Antituberculous activity of some aryl semicarbazone derivatives

Bioorg Med Chem Lett. 2004 Aug 2;14(15):3923-4. doi: 10.1016/j.bmcl.2004.05.060.

Abstract

During the course of our work on the synthesis and screening of new drugs for tuberculosis, we have identified N1-(4-acetamido phenyl)-N4-(2-nitro benzylidene) semicarbazone (1b), which inhibited in vitro Mycobacterium tuberculosis H(37)Rv; 100% inhibition at 1.56 microg/mL. This paper is first of its kind in which aryl semicarbazones are reported to possess antimycobacterials potency greater than p-aminosalicylic acid, ethionamide, ethambutol, ciprofloxacin and kanamycin.

MeSH terms

  • Antitubercular Agents / chemical synthesis*
  • Antitubercular Agents / pharmacology
  • Microbial Sensitivity Tests
  • Molecular Conformation
  • Molecular Structure
  • Mycobacterium tuberculosis / drug effects*
  • Semicarbazones / chemical synthesis*
  • Semicarbazones / pharmacology
  • Structure-Activity Relationship

Substances

  • Antitubercular Agents
  • Semicarbazones