Recherche de Sous-structure

27632

Br.NCC(=O)N[C@H]1CCCC[C@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #77832
N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccccc1.Nc1ccc(I)cc1C(=O)NCC(=O)N[C@@H]1CCCC[C@@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #77833
benzamide 2-amino-N-{2-[((cis)-2-{[4-(aminosulfonyl)benzoyl]amino}cyclohexyl)amino]-2-oxoethyl}-5-iodobenzamide
Rendement 12.3%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(C(=O)N[C@@H]2CCCC[C@@H]2NC(=O)CNC(=O)Nc2ccccc2C(F)(F)F)cc1
Reaction #77834
benzamide
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(C(=O)N[C@@H]2CCCC[C@@H]2NC(=O)CNS(=O)(=O)c2cccc(Cl)c2)cc1
Reaction #77835
benzamide
Rendement 29.4%DOI: 10.6084/m9.figshare.5104873.v1
Br.NCC(=O)N[C@H]1CCCC[C@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #1912211
N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccccc1.Nc1ccc(I)cc1C(=O)NCC(=O)N[C@@H]1CCCC[C@@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #1912212
benzamide 2-amino-N-{2-[((cis)-2-{[4-(aminosulfonyl)benzoyl]amino}cyclohexyl)amino]-2-oxoethyl}-5-iodobenzamide
Rendement 12.3%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(C(=O)N[C@@H]2CCCC[C@@H]2NC(=O)CNC(=O)Nc2ccccc2C(F)(F)F)cc1
Reaction #1912213
benzamide
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(C(=O)N[C@@H]2CCCC[C@@H]2NC(=O)CNS(=O)(=O)c2cccc(Cl)c2)cc1
Reaction #1912214
benzamide
Rendement 29.4%DOI: 10.6084/m9.figshare.5104873.v1
Br.NCC(=O)N[C@H]1CCCC[C@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #2188606
N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccccc1.Nc1ccc(I)cc1C(=O)NCC(=O)N[C@@H]1CCCC[C@@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #2188607
benzamide 2-amino-N-{2-[((cis)-2-{[4-(aminosulfonyl)benzoyl]amino}cyclohexyl)amino]-2-oxoethyl}-5-iodobenzamide
Rendement 12.3%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(C(=O)N[C@@H]2CCCC[C@@H]2NC(=O)CNC(=O)Nc2ccccc2C(F)(F)F)cc1
Reaction #2188608
benzamide
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(C(=O)N[C@@H]2CCCC[C@@H]2NC(=O)CNS(=O)(=O)c2cccc(Cl)c2)cc1
Reaction #2188609
benzamide
Rendement 29.4%DOI: 10.6084/m9.figshare.5104873.v1