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2,3-二芳基丙烯腈衍生物作为潜在抗癌剂的合成与生物活性评价

Synthesis and bioactivity evaluation of 2,3-diaryl acrylonitrile derivatives as potential anticancer agents.

作者信息

Ma Jun, Li Jiajun, Tian Yu-Shun

机构信息

Yanbian University, College of Pharmacy, Yanji City, Jinlin Province 133002, PR China.

Yanbian University, College of Pharmacy, Yanji City, Jinlin Province 133002, PR China.

出版信息

Bioorg Med Chem Lett. 2017 Jan 1;27(1):81-85. doi: 10.1016/j.bmcl.2016.11.025. Epub 2016 Nov 15.

Abstract

Thirty novel derivatives of 2,3-diaryl acrylonitrile were synthesized and evaluated for biological activity. Preliminary investigations of antitumor activity in vitro showed that most of the synthesized compounds have significant antiproliferative effects on human cancer cell lines, such as BEL-7402, HeLa, and HCT116 with IC values in the range of 0.13-60.23μM without significant toxic effects on the non-cancerous human liver cell line L-02. In particular, compounds 4d and 4p were found to be the most potent against HeLa (4.20μM) and HCT116 cells (0.13μM), respectively, with superior or similar in vitro efficacy to that of the broad-spectrum anticancer drug taxol.

摘要

合成了30种2,3-二芳基丙烯腈的新型衍生物,并对其生物活性进行了评估。体外抗肿瘤活性的初步研究表明,大多数合成化合物对人类癌细胞系,如BEL-7402、HeLa和HCT116具有显著的抗增殖作用,IC值在0.13-60.23μM范围内,对非癌性人类肝细胞系L-02无明显毒性作用。特别是,发现化合物4d和4p分别对HeLa细胞(4.20μM)和HCT116细胞(0.13μM)最有效,其体外疗效优于或类似于广谱抗癌药物紫杉醇。

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