子结构搜索

CSCCC(C(=O)O)N

COC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1C
Reaction #5180
title compound
收率 27.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(=O)O)N(C)C2)cc1
Reaction #5181
(2S, 4S)-2-carboxy-4-(4-methoxybenzylthio)-1-methylpyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1C
Reaction #5190
title compound
收率 55.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(=O)O)N(C)C2)cc1
Reaction #5191
(2S, 4S)-2-carboxy-4-(4-methoxybenzylthio)-1-methylpyrrolidine
收率 120.2%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
收率 32.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CCSC)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47613
(S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methylsulfanyl-butyric acid methyl ester
收率 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](C(=O)O)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47614
(S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methylsulfanyl-butyric acid
收率 89.0%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
CC[C@H](C)[C@H](N)CN[C@H](C(=O)OC)[C@H](CSC)C(=O)C1NCCc2ccccc21
Reaction #83386
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCS(=O)(=O)CC1=O
Reaction #84689
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)O)C(=COC(C)=O)CSC12)c1csc(N)n1
Reaction #177241
DOI: 10.1039/C8SC04228D
COC(=O)C(CCSC)NC(=O)c1ccc(CC(=O)Nc2ccccn2)cc1-c1ccccc1
Reaction #181124
DOI: 10.1039/C8SC04228D
C=CCCCCCC1(S(=O)(=O)NC(=O)C2(NC(=O)C3CC(SCC=C)(c4ccc(-c5ccccc5)cc4)CN3C(=O)C(NC(=O)OC(C)(C)C)C(C)(C)C)CC2C(F)F)CC1
Reaction #183181
DOI: 10.1039/C8SC04228D
COC(=O)C(CCSC)NC(=O)c1ccc(CC(=O)Nc2ccccn2)cc1-c1ccccc1
Reaction #183540
DOI: 10.1039/C8SC04228D
COc1ccc(CSC2CC(C(=O)N3CCN(C(=N)NC(=O)OCc4ccc([N+](=O)[O-])cc4)CC3)N(C)C2)cc1
Reaction #184621
DOI: 10.1039/C8SC04228D
C=CCSC1(c2ccc(-c3ccccc3)cc2)CC(C(=O)NC2(C(=O)NS(=O)(=O)C3CC3)CC2C=C)N(C(=O)C(NC(=O)OC(C)(C)C)C(C)(C)C)C1
Reaction #188649
DOI: 10.1039/C8SC04228D
CCOP(=O)(CCCCc1ccccc1)CC(=O)N1CC2(CC1C(=O)O)SCCS2
Reaction #193878
DOI: 10.1039/C8SC04228D
CSCCC(NC(=O)CNC(=O)OC(C)(C)C)C(=O)NO
Reaction #196758
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
COc1ccc(CSC2CC(C(=O)N3CCN(C)CC3)N(C)C2)cc1
Reaction #197643
DOI: 10.1039/C8SC04228D
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