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Updated: Jun 12, 2026

Transient Expression in Nicotiana Benthamiana Leaves for Triterpene Production at a Preparative Scale
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Terpenoids from Salvia trijuga.

Zheng-Hong Pan1, Yuan-Yuan Wang, Ming-Ming Li

  • 1State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650204, People's Republic of China.

Journal of Natural Products
|June 3, 2010
PubMed
Summary

Researchers isolated nine new germacrane sesquiterpenes and a lupane triterpenoid from Salvia trijuga. Some compounds showed moderate cytotoxicity against human tumor cell lines, indicating potential for further study.

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Published on: October 4, 2019

Area of Science:

  • Natural Product Chemistry
  • Phytochemistry
  • Pharmacology

Background:

  • Salvia trijuga is a plant species known to produce diverse secondary metabolites.
  • Terpenoids, including sesquiterpenes and triterpenoids, are classes of natural products with a wide range of biological activities.
  • Investigating the chemical constituents of medicinal plants can lead to the discovery of novel bioactive compounds.

Purpose of the Study:

  • To isolate and characterize new terpenoid compounds from Salvia trijuga.
  • To evaluate the cytotoxic effects of the isolated compounds against human tumor cell lines.

Main Methods:

  • Phytochemical investigation involving extraction and chromatographic separation techniques.
  • Structure elucidation of new compounds using spectroscopic methods, including single-crystal X-ray diffraction.
  • Cytotoxicity assays were performed on five human tumor cell lines.

Main Results:

  • Nine new germacrane sesquiterpenes (trijugins A-I) and one new lupane triterpenoid were isolated.
  • Twenty-four known terpenoids were also identified.
  • Compounds 9 and 32 demonstrated moderate cytotoxic activity against several tested human tumor cell lines.

Conclusions:

  • Salvia trijuga is a rich source of novel terpenoid natural products.
  • The isolated compounds, particularly trijugin I and compound 32, show potential as cytotoxic agents.
  • Further research is warranted to explore the therapeutic potential of these compounds.