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ASS234, As a New Multi-Target Directed Propargylamine for Alzheimer's Disease Therapy

Highlights: ASS2324 is a hybrid compound resulting from the juxtaposition of donepezil and the propargylamine PF9601N. ASS2324 is a multi-target directed propargylamine able to bind to all the AChE/BuChE and MAO A/B enzymes. ASS2324 shows antioxidant, neuroprotective and suitable permeability proper...

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Detalles Bibliográficos
Autores principales: Marco-Contelles, José, Unzeta, Mercedes, Bolea, Irene, Esteban, Gerard, Ramsay, Rona R., Romero, Alejandro, Martínez-Murillo, Ricard, Carreiras, M. Carmo, Ismaili, Lhassane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923252/
https://www.ncbi.nlm.nih.gov/pubmed/27445665
http://dx.doi.org/10.3389/fnins.2016.00294
Descripción
Sumario:Highlights: ASS2324 is a hybrid compound resulting from the juxtaposition of donepezil and the propargylamine PF9601N. ASS2324 is a multi-target directed propargylamine able to bind to all the AChE/BuChE and MAO A/B enzymes. ASS2324 shows antioxidant, neuroprotective and suitable permeability properties. ASS2324 restores the scopolamine-induced cognitive impairment to the same extent as donepezil, and is less toxic. ASS2324 prevents β-amyloid induced aggregation in the cortex of double transgenic mice. ASS2324 is the most advanced anti-Alzheimer agent for pre-clinical studies that we have identified in our laboratories. The complex nature of Alzheimer's disease (AD) has prompted the design of Multi-Target-Directed Ligands (MTDL) able to bind to diverse biochemical targets involved in the progress and development of the disease. In this context, we have designed a number of MTD propargylamines (MTDP) showing antioxidant, anti-beta-amyloid, anti-inflammatory, as well as cholinesterase and monoamine oxidase (MAO) inhibition capacities. Here, we describe these properties in the MTDL ASS234, our lead-compound ready to enter in pre-clinical studies for AD, as a new multipotent, permeable cholinesterase/monoamine oxidase inhibitor, able to inhibit Aβ-aggregation, and possessing antioxidant and neuroprotective properties.