| Literature DB >> 27384289 |
Fan Li1, Zhi-Min Wang1, Jia-Jia Wu1, Jin Wang1, Sai-Sai Xie1, Jin-Shuai Lan1, Wei Xu1, Ling-Yi Kong1, Xiao-Bing Wang1.
Abstract
In a continuing effort to develop multitargeted compounds as potential treatment agents against Alzheimer's disease (AD), a series of donepezil-like compounds were designed, synthesized and evaluated. In vitro studies showed that most of the designed compounds displayed potent inhibitory activities toward AChE, BuChE, MAO-B and MAO-A. Among them, w18 was a promising agent with balanced activities, which exhibited a moderate cholinesterase inhibition (IC50, 0.220 μM for eeAChE; 1.23 μM for eqBuChE; 0.454 μM for hAChE) and an acceptable inhibitory activity against monoamine oxidases (IC50, 3.14 μM for MAO-B; 13.4 μM for MAO-A). Moreover, w18 could also be a metal-chelator, and able to cross the blood-brain barrier with low cell toxicity on PC12 cells. Taken together, these results suggested that w18 might be a promising multitargeted compound for AD treatment.Entities:
Keywords: Alzheimer’s disease; cholinesterase; donepezil; molecular modeling; monoamine oxidase
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Year: 2016 PMID: 27384289 DOI: 10.1080/14756366.2016.1201814
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051