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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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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
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author Marco-Contelles, José
Unzeta, Mercedes
Bolea, Irene
Esteban, Gerard
Ramsay, Rona R.
Romero, Alejandro
Martínez-Murillo, Ricard
Carreiras, M. Carmo
Ismaili, Lhassane
author_facet Marco-Contelles, José
Unzeta, Mercedes
Bolea, Irene
Esteban, Gerard
Ramsay, Rona R.
Romero, Alejandro
Martínez-Murillo, Ricard
Carreiras, M. Carmo
Ismaili, Lhassane
author_sort Marco-Contelles, José
collection PubMed
description 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.
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spelling pubmed-49232522016-07-21 ASS234, As a New Multi-Target Directed Propargylamine for Alzheimer's Disease Therapy Marco-Contelles, José Unzeta, Mercedes Bolea, Irene Esteban, Gerard Ramsay, Rona R. Romero, Alejandro Martínez-Murillo, Ricard Carreiras, M. Carmo Ismaili, Lhassane Front Neurosci Pharmacology 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. Frontiers Media S.A. 2016-06-28 /pmc/articles/PMC4923252/ /pubmed/27445665 http://dx.doi.org/10.3389/fnins.2016.00294 Text en Copyright © 2016 Marco-Contelles, Unzeta, Bolea, Esteban, Ramsay, Romero, Martínez-Murillo, Carreiras and Ismaili. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Marco-Contelles, José
Unzeta, Mercedes
Bolea, Irene
Esteban, Gerard
Ramsay, Rona R.
Romero, Alejandro
Martínez-Murillo, Ricard
Carreiras, M. Carmo
Ismaili, Lhassane
ASS234, As a New Multi-Target Directed Propargylamine for Alzheimer's Disease Therapy
title ASS234, As a New Multi-Target Directed Propargylamine for Alzheimer's Disease Therapy
title_full ASS234, As a New Multi-Target Directed Propargylamine for Alzheimer's Disease Therapy
title_fullStr ASS234, As a New Multi-Target Directed Propargylamine for Alzheimer's Disease Therapy
title_full_unstemmed ASS234, As a New Multi-Target Directed Propargylamine for Alzheimer's Disease Therapy
title_short ASS234, As a New Multi-Target Directed Propargylamine for Alzheimer's Disease Therapy
title_sort ass234, as a new multi-target directed propargylamine for alzheimer's disease therapy
topic Pharmacology
url 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
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