| Literature DB >> 25815144 |
Rieko Takano1, Masao Yoshida1, Masahiro Inoue1, Takeshi Honda1, Ryutaro Nakashima1, Koji Matsumoto1, Tatsuya Yano1, Tsuneaki Ogata1, Nobuaki Watanabe1, Masakazu Hirouchi1, Tomoko Yoneyama2, Shuichiro Ito2, Narihiro Toda1.
Abstract
GPR40 is a G protein-coupled receptor that is predominantly expressed in pancreatic β-cells. GPR40 agonists stimulate insulin secretion in the presence of high glucose concentration. On the basis of this mechanism, GPR40 agonists are possible novel insulin secretagogues with reduced or no risk of hypoglycemia. The improvement of in vitro activity and metabolic stability of compound 1 led to the discovery of 13, (3S)-3-ethoxy-3-(4-{[(1R)-4-(trifluoromethyl)-2,3-dihydro-1H-inden-1-yl]oxy}phenyl)propanoic acid, as a potent and orally available GPR40 agonist. Compound 13 (DS-1558) was found to have potent glucose lowering effects during an oral glucose tolerance test in ZDF rats.Entities:
Keywords: GPR40; agonist; diabetes; glucose lowering; insulin secretagogue
Year: 2015 PMID: 25815144 PMCID: PMC4360146 DOI: 10.1021/ml500391n
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345