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Synthesis, structure and antibiotic activity of aryl-substituted LpxC inhibitors

The zinc-dependent deacetylase LpxC catalyzes the committed step of lipid A biosynthesis in Gram-negative bacteria and is a validated target for development of novel antibiotics to combat multidrug-resistant Gram-negative infections. Many potent LpxC inhibitors contain an essential threonyl-hydroxam...

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Autores principales: Liang, Xiaofei, Lee, Chul-Jin, Zhao, Jinshi, Toone, Eric J., Zhou, Pei
Formato: Artigo
Lenguaje:Inglês
Publicado: 2013
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3941642/
https://ncbi.nlm.nih.gov/pubmed/23914798
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jm4007774
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