Design, synthesis and anticancer activity of shikonin and alkannin derivatives with different substituents on the naphthazarin scaffold

Xu Zhang , Jiahua Cui , Wen Zhou , Shaoshun Li

Chemical Research in Chinese Universities ›› 2015, Vol. 31 ›› Issue (3) : 394 -400.

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Chemical Research in Chinese Universities ›› 2015, Vol. 31 ›› Issue (3) : 394 -400. DOI: 10.1007/s40242-015-4385-y
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Design, synthesis and anticancer activity of shikonin and alkannin derivatives with different substituents on the naphthazarin scaffold

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Abstract

Based on the asymmetric reduction of alkannin ketone derivative 4 by diisopinocampheylchloroborane(DIP-Cl), 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.

Keywords

Shikonin and alkannin oxime derivative / Asymmetric reduction / Anticancer / Apoptosis / Cell cycle

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Xu Zhang, Jiahua Cui, Wen Zhou, Shaoshun Li. Design, synthesis and anticancer activity of shikonin and alkannin derivatives with different substituents on the naphthazarin scaffold. Chemical Research in Chinese Universities, 2015, 31(3): 394-400 DOI:10.1007/s40242-015-4385-y

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