Abstract
Novel inhibitors of Trypanosoma brucei and mammalian UDP-Glc 4'-epimerase were identified by screening a small library of natural products and commercially available drug-like molecules. The inhibitors possess low micromolar potency against the T. brucei and human enzymes in vitro, display a degree of selectivity between the two enzymes, and are cytotoxic to cultured T. brucei and mammalian cells.
Publication types
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Research Support, Non-U.S. Gov't
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Validation Study
MeSH terms
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Animals
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology*
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Humans
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Models, Chemical
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Trypanocidal Agents / chemistry
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Trypanocidal Agents / pharmacology*
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Trypanocidal Agents / therapeutic use
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Trypanosoma brucei brucei / drug effects*
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Trypanosoma brucei brucei / growth & development
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Trypanosomiasis, African / drug therapy*
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UDPglucose 4-Epimerase / antagonists & inhibitors*
Substances
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Enzyme Inhibitors
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Trypanocidal Agents
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UDPglucose 4-Epimerase