Synthesis and antitubercular activity of monocyclic nitroimidazoles: insights from econazole

Bioorg Med Chem Lett. 2011 Mar 1;21(5):1515-8. doi: 10.1016/j.bmcl.2010.12.128. Epub 2011 Jan 5.

Abstract

We have designed and synthesized econazole-derived nitroimidazoles to investigate the antitubercular activity of the nitroimidazole compounds. The introduction of a nitro group at the 4-position of the imidazole on econazole abolished the antitubercular activity. However, alcoholic nitroimidazoles 4 and 6 compounds were active against Mycobacterium tuberculosis (Mtb). While the MIC value of econazole was 16 μg/mL, the MIC of 6a and 6f turned out to be 0.5 μg/mL. In particular, the activity of 6f against non-replicating Mtb was as good as PA-824, which is currently in clinical phase II studies as an antitubercular agent. Overall, alcohol compounds 4 and 6 tend to be more active than ether compounds 5 and 7.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / pharmacology
  • Antitubercular Agents / chemical synthesis*
  • Antitubercular Agents / pharmacology
  • Cyclization
  • Drug Design*
  • Econazole / chemistry*
  • Econazole / pharmacology
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Nitroimidazoles / chemical synthesis*
  • Nitroimidazoles / pharmacology

Substances

  • Antifungal Agents
  • Antitubercular Agents
  • Nitroimidazoles
  • Econazole