| Literature DB >> 30396115 |
Zahra Najafi1, Mohammad Mahdavi2, Mina Saeedi3, Elahe Karimpour-Razkenari4, Najmeh Edraki5, Mohammad Sharifzadeh6, Mahnaz Khanavi7, Tahmineh Akbarzadeh8.
Abstract
A new series of tacrine-coumarin hybrids linked to 1,2,3-triazole were designed, synthesized, and tested as potent dual binding site cholinesterase inhibitors (ChEIs) for the treatment of Alzheimer's disease (AD). Among them, compound 8e was the most potent anti-AChE derivative (IC50 = 27 nM) and compound 8m displayed the best anti-BChE activity (IC50 = 6 nM) much more active than tacrine and donepezil as the reference drugs. Compound 8e was also evaluated for its BACE1 inhibitory activity and neuroprotectivity against PC12 cells exposed to Aβ25-35 which indicated low activity. Finally, in vivo studies by Morris water maze task showed that compound 8e significantly reversed scopolamine-induced memory deficit in rats.Entities:
Keywords: 1,2,3-Triazole; Alzheimer’s disease; Docking study; Dual binding site; Morris water maze; Tacrine-Coumarins
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Year: 2018 PMID: 30396115 DOI: 10.1016/j.bioorg.2018.10.056
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275