(+/-)-BIGI-3h: Pentatarget-Directed Ligand combining Cholinesterase, Monoamine Oxidase, and Glycogen Synthase Kinase 3 beta Inhibition with Calcium Channel Antagonism and Antiaggregating Properties for Alzheimer's Disease
Affiliation auteurs | !!!! Error affiliation !!!! |
Titre | (+/-)-BIGI-3h: Pentatarget-Directed Ligand combining Cholinesterase, Monoamine Oxidase, and Glycogen Synthase Kinase 3 beta Inhibition with Calcium Channel Antagonism and Antiaggregating Properties for Alzheimer's Disease |
Type de publication | Journal Article |
Year of Publication | 2021 |
Auteurs | Ismaili L, Monnin J, Etievant A, Arribas RL, Viejo L, Refouvelet B, Soukup O, Janockova J, Hepnarova V, Korabecny J, Kucera T, Jun D, Andrys R, Musilek K, Baguet A, Garcia-Frutos EM, De Simone A, Andrisano V, Bartolini M, Rios Cde los, Marco-Contelles J, Haffen E |
Journal | ACS CHEMICAL NEUROSCIENCE |
Volume | 12 |
Pagination | 1328-1342 |
Date Published | APR 21 |
Type of Article | Article |
ISSN | 1948-7193 |
Mots-clés | Alzheimer's disease, Biginelli reaction, calcium channel, cholinesterases, GSK 3 beta, MAO |
Résumé | 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 3 beta 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 t protein and beta-amyloid peptide. The in vivo studies have shown that (+/-)-BIGI-3h (10 mg/kg intraperitoneally) significantly reduces scopolamine-induced cognitive deficits. |
DOI | 10.1021/acschemneuro.0c00803 |