Back to Search Start Over

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

Authors :
Marco-Contelles J
Unzeta M
Bolea I
Esteban G
Ramsay RR
Romero A
Martínez-Murillo R
Carreiras MC
Ismaili L
Source :
Frontiers in neuroscience [Front Neurosci] 2016 Jun 28; Vol. 10, pp. 294. Date of Electronic Publication: 2016 Jun 28 (Print Publication: 2016).
Publication Year :
2016

Abstract

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 enzymesASS2324 shows antioxidant, neuroprotective and suitable permeability propertiesASS2324 restores the scopolamine-induced cognitive impairment to the same extent as donepezil, and is less toxicASS2324 prevents β-amyloid induced aggregation in the cortex of double transgenic miceASS2324 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.

Details

Language :
English
ISSN :
1662-4548
Volume :
10
Database :
MEDLINE
Journal :
Frontiers in neuroscience
Publication Type :
Academic Journal
Accession number :
27445665
Full Text :
https://doi.org/10.3389/fnins.2016.00294