Recherche de Sous-structure

620822

CCN(CC)CCS(=O)(=O)CC(Cc1ccccc1)C(=O)O
Reaction #65028
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(=O)C(c2cccc(F)c2F)N(c2ccc3[nH]cnc3c2)C1=O
Reaction #70028
Ethyl 1-(1H-benzo[d]imidazol-5-yl)-2,4-dioxo-5-(2,3-difluorophenyl)pyrrolidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCN(C(=O)c1ccc2c(c1)nc(CCc1ccc(C(=N)N)cc1)n2C)c1ccccc1.Cl.Cl
Reaction #78521
1-Methyl-2-[2-(4-amidinophenyl)ethyl]benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(3-methoxycarbonylpropyl)amide dihydrochloride
Rendement 83.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(CNc2ccc(C#N)cc2)nc2cc(C(=O)N(CCCC(=O)OC(C)(C)C)c3ccccc3)ccc21
Reaction #78522
1-Methyl-2-[N-(4-cyanophenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(3-tert-butyloxycarbonylpropyl)amide
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCN(C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1)n2C)c1ccccc1.Cl.Cl
Reaction #78523
1-Methyl-2-[N-(4-amidinophenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(3-ethoxycarbonylpropyl)amide dihydrochloride
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1)n2C)c1cccc(C)c1.Cl
Reaction #78571
1-Methyl-2-[N-(4-amidinophenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-(3-methylphenyl)-N-(2-ethoxycarbonylethyl)amide hydrochloride
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1)n2C1CC1)c1ccccc1.Cl
Reaction #78624
1-Cyclopropyl-2-[N-(4-amidinophenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide hydrochloride
Rendement 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(Cc1nc2cc(C(=O)N(CCC(=O)OCC)c3ccccc3)ccc2n1C)c1ccc(C(=N)N)cc1.Cl
Reaction #78626
1-Methyl-2-[N-(4-amidinophenyl)-N-(n-butyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide hydrochloride
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1CC)n2C)c1ccccc1.Cl
Reaction #78629
1-Methyl-2-[N-(4-amidino-2-ethylphenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide hydrochloride
Rendement 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1cc(CCNC(=O)OC(C)(C)C)cc(Cc2ccc(F)cc2)c1
Reaction #81608
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1cc(CCN)cc(Cc2ccc(F)cc2)c1
Reaction #81609
title compound
Rendement 62.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #87144
(2S,3R)-benzyl 2-((tert-butoxycarbonyl)amino)-3-hydroxy-3-(4-methoxyphenyl)propanoate
Rendement 71.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](N)C(=O)OCc2ccccc2)cc1
Reaction #87145
(2S,3R)-benzyl 2-amino-3-hydroxy-3-(4-methoxyphenyl)propanoate
Rendement 101.8%DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)CN(Cc1ccccc1)[C@@H](CC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Reaction #89694
(2S)-[benzyl-(2-chloromethyl-allyl)-amino]-succinic acid 1-benzyl ester 4-tert-butyl ester
Rendement 58.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cc(F)ccc2OC)cc1)NC(=O)CCC(=O)O
Reaction #158008
(R)-4-(4-ethoxy-1-(5′-fluoro-2′-methoxybiphenyl-4-yl)-4-oxobutan-2-ylamino)-4-oxobutanoic acid
Rendement 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(N)Cc1ccc(-c2ccccc2)cc1.Cl
Reaction #158015
3-amino-4-biphenyl-4-yl-butyric acid tert-butyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)cc1-c1ccc(C[C@H](CC(=O)O)NC(=O)CCC(=O)O)cc1
Reaction #158028
(R)-4-(1-carboxy-3-(5′-fluoro-2′-methoxybiphenyl-4-yl)propan-2-ylamino)-4-oxobutanoic acid
Rendement 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)CCC(=O)O
Reaction #158042
(R)-4-(1-(biphenyl-4-yl)-4-tert-butoxy-4-oxobutan-2-ylamino)-4-oxobutanoic acid
Rendement 36.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(Cc1ccc(-c2ccccc2)cc1)NC(=O)OC(C)(C)C
Reaction #158066
tert-butyl 4-(biphenyl-4-yl)-3-(tert-butoxycarbonylamino)butanoate
Rendement 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2ccc(F)c(-c3nc4cc(C)ccc4n3C(=O)OC(C)(C)C)c2)CC1
Reaction #164263
title compound
Rendement 99.5%DOI: 10.6084/m9.figshare.5104873.v1
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