Journal of Natural Products · 2008 · 34 citations · 30 references
PharmacyMedicinal ChemistryPharmacologyBiochemical PharmacologyCancer PharmacologyDrug DiscoveryBioactive Small MoleculesEnzyme InhibitionNatural Product Drug DiscoveryNatural Product-based Drug DesignTyrosine Kinase InhibitorsAbsolute Configuration AssignmentAbsolute Configuration DeterminationAnticancer Compound ScreeningBioactive Compound LibrariesHeterocyclic Natural ProductsTyrosine-derived Natural ProductsTyrosine-targeted Inhibitors
Exploration of actinomycetes for isolation of natural products for abrogating TRAIL resistance led to the isolation of two new tyrosine derivatives (1 and 2) along with novobiocin (3). The structures of 1 and 2 were determined by spectroscopic methods, while the absolute configuration was determined by analyzing CD spectra and by a modified Marfey's method. Compounds 1 (150 μM) and 3 (37.5 and 75 μM) in combination with TRAIL showed synergistic activity in sensitizing TRAIL-resistant human gastric adenocarcinoma cells.
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Kiyonaga Fujii, Yoshitomo Ikai, Hisao Oka et al. · Analytical Chemistry · 1997 · 468 citations
Kiyonaga Fujii, Yoshitomo Ikai, Tsuyoshi Mayumi et al. · Analytical Chemistry · 1997 · 343 citations