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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...

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Autores principales: Rbaa, Mohamed, Jabli, Siham, Lakhrissi, Younes, Ouhssine, Mohamed, Almalki, Faisal, Ben Hadda, Taibi, Messgo-Moumene, Saida, Zarrouk, Abbelkader, Lakhrissi, Brahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
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).
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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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