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
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antimony Sodium Gluconate / pharmacology
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Antiprotozoal Agents / chemistry
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Antiprotozoal Agents / isolation & purification*
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Antiprotozoal Agents / therapeutic use*
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Female
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Flavonoids / chemistry
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Flavonoids / isolation & purification*
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Flavonoids / therapeutic use*
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Galactosides / pharmacology
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Kaempferols / pharmacology
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Leishmania / drug effects*
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Leishmaniasis / drug therapy*
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Meglumine / pharmacology
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Meglumine Antimoniate
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Molecular Structure
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Organometallic Compounds / pharmacology
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Ranunculaceae / chemistry*
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Rats
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Rats, Inbred Strains
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Turkey
Substances
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Antiprotozoal Agents
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Flavonoids
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Galactosides
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Kaempferols
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Organometallic Compounds
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kaempferol-3-O-galactoside
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Meglumine
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kaempferol
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Meglumine Antimoniate
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Antimony Sodium Gluconate