Design, Synthesis and Anticancer Activity of Shikonin and Alkannin Derivatives with Different Substituents on the Naphthazarin Scaffold

被引:10
作者
Zhang Xu [1 ]
Cui Jiahua [1 ]
Zhou Wen [1 ]
Li Shaoshun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Shikonin and alkannin oxime derivative; Asymmetric reduction; Anticancer; Apoptosis; Cell cycle; ANTITUMOR-ACTIVITY; MECHANISMS;
D O I
10.1007/s40242-015-4385-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Based on the asymmetric reduction of alkannin ketone derivative 4 by diisopinocampheylchloroborane(DIP-CI), a series of shikonin and alkannin derivatives was designed, synthesized and their anticancer activities against various kinds of cell lines were evaluated. The in vitro biological experiments demonstrated that compound S-10, a 5,8-O-dimethyl-1,4-dioxime alkannin derivative, not only displayed excellent antiproliferative activity against cancer cells, but also exhibited low toxicity towards normal cells. It could induce HCT-116 cell apoptosis, but had no impact on the cell cycle. The underlying anticancer mechanism of S-10 is most likely different from other shikonin and alkannin derivatives.
引用
收藏
页码:394 / 400
页数:7
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