Synthesis and antimycobacterial evaluation of new trans-cinnamic acid hydrazide derivatives

Bioorg Med Chem Lett. 2008 Jan 15;18(2):538-41. doi: 10.1016/j.bmcl.2007.11.091. Epub 2007 Nov 28.

Abstract

In this work, we report the synthesis and the antimycobacterial evaluation of new trans-cinnamic acid derivatives of isonicotinic acid series (5) and benzoic acid series (6), designed by exploring the molecular hybridization approach between isoniazid (1) and trans-cinnamic acid derivative (3). The minimum inhibitory concentration (MIC) of the compounds 5a-d and 6c exhibited activity between 3.12 and 12.5 microg/mL and could be a good start point to find new lead compounds against multi-drug resistant tuberculosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antitubercular Agents / chemical synthesis*
  • Antitubercular Agents / chemistry
  • Antitubercular Agents / pharmacology*
  • Cinnamates / chemistry*
  • Hydrazines / chemistry*
  • Magnetic Resonance Spectroscopy
  • Microbial Sensitivity Tests
  • Mycobacterium tuberculosis / drug effects*
  • Mycobacterium tuberculosis / growth & development

Substances

  • Antitubercular Agents
  • Cinnamates
  • Hydrazines
  • cinnamic acid