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An Efficient and Rapid HPLC-QQQ-MS Method for the Quantitation of Tropane Alkaloids in Medicinal Plants
Published on: June 12, 2026
Cytotoxic triterpenoid alkaloids from Buxus microphylla
Yu-Xin Yan1, Xiao-Dong Hu, Jian-Chao Chen
1State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650204, Yunnan, People's Republic of China.
Journal of Natural Products
|January 13, 2009
Summary
Five new triterpenoid alkaloids were discovered in Buxus microphylla. Some compounds showed significant cytotoxicity against liver (HepG2) and leukemia (K562) cancer cell lines.
Area of Science:
- Natural Product Chemistry
- Medicinal Chemistry
- Pharmacology
Background:
- Buxus microphylla is a plant species known to produce various bioactive compounds.
- Triterpenoid alkaloids represent a class of natural products with diverse pharmacological activities.
Purpose of the Study:
- To isolate and characterize new triterpenoid alkaloids from Buxus microphylla.
- To evaluate the cytotoxic potential of isolated compounds against cancer cell lines.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation through Nuclear Magnetic Resonance (NMR) and Mass Spectrometry (MS).
- Determination of relative stereochemistry via single-crystal X-ray crystallography.
- Cytotoxicity assays using HepG2 and K562 cell lines.
Main Results:
- Five new triterpenoid alkaloids, buxmicrophyllines E-I (1-5), were identified alongside six known compounds (6-11).
- The structures of compounds 1-5 were fully characterized.
- Compound 3 exhibited potent cytotoxicity against HepG2 cells (IC50 = 0.89 μM), and compound 9 showed similar activity (IC50 = 0.78 μM).
- Compounds 2, 3, 7, 8, and 9 demonstrated cytotoxicity against K562 cells, with IC50 values ranging from 0.37 to 4.44 μM.
Conclusions:
- Buxus microphylla is a rich source of novel triterpenoid alkaloids.
- Several isolated compounds, particularly buxmicrophyllines, possess significant cytotoxic activity against human cancer cell lines, warranting further investigation for therapeutic potential.
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