中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Structure-based de novo design, synthesis, and biological evaluation of the indole-based PPAR gamma ligands (I)

文献类型:期刊论文

作者Dong, Xiaochun; Zhang, Zhenshan; Wen, Ren; Shen, Jianhua; Shen, Xu; Jiang, Hualiang
刊名BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
出版日期2006-11-15
卷号16期号:22页码:5913-5916
关键词de novo drug design PPAR gamma ligand type II diabetes indole compounds
ISSN号0960-894X
DOI10.1016/j.bmcl.2006.06.093
文献子类Article
英文摘要MCSS and LeapFrog, two de novo drug design programs, were used for the novel indole-based PPAR gamma ligands' study. The designed compounds were synthesized and tested for the PPAR gamma protein binding activities in vitro. Out of the compounds that were synthesized, two molecules (compounds 14d and 7d) possessed potent PPAR gamma protein binding activity close to rosiglitazone in vitro. (c) 2006 Elsevier Ltd. All rights reserved.
WOS关键词ACTIVATED RECEPTOR-GAMMA ; AGONISTS ; BINDING ; SERIES ; AGENTS
WOS研究方向Pharmacology & Pharmacy ; Chemistry
语种英语
WOS记录号WOS:000241850400042
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://119.78.100.183/handle/2S10ELR8/273444]  
专题中国科学院上海药物研究所
通讯作者Wen, Ren
作者单位1.Fudan Univ, Dept Med Chem, Shanghai 200032, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
推荐引用方式
GB/T 7714
Dong, Xiaochun,Zhang, Zhenshan,Wen, Ren,et al. Structure-based de novo design, synthesis, and biological evaluation of the indole-based PPAR gamma ligands (I)[J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,2006,16(22):5913-5916.
APA Dong, Xiaochun,Zhang, Zhenshan,Wen, Ren,Shen, Jianhua,Shen, Xu,&Jiang, Hualiang.(2006).Structure-based de novo design, synthesis, and biological evaluation of the indole-based PPAR gamma ligands (I).BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,16(22),5913-5916.
MLA Dong, Xiaochun,et al."Structure-based de novo design, synthesis, and biological evaluation of the indole-based PPAR gamma ligands (I)".BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 16.22(2006):5913-5916.

入库方式: OAI收割

来源:上海药物研究所

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