中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Novel indole alpha-methylene-gamma-lactones as potent inhibitors for AKT-mTOR signaling pathway kinases

文献类型:期刊论文

作者Ding, HS; Zhang, C; Wu, XH; Yang, CH; Zhang, XW; Ding, J; Xie, YY
刊名BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
出版日期2005-11-01
卷号15期号:21页码:4799-4802
关键词indole alpha-methylene-gamma-lactones AKT-mTOR signaling pathway kinase inhibitors
ISSN号0960-894X
DOI10.1016/j.bmcl.2005.07.050
文献子类Article
英文摘要In an effort to generate novel anticancer agents, a series of hybrids of alpha-methylene-gamma-lactones and 2-phenyl indoles has been synthesized and evaluated for inhibition activities on the phosphorylation of AKT, mTOR, p70S6 kinase, and 4E-BP1. The results indicate that substitutes on the gamma-position of lactones have a rather significant influence on inhibition activities. (c) 2005 Elsevier Ltd. All rights reserved.
WOS关键词TRANSLATION
WOS研究方向Pharmacology & Pharmacy ; Chemistry
语种英语
WOS记录号WOS:000232465900030
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://119.78.100.183/handle/2S10ELR8/273777]  
专题药物化学研究室
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Yang, CH
作者单位Chinese Acad Sci, State Key Lab Drug Res, Shanghai Inst Mat Med, Shanghai Inst Biol Sci,Grad Sch, Shanghai 201203, Peoples R China
推荐引用方式
GB/T 7714
Ding, HS,Zhang, C,Wu, XH,et al. Novel indole alpha-methylene-gamma-lactones as potent inhibitors for AKT-mTOR signaling pathway kinases[J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,2005,15(21):4799-4802.
APA Ding, HS.,Zhang, C.,Wu, XH.,Yang, CH.,Zhang, XW.,...&Xie, YY.(2005).Novel indole alpha-methylene-gamma-lactones as potent inhibitors for AKT-mTOR signaling pathway kinases.BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,15(21),4799-4802.
MLA Ding, HS,et al."Novel indole alpha-methylene-gamma-lactones as potent inhibitors for AKT-mTOR signaling pathway kinases".BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 15.21(2005):4799-4802.

入库方式: OAI收割

来源:上海药物研究所

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