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• W2947671824 startingPage "372" @default.
• W2947671824 abstract "According to recent research advance, it is interesting to identify new, potent and selective inhibitors of human butyrylcholinesterase (BChE) for therapeutic treatment of both the Alzheimer's disease (AD) and heroin abuse. In this study, we carried out a structure-based virtual screening followed by in vitro activity assays, with the goal to identify new inhibitors that are selective for BChE over acetylcholinesterase (AChE). As a result, a set of new, selective inhibitors of human BChE were identified from natural products with solanaceous alkaloid scaffolds. The most active one of the natural products (compound 1) identified has an IC50 of 16.8 nM against BChE. It has been demonstrated that the desirable selectivity of these inhibitors for BChE over AChE is mainly controlled by three key residues in the active site cavity, i.e. residues Q119, A277, and A328 in BChE versus the respective residues Y124, W286, and Y337 in AChE. Based on this structural insight, future rational design of new, potent and selective BChE inhibitors may focus on these key structural differences in the active site cavity." @default.
• W2947671824 created "2019-06-07" @default.
• W2947671824 creator A5001124751 @default.
• W2947671824 creator A5029028746 @default.
• W2947671824 creator A5046372700 @default.
• W2947671824 creator A5046581115 @default.
• W2947671824 date "2019-08-01" @default.
• W2947671824 modified "2023-10-13" @default.
• W2947671824 title "Structure-based virtual screening leading to discovery of highly selective butyrylcholinesterase inhibitors with solanaceous alkaloid scaffolds" @default.
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• W2947671824 doi "https://doi.org/10.1016/j.cbi.2019.05.051" @default.
• W2947671824 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6613991" @default.
• W2947671824 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31152736" @default.
• W2947671824 hasPublicationYear "2019" @default.
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