Antiprotozoal activity of dicationic 3,5-diphenylisoxazoles, their prodrugs and aza-analogues

Bioorg Med Chem. 2014 Jan 1;22(1):559-76. doi: 10.1016/j.bmc.2013.10.050. Epub 2013 Nov 9.

Abstract

Fifty novel prodrugs and aza-analogues of 3,5-bis(4-amidinophenyl)isoxazole and its derivatives were prepared. Eighteen of the 24 aza-analogues exhibited IC₅₀ values below 25 nM against Trypanosoma brucei rhodesiense or Plasmodium falciparum. Six compounds had antitrypanosomal IC₅₀ values below 10 nM. Twelve analogues showed similar antiplasmodial activities, including three with sub-nanomolar potencies. Forty-four diamidines (including 16 aza-analogues) and the 26 prodrugs were evaluated for efficacy in mice infected with T. b. rhodesiense STIB900. Six diamidines cured 4/4 mice at daily 5 mg/kg intraperitoneal doses for 4 days, giving results far superior to pentamidine and furamidine. One prodrug attained 3/4 cures at daily 25 mg/kg oral doses for 4 days.

Keywords: Antiprotozoal; Antitrypanosomal; Diamidine; Diarylisoxazole; Prodrug.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiprotozoal Agents / pharmacology
  • Antiprotozoal Agents / therapeutic use*
  • Isoxazoles / chemical synthesis*
  • Isoxazoles / chemistry
  • Isoxazoles / pharmacology
  • Mice
  • Molecular Structure
  • Plasmodium falciparum / drug effects*
  • Prodrugs / therapeutic use*
  • Structure-Activity Relationship
  • Trypanosomiasis, African / drug therapy*

Substances

  • Antiprotozoal Agents
  • Isoxazoles
  • Prodrugs