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β-榄香烯聚乙二醇衍生物的合成及体外抗癌活性
Synthesis and in vitro Antiproliferative Activity ofβ-Elemene Polyethylene Glycol Derivatives
【摘要】 以中草药有效成分β-榄香烯为起始原料,在碱性条件下与氨基化的聚乙二醇(PEG)反应合成了一系列β-榄香烯单取代PEG衍生物,利用IR,1H NMR及13C NMR对其结构进行了表征.并采用WST-1法观察其对人宫颈癌细胞(Hela)、人白血病细胞(K562)的抑制作用,探讨其体外抗肿瘤活性.细胞实验结果表明经PEG修饰的β-榄香烯的抗癌活性有不同程度的增强.
【Abstract】 A series ofβ-elemene monosubstituted polyethylene glycol(PEG)derivatives were prepared by the reaction ofβ-elemene with aminated PEG and characterized by IR,1H NMR and 13C NMR spectra.Their in vitro antiproliferative activities towards K562 cell and Hela cell lines were evaluated by a WST-1 method, showing that their antiproliferative activities were improved compared to that ofβ-elemene.
【关键词】 β-榄香烯;
聚乙二醇;
抗癌活性;
【Key words】 β-elemene derivative; polyethylene glycol; antiproliferative activity;
【Key words】 β-elemene derivative; polyethylene glycol; antiproliferative activity;
【基金】 中国科学院“百人计划”(No.26200601)资助项目
- 【文献出处】 有机化学 ,Chinese Journal of Organic Chemistry , 编辑部邮箱 ,2008年01期
- 【分类号】R914;R73-3
- 【被引频次】8
- 【下载频次】349