SAR, Pharmacokinetics, Safety, and Efficacy of Glucokinase Activating 2-(4-Sulfonylphenyl)-N-thiazol-2-ylacetamides: Discovery of PSN-GK1
摘要:
Allosteric activators of the glucose-sensing enzyme glucokinase (GK) are currently attracting much interest as potential antidiabetic therapies because they can achieve powerful blood glucose lowering through actions in multiple organs. Here, the optimization of a weakly active high-throughput screening hit to (2R)-2-(4-cyclopropanesulfonylphenyl)-N-(5-fluorothiazol-2-yl)-3-(tetrahydropyran-4-yl)propionamide (PSN-GK1), a potent GK activator with an improved pharmacokinetic and safety profile, is described. Following oral administration, this compound elicited robust glucose lowering in rats.
Compounds of Formula (I):
1
or pharmaceutically acceptable salts thereof, are useful in the prophylactic and therapeutic treatment of hyperglycemia and diabetes.
公式(I)化合物或其药学上可接受的盐,可用于预防和治疗高血糖和糖尿病。
TRI(CYCLO) SUBSTITUTED AMIDE COMPOUNDS
申请人:Fyfe Colin Thor Matthew
公开号:US20070281946A1
公开(公告)日:2007-12-06
Compounds of Formula (I):
or pharmaceutically acceptable salts thereof, are useful in the prophylactic and therapeutic treatment of hyperglycemia and diabetes.
式(I)的化合物或其药学上可接受的盐,在预防和治疗高血糖和糖尿病方面是有用的。
PHENYLACETAMIDES AND THEIR USE AS GLUCOKINASE MODULATORS