| Literature DB >> 29348809 |
Danqing Feng1, Tesfaye Biftu1, F Anthony Romero1, Ahmet Kekec1, James Dropinski1, Andrew Kassick1, Shiyao Xu1, Marc M Kurtz1, Anantha Gollapudi1, Qing Shao1, Xiaodong Yang1, Ku Lu1, Gaochao Zhou1, Daniel Kemp1, Robert W Myers1, Hong-Ping Guan1, Maria E Trujillo1, Cai Li1, Ann Weber1, Iyassu K Sebhat1.
Abstract
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.Entities:
Year: 2017 PMID: 29348809 PMCID: PMC5767883 DOI: 10.1021/acsmedchemlett.7b00417
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345