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Trigoxyphins A-G: diterpenes from Trigonostemon xyphophylloides
Bing-Dong Lin1, Mei-Ling Han, Yin-Chun Ji
1State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 555 Zu Chong Zhi Road, Zhangjiang Hi-Tech Park, Shanghai, People's Republic of China.
Six new daphnane-type diterpenoids and one phenanthrene-type diterpenoid were isolated from Trigonostemon xyphophylloides. Two compounds showed significant cytotoxic activity against human tumor cell lines, indicating potential anticancer properties.
Area of Science:
- Natural Product Chemistry
- Phytochemistry
- Medicinal Chemistry
Background:
- Trigonostemon xyphophylloides is a plant source of bioactive compounds.
- Diterpenoids are a class of natural products with diverse biological activities.
Purpose of the Study:
- To isolate and characterize new diterpenoids from Trigonostemon xyphophylloides.
- To evaluate the cytotoxic activity of isolated compounds against cancer cell lines.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation using spectroscopic methods (NMR, MS).
- Cytotoxicity assays against HL60 and A549 cell lines.
Main Results:
- Six new oxygenated daphnane-type diterpenoids (trigoxyphins A-F) and one phenanthrene-type diterpenoid (trigoxyphin G) were identified.
- Compounds 1 and 2 demonstrated potent cytotoxic effects against HL60 and A549 tumor cell lines with low IC(50) values.
- Two known compounds were also isolated and identified.
Conclusions:
- Trigonostemon xyphophylloides is a rich source of novel diterpenoids.
- Trigoxyphins A and B possess significant cytotoxic potential, warranting further investigation as anticancer drug leads.
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