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萘醌衍生物的设计、合成及抗癌活性。

Design, synthesis and anticancer activity of naphthoquinone derivatives.

机构信息

School of Pharmacy, Anhui Medical University, Hefei, PR China.

Engineering Research Center of Biomass Conversion and Pollution Prevention of Anhui Educational Institutions, Fuyang Normal University, Fuyang, PR China.

出版信息

J Enzyme Inhib Med Chem. 2020 Dec;35(1):773-785. doi: 10.1080/14756366.2020.1740693.

Abstract

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 : 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 IC against SGC-7901 was 4.1 ± 2.6 μM. Meanwhile the anticancer mechanism of compound 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.

摘要

基于萘醌部分的分子对接和药效团分析,共设计和合成了 23 种化合物。借助反向靶标搜索,初步评估了它们的抗癌活性,其中大多数对某些肿瘤细胞有效,特别是化合物:1-(5,8-二羟基-1,4-二氧代-1,4-二氢萘-2-基)-4-甲基戊-3-烯-1-基-4-氧代-4-((4-苯氧基苯基)氨基)丁基-4-氧代丁酸酯,其对 SGC-7901 的 IC 值为 4.1±2.6μM。同时,通过 AnnexinV/PI 染色、免疫荧光、Western blot 检测和分子对接研究了化合物的抗癌机制。结果表明,该化合物可能通过调节 PI3K 信号通路诱导细胞凋亡和细胞自噬。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c6f/7144209/2b895ce8757e/IENZ_A_1740693_F0001_C.jpg

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