@article{92d6a27ee489435eb2d3eba2952f15ac,
title = "UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase (LpxC) inhibitors: A new class of antibacterial agents",
keywords = "Biosynthesis, FtsH, Gram-negative bacteria, Lipid A, LpxC, LpxC Inhibitors, MDR, Structure",
author = "J. Zhang and L. Zhang and X. Li and W. Xu",
note = "The rapid increase of health-threatening infections by Gram-negative pathogens along with the emergence of multidrugresistant bacterial strains demands the development of novel antibiotics directed against the previously unexploited targets. One of the promising targets in Gram-negative bacteria is the zinc-dependent metalloamidase, UDP-3-O-(R-3-hydroxymyristoyl)-Nacetylglucosamine deacetylase (LpxC).",
year = "2012",
month = may,
doi = "10.2174/092986712800167374",
language = "English",
volume = "19",
pages = "2038--2050",
journal = "Current Medicinal Chemistry",
issn = "0929-8673",
number = "13",
}