| Literature DB >> 25203462 |
Ronald J Hinklin1, Thomas D Aicher, Deborah A Anderson, Brian R Baer, Steven A Boyd, Kevin R Condroski, Walter E DeWolf, Christopher F Kraser, Maralee McVean, Susan P Rhodes, Hillary L Sturgis, Walter C Voegtli, Lance Williams, Jonathan B Houze.
Abstract
Glucokinase (GK) is the rate-limiting step for insulin release from the pancreas in response to high levels of glucose. Flux through GK also contributes to reducing hepatic glucose output. Since many individuals with type 2 diabetes appear to have an inadequacy or defect in one or both of these processes, identifying compounds that can allosterically activate GK may address this issue. Herein we report the identification and initial optimization of a novel series of glucokinase activators (GKAs). Optimization led to the identification of 33 as a compound that displayed activity in an oral glucose tolerance test (OGTT) in normal and diabetic mice.Entities:
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Year: 2014 PMID: 25203462 DOI: 10.1021/jm501204z
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446