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Compounds Containing 2,3-Bis(phenylamino) Quinoxaline Exhibit Activity Against Methicillin-Resistant Staphylococcus aureus, Enterococcus faecalis, and Their Biofilms
G. Padalino, K. Duggan, LAJ. Mur, JY. Maillard, A. Brancale, KF. Hoffmann
Language English Country England, Great Britain
Document type Journal Article
Grant support
This work was supported by Aberystwyth University (Technology Transfer Grant Development Award) and the Life Sciences Wales Research Network (a Welsh Government Ser Cymru initiative).
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PubMed
39665231
DOI
10.1002/mbo3.70011
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents * pharmacology MeSH
- Biofilms * drug effects growth & development MeSH
- Quinoxalines * pharmacology MeSH
- Enterococcus faecalis * drug effects MeSH
- Humans MeSH
- Methicillin-Resistant Staphylococcus aureus * drug effects MeSH
- Microbial Sensitivity Tests * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Antimicrobial resistance remains a global issue, hindering the control of bacterial infections. This study examined the antimicrobial properties of 2,3-N,N-diphenyl quinoxaline derivatives against Gram-positive, Gram-negative, and Mycobacterium species. Two quinoxaline derivatives (compounds 25 and 31) exhibited significant activity against most strains of Staphylococcus aureus, Enterococcus faecium, and Enterococcus faecalis tested, with MIC values ranging from 0.25 to 1 mg/L. These compounds also showed effective antibacterial activity against methicillin-resistant S. aureus (MRSA) and vancomycin-resistant E. faecium/E. faecalis (VRE) strains. They demonstrated comparable or superior activity to four current antibiotics (vancomycin, teicoplanin, daptomycin, and linezolid) against a wide range of clinically relevant isolates. Additionally, they were more effective in preventing S. aureus and E. faecalis biofilm formation compared to several other antibiotics. In summary, these two quinoxaline derivatives have potential as new antibacterial agents.
Department of Life Sciences Aberystwyth University Aberystwyth UK
Department of Organic Chemistry UCT Prague Prague Czech Republic
School of Pharmacy and Pharmaceutical Sciences Cardiff University Cardiff UK
References provided by Crossref.org
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