Memantine Derivatives as Multitarget Agents in Alzheimer's Disease.
Alzheimer’s disease
hybrid structures
memantine
multi target directed ligand
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
02 Sep 2020
02 Sep 2020
Historique:
received:
10
07
2020
revised:
31
08
2020
accepted:
01
09
2020
entrez:
5
9
2020
pubmed:
6
9
2020
medline:
11
3
2021
Statut:
epublish
Résumé
Memantine (3,5-dimethyladamantan-1-amine) is an orally active, noncompetitive N-methyl-D-aspartate receptor (NMDAR) antagonist approved for treatment of moderate-to-severe Alzheimer's disease (AD), a neurodegenerative condition characterized by a progressive cognitive decline. Unfortunately, memantine as well as the other class of drugs licensed for AD treatment acting as acetylcholinesterase inhibitors (AChEIs), provide only symptomatic relief. Thus, the urgent need in AD drug development is for disease-modifying therapies that may require approaching targets from more than one path at once or multiple targets simultaneously. Indeed, increasing evidence suggests that the modulation of a single neurotransmitter system represents a reductive approach to face the complexity of AD. Memantine is viewed as a privileged NMDAR-directed structure, and therefore, represents the driving motif in the design of a variety of multi-target directed ligands (MTDLs). In this review, we present selected examples of small molecules recently designed as MTDLs to contrast AD, by combining in a single entity the amantadine core of memantine with the pharmacophoric features of known neuroprotectants, such as antioxidant agents, AChEIs and Aβ-aggregation inhibitors.
Identifiants
pubmed: 32887400
pii: molecules25174005
doi: 10.3390/molecules25174005
pmc: PMC7504780
pii:
doi:
Substances chimiques
Antioxidants
0
Cholinesterase Inhibitors
0
Memantine
W8O17SJF3T
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Ministero dell'Istruzione, dell'Università e della Ricerca
ID : PRIN 2017 (2017MT3993_007)
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