Graveoline Analogs Exhibiting Selective Acetylcholinesterase Inhibitory Activity as Potential Lead Compounds for the Treatment of Alzheimer’s Disease

This study designed and synthesized a series of new graveoline analogs on the basis of the structural characteristics of acetylcholinesterase (AChE) dual-site inhibitors. The activity of these analogs was also evaluated. Results showed that the synthesized graveoline analogs displayed stronger inhib...

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Bibliographic Details
Main Authors: Zeng Li, Chaoyu Mu, Bin Wang, Juan Jin
Format: Article
Language:English
Published: MDPI AG 2016-01-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/21/2/132