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Synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives
New heterocyclic derivatives of 8-hydroxyquinoline were prepared and screened as antimicrobial agents. Chemical structures were elucidated and confirmed using different spectroscopic methods such as elemental analysis data, Infrared, Nuclear Magnetic Resonance Spectroscopy. In order to explore their...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820249/ https://www.ncbi.nlm.nih.gov/pubmed/31687516 http://dx.doi.org/10.1016/j.heliyon.2019.e02689 |
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author | Rbaa, Mohamed Jabli, Siham Lakhrissi, Younes Ouhssine, Mohamed Almalki, Faisal Ben Hadda, Taibi Messgo-Moumene, Saida Zarrouk, Abbelkader Lakhrissi, Brahim |
author_facet | Rbaa, Mohamed Jabli, Siham Lakhrissi, Younes Ouhssine, Mohamed Almalki, Faisal Ben Hadda, Taibi Messgo-Moumene, Saida Zarrouk, Abbelkader Lakhrissi, Brahim |
author_sort | Rbaa, Mohamed |
collection | PubMed |
description | New heterocyclic derivatives of 8-hydroxyquinoline were prepared and screened as antimicrobial agents. Chemical structures were elucidated and confirmed using different spectroscopic methods such as elemental analysis data, Infrared, Nuclear Magnetic Resonance Spectroscopy. In order to explore their potential biological activity, the “in vitro” antibacterial activity was investigated against [E. coli (ATCC35218), S. aureus (ATCC29213), V. parahaemolyticus (ATCC17802), and P. aeruginosa (ATCC27853)]. The studied compounds exhibited a remarkable antibacterial activity superior to the standard antibiotic (Penicillin G). These new heterocyclic derivatives of 8-hydroxyquinoline, which proved to be potentially effective, can be used as alternative chemical antimicrobial agents applications. It was very interesting to observe that POM (Petra/Osiris/Molinspiration) bioinformatic analyses of the 8-hydroxyquinoline derivative (5) exhibited more important antibacterial activity (MIC = 10(−6) mg/mL against V.p and S.a bacteria) and good drug score (DS = 0.71) when compared with Penicillin (DS = 0.33; MIC = 10(−3) mg/mL). |
format | Online Article Text |
id | pubmed-6820249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68202492019-11-04 Synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives Rbaa, Mohamed Jabli, Siham Lakhrissi, Younes Ouhssine, Mohamed Almalki, Faisal Ben Hadda, Taibi Messgo-Moumene, Saida Zarrouk, Abbelkader Lakhrissi, Brahim Heliyon Article New heterocyclic derivatives of 8-hydroxyquinoline were prepared and screened as antimicrobial agents. Chemical structures were elucidated and confirmed using different spectroscopic methods such as elemental analysis data, Infrared, Nuclear Magnetic Resonance Spectroscopy. In order to explore their potential biological activity, the “in vitro” antibacterial activity was investigated against [E. coli (ATCC35218), S. aureus (ATCC29213), V. parahaemolyticus (ATCC17802), and P. aeruginosa (ATCC27853)]. The studied compounds exhibited a remarkable antibacterial activity superior to the standard antibiotic (Penicillin G). These new heterocyclic derivatives of 8-hydroxyquinoline, which proved to be potentially effective, can be used as alternative chemical antimicrobial agents applications. It was very interesting to observe that POM (Petra/Osiris/Molinspiration) bioinformatic analyses of the 8-hydroxyquinoline derivative (5) exhibited more important antibacterial activity (MIC = 10(−6) mg/mL against V.p and S.a bacteria) and good drug score (DS = 0.71) when compared with Penicillin (DS = 0.33; MIC = 10(−3) mg/mL). Elsevier 2019-10-21 /pmc/articles/PMC6820249/ /pubmed/31687516 http://dx.doi.org/10.1016/j.heliyon.2019.e02689 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Rbaa, Mohamed Jabli, Siham Lakhrissi, Younes Ouhssine, Mohamed Almalki, Faisal Ben Hadda, Taibi Messgo-Moumene, Saida Zarrouk, Abbelkader Lakhrissi, Brahim Synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives |
title | Synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives |
title_full | Synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives |
title_fullStr | Synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives |
title_full_unstemmed | Synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives |
title_short | Synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives |
title_sort | synthesis, antibacterial properties and bioinformatics computational analyses of novel 8-hydroxyquinoline derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820249/ https://www.ncbi.nlm.nih.gov/pubmed/31687516 http://dx.doi.org/10.1016/j.heliyon.2019.e02689 |
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