| Literature DB >> 26166578 |
Tiantong Ou1, Xumin Hou1, Shaofeng Guan1, Jinjie Dai1, Wenzheng Han1, Ruogu Li1, Wenxia Wang1, Xinkai Qu1, Min Zhang1.
Abstract
An integration of virtual screening and kinase assay was reported to identify AMPK kinase inhibitors from various natural medicines.The activation of AMP-activated protein kinase (AMPK) signalling pathway plays a central role in the pathologic progression of atherosclerosis (AS). Targeting the AMPK is thus considered as a potential therapeutics to attenuate AS. Here, we report the establishment of a synthetic pipeline that integrates in silico virtual screening and in vitro kinase assay to discover new lead compounds of AMPK inhibitors. The screening is performed against a large-size pool of structurally diverse natural products, from which a number of compounds are inferred as promising candidates, and few of them are further tested in vitro by using a standard kinase assay protocol to determine their inhibitory potency against AMPK. With this scheme we successfully identify five potent AMPK inhibitors with IC50 values at micromolar level. We also examine the structural basis and molecular mechanism of nonbonded interaction network across the modelled complex interface of AMPK kinase domain with a newly identified natural medicine.Entities:
Keywords: AMP-activated protein kinase; atherosclerosis; inhibitor; natural product
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Year: 2015 PMID: 26166578 DOI: 10.1080/14786419.2015.1050672
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861