Synthesis and potent antiprotozoal activity of mono/di amidino 2-anilinobenzimidazoles versus Plasmodium falciparum and Trypanosoma brucei rhodesiense

Bioorg Med Chem. 2016 Sep 15;24(18):4038-4044. doi: 10.1016/j.bmc.2016.06.047. Epub 2016 Jun 25.

Abstract

A series of mono and dicationic new 2-anilinobenzimidazole carboxamidines were prepared in a four step process starting from 4-amino-3-nitrobenzonitrile and corresponding o-phenylenediamines. Their antiparasitic activity against Plasmodium falciparum (P. falciparum) and Trypanosoma brucei rhodesiense (T.b. rhodesiense) were evaluated in vitro. Some of the dicationic compounds (10,12,14) showed equal or very close activity against T.b. rhodesiense with melarsoprol and also showed promising activity against P. falciparum as compared to chloroquine. Among the monocationic derivatives compound 21 exhibited best inhibitory activity against P. falciparum.

Keywords: Anilinobenzimidazoles; Antiparasitic agents; Carboxamidines; Plasmodium falciparum; Trypanosoma brucei rhodesiense.

MeSH terms

  • Aniline Compounds / chemical synthesis
  • Aniline Compounds / chemistry
  • Aniline Compounds / pharmacology
  • Animals
  • Antiprotozoal Agents / chemical synthesis
  • Antiprotozoal Agents / chemistry*
  • Antiprotozoal Agents / pharmacology*
  • Benzimidazoles / chemical synthesis
  • Benzimidazoles / chemistry*
  • Benzimidazoles / pharmacology*
  • Cell Line
  • Humans
  • Malaria, Falciparum / drug therapy
  • Parasitic Sensitivity Tests
  • Plasmodium falciparum / drug effects*
  • Rats
  • Structure-Activity Relationship
  • Trypanosoma brucei rhodesiense / drug effects*
  • Trypanosomiasis, African / drug therapy

Substances

  • Aniline Compounds
  • Antiprotozoal Agents
  • Benzimidazoles