Substructure Search

17438

CC(C)CC(C(=O)OC(C)(C)C)N1Cc2ccccc2CC(NC(=O)C(S)Cc2ccccc2)C1=O
Reaction #2798
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)c1cccnc1SSc1ncccc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3352
title compound
Yield 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(C3(C(=O)O)CCCCC3)CC2)c2ccccc21.Cl
Reaction #44884
1-[4-({[(3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]cyclohexanecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@H](N)CC1CCCCC1
Reaction #49774
H-DCha-Pro-OtBu
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CN2C(=O)CCC2=O)cc(OC)c1-c1ccc(C[C@H](NC(=O)c2c(Cl)cccc2Cl)C(=O)OC(C)(C)C)cc1
Reaction #52973
N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(succinimidomethyl)phenyl]-L-phenylalanine tert-butyl ester
Yield 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)CN1CCC[C@H]1C(=O)OC(C)(C)C
Reaction #82327
N-[[N-[N-(4-methylvaleryl)-L-asparaginyl]-L-phenylalanyl]methyl]-L-proline tert.butyl ester
Yield 27.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)CN1CCC[C@H]1C(=O)OC(C)(C)C
Reaction #82328
N-[[N-[N-(benzyloxycarbonyl)-L-alanyl]-L-phenylalanyl]methyl]-L-proline tert.butyl ester
Yield 36.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1
Reaction #82329
L-proline tert.butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1
Reaction #82330
L-proline tert.butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1
Reaction #82334
L-proline tert.butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(N)=O)NC(=O)c1ccc2ccccc2c1
Reaction #82336
N-[2(R)-hydroxy-3(S)-[[N-(2-naphthoyl)-L-asparaginyl]amino]-4-phenylbutyl]-L-proline tert.butyl ester
Yield 64.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1C[C@@H](O)[C@H](Cc1ccc(F)cc1)NC(=O)[C@H](CC(N)=O)NC(=O)OCc1ccccc1
Reaction #82347
N-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-4-(4-fluorophenyl)-2(R)-hydroxybutyl]-L-proline tert.butyl ester
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)OCc2ccccc2)[C@H](O)CN2CCC[C@H]2C(=O)OC(C)(C)C)cc1
Reaction #82348
N-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-(4-methoxyphenyl)butyl]-L-proline tert.butyl ester
Yield 10.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@H](CCCCNC(=O)OCc1ccccc1)NC(=O)N[C@@H](CCC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
Reaction #84599
(9S,13S)-15-benzyl 13,9-di-tert-butyl 3,11-dioxo-1-phenyl-2-oxa-4,10,12-triazapentadecane-9,13,15-tricarboxylate
Yield 229.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@H](CCCCN)NC(=O)N[C@@H](CCC(=O)O)C(=O)OC(C)(C)C
Reaction #84600
(S)-4-(3-((S)-6-amino-1-tert-butoxy-1-oxohexan-2-yl)ureido)-5-tert-butoxy-5-oxopentanoic acid
Yield 142.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)OC(C)(C)C)n1ccc(-c2cc(Cl)ccc2C#N)cc1=O
Reaction #84930
tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]butanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)O)n1ccc(-c2cc(Cl)ccc2C#N)cc1=O
Reaction #84931
2-[4-(5-Chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(CC1CC1)n1cc(Cl)c(-c2cc(Cl)ccc2C#N)cc1=O
Reaction #84980
tert-Butyl 2-[5-chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]-3-cyclopropylpropanoate
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Cl)cc1-c1cc(=O)n(C(CC2CC2)C(=O)O)cc1Cl
Reaction #84981
2-[5-Chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]-3-cyclopropylpropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(CC2CC2)C(=O)OC(C)(C)C)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85022
tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-cyclopropylpropanoate
DOI: 10.6084/m9.figshare.5104873.v1
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