Marine Drugs · 2011 · 61 citations · 14 references
Life SciencesBiochemistryPharmacologyBiochemical PharmacologyDrug DiscoveryStructure-activity RelationshipsAntioxidant DefenseEnzyme InhibitionMarine Bioactive CompoundsMarine Natural ProductsReactive Oxygen SpeciesVenom BiologyAntioxidant Activity AssaysAntioxidant Marine CompoundsBioactive Compounds From Marine SpongesIndole DerivativesMarine Sponge MetabolitesMarine-derived AntioxidantsPhospholipase A2 InhibitionPhospholipase A2 Pathway
Indole derivatives including bromoindoles have been isolated from the South Pacific marine sponges Rhopaloeides odorabile and Hyrtios sp. Their structures were established through analysis of mass spectra and 1D and 2D NMR spectroscopic data. Their potential inhibitory phospholipase A₂ (PLA₂), antioxidant and cytotoxic activities were evaluated. The new derivative 5,6-dibromo-L-hypaphorine (9) isolated from Hyrtios sp. revealed a weak bee venom PLA₂ inhibition (IC₅₀ 0.2 mM) and a significant antioxidant activity with an Oxygen Radical Absorbance Capacity (ORAC) value of 0.22. The sesquiterpene aureol (4), also isolated from Hyrtios sp., showed the most potent antioxidant activity with an ORAC value of 0.29.
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