1H),7.40-7.42(d,J=7.82Hz,2H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.15(s,3H),2.85-2.90(dd,J=14.67,7.82Hz,1H),3.07-3.11(dd,J=14.67,6.84Hz,1H),4.28-4.31(t,J=7.33Hz,1H),6.89-6.92(t,J=7.33Hz,1H),7.01-7.06(m,4H),7.26-7.28(d,J=8.31Hz,1H),7.40-7.42(d,J=7.82Hz,1H),7.45-7.47(d,J=8.31Hz,2H),7.78-7.80(m,3H),8.06-8.08(d,J=8.31Hz,2H),8.27(brs,1H),10.78(s,1H),12.39(brs,1H)
(s)-N-(2-(1H-吲哚-3-基)乙基)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,CD3OD)δ2.72-2.84(m,3H),3.14-3.18(dd,J=14.67,5.38Hz,1H),3.27-3.30(m,1H),3.38-3.42(m,1H),3.92-3.95(dd,9.29,5.38Hz,1H),6.93-6.96(m,2H),6.99-7.03(m,2H),7.07-7.11(m,2H),7.22-7.24(m,2H),7.27-7.29(m,3H),7.32-7.36(dd,J=7.82,4.40Hz,2H),7.52-7.53(d,J=7.82Hz,1H)
(S)-N-(3-(1H-吲哚-3-基)-1-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-1-氧代丙-2-基)-4-甲基苯甲酰胺
1H-NMR(500MHz,DMSO-d6)δ2.33(s,3H),3.23-3.34(m,2H),3.78(s,3H),4.95-4.99(m,1H),6.97-7.00(m,3H),7.04-7.07(t,J=7.82Hz,1H),7.24-7.26(d,J=7.82Hz,2H),7.30-7.32(m,2H),7.45(s,1H),7.73-7.75(d,J=7.82Hz,2H),7.83-7.84(d,J=8.80Hz,3H),8.62-8.63(d,J=7.82Hz,1H),10.84(s,1H),12.64(s,1H)
(S)-2-(4-氯苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.86-2.91(dd,J=14.18,8.80Hz,1H),3.08-3.12(dd,J=14.67,6.35Hz,1H),3.78(s,3H),4.33(brs,1H),6.90-6.93(t,J=7.33Hz,1H),6.97-6.99(d,J=8.80Hz,2H),7.02-7.05(t,J=7.33Hz,1H),7.08(d,J=1.95Hz,1H),7.22-7.24(d,J=8.80Hz,2H),7.26-7.27(d,J=8.31Hz,1H),7.43(s,1H),7.46-7.48(d,J=8.80Hz,3H),7.79-7.81(d,J=8.80Hz,2H),8.50(brs,1H),10.78(s,1H),12.44(brs,1H)
(S)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-(三氟甲基)苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.88-2.93(dd,J=14.67,9.29Hz,1H),3.09-3.13(dd,J=14.18,5.18Hz,1H),3.78(s,3H),4.37(brs,1H),6.88-6.91(t,J=7.33Hz,1H),6.97-7.02(m,3H),7.10(d,J=1.95Hz,1H),7.22-7.24(d,J=8.31Hz,1H),7.42(s,1H),7.48-7.53(m,3H),7.65-7.67(d,J=7.82Hz,2H),7.79-7.80(d,J=8.31Hz,2H),8.70(brs,1H),10.77(s,1H),12.46(brs,1H)
(S)-2-(4-氟苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,CD3OD)δ2.87-2.92(dd,J=14.67,8.80,Hz,1H),3.08-3.12(dd,J=14.18,6.35Hz,1H),3.76(s,3H),4.28-4.31(dd,J=8.31,6.84Hz,1H),6.89-6.92(m,1H),6.96-7.06(m,4H),7.08(s,1H),7.26-7.28(m,1H),7.39(s,1H),7.46-7.47(d,J=7.82Hz,1H),7.54-7.58(m,2H),7.78-7.81(m,2H),10.82(brs,1H)
(S)-2-(4-溴苯基磺酰胺基)-N-((1r,3R,5S,7S)-3,5-二甲基金刚烷-1-基)-3-(1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,CDCl3)δ0.80(s,6H),1.08(s,2H),1.22-1.43(m,8H),1.59(s,2H),2.07(s,1H),3.03-3.07(dd,J=14.67,7.33Hz,1H),3.16-3.20(dd,J=14.67,6.84Hz,1H),3.77-3.80(m,1H),5.36-5.37(d,J=6.35Hz,1H),5.70(s,1H),6.97(s,1H),7.03-7.06(t,J=7.33Hz,1H),7.20-7.23(t,J=7.33Hz,1H),7.32-7.38(m,4H),7.63-7.64(d,J=8.80Hz,1H),7.77-7.79(d,J=8.31Hz,1H),8.20(s,1H)
(S)-2-(4-氰基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.85-2.90(dd,J=14.67,9.78Hz,1H),3.05-3.09(dd,J=14.18,5.38Hz,1H),3.78(s,3H),4.34(brs,1H),6.89-6.92(t,J=7.82Hz,1H),6.98-7.04(m,3H),7.07-7.08(d,J=1.95Hz,1H),7.22-7.23(d,J=8.31Hz,1H),7.46-7.52(m,6H),7.82-7.83(d,J=8.80Hz,2H),8.74(brs,1H),10.72-10.72(d,J=1.46Hz,1H),12.58(brs,1H)
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯甲酰胺基)丙酸苄酯
1H-NMR(500MHz,CDCl3)δ3.36-3.43(m,2H),5.03-5.10(m,2H),5.15-5.18(dt,J=7.82,5.38x2Hz,1H),6.69-6.70(d,J=2.44Hz,1H),6.76-6.78(d,J=7.82Hz,1H),7.01-7.04(t,J=7.33Hz,1H),7.07-7.08(d,J=8.31Hz,2H),7.10-7.13(t,J=7.33Hz,1H),7.21-7.31(m,6H),7.50-7.51(d,J=7.82Hz,1H),7.53-7.54(d,J=8.31Hz,2H),8.64(brs,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(5-羟基-1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.79-2.83(dd,J=14.18,8.31Hz,1H),2.99-3.03(dd,J=14.18,6.84Hz,1H),3.77(s,3H),4.31-4.34(q,J=8.31,7.82,7.33Hz,1H),6.58-6.60(dd,J=8.80,2.44Hz,1H),6.86(d,J=1.95Hz,1H),6.97-6.99(m,3H),7.06-7.07(d,J=8.80Hz,1H),7.40-7.46(m,4H),7.77-7.84(m,2H),8.46-8.48(d,J=8.31Hz,1H),8.61(brs,1H),10.47-10.48(d,J=1.95Hz,1H),12.4(s,1H)
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-3-(5-甲基-1H-吲哚-3-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.33(s,3H),2.82-2.86(dd,J=14.18,8.31Hz,1H),3.04-3.09(dd,J=14.67,6.84Hz,1H),3.77(s,3H),4.29(brs,1H),6.84-6.86(d,J=8.31Hz,1H),6.97-7.02(m,3H),7.14-7.16(m,2H),7.41-7.45(m,5H),7.79-7.81(d,J=8.31Hz,2H),8.47(brs,1H),10.64(s,1H),12.40(brs,1H)
(S)-2-(4-溴苯基磺酰胺基)-3-(5-氟-1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.97-3.02(dd,J=14.18,8.80Hz,1H),3.17-3.22(dd,J=14.18,5.86Hz,1H),3.81(s,3H),4.24-4.27(dd,J=8.80,6.35Hz,1H),4.62(s,1H),6.81-6.85(td,J=9.29x2,2.44Hz,1H),6.92-6.94(d,J=8.80Hz,2H),7.08(s,1H),7.12-7.14(dd,J=10.27,1.95Hz,1H),7.17(s,1H),7.21-7.22(dd,J=8.80,4.40Hz,1H),7.27-7.29(d,J=8.31Hz,2H),7.41-7.43(d,J=8.31Hz,2H),7.77-7.79(d,J=8.31Hz,2H)
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)乙基)苯甲酸
1H-NMR(500MHz,DMSO-d6)δ2.28(s,3H),2.54-2.64(m,2H),2.80-2.85(dd,J=14.18,7.82Hz,1H),3.09-3.20(m,2H),3.26-3.30(dd,J=13.20,6.35Hz,1H),3.86-3.89(dd,J=7.82,6.35Hz,1H),6.90-6.93(t,J=7.82Hz,1H),6.95(s,1H),7.00-7.02(d,J=8.31Hz,2H),7.04-7.07(t,J=6.84Hz,1H),7.14-7.15(d,J=8.31Hz,2H),7.26-7.27(d,J=7.82Hz,1H),7.31-7.32(d,J=7.82Hz,1H),7.40-7.41(d,J=8.31Hz,2H),7.90-7.91(d,J=7.82Hz,3H),10.22(s,1H)
(S)-N-(4-溴苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.27(s,3H),2.36-2.43(m,2H),2.69-2.73(dd,J=14.18,7.82Hz,1H),2.88-2.98(m,2H),3.03-3.08(dt,J=13.20,6.84,6.35Hz,1H),3.82-3.85(t,J=6.84Hz,1H),6.89-6.92(t,J=7.33Hz,1H),6.97-6.99(d,8.31Hz,2H),7.01.7.04(t,J=7.33Hz,2H),7.12-7.14(d,J=8.31Hz,2H),7.28-7.32(dd,J=11.24,8.31Hz,2H),7.37-7.39(d,J=7.33Hz,2H),7.44-7.46(d,J=7.82Hz,2H),7.91-7.93(t,J=5.38Hz,2H),10.75(brs,1H)
(S)-N-(2-(1H-吲哚-3-基)乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500Mz,CD3OD)δ2.24(s,3H),2.64-2.76(m,2H),2.82-2.86(dd,J=14.67,8.31Hz,1H),3.11-3.15(dd,J=14.67,5.86Hz,1H),3.20-3.26(m,1H),3.30-3.36(m,1H),3.89-3.91(dd,J=8.31,6.35Hz,1H),6.91-7.01(m,6H),7.04-7.10(m,2H),7.25-7.27(d,J=7.82Hz,1H),7.32-7.35(m,2H),7.36-7.38(d,J=8.31Hz,2H),7.48-7.49(d,J=7.82Hz,1H)
(S)-3-(1H-吲哚-3-基)-N-(4-甲基苯乙基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,CD3OD)δ2.27-2.27(d,J=4.89Hz,6H),2.43-2.54(m,2H),2.80-2.85(dd,J=14.18,8.13Hz,1H),3.07-3.14(m,2H),3.21-3.26(m,1H),3.86-3.89(t,J=6.84Hz,1H),6.91-7.07(m,9H),7.25-7.27(d,J=7.82Hz,1H),7.32-7.33(d,J=7.82Hz,1H),7.40-7.41(d,J=7.82Hz,2H)
2-((S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-(1H-吲哚-3-基)丙酸乙酯
1H-NMR(500MHz,CD3OD)δ1.07-1.10(t,J=7.33Hz,3H),2.18(s,3H),2.80-2.85(dd,J=14.67,8.80Hz,1H),3.06-3.18(m,3H),3.97-4.05(m,3H),4.53-4.55(t,J=6.84Hz,1H),6.82-6.84(d,J=7.82Hz,2H),6.90-6.94(m,1H),6.96(s,1H),7.00.7.06(m,3H),7.10-7.13(td,J=7.82,7.33Hz,1H),7.24-7.26(d,J=7.82Hz,1H),7.29-7.30(d,J=8.31Hz,2H),7.34-7.36(dt,J=8.31x2Hz,2H),7.45-7.46(d,J=7.82Hz,1H)
(S)-N-(4-氯苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,CD3OD)δ2.29(s,3H),2.46-2.57(m,2H),2.80-2.84(dd,J=14.18,7.82Hz,1H),3.07-3.14(m,2H),3.24-3.29(m,1H),3.86-3.89(t,J=6.35Hz,1H),6.91-6.96(m,2H),7.02-7.08(m,5H),7.19-7.21(d,J=8.31Hz,2H),7.26-7.28(d,J=7.82Hz,1H),7.31-7.33(d,J=7.82Hz,1H),7.41-7.42(d,J=7.82Hz,2H)
2-((S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-(1H-吲哚-3-基)丙酸
1H-NMR(500MHz,CD3OD)δ2.18(s,3H),2.57-2.62(dd,J=14.67,10.27,Hz,1H),3.12-3.21(dd,J=14.67,3.42Hz,1H),3.21-3.25(dd,J=14.67,6.35Hz,1H),3.37-3.41(dd,J=14.67,4.89Hz,1H),3.87-3.89(dd,J=9.78,3.91Hz,1H),4.51-4.53(t,J=5.86Hz,1H),6.72-6.74(d,J=8.31Hz,2H),6.84(s,1H),6.86-6.89(t,J=7.82Hz,1H),6.97-7.00(t,J=7.82Hz,1H),7.02.7.09(m,2H),7.13-7.15(m,3H),7.20-7.21(d,J=7.82Hz,1H),7.29-7.32(dd,J=7.33,6.84Hz,2H),7.59-7.61(d,J=7.82Hz,1H)
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸甲酯
1H-NMR(500MHz,DMSO-d6)δ2.16(s,3H),2.49-2.50(dd,J=14.18,7.82,6.35Hz,1H),3.07-3.11(dd,J=14.18,7.33,6.84Hz,1H),3.85(s,3H),4.30(brs,1H),6.89-6.92(t,J=7.33Hz,1H),7.01-7.07(m,4H),7.26-7.28(d,J=7.82Hz,1H),7.41-7.42(d,J=7.82Hz,1H),7.45-7.47(d,J=8.31Hz,2H),7.80(s,1H),8.01(s,4H),8.27(brs,1H),10.79(s,1H),12.41(brs,1H)
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸
1H-NMR(500MHz,DMSO-d6)δ2.18(s,3H),2.87-2.91(dd.J=14.18,7.82Hz,1H),3.09-3.13(dd,J=14.18,6.84Hz,1H),4.31-4.36(q,J=7.82x3Hz,1H),6.91-6.94(t,J=7.33Hz,1H),7.03-7.09(m,4H),7.28-7.30(d,J=7.82Hz,1H),7.43-7.44(d,J=7.82Hz,1H),7.47-7.49(d,J=7.82Hz,2H),7.80(s,1H),7.99-8.03(m,4H),8.28-8.30(d,J=8.80Hz,1H),10.81(s,1H),12.43(s,1H),12.98(brs,1H)
(S)-3-(苯并[d]噁唑-2-基氨基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-甲基苯基磺酰胺基)丙酰胺
1H-NMR(500MHz,DMSO-d6)δ2.13(s,3H),3.51-3.55(m,2H),3.79(s,3H),4.35-4.36(d,J=5.38Hz,1H),6.98-7.01(m,3H),7.11-7.15(m,3H),7.22-7.24(d,J=7.82Hz,1H),7.30-7.32(d,J=7.82Hz,1H),7.44(s,1H),7.65-7.66(d,J=8.31Hz,2H),7.80-7.82(d,J=8.31Hz,2H),7.99-8.01(t,J=6.35Hz,1H),8.20-8.21(d,J=5.86Hz,1H),12.33(brs,1H)
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)苯甲酰胺
1H-NMR(500MHz,CD3OD)δ2.20(s,3H),3.63-3.67(m,1H),3.73-3.75(m,1H),3.88(s,3H),4.33-4.35(t,J=6.35Hz,1H),6.99-7.01(d,J=8.80Hz,2H),7.17-7.18(d,J=7.82Hz,2H),7.24(s,1H),7.47-7.50(m,2H),7.57-7.60(m,1H),7.74-7.78(dd,J=14.18,7.82Hz,4H),7.85-7.86(d,J=8.31Hz,2H)
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)烟酰胺
1H-NMR(500MHz,DMSO-d6)δ2.14(s,3H),3.48-3.53(dt,J=13.20,6.84,6.35Hz,1H),3.56-3.63(m,1H),3.78(s,3H),4.23-4.26(t,J=6.84Hz,1H),6.97-6.99(d,J=8.80Hz,2H),7.14-7.16(d,J=8.31Hz,2H),7.42(s,1H),7.45-7.48(dd,J=7.82,4.89,2.93Hz,1H),7.64-7.66(d,J=8.31Hz,2H),7.79-7.80(d,J=8.80Hz,2H),8.01-8.03(dt,J=7.82,1.95x2Hz,1H),8.11(brs,1H),8.65-8.68(m,2H),8.84-8.85(d,J=1.46Hz,1H),12.28(brs,1H)
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)嘧啶-5-甲酰胺
1H-NMR(500MHz,DMSO-d6)δ2.16(s,3H),3.49-3.53(dt,J=13.69,6.84x2Hz,1H),3.57-3.63(dt,J=13.20,6.35x2Hz,1H),3.79(s,3H),4.23-4.26(m,1H),6.98-7.00(d,J=8.80Hz,2H),7.17-7.19(d,J=8.31Hz,2H),7.45(s,1H),7.65-7.67(d,J=8.31Hz,2H),7.79-7.81(d,J=8.80Hz,2H),8.18-8.19(d,J=7.82Hz,1H),8.87-8.89(t,J=5.86Hz,1H),9.00(s,2H),9.31(s,1H),12.31(brs,1H).
实施例2:DX2-Nanoluc荧光素酶活性(40uM)和细胞活力(%抑制)
将DX2克隆到表达nano1uc荧光素酶的质粒中后,将质粒转染到A549细胞中。将转染的细胞以每孔1X104接种在96孔板中并稳定12小时。将化合物处理4小时,然后通过萤光素酶试验观察DX2的表达变化。在A549细胞中用各个浓度的化合物处理72小时后,通过MTT方法测量细胞活力。
结果如上表1所示。
实施例3:AIMP2-DX2和AIMP2抑制评估(nanoluc荧光素酶试验)
从表1中显示出优异效果的化合物中选择化合物63,并进行以下实验。
为了计算化合物63的IC50,将表达nanoluc荧光素酶-DX2或-AIMP2的A549细胞用各个浓度的化合物63处理4小时,然后测量荧光。
其结果示于图1。
如图1所示,证实了化合物63对AIMP2-DX2和AIMP2的抑制率表明对AIMP2-DX2的选择性是100倍或以上(DX2 IC50=0.92μM,AIMP2 IC50>100μM)。
实施例4:AIMP2-DX2抑制机制研究
如之前报道,AIMP2-DX2通过与HSP70结合而稳定。因此,本发明人检查了表现出最佳AIMP2-DX2抑制能力的化合物63是否能够抑制AIMP2-DX2和HSP70的结合。具体地,使用纯化的AIMP2-DX2和HSP70蛋白质在化合物63存在下进行体外拉下试验。
其结果示于图2。
如图2所示,证实化合物63以浓度依赖性方式抑制AIMP2-DX2与HSP70的结合。
实施例5:体内抗癌功效评价
接下来,在移植有H460细胞的小鼠模型中评估了化合物63的抗癌功效。
具体地,将化合物63以50mg/kg向移植有H460细胞的小鼠腹膜内给药,每两天一次,持续总共15天。
结果示于图3a至3d中。
如图3a至3d所示,化合物63显着抑制肿瘤的生长,并且证实了给药期间动物体重没有变化。
实施例6:化合物55和化合物89对体内癌症生长的抑制作用
另外,从表1中选取化合物55和化合物88,进行了体内癌症生长抑制效果实验。
将H460细胞(2X107)皮下植入7周龄BALB/cAnCr雌性大鼠,然后腹腔给药化合物55或化合物89(50mg/kg)和紫杉醇(10mg/kg),每2天一次。给药16天,给药期间测量肿瘤大小和动物体重。16天后,处死动物并测量移除的肿瘤的大小和重量。
其结果示于图4。
在治疗浓度下,化合物55在治疗期间表现出约50%的癌症生长抑制效果,并且由于治疗期间动物体重没有变化,所以判断该化合物没有副作用。
工业实用性
本发明由式1表示的化合物在抑制AIMP2-DX2的表达方面非常有效,因此可以非常有用地在AIMP2-DX2引起的各种疾病的发展中使用,特别是用作癌症的治疗剂。
Claims (15)
1.由下式1表示的化合物或其药学上可接受的盐:
<式1>
在式1中,
R1是氢;被一个或多个选自羟基、取代或未取代的苯基、巯基和C1~C5烷硫基的取代基取代或未取代的C1~C5直链或支链烷基;未取代的或被一个或多个选自C1~C5烷基、羟基、羟基羰基和甲酰基的取代基取代的吲哚基甲基;C1~C5羧甲基;C7~C10羟基苯基烷基;取代或未取代的C3~C8环烷基;取代或未取代的C1~C5氨基烷基;
R2是氢;未取代的或被一个或多个选自C1~C5直链或支链烷基、硝基、胺基、卤素、-CF3、C1~C5烷基羰基氨基、-COOH、C1~C5烷氧基、苯基、-OCH2Ph、羟基、-COOCH2Ph、C1~C5烷氧基羰基、-CONHCH3和腈的取代基取代的苯磺酰基;萘磺酰基;苄基磺酰基;未取代的或被一个或多个选自C1~C5直链或支链烷基和C1~C5直链或支链烷基胺基的取代基取代的苯甲酰基;噻吩磺酰基;C1~C5烷氧基羰基;或苯基氨基羰基;
5.权利要求1的化合物或其药学上可接受的盐,
其中所述式1的化合物为
(S)-4-甲基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺,
(R)-4-甲基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺,
(S)-4-甲基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺,
(R)-4-甲基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)-戊-2-基)苯磺酰胺,
(S)-N-(1-(1,1-二氧化硫代吗啉代)-4-甲基-1-氧代戊-2-基)-4-甲基苯磺酰胺,
(N-((S)-1-((R)-2-(羟甲基)吡咯烷-1-基)-4-甲基-1-氧代戊-2-基)-4-甲基苯磺酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(哌啶-1-基)苯基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-甲基哌啶-1-基)苯基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-(4-甲基哌啶-1-基)吡啶-3-基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-(4-甲基哌啶-1-基)嘧啶-4-基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(6-吗啉代吡啶-3-基)戊酰胺,
(S)-N-(6-((2S,6R)-2,6-二甲基吗啉代)吡啶-3-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(3-氟-4-吗啉代苯基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(4-(1,1-二氧化硫代吗啉代)苯基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-(5-(4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺基)吡啶-2-基)哌嗪-1-甲酸叔丁酯,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(吡咯烷-1-基)苯基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(2-吗啉代乙基)戊酰胺,
(S)-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-硝基苯磺酰胺,
(S)-3-氨基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯磺酰胺,
(S)-2-(4-氟苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-2-(4-溴苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(4-(三氟甲基)苯基磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(3-硝基苯基磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(萘-1-磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(萘-2-磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(苯基磺酰胺基)戊酰胺,
(S)-4-甲基-2-(3-(苯基磺酰基)丙酰胺基)戊酸苄酯,
(S)-2-(4-甲氧基苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(噻吩-2-磺酰胺基)戊酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(4-硝基苯基磺酰胺基)戊酰胺,
(S)-2-(4-异丙基苯基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-2-(联苯-4-基磺酰胺基)-4-甲基-N-(4-吗啉代苯基)戊酰胺,
(S)-4-(苄基氧基)-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺,(S)-4-羟基-N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)苯磺酰胺,
(S)-4-(N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)氨磺酰基)苯甲酸苄酯,
(S)-3-(4-甲基苯基磺酰胺基)-4-吗啉代-4-氧代丁酸叔丁酯,
(S)-4-甲基-N-(1-吗啉代-1-氧代-3-苯基丙-2-基)苯磺酰胺,
(S)-N-(3-羟基-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-4-甲基-N-(3-甲基-1-吗啉代-1-氧代丁-2-基)苯磺酰胺,
(R)-N-(3-巯基-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(2S,3S)-3-羟基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丁酰胺,
(2S,3S)-3-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)戊酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-4-(甲硫基)-N-(4-吗啉代苯基)丁酰胺,
(S)-3-(1H-吲哚-2-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1-甲基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-苯基丙酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酸苄酯,
(S)-4-甲基-2-(4-甲基苯甲酰胺基)戊酸苄酯,
(S)-2-(4-叔丁基苯甲酰胺基)-4-甲基戊酸苄酯,
(S)-2-(苯并[d][1,3]二氧杂环戊烯-5-甲酰胺基)-4-甲基戊酸苄酯,
(S)-2-(4-(叔丁氧基羰基氨基)苯甲酰胺基)-4-甲基戊酸苄酯,
(S)-4-甲基-2-(3-(苯基磺酰基)丙酰胺基)戊酸苄酯,
(S)-N-(4-(4-甲氧基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-1-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-苯基脲,
(S)-4-叔丁基-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)苯甲酰胺,
(S)-N-(4-甲基-1-吗啉代-1-氧代戊-2-基)-3-(苯基磺酰基)丙酰胺,
(S)-4-叔丁基-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯甲酰胺,
(S)-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯并[d][1,3]二氧杂环戊烯-5-甲酰胺,
(S)-4-甲基-N-(4-吗啉代苯基)-2-(3-(苯基磺酰基)丙酰胺基)戊酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(2-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(3-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-2-(3,5-二甲基苯基磺酰胺基)-3-(1H-吲哚-3-基)N-(4吗啉代苯基)丙酰胺,
(S)-2-(4-氟苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(4-(三氟甲基)苯基磺酰胺基)丙酰胺,
(S)-3-(5-羟基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-吗啉代-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(5-吗啉代噻唑-2-基)丙酰胺,
(S)-2-(2,4-二甲基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
3-(3-乙氧基-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)-1H-吲哚-5-羧酸,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-(1-甲苯磺酰基-1H-咪唑-4-基)丙酰胺,
(S)-N-(6-((2S,6R)-2,6-二甲基吗啉代)吡啶-3-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙烯酰胺,
(R)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-N-(3-氟-4-吗啉代苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(4-硝基苯基磺酰胺基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲氧基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-异丙基苯基磺酰胺基)-N-(4吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-异丙基苯基磺酰胺基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙烯酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-甲基噻唑-2-基)丙酰胺,
(S)-N-(苯并[d]噻唑-2-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酸,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(5-吗啉代噻唑-2-基)戊酰胺,
(S)-N-(5-(4-甲氧基苯基)-1,3,4-噻二唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(5-(4-甲氧基苯基)异噁唑-3-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(3-(4-甲氧基苯基)异噁唑-5-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)戊酰胺,
(S)-N-(4-(3,4-二甲氧基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-N-(4-(2-溴-4-氟苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-(2-氨基噻唑-4-基)苯基-4-甲基-2-(4-甲基苯基磺酰胺基)戊酸酯,
(S)-N-(4-(4-氟苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲氧基)苯基)噻唑-2-基)戊酰胺,
(S)-N-(4-(4-羟基苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-对甲苯基噻唑-2-基)戊酰胺,
(S)-N-(4-(4-((S)-1-甲氧基丙-2-基氧基)苯基)噻唑-2-基)-4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-4-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-(4-吗啉代苯基)噻唑-2-基)戊酰胺,
(S)-甲基-4-(2-(4-甲基-2-(4-甲基苯基磺酰胺基)戊酰胺基)噻唑-4-基)苯甲酸酯,
(S)-4-(2-(4-甲基苯基磺酰胺基)-3-(4-吗啉代苯基氨基)-3-氧代丙基)苯基4-甲基苯磺酸酯,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-咪唑-4-基)N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-N-甲氧基-N,4-二甲基-2-(4-甲基苯基磺酰胺基)戊酰胺,
(S)-3-(1H-吲哚-3-基)-N-甲氧基-N-甲基-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)丙-2-基)-4-甲基苯磺酰胺,
(S)-2-(4-叔丁基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(2-氯苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(2,4-二甲氧基苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(噻唑-2-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(5-甲基噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-甲基噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(5-甲基噻唑-2-基)丙酰胺,
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸甲酯,
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸乙酯,
(S)-3-(4-苯甲酰基苯基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)-N-甲基苯甲酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-(萘-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基氨基甲酸叔丁酯,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酸,
(S)-4-(4-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-甲氧基苯基)哌嗪-1-甲酸叔丁酯,
(S)-3-(1H-吲哚-3-基)-N-(2-甲氧基-4-(哌嗪-1-基)苯基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-4-(4-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)苯基)哌嗪-1-甲酸叔丁酯,
(S)-3-(1H-吲哚-3-基)-N-(2-甲氧基-4-吗啉代苯基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(哌嗪-1-基)苯基)丙酰胺,
(S)-3-(1-甲酰基-1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(3-(4-甲氧基苯基)异噁唑-5-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酸苄酯,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯甲酰胺基)丙酸苄酯,
(S)-N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)-4-甲基苯甲酰胺,
(S)-3-羟基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-甲基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丁酰胺,
(S)-1-(3-(1H-吲哚-3-基)-1-吗啉代-1-氧代丙-2-基)-3-苯基脲,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(6-吗啉代吡啶-3-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(2-吗啉代嘧啶-5-基)丙酰胺,
(S)-2-(4-氰基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)-2-(6-(三氟甲基)吡啶-3-磺酰胺基)丙酰胺,
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸甲酯,
(S)-3-(1H-苯并[d]咪唑-1-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(R)-3-(2,3-二氧代-3,4-二氢喹喔啉-1(2H)-基)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)丙酰胺,
(S)-N-(5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基)-5-(三氟甲基)吡啶甲酰胺,
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸苄酯,
(S)-3-(4-甲基苯基磺酰胺基)-4-(4-吗啉代苯基氨基)-4-氧代丁酸苄酯,
(S)-4-甲基-N-(4-甲基-1-(4-吗啉代苯基氨基)-1-氧代戊-2-基)苯甲酰胺,
2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)乙酰胺,
(S)-3-(4-甲基苯基磺酰胺基)-4-(4-吗啉代苯基氨基)-4-氧代丁酸,
(S)-4-(4-甲基苯基磺酰胺基)-5-(4-吗啉代苯基氨基)-5-氧代戊酸,
(S)-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)-3-苯基丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-苯基丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-苯基丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(噻吩-2-基甲基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(噻吩-2-基甲基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(2-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-N-(3-(N-(4-甲基-1-吗啉代-1-氧代戊-2-基)氨磺酰基)苯基)乙酰胺,
(S)-4-甲基-2-(3-苯基脲基)戊酸苄酯,
4-甲基-N-(2-吗啉代-2-氧代乙基)苯磺酰胺,
4-甲基-N-(1-(吗啉-4-羰基)环己基)苯磺酰胺,
(S)-4-(N-(4-甲基-1-氧代-1-(1,4,7-三氧杂-10-氮杂环十二烷-10-基)戊-2-基)氨磺酰基)苯甲酸,
(S)-2-(4-羟基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙烯酰胺,
(S)-4-(N-(3-(1H-吲哚-3-基)-1-(4-吗啉代苯基氨基)-1-氧代丙-2-基)氨磺酰基)苯甲酸,
(S)-2-氨基-3-(1H-吲哚-3-基)-N-(4-吗啉代苯基)丙烯酰胺,
(S)-N-(4-(4-乙酰基哌嗪-1-基)-2-甲氧基苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙烯酰胺,
(S)-N-(4-(4-乙酰基哌嗪-1-基)苯基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙烯酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-吗啉代苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(4-吗啉代苯基)噻唑-2-基)丙酰胺,
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸甲酯,
(S)-3-(1H-吲哚-3-基)-2-(6-(三氟甲基)吡啶-3-磺酰胺基)丙酸苄酯,
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-(4-硝基苯基)戊二酰胺,
(S)-5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基氨基甲酸苄酯,
(S)-6-氨基-2-(4-甲基苯基磺酰胺基)-N-(4-吗啉代苯基)己酰胺,
(S)-3,5-二甲氧基-N-(5-(4-甲基苯基磺酰胺基)-6-(4-吗啉代苯基氨基)-6-氧代己基)苯甲酰胺,
(S)-N5-(4-甲氧基苄基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-苯基戊二酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-5-吗啉代-N-(4-吗啉代苯基)-5-氧代戊酰胺,
S)-N5-(4-氟苯基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺,
(S)-N5-(4-叔丁基苯基)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)戊二酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N5-(4-(三氟甲基)苯基)戊二酰胺,
(S)-2-(4-甲基苯基磺酰胺基)-N1-(4-吗啉代苯基)-N4-(4-硝基苯基)琥珀酰胺,
(S)-N-(呋喃-2-基甲基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(呋喃-2-基甲基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-异丙基-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-异丙基丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-甲氧基苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰基)-N-(4-甲氧基苯基)肼甲酰胺,
(S)-4-溴-N-(1-(3,5-二甲基-1H-吡唑-1-基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-氧代-1-(3-苯基-1H-吡唑-1-基)丙-2-基)-4-溴苯磺酰胺,
N-((S)-1-(2-((3S,5S,7S)-金刚烷-1-羰基)肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(对甲苯基)噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-苯乙基丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-氟苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-硝基苯基)噻唑-2-基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(2-(4-甲氧基苯甲酰基)肼基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-氰基苯基)噻唑-2-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)丙酰胺,
(S)-4-溴-N-(1-(2-十二酰基肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺,
(S)-4-溴-N-(1-(2-癸酰基肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)苯磺酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-苯乙基丙酰胺,
N-((S)-1-(2-((3S,5S,7S)-金刚烷-1-羰基)肼基)-3-(1H-吲哚-3-基)-1-氧代丙-2-基)-4-溴苯磺酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-氟苯乙基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-甲氧基苯乙基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(3-苯基丙基)丙酰胺,
(S)-N-((3R,5R,7R)-金刚烷-1-基)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(4-(4-甲氧基苯基)哌嗪-1-基)-1-氧代丙-2-基)-4-溴苯磺酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-(4-(4-甲氧基苯基)哌嗪-1-基)-1-氧代丙-2-基)-4-甲基苯磺酰胺,
(S)-N-((3R,5R,7R)-金刚烷-1-基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-甲氧基苯乙基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(3-苯基丙基)丙酰胺,
(S)-N-(4-氟苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)-N-(4-(4-(三氟甲基)苯基)噻唑-2-基)丙酰胺,
(S)-N-(2-(1H-吲哚-3-基)乙基)-2-(4-溴苯基磺酰胺基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-N-(3-(1H-吲哚-3-基)-1-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-1-氧代丙-2-基)-4-甲基苯甲酰胺,
(S)-2-(4-氯苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-(三氟甲基)苯基磺酰胺基)丙酰胺,
(S)-2-(4-氟苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-((1r,3R,5S,7S)-3,5-二甲基金刚烷-1-基)-3-(1H-吲哚-3-基)丙酰胺,
(S)-2-(4-氰基苯基磺酰胺基)-3-(1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-3-(1H-吲哚-3-基)-2-(4-甲基苯甲酰胺基)丙酸苄酯,
(S)-2-(4-溴苯基磺酰胺基)-3-(5-羟基-1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-2-(4-溴苯基磺酰胺基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-3-(5-甲基-1H-吲哚-3-基)丙烯酰胺,
(S)-2-(4-溴苯基磺酰胺基)-3-(5-氟-1H-吲哚-3-基)-N-(4-(4-甲氧基苯基)噻唑-2-基)丙酰胺,
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)乙基)苯甲酸,
(S)-N-(4-溴苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-N-(2-(1H-吲哚-3-基)乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙烯酰胺,
(S)-3-(1H-吲哚-3-基)-N-(4-甲基苯乙基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
2-((S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-(1H-吲哚-3-基)丙酸乙酯,
(S)-N-(4-氯苯乙基)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
2-((S)-3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)-3-(1H-吲哚-3-基)丙酸,
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸甲酯,
(S)-4-(2-(3-(1H-吲哚-3-基)-2-(4-甲基苯基磺酰胺基)丙酰胺基)噻唑-4-基)苯甲酸,
(S)-3-(苯并[d]噁唑-2-基氨基)-N-(4-(4-甲氧基苯基)噻唑-2-基)-2-(4-甲基苯基磺酰胺基)丙酰胺,
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)苯甲酰胺,
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)烟酰胺,或
(S)-N-(3-((4-(4-甲氧基苯基)噻唑-2-基)氨基)-2-(4-甲基苯基磺酰胺基)-3-氧代丙基)嘧啶-5-甲酰胺。
6.权利要求1-5中任一项的化合物,其中所述化合物或其药学上可接受的盐抑制AIMP2-DX2的表达。
8.用于预防或治疗癌症的药物组合物,其包含权利要求1-5中任一项的化合物或其药学上可接受的盐作为活性成分。
9.权利要求8的药物组合物,其中所述癌症选自白血病、脑瘤、肾癌、胃癌、皮肤癌、膀胱癌、乳腺癌、子宫癌、黑色素瘤、甲状腺癌、头颈癌、淋巴瘤、胆囊癌、食管癌、肺癌、结肠癌、前列腺癌、卵巢癌、肝癌、结直肠癌、腹膜癌、腹膜转移癌和胰腺癌。
10.用于预防或治疗炎症性疾病的药物组合物,其包含权利要求1-5中任一项的化合物或其药学上可接受的盐作为活性成分。
11.权利要求10的药物组合物,其中所述炎症性疾病选自炎症性皮肤病、克罗恩病、溃疡性结肠炎、腹膜炎、骨髓炎、蜂窝织炎、脑膜炎、脑炎、胰腺炎、创伤性休克、支气管哮喘、变应性鼻炎、囊性纤维化、中风、急性支气管炎、慢性支气管炎、急性细支气管炎、慢性细支气管炎、骨关节炎、痛风、脊椎关节病、强直性脊柱炎、莱特尔氏综合征、牛皮癣性关节病、肠脊椎炎、青少年关节病、青少年强直性脊柱炎、反应性关节病、感染性关节炎、感染后关节炎、淋球菌性关节炎、结核性关节炎、病毒性关节炎、真菌性关节炎、梅毒性关节炎、莱姆病、与“血管炎综合征”相关的关节炎、结节性多动脉炎、过敏性血管炎、卢伽雷肉芽肿病、风湿性多肌痛、关节细胞动脉炎、钙结晶沉积性关节病、假性痛风、非关节风湿病、滑囊炎、肌腱炎、上髁炎(网球肘)、神经性关节病(夏科氏关节)、关节积血、过敏性紫癜、肥大性骨关节病、多中心网状细胞瘤、腹股沟炎、血色素沉着病、镰刀形细胞病和其他血红蛋白病、高蛋白血症、低丙球蛋白血症、家族性地中海贫血、Behat′s病、系统性红斑狼疮、回归热、银屑病、多发性硬化症、败血症、感染性休克、多器官功能障碍综合征、急性呼吸窘迫综合征、慢性阻塞性肺病、类风湿性关节炎、急性肺损伤和支气管肺发育不良。
12.权利要求1-5中任一项的化合物或其药学上可接受的盐在制备用于预防或治疗癌症的药剂中的用途。
13.治疗癌症的方法,其包括向需要其的个体给药有效量的包含权利要求1-5中任一项的化合物或其药学上可接受的盐作为活性成分的组合物。
14.权利要求1-5中任一项的化合物或其药学上可接受的盐在制备用于预防或治疗炎症性疾病的药剂中的用途。
15.治疗炎症性疾病的方法,其包括向需要其的个体给药有效量的包含权利要求1-5中任一项的化合物或其药学上可接受的盐作为活性成分的组合物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2019-0037271 | 2019-03-29 | ||
KR20190037271 | 2019-03-29 | ||
PCT/KR2020/004364 WO2020204548A1 (ko) | 2019-03-29 | 2020-03-30 | 항암활성을 갖는 신규한 화합물 및 이의 제조방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113874361A true CN113874361A (zh) | 2021-12-31 |
CN113874361B CN113874361B (zh) | 2024-07-12 |
Family
ID=72666766
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202080039308.0A Active CN113874361B (zh) | 2019-03-29 | 2020-03-30 | 具有抗癌活性的化合物及其制备方法 |
Country Status (6)
Country | Link |
---|---|
US (1) | US20220204497A1 (zh) |
EP (1) | EP3939968A4 (zh) |
JP (1) | JP2022528950A (zh) |
KR (1) | KR102520437B1 (zh) |
CN (1) | CN113874361B (zh) |
WO (1) | WO2020204548A1 (zh) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20050104045A (ko) * | 2004-04-27 | 2005-11-02 | 재단법인서울대학교산학협력재단 | 종양 억제자로 작용하는 aim3의 신규 용도 |
CN102834098A (zh) * | 2009-11-05 | 2012-12-19 | 首尔大学产学协力团 | 苯并杂环衍生物的用于癌预防及治疗或抑制癌转移的用途 |
JP2014118360A (ja) * | 2012-12-13 | 2014-06-30 | Ktn Biotech Co Ltd | 新規抗癌剤 |
EP3020399A1 (en) * | 2013-06-14 | 2016-05-18 | Medicinal Bioconvergence Research Center | Novel pharmaceutical composition for preventing or treating cancer |
WO2016119690A1 (zh) * | 2015-01-28 | 2016-08-04 | 中国科学院广州生物医药与健康研究院 | 一种2-氧代-1,2-二氢苯并[cd]吲哚类化合物及其应用 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2508444B2 (ja) * | 1987-06-25 | 1996-06-19 | ソニー株式会社 | カラ−陰極線管 |
UA73543C2 (uk) * | 1999-12-07 | 2005-08-15 | Тераванс, Інк. | Похідні сечовини, фармацевтична композиція та застосування похідного при приготуванні лікарського засобу для лікування захворювання, яке опосередковується мускариновим рецептором |
US7459529B2 (en) | 2004-11-24 | 2008-12-02 | Seoul National University Industry Foundation | AIMP2-DX2 and its uses |
KR101067816B1 (ko) | 2007-11-09 | 2011-09-27 | (주)네오믹스 | Aimp2-dx2의 억제제를 유효성분으로 포함하는 염증성질환 예방 및 치료용 조성물 |
CN103403018B (zh) * | 2010-12-21 | 2015-08-19 | 医药公司(莱比锡)有限公司 | 胰蛋白酶样丝氨酸蛋白酶抑制剂,它们的制备以及作为凝结因子IIa和Xa的选择性抑制剂的用途 |
CN117986372A (zh) | 2016-07-29 | 2024-05-07 | 中外制药株式会社 | 显示增加的备选fviii辅因子功能活性的双特异性抗体 |
WO2018102006A1 (en) * | 2016-11-30 | 2018-06-07 | Ensemble Therapeutics Corporation | Compounds for the inhibition of indoleamine-2,3-dioxygenase activity and use thereof |
-
2020
- 2020-03-30 US US17/599,931 patent/US20220204497A1/en active Pending
- 2020-03-30 EP EP20784904.3A patent/EP3939968A4/en active Pending
- 2020-03-30 WO PCT/KR2020/004364 patent/WO2020204548A1/ko unknown
- 2020-03-30 CN CN202080039308.0A patent/CN113874361B/zh active Active
- 2020-03-30 KR KR1020200038419A patent/KR102520437B1/ko active IP Right Grant
- 2020-03-30 JP JP2021560303A patent/JP2022528950A/ja active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20050104045A (ko) * | 2004-04-27 | 2005-11-02 | 재단법인서울대학교산학협력재단 | 종양 억제자로 작용하는 aim3의 신규 용도 |
CN102834098A (zh) * | 2009-11-05 | 2012-12-19 | 首尔大学产学协力团 | 苯并杂环衍生物的用于癌预防及治疗或抑制癌转移的用途 |
JP2014118360A (ja) * | 2012-12-13 | 2014-06-30 | Ktn Biotech Co Ltd | 新規抗癌剤 |
EP3020399A1 (en) * | 2013-06-14 | 2016-05-18 | Medicinal Bioconvergence Research Center | Novel pharmaceutical composition for preventing or treating cancer |
WO2016119690A1 (zh) * | 2015-01-28 | 2016-08-04 | 中国科学院广州生物医药与健康研究院 | 一种2-氧代-1,2-二氢苯并[cd]吲哚类化合物及其应用 |
Non-Patent Citations (3)
Title |
---|
M. M. GARAZD ET AL., 《CHEM. HETEROCYCL. COMPD》, vol. 35, no. 6, pages 658 - 662 * |
MARGRITH E. MATTMANN ET AL., 《BIOORGANIC & MEDICINAL CHEMISTRY LETTERS》, vol. 22, pages 5936 - 5941 * |
VASSILIKI THEODOROU-KASSIOUMIS ET AL., 《TETRAHEDRON LETTERS》, vol. 26, no. 42, pages 4439 - 4442 * |
Also Published As
Publication number | Publication date |
---|---|
US20220204497A1 (en) | 2022-06-30 |
EP3939968A1 (en) | 2022-01-19 |
EP3939968A4 (en) | 2022-12-14 |
CN113874361B (zh) | 2024-07-12 |
JP2022528950A (ja) | 2022-06-16 |
KR102520437B1 (ko) | 2023-04-12 |
WO2020204548A1 (ko) | 2020-10-08 |
KR20200116065A (ko) | 2020-10-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES2560612T3 (es) | Derivados bencilamina como inhibidores de la calicreina plasmática | |
US8461209B2 (en) | Malonic acid sulfonamide derivative and pharmaceutical use thereof | |
AU2016206369B2 (en) | N-acyloxysulfonamide and n-hydroxy-n-acylsulfonamide derivatives | |
US7166590B2 (en) | Amino acid derivatives | |
US6593327B2 (en) | Compounds and compositions as protease inhibitors | |
US8822530B2 (en) | Sulfur derivatives as chemokine receptor modulators | |
CA2972366C (en) | Necrosis inhibitors | |
CA2634005C (en) | N-hydroxyamide derivatives possessing antibacterial activity | |
PT832061E (pt) | Derivados de banzamida e sua utilizacao como antagonistas da vasopressina | |
WO1996018608A1 (fr) | Derives d'aniline a activite inhibant la monoxyde d'azote synthase | |
BRPI0912878A2 (pt) | derivados de indazóis substituídos por fenila e benzodioxinila | |
AU2010328230A1 (en) | Bis-acylated hydroxylamine derivatives | |
EA009735B1 (ru) | Сульфонамидные производные для лечения заболеваний | |
AU2021394226B2 (en) | Benzylamine or benzyl alcohol derivative and use thereof | |
WO2008053913A1 (fr) | Dérivé de sulfonylurée capable d'inhiber sélectivement mmp-13 | |
KR20070112240A (ko) | 히스톤 탈아세틸화효소 저해제로서 하이드록사메이트 및이를 함유하는 약학적 제제 | |
CN113874361B (zh) | 具有抗癌活性的化合物及其制备方法 | |
ES2213563T3 (es) | Compuestos de tiopirano como inhibidores de mmp. | |
EP3325452B1 (en) | Substituted hydrophobic benzene sulfonamide thiazole compounds for use in treating cancer | |
JP2006528964A (ja) | グリオキサラーゼ阻害物質 | |
JP2004508350A (ja) | 置換フェニルシクロヘキサンカルボン酸アミドおよびその使用 | |
WO1999012912A1 (en) | Thiourea derivatives or non-toxic salts thereof for inhibitng ras-transformed cell growth | |
WO2012047926A2 (en) | Sulfonamide-containing compounds |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |