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A Versatile Strategy for the Synthesis of 4,5-Dihydroxy-2,3-Pentanedione (DPD) and Related Compounds as Potential Modulators of Bacterial Quorum Sensing

Resistance to antibiotics is an increasingly serious threat to global public health and its management translates to significant health care costs. The validation of new Gram-negative antibacterial targets as sources for potential new antibiotics remains a challenge for all the scientists working in...

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Autores principales: Stotani, Silvia, Gatta, Viviana, Medda, Federico, Padmanaban, Mohan, Karawajczyk, Anna, Tammela, Päivi, Giordanetto, Fabrizio, Tzalis, Dimitrios, Collina, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222300/
https://www.ncbi.nlm.nih.gov/pubmed/30301207
http://dx.doi.org/10.3390/molecules23102545
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author Stotani, Silvia
Gatta, Viviana
Medda, Federico
Padmanaban, Mohan
Karawajczyk, Anna
Tammela, Päivi
Giordanetto, Fabrizio
Tzalis, Dimitrios
Collina, Simona
author_facet Stotani, Silvia
Gatta, Viviana
Medda, Federico
Padmanaban, Mohan
Karawajczyk, Anna
Tammela, Päivi
Giordanetto, Fabrizio
Tzalis, Dimitrios
Collina, Simona
author_sort Stotani, Silvia
collection PubMed
description Resistance to antibiotics is an increasingly serious threat to global public health and its management translates to significant health care costs. The validation of new Gram-negative antibacterial targets as sources for potential new antibiotics remains a challenge for all the scientists working in this field. The interference with bacterial Quorum Sensing (QS) mechanisms represents a potentially interesting approach to control bacterial growth and pursue the next generation of antimicrobials. In this context, our research is focused on the discovery of novel compounds structurally related to (S)-4,5-dihydroxy-2,3-pentanedione, commonly known as (S)-DPD, a small signaling molecule able to modulate bacterial QS in both Gram-negative and Gram-positive bacteria. In this study, a practical and versatile synthesis of racemic DPD is presented. Compared to previously reported syntheses, the proposed strategy is short and robust: it requires only one purification step and avoids the use of expensive or hazardous starting materials as well as the use of specific equipment. It is therefore well suited to the synthesis of derivatives for pharmaceutical research, as demonstrated by four series of novel DPD-related compounds described herein.
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spelling pubmed-62223002018-11-13 A Versatile Strategy for the Synthesis of 4,5-Dihydroxy-2,3-Pentanedione (DPD) and Related Compounds as Potential Modulators of Bacterial Quorum Sensing Stotani, Silvia Gatta, Viviana Medda, Federico Padmanaban, Mohan Karawajczyk, Anna Tammela, Päivi Giordanetto, Fabrizio Tzalis, Dimitrios Collina, Simona Molecules Article Resistance to antibiotics is an increasingly serious threat to global public health and its management translates to significant health care costs. The validation of new Gram-negative antibacterial targets as sources for potential new antibiotics remains a challenge for all the scientists working in this field. The interference with bacterial Quorum Sensing (QS) mechanisms represents a potentially interesting approach to control bacterial growth and pursue the next generation of antimicrobials. In this context, our research is focused on the discovery of novel compounds structurally related to (S)-4,5-dihydroxy-2,3-pentanedione, commonly known as (S)-DPD, a small signaling molecule able to modulate bacterial QS in both Gram-negative and Gram-positive bacteria. In this study, a practical and versatile synthesis of racemic DPD is presented. Compared to previously reported syntheses, the proposed strategy is short and robust: it requires only one purification step and avoids the use of expensive or hazardous starting materials as well as the use of specific equipment. It is therefore well suited to the synthesis of derivatives for pharmaceutical research, as demonstrated by four series of novel DPD-related compounds described herein. MDPI 2018-10-06 /pmc/articles/PMC6222300/ /pubmed/30301207 http://dx.doi.org/10.3390/molecules23102545 Text en © 2018 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
Stotani, Silvia
Gatta, Viviana
Medda, Federico
Padmanaban, Mohan
Karawajczyk, Anna
Tammela, Päivi
Giordanetto, Fabrizio
Tzalis, Dimitrios
Collina, Simona
A Versatile Strategy for the Synthesis of 4,5-Dihydroxy-2,3-Pentanedione (DPD) and Related Compounds as Potential Modulators of Bacterial Quorum Sensing
title A Versatile Strategy for the Synthesis of 4,5-Dihydroxy-2,3-Pentanedione (DPD) and Related Compounds as Potential Modulators of Bacterial Quorum Sensing
title_full A Versatile Strategy for the Synthesis of 4,5-Dihydroxy-2,3-Pentanedione (DPD) and Related Compounds as Potential Modulators of Bacterial Quorum Sensing
title_fullStr A Versatile Strategy for the Synthesis of 4,5-Dihydroxy-2,3-Pentanedione (DPD) and Related Compounds as Potential Modulators of Bacterial Quorum Sensing
title_full_unstemmed A Versatile Strategy for the Synthesis of 4,5-Dihydroxy-2,3-Pentanedione (DPD) and Related Compounds as Potential Modulators of Bacterial Quorum Sensing
title_short A Versatile Strategy for the Synthesis of 4,5-Dihydroxy-2,3-Pentanedione (DPD) and Related Compounds as Potential Modulators of Bacterial Quorum Sensing
title_sort versatile strategy for the synthesis of 4,5-dihydroxy-2,3-pentanedione (dpd) and related compounds as potential modulators of bacterial quorum sensing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222300/
https://www.ncbi.nlm.nih.gov/pubmed/30301207
http://dx.doi.org/10.3390/molecules23102545
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