| Literature DB >> 29571571 |
Jordan G Sheppard1, Keely R Frazier1, Pushkar Saralkar2, Mohammad F Hossain1, Werner J Geldenhuys2, Timothy E Long3.
Abstract
Sixteen disulfides derived from disulfiram (Antabuse™) were evaluated as antibacterial agents. Derivatives with hydrocarbon chains of seven and eight carbons in length exhibited antibacterial activity against Gram-positive Staphylococcus, Streptococcus, Enterococcus, Bacillus, and Listeria spp. A comparison of the cytotoxicity and microsomal stability with disulfiram further revealed that the eight carbon chain analog was of lower toxicity to human hepatocytes and has a longer metabolic half-life. In the final analysis, this investigation concluded that the S-octylthio derivative is a more effective growth inhibitor of Gram-positive bacteria than disulfiram and exhibits more favorable cytotoxic and metabolic parameters over disulfiram.Entities:
Keywords: Antibiotic; Disulfides; Disulfiram; MRSA; Staphylococcus; VISA; VRSA
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Year: 2018 PMID: 29571571 PMCID: PMC5893419 DOI: 10.1016/j.bmcl.2018.03.023
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823