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Updated: Mar 28, 2026

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Bioactive spirostane glycosides from Tacca plantaginea
Zhen-Hua Liu1, Huan Yan2, Yong-Ai Si1
1State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Eight new spirostane glycosides were identified from Tacca plantaginea, with compound 1 showing significant cytotoxic activity against cancer cells. Some compounds also demonstrated platelet aggregation effects.
Area of Science:
- Natural Products Chemistry
- Pharmacognosy
- Medicinal Chemistry
Background:
- Tacca plantaginea is a plant source of bioactive compounds.
- Spirostanoid glycosides are a class of natural products with diverse biological activities.
Purpose of the Study:
- To isolate and characterize new spirostane glycosides from Tacca plantaginea.
- To evaluate the cytotoxic and platelet aggregation activities of these compounds.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation via spectroscopic methods (MS, 1D and 2D NMR) and chemical analysis.
- In vitro cytotoxicity assays against HEK293 and HepG2 cell lines.
- Platelet aggregation assays for selected compounds.
Main Results:
- Eight new spirostane glycosides (taccaosides E-L) and seven known analogs were isolated.
- Compound 1 exhibited potent cytotoxicity against both tested cancer cell lines (IC50 values 1.7 μM and 1.2 μM).
- Spirostanoid glycosides with a 17α-hydroxyl group were assessed for platelet aggregation activity.
Conclusions:
- Tacca plantaginea is a rich source of structurally diverse spirostane glycosides.
- Compound 1 represents a promising lead for further investigation as an anticancer agent.
- The study contributes to understanding the structure-activity relationships of spirostane glycosides.
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