Abstract
Two new 11-hydroxyeunicellin diterpenoids, cladieunicellin F (1) and (-)-solenopodin C (2), were isolated from an Indonesian octocoral Cladiella sp. The structures of eunicellins 1 and 2 were established by spectroscopic methods, and eunicellin 2 was found to be an enantiomer of the known eunicellin solenopodin C (3). Eunicellin 2 displayed inhibitory effects on the generation of superoxide anion and the release of elastase by human neutrophils. The previously reported structures of two eunicellin-based compounds, cladielloides A and B, are corrected in this study.
Keywords:
Cladiella; cladieunicellin; elastase; eunicellin; octocoral; superoxide anion.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Anthozoa / chemistry*
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Anti-Inflammatory Agents, Non-Steroidal / chemistry*
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Anti-Inflammatory Agents, Non-Steroidal / isolation & purification
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Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
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Diterpenes / chemistry*
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Diterpenes / isolation & purification
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Diterpenes / pharmacology*
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Humans
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Indonesia
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Neutrophils / drug effects
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Neutrophils / enzymology
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Neutrophils / metabolism
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Nuclear Magnetic Resonance, Biomolecular
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Pancreatic Elastase / metabolism
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Spectrum Analysis / methods
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Superoxides / metabolism
Substances
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Anti-Inflammatory Agents, Non-Steroidal
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Diterpenes
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eunicellin
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Superoxides
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Pancreatic Elastase