Synthesis and anticancer activity evaluation of novel azacalix[2]arene[2]pyrimidines

被引:26
作者
Addepalli, Yesu
Yang, Xiaohong
Zhou, Minghui
Reddy, D. Prabhakar
Zhang, Shao-Lin
Wang, Zhen [1 ]
He, Yun [1 ]
机构
[1] Chongqing Univ, Sch Pharmaceut Sci, 55 Daxuecheng South Rd, Chongqing 401331, Peoples R China
基金
中国国家自然科学基金;
关键词
2,4-diaminopyrimidine; Calixarene; Azacalix[2]arene[2]pyrimidines; Anticancer activity; Antiproliferation; ANTIPROLIFERATIVE ACTIVITY; DERIVATIVES; DESIGN; PROTEIN; AETHERAMIDES; DISCOVERY; APOPTOSIS; KINASES; DEATH;
D O I
10.1016/j.ejmech.2018.02.079
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel azacalix[2]arene[2]pyrimidines were synthesized, and evaluated for their anti proliferative activities against A549, MCF7, SH-SY5Y and CNE human cancer cell lines in vitro by using the CCK-8 assay. A number of compounds showed low micromolar antiproliferative activities against MCF7 cell line. Compound 4j, containing a pyrrolidine moiety, exhibited the strongest inhibitory activity with an IC50 value of 0.58 mu M. Furthermore, breast cancer cells were used to explore the inhibition mechanism of these azacalix[2]arene[2]pyrimidines. The results suggested these compounds were involved in inducing cell apoptosis via up-regulation of caspase-3 and caspase-9 protein expression, and the cell cycle was arrested at the S phase. Our reports here represent the first studies on the biological activities of azacalix[2]arene[2]pyrimidines. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:214 / 225
页数:12
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