Journal of Natural Products · 2000 · 89 citations · 14 references
Life SciencesBotanyPlant SciencesDrug DiscoveryPlant BiochemistryCytotoxicity AssessmentCytotoxicity EvaluationMedicinal Plant KnowledgeMedicinal PlantsNatural Product Drug DiscoveryBioactive Plant CompoundsBotanical BioassaysCytotoxicity AssaysExtractPharmacological ScreeningPlant-derived Natural ProductsSpectroscopic IdentificationToxicology Of Medicinal Plants
Bioassay-guided fractionation of a leaf extract of G. bracteata has yielded six new prenylxanthones, bractatin (1), isobractatin (2), 1-O-methylbractatin (3), 1-O-methylisobractatin (4), 1-O-methyl-8-methoxy-8,8a-dihydrobractatin (5), and 1-O-methylneobractatin (6). The structures of these compounds have been elucidated by spectroscopic means (NMR, MS), literature data, and X-ray crystallographic analysis of 2. These compounds possess significant cytotoxicity against the KB cell line.
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Inhibition of purified p21 farnesyl:protein transferase by Cys-AAX tetrapeptides
Yuval Reiss, Joseph L. Goldstein, Miguel C. Seabra et al. · Cell · 1990 · 815 citations
Cytotoxic xanthones from Garcinia hanburyi
Jun Asano, Kazuhiro Chiba, Masahiro Tada et al. · Phytochemistry · 1996 · 193 citations