Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Oct 8;15(1):35200.
doi: 10.1038/s41598-025-19109-0.

Secoisopimaranes from Salvia elegans Vahl leaves as antibacterial agents against Staphylococcus aureus

Affiliations

Secoisopimaranes from Salvia elegans Vahl leaves as antibacterial agents against Staphylococcus aureus

Gabin Thierry M Bitchagno et al. Sci Rep. .

Abstract

The genus Salvia contains around 1000 species and is primarily known to produce caffeic acid polymers and diterpenes. Of the bi- and tricyclic classes of diterpenes found in Salvia, isopimaranes are the least represented. The bio-guided metabolomic analysis of the leaves of Salvia elegans Vahl revealed the occurrences of three secoisopimaranes (1-3), of which the known 3,4-secoisopimara-7,15-dien-3-oic acid was the most abundant and showed potent antimicrobial activity against Staphylococcus aureus with a MIC = 15.6 µg/mL (51.6 µM). All three diterpenes were detected in domesticated and wild specimens of the closely related species Salvia cinnabarina M.Martens & Galeotti, but not in other species reportedly to be closely related to S. elegans. Diterpenoids from Salvia are an interesting group of biologically active molecules and their distribution within the genus justifies further study.

Keywords: Salvia; Staphylococcus aureus; Lamiaceae; Metabolomic; Secoisopimarane; Structure elucidation.

PubMed Disclaimer

Conflict of interest statement

Declarations. Competing interests: The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Structures of isolated compounds 15.
Fig. 2
Fig. 2
Selected COSY (bold lines), HMBC (blue arrows) and NOESY (red double arrows) correlations in compounds 2 and 3.
Fig. 3
Fig. 3
Proposed biosynthesis route to compounds 13.

References

    1. Herrera-Ruiz, M. et al. Antidepressant and anxiolytic effects of hydroalcoholic extract from Salvia elegans. J. Ethnopharmacol.107, 53–58 (2006). - PubMed
    1. González-Cortazar, M. et al. Isosakuranetin-5-O-rutinoside: A new Flavanone with antidepressant activity isolated from Salvia elegans Vahl. Molecules18, 13260–13270 (2013). - PMC - PubMed
    1. Wu, Y. B. et al. Constituents from species and their biological activities. Chem. Rev.112, 5967–6026 (2012). - PubMed
    1. Bonito, M. C. et al. Biological activity of bicyclic and tricyclic diterpenoids from Salvia species of immediate Pharmacological and pharmaceutical interest. Nat. Prod. Commun.6, 1205–1215 (2011). - PubMed
    1. Romussi, G. et al. A new diterpenoid with antispasmodic activity from Salvia cinnabarina. Planta Med.67, 153–155 (2001). - PubMed

MeSH terms

LinkOut - more resources