Busqueda de Subestructura

697027

COc1cc(NC(=O)c2ccccc2C)ccc1C(=O)N1CCCC(OC(=O)[C@H](CCSC)NC(=O)OC(C)(C)C)c2cc(Cl)ccc21
Reaction #5677
5-(N-tert-butoxycarbonyl-L-methionyloxy)-7-chloro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine
Rendimiento 121.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=O)c2ccccc2C)ccc1C(=O)N1CCCC(OC(=O)[C@@H](N)CCSC)c2cc(Cl)ccc21
Reaction #5682
5-(L-methionyloxy)-7-chloro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine
Rendimiento 32.2%DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@H](NC(=O)Cc1ccccc1)C(=O)OCC(C)C
Reaction #51375
N-(phenylacetyl)-L-methionine iso-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](CCSC)NC(=O)Cc1cccc([N+](=O)[O-])c1
Reaction #51388
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=O)c2ccccc2C)ccc1C(=O)N1CCCC(OC(=O)[C@H](CCSC)NC(=O)OC(C)(C)C)c2cc(Cl)ccc21
Reaction #83024
5-(N-tert-butoxycarbonyl-L-methionyloxy)-7-chloro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=O)c2ccccc2C)ccc1C(=O)N1CCCC(OC(=O)[C@@H](N)CCSC)c2cc(Cl)ccc21
Reaction #83029
5-(L-methionyloxy)-7-chloro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(Cl)CS[C@@H]2C(NC(=O)COc3ccccc3)C(=O)N2C1C(=O)O
Reaction #94054
7-phenoxyacetoamido-3-chloro-3-methyl-cepham-4-carboxylic acid
Rendimiento 51.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCC(Cl)(Cl)Cl)C(=O)CS[C@H]12
Reaction #96120
2,2,2-trichloroethyl 7-phenoxyacetamido-3-oxocepham-4-carboxylate
Rendimiento 124.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)CS[C@H]12
Reaction #96125
p-nitrobenzyl 3-oxo-7-phenoxyacetamidocepham-4-carboxylate
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CSCCC(NC(=O)Cc1ccccc1)C(=O)OCC(C)C
Reaction #175279
DOI: 10.1039/C8SC04228D
CON=C(C(=O)NC1C(=O)N2C(C(=O)O)C(=COC(C)=O)CSC12)c1csc(N)n1
Reaction #177241
DOI: 10.1039/C8SC04228D
Cc1onc(-c2ccccc2Cl)c1C(=O)NC1C(=O)N2C1SC(C)(CSc1nnnn1C)C2C(=O)OCC(Cl)(Cl)Cl
Reaction #187841
DOI: 10.1039/C8SC04228D
CC1(CSC#N)SC2C(NC(=O)Cc3ccccc3)C(=O)N2C1C(=O)OCC(Cl)(Cl)Cl
Reaction #197072
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCSC)NC(=O)C(CC1(NCCCl)C=CC=C(NCCCl)C1)NC(=O)C(Cc1ccc(F)cc1)NC=O
Reaction #197096
DOI: 10.1039/C8SC04228D
C=C1CS(=O)C2C(NC(=O)COc3ccccc3)C(=O)N2C1C(=O)OCc1ccc([N+](=O)[O-])cc1
Reaction #207768
DOI: 10.1039/C8SC04228D
CC(=O)SCC1(C)SC2C(NC(=O)Cc3ccccc3)C(=O)N2C1C(=O)OCC(Cl)(Cl)Cl
Reaction #211314
DOI: 10.1039/C8SC04228D
CSCC[C@H](NC(=O)Cc1ccccc1)C(=O)OCC(C)C
Reaction #220561
N-(phenylacetyl)-L-methionine iso-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](CCSC)NC(=O)Cc1cccc([N+](=O)[O-])c1
Reaction #220573
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSCCC(NC(=O)c1ccc(C(OCCn2ccnc2)c2ccc(F)cc2)cc1-c1ccc(F)cc1)C(=O)OC1CCN(C)CC1
Reaction #231357
DOI: 10.1039/C8SC04228D
CSCCC(NC(=O)c1cc(OC(Cn2ccnc2)c2ccc(F)cc2)ccc1CCc1ccc(F)cc1)C(=O)OC1CCCC1
Reaction #239718
DOI: 10.1039/C8SC04228D
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