Enhanced pneumocystis carinii activity of new primaquine analogues

Bioorg Med Chem Lett. 2000 Oct 2;10(19):2205-8. doi: 10.1016/s0960-894x(00)00436-4.

Abstract

New analogues of the venerable antimalarial drug primaquine have been synthesized and bioassayed in vivo against Pneumocystis carinii, a life-threatening infection common among immunosuppressed patients. Two of these new compounds are significantly more active than primaquine itself, and provide new information for future drug design and development in this area.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / chemistry
  • Antifungal Agents / pharmacology
  • Antifungal Agents / therapeutic use*
  • Dose-Response Relationship, Drug
  • Drug Design
  • Female
  • Humans
  • Molecular Structure
  • Pneumocystis / drug effects
  • Pneumocystis Infections / drug therapy*
  • Primaquine / analogs & derivatives*
  • Primaquine / chemical synthesis
  • Primaquine / chemistry
  • Primaquine / pharmacology
  • Primaquine / therapeutic use*
  • Rats
  • Structure-Activity Relationship

Substances

  • Antifungal Agents
  • Primaquine