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Design, synthesis and anticancer activity of naphthoquinone derivatives

机译:萘醌衍生物的设计,合成和抗癌活性

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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 ICsub50/sub against SGC-7901 was 4.1?±?2.6?μM. 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.
机译:基于萘醌部分的分子对接和药物光学分析,设计并合成了共23种化合物。在逆向目标搜索的帮助下,初步评估抗癌活性,其中大多数对某些肿瘤细胞有效,特别是化合物12:1-(5,8-二羟基-1,4-二氧化硅-1,4-二氢萘-1,4-二氢萘-1,4-二氢萘碱-2-y1)-4-甲基戊-3-烯-1-基-4-氧代-4-((4-苯氧基苯基)氨基)丁酸盐,其IC 50 对SGC-7901是4.1? ±2.6?μm。同时,通过annexinv / pi染色,免疫荧光,蛋白质印迹测定和分子对接研究了化合物12的抗癌机制。结果表明,通过调节PI3K信号途径,该化合物可以诱导细胞凋亡和细胞自噬。

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