| Literature DB >> 33797877 |
Lhassane Ismaili1, Julie Monnin1, Adeline Etievant1, Raquel L Arribas2,3, Lucía Viejo2,3, Bernard Refouvelet1, Ondrej Soukup4, Jana Janockova4, Vendula Hepnarova5, Jan Korabecny4, Tomas Kucera5, Daniel Jun5, Rudolf Andrys6, Kamil Musilek6, Aurelie Baguet7, Eva M García-Frutos8, Angela De Simone9, Vincenza Andrisano9, Manuela Bartolini10, Cristóbal de Los Ríos2,3, José Marco-Contelles11, Emmanuel Haffen1.
Abstract
Multitarget-directed ligands (MTDLs) are considered a promising therapeutic strategy to address the multifactorial nature of Alzheimer's disease (AD). Novel MTDLs have been designed as inhibitors of human acetylcholinesterases/butyrylcholinesterases, monoamine oxidase A/B, and glycogen synthase kinase 3β and as calcium channel antagonists via the Biginelli multicomponent reaction. Among these MTDLs, (±)-BIGI-3h was identified as a promising new hit compound showing in vitro balanced activities toward the aforementioned recognized AD targets. Additional in vitro studies demonstrated antioxidant effects and brain penetration, along with the ability to inhibit the aggregation of both τ protein and β-amyloid peptide. The in vivo studies have shown that (±)-BIGI-3h (10 mg/kg intraperitoneally) significantly reduces scopolamine-induced cognitive deficits.Entities:
Keywords: Alzheimer’s disease; Biginelli reaction; GSK 3β; MAO; calcium channel; cholinesterases
Year: 2021 PMID: 33797877 DOI: 10.1021/acschemneuro.0c00803
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418