Phytochemical Analysis · 2009 · 17 citations · 3 references
PharmacyMedicinal ChemistryFood AnalysisMass Spectrometric AnalysisMetabolomicsAnalytical ChromatographyAromatic PlantsChromatographic Food AnalysisInstrumental AnalysisBioactive ConstituentsBioanalytical ChromatographyFragmentationFragmentation BehaviorPharmacological ScreeningQuantitative Chromatography-mass SpectrometryTraditional Chinese Medicine
INTRODUCTION: The aerial part Eupatorium lindleyanum is commonly used as an antipyretic and detoxicant clinically in traditional Chinese medicine. Our previous research showed that germacrane sesquiterpene lactones were its main active constituents, so the development of rapid and accurate methods for the identification of the sesquiterpene lactones is of great significance. OBJECTIVE: To develop an HPLC-PDA-ESI-MS/MS method capable for simple and rapid analysis of germacrane sesquiterpene lactones in the aerial part E. lindleyanum. METHODOLOGY: High-performance liquid chromatography-photodiode array detection-electrospray ionization-tandem mass spectrometry was used to analyze germacrane sesquiterpene lactones of Eupatorium lindleyanum. The fragmentation behavior of germacrane sesquiterpene lactones in a Micromass Q/TOF Mass Spectrometer was discussed, and 9 germacrane sesquiterpene lactones were identified by comparison of their characteristic data of HPLC and MS analyses with those obtained from reference compounds. RESULTS: The investigated germacrane sesquiterpene lactones were identified as eupalinolides C (1), 3beta-acetoxy-8beta-(4'-hydroxy-tigloyloxy)-14-hydroxy-costunolide (2), eupalinolides A (3), eupalinolides B (4), eupalinolides E (5), 3beta-acetoxy-8beta-(4'-oxo-tigloyloxy)-14-hydroxy-heliangolide (6), 3beta-acetoxy-8beta-(4'-oxo- tigloyloxy)-14-hydroxy-costunolide (7), hiyodorilactone B (8), and 3beta-acetoxy-8beta-(4'-hydroxy-tigloyloxy)- costunolide (9). Compounds 6, 7 and 9 were reported for the first time. CONCLUSION: HPLC-PDA-ESI-MS/MS provides a new powerful approach to identify germacrane sesquiterpene lactones in E. lindleyanum rapidly and accurately.
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Cytotoxic sesquiterpene lactones from<i>Eupatorium lindleyanum</i>
Na Yang, Shan Qian, Jin Ao Duan et al. · Journal of Asian Natural Products Research · 2007 · 27 citations
Motoo Tori, Norie Morishita, Naoko Hirota et al. · Chemical and Pharmaceutical Bulletin · 2008 · 16 citations · Full text
[Study on the flavonoids of Eupatorium lindleyanum].
Shihui Qian, Nian‐Yun Yang, Jin‐Ao Duan et al. · PubMed · 2004 · 10 citations