Lead Selection of a New Aminomethylphenol, JPC-3210, for Malaria Treatment and Prevention

Antimicrob Agents Chemother. 2016 Apr 22;60(5):3115-8. doi: 10.1128/AAC.03066-15. Print 2016 May.

Abstract

Structure-activity relationship studies of trifluoromethyl-substituted pyridine and pyrimidine analogues of 2-aminomethylphenols (JPC-2997, JPC-3186, and JPC-3210) were conducted for preclinical development for malaria treatment and/or prevention. Of these compounds, JPC-3210 [4-(tert-butyl)-2-((tert-butylamino)methyl)-6-(5-fluoro-6-(trifluoromethyl)pyridin-3-yl)phenol] was selected as the lead compound due to superior in vitro antimalarial activity against multidrug-resistant Plasmodium falciparum lines, lower in vitro cytotoxicity in mammalian cell lines, longer plasma elimination half-life, and greater in vivo efficacy against murine malaria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimalarials / therapeutic use*
  • Cell Line
  • Cricetinae
  • HEK293 Cells
  • Hep G2 Cells
  • Humans
  • Malaria / drug therapy*
  • Malaria, Falciparum / drug therapy*
  • Mefloquine / therapeutic use
  • Mice
  • Phenols / therapeutic use*
  • Plasmodium falciparum / drug effects
  • Plasmodium falciparum / pathogenicity
  • Pyridines / therapeutic use

Substances

  • Antimalarials
  • JPC-2997
  • Phenols
  • Pyridines
  • Mefloquine