首页> 外文期刊>Journal of Asian natural products research >'Click' reaction mediated synthesis of costunolide and dehydrocostuslactone derivatives and evaluation of their cytotoxic activity
【24h】

'Click' reaction mediated synthesis of costunolide and dehydrocostuslactone derivatives and evaluation of their cytotoxic activity

机译:“点击”反应介导的木香酚内酯和脱氢木香内酯衍生物的合成及其细胞毒性活性的评估

获取原文
获取原文并翻译 | 示例
       

摘要

As part of pharmacological-phytochemical integrated studies on medicinal plants from Indian flora, costunolide (1) and dehydrocostus lactone (2), were isolated as major phytochemicals from Saussurea lappa, a plant traditionally used in different Asian systems of medicine. A series of 1,4-disubstituted-1,2,3-triazoles conjugates were synthesized through diastereo selective Michael addition followed by regioselective Huisgen 1,3-dipolar cycloaddition reactions. All these triazolyl derivatives (5a-5j) & (7a-7j) were well characterized using modern spectroscopic techniques and evaluated for their anticancer activity against a panel of five human cancerous celllines. The results indicated that all the analogs displayed moderate cytotoxic activity.
机译:作为对来自印度植物群的药用植物进行药理学-植物化学综合研究的一部分,从传统的亚洲不同医学体系中使用的雪莲(Sausurea lappa)中分离了木香酚内酯(1)和脱氢木耳内酯(2)作为主要植物化学物质。通过非对映选择性迈克尔加成,然后区域选择性Huisgen 1,3-偶极环加成反应,合成了一系列1,4-二取代-1,2,3-三唑共轭物。使用现代光谱技术对所有这些三唑基衍生物(5a-5j)和(7a-7j)进行了很好的表征,并评估了它们对五种人类癌细胞系的抗癌活性。结果表明,所有类似物均显示出中等的细胞毒活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号