Busqueda de Subestructura

1178622

COC(=O)c1nc(-c2cscc2N)nc(O)c1O.O=C(O)C(F)(F)F
Reaction #8802
methyl 2-(3-amino-4-thienyl)-4,5-dihydroxy-pyrimidine-6-carboxylate trifluoroacetate
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1NC(=O)COc1ccc(-c2ccc(F)cc2)cc1
Reaction #42868
title compound
Rendimiento 124.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc(-c2ccc(F)cc2)cc1)Nc1cscc1C(=O)O
Reaction #42869
title compound
Rendimiento 96.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1NC(=O)COc1ccc(-c2ccccc2)cc1
Reaction #42870
title compound
Rendimiento 101.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc(-c2ccccc2)cc1)Nc1cscc1C(=O)O
Reaction #42871
title compound
Rendimiento 104.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCc1ccccc1)Nc1cscc1C(=O)O
Reaction #42872
title compound
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1NC(=O)CCCOc1ccccc1Cl
Reaction #42878
title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCOc1ccccc1Cl)Nc1cscc1C(=O)O
Reaction #42879
title compound
Rendimiento 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1NC(=O)COc1ccc(Cl)c(Cl)c1
Reaction #42880
title compound
Rendimiento 70.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc(Cl)c(Cl)c1)Nc1cscc1C(=O)O
Reaction #42881
title compound
Rendimiento 80.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1NC(=O)COc1ccc(-c2ccccc2Cl)cn1
Reaction #42883
4-{2-[5-(2-chloro-phenyl)-pyridin-2-yloxy]-acetylamino}-thiophene-3-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc(-c2ccccc2Cl)cn1)Nc1cscc1C(=O)O
Reaction #42884
4-{2-[5-(2-chloro-phenyl)-pyridin-2-yloxy]-acetylamino}-thiophene-3-carboxylic acid
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc(C2CCCCC2)cc1)Nc1cscc1C(=O)O
Reaction #42885
4-[2-(4-cyclohexyl-phenoxy)-acetylamino]-thiophene-3-carboxylic acid
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1NC(=O)COc1ccc(-c2ncccn2)cc1
Reaction #42886
title compound
Rendimiento 59.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc(-c2ncccn2)cc1)Nc1cscc1C(=O)O
Reaction #42887
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(OC(F)C(=O)Nc2cscc2C(=O)O)cc1
Reaction #42895
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccsc2)CC1
Reaction #48152
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2c(Nc3ccccc3)csc2n1-c1ccccc1
Reaction #58701
title compound
Rendimiento 53.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(=O)N(c2cc(C#CC(C)(C)C)sc2C(=O)O)C2CCN(C(=O)O[C@H]3COC4OCCC43)CC2)CC1
Reaction #67572
4-[[2-carboxy-5-(3,3-dimethyl-but-1-ynyl)-thiophen-3-yl]-(4-methyl-cyclohexanecarbonyl)-amino]-piperidine-1-carboxylic acid hexahydro-furo[2,3-b]furan-3-(R)-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(=O)N(c2cc(C#CC(C)(C)C)sc2C(=O)O)N(C)C2CCNCC2)CC1
Reaction #67588
title compound
Rendimiento 0.0%DOI: 10.6084/m9.figshare.5104873.v1
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