| Literature DB >> 18489104 |
Priscila de Almeida Leone1, Anthony R Carroll, Leanne Towerzey, Gordon King, Bernadette M McArdle, Gunther Kern, Stewart Fisher, John N A Hooper, Ronald J Quinn.
Abstract
Bioassay-guided fractionation of the methanol extract of the Australian sponge Neopetrosia exigua led to the isolation of exiguaquinol (2), a new pentacyclic hydroquinone that inhibited Helicobacter pylori glutamate racemase (MurI) with an IC(50) of 4.4 microM. Its structure and relative configuration were assigned on the basis of spectroscopic data. Exiguaquinol (2), bearing a novel pentacyclic ring skeleton, is the first natural product to show inhibition of H. pylori MurI. Its protein-ligand modeling is also discussed.Entities:
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Year: 2008 PMID: 18489104 DOI: 10.1021/ol800898z
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005