Substructure Search

82983

COc1ccc(C(CC(=O)Nc2ccc(NC(=O)Nc3ccccc3C)cc2)NC(=O)c2ccc(C(=O)O)cc2)cc1OC
Reaction #9401
4-{[(1-(3,4-Dimethoxyphenyl)-3-{[4-({[(2-methylphenyl)amino]carbonyl}amino)phenyl]amino}-3-oxopropyl)amino]carbonyl}benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Cl)c1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #178503
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(NC(=O)CC(C(=O)Nc2ccc(NC(=O)Nc3ccccc3C)cc2)c2ccccc2)cc1
Reaction #207141
DOI: 10.1039/C8SC04228D
CC(C)c1cccc(C(C)C)c1NC(=O)N(Cc1ccc(N(C)C)cc1)c1ccc(N(C)C)cc1
Reaction #264913
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc([N+](=O)[O-])cc1O)Nc1ccccc1C(F)(F)F
Reaction #410215
title compound
Yield 52.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc([N+](=O)[O-])cc1O)Nc1ccccc1-c1ccccc1
Reaction #410220
title compound
Yield 19.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccccc1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #410225
title compound
Yield 45.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #410238
title compound
Yield 66.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Oc2ccc3nc(COc4ccc(CC5SC(=O)NC5=O)cc4)n(C)c3c2)cc(C)c1NC(=O)Nc1ccc([N+](=O)[O-])cc1
Reaction #499512
title compound
Yield 54.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc([N+](=O)[O-])cc1O)Nc1ccccc1C(F)(F)F
Reaction #655157
title compound
Yield 52.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc([N+](=O)[O-])cc1O)Nc1ccccc1-c1ccccc1
Reaction #655162
title compound
Yield 19.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccccc1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #655168
title compound
Yield 45.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Cl)c1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #655171
desired compound
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #655183
title compound
Yield 66.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc([N+](=O)[O-])cc1O)Nc1ccccc1C(F)(F)F
Reaction #699820
title compound
Yield 52.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc([N+](=O)[O-])cc1O)Nc1ccccc1-c1ccccc1
Reaction #699824
title compound
Yield 19.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccccc1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #699830
title compound
Yield 45.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Cl)c1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #699833
desired compound
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #699843
title compound
Yield 66.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc([N+](=O)[O-])cc1O)Nc1ccccc1C(F)(F)F
Reaction #760070
DOI: 10.1039/C8SC04228D
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