Title:UDP-3-O-(R-3-hydroxymyristoyl)-N-Acetylglucosamine Deacetylase (LpxC) Inhibitors: A New Class of Antibacterial Agents
VOLUME: 19 ISSUE: 13
Author(s):J. Zhang, L. Zhang, X. Li and W. Xu
Affiliation:Department of Medicinal Chemistry, School of Pharmaceutical Sciences, Shandong University, Ji’nan, Shandong 250012, China.
Keywords:Gram-negative bacteria, MDR, lipid A, biosynthesis, LpxC, Structure, FtsH, LpxC Inhibitors
Abstract: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). LpxC catalyzes the first committed, second overall step in the biosynthetic pathway of lipid A.
Thus, research on LpxC inhibitors as antibacterial agents has become an attractive field in the development of the novel antibiotic therapy
of Gram-negative bacteria. In this review, we will summarize the recent progress in the studies on the structure, catalytic mechanism and
regulation of LpxC and the current development of LpxC inhibitors.
