中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Recent research progress in small molecule AMPK direct activators

文献类型:期刊论文

作者Wei Qiangqiang2; Duan Wenhu1; Zhou Jinpei2; Zhang Huibin2
刊名Journal of China Pharmaceutical University
出版日期2015
卷号46期号:4页码:406-415
关键词AMP-activated protein kinase AMPK direct activators structure-activity relationship type 2 diabetes new target advances
ISSN号1000-5048
其他题名小分子AMPK直接激动剂的最新研究进展
文献子类Review
英文摘要Type 2 diabetes,an epidemic disorder characterized by high blood glucose level associated with microvascular complications,is one of the main causes of human suffer across the globe,with no effective medicine up to now.AMP-activated protein kinase(AMPK),a highly conserved serine/threonine protein kinase,is a key sensor and regulator of intracellular and whole-body energy metabolism.Small molecule AMPK direct activators have been proven to lower blood-glucose,which is a promising candidate for the treatment of type 2 diabetes.The progress on the research of small molecule AMPK direct activators in recent years is summarized in this paper.
WOS研究方向General & Internal Medicine (provided by Clarivate Analytics)
语种中文
CSCD记录号CSCD:5471872
源URL[http://119.78.100.183/handle/2S10ELR8/269277]  
专题药物化学研究室
作者单位1.Department of Medicinal Chemistry, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201203, China.
2.Center of New Drug Research, China Pharmaceutical University, Nanjing, Jiangsu 210009, China.;
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Wei Qiangqiang,Duan Wenhu,Zhou Jinpei,et al. Recent research progress in small molecule AMPK direct activators[J]. Journal of China Pharmaceutical University,2015,46(4):406-415.
APA Wei Qiangqiang,Duan Wenhu,Zhou Jinpei,&Zhang Huibin.(2015).Recent research progress in small molecule AMPK direct activators.Journal of China Pharmaceutical University,46(4),406-415.
MLA Wei Qiangqiang,et al."Recent research progress in small molecule AMPK direct activators".Journal of China Pharmaceutical University 46.4(2015):406-415.

入库方式: OAI收割

来源:上海药物研究所

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