首页 | 本学科首页   官方微博 | 高级检索  
检索        

九节龙皂苷衍生物的合成及其抗肿瘤活性
引用本文:王丽,王荣,校鑫,匡永清,王晓娟.九节龙皂苷衍生物的合成及其抗肿瘤活性[J].中国药师,2013,16(1):6-8.
作者姓名:王丽  王荣  校鑫  匡永清  王晓娟
作者单位:湖南大学化学化工学院;第四军医大学口腔医院
基金项目:国家自然科学基金项目(编号:30973623);陕西省资源主导型产业关键技术(链)项目(编号:2011KTCL03-01);第四军医大学优秀文职人员培养基金(编号:00003383)
摘    要:目的:合成九节龙皂苷衍生物并研究其抗肿瘤活性。方法:以九节龙皂苷Ⅰ为先导物,对其30位醛基进行结构修饰,合成一系列衍生物,通过体外细胞培养方法检测其对9种常见肿瘤细胞系的抗肿瘤活性。结果:获得了3个新的皂苷修饰物,其中化合物1和化合物3对常见的9种瘤株的IC50与原皂苷相比均降低(P<0.05),化合物1和化合物3对肿瘤细胞的抑制率较原皂苷增强。结论:通过对九节龙皂苷进行结构修饰,能增加其抗肿瘤活性。

关 键 词:九节龙皂苷  结构修饰  抗肿瘤活性
收稿时间:2012/8/29 0:00:00
修稿时间:2012/10/17 0:00:00

Synthesis and Anti-tumor Activities of Ardipusilloside Derivatives
Wang Li,Wang Rong,Xiao Xin,Kuang Yongqing and Wang Xiaojuan.Synthesis and Anti-tumor Activities of Ardipusilloside Derivatives[J].China Pharmacist,2013,16(1):6-8.
Authors:Wang Li  Wang Rong  Xiao Xin  Kuang Yongqing and Wang Xiaojuan
Institution:1.College of Chemistry and Chemical Engineering,Hunan University, Changsha 410082,China;2.Department of Pharmacology,College of Stomatology,the Fourth Military Medical University)
Abstract:ABSTRACT Objective: To synthesize ardipusilloside (ADS) derivatives and evaluate their anti-tumor activities. Method:A series of chemical compounds were synthesized by the modification of 30-aldehyde group in ardipusilloside, and the anti-tumor activities of the three compounds were studied. Result:Three new compounds were synthesized, and two of which could enhance the anti-tumor activity when compared with ADS. Conclusion:The study establishes a synthetic method for ardipusilloside derivatives and the anti-tumor activities are worthy of further study.
Keywords:
本文献已被 CNKI 等数据库收录!
点击此处可从《中国药师》浏览原始摘要信息
点击此处可从《中国药师》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号