Recherche de Sous-structure

5297

COc1ccc(C(=O)NC(CC(C)C)C(=O)O)c(SSc2cc(OC)ccc2C(=O)NC(CC(C)C)C(=O)O)c1
Reaction #3349
title compound
Rendement 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)c1cc(F)ccc1SSc1ccc(F)cc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc([SH](Sc2cc(C)ccc2C(=O)NC(CC(C)C)C(=O)O)C(=O)NC(CC(C)C)C(=O)O)c1
Reaction #3351
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)c1cccnc1SSc1ncccc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3352
title compound
Rendement 77.4%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(N)ccc1SSc1ccc(N)cc1C(N)=O
Reaction #3354
2,2'-Dithiobis(5-aminobenzamide)
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NS(=O)(=O)c1ccc(NC(=O)c2ccccc2SSc2ccccc2C(=O)Nc2ccc(S(=O)(=O)NC(C)=O)cc2)cc1
Reaction #3355
2,2'-Dithiobis[N-[4-[(acetylamino)sulfonyl]phenyl]benzamide]
Rendement 8.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)c1ccccc1SSc1ccccc1C(=O)NC(C(=O)O)C(C)C)C(=O)O
Reaction #3356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCNC(=O)c1ccccc1SSc1ccccc1C(=O)NCCCC(=O)O
Reaction #3357
title compound
Rendement 49.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(C(=O)O)n1sc2ccccc2c1=O
Reaction #3364
title compound
Rendement 0.1%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(CNC(=O)c2ccccc2SSc2ccccc2C(=O)NCc2ccc(S(N)(=O)=O)cc2)cc1
Reaction #3791
title compound
Rendement 35.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(S(=O)(=O)Nc2ncccn2)cc1)c1ccccc1SSc1ccccc1C(=O)Nc1ccc(S(=O)(=O)Nc2ncccn2)cc1
Reaction #3792
title compound
Rendement 58.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)c1ccc(F)cc1SSc1cc(F)ccc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3795
title compound
Rendement 62.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)c1cc(F)ccc1SSc1ccc(F)cc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3796
title compound
Rendement 17.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(SSc2ccc(OC)cc2C(=O)NC(CC(C)C)C(=O)O)c(C(=O)NC(CC(C)C)C(=O)O)c1
Reaction #3797
title compound
Rendement 34.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C(=O)NC(CC(C)C)C(=O)O)c1SSc1c(C)cccc1C(=O)NC(CC(C)C)C(=O)O
Reaction #3798
title compound
Rendement 54.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(SSc2ccc(NC(C)=O)cc2C(=O)NC(CC(C)C)C(=O)O)c(C(=O)NC(CC(C)C)C(=O)O)c1
Reaction #3800
title compound
Rendement 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(SSc2ccc(NCC)cc2C(=O)N[C@H](C(=O)O)[C@@H](C)CC)c(C(=O)N[C@H](C(=O)O)[C@@H](C)CC)c1
Reaction #3801
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCC(NC(=O)c1ccccc1SSc1ccccc1C(=O)NC(CCCC(=O)O)C(=O)O)C(=O)O
Reaction #3802
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCNC(=O)c1ccccc1SSc1ccccc1C(=O)NCCCC(=O)O
Reaction #3803
title compound
Rendement 139.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(C(=O)O)c1ccccc1)c1ccccc1SSc1ccccc1C(=O)NC(C(=O)O)c1ccccc1
Reaction #3804
title compound
Rendement 42.5%DOI: 10.6084/m9.figshare.5104873.v1
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