Abstract
The structures of pentacecilides, new inhibitors of lipid droplet formation in mouse macrophages produced by Penicillium cecidicola FKI-3765-1, were elucidated by spectroscopic studies, including various NMR experiments. Pentacecilides have a common pentacyclic meroterpene core, which contains an aromatic ring and a delta-lactone ring.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Animals
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Hypolipidemic Agents / pharmacology*
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Lipid Metabolism / drug effects*
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Magnetic Resonance Spectroscopy
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Mice
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Molecular Conformation
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Molecular Weight
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Sesquiterpenes / pharmacology*
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Spectrometry, Mass, Electrospray Ionization
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Spectrophotometry, Infrared
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Spectrophotometry, Ultraviolet
Substances
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Hypolipidemic Agents
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Sesquiterpenes
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pentacecilide A
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pentacecilide B
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pentacecilide C