Furosemide analogues as potent inhibitors of the new permeability pathways of Plasmodium falciparum-infected human erythrocytes

Mol Biochem Parasitol. 2004 Feb;133(2):315-8. doi: 10.1016/j.molbiopara.2003.10.009.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport / drug effects
  • Cell Membrane Permeability / drug effects*
  • Choline / metabolism*
  • Dose-Response Relationship, Drug
  • Erythrocytes / metabolism
  • Erythrocytes / parasitology*
  • Furosemide / analogs & derivatives*
  • Furosemide / pharmacology*
  • Humans
  • Plasmodium falciparum / growth & development
  • Plasmodium falciparum / pathogenicity*

Substances

  • Furosemide
  • Choline