Hinklin Ronald J, Aicher Thomas D, Anderson Deborah A, Baer Brian R, Boyd Steven A, Condroski Kevin R, DeWolf Walter E, Kraser Christopher F, McVean Maralee, Rhodes Susan P, Sturgis Hillary L, Voegtli Walter C, Williams Lance, Houze Jonathan B
Array BioPharma Inc. , 3200 Walnut Street, Boulder, Colorado 80301, United States.
J Med Chem. 2014 Oct 9;57(19):8180-6. doi: 10.1021/jm501204z. Epub 2014 Sep 17.
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.
葡萄糖激酶(GK)是胰腺在高血糖水平下释放胰岛素的限速步骤。通过GK的通量也有助于降低肝脏葡萄糖输出。由于许多2型糖尿病患者在这两个过程中的一个或两个方面似乎存在不足或缺陷,因此鉴定能够变构激活GK的化合物可能解决这一问题。在此,我们报告了一系列新型葡萄糖激酶激活剂(GKA)的鉴定和初步优化。优化后鉴定出化合物33,其在正常和糖尿病小鼠的口服葡萄糖耐量试验(OGTT)中显示出活性。