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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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Detalles Bibliográficos
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
Descripción
Sumario:[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.