One-pot synthesis and antiproliferative activity of novel 2,4-diaminopyrimidine derivatives bearing piperidine and piperazine moieties

被引:25
|
作者
Ma, Wei-Feng [2 ]
Yang, Hai-Kui [1 ]
Hu, Meng-Jin [1 ]
Li, Qian [1 ]
Ma, Tian-Zhu [1 ]
Zhou, Zhong-Zhen [1 ]
Liu, Rui-Yuan [1 ]
You, Wen-Wei [1 ]
Zhao, Pei-Liang [1 ]
机构
[1] Southern Med Univ, Sch Pharmaceut Sci, Dept Chem, Guangzhou 510515, Guangdong, Peoples R China
[2] Southern Med Univ, Sch Publ Hlth & Trop Med, Dept Microbiol, Guangzhou 510515, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
2,4-Diaminopyrimidines; Piperidine; Piperazine; Antiproliferative activity; One-pot synthesis; INHIBITORS; DESIGN; CANCER; IDENTIFICATION; DISCOVERY;
D O I
10.1016/j.ejmech.2014.07.017
中图分类号
R914 [药物化学];
学科分类号
100701 ;
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 mu M, respectively. Further flow-activated cell sorting analysis revealed that the most promising compound 28 displayed a significant effect on G(2)/M cell-cycle arrest in a dose-dependent manner in MDA-MB-231 cells. (c) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:127 / 134
页数:8
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