Design and Synthesis of New Donepezil-Based Chalcones As Multi-Target-Directed Ligands Against Alzheimer's Disease: Biological Evaluation, Molecular Dynamics, and Zebrafish Model Studies Publisher



Geraiely B ; Kianmehr E ; Iraji A ; Bukhari S N A ; Mohammadi H ; Mojtabavi S ; Mahdavi M ; Saeedi M
Source: RSC Advances Published:2026

Abstract

Alzheimer's disease (AD) is a multifactorial neurodegenerative disease characterized by several hallmarks, including cholinergic dysfunction, aggregation of amyloid beta (Aβ), oxidative stress, and metal ion dyshomeostasis. A series of donepezil-derived chalcones 7a–q were synthesized and tested for their ability to inhibit cholinesterase (ChE) and amyloid beta (Aβ) aggregation, antioxidant properties, and metal chelation. Of these, compound 7j with a 2-chloroaryl moiety showed moderate anti-AChE activity (IC50 = 17.96 µM) and showed potent inhibition of Aβ aggregation, both in the presence of self-induced (72.5%) and AChE-induced (77.6%) conditions, and had good Cu2+ chelation ability, which was confirmed by ultraviolet-visible (UV-vis) spectroscopy. Compound 7p, an analog containing furan, exhibited both anti-ChE activity (IC50 = 22.70 µM for AChE and 19.14 µM for BuChE, respectively) and moderate anti-Aβ aggregation activity, as well as moderate antioxidant activity. The two compounds were found to be safe, also in PC12 cells and SH-SY5Y cells. Their results are all encouraging for their use as multi-target directed ligands (MTDLs) against AD. Finally, the molecular dynamics simulations in the active site of AChE of compound 7j showed stable binding for 100 nanoseconds. In vivo experiments in zebrafish showed that compound 7p markedly enhanced locomotor and exploratory behavior, with a therapeutic profile compared to the standard drug donepezil, and compound 7j exhibited moderate therapeutic effects. This journal is © The Royal Society of Chemistry, 2026.