4.5 Article

Four new macrocyclic trichothecenes from two strains of marine-derived fungi of the genus Myrothecium

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JOURNAL OF ANTIBIOTICS
卷 59, 期 8, 页码 451-455

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JAPAN ANTIBIOTICS RESEARCH ASSOC
DOI: 10.1038/ja.2006.63

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Myrothecium roridum; marine-derived fungus; roridin Q; roridin R; macrocyclic trichothecene; cytotoxicity; L1210

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Three new macrocyclic trichothecenes, named 12'-hydroxyroridin E (1), roridin Q (2), and 2',3'-deoxyroritoxin D (3), were isolated from the marine-derived fungus Myrothecium roridum TUF 98F42, and a new macrocyclic trichothecene, named roridin R (4), was isolated from Myrothecium sp. TUF 02176 together with foridins A and H and isororidin E. The structures of new compounds were determined on the basis of their spectral data. Compound 2 possessed a unique ether moiety at the 13' position of 1. Compound 4 was a 2',3'-dihydro-2'-hydroxy derivative of roridin H. The IC50 values of compounds 1, 2, and 4 against the murine leukemia cell line L1210 were 0.19, 31.2, and 0.45 mu M, respectively. Compound 3 showed antiyeast activity to Saccharomyces cerevisiae at 1 mu g/disc (inhibition zone: 12.2 mm), which was about 10 time more active than roritoxin D (10.2 mm at 10 mu g/disc).

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