子结构搜索

COC(=O)C(N)Cc1ccccc1

COC(=O)[C@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)C1Cc2cc3c(cc2CN1C(=O)OC(C)C)O[C@@H](c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)C(=O)N3
Reaction #41883
(S)-7-((S)-2-biphenyl-4-yl-1-methoxycarbonyl-ethylcarbamoyl)-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6-carboxylic acid isopropyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2CNc2ccccc2)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52923
N-(2,6-dichlorobenzoyl)-4-[2-[(phenylamino)methyl]phenyl]-L-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2CO)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52925
N-(2,6-dichlorobenzoyl)-4-[2-(hydroxymethyl)phenyl]-L-phenylalanine methyl ester
收率 103.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2CBr)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52926
N-(2,6-dichlorobenzoyl)-4-[2-(bromomethyl)phenyl]-L-phenylalanine methyl ester
收率 70.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1ccc(C[C@H](NC(C)=O)C(=O)O)cc1
Reaction #66043
title compound
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(I)cc1)NC(C)=O
Reaction #66047
title compound
收率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)N1CCc2cc3c(cc2C1)OC(c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)C(=O)N3
Reaction #67359
3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6-carboxylic acid isopropyl ester
收率 136.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H](Cc1cccc([N+](=O)[O-])c1)C(=O)O
Reaction #75985
3-nitrophenylalanine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1Cc2ccccc2N1C
Reaction #83750
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2CC1CO
Reaction #83751
title compound
收率 100.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)Cc1ccc2c(c1)CCCN2
Reaction #162000
#215
收率 85.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccccc1)NC(=O)c1ccc(OCc2c(-c3ccccc3)noc2C)nc1
Reaction #170525
title compound
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N[C@@H](Cc2ccccc2)C(=O)O)cn1
Reaction #170526
title compound
收率 95.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1conc1-c1ccccn1
Reaction #170634
title compound
收率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CNC(Cc1ccc([N+](=O)[O-])cc1)C(=O)OC
Reaction #175771
DOI: 10.1039/C8SC04228D
COC(=O)C(N)Cc1ccc([N+](=O)[O-])cc1
Reaction #180446
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc([N+](=O)[O-])cc1)NCc1c(Cl)cccc1Cl
Reaction #182663
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(NC(=O)c2cc(Cl)cc(Cl)c2OC2CCC2)Cc2ccc(F)cc2C1
Reaction #184611
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc([N+](=O)[O-])cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #188988
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1cccc2ccccc12)NC(=O)C(C)NC(=O)Cc1cc(F)cc(F)c1
Reaction #189347
DOI: 10.1039/C8SC04228D
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