Diverse metabolites of coral reef organisms

A detailed mechanism for the spontaneous transformation of 2-chloro-1-hydroxyoctoda-3(8),5-dien-4-one, a metabolite of , into 4,5-dimethylbenzo[ ]furan was presented. Five new terpenoids have been isolated from the red alga . Five species of sponges yielded various metabolites: furanosesterterpenes...

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Veröffentlicht in:Pure and applied chemistry 2005-01, Vol.77 (1), p.83-89
Hauptverfasser: Tanaka, Junichi, Kuniyoshi, Masayuki, Tanaka, Chiaki, Issa, Hamad H., Balansa, Walter, Otsuka, Masahito, Githige, Wahome P., Higa, Tatsuo
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Sprache:eng
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Zusammenfassung:A detailed mechanism for the spontaneous transformation of 2-chloro-1-hydroxyoctoda-3(8),5-dien-4-one, a metabolite of , into 4,5-dimethylbenzo[ ]furan was presented. Five new terpenoids have been isolated from the red alga . Five species of sponges yielded various metabolites: furanosesterterpenes from sp., scalarane derivatives from sp., polyketides from cf. , a polyacetylene from sp., and cyclic depsipeptides from . Other new metabolites were sponge-derived secomanoalide derivative and imidazole alkaloids from nudibranchs, briarane class diterpenes from octocorals, and cyclofarnesylated hydroquinones, floresolides A-C, from an ascidian, sp. Many of these compounds showed cytotoxicity.
ISSN:0033-4545
1365-3075
DOI:10.1351/pac200577010083