An efficient step-by-step approach to select pleiotropic drug candidates against Alzheimer's disease: The discovery of neocopride

BackgroundThe selection of novel chemical entities that have a reasonable chance of showing clinical efficacy in AD patients is challenging.ObjectiveThe aim of this article is to outline the steps involved in a selection process that can result in the identification of potential preclinical candidates.MethodsWe used a cellular model of injured hippocampal neurons, for the validation of the association of the targets considered (acetylcholinesterase and 5-HT<sub>4</sub> receptor) and for the selection of multi-target ligands active <i>in cellulo</i>. The mechanism of the plural action of the best compound, we called neocopride, was deciphered using several <i>in cellulo</i> approaches. Finally, the protective effect of neocopride against short-term memory impairment was investigated in mice intoxicated with amyloid- β peptide.ResultsOur results show that neocopride displays strong protective effects against short-term memory disorders after oral administration at a dose of 3 mg/kg.ConclusionsThe findings suggest that neocopride is a promising drug candidate It is currently undergoing preclinical regulatory trials for AD.

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Publication Details

Journal
Journal of Alzheimer s Disease
Published
2026-03-13
DOI
https://doi.org/10.1177/13872877261424925
Primary Topic
Cholinesterase and Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
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article

An efficient step-by-step approach to select pleiotropic drug candidates against Alzheimer's disease: The discovery of neocopride

Emilie Duval, Georgia R. Culley, Patrick Dallemagne, Cédric Lecoutey et al.
Journal of Alzheimer s Disease
Cholinesterase and Neurodegenerative Diseases
article

An efficient step-by-step approach to select pleiotropic drug candidates against Alzheimer's disease: The discovery of neocopride

Emilie Duval, Georgia R. Culley, Patrick Dallemagne, Cédric Lecoutey, Audrey Davis, Romain Legrand, Thomas Curel, Sylvie Claeysen, Christophe Rochais, Alexandre Henriques, Noëlle Callizot, Laura Rouvière
article en

Abstract

BackgroundThe selection of novel chemical entities that have a reasonable chance of showing clinical efficacy in AD patients is challenging.ObjectiveThe aim of this article is to outline the steps involved in a selection process that can result in the identification of potential preclinical candidates.MethodsWe used a cellular model of injured hippocampal neurons, for the validation of the association of the targets considered (acetylcholinesterase and 5-HT<sub>4</sub> receptor) and for the selection of multi-target ligands active <i>in cellulo</i>. The mechanism of the plural action of the best compound, we called neocopride, was deciphered using several <i>in cellulo</i> approaches. Finally, the protective effect of neocopride against short-term memory impairment was investigated in mice intoxicated with amyloid- β peptide.ResultsOur results show that neocopride displays strong protective effects against short-term memory disorders after oral administration at a dose of 3 mg/kg.ConclusionsThe findings suggest that neocopride is a promising drug candidate It is currently undergoing preclinical regulatory trials for AD.

Journal of Alzheimer s Disease
Centre National de la Recherche Scientifique (FR), Inserm (FR), Université de Montpellier (FR), École Supérieure d'Ingénieurs en Génie Électrique (FR), Center for Neuro-Oncology (US), Normandie Université (FR)
Good health and well-being
Openalex Percentile: Top 22%
Cholinesterase and Neurodegenerative Diseases
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