CORC  > 北京大学  > 化学与分子工程学院
Searching for more effective HCVNS3 protease inhibitors via modification of corilagin
Wang, Y ; Yang, XS ; Li, ZQ ; Zhang, W ; Chen, LR ; Xu, XJ
刊名progress in natural science
2005
关键词corilagin synthesis HCVNS3 serine protease molecular docking VIRUS NS3/4A PROTEASE HEPATITIS-C SERINE-PROTEASE
DOI10.1080/10020070512331343080
英文摘要Corilagin was seperated from extract of Phyllanthus urinaria L. and used as the precursor of inhibitors of hepatitis C virus (HCV) NS3 serine protease. Six derivatives were obtained through the chemical modification of corilagin and their structures were elucidated by the spectra analysis. Bioassay of these compounds showed that two of them had improved inhibitory efficiency than the precursor, with IC50 values of 2.28 mu mol/L and 1.52 mu mol/L, respectively. The binding mode of two active compounds with substrate binding site of HCV NS3 protease was also investigated by molecular docking method.; Materials Science, Multidisciplinary; Multidisciplinary Sciences; SCI(E); EI; 3; ARTICLE; 10; 896-901; 15
语种英语
内容类型期刊论文
源URL[http://ir.pku.edu.cn/handle/20.500.11897/399581]  
专题化学与分子工程学院
推荐引用方式
GB/T 7714
Wang, Y,Yang, XS,Li, ZQ,et al. Searching for more effective HCVNS3 protease inhibitors via modification of corilagin[J]. progress in natural science,2005.
APA Wang, Y,Yang, XS,Li, ZQ,Zhang, W,Chen, LR,&Xu, XJ.(2005).Searching for more effective HCVNS3 protease inhibitors via modification of corilagin.progress in natural science.
MLA Wang, Y,et al."Searching for more effective HCVNS3 protease inhibitors via modification of corilagin".progress in natural science (2005).
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace