Publication | Open Access
Discovery of MK-8722: A Systemic, Direct Pan-Activator of AMP-Activated Protein Kinase
56
Citations
9
References
2017
Year
Early Generation CompoundsMetabolic RemodelingInsulin SignalingMetabolic SyndromeMolecular PharmacologySignaling PathwayAmp-activated Protein KinaseDirect Pan-activatorMetabolic SignalingCell SignalingSystems BiologyMolecular PhysiologyProtein FunctionBiochemistryG Protein-coupled ReceptorInsulin ManagementMetabolic ControlMammalian Energy HomeostasisPharmacologyCell BiologyProtein PhosphorylationSignal TransductionNatural SciencesDiabetesPhysiologyMetabolic RegulationDiabetes MellitusCellular BiochemistryMetabolismMedicine
5'-Adenosine monophosphate-activated protein kinase (AMPK) is a key regulator of mammalian energy homeostasis and has been implicated in mediating many of the beneficial effects of exercise and weight loss including lipid and glucose trafficking. As such, the enzyme has long been of interest as a target for the treatment of Type 2 Diabetes Mellitus. We describe the optimization of β1-selective, liver-targeted AMPK activators and their evolution into systemic pan-activators capable of acutely lowering glucose in mouse models. Identifying surrogates for the key acid moiety in early generation compounds proved essential in improving β2-activation and in balancing improvements in plasma unbound fraction while avoiding liver sequestration.
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