GPR40 agonist;
Antidiabetics;
Type 2 diabetes mellitus;
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摘要:
With growing needs for new antidiabetic drugs which are safe and effective alone or in combination with existing drugs, G-protein coupled receptor 40 (GPR40) has drawn a considerable attention as a potential therapeutic target for type 2 diabetes. As GPR40 agonist may offer advantages to commonly used agents, by acting ambient glucose dependent manner which mechanistically leads to reduced risk of developing hypoglycemia. Since deorphanization in 2003, development of small molecule GPR40 agonists has been spurred by several research groups. There are a number of lead molecules targeting GPR40, and among these molecules TAK-875 (full agonist) and AMG 837 (partial agonist) advanced into clinical stage.
机构:
School of Life Science and Engineering, Southwest Jiao Tong UniversitySchool of Life Science and Engineering, Southwest Jiao Tong University
Jing Huang
Bin Guo
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机构:
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of SciencesSchool of Life Science and Engineering, Southwest Jiao Tong University
Bin Guo
Wen-Jing Chu
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机构:
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of SciencesSchool of Life Science and Engineering, Southwest Jiao Tong University
Wen-Jing Chu
Xin Xie
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机构:
CAS Key Laboratory of Receptor Research, The National Center for Drug Screening, Shanghai Institute of Materia Medica, Chinese Academy of SciencesSchool of Life Science and Engineering, Southwest Jiao Tong University
Xin Xie
Yu-She Yang
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机构:
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of SciencesSchool of Life Science and Engineering, Southwest Jiao Tong University
Yu-She Yang
Xian-Li Zhou
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机构:
School of Life Science and Engineering, Southwest Jiao Tong UniversitySchool of Life Science and Engineering, Southwest Jiao Tong University
机构:
Southwest Jiao Tong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R ChinaSouthwest Jiao Tong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
Huang, Jing
Guo, Bin
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机构:
Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R ChinaSouthwest Jiao Tong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
Guo, Bin
Chu, Wen-Jing
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机构:
Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R ChinaSouthwest Jiao Tong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
Chu, Wen-Jing
Xie, Xin
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机构:
Chinese Acad Sci, Shanghai Inst Mat Med, Natl Ctr Drug Screening, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R ChinaSouthwest Jiao Tong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
Xie, Xin
Yang, Yu-She
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h-index: 0
机构:
Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R ChinaSouthwest Jiao Tong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
Yang, Yu-She
Zhou, Xian-Li
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机构:
Southwest Jiao Tong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R ChinaSouthwest Jiao Tong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China