哌嗪
化学
哌啶
A549电池
细胞生长
立体化学
IC50型
细胞周期
吗啉
细胞培养
组合化学
体外
细胞
生物化学
药物化学
有机化学
生物
遗传学
作者
Weifeng Ma,Hai‐Kui Yang,Meng‐Jin Hu,Qian Li,Tianzhu Ma,Zhong‐Zhen Zhou,Ruiyuan Liu,Wen‐Wei You,Pei‐Liang Zhao
标识
DOI:10.1016/j.ejmech.2014.07.017
摘要
A series of novel 2,4-diaminopyrimidines containing piperidine and piperazine moieties were synthesized via an efficient one-pot methodology. The bioassay tests demonstrated that compounds 27 and 28 displayed much stronger antitumor activities against four human cancer cell lines (HepG2, A549, MDA-MB-231 and MCF-7) than positive control fluorouracil. Particularly, compound 28 showed a two-fold improvement compared to fluorouracil in inhibiting MDA-MB-231 and A549 cell proliferation with IC50 values of 7.46 and 12.78 μM, respectively. Further flow-activated cell sorting analysis revealed that the most promising compound 28 displayed a significant effect on G2/M cell-cycle arrest in a dose-dependent manner in MDA-MB-231 cells.
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