Design, synthesis, and evaluation of multitarget-directed ligands against Alzheimer’s disease based on the fusion of donepezil and curcumin

[Display omitted] By fusing donepezil and curcumin, a novel series of compounds were obtained as multitarget-directed ligands against Alzheimer’s disease. Among them, compound 11b displayed potent acetylcholinesterase (AChE) inhibition (IC50=187nM) and the highest BuChE/AChE selectivity (66.3). Comp...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2017-06, Vol.25 (12), p.2946-2955
Hauptverfasser: Yan, Jun, Hu, Jinhui, Liu, Anqiu, He, Lin, Li, Xingshu, Wei, Hui
Format: Artikel
Sprache:eng
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Zusammenfassung:[Display omitted] By fusing donepezil and curcumin, a novel series of compounds were obtained as multitarget-directed ligands against Alzheimer’s disease. Among them, compound 11b displayed potent acetylcholinesterase (AChE) inhibition (IC50=187nM) and the highest BuChE/AChE selectivity (66.3). Compound 11b also inhibited 45.3% Aβ1–42 self-aggregation at 20μM and displayed remarkable antioxidant effects. The metal-chelating property of compound 11b was elucidated by determining the 1:1 stoichiometry for the 11b–Cu(II) complex. The excellent blood–brain barrier permeability of 11b also indicated the potential for the compound to penetrate the central nervous system.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2017.02.048