In vitro activity of wALADin benzimidazoles against different life cycle stages of Plasmodium parasites

Antimicrob Agents Chemother. 2015 Jan;59(1):654-8. doi: 10.1128/AAC.02383-14. Epub 2014 Oct 13.

Abstract

wALADin1 benzimidazoles are specific inhibitors of δ-aminolevulinic acid dehydratase from Wolbachia endobacteria of filarial nematodes. We report that wALADin1 and two derivatives killed blood stage Plasmodium falciparum in vitro (50% inhibitory concentrations, 39, 7.7, and 12.8 μM, respectively). One of these derivatives inhibited gliding motility of Plasmodium berghei ANKA infectious sporozoites with nanomolar affinity and blocked invasion into hepatocytes but did not affect intrahepatocytic replication. Hence, wALADin1 benzimidazoles are tools to study gliding motility and potential antiplasmodial drug candidates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimalarials / pharmacology*
  • Benzimidazoles / chemistry
  • Benzimidazoles / pharmacology*
  • Humans
  • Inhibitory Concentration 50
  • Plasmodium berghei / drug effects
  • Plasmodium falciparum / drug effects*
  • Plasmodium falciparum / physiology
  • Porphobilinogen Synthase / antagonists & inhibitors*
  • Thiophenes / chemistry
  • Thiophenes / pharmacology
  • Toxoplasma / drug effects

Substances

  • Antimalarials
  • Benzimidazoles
  • Thiophenes
  • wALADin1 compound
  • Porphobilinogen Synthase