Journal of Natural Products · 2015 · 31 citations · 11 references
Life SciencesBiochemistryChemistryMycologyOrganic ChemistryStructure-activity RelationshipsFungal BiochemistryFungal Secondary MetabolitesTerpenoid BiosynthesisAnti-inflammatory ActivityAnti-inflammatory ResponseBioactive Compounds From Marine FungiBioactive Fungal MetabolitesCircular DichroismFungal Bioactive CompoundsMarine Fungal MetabolitesMarine Fungal Natural Products
Aspertetranones A-D (1-4), four new highly oxygenated putative rearranged triketide-sesquiterpenoid meroterpenes, were isolated from the marine algal-associated fungus Aspergillus sp. ZL0-1b14. On the basis of a comprehensive spectroscopic analysis, the planar structures of aspertetranones were determined to possess an unusual skeleton in the terpenoid part. The relative and absolute configurations of the aspertetranones were assigned on the basis of NOESY analysis, X-ray crystallography, and circular dichroism spectroscopy. Compounds 1-4 were evaluated for anti-inflammatory activity in LPS-stimulated RAW264.7 macrophages. Aspertetranone D exhibited an inhibitory effect against IL-6 production with 69% inhibition at 40 μM.
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A short history of<i>SHELX</i>
George M. Sheldrick · Acta Crystallographica Section A Foundations of Crystallography · 2007 · 87.4K citations · Full text
Anti-inflammatory Triterpenes from the Leaves of <i>Rosa laevigata</i>
Na Zeng, Yang Shen, Ling-Zhi Li et al. · Journal of Natural Products · 2011 · 69 citations
Life Sciences, Botany, Pharmacology +16