吲哚嗪
法尼酰转移酶
化学
法尼酰转移酶抑制剂
细胞培养
体外
铅化合物
衍生工具(金融)
癌细胞系
IC50型
组合化学
生物化学
立体化学
癌细胞
预酸化
癌症
酶
经济
内科学
金融经济学
生物
医学
遗传学
作者
Liliana Lucescu,Alina Ghinet,Dalila Belei,Joëlle Dubois,Alina Ghinet
出处
期刊:Letters in Drug Design & Discovery
[Bentham Science]
日期:2016-06-18
卷期号:13 (6): 479-488
被引量:4
标识
DOI:10.2174/1570180812666151022221628
摘要
A new series of indolizine derivatives were synthesized and screened for the antiproliferative potential against NCI 60 tumor cell line panel. The results of the study revealed a selective and good antitumor growth inhibitory activity against SNB-75 CNS cancer cell line for 1-cyanoindolizine derivative 10b. Moreover, a supplementary in vitro biological evaluation showed that compound 9d exhibited a significant farnesyltransferase inhibition activity (IC50 = 1.07 ± 0.34 µM) and could represent a lead for the development of new antitumoral chemical entities. Keywords: Indolizine, farnesyltransferase, anticancer agent.
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