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首页> 外文期刊>Bulletin of the Korean Chemical Society >Naphthofuroquinone Derivatives: DNA Topoisomerase-I Inhibition and Cytotoxicity
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Naphthofuroquinone Derivatives: DNA Topoisomerase-I Inhibition and Cytotoxicity

机译:萘呋喃醌衍生物:DNA拓扑异构酶-I抑制和细胞毒性

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摘要

The naphthoquinone skeleton is found in many natural products and has been employed as a synthetic intermediate for the preparation of numerous heterocyclic compounds with interesting biological properties such as antitumor,antibacterial,antifungal and antiinflammatory agents.The quinone core of streptonigrin and lavendamycin has been proposed to be a determining factor in their antitumor activity.Recently,the linearly substituted quinolinediones have revealed the importance of the quinone framework for potent antitumor activity against the cell lines.
机译:萘醌骨架存在于许多天然产物中,已被用作合成中间体,用于制备许多具有令人感兴趣的生物学特性的杂环化合物,例如抗肿瘤药,抗菌药,抗真菌药和抗炎药。链霉菌素和拉文达霉素的醌核已被建议用于近年来,线性取代的喹啉二酮已经显示出醌骨架对于针对细胞系的有效抗肿瘤活性的重要性。

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