بحث البنية الفرعية

15669

CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nc(=S)o[nH]2)cc1
Reaction #5339
prisms
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(N3CCc4c(ncn4Cc4ccccc4)C3)[nH]c(=O)c2cc1OC
Reaction #8817
2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-one
المردود 29.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1
Reaction #11900
candesartan cilexetil
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1
Reaction #11901
candesartan cilexetil
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1
Reaction #11902
candesartan cilexetil
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1
Reaction #11903
candesartan cilexetil
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)c1ccc(C(Cl)CCc2cn(C(c3ccccc3)(c3ccccc3)c3ccccc3)cn2)cc1
Reaction #50841
4-[3-(4-tert-butylaminocarbonylphenyl)-3-chloroprop-1-yl]-1-tritylimidazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)c1ccc(C(=O)CCCc2cn(C(c3ccccc3)(c3ccccc3)c3ccccc3)cn2)cc1
Reaction #50848
1-(p-N-tert-butylaminocarbonylphenyl)-4-(1-trityl-4-imidazolyl)-1-butanone
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)CCCc2c[nH]cn2)cc1
Reaction #50849
1-(p-cyanophenyl)-4-(4-imidazolyl)-1-butanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(C)(O)CC)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81175
title compound
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(C)(O)CC)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81176
title compound
المردود 99.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(O)CC)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81178
title compound
المردود 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(=O)OCC)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81182
title compound
المردود 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(CO)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81183
title compound
المردود 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCOC(=O)C(C)(C)C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81235
title compound
المردود 48.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCOC(=O)OC(C)C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81238
title compound
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(C)(C)O)nc(CC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81240
title compound
المردود 64.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(C)(C)O)nc(CC)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81241
title compound
المردود 97.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)O)c(C(=O)OCOC(=O)C(C)(C)C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #81245
title compound
المردود 60.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(O)C(C)(C)C)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81247
title compound
المردود 96.2%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي