| Literature DB >> 28197316 |
Christopher W Plummer1, Matthew J Clements1, Helen Chen1, Murali Rajagopalan1, Hubert Josien1, William K Hagmann1, Michael Miller1, Maria E Trujillo1, Melissa Kirkland1, Daniel Kosinski1, Joel Mane1, Michele Pachanski1, Boonlert Cheewatrakoolpong1, Andrew F Nolting1, Robert Orr1, Melodie Christensen1, Louis-Charles Campeau1, Michael J Wright1, Randal Bugianesi1, Sarah Souza1, Xiaoping Zhang1, Jerry Di Salvo1, Adam B Weinglass1, Richard Tschirret-Guth1, Ravi Nargund1, Andrew D Howard1, Steven L Colletti1.
Abstract
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 24 demonstrated sustained glucose lowering in a chronic study of Goto Kakizaki rats, showing no signs of tachyphylaxis for this mechanism.Entities:
Keywords: FFA1; GPCR; GPR40; agoPAM; chroman; diabetes; insulin secretogogue
Year: 2017 PMID: 28197316 PMCID: PMC5304298 DOI: 10.1021/acsmedchemlett.6b00443
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345