A novel cyclodepsipeptide, neosiphoniamolide A (I), has been isolated from the sponge Neosiphonia superstes. The structure of I, which contains a 12-carbon hydroxy acid, glycine, valine, and a halogenated tyrosine residue is an 18- membered ring, is related to jaspamide and the geodiamolides, previously isolated from sponges. The structure was solved by spectroscopic analysis.

Neosiphoniamolide A, a novel cyclodepsipeptide, with antifungal activity from the marine spongeNeosiphonia superstes / D'Auria, MARIA VALERIA; Gomez Paloma, L.; Minale, L.; Zampella, Angela; Debitus, C.; Perez, J.. - In: JOURNAL OF NATURAL PRODUCTS. - ISSN 0163-3864. - STAMPA. - 58:1(1995), pp. 121-123. [10.1021/np50115a017]

Neosiphoniamolide A, a novel cyclodepsipeptide, with antifungal activity from the marine spongeNeosiphonia superstes

D'AURIA, MARIA VALERIA;ZAMPELLA, ANGELA;
1995

Abstract

A novel cyclodepsipeptide, neosiphoniamolide A (I), has been isolated from the sponge Neosiphonia superstes. The structure of I, which contains a 12-carbon hydroxy acid, glycine, valine, and a halogenated tyrosine residue is an 18- membered ring, is related to jaspamide and the geodiamolides, previously isolated from sponges. The structure was solved by spectroscopic analysis.
1995
Neosiphoniamolide A, a novel cyclodepsipeptide, with antifungal activity from the marine spongeNeosiphonia superstes / D'Auria, MARIA VALERIA; Gomez Paloma, L.; Minale, L.; Zampella, Angela; Debitus, C.; Perez, J.. - In: JOURNAL OF NATURAL PRODUCTS. - ISSN 0163-3864. - STAMPA. - 58:1(1995), pp. 121-123. [10.1021/np50115a017]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/415384
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