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Updated: Mar 7, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Ent-Abietanoids Isolated from Isodon serra.
Jun Wan1,2, Hua-Yi Jiang3,4, Jian-Wei Tang5,6
1State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China. wanjun@imm.ac.cn.
Researchers isolated four new ent-abietane diterpenoids from Isodon serra, a traditional Chinese medicine. One compound, serrin K, demonstrated significant nitric oxide (NO) inhibition in immune cells.
Area of Science:
- Natural Product Chemistry
- Pharmacology
- Medicinal Chemistry
Background:
- Isodon serra is a traditional Chinese folk medicine.
- Diterpenoids are a class of natural products with diverse biological activities.
Purpose of the Study:
- To isolate and characterize new ent-abietane diterpenoids from Isodon serra.
- To evaluate the biological activities of the isolated compounds.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation through extensive spectroscopic analysis (NMR, MS).
- In vitro assays to assess inhibitory activity against nitric oxide (NO) production and cytotoxicity.
Main Results:
- Four new ent-abietane diterpenoids (serrin K, xerophilusin XVII, enanderianins Q and R) and four known compounds were isolated.
- Serrin K (1) exhibited significant inhibitory activity against NO production in lipopolysaccharide (LPS)-stimulated RAW264.7 cells (IC50 = 1.8 μM).
- Compound 1 showed weak cytotoxicity against a panel of human tumor cell lines.
Conclusions:
- The study successfully identified novel diterpenoids from Isodon serra.
- Serrin K represents a promising candidate for further investigation in the context of inflammatory conditions.
- The findings contribute to the understanding of the chemical constituents and potential therapeutic applications of Isodon serra.
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