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Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease

[Image: see text] The multifactorial nature of Alzheimer’s disease (AD) is a reason for the lack of effective drugs as well as a basis for the development of “multi-target-directed ligands” (MTDLs). As cases increase in developing countries, there is a need of new drugs that are not only effective b...

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Autores principales: Rossi, Michele, Freschi, Michela, de Camargo Nascente, Luciana, Salerno, Alessandra, de Melo Viana Teixeira, Sarah, Nachon, Florian, Chantegreil, Fabien, Soukup, Ondrej, Prchal, Lukáš, Malaguti, Marco, Bergamini, Christian, Bartolini, Manuela, Angeloni, Cristina, Hrelia, Silvana, Soares Romeiro, Luiz Antonio, Bolognesi, Maria Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154578/
https://www.ncbi.nlm.nih.gov/pubmed/33829779
http://dx.doi.org/10.1021/acs.jmedchem.1c00048
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author Rossi, Michele
Freschi, Michela
de Camargo Nascente, Luciana
Salerno, Alessandra
de Melo Viana Teixeira, Sarah
Nachon, Florian
Chantegreil, Fabien
Soukup, Ondrej
Prchal, Lukáš
Malaguti, Marco
Bergamini, Christian
Bartolini, Manuela
Angeloni, Cristina
Hrelia, Silvana
Soares Romeiro, Luiz Antonio
Bolognesi, Maria Laura
author_facet Rossi, Michele
Freschi, Michela
de Camargo Nascente, Luciana
Salerno, Alessandra
de Melo Viana Teixeira, Sarah
Nachon, Florian
Chantegreil, Fabien
Soukup, Ondrej
Prchal, Lukáš
Malaguti, Marco
Bergamini, Christian
Bartolini, Manuela
Angeloni, Cristina
Hrelia, Silvana
Soares Romeiro, Luiz Antonio
Bolognesi, Maria Laura
author_sort Rossi, Michele
collection PubMed
description [Image: see text] The multifactorial nature of Alzheimer’s disease (AD) is a reason for the lack of effective drugs as well as a basis for the development of “multi-target-directed ligands” (MTDLs). As cases increase in developing countries, there is a need of new drugs that are not only effective but also accessible. With this motivation, we report the first sustainable MTDLs, derived from cashew nutshell liquid (CNSL), an inexpensive food waste with anti-inflammatory properties. We applied a framework combination of functionalized CNSL components and well-established acetylcholinesterase (AChE)/butyrylcholinesterase (BChE) tacrine templates. MTDLs were selected based on hepatic, neuronal, and microglial cell toxicity. Enzymatic studies disclosed potent and selective AChE/BChE inhibitors (5, 6, and 12), with subnanomolar activities. The X-ray crystal structure of 5 complexed with BChE allowed rationalizing the observed activity (0.0352 nM). Investigation in BV-2 microglial cells revealed antineuroinflammatory and neuroprotective activities for 5 and 6 (already at 0.01 μM), confirming the design rationale.
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spelling pubmed-81545782021-05-27 Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease Rossi, Michele Freschi, Michela de Camargo Nascente, Luciana Salerno, Alessandra de Melo Viana Teixeira, Sarah Nachon, Florian Chantegreil, Fabien Soukup, Ondrej Prchal, Lukáš Malaguti, Marco Bergamini, Christian Bartolini, Manuela Angeloni, Cristina Hrelia, Silvana Soares Romeiro, Luiz Antonio Bolognesi, Maria Laura J Med Chem [Image: see text] The multifactorial nature of Alzheimer’s disease (AD) is a reason for the lack of effective drugs as well as a basis for the development of “multi-target-directed ligands” (MTDLs). As cases increase in developing countries, there is a need of new drugs that are not only effective but also accessible. With this motivation, we report the first sustainable MTDLs, derived from cashew nutshell liquid (CNSL), an inexpensive food waste with anti-inflammatory properties. We applied a framework combination of functionalized CNSL components and well-established acetylcholinesterase (AChE)/butyrylcholinesterase (BChE) tacrine templates. MTDLs were selected based on hepatic, neuronal, and microglial cell toxicity. Enzymatic studies disclosed potent and selective AChE/BChE inhibitors (5, 6, and 12), with subnanomolar activities. The X-ray crystal structure of 5 complexed with BChE allowed rationalizing the observed activity (0.0352 nM). Investigation in BV-2 microglial cells revealed antineuroinflammatory and neuroprotective activities for 5 and 6 (already at 0.01 μM), confirming the design rationale. American Chemical Society 2021-04-08 2021-04-22 /pmc/articles/PMC8154578/ /pubmed/33829779 http://dx.doi.org/10.1021/acs.jmedchem.1c00048 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Rossi, Michele
Freschi, Michela
de Camargo Nascente, Luciana
Salerno, Alessandra
de Melo Viana Teixeira, Sarah
Nachon, Florian
Chantegreil, Fabien
Soukup, Ondrej
Prchal, Lukáš
Malaguti, Marco
Bergamini, Christian
Bartolini, Manuela
Angeloni, Cristina
Hrelia, Silvana
Soares Romeiro, Luiz Antonio
Bolognesi, Maria Laura
Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease
title Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease
title_full Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease
title_fullStr Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease
title_full_unstemmed Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease
title_short Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease
title_sort sustainable drug discovery of multi-target-directed ligands for alzheimer’s disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154578/
https://www.ncbi.nlm.nih.gov/pubmed/33829779
http://dx.doi.org/10.1021/acs.jmedchem.1c00048
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