Helvetica Chimica Acta · 2008 · 18 citations · 18 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsMedicinal Plant KnowledgeMedicinal PlantsStructure-activity Relationship AnalysisAnticancer ActivityAnticancer Natural ProductsChemical Structure-activity RelationshipsCytotoxicity AssaysMedicinal Plant ResourcesPharmacological ScreeningTerpenoid Profiling
Abstract Bioassay‐guided fractionation of ethanolic extract from the root tuber of Curcuma wenyujin afforded three new diterpenes, curcumrinols A–C ( 1 – 3 ), where 2 is the (14 S ) ‐ epimer of 1 . The structures of 1 – 3 were established on the basis of spectroscopic analysis, mainly NMR and MS. 1 – 3 were tested in vitro for their cytotoxic activity against the HL‐60 and K562 cancer cells. Among the compounds tested, 1 exhibited medium cytotoxicity against K‐562 and HL60 human cancer cells with IC 50 values of 11.2 and 3.2 μg/ml, respectively. However, 2 showed only weak activity against the above cancers cells, which suggested that C(14) may be an important position for cytotoxic activity.
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So‐Young Park, Darrick S. H. L. Kim · Journal of Natural Products · 2002 · 280 citations
Fumiyuki Kiuchi, Yoshihisa Goto, Naoki Sugimoto et al. · Chemical and Pharmaceutical Bulletin · 1993 · 254 citations · Full text