铅化合物
激酶
体外
化学
药理学
癌细胞系
细胞培养
行动方式
活性化合物
立体化学
组合化学
生物化学
癌症
癌细胞
生物
医学
内科学
遗传学
作者
Ibrahim M. El‐Deeb,Dong Keun Han,In-Tae Kim,So Ha Lee
标识
DOI:10.5012/bkcs.2010.31.7.1848
摘要
Phenylaminopyrimidines represent a large group of new selective anticancer agents, the majority of which exert their action through the inhibition of specific kinases. In this study, a new series of N-substituted-2-aminopyrimidines has been designed and synthesized. A selected group of the synthesized derivatives was screened at a single dose concentration of 10 ${\mu}M$ over a panel of 60 cancer cell-lines. Compound 12e has showed great inhibitory and strong lethal effect over almost all of the 60 cell-lines and accordingly was further tested in a 5-dose testing mode to determine its $IC_{50}$ values, where it showed great efficacies with intermediate potencies over the tested cell-lines. The compound was also tested over a panel of 52 kinases to explore its kinase inhibitory profile, and was found to be a selective but moderate inhibitor over FLT3 kinase.
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