Journal of Natural Products · 2010 · 67 citations · 19 references
Life SciencesMedicinal ChemistryOncologyCancer PharmacologySteroid BiochemistryStructure-activity RelationshipsMedicinal PlantsSteroid StructureAnticancer ActivityAnticancer Compound ScreeningFruit Bioactive CompoundsFruit PhytochemicalsInsecticidal Activity AssaysPharmacological ScreeningRelative Configuration DeterminationSingle-crystal Diffraction
Ten new triterpenoids, named meliasenins I-R (1-10), one new steroid (11), and 11 related known compounds (12-22) were isolated from fruits of Melia toosendan. The structures of the new compounds were established on the basis of spectroscopic methods, including 2D NMR techniques and mass spectrometry. The relative configuration of 1, (20R*,23E)-25-hydroperoxyeupha-7,23-diene-3β,16β-diol (meliasenin I), was confirmed by single-crystal X-ray diffraction analysis. All isolated triterpenoids (1-10, 12-15) and two steroids (11, 20) were tested for their cytotoxicity against U20S human osteosarcoma and MCF-7 human breast cancer cells using the MTT assay, and some of them were significantly cytotoxic (IC(50) <10 μg/mL). The insecticidal properties of compounds 1-15 and 20 were also briefly evaluated.
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Sterols and Steryl Glycosides from Urtica dioica
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Agladupols A–E, Triterpenoids from Aglaia duperreana
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