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Published on: December 27, 2016
Versilulins A-D, Spiroketals, and Diphenyl Ether Derivatives from Marine-Derived Aspergillus versicolor 347 with
Biao Wang1,2, Xiao Yang1,3, Rongfa Song1,3
1State Key Laboratory of Agricultural and Forestry Biosecurity, State & Local Joint Engineering Research Center of Green Pesticide Invention and Application, College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, P. R. China.
Abstract:
Four unreported compounds, including two pairs of spiroketal racemates, (±)-versilulin A (1a and 1b) and (±)-versilulin B (2a and 2b), and two diphenyl ether derivatives, versilulins C and D (3 and 4), together with four known compounds (5-8), were isolated from the endophytic fungus Aspergillus versicolor 347. The assignment of their structures was accomplished by spectroscopic analysis, including HRESIMS, NMR, chiral analysis, ECD calculation, and X-ray diffraction. Among them, compounds 1 and 2 possess an unprecedented 6/5/6/6 tetracyclic polyketide with a unique 1,4-dioxospiro[4.5]decan-8-one core skeleton. Compound 3 was characterized by an unusual 6/6/6/6/6/6 hexacyclic ring system featuring a rare 9-oxospiro[5.5]undecan-3-one. Compound 4 contains a novel 6/8/6/6/6/6 hexacyclic fused ring system. Biological assays revealed that compounds 3 and 5 displayed modest antibacterial activity against Staphylococcus aureus with an equal MIC value of 32 μg/mL.
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