Synthesis and antimicrobial activities of structurally novel S,S'-bis(heterosubstituted) disulfides

Bioorg Med Chem Lett. 2012 Jun 1;22(11):3623-31. doi: 10.1016/j.bmcl.2012.04.056. Epub 2012 Apr 19.

Abstract

The central focus of this study is on the antibacterial and antifungal properties of synthetically produced S,S'-bis(heterosubstituted) disulfides as a means to control the growth of various infection-causing pathogens. Staphylococcus aureus, Francisella tularensis and Candida albicans were each found to be highly susceptible to several of these compounds by agar or broth dilution and Kirby-Bauer diffusion assays. These structurally simple, low molecular weight disulfides have shown promising bioactivities and may serve as leads to the development of effective new antibacterials for pathogenic bacteria such as methicillin-resistant S. aureus and F. tularensis.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Anti-Infective Agents / chemical synthesis*
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / pharmacology
  • Candida albicans / drug effects
  • Disulfides / chemical synthesis
  • Disulfides / chemistry*
  • Disulfides / pharmacology
  • Francisella tularensis / drug effects
  • Methicillin-Resistant Staphylococcus aureus / drug effects
  • Microbial Sensitivity Tests
  • Structure-Activity Relationship

Substances

  • Anti-Infective Agents
  • Disulfides