Identification of oxadiazoles as new drug leads for the control of schistosomiasis.

Therapeutic Approaches

Abstract

Treatment for schistosomiasis, which is responsible for more than 280,000 deaths annually, depends almost exclusively on praziquantel. Millions of people are treated annually with praziquantel, and drug-resistant parasites thus are likely to evolve. Phosphinic amides and oxadiazole 2-oxides, identified from a quantitative high-throughput screen, were shown to inhibit a parasite enzyme, thioredoxin glutathione reductase (TGR), with activities in the low micromolar to low nanomolar range. Incubation of parasites with these compounds led to rapid inhibition of TGR activity and parasite death. The activity of the oxadiazole 2-oxides was associated with a donation of nitric oxide. Treatment of schistosome-infected mice with 4-phenyl-1,2,5-oxadiazole-3-carbonitrile-2-oxide led to marked reductions in worm burdens from treatments against multiple parasite stages and egg-associated pathologies. The compound was active against the three major schistosome species infecting humans. These protective effects exceed benchmark activity criteria set by the World Health Organization for lead compound development for schistosomiasis.

Authors

Sayed, Ahmed A; Simeonov, Anton; Thomas, Craig; Inglese, James; Austin, Christopher; Williams, David L;

Keywords

  • Amides/ chemistry
  • Amides/ pharmacology
  • Animals
  • Drug Design
  • Enzyme Inhibitors/ chemistry
  • Enzyme Inhibitors/ pharmacology
  • Humans
  • Mice
  • Multienzyme Complexes/ antagonists & inhibitors
  • NADH, NADPH Oxidoreductases/ antagonists & inhibitors
  • Nitric Oxide Donors/ chemistry
  • Nitric Oxide Donors/ pharmacology
  • Oxadiazoles/ chemistry
  • Oxadiazoles/ pharmacology
  • Schistosoma mansoni/ drug effects
  • Schistosoma mansoni/ enzymology
  • Schistosomiasis mansoni/ drug therapy
  • Schistosomicides/ chemistry
  • Schistosomicides/ pharmacology
  • Structure-Activity Relationship

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