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Pseudoceratina purpurea, ceratinamides

Other biologically active bromotyrosine-derived metabolites of marine origin include aeroplysinin, Fig. (48) as cytotoxic and tyrosine kinase inhibitor [382,383], fistularin isolated from Aplysina circheri which exhibited antiviral activity [384], and ceratinamides A and B, antifouling metabolites from Pseudoceratina purpurea [385],... [Pg.720]

The bromotyramine derivatives ceratinamide A (136) and psammaplysin A (137) from the sponge Pseudoceratina purpurea inhibit the settlement and metamorphosis of cyprid larvae of the barnacle Balanus amphitrite (ED50 0.10 and 0.27 (Jg/ml). Interestingly, psammaplysin A induces larval metamorphosis of the ascidian Halocynthia roretzi (ED 0o 1.2 (Jg/ml) [74]. [Pg.784]

Tsukamoto S, Kato H, Hirota H, Fusetani N (1996) Ceratinamides A and B New Antifouling Dibromotyrosine Derivatives from the Marine Sponge Pseudoceratina purpurea. Tetrahedron 52 8181... [Pg.467]

Tsukamoto, S., Kato, H., Hirota, H., and Fusetani, N., Ceratinamides A and B new antifouling dibromotyrosine derivatives from the marine sponge Pseudoceratina purpurea, Tetrahedron, 52, 8181, 1996. [Pg.562]

Ceratinamides A (68) and B (69), antifouling bromotyrosine derivatives, were isolated from marine sponge Pseudoceratina purpurea through a bioassay -guided isolation (Figure 4) [38]. Ceratinamide A (68) is structurally similar to psammaplysin A (27) and has one formyl group at the A-terminus. [Pg.84]

Ceratinamides A and B new antifouling dibromotyrosine derivatives from the marine sponge Pseudoceratina purpurea. Tetrahedron, 52, 8181-8186. [Pg.2073]


See other pages where Pseudoceratina purpurea, ceratinamides is mentioned: [Pg.303]    [Pg.246]   
See also in sourсe #XX -- [ Pg.303 ]




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Ceratinamide

Pseudoceratina

Pseudoceratina purpurea

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