Synthesis and antimalarial activity of novel chiral and achiral benzenesulfonamides bearing 1, 3, 4-oxadiazole moieties

J Enzyme Inhib Med Chem. 2007 Jun;22(3):301-8. doi: 10.1080/14756360601114569.

Abstract

A series of new benzenesulfonamides, most of which are chiral, incorporating 1, 3, 4-oxadiazole and amino acid moieties have been synthesized. Some of these compounds were screened for antimalarial activity and also evaluated for their ability to inhibit hem polymerization. The electrophoretic analysis indicated that one compound was effective in inhibiting the degradation of hemoglobin. The synthesized compounds were tested in mice infected with Plasmodium berghei. These derivatives have the potential for the development of novel antimalarial lead compounds.

MeSH terms

  • Animals
  • Antimalarials / chemical synthesis*
  • Antimalarials / chemistry
  • Antimalarials / pharmacology*
  • Crystallization
  • Drug Evaluation, Preclinical
  • Hemoglobins / chemistry
  • Hemoglobins / drug effects
  • In Vitro Techniques
  • Magnetic Resonance Spectroscopy
  • Malaria / drug therapy
  • Malaria / parasitology
  • Male
  • Mice
  • Oxadiazoles / chemical synthesis
  • Oxadiazoles / chemistry
  • Oxadiazoles / pharmacology
  • Plasmodium berghei
  • Spectrometry, Mass, Electrospray Ionization
  • Spectrophotometry, Infrared
  • Stereoisomerism
  • Structure-Activity Relationship
  • Sulfonamides / chemical synthesis*
  • Sulfonamides / chemistry
  • Sulfonamides / pharmacology*

Substances

  • Antimalarials
  • Hemoglobins
  • Oxadiazoles
  • Sulfonamides