Antileishmaniasis activity of flavonoids from Consolida oliveriana

J Nat Prod. 2009 Jun;72(6):1069-74. doi: 10.1021/np8008122.

Abstract

A set of flavonoids from Consolida oliveriana, kaempferol (1), quercetin (2), trifolin (3), and acetyl hyperoside (5) and their O-acetyl derivatives (1a, 2a, 3a), and octa-O-acetylhyperoside (4) showed leishmanicidal activity against promastigote as well as amastigote forms of Leishmania spp. The cellular proliferation, metabolic, and ultrastructural studies showed that the acetylated compounds 2a, 3a, and 4 were highly active against Leishmania (V.) peruviana, while 2a as well as 4 were effective against Leishmania (V.) braziliensis. These compounds were not cytotoxic and are effective at similar concentrations up to or lower than the reference drugs (pentostam and glucantim).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimony Sodium Gluconate / pharmacology
  • Antiprotozoal Agents / chemistry
  • Antiprotozoal Agents / isolation & purification*
  • Antiprotozoal Agents / therapeutic use*
  • Female
  • Flavonoids / chemistry
  • Flavonoids / isolation & purification*
  • Flavonoids / therapeutic use*
  • Galactosides / pharmacology
  • Kaempferols / pharmacology
  • Leishmania / drug effects*
  • Leishmaniasis / drug therapy*
  • Meglumine / pharmacology
  • Meglumine Antimoniate
  • Molecular Structure
  • Organometallic Compounds / pharmacology
  • Ranunculaceae / chemistry*
  • Rats
  • Rats, Inbred Strains
  • Turkey

Substances

  • Antiprotozoal Agents
  • Flavonoids
  • Galactosides
  • Kaempferols
  • Organometallic Compounds
  • kaempferol-3-O-galactoside
  • Meglumine
  • kaempferol
  • Meglumine Antimoniate
  • Antimony Sodium Gluconate