| Literature DB >> 29795759 |
Santhosh F Neelamkavil1, Andrew W Stamford1, Timothy Kowalski1, Dipshikha Biswas1, Craig Boyle1, Samuel Chackalamannil1, Yan Xia1, Charles Jayne1, Bernard Neustadt1, Jinsong Hao1, Hong Liu1, Xing Dai1, Hana Baker1, Brian Hawes1, Kim O'Neill1, Huadong Tang1, William J Greenlee1.
Abstract
The ever-growing prevalence of type 2 diabetes in the world has necessitated an urgent need for multiple orally effective agents that can regulate glucose homeostasis with a concurrent reduction in body weight. G-Protein coupled receptor 119 (GPR119) is a GPCR target at which agonists have demonstrated glucose-dependent insulin secretion and shows beneficial effects on glycemic control. Herein, we describe our efforts leading to the identification of a potent, oral GPR-119 agonist, MK-8282, which shows improved glucose tolerance in multiple animal models and has excellent off-target profile. The key design elements in the compounds involved a combination of a fluoro-pyrimidine and a conformationally constrained bridged piperidine to impart good potency and efficacy.Entities:
Year: 2018 PMID: 29795759 PMCID: PMC5949837 DOI: 10.1021/acsmedchemlett.8b00073
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345