Organic Letters · 2014 · 26 citations · 14 references
Life SciencesBiochemistryChemistryCoral Reef BiologyDrug DiscoveryStructure-activity RelationshipsCoral PhysiologyMarine Bioactive CompoundsMarine Natural Product BiosynthesisMarine Natural ProductsReef-building CoralsTerpenoid BiosynthesisAbsolute Configuration AssignmentAbsolute Configuration DeterminationBioactive Compounds From Marine CoralsMarine Compound Structure ElucidationMarine-derived Anti-inflammatory CompoundsSecondary MetabolitesSoft Coral MetabolitesStructure Elucidation Of Marine Natural Products
Tortuosenes A and B (1 and 2), possessing new diterpenoid molecular structures, were isolated from the Formosan soft coral Sarcophyton tortuosum along with a known cembrane, emblide (3). The structures of 1 and 2 were established by extensive spectroscopic analysis, and the absolute configuration of 1 was determined by TDDFT ECD calculations. Tortuosene A was found to display significant inhibitory effects on the generation of the superoxide anion in N-formyl-methionyl-leucyl-phenylalanine/cytochalasin B (fMLP/CB)-induced neutrophils.
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Tsong‐Long Hwang, Guo-Long Li, Yu-Hsuan Lan et al. · Free Radical Biology and Medicine · 2008 · 92 citations