Abstract
A marine fungal isolate, identified as Wardomyces anomalus, was cultivated and found to produce two new xanthone derivatives, 2,3,6,8-tetrahydroxy-1-methylxanthone (1) and 2,3,4,6,8-pentahydroxy-1-methylxanthone (2), in addition to the known xanthone derivative 3,6,8-trihydroxy-1-methylxanthone (3) and the known fungal metabolite 5-(hydroxymethyl)-2-furanocarboxylic acid (4). The structures of all compounds were determined on the basis of extensive spectroscopic measurements (1D and 2D NMR, MS, UV, and IR). Compounds 1 and 4 showed significant antioxidant activities. The total extract and 1, 3, and 4 were shown to be inhibitors of p56(lck)tyrosine kinase.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antioxidants / chemistry
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Antioxidants / isolation & purification*
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Antioxidants / pharmacology
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Fungi / chemistry*
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Fungi / classification
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HIV Reverse Transcriptase / drug effects*
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Lymphocyte Specific Protein Tyrosine Kinase p56(lck) / drug effects*
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Molecular Structure
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Nuclear Magnetic Resonance, Biomolecular
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Xanthenes / chemistry
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Xanthenes / isolation & purification*
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Xanthenes / pharmacology
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Xanthones*
Substances
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2,3,4,6,8-pentahydroxy-1-methylxanthone
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2,3,6,8-tetrahydroxy-1-methylxanthone
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Antioxidants
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Xanthenes
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Xanthones
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xanthone
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Lymphocyte Specific Protein Tyrosine Kinase p56(lck)
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HIV Reverse Transcriptase