Discovery of AM-1638: A Potent and Orally Bioavailable GPR40/FFA1 Full Agonist

Sean P. Brown(Amgen (United States)), Paul J. Dransfield(Amgen (United States)), Marc Vimolratana(Amgen (United States)), Xian‐Yun Jiao(Amgen (United States)), Liusheng Zhu(Amgen (United States)), Vatee Pattaropong(Amgen (United States)), Ying Sun(Amgen (United States)), Jinqian Liu(Amgen (United States)), Jian Luo(Amgen (United States)), Jane Zhang(Amgen (United States)), Simon Wong(Amgen (United States)), Run Zhuang(Amgen (United States)), Qi Guo(Amgen (United States)), Frank Li(Amgen (United States)), Julio C. Medina(Amgen (United States)), Gayathri Swaminath(Amgen (United States)), Daniel C.-H. Lin(Amgen (United States)), Jonathan B. Houze(Amgen (United States))
ACS Medicinal Chemistry Letters
August 15, 2012
Cited by 89Open Access
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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.


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