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746179

COC(=O)CCCNC(=O)C(CSC(C)=O)Cc1ccccc1
Reaction #3852
(±)-4-[[2-[(Acetylthio)methyl]-1 oxo-3-phenylpropyl]amino]butanoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)CS
Reaction #50703
title compound
Выход 82.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@H](C)SC(C)=O
Reaction #50704
title compound
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CSC(=O)[C@@H]2CCCN2C1=O
Reaction #56345
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)C(C)SC(C)=O
Reaction #71583
objective compound
Выход 93.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)C(C)S
Reaction #71584
objective compound
Выход 56.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)C(C)SC(C)=O
Reaction #71585
ethyl 3-acetylthio-2-methylbutyrate
DOI: 10.6084/m9.figshare.5104873.v1
CSCC(CSC(C)=O)C(=O)N1CCC[C@H]1C(=O)O
Reaction #75204
1-[3-(acetylthio)-2-(methylthiomethyl)propanoyl]-L-proline
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC(CCC(=O)C(C)C)C(=O)N1CCC[C@H]1C(=O)OC(C)(C)C
Reaction #75207
(2-(Acetylthiomethyl)-5-oxo-6-methylheptanoyl]-L-proline tert.butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CSCC(CSC(C)=O)C(=O)N1CCC[C@H]1C(=O)O
Reaction #75410
1-[3-(acetylthio)-2-(methylthiomethyl)propanoyl]-L-proline
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC(CCC(=O)C(C)C)C(=O)N1CCC[C@H]1C(=O)OC(C)(C)C
Reaction #75413
1-[2-(Acetylthiomethyl)-5-oxo-6-methylheptanoyl]-L-proline tert.butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@](O)(NC(=O)CCS)C(=O)O
Reaction #75423
2-hydroxy-3-mercaptopropanoyl-L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCCC(=O)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80405
title compound
Выход 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCCC(=O)OC(=O)CO
Reaction #93189
O-(3-Acetylthiopropanoyl)glycolic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CO)OC(=O)CCS
Reaction #93190
O-(3-Mercaptopropanoyl)glycolic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC(C)C(=O)OC(=O)CO
Reaction #93191
O-[3-(Acetylthio)-2-methylpropanoyl]glycolic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(S)(OC(=O)C(O)c1ccccc1)C(=O)c1ccccc1
Reaction #93192
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(C(=O)SCC2C(=O)OCC2c2ccccc2)cc1
Reaction #93538
title compound
Выход 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(SCC1C(=O)OCC1c1ccc(Cl)cc1)c1ccccc1
Reaction #93539
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(SCC1C(=O)OCC1c1ccccc1)c1ccccc1F
Reaction #93540
title compound
Выход 67.2%DOI: 10.6084/m9.figshare.5104873.v1
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