Abstract
The fungus Epicoccum sp., was isolated from the marine brown alga Fucus vesiculosus. After cultivation the fungus was investigated for its secondary metabolite content,
and found to contain the new natural product 4,5,6-trihydroxy-7-methylphthalide (1, epicoccone), together with 5-(acetoxymethyl)-furan-2-carboxylic acid (2), furan-2-carboxylic acid (3), 5-(hydroxymethyl)-furan-2-carboxylic acid (4), (-)-(3R,4S)-4-hydroxymellein (5), and (-)-(3R)-5-hydroxymellein (6). The structures of all compounds were determined by interpretation of their spectroscopic
data (1D and 2D NMR, MS, UV, optical rotation and IR). Each isolate was tested for
its antioxidative properties. Compound 1 was found to be potently active, showing 95 % DPPH radical scavenging effects at
25 μg/mL. Compound 1 also inhibited the peroxidation of linolenic acid in the TBARS assay (62 % inhibition
at 37 μg/mL).
Key words
Antioxidant - isobenzofuranone - epicoccone - marine fungus -
Epicoccum sp.
- Ascomycota - Leptosphaeriaceae
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Prof. Dr. Gabriele M. König
Institute for Pharmaceutical Biology
University of Bonn
Nussallee 6
53115 Bonn
Germany
Phone: +49-228-733747
Fax: +49-228-733250
Email: g-koenig@uni-bonn.de