Synthesis and in vitro antimicrobial activities of new (cyano-NNO-azoxy)pyrazole derivatives

Bioorg Med Chem Lett. 2011 Jun 1;21(11):3431-4. doi: 10.1016/j.bmcl.2011.03.101. Epub 2011 Apr 5.

Abstract

The antibacterial and antifungal activity of a series of products, in which the 1,5-dimethyl-4-(cyano-NNO-azoxy)pyrazol-3-yl and 1,3-dimethyl-4-(cyano-NNO-azoxy)pyrazol-5-yl moieties were linked to pyridine, pyrazole, isoxazole, thiophene and the furan ring, were examined. No molecule displayed activity against the gram-negative bacteria tested. Conversely, some compounds displayed activity against two Staphylococcus aureus strains, including the methicillin resistant strain. All compounds displayed interesting antifungal activity, the most active compound of the series being the thiophene derivative 7a. This compound's activity against Candida krusei and Candida glabrata (MIC=0.25 and 0.5 μg/mL, respectively), two fungal species resistant to azoles, is noteworthy. The presence of the cyano function appeared essential for activity.

MeSH terms

  • Anti-Infective Agents / chemical synthesis*
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / pharmacology*
  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / chemistry
  • Antifungal Agents / pharmacology
  • Azo Compounds / chemical synthesis*
  • Azo Compounds / chemistry
  • Azo Compounds / pharmacology*
  • Candida / drug effects*
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Nitriles / chemistry
  • Pyrazoles / chemical synthesis*
  • Pyrazoles / chemistry
  • Pyrazoles / pharmacology
  • Staphylococcus aureus / drug effects*

Substances

  • Anti-Infective Agents
  • Antifungal Agents
  • Azo Compounds
  • Nitriles
  • Pyrazoles
  • phenylazoxycyanide