Plummer Christopher W, Clements Matthew J, Chen Helen, Rajagopalan Murali, Josien Hubert, Hagmann William K, Miller Michael, Trujillo Maria E, Kirkland Melissa, Kosinski Daniel, Mane Joel, Pachanski Michele, Cheewatrakoolpong Boonlert, Nolting Andrew F, Orr Robert, Christensen Melodie, Campeau Louis-Charles, Wright Michael J, Bugianesi Randal, Souza Sarah, Zhang Xiaoping, Di Salvo Jerry, Weinglass Adam B, Tschirret-Guth Richard, Nargund Ravi, Howard Andrew D, Colletti Steven L
Departments of Discovery Chemistry, Process Chemistry, Drug Metabolism and Pharmacokinetics, In Vivo Pharmacology, and In Vitro Pharmacology, Merck Research Laboratories , Kenilworth, New Jersey 07033, United States.
ACS Med Chem Lett. 2017 Jan 23;8(2):221-226. doi: 10.1021/acsmedchemlett.6b00443. eCollection 2017 Feb 9.
GPR40 is a G-protein-coupled receptor expressed primarily in pancreatic islets and intestinal L-cells that has been a target of significant recent therapeutic interest for type II diabetes. Activation of GPR40 by partial agonists elicits insulin secretion only in the presence of elevated blood glucose levels, minimizing the risk of hypoglycemia. GPR40 agoPAMs have shown superior efficacy to partial agonists as assessed in a glucose tolerability test (GTT). Herein, we report the discovery and optimization of a series of potent, selective GPR40 agoPAMs. Compound demonstrated sustained glucose lowering in a chronic study of Goto Kakizaki rats, showing no signs of tachyphylaxis for this mechanism.
GPR40是一种主要在胰岛和肠道L细胞中表达的G蛋白偶联受体,它已成为近期II型糖尿病治疗的重要靶点。部分激动剂激活GPR40仅在血糖水平升高时引发胰岛素分泌,从而将低血糖风险降至最低。在葡萄糖耐量试验(GTT)中评估发现,GPR40 agoPAMs比部分激动剂具有更高的疗效。在此,我们报告了一系列强效、选择性GPR40 agoPAMs的发现和优化。化合物在对Goto Kakizaki大鼠的长期研究中显示出持续的血糖降低作用,且该机制未出现快速耐受的迹象。