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Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors
The enormous burden of the COVID-19 pandemic in economic and healthcare terms has cast a shadow on the serious threat of antimicrobial resistance, increasing the inappropriate use of antibiotics and shifting the focus of drug discovery programmes from antibacterial and antifungal fields. Thus, there...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956313/ https://www.ncbi.nlm.nih.gov/pubmed/35322729 http://dx.doi.org/10.1080/14756366.2022.2055009 |
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author | D’Agostino, Ilaria Mathew, Githa Elizabeth Angelini, Paola Venanzoni, Roberto Angeles Flores, Giancarlo Angeli, Andrea Carradori, Simone Marinacci, Beatrice Menghini, Luigi Abdelgawad, Mohamed A. Ghoneim, Mohammed M. Mathew, Bijo Supuran, Claudiu T. |
author_facet | D’Agostino, Ilaria Mathew, Githa Elizabeth Angelini, Paola Venanzoni, Roberto Angeles Flores, Giancarlo Angeli, Andrea Carradori, Simone Marinacci, Beatrice Menghini, Luigi Abdelgawad, Mohamed A. Ghoneim, Mohammed M. Mathew, Bijo Supuran, Claudiu T. |
author_sort | D’Agostino, Ilaria |
collection | PubMed |
description | The enormous burden of the COVID-19 pandemic in economic and healthcare terms has cast a shadow on the serious threat of antimicrobial resistance, increasing the inappropriate use of antibiotics and shifting the focus of drug discovery programmes from antibacterial and antifungal fields. Thus, there is a pressing need for new antimicrobials involving innovative modes of action (MoAs) to avoid cross-resistance rise. Thiosemicarbazones (TSCs) stand out due to their easy preparation and polypharmacological application, also in infectious diseases. Recently, we reported a small library of TSCs (1–9) that emerged for their non-cytotoxic behaviour. Inspired by their multifaceted activity, we investigated the antibacterial, antifungal, and antidermatophytal profiles of derivatives 1–9, highlighting a new promising research line. Furthermore, the ability of these compounds to inhibit selected microbial and human carbonic anhydrases (CAs) was assessed, revealing their possible involvement in the MoA and a good selectivity index for some derivatives. |
format | Online Article Text |
id | pubmed-8956313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-89563132022-03-26 Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors D’Agostino, Ilaria Mathew, Githa Elizabeth Angelini, Paola Venanzoni, Roberto Angeles Flores, Giancarlo Angeli, Andrea Carradori, Simone Marinacci, Beatrice Menghini, Luigi Abdelgawad, Mohamed A. Ghoneim, Mohammed M. Mathew, Bijo Supuran, Claudiu T. J Enzyme Inhib Med Chem Short Communication The enormous burden of the COVID-19 pandemic in economic and healthcare terms has cast a shadow on the serious threat of antimicrobial resistance, increasing the inappropriate use of antibiotics and shifting the focus of drug discovery programmes from antibacterial and antifungal fields. Thus, there is a pressing need for new antimicrobials involving innovative modes of action (MoAs) to avoid cross-resistance rise. Thiosemicarbazones (TSCs) stand out due to their easy preparation and polypharmacological application, also in infectious diseases. Recently, we reported a small library of TSCs (1–9) that emerged for their non-cytotoxic behaviour. Inspired by their multifaceted activity, we investigated the antibacterial, antifungal, and antidermatophytal profiles of derivatives 1–9, highlighting a new promising research line. Furthermore, the ability of these compounds to inhibit selected microbial and human carbonic anhydrases (CAs) was assessed, revealing their possible involvement in the MoA and a good selectivity index for some derivatives. Taylor & Francis 2022-03-24 /pmc/articles/PMC8956313/ /pubmed/35322729 http://dx.doi.org/10.1080/14756366.2022.2055009 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication D’Agostino, Ilaria Mathew, Githa Elizabeth Angelini, Paola Venanzoni, Roberto Angeles Flores, Giancarlo Angeli, Andrea Carradori, Simone Marinacci, Beatrice Menghini, Luigi Abdelgawad, Mohamed A. Ghoneim, Mohammed M. Mathew, Bijo Supuran, Claudiu T. Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors |
title | Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors |
title_full | Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors |
title_fullStr | Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors |
title_full_unstemmed | Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors |
title_short | Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors |
title_sort | biological investigation of n-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956313/ https://www.ncbi.nlm.nih.gov/pubmed/35322729 http://dx.doi.org/10.1080/14756366.2022.2055009 |
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