| Literature DB >> 24900539 |
Sean P Brown1, Paul J Dransfield1, Marc Vimolratana1, XianYun Jiao1, Liusheng Zhu1, Vatee Pattaropong1, Ying Sun1, Jinqian Liu1, Jian Luo1, Jane Zhang1, Simon Wong1, Run Zhuang1, Qi Guo1, Frank Li1, Julio C Medina1, Gayathri Swaminath1, Daniel C-H Lin1, Jonathan B Houze1.
Abstract
GPR40 (FFA1) is a G-protein-coupled receptor, primarily expressed in pancreatic islets, the activation of which elicits increased insulin secretion only in the presence of elevated glucose levels. A potent, orally bioavailable small molecule GPR40 agonist is hypothesized to be an effective antidiabetic posing little or no risk of hypoglycemia. We recently reported the discovery of AMG 837 (1), a potent partial agonist of GPR40. Herein, we present the optimization from the GPR40 partial agonist 1 to the structurally and pharmacologically distinct GPR40 full agonist AM-1638 (21). Moreover, we demonstrate the improved in vivo efficacy that GPR40 full agonist 21 exhibits in BDF/DIO mice as compared to partial agonist 1.Entities:
Keywords: AM-1638; AMG 837; FFA1; GPR40; full agonist; insulin secretagogue
Year: 2012 PMID: 24900539 PMCID: PMC4025659 DOI: 10.1021/ml300133f
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345