Cytotoxic abietane-type diterpenoids from roots of Salvia spinosa and their in Silico pharmacophore modeling

Nat Prod Res. 2022 Jun;36(12):3183-3188. doi: 10.1080/14786419.2021.1952202. Epub 2021 Jul 22.

Abstract

The roots of Salvia spinosa L. (Lamiaceae) were extracted with hexane, dichloromethane (DCM) and ethyl acetate. The DCM extract exhibited cytotoxic activity (IC50 32.7 µg/mL) against MFC-7 breast cancer cell line in MTT colorimetric bioassay. Ferruginol (1), taxodione (2), 12-deoxy-6-hydroxy-6,7-dehydroroyleanone (3), 14-deoxycoleon U (4), 15-deoxyfuerstione (5) and taxodone (6) were isolated from the DCM roots extract. Their structures were elucidated by a combination of spectroscopic analyses including EIMS and 1H- and 13C NMR spectra. The cytotoxicity of compound 3 was determined against MCF-7 and K562 cell lines and compared with the other compounds. A pharmacophore model was built based on potent input compounds to resolve important pharmacophore features responsible for cytotoxic activity of the isolated compounds.

Keywords: Abietane diterpenoids; Salvia spinosa L.; cytotoxic diterpenoids.

MeSH terms

  • Abietanes / chemistry
  • Abietanes / pharmacology
  • Antineoplastic Agents* / analysis
  • Antineoplastic Agents, Phytogenic* / chemistry
  • Diterpenes* / chemistry
  • Humans
  • MCF-7 Cells
  • Molecular Structure
  • Plant Extracts / analysis
  • Plant Roots / chemistry
  • Salvia* / chemistry

Substances

  • Abietanes
  • Antineoplastic Agents
  • Antineoplastic Agents, Phytogenic
  • Diterpenes
  • Plant Extracts