| Literature DB >> 30392371 |
Trent Kunkle1, Sanofar Abdeen1, Nilshad Salim1, Anne-Marie Ray1, Mckayla Stevens1, Andrew J Ambrose2, José Victorino1, Yangshin Park1,3,4, Quyen Q Hoang1,3,4, Eli Chapman2, Steven M Johnson1.
Abstract
We recently reported the identification of a GroEL/ES inhibitor (1, N-(4-(benzo[ d]thiazol-2-ylthio)-3-chlorophenyl)-3,5-dibromo-2-hydroxybenzamide) that exhibited in vitro antibacterial effects against Staphylococcus aureus comparable to vancomycin, an antibiotic of last resort. To follow up, we have synthesized 43 compound 1 analogs to determine the most effective functional groups of the scaffold for inhibiting GroEL/ES and killing bacteria. Our results identified that the benzothiazole and hydroxyl groups are important for inhibiting GroEL/ES-mediated folding functions, with the hydroxyl essential for antibacterial effects. Several analogs exhibited >50-fold selectivity indices between antibacterial efficacy and cytotoxicity to human liver and kidney cells in cell culture. We found that MRSA was not able to easily generate acute resistance to lead inhibitors in a gain-of-resistance assay and that lead inhibitors were able to permeate through established S. aureus biofilms and maintain their bactericidal effects.Entities:
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Year: 2018 PMID: 30392371 PMCID: PMC6467803 DOI: 10.1021/acs.jmedchem.8b01293
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446