| Literature DB >> 29131575 |
Ashleigh S Paparella1, Kwang Jun Lee2, Andrew J Hayes1, Jiage Feng2,3, Zikai Feng1, Danielle Cini4, Sonali Deshmukh1, Grant W Booker1, Matthew C J Wilce4, Steven W Polyak1, Andrew D Abell2,3.
Abstract
We report the synthesis and evaluation of 5-halogenated-1,2,3-triazoles as inhibitors of biotin protein ligase from Staphylococcus aureus. The halogenated compounds exhibit significantly improved antibacterial activity over their nonhalogenated counterparts. Importantly, the 5-fluoro-1,2,3-triazole compound 4c displays antibacterial activity against S. aureus ATCC49775 with a minimum inhibitory concentration (MIC) of 8 μg/mL.Entities:
Keywords: Staphylococcus aureus; antibiotic; biotin protein ligase; enzyme inhibitor
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Year: 2017 PMID: 29131575 DOI: 10.1021/acsinfecdis.7b00134
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084