بحث البنية الفرعية

Cc1ccc(N)cc1

CCCNC(=O)NCCCCCCN1CC[C@@H](CNC(=O)c2cc(Cl)c(N)cc2OC)C1
Reaction #431515
4-amino-5-chloro-2-methoxy-N-((3S)-1-(6-(3-n-propylureido)hexyl)pyrrolidin-3-ylmethyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(Cl)cc1C(=O)NCCCCCN1CC[C@H](CNC(=O)c2cc(Cl)c(N)cc2OC)C1
Reaction #431537
4-amino-N-((3R)-1-(5-(4-amino-5-chloro-2-methoxybenzoylamino)pentyl)pyrrolidin-3-ylmethyl)-5-chloro-2-methoxybenzamide
المردود 35.1%DOI: 10.6084/m9.figshare.5104873.v1
CNc1c(F)cc2c(=O)c(C(=O)O)cn(-c3cc(N)c(F)cc3C)c2c1Cl
Reaction #456405
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1SC(=O)N(Cc2ccc(NC(=O)C(F)(F)F)cc2)N=C1c1ccc(OC)c(OC)c1
Reaction #464349
3-(4-trifluoroacetamidobenzyl)-5(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(O)c(NC(=O)N2CCN(c3cc(F)cc(F)c3)CC2)cc1C
Reaction #465122
titled compound
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(c1ccc(C#N)cc1)c1cccc2c1CCCC2
Reaction #468789
N-(4-cyanophenyl)-N-(5,6,7,8-tetrahydro-1-naphthyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ncco2)cc1-c1ccc(NS(=O)(=O)c2c(F)cccc2F)cc1
Reaction #489038
Compound 1
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(NC(=O)Nc3ccc(-c4nc(N5CCOCC5)nc(N5CCOCC5)n4)cc3)cc2)CC1
Reaction #491623
1-(4-(4,6-dimorpholino-1,3,5-triazin-2-yl)phenyl)-3-(4-(4-methylpiperazine-1-carbonyl)phenyl)urea
المردود 54.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(NC(=O)Nc3ccc(-c4nc(N5CCOCC5)nc(N5CCOCC5)n4)cc3)cc2)CC1.Cl
Reaction #491624
product
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCN(C(=O)c2ccc(NC(=O)Nc3ccc(-c4nc(N5CCOCC5)nc(N5CCOCC5)n4)cc3)cc2)CC1
Reaction #491631
product
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)Nc1ccc(-c2nc(-c3ccc(NC(=O)Nc4cccc(C(N)=O)c4)cc3)nc(N3C(C)COCC3C)n2)cc1
Reaction #491689
title compound
المردود 4.1%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)Nc1ccc(-c2nc(-c3ccc(NC(=O)Nc4ccc(C(N)=O)cc4)cc3)nc(N3C(C)COCC3C)n2)cc1
Reaction #491690
title compound
المردود 12.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCNC(=O)c1ccc(-c2ccccc2CNc2ccc(-c3ccccc3)cc2)cn1
Reaction #492293
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)c1ccc(-c2cc(C(F)(F)F)cc(Cl)c2CNc2ccc(-c3ccc(Cl)cc3Cl)cc2)cn1
Reaction #492372
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCNC(=O)c1ccc(-c2cc(C(F)(F)F)cc(Cl)c2CNc2ccc(-c3ccc(Cl)cc3Cl)cc2)cn1
Reaction #492373
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)c1ccc(-c2cc(C(F)(F)F)cc(Cl)c2CNc2ccc(-c3ccc(Cl)cc3)c(C)c2)cn1
Reaction #492376
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NCc2c(Cl)cc(C(F)(F)F)cc2-c2ccc(C(=O)NCCC(=O)O)nc2)ccc1-c1ccc(Cl)cc1
Reaction #492377
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(CC(=O)O)n(-c2ccc(CC(=O)O)cc2)c2ccc(Oc3ccc(C(F)(F)F)cc3)cc12
Reaction #508095
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1c(C(=O)OCC)c2cc(Oc3ccc(C(F)(F)F)cc3)ccc2n1-c1ccc(C2CCNCC2)cc1
Reaction #508106
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1c(C(=O)OCC)c2cc(Oc3ccc(Cl)cc3)ccc2n1-c1ccc(C(C)C)cc1
Reaction #508142
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
السابقالصفحة 5التالي