部分構造検索

131059

Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCCc4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #78721
title compound
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCC(=O)c4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #78722
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(N)nc4c(C)cc(C)nc43)cc2)cc1.Cl.Cl
Reaction #78732
title compound
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)Nc1c(C)cc(C)nc1Nc1ccc(CCNC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #78733
N-{[(2-{4-[(4,6-dimethyl-{[(methylamino)carbonothioyl]amino}-2-pyridinyl)amino]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)Nc1c(C)cc(C)nc1Nc1ccc(CCNC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #273139
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(Nc3nc(C)cc(C)c3[N+](=O)[O-])cc2)cc1
Reaction #811297
title compound
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(Nc3nc(C)cc(C)c3N)cc2)cc1
Reaction #811298
title compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCC(=O)c4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #811311
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(N)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #811348
title compound
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)Nc1c(C)cc(C)nc1Nc1ccc(CCNC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #811349
N-{[(2-{4-[(4,6-dimethyl-{[(methylamino)carbonothioyl]amino}-2-pyridinyl)amino]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(Nc3nc(C)cc(C)c3[N+](=O)[O-])cc2)cc1
Reaction #945655
title compound
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCC(=O)c4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #945666
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(N)nc4c(C)cc(C)nc43)cc2)cc1.Cl.Cl
Reaction #945699
title compound
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)Nc1c(C)cc(C)nc1Nc1ccc(CCNC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #945700
N-{[(2-{4-[(4,6-dimethyl-{[(methylamino)carbonothioyl]amino}-2-pyridinyl)amino]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(Nc3nc(C)cc(C)c3[N+](=O)[O-])cc2)cc1
Reaction #1541847
title compound
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(Nc3nc(C)cc(C)c3N)cc2)cc1
Reaction #1541848
title compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCCc4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #1541856
title compound
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCC(=O)c4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #1541857
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(N)nc4c(C)cc(C)nc43)cc2)cc1.Cl.Cl
Reaction #1541890
title compound
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)Nc1c(C)cc(C)nc1Nc1ccc(CCNC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #1541891
N-{[(2-{4-[(4,6-dimethyl -{[(methylamino)carbonothioyl]amino}-2-pyridinyl)amino]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
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