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B环三氟甲基取代的白杨素衍生物合成及其抗癌活性
Synthesis and Anticancer Activities of B-Ring Trifluoromethylated Chrysin Derivatives
【摘要】 目的研究B环三氟甲基取代白杨素衍生物的体外抗癌活性。方法合成B环三氟甲基取代的白杨素衍生物,并通过MTT法检测其对人急性粒细胞性白血病(HL-60)细胞、人结肠癌(HT-29)细胞和人胃癌(SGC-7901)细胞增殖的抑制作用。结果合成了3个三氟甲基B环取代白杨素衍生物,其中化合物6对HL-60、HT-29细胞增殖的抑制作用最强。结论化合物6(7-羟基-4’-三氟甲基-黄酮)具有良好的抗癌活性。
【Abstract】 Objective To study the anticancer activity of B-ring trifluoromethylated chrysin derivatives. Methods B-ring trifluoromethylated chrysin derivatives were prepared and their anticancer activities in vitro were evaluated by the standard MTT method. Results Compound 6 showed the strongest activity against HL-60 and HT-29 cells. Conclusion Compound 6(7-hydroxyl-4’-trifluoromethyl-flavone) possessed the potent anticancer activity.
【关键词】 白杨素;
衍生物;
三氟甲基;
抗癌活性;
【Key words】 chrysin; derivatives; trifluoromethylated; anticancer activities;
【Key words】 chrysin; derivatives; trifluoromethylated; anticancer activities;
【基金】 湖南省教育厅优秀青年基金(07B065);湖南省大学生研究性学习和创新性试验计划项目(2008-269-132)资助
- 【文献出处】 南华大学学报(医学版) ,Journal of University of South China(Medical Edition) , 编辑部邮箱 ,2009年02期
- 【分类号】R284
- 【被引频次】5
- 【下载频次】274