Molecules · 2010 · 16 citations · 12 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsCytotoxicity AssessmentCytotoxicity EvaluationMedicinal Plant KnowledgeMedicinal PlantsAnticancer ActivityAnticancer Compound ScreeningAnticancer Natural ProductsApoptotic Morphological ChangesApoptotic MorphologyBioactive Plant CompoundsChemical Structure-activity RelationshipsPharmacological Screening
Compounds were isolated from a methanol extract of the dried stem barks of Viburnum sargentii Koehne. The structures of the compounds, namely 9'-O-methylvibsanol (3), furcatoside A (4) and lareciresinol (5) were elucidated by analysis of spectroscopic data and comparison with values for previously known analogues. In addition, (+)-catechin (1), (+)-epicatechin (2) were also isolated. This work also examined the cytotoxic effects of three compounds 3-5 (25-100 microM) in MCF-7 and A549 cells after 24, 48 and 72 h of exposure. Our results showed that 9'-O-methylvibsanol (3) exhibited strong concentration-dependent anticancer effects according to the MTT assay and produced morphological changes consistent with apoptosis, as confirmed by Ho3342 staining analysis revealed that more apoptotic cells were observed after 9'-Omethylvibsanol (3) treatment.
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Iridoids. An Updated Review. Part I.
Christie A. Boros, Frank R. Stermitz · Journal of Natural Products · 1990 · 277 citations
Iridoids. An Updated Review, Part II
Christie A. Boros, Frank R. Stermitz · Journal of Natural Products · 1991 · 226 citations