Design, synthesis and anticancer activity of naphthoquinone derivatives

被引:21
作者
Shen, Xiao-bao [1 ,2 ]
Wang, Yang [1 ]
Han, Xuan-zhen [2 ]
Sheng, Liang-quan [2 ]
Wu, Fu-fang [1 ,2 ]
Liu, Xinhua [1 ]
机构
[1] Anhui Med Univ, Sch Pharm, Hefei 230032, Peoples R China
[2] Fuyang Normal Univ, Engn Res Ctr Biomass Convers & Pollut Prevent, Anhui Educ Inst, Fuyang, Peoples R China
基金
中国国家自然科学基金;
关键词
Naphthoquinone moiety; anticancer activity; autophagy; ER-STRESS; BIOLOGICAL EVALUATION; INDUCED AUTOPHAGY; CELL-DEATH; SHIKONIN; APOPTOSIS; INHIBITION; PI3K/AKT/MTOR; COMPLEXES; MIGRATION;
D O I
10.1080/14756366.2020.1740693
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Basis on molecular docking and pharmacophore analysis of naphthoquinone moiety, a total of 23 compounds were designed and synthesised. With the help of reverse targets searching, anti-cancer activity was preliminarily evaluated, most of them are effective against some tumour cells, especially compound 12: 1-(5,8-dihydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-4-methylpent-3-en-1-yl-4-oxo-4-((4-phenoxyphenyl)amino) butanoate whose IC50 against SGC-7901 was 4.1 +/- 2.6 mu M. Meanwhile the anticancer mechanism of compound 12 had been investigated by AnnexinV/PI staining, immunofluorescence, Western blot assay and molecular docking. The results indicated that this compound might induce cell apoptosis and cell autophagy through regulating the PI3K signal pathway.
引用
收藏
页码:773 / 785
页数:13
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