| Literature DB >> 19124251 |
Nicolas Desroy1, François Moreau, Sophia Briet, Géraldine Le Fralliec, Stephanie Floquet, Lionel Durant, Vanida Vongsouthi, Vincent Gerusz, Alexis Denis, Sonia Escaich.
Abstract
Gram-negative bacteria lacking heptoses in their lipopolysaccharide (LPS) display attenuated virulence and increased sensitivity to human serum and to some antibiotics. Thus inhibition of bacterial heptose synthesis represents an attractive target for the development of new antibacterial agents. HldE is a bifunctional enzyme involved in the synthesis of bacterial heptoses. Development of a biochemical assay suitable for high-throughput screening allowed the discovery of inhibitors 1 and 2 of HldE kinase. Study of the structure-activity relationship of this series of inhibitors led to highly potent compounds.Entities:
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Year: 2008 PMID: 19124251 DOI: 10.1016/j.bmc.2008.12.021
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641