首页> 外文期刊>Organic letters >Synthesis and Cytotoxic Activities of a New Benzo[c]phenanthridine Alkaloid, 7-Hydroxynitidine, and Some 9-Oxygenated Benzo[c]phenanthridine Derivatives
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Synthesis and Cytotoxic Activities of a New Benzo[c]phenanthridine Alkaloid, 7-Hydroxynitidine, and Some 9-Oxygenated Benzo[c]phenanthridine Derivatives

机译:新型苯并[c]菲啶生物碱,7-羟基亚硝胺和一些9-氧合苯并[c]菲啶衍生物的合成及细胞毒活性

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摘要

A new benzo[c]phenanthridine alkaloid, 7-hydroxynitidine, was synthesized by a novel synthetic procedure. The cytotoxic activity of this compound against HeLa S3 cells was strong, but not greater than those of its mother compounds, nitidine and NK 109. We also synthesized other 9-oxygenated benzo[c]phenanthridine alkaloids, 7-methoxynitidine, 9-demethylnitidine, nitidine, and fagaronine, and tested their cytotoxic activities. These results suggest that the 7-hydroxy group enhances antitumor activity and an 8- or 9-hydroxy group weakens this activity.
机译:通过新颖的合成方法合成了新的苯并[c]菲啶生物碱7-羟基亚硝胺。该化合物对HeLa S3细胞的细胞毒性很强,但不超过其母体化合物nitidine和NK 109。尼替丁和法加宁,并测试了它们的细胞毒活性。这些结果表明7-羟基增强了抗肿瘤活性,而8或9-羟基则减弱了该活性。

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