Chemical Communications · 2011 · 30 citations · 16 references
Life SciencesBiochemistryMicrobiologyMycologyNatural Product BiosynthesisOrganic ChemistryFungal BiochemistryFungal Natural Product BiosynthesisFungal Secondary MetabolitesAbsolute Configuration AssignmentAbsolute Configuration DeterminationFungal Bioactive CompoundsMacrophage-fungus Interactions
Cyclopenicillone (1), possessing a unique 2,5-dimethylcyclopent-2-enone carbon skeleton, has been isolated from the cultures broth of the fungus Penicillium decumbens. The structure and absolute configuration of 1 were elucidated using a combination of NMR spectroscopy, CD data and computational approaches. Cyclopenicillone (1) demonstrated a dose-dependent (10-100 μM) inhibition against LPS-induced NO production in RAW264.7 macrophages.
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Nobuaki Matsumori, Daisuke Kaneno, Michio Murata et al. · The Journal of Organic Chemistry · 1999 · 769 citations
Absolute Stereochemistry of Citrinadins A and B from Marine-Derived Fungus
Takao Mugishima, Masashi Tsuda, Yuu Kasai et al. · The Journal of Organic Chemistry · 2005 · 217 citations