Anti-plasmodial activities and X-ray crystal structures of rotenoids from Millettia usaramensis subspecies usaramensis

Phytochemistry. 2003 Oct;64(3):773-9. doi: 10.1016/s0031-9422(03)00373-x.

Abstract

The dichloromethane extract of the stem bark of Millettia usaramensis subspecies usaramensis showed anti-plasmodial activity against the chloroquine sensitive (D6) and chloroquine resistant (W2) strains of Plasmodium falciparum. Chromatographic separation of the extract led to the identification of a new rotenoid, (6aR,12aS)-2,3-methylenedioxy-9-methoxy-8-(3,3-dimethylallyl)-12a-hydroxyrotenoid (trivial name, usararotenoid C) along with known flavonoids (usararotenoid A, 12a-epimillettosin, 6a,12a-dehydromillettone, barbigerone and 4'-O-geranylisoliquiritigenin) as the anti-plasmodial principles. The structures were determined by spectroscopic analyses. CD and X-ray analyses established absolute configurations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimalarials / chemistry*
  • Antimalarials / isolation & purification
  • Antimalarials / pharmacology*
  • Chloroquine / pharmacology
  • Crystallography, X-Ray
  • Drug Resistance
  • Flavonoids / chemistry
  • Flavonoids / isolation & purification
  • Inhibitory Concentration 50
  • Magnetic Resonance Spectroscopy
  • Millettia / chemistry*
  • Molecular Structure
  • Plant Bark / chemistry
  • Plant Stems / chemistry
  • Plasmodium falciparum / drug effects
  • Plasmodium falciparum / genetics
  • Rotenone / chemistry*
  • Rotenone / isolation & purification
  • Rotenone / pharmacology*

Substances

  • Antimalarials
  • Flavonoids
  • Rotenone
  • Chloroquine