Mar 1, 1992

(-)-agelasidine C and (-)-agelasidine D, two new hypotaurocyamine diterpenoids from the Caribbean sea sponge Agelas clathrodes

Journal of Natural Products
J J Morales, A D Rodríguez

Abstract

Two new diterpene derivatives of hypotaurocyamine, (-)-agelasidine C [3] and (-)-agelasidine D [5], have been isolated from the Caribbean sea sponge Agelas clathrodes. The structures of 3 and 5 have been established by interpretation and comparison of their spectral data to those of the known antipode (+)-agelasidine C [1].

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Mentioned in this Paper

In Vivo NMR Spectroscopy
Antineoplastic Agents
Diterpenes
Derivatives
Bacteriocidal Agents
Agelasidine C
Agelas clathrodes
Demospongiae
Diterpenes, Labdane
Guanidines

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