Pentacyclic triterpenoids from spikes of Prunella vulgaris L. with thyroid tumour cell cytostatic bioactivities

Nat Prod Res. 2023 May;37(9):1518-1526. doi: 10.1080/14786419.2021.2024532. Epub 2022 Jan 18.

Abstract

Five new triterpenoids, including four ursane types (1-4) and one oleanane type (5), together with 15 known ursane types pentacyclic triterpenoids (6-20) were isolated from the fruit spikes of Prunella vulgaris L., a traditional Chinese herbal medicine. Their structures were elucidated based on IR, HR-ESI-MS, and NMR spectroscopic data. The SW579 cell line was used to evaluate anti-thyroid cancer activities of (1-20). The results indicated that (7-9), (16), and (19) exhibited apparent inhibitory activity with IC50 values of 25.73-71.41 μM (cisplatin as positive control, IC50 14.49 ± 0.97 μM). Network pharmacology and molecular docking were also used for the prediction of the synergistic actions and the underlying mechanisms. Accordingly, four potential targets have been characterized.

Keywords: Labiatae; PI3KCA; Prunella vulgaris L.; SW579; pentacyclic triterpenoid.

MeSH terms

  • Cytostatic Agents*
  • Humans
  • Molecular Docking Simulation
  • Molecular Structure
  • Pentacyclic Triterpenes / chemistry
  • Prunella* / chemistry
  • Thyroid Neoplasms*
  • Triterpenes* / pharmacology

Substances

  • ursane
  • Cytostatic Agents
  • Pentacyclic Triterpenes
  • Triterpenes