Journal of Natural Products · 2009 · 29 citations · 13 references
MedicineMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryMolecular PharmacologyCancer MetabolismOncology PharmacologyAdme ProfilingBiological Activity FeaturesCancer Cell Line ModelsCancer Cell Proliferation InhibitionG1 Cell-cycle ArrestG1 Phase ArrestMarine-derived Anticancer CompoundsPharmacological Profiling
A new adenine-substituted bromotyrosine-derived metabolite designated as aphrocallistin (1) has been isolated from the deep-water Hexactinellida sponge Aphrocallistes beatrix. Its structure was elucidated on the basis of spectral data and confirmed through a convergent, modular total synthetic route that is amenable toward future analogue preparation. Aphrocallistin inhibits the growth of a panel of human tumor cell lines with IC(50) values ranging from 7.5 to >100 microM and has been shown to induce G1 cell cycle arrest in the PANC-1 pancreatic carcinoma cell line. Aphrocallistin has been fully characterized in the NCI cancer cell line panel and has undergone in vitro ADME pharmacological profiling.
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