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Crystal structure, quantum chemical insights, and molecular docking studies of aryl-2-(-) acetamide compounds: potential inhibitors for neurodegenerative enzymes. | LitMetric

Crystal structure, quantum chemical insights, and molecular docking studies of aryl-2-(-) acetamide compounds: potential inhibitors for neurodegenerative enzymes.

RSC Adv

Laboratorio Síntesis Orgánica y Actividad Biológica (LSO-Act-Bio), Instituto de Química de Recursos Naturales, Universidad de Talca Casilla 747 Talca 3460000 Chile

Published: February 2024

AI Article Synopsis

Article Abstract

The increase in and concern about neurodegenerative diseases continue to grow in an increasingly long-lived world population. Therefore, the search for new drugs continues to be a priority for medicinal chemistry. We present here the synthesis of a series of compounds with acetamide nuclei. Their structures were established using UV-Visible, NMR, HRMS and IR techniques. Furthermore, we report the crystal structures that were obtained from compounds 5a-5d by X-ray diffraction. The compounds were evaluated as potential inhibitors of the monoxidase enzymes; A (MAO-A) and B (MAO-B), and cholinesterases; acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) through studies using the induced fit docking (IFD) method and binding free energy (Δ) calculations by the MMGBSA method. Interestingly, compounds 5b, 5c and 5d showed much better Δ than the reference drug Zonisamide. Compound 5c is the best in the series, which indicates a potential selective affinity of our compounds against MAO-B, which could be a promising finding in the search for new drugs for Parkinson's disease treatment. The acetamide crystal exhibits moderate NLO properties suggesting that it could be considered a potential candidate for application in nonlinear optical devices.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10853808PMC
http://dx.doi.org/10.1039/d3ra08649fDOI Listing

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