Journal of Natural Products · 2007 · 42 citations · 21 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsAnti-inflammatory PharmacologyMedicinal Plant KnowledgeMedicinal PlantsStructure-activity Relationship AnalysisAnti-inflammatory ResponseBioactive Plant CompoundsMass Spectral Data AnalysisMedicinal Aromatic Plants
Cytotoxicity-guided phytochemical investigation of a methanolic extract of Croton tonkinensis afforded two new kaurane diterpenoids (1, 2) and 10 known ent-kaurane-type diterpenoids (3- 12). The structures of 1 and 2 were based on analysis of spectroscopic and mass spectral data. Compounds 3- 12 were identified by comparison of their spectroscopic and physical data with those reported in the literature. Selected compounds from this plant were examined for cytotoxic and anti-inflammatory activities. Compounds 4 and 9 showed the highest cytotoxic activity against the tested tumor cell lines. Compounds 3, 4, 6, 8, 9, and 11 had IC 50 values less than 5 microM and were more potent than the nonspecific NOS inhibitor L-NAME in inhibiting LPS-induced NO production.
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Jianrong Li, Olivier Baud, Timothy Vartanian et al. · Proceedings of the National Academy of Sciences · 2005 · 365 citations · Full text
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Xihong Wang, Kenneth F. Bastow, Chang-Ming Sun et al. · Journal of Medicinal Chemistry · 2004 · 213 citations
Medicine, Oncology, Pharmacology +11
Cytotoxicity of sesquiterpene lactones.
Kuo‐Hsiung Lee, Eng‐Shang Huang, Claude A. Piantadosi et al. · PubMed · 1971 · 211 citations