| Literature DB >> 26435072 |
Jonas Thelemann1, Boris Illarionov2, Konstantin Barylyuk1, Julie Geist1, Johannes Kirchmair3, Petra Schneider4, Lucile Anthore1, Katharina Root1, Nils Trapp1, Adelbert Bacher5, Matthias Witschel6, Renato Zenobi7, Markus Fischer8, Gisbert Schneider9, François Diederich10.
Abstract
2-Methylerythritol 2,4-cyclodiphosphate synthase (IspF) is an essential enzyme for the biosynthesis of isoprenoid precursors in plants and many human pathogens. The protein is an attractive target for the development of anti-infectives and herbicides. Using a photometric assay, a screen of 40 000 compounds on IspF from Arabidopsis thaliana afforded symmetrical aryl bis-sulfonamides that inhibit IspF from A. thaliana (AtIspF) and Plasmodium falciparum (PfIspF) with IC50 values in the micromolar range. The ortho-bis-sulfonamide structural motif is essential for inhibitory activity. The best derivatives obtained by parallel synthesis showed IC50 values of 1.4 μm against PfIspF and 240 nm against AtIspF. Substantial herbicidal activity was observed at a dose of 2 kg ha(-1) . Molecular modeling studies served as the basis for an in silico search targeted at the discovery of novel, non-symmetrical sulfonamide IspF inhibitors. The designed compounds were found to exhibit inhibitory activities in the double-digit micromolar IC50 range.Entities:
Keywords: P. falciparum; bis-sulfonamides; docking; inhibitors; isoprenoid biosynthesis; non-mevalonate pathway
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Year: 2015 PMID: 26435072 DOI: 10.1002/cmdc.201500382
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466