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1.
Peptides ; 27(9): 2058-64, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16781016

ABSTRACT

Barettin (cyclo [(6-bromo-8-en-tryptophan) arginine]), a diketopiperazine isolated from the marine sponge Geodia barretti, is a potent inhibitor of barnacle larvae settlement with an EC50-value of 0.9 microM. In the present study, 14 analogs of barettin and its structural congener dipodazine were synthezised and tested for their ability to inhibit larval settlement. Two of the analogs have an intact barettin skeleton. The remaining analogs have a dipodazine skeleton (a diketopiperazine where arginine is replaced with glycine). Six of the tested synthetic analogs displayed significant settlement inhibition with the most potent inhibitor being benzo[g]dipodazine, which displayed even stronger activity than barettin (EC50-value 0.034 microM). The effect of benzo[g]dipodazine was also shown to be readily reversible, when cyprids were transferred to filtered seawater (FSW).


Subject(s)
Peptides, Cyclic/chemistry , Peptides, Cyclic/pharmacology , Porifera/chemistry , Animals , Diketopiperazines , Glycine/chemical synthesis , Glycine/chemistry , Indoles/chemical synthesis , Indoles/chemistry , Indoles/pharmacology , Larva/cytology , Larva/drug effects , Larva/metabolism , Peptides, Cyclic/chemical synthesis , Piperazines/chemical synthesis , Piperazines/chemistry , Piperazines/pharmacology , Porifera/cytology , Porifera/metabolism , Stereoisomerism , Structure-Activity Relationship , Thoracica/cytology , Thoracica/drug effects
2.
J Nat Prod ; 67(3): 368-72, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15043412

ABSTRACT

In this work, we show the potent antifouling effects of two compounds, barettin (cyclo[(6-bromo-8-entryptophan)arginine]) (1), isolated as a Z/E mixture (87/13), and 8,9-dihydrobarettin (cyclo[(6-bromotryptophan)arginine]) (2), isolated from the marine sponge Geodia barretti. The compounds were isolated guided by their ability to inhibit the settlement of cyprid larvae of the barnacle Balanusimprovisus, and their structures were determined by means of mass spectrometry, NMR, and quantitative amino acid analysis. The activities of these brominated diketopiperazine-like cyclic dipeptides are in the range of antifouling agents in use today, as shown by their EC(50) values of 0.9 and 7.9 microM, respectively. However, contrary to today's antifouling agents, the effects of barettin and 8,9-dihydrobarettin are nontoxic and reversible. A small set of synthetic analogues, including l-arginine, l-tryptophan, 5-bromo-d,l-tryptophan, 6-bromo-d,l-tryptophan, and 6-fluoro-d,l-tryptophan, were tested for possible structure-activity relationships. None of these compounds showed any effect at a concentration of 10 microM. We hypothesize that the isolated compounds are part of the sponge's chemical defense to deter fouling organisms. This theory is supported by the fact that barettin is found in water exposed to living specimens of G. barretti in concentrations that completely inhibit barnacles from settling.


Subject(s)
Marine Biology , Peptides, Cyclic/isolation & purification , Porifera/chemistry , Animals , Dose-Response Relationship, Drug , Larva/drug effects , Molecular Structure , Oceans and Seas , Peptides, Cyclic/chemistry , Peptides, Cyclic/pharmacology , Stereoisomerism , Thoracica/drug effects
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