Enone- and chalcone-chloroquinoline hybrid analogues: In silico guided design, synthesis, antiplasmodial activity, in vitro metabolism, and mechanistic studies

导出原文传递

翻译打印收藏纠错

作者： Guantai, E.M. ^[1] ; Ncokazi, K. ^[2] ; Egan, T.J. ^[3] ; Gut, J. ^[4] ; Rosenthal, P.J. ; Bhampidipati, R. ; Kopinathan, A. ; Smith, P.J. ; Chibale, K.

作者单位： Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa ^[1] Centre for Drug Candidate Optimisation, Monash Institute of Pharmaceutical Sciences, Monash University (Parkville Campus), 381 Royal Parade, Parkville, VIC 3052, Australia ^[2] Department of Medicine, San Francisco General Hospital, University of California at San Francisco, San Francisco, CA 94143, United States ^[3] Division of Pharmacology, University of Cape Town, Observatory 7925, South Africa ^[4]

发布时间 2013-11-20

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览0

Journal of Medicinal Chemistry

2011年54卷10期

3637-3649页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

Enone- and chalcone-chloroquinoline hybrid analogues: In silico guided design, synthesis, antiplasmodial activity, in vitro metabolism, and mechanistic studies

Journal of Medicinal Chemistry

相似文献

Journal of Medicinal Chemistry

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

Enone- and chalcone-chloroquinoline hybrid analogues: In silico guided design, synthesis, antiplasmodial activity, in vitro metabolism, and mechanistic studies

Journal of Medicinal Chemistry

相似文献

Journal of Medicinal Chemistry

相关期刊

检索历史清除