Abstract
Paraherquamide and six novel analogs were isolated from the fermentation of Penicillium charlesii (ATCC 20841). All seven natural products displayed potent antinematodal activity against Caenorhabditis elegans. None of the novel analogs were more potent than paraherquamide.
MeSH terms
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Animals
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Anthelmintics / isolation & purification*
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Anthelmintics / pharmacology
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Antinematodal Agents / isolation & purification*
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Antinematodal Agents / pharmacology
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Caenorhabditis / drug effects*
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Chromatography, High Pressure Liquid
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Chromatography, Thin Layer
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Culture Media
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Fermentation
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Indolizines / isolation & purification*
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Indolizines / pharmacology
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Penicillium / metabolism*
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Soil Microbiology
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Spiro Compounds / isolation & purification*
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Spiro Compounds / pharmacology
Substances
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Anthelmintics
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Antinematodal Agents
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Culture Media
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Indolizines
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Spiro Compounds
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paraherquamide