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New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking
Sortase A inhibition is a well establish strategy for decreasing bacterial virulence by affecting numerous key processes that control biofilm formation, host cell entry, evasion and suppression of the immune response and acquisition of essential nutrients. A meta-analysis of structures known to act...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150342/ https://www.ncbi.nlm.nih.gov/pubmed/29077016 http://dx.doi.org/10.3390/molecules22111827 |
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author | Oniga, Smaranda Dafina Araniciu, Cătălin Palage, Mariana Doina Popa, Marcela Chifiriuc, Mariana Carmen Marc, Gabriel Pirnau, Adrian Stoica, Cristina Ioana Lagoudis, Ioannis Dragoumis, Theodoros Oniga, Ovidiu |
author_facet | Oniga, Smaranda Dafina Araniciu, Cătălin Palage, Mariana Doina Popa, Marcela Chifiriuc, Mariana Carmen Marc, Gabriel Pirnau, Adrian Stoica, Cristina Ioana Lagoudis, Ioannis Dragoumis, Theodoros Oniga, Ovidiu |
author_sort | Oniga, Smaranda Dafina |
collection | PubMed |
description | Sortase A inhibition is a well establish strategy for decreasing bacterial virulence by affecting numerous key processes that control biofilm formation, host cell entry, evasion and suppression of the immune response and acquisition of essential nutrients. A meta-analysis of structures known to act as Sortase A inhibitors provided the starting point for identifying a new potential scaffold. Based on this template a series of new potential Sortase A inhibitors, that contain the 2-phenylthiazole moiety, were synthesized. The physicochemical characterisation confirmed the identity of the proposed structures. Antibacterial activity evaluation showed that the new compounds have a reduced activity against bacterial cell viability. However, the compounds prevent biofilm formation at very low concentrations, especially in the case of E. faecalis. Molecular docking studies performed estimate that this is most likely due to the inhibition of Sortase A. The new compounds could be used as add-on therapies together with known antibacterial agents in order to combat multidrug-resistance enterococcal infections. |
format | Online Article Text |
id | pubmed-6150342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61503422018-11-13 New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking Oniga, Smaranda Dafina Araniciu, Cătălin Palage, Mariana Doina Popa, Marcela Chifiriuc, Mariana Carmen Marc, Gabriel Pirnau, Adrian Stoica, Cristina Ioana Lagoudis, Ioannis Dragoumis, Theodoros Oniga, Ovidiu Molecules Article Sortase A inhibition is a well establish strategy for decreasing bacterial virulence by affecting numerous key processes that control biofilm formation, host cell entry, evasion and suppression of the immune response and acquisition of essential nutrients. A meta-analysis of structures known to act as Sortase A inhibitors provided the starting point for identifying a new potential scaffold. Based on this template a series of new potential Sortase A inhibitors, that contain the 2-phenylthiazole moiety, were synthesized. The physicochemical characterisation confirmed the identity of the proposed structures. Antibacterial activity evaluation showed that the new compounds have a reduced activity against bacterial cell viability. However, the compounds prevent biofilm formation at very low concentrations, especially in the case of E. faecalis. Molecular docking studies performed estimate that this is most likely due to the inhibition of Sortase A. The new compounds could be used as add-on therapies together with known antibacterial agents in order to combat multidrug-resistance enterococcal infections. MDPI 2017-10-27 /pmc/articles/PMC6150342/ /pubmed/29077016 http://dx.doi.org/10.3390/molecules22111827 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Oniga, Smaranda Dafina Araniciu, Cătălin Palage, Mariana Doina Popa, Marcela Chifiriuc, Mariana Carmen Marc, Gabriel Pirnau, Adrian Stoica, Cristina Ioana Lagoudis, Ioannis Dragoumis, Theodoros Oniga, Ovidiu New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking |
title | New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking |
title_full | New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking |
title_fullStr | New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking |
title_full_unstemmed | New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking |
title_short | New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking |
title_sort | new 2-phenylthiazoles as potential sortase a inhibitors: synthesis, biological evaluation and molecular docking |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150342/ https://www.ncbi.nlm.nih.gov/pubmed/29077016 http://dx.doi.org/10.3390/molecules22111827 |
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