بحث البنية الفرعية

Cc1ccc(S)cc1

C[C@H](NC(=O)C(F)(F)F)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccc(SC2CC2)cc1
Reaction #41296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)n1ccc(S(=O)(=O)c2c(C)cc(C)cc2C)n1
Reaction #49880
title compound
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)Sc2cc(N)c(N)cc2C(C)C)cc1
Reaction #51769
Toluene-4-thiosulfonic acid S-(4,5-diamino-2-isopropyl-phenyl)ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Nc2nccc(-c3ccc(SCCCCO)cc3)n2)cc1)N1CCN(C(=O)c2ccco2)CC1
Reaction #61737
[4-(Furan-2-carbonyl)-piperazin-1-yl]-(4-{4-[4-(4-hydroxybutylsulfanyl)phenyl]pyrimidin-2-ylamino}phenyl)methanone
المردود 9.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2ncc3c(-c4nnc(CN5CCOCC5)o4)cc(Br)cc32)cc1
Reaction #67090
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2ncc3c(-c4nnc(CN5CCOCC5)o4)cc(-c4cccc5[nH]ccc45)cc32)cc1
Reaction #67091
title compound
المردود 29.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2ncc3c(-c4nnc(CCl)o4)cc(-c4cnc(Cl)c(NS(C)(=O)=O)c4)cc32)cc1
Reaction #67095
title compound
المردود 23.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2ncc3c(-c4nnc(CN5CCOCC5)o4)cc(-c4cnc(Cl)c(NS(C)(=O)=O)c4)cc32)cc1
Reaction #67096
title compound
المردود 96.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2ncc3c(-c4nnc(C)o4)cc(-c4cnc(Cl)c(NS(C)(=O)=O)c4)cc32)cc1
Reaction #67119
title compound
المردود 31.1%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(-c2cc(-c3nnc(CN4CCOCC4)o3)c3cn[nH]c3c2)c2cc[nH]c2c1
Reaction #67138
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(Cc2nnc(-c3cc(-c4cnc(Cl)c(NS(C)(=O)=O)c4)cc4[nH]ncc34)o2)CC1
Reaction #67142
title compound
المردود 17.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2nnc(-c3cc(-c4cnc(Cl)c(NS(C)(=O)=O)c4)cc4[nH]ncc34)o2)C[C@H](C)O1
Reaction #67143
title compound
المردود 27.6%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cc(-c2cc(-c3nnc(CN4CCOCC4)o3)c3cn[nH]c3c2)cnc1Cl
Reaction #67144
title compound
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(-c2cc(-c3cnc(Cl)c(NS(C)(=O)=O)c3)cc3[nH]ncc23)o1
Reaction #67154
title compound
المردود 85.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC[C@@H](O)CCc2ccc3ncccc3c2O)cc1
Reaction #76237
(2S)-2-hydroxy-4-(5-hydroxy-quinolin-6-yl)butyl 4-methylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)n1cnc(S(=O)(=O)c2ccc(C(F)(F)F)cc2Cl)n1
Reaction #173023
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)n2ccc3c(-c4c(-c5ccc(F)cc5)nc5ccc(N6CCC(N7CCCC7)CC6)nn45)ccnc32)cc1
Reaction #176559
DOI: 10.1039/C8SC04228D
O=C(c1ccc(Nc2nccc(-c3ccc(SCCCCO)cc3)n2)cc1)N1CCN(C(=O)c2ccco2)CC1
Reaction #178295
DOI: 10.1039/C8SC04228D
COC(=O)c1sccc1NS(=O)(=O)c1c(Cl)cc(C(F)(F)F)cc1Cl
Reaction #193324
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C(=O)c1ccc(F)cc1)c1ccc(SC)cc1
Reaction #193525
DOI: 10.1039/C8SC04228D
الصفحة 1التالي