Abstract
A novel series of tacrine-selegiline hybrids was synthesised and evaluated for application as inhibitors of cholinesterase (AChE/BuChE) and monoamine oxidase (MAO-A/B). The results demonstrate that most of the synthesised compounds exhibit high inhibitory activity. Among these compounds, compound 8g provided a good balance of activity towards all targets (with IC50 values of 22.6 nM, 9.37 nM, 0.3724 μM, and 0.1810 μM for AChE, BuChE, MAO-A and MAO-B, respectively). These results indicated that 8g has the potential to be a multi-functional candidate for Alzheimer's disease.
Copyright © 2013 Elsevier Masson SAS. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetylcholinesterase / metabolism*
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Alzheimer Disease / drug therapy*
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Alzheimer Disease / enzymology
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Butyrylcholinesterase / metabolism*
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Dose-Response Relationship, Drug
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Enzyme Inhibitors / chemical synthesis
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology*
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Humans
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Models, Molecular
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Molecular Structure
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Monoamine Oxidase / metabolism*
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Recombinant Proteins / antagonists & inhibitors
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Recombinant Proteins / metabolism
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Selegiline / chemistry
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Structure-Activity Relationship
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Tacrine / chemistry
Substances
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Enzyme Inhibitors
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Recombinant Proteins
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Selegiline
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Tacrine
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Monoamine Oxidase
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Acetylcholinesterase
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Butyrylcholinesterase