بحث البنية الفرعية

17953

Fc1cc(I)ccc1Nc1nc2ccc(Cl)cc2s1
Reaction #9683
desired product
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CCc1ccccc1)C(=O)O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #9689
desired product
المردود 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1)C(=O)O
Reaction #9690
desired product
المردود 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCC(CC(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1)C(=O)O
Reaction #9692
desired product
المردود 16.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #9707
trans-2-({4′-[(6-chloro-1,3-benzothiazol-2-yl) amino]-1,1′-biphenyl-4-yl}carbonyl)cyclobutanecarboxylic acid
المردود 10.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #9714
trans-2-({4′-[(6-chloro-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclohexanecarboxylic acid
المردود 15.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H]1CCC[C@@H](C(=O)c2ccc(-c3ccc(Nc4nc5ccc(Cl)cc5s4)cc3)cc2)C1
Reaction #9717
cis-3-[4′-(6-chloro-benzothiazol-2-ylamino)-biphenyl-4-carbonyl]-cyclohexanecarboxylic acid
المردود 23.4%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(I)ccc1Nc1nc2ccc(Cl)cc2s1
Reaction #59181
desired product
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CCc1ccccc1)C(=O)O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #59188
desired product
المردود 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1)C(=O)O
Reaction #59189
desired product
المردود 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCC(CC(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1)C(=O)O
Reaction #59191
desired product
المردود 16.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #59206
trans-2-({4′-[(6-chloro-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclobutanecarboxylic acid
المردود 10.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #59214
trans-2-({4′-[(6-chloro-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclohexanecarboxylic acid
المردود 15.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H]1CCC[C@@H](C(=O)c2ccc(-c3ccc(Nc4nc5ccc(Cl)cc5s4)cc3)cc2)C1
Reaction #59217
cis-3-[4′-(6-chloro-benzothiazol-2-ylamino)-biphenyl-4-carbonyl]-cyclohexanecarboxylic acid
المردود 23.4%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(-c2nc(NCCNc3nc4ccc(Cl)cc4s3)ncc2-c2ncc[nH]2)c(Cl)c1
Reaction #60121
[4-(2,4-dichlorophenyl)-5-imidazolylpyrimidin-2-yl]{2-[(6-chlorobenzothiazo 1-2-yl)amino]ethyl}amine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2nc(N3CCNCC3)sc2c1
Reaction #61416
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2nc(N3CCNCC3)sc2c1
Reaction #61874
desired product
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCN1c1nc2ccc(Cl)cc2s1
Reaction #181272
DOI: 10.1039/C8SC04228D
Clc1ccc2nc(Nc3ccc(Br)cc3)sc2c1
Reaction #182834
DOI: 10.1039/C8SC04228D
Nc1cc(Cl)c(Oc2nc3ccc(Cl)cc3s2)c(Cl)c1
Reaction #191154
DOI: 10.1039/C8SC04228D
الصفحة 1التالي