Multitarget compounds bearing tacrine- and donepezil-like structural and functional motifs for the potential treatment of Alzheimer's disease

Affiliation auteurs!!!! Error affiliation !!!!
TitreMultitarget compounds bearing tacrine- and donepezil-like structural and functional motifs for the potential treatment of Alzheimer's disease
Type de publicationJournal Article
Year of Publication2017
AuteursIsmaili L, Refouvelet B, Benchekroun M, Brogi S, Brindisi M, Gemma S, Campiani G, Filipic S, Agbaba D, Esteban G, Unzeta M, Nikolic K, Butini S, Marco-Contelles J
JournalPROGRESS IN NEUROBIOLOGY
Volume151
Pagination4-34
Date PublishedAPR
Type of ArticleReview
ISSN0301-0082
Mots-clésAcetylcholinesterase, Alzheimer's disease, Beta secretase, beta-Amyloid, Butyrylcholinesterase, cholinesterases, Histamine receptor, Monoamine oxidases, Multi-target-directed ligand, Nitric oxide, Reactive oxygen species, Serotonin receptors
Résumé

Alzheimer's disease is a multifactorial and fatal neurodegenerative disorder characterized by decline of cholinergic function, deregulation of other neurotransmitter systems, beta-amyloid fibril deposition, and beta-amyloid oligomers formation. Based on the involvement of a relevant number of biological systems in Alzheimer's disease progression, multitarget compounds may enable therapeutic efficacy. Accordingly, compounds possessing, besides anticholinergic activity and beta-amyloid aggregation inhibition properties, metal chelating and/or nitric oxide releasing properties with additional antioxidant capacity were developed. Other targets relevant to Alzheimer's disease have also been considered in the last years for producing multitarget compounds such as beta-secretase, monoamino oxidases, serotonin receptors and sigma 1 receptors. The purpose of this review will be to highlight recent reports on the development of multitarget compounds for Alzheimer's disease published within the last years focusing on multifunctional ligands characterized by tacrine-like and donepezil-like structures. (C) 2016 Elsevier Ltd. All rights reserved.

DOI10.1016/j.pneurobio.2015.12.003