The Selectivity of Butyrylcholinesterase Inhibitors Revisited

Resource type
Authors/contributors
Title
The Selectivity of Butyrylcholinesterase Inhibitors Revisited
Abstract
Acetylcholinesterase (AChE) inhibitors are the primary target for single-molecule anti-Alzheimer’s disease (AD) therapeutics. Though AChE has historically been the focus of investigation for small-molecule inhibitors, interest in another cholinergic enzyme, butyrylcholinesterase (BChE), has grown in recent years. Attention stems from BChE’s role in β-amyloid (Aβ) protein aggregation and an increase in BChE concentration during the late stages of AD, where a decrease in AChE concentration is also observed. Currently, five FDA-approved drugs are on the market for inhibiting AChE, though no BChE-selective drugs have been approved so far. In this review, we focus on newly identified BChE selective inhibitors and present the ideas behind these discoveries. © 2025 by the authors.
Publication
Molecules
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Date
2025
Volume
30
Issue
21
Journal Abbr
Molecules
Citation Key
gambardellaSelectivityButyrylcholinesteraseInhibitors2025
ISSN
1420-3049
Language
English
Library Catalog
Scopus
Citation
Gambardella, M. D., Wang, Y., & Pang, J. (2025). The Selectivity of Butyrylcholinesterase Inhibitors Revisited. Molecules, 30(21). https://doi.org/10.3390/molecules30214201