Synthesis and in vitro anti Mycobacterium tuberculosis activity of a series of phthalimide derivatives

Bioorg Med Chem. 2009 Jun 1;17(11):3795-9. doi: 10.1016/j.bmc.2009.04.042. Epub 2009 May 3.

Abstract

New phthalimide derivatives were easily prepared through condensation of phthalic anhydride and selected amines with variable yields (70-90%). All compounds (3a-l) were evaluated against Mycobacterium tuberculosis H(37)Rv using Alamar Blue susceptibility. The compounds 3c, 3i, and 3l have the minimum inhibitory concentrations (MICs) of 3.9, 7.8, and 5.0 microg/mL, respectively, and could be considered new lead compounds in the treatment of tuberculosis and multi-drug resistant tuberculosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antitubercular Agents / chemical synthesis*
  • Antitubercular Agents / pharmacology*
  • Cell Line
  • Mice
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Mycobacterium tuberculosis / drug effects*
  • Phthalimides / chemistry*

Substances

  • Antitubercular Agents
  • Phthalimides
  • phthalimide