Disulfiram-based disulfides as narrow-spectrum antibacterial agents.
Ontology highlight
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.
SUBMITTER: Sheppard JG
PROVIDER: S-EPMC5893419 | biostudies-literature | 2018 May
REPOSITORIES: biostudies-literature
ACCESS DATA