Organic Letters · 2011 · 85 citations · 21 references
Natural SciencesBiochemistryMedicinal ChemistryCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsCircular Dichroism SpectroscopyEnzyme InhibitionMarine Bioactive CompoundsMarine Drug DiscoveryMarine Natural ProductsSpectroscopy Of BiomoleculesAnticancer Marine CompoundsBioactive Compounds From Marine SpongesBioactive Marine MetabolitesElectronic Circular DichroismMarine Compound Structure ElucidationMarine Sponge MetabolitesSponges As Drug SourcesSponges-derived Metabolites
Dysidavarones A-D (1-4), four new sesquiterpene quinones possessing the unprecedented "dysidavarane" carbon skeleton, were isolated from the South China Sea sponge Dysidea avara. The structures were established by spectroscopic methods, and the absolute configurations were determined using quantum mechanical calculation of the electronic circular dichroic (ECD) spectrum and exciton chirality CD method. Their cytotoxic activity against four human cancer cell lines and PTP1B inhibitory activity were also evaluated.
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Nobuaki Matsumori, Daisuke Kaneno, Michio Murata et al. · The Journal of Organic Chemistry · 1999 · 769 citations
Naoya Oku, Kentaro Takada, Richard W. Fuller et al. · Journal of the American Chemical Society · 2010 · 91 citations · Full text
Quinone/Hydroquinone Sesquiterpenes
Isidro S. Marcos, A. Conde, Rosalina F. Moro et al. · Mini-Reviews in Organic Chemistry · 2010 · 83 citations