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Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics
Gram-negative bacteria’s resistance such as Pseudomonas aeruginosa and the Burkholderia group to conventional antibiotics leads to therapeutic failure. Use of siderophores as Trojan horses to internalize antibacterial agents or toxic metals within bacteria is a promising strategy to overcome resista...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958365/ https://www.ncbi.nlm.nih.gov/pubmed/31652873 http://dx.doi.org/10.3390/ph12040160 |
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author | Loupias, Pauline Dechamps-Olivier, Isabelle Dupont, Laurent Vanlemmens, Pierre Mullié, Catherine Taudon, Nicolas Bouchut, Anne Dassonville-Klimpt, Alexandra Sonnet, Pascal |
author_facet | Loupias, Pauline Dechamps-Olivier, Isabelle Dupont, Laurent Vanlemmens, Pierre Mullié, Catherine Taudon, Nicolas Bouchut, Anne Dassonville-Klimpt, Alexandra Sonnet, Pascal |
author_sort | Loupias, Pauline |
collection | PubMed |
description | Gram-negative bacteria’s resistance such as Pseudomonas aeruginosa and the Burkholderia group to conventional antibiotics leads to therapeutic failure. Use of siderophores as Trojan horses to internalize antibacterial agents or toxic metals within bacteria is a promising strategy to overcome resistance phenomenon. To combat the Pseudomonas sp, we have synthesized and studied two piperazine-based siderophore mimetics carrying either catecholate moieties (1) or hydroxypyridinone groups (2) as iron chelators. These siderophore-like molecules were prepared in no more than four steps with good global yields. The physicochemical study has highlighted a strong iron affinity since their pFe values were higher than 20. 1 possesses even a pFe value superior than those of pyoverdine, the P. aeruginosa endogenous siderophore, suggesting its potential ability to compete with it. At physiological pH, 1 forms mainly a 2:3 complex with iron, whereas two species are observed for 2. Unfortunately, the corresponding Ga(III)-1 and 2 complexes showed no antibacterial activity against P. aeruginosa DSM 1117 strain. The evaluation of their siderophore-like activity showed that 1 and 2 could be internalized by the bacteria. |
format | Online Article Text |
id | pubmed-6958365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69583652020-01-23 Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics Loupias, Pauline Dechamps-Olivier, Isabelle Dupont, Laurent Vanlemmens, Pierre Mullié, Catherine Taudon, Nicolas Bouchut, Anne Dassonville-Klimpt, Alexandra Sonnet, Pascal Pharmaceuticals (Basel) Article Gram-negative bacteria’s resistance such as Pseudomonas aeruginosa and the Burkholderia group to conventional antibiotics leads to therapeutic failure. Use of siderophores as Trojan horses to internalize antibacterial agents or toxic metals within bacteria is a promising strategy to overcome resistance phenomenon. To combat the Pseudomonas sp, we have synthesized and studied two piperazine-based siderophore mimetics carrying either catecholate moieties (1) or hydroxypyridinone groups (2) as iron chelators. These siderophore-like molecules were prepared in no more than four steps with good global yields. The physicochemical study has highlighted a strong iron affinity since their pFe values were higher than 20. 1 possesses even a pFe value superior than those of pyoverdine, the P. aeruginosa endogenous siderophore, suggesting its potential ability to compete with it. At physiological pH, 1 forms mainly a 2:3 complex with iron, whereas two species are observed for 2. Unfortunately, the corresponding Ga(III)-1 and 2 complexes showed no antibacterial activity against P. aeruginosa DSM 1117 strain. The evaluation of their siderophore-like activity showed that 1 and 2 could be internalized by the bacteria. MDPI 2019-10-23 /pmc/articles/PMC6958365/ /pubmed/31652873 http://dx.doi.org/10.3390/ph12040160 Text en © 2019 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 Loupias, Pauline Dechamps-Olivier, Isabelle Dupont, Laurent Vanlemmens, Pierre Mullié, Catherine Taudon, Nicolas Bouchut, Anne Dassonville-Klimpt, Alexandra Sonnet, Pascal Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics |
title | Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics |
title_full | Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics |
title_fullStr | Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics |
title_full_unstemmed | Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics |
title_short | Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics |
title_sort | study of iron piperazine-based chelators as potential siderophore mimetics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958365/ https://www.ncbi.nlm.nih.gov/pubmed/31652873 http://dx.doi.org/10.3390/ph12040160 |
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