Journal of Natural Products · 2011 · 76 citations · 30 references
Life SciencesBotanyMicrobiologyDrug DiscoveryMycologyPlant BiochemistryFungal BiochemistryFungal DiversityFungal Natural Product BiosynthesisFungal Secondary MetabolitesMetabolite IdentificationAbsolute Configuration AssignmentAbsolute Configuration DeterminationBioactive Fungal MetabolitesEndophytic Fungal MetabolitesFungal Bioactive CompoundsLegionella InfectionPlant-associated Fungal MetabolitesStructure Elucidation Of Fungal Metabolites
Chemical investigation of the fungal strain Microdiplodia sp. isolated from the shrub Lycium intricatum led to the isolation of four new compounds: a hexahydroxanthone (2), a 2,3-dihydrochroman-4-one (3), a 7-oxoxanthone derivative (4), and a 1,4-oxazepan-7-one (5). The relative configurations of the new compounds were determined by intensive NMR investigations, notably NOESY experiments at different temperatures. The absolute configurations of the well-known fungal metabolite diversonol (1) and of other xanthone derivatives (3, 4) were established by means of TDDFT ECD calculations. Most of the metabolites were biologically active, with antibacterial activity against Legionella pneumophila and/or antifungal activity against Microbotryum violaceum.
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