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Published on: August 16, 2018
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Lupane- and Friedelane-Type Triterpenoids from Celastrus stylosus
You-Min Ying1,2, Cui-Yu Li1, Yan Chen1
1College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, P. R. China, (phone/fax: +86-571-88871075 (Z.-J. Zhan), +86-571-88320554 (W.-G. Shan); , (Z.-J. Zhan), (W.-G. Shan)).
Chemistry & Biodiversity
|August 13, 2015
Summary
Researchers isolated novel triterpenoids from Celastrus stylosus roots, finding some compounds show significant antiproliferative activity against human cancer cell lines, comparable to taxol.
Area of Science:
- Natural Product Chemistry
- Pharmacology
- Medicinal Chemistry
Background:
- Celastrus stylosus is a plant species with potential medicinal properties.
- Triterpenoids are a class of natural compounds known for diverse biological activities.
- The chemical constituents and bioactivities of C. stylosus have not been previously investigated.
Purpose of the Study:
- To isolate and characterize chemical constituents from the roots of Celastrus stylosus.
- To evaluate the antiproliferative activities of the isolated compounds against human cancer cell lines.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation of new compounds via spectroscopic analyses (e.g., NMR, MS).
- In vitro antiproliferative assays against six human cancer cell lines (PANC-1, A549, PC-3, HepG2, SGC-7901, HCCLM3).
Main Results:
- Two new triterpenoids, 30-hydroxylup-20(29)-ene 3β-caffeate (1) and 24-nor-friedelan-6α,10-dihydroxy-1,2-dioxo-4,7-dien-29-oic acid (2), were identified.
- Eight known compounds (3-10) were also isolated and characterized.
- Compounds 3, 4, and 10 demonstrated antiproliferative activity against PC-3 and HCCLM3 cell lines, comparable to the positive control, taxol.
Conclusions:
- This study reports the first chemical investigation of Celastrus stylosus roots.
- Novel and known triterpenoids were successfully isolated and identified.
- Certain isolated triterpenoids exhibit promising antiproliferative potential against specific human cancer cell lines.

