Abstract
Previous studies have shown that fosmidomycin, risedronate, and nerolidol exert antimalarial activity in vitro. We included squalestatin, an inhibitor of the isoprenoid metabolism in Erwinia uredovora, and found that combinations of compounds which act on different targets of the plasmodial isoprenoid pathway possess important supra-additivity effects.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antimalarials / pharmacology*
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Biosynthetic Pathways / drug effects*
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Bridged Bicyclo Compounds, Heterocyclic / pharmacology
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Drug Interactions
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Fosfomycin / analogs & derivatives
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Fosfomycin / pharmacology
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Malaria / drug therapy
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Parasitic Sensitivity Tests
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Plasmodium falciparum / drug effects*
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Plasmodium falciparum / metabolism
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Risedronic Acid / pharmacology
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Sesquiterpenes / pharmacology
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Terpenes / metabolism*
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Tricarboxylic Acids / pharmacology
Substances
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Antimalarials
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Bridged Bicyclo Compounds, Heterocyclic
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Sesquiterpenes
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Terpenes
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Tricarboxylic Acids
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squalestatin 1
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Fosfomycin
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fosmidomycin
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Risedronic Acid
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nerolidol