بحث البنية الفرعية

SCCc1ccccc1

Cc1ccc(-c2c(Cl)nc(-c3ccncc3)nc2NS(=O)(=O)CCc2ccccc2)cc1
Reaction #8692
2-phenyl-ethanesulfonic acid (6-chloro-2-pyridin-4-yl-5-p-tolyl-pyrimidin-4-yl)-amide
المردود 21.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)CCc3ccccc3)nc(-c3ccncc3)nc2OCCO)cc1
Reaction #8693
2-phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-2-pyridin-4-yl-5-p-tolyl-pyrimidin-4-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1Oc1c(Cl)nc(-c2ccncc2)nc1NS(=O)(=O)CCc1ccccc1
Reaction #8698
2-phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide
المردود 78.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1Oc1c(NS(=O)(=O)CCc2ccccc2)nc(-c2ccncc2)nc1OCCO
Reaction #8699
2-phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1Oc1c(Cl)nc(-c2ncccn2)nc1NS(=O)(=O)CCc1ccccc1
Reaction #8700
2-Phenylethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)CCc3ccccc3)ncnc2OCCOc2ccc(Br)cc2)cc1
Reaction #8714
2-phenyl-ethanesulfonic acid {6-[2-(4-bromo-phenoxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide
المردود 86.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=N)Nc1cccc(C2CSC(N)=N2)c1
Reaction #75995
[3-(2-amino-4,5-dihydrothiazol-4-yl)phenyl]-(1-iminoethyl)amine
المردود 58.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(Nc2ccc(C(=N)N)cc2)c2nn(-c3ccsc3C(=O)O)c(=O)[nH]2)c(F)c2c1OCC2
Reaction #174724
DOI: 10.1039/C8SC04228D
CNC(=O)NS(=O)(=O)c1cccc2c1OS(=O)(=O)C(C)C2
Reaction #191713
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(NC2=NCCN2)cc2c1SCC2(C)C
Reaction #192165
DOI: 10.1039/C8SC04228D
COc1cc(O)cc(Nc2c(C#N)cnc3ccc4c(c23)CCS4(=O)=O)c1
Reaction #212865
DOI: 10.1039/C8SC04228D
COc1ccccc1Oc1c(Cl)nc(-c2ncccn2)nc1NS(=O)(=O)CCc1ccccc1
Reaction #213506
DOI: 10.1039/C8SC04228D
CC(Nc1ccc(C(=O)CS(=O)(=O)c2ccccc2)cc1)C1CCCC1
Reaction #215508
4'-(1cyclopentylethylamino)-2-(phenylsulfonyl)acetophenone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CCC(C)(COc1ccc(CC3SC(=O)NC3=O)cc1)O2.O=C1CCC(=O)N1
Reaction #216081
CS-045 succinimide
DOI: 10.6084/m9.figshare.5104873.v1
O=S1(=O)CCc2ccc(I)cc21
Reaction #222353
DOI: 10.1039/C8SC04228D
CON=C1CC(C)(COc2ccc(CC3SC(=O)NC3=O)cc2)Oc2c(C)c(C)c(O)c(C)c21
Reaction #223677
DOI: 10.1039/C8SC04228D
COc1ccccc1Oc1c(NS(=O)(=O)CCc2ccccc2)nc(-c2ccncc2)nc1OCCO
Reaction #233275
DOI: 10.1039/C8SC04228D
CCN1C(=O)SC(Cc2ccc(OCC3(C)CCc4c(C)c(O)c(C)c(C)c4O3)cc2)C1=O
Reaction #262131
DOI: 10.1039/C8SC04228D
Cc1c(C)c2c(c(C)c1O)C(=NOCC(=O)O)CC(C)(COc1ccc(CC3SC(=O)NC3=O)cc1)O2
Reaction #262551
DOI: 10.1039/C8SC04228D
CCCCCC(C)C(C)c1cc(OC(=O)C(C)(C)CCN2CCCCC2)c2c(c1)OC(C)(C)C1=C2CSC1
Reaction #268819
DOI: 10.1039/C8SC04228D
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