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G-protein coupled receptor 40 agonists as novel therapeutics for type 2 diabetes

Authors
Choi, Yun JungShin, DongyunLee, Ju-Yeun
Issue Date
Apr-2014
Publisher
PHARMACEUTICAL SOC KOREA
Keywords
GPR40 agonist; Antidiabetics; Type 2 diabetes mellitus
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.37, no.4, pp.435 - 439
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
37
Number
4
Start Page
435
End Page
439
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12744
DOI
10.1007/s12272-013-0283-3
ISSN
0253-6269
Abstract
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.
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