| Literature DB >> 27571880 |
Janish Desai1, Yang Wang2, Ke Wang2, Satish R Malwal2, Eric Oldfield1,2.
Abstract
We synthesized potential inhibitors of farnesyl diphosphate synthase (FPPS), undecaprenyl diphosphate synthase (UPPS), or undecaprenyl diphosphate phosphatase (UPPP), and tested them in bacterial cell growth and enzyme inhibition assays. The most active compounds were found to be bisphosphonates with electron-withdrawing aryl-alkyl side chains which inhibited the growth of Gram-negative bacteria (Acinetobacter baumannii, Klebsiella pneumoniae, Escherichia coli, and Pseudomonas aeruginosa) at ∼1-4 μg mL-1 levels. They were found to be potent inhibitors of FPPS; cell growth was partially "rescued" by the addition of farnesol or overexpression of FPPS, and there was synergistic activity with known isoprenoid biosynthesis pathway inhibitors. Lipophilic hydroxyalkyl phosphonic acids inhibited UPPS and UPPP at micromolar levels; they were active (∼2-6 μg mL-1 ) against Gram-positive but not Gram-negative organisms, and again exhibited synergistic activity with cell wall biosynthesis inhibitors, but only indifferent effects with other inhibitors. The results are of interest because they describe novel inhibitors of FPPS, UPPS, and UPPP with cell growth inhibitory activities as low as ∼1-2 μg mL-1 .Entities:
Keywords: Gram-negative pathogens; Staphylococcus aureus; cell wall biosynthesis; drug discovery; membrane proteins
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Year: 2016 PMID: 27571880 PMCID: PMC5160999 DOI: 10.1002/cmdc.201600343
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466