Journal of Natural Products · 2005 · 28 citations · 4 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DesignDrug DiscoveryCytotoxicity AssessmentCytotoxicity EvaluationMetabolite IdentificationBioactivity ScreeningBotanical BioassaysChemical Structure-activity RelationshipsCytotoxicity AssaysDrug Cytotoxicity TestingPharmacological ScreeningThree-dimensional Nmr SpectroscopyTwo-dimensional Nmr Spectroscopy
Bioassay-guided fractionation of an ethanol extract of a Madagascar collection of Schizolaena hystrix afforded three new flavanones, schizolaenone A (1), schizolaenone B (2), and 4'-O-methylbonannione A (3), as well as three known flavanones, nymphaeol A, bonannione A, and macarangaflavanone B, and the flavanol bonanniol A. The structures of compounds 1-3 were determined by various one- and two-dimensional NMR techniques. All of the isolates were tested for cytotoxicity against the A2780 human ovarian cancer cell line. Nymphaeol A (IC(50) = 5.5 microg/mL) exhibited the greatest cytotoxicity, while the other flavanones were found to be only weakly active.
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Prenylated flavanones from leaves of Macaranga pleiostemona
Barbara A. Schütz, Anthony D. Wright, Topul Rali et al. · Phytochemistry · 1995 · 65 citations
New Flavonoids from Bonannia graeca (L.) Halacsy
Maurizio Bruno, Giuseppe Savona, Liliana Lamartina et al. · Heterocycles · 1985 · 24 citations · Full text