Four Prenylflavone Derivatives with Antiplasmodial Activities from the Stem of Tephrosia purpurea subsp. leptostachya

Molecules. 2017 Sep 10;22(9):1514. doi: 10.3390/molecules22091514.

Abstract

Four new flavones with modified prenyl groups, namely (E)-5-hydroxytephrostachin (1), purleptone (2), (E)-5-hydroxyanhydrotephrostachin (3), and terpurlepflavone (4), along with seven known compounds (5-11), were isolated from the CH₂Cl₂/MeOH (1:1) extract of the stem of Tephrosia purpurea subsp. leptostachya, a widely used medicinal plant. Their structures were elucidated on the basis of NMR spectroscopic and mass spectrometric evidence. Some of the isolated compounds showed antiplasmodial activity against the chloroquine-sensitive D6 strains of Plasmodium falciparum, with (E)-5-hydroxytephrostachin (1) being the most active, IC50 1.7 ± 0.1 μM, with relatively low cytotoxicity, IC50 > 21 μM, against four cell-lines.

Keywords: Tephrosia purpurea subsp. leptostachya; antiplasmodial; cytotoxicity; flavone; stem.

MeSH terms

  • A549 Cells
  • Antimalarials / chemistry
  • Antimalarials / isolation & purification*
  • Antimalarials / pharmacology
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Cells, Cultured
  • Chloroquine / pharmacology
  • Drug Resistance / drug effects
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Erythrocytes / drug effects
  • Erythrocytes / parasitology
  • Flavones / chemistry
  • Flavones / isolation & purification*
  • Flavones / pharmacology
  • Hep G2 Cells
  • Humans
  • Organ Specificity
  • Plant Extracts / chemistry
  • Plant Stems / chemistry*
  • Plants, Medicinal
  • Plasmodium falciparum / drug effects*
  • Plasmodium falciparum / growth & development
  • Structure-Activity Relationship
  • Tephrosia / chemistry*

Substances

  • Antimalarials
  • Flavones
  • Plant Extracts
  • Chloroquine