Cinnamic acid/chloroquinoline conjugates as potent agents against chloroquine-resistant Plasmodium falciparum

ChemMedChem. 2012 Sep;7(9):1537-40. doi: 10.1002/cmdc.201200257. Epub 2012 Jun 29.

Abstract

Cinnamic acid derivatives containing a 4-amino-7-chloroquinoline scaffold (blue) and substituted cinnamoyl building blocks (green) linked through an alkylamine chain (red) were found to have potent (11-59 nM) in vitro activities against erythrocytic chloroquine- resistant Plasmodium falciparum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimalarials / chemistry*
  • Antimalarials / pharmacology*
  • Chloroquine / analogs & derivatives*
  • Chloroquine / pharmacology*
  • Cinnamates / chemistry*
  • Cinnamates / pharmacology*
  • Drug Resistance
  • Erythrocytes / parasitology
  • Humans
  • Malaria, Falciparum / drug therapy
  • Plasmodium falciparum / drug effects*

Substances

  • Antimalarials
  • Cinnamates
  • cinnamic acid
  • Chloroquine