Journal of Natural Products · 2004 · 25 citations · 11 references
MedicineMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsAntibacterial AgentsAntibacterial PharmacologyAntifungal AgentsMedicinal PlantsMetabolite IdentificationStructure-activity Relationship AnalysisAntimalarial AgentsAntimalarial ChemotherapyBioactive Fungal MetabolitesBioactive Plant CompoundsCytotoxicity AssaysPharmacological ScreeningX-ray Diffraction AnalysisX-ray Spectral Analysis
Two new flavanones (1 and 2), a new flavan (3), and a new rare dibenzocycloheptene derivative (4) together with a known flavan, 4'-hydroxy-2' ',2' 'dimethyl-pyranoflavan (5), were isolated from the roots of Dendrolobium lanceolatum. Their structures were established on the basis of spectral evidence, and an X-ray analysis was performed to confirm the structure of 4. Compounds 1-3 exhibited antimalarial activity with IC50 values of 2.6, 3.3, and 3.1 microg/mL, respectively. Compounds 1-5 showed moderate antimycobacterial activity with MIC values of 6.3, 12.5, 25, 25, and 50 microg/mL, respectively. In addition, 1 showed strong cytotoxicity against cancer cell lines KB, BC, and NCI-H187 with IC50 values of 1.2, 1.6, and 0.6 microg/mL, respectively, while 2 showed moderate cytotoxicity against the NCI-H187 cell line with an IC50 value of 8.1 microg/ mL.
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New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
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