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(+/-)-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

dc.contributor.authorIsmaili, Lhassane
dc.contributor.authorMonnin, Julie
dc.contributor.authorEtievant, Adeline
dc.contributor.authorArribas, Raquel L
dc.contributor.authorViejo, Lucia
dc.contributor.authorRefouvelet, Bernard
dc.contributor.authorSoukup, Ondrej
dc.contributor.authorJanockova, Jana
dc.contributor.authorHepnarova, Vendula
dc.contributor.authorKorabecny, Jan
dc.contributor.authorKucera, Tomas
dc.contributor.authorJun, Daniel
dc.contributor.authorAndrýs, Rudolf
dc.contributor.authorMusílek, Kamil
dc.contributor.authorBaguet, Aurelie
dc.contributor.authorGarcia-Frutos, Eva M
dc.contributor.authorDe Simone, Angela
dc.contributor.authorAndrisano, Vincenza
dc.contributor.authorBartolini, Manuela
dc.contributor.authorde Los Rios, Cristobal
dc.contributor.authorMarco-Contelles, Jose
dc.contributor.authorHaffen, Emmanuel
dc.date.accessioned2025-12-05T09:59:08Z
dc.date.available2025-12-05T09:59:08Z
dc.date.issued2021
dc.description.abstractMultitarget-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.eng
dc.formatp. 1328-1342
dc.identifier.doi10.1021/acschemneuro.0c00803
dc.identifier.issn1948-7193
dc.identifier.obd43877684
dc.identifier.scopus2-s2.0-85104920488
dc.identifier.urihttp://hdl.handle.net/20.500.12603/1249
dc.identifier.wos000643598600005
dc.language.isoeng
dc.peerreviewedyes
dc.publicationstatuspostprint
dc.publisherAmerican chemical society
dc.relation.ispartofACS Chemical Neuroscience, volume 12, issue: 8eng
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/acschemneuro.0c00803
dc.rights.accessOpen Access
dc.rights.licenseCC BY
dc.source.urlhttps://pubs.acs.org/doi/10.1021/acschemneuro.0c00803
dc.subjectAlzheimer's diseaseeng
dc.subjectcalcium channeleng
dc.subjectGSK 3 betaeng
dc.subjectMAOeng
dc.subjectcholinesteraseseng
dc.subjectBiginelli reactioneng
dc.title(+/-)-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 Diseaseeng
dc.typearticle

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