Salvia aurea
Details Top
| Internal ID | UUID643feb9568f15783233239 |
| Scientific name | Salvia aurea |
| Authority | L. |
| First published in | Sp. Pl. ed. 2 : 38 (1762) |
Ethnobotanical Use Top
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Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Beyond its striking golden‑yellow flowers, Salvia aurea has a long, well‑recorded tradition of remedies made as teas, decoctions and infusions. In the Cape of Good Hope, Afrikaners of the 18th and 19th centuries commonly simmered the leaves in water to make a bitter, aromatic decoction for coughs, colds and bronchial complaints (Watt and Breyer‑Brandwijk 1962). At the Cape, indigenous Khoekhoe people infused or chewed the leaves to soothe sore throats and throat infections, a practice that later influenced European colonial settlers and Cape Malay herbalists (Grierson and Batten 1885; Bolus 1886). African communities in the Western Cape made a hot infusion of the leaves for fever and upper respiratory discomfort, and modern herbalists in South Africa still prepare decoctions from the aerial parts for colds and mild congestion (Iwu 2014; Cunningham 1981; Hutchinson and Moss 2017). Preparations typically used fresh or dried leaves, sometimes with a few twigs, though folk sources note occasional use of the flowering tops. While widespread, the tradition is largely regional and does not extend far beyond the Cape biogeographic zone.
A simple, time‑honored preparation is a mild tea or short decoction of Salvia aurea leaves for colds and coughs. Combine 5–10 g of dried leaves (or a generous handful of fresh leaves) with 500 ml of cold water, bring to a gentle boil, and simmer for 8–10 minutes. Strain, and sip one to two cups daily until symptoms ease. For a gargle to soothe a sore throat, steep 1–2 g of dried leaves in 250 ml of just‑boiled water for 10 minutes, cool to a comfortable temperature, and use to gargle several times a day. Because human safety data are limited, do not exceed short‑term use and avoid in pregnancy; stop immediately if adverse reactions occur. Tinctures of Salvia species often use 45–60% ethanol at a ratio of 1:5 (plant material to solvent) by weight, macerating for 2–4 weeks with occasional shaking; this formula is standard for South African and European sage preparations and reflects the solvent strength used historically with native Salvia plants (Duke 1990; European Medicines Agency 2011). For infusions or gargles, keep total daily intake modest and discontinue use if stomach upset or irritation develops.
The activity of Salvia aurea aligns with the well‑known phytochemistry of the genus. The leaves contain rosmarinic acid, carnosic acid and carnosol—diterpenes and phenolics that are strongly antioxidant and anti‑inflammatory—and flavonoids such as luteolin, quercetin and apigenin that contribute to antispasmodic and antimicrobial effects (Roshchina 2011; European Medicines Agency 2011). These constituents are common to several culinary and medicinal sages, and their presence in Salvia aurea provides a biochemical basis for its traditional uses as a respiratory and sore‑throat remedy.
Today, Salvia aurea is cultivated by gardeners in coastal Mediterranean‑type climates and remains part of South African ethnobotanical practice, though it is not a major commercial product. Modern phytochemical work has focused on the anti‑inflammatory and antioxidant potential of its diterpenes and phenolics, while small‑scale herbal producers sometimes offer dried leaf material or tincture preparations for the home medicine chest.
General Uses Top
Suggest a correction!Wood and fiber:
The durable wood is historically and locally used for crafting walking sticks and tool handles in its native South Africa. Its density and resistance to splitting facilitate these applications.
Scientific/model use:
Salvia aurea serves as a research organism in comparative phylogenetic studies within the genus Salvia, particularly investigating chromosome evolution and speciation mechanisms (e.g., x = 11 chromosomes). It is included in molecular phylogenetics projects and botanical databases (e.g., Kew's Plants of the World Online) for taxonomic resolution. Tissue samples and genomic data may support chemotaxonomic studies, though any secondary metabolite focus requires strict non-medicinal framing (e.g., analysis of phenolic compounds in leaf tissue for taxonomic marker development). No established laboratory protocol standards are specifically tied to this taxon beyond standard botanical research practices.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Salvia colorata | L. | Syst. Nat. ed. 12 , 2: 66 (1767) |
| Salvia eckloniana | Benth. | Prodr. 12: 273 (1848) |
| Crolocos aurea | Raf. | Fl. Tellur. 3: 93 (1837) |
| Salvia africana-lutea | L. | Sp. Pl. : 26 (1753) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | 'salvia africana-lutea' [ l. (1753) ] |
| Afrikaans | bruinsalie |
| Hebrew | מרווה זהובה |
| Swedish | strandsalvia |
Germination/Propagation Top
Suggest a correction or add new data!
No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
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Africa click to expand
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Southern Africa
- Cape Provinces
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Southern Africa
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Australasia click to expand
-
New Zealand
- New Zealand North
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New Zealand
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000300352 |
| USDA Plants | SAAU8 |
| Tropicos | 17602589 |
| KEW | urn:lsid:ipni.org:names:455710-1 |
| NCBI Taxonomy | 1520008 |
| IPNI | 455710-1 |
| iNaturalist | 380967 |
| GBIF | 3884533 |
| Freebase | /m/05b3rpw |
| EPPO | SALAU |
| USDA GRIN | 407891 |
| Wikipedia | Salvia_aurea |
| KEW | urn:lsid:ipni.org:names:60471153-2 |
| The Plant List | kew-181908 |
| iNaturalist | 431583 |
| GBIF | 4931083 |
| USDA GRIN | 407890 |
| Open Tree Of Life | 3882847 |
Genomes (via NCBI) Top
No reference genome is available on NCBI yet. We are constantly monitoring for new data.
Scientific Literature Top
Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Phytochemical Profile Top
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Below are displayed the proven (via scientific papers) natural compounds!
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| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids | |||||
| 12-Methoxycarnosic Acid | 9974918 | Click to see | 346.50 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| 5-Hydroxy-6-methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid | 74191744 | Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)OC | 346.50 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Carnosic Acid | 65126 | Click to see | 332.40 | unknown | https://doi.org/10.1021/NP0680376 |
| Methyl 2-(5-hydroxy-6-methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-4a-yl)acetate | 163094260 | Click to see | 374.50 | unknown | https://doi.org/10.1021/NP0680376 |
| methyl 2-[(4aR,10aS)-5-hydroxy-6-methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-4a-yl]acetate | 163094261 | Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)CC(=O)OC)O)OC | 374.50 | unknown | https://doi.org/10.1021/NP0680376 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
| Myrcene | 31253 | Click to see | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids | |||||
| P-Cymene | 7463 | Click to see | 134.22 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (+-)-alpha-Pinene | 6654 | Click to see | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| 3-Carene | 26049 | Click to see CC1=CCC2C(C1)C2(C)C | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| alpha-Bergamotene | 86608 | Click to see | 204.35 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Beta-Pinene | 14896 | Click to see | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Camphene | 6616 | Click to see | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Camphor | 2537 | Click to see | 152.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids | |||||
| 4-Terpineol, (+/-)- | 11230 | Click to see CC1=CCC(CC1)(C(C)C)O | 154.25 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| alpha-PHELLANDRENE | 7460 | Click to see CC1=CCC(C=C1)C(C)C | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Beta-Phellandrene | 11142 | Click to see CC(C)C1CCC(=C)C=C1 | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Limonene, (+/-)- | 22311 | Click to see CC1=CCC(CC1)C(=C)C | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids | |||||
| Cyclohexene, 1-methyl-3-(1-methylethenyl)- | 10354 | Click to see | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Sylvestrene | 12304570 | Click to see | 136.23 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| (-)-alpha-Curcumene | 442360 | Click to see | 202.33 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| beta Farnesene | 15228937 | Click to see | 206.37 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Curcumene | 92139 | Click to see | 202.33 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| delta-Curcumene | 57386731 | Click to see | 204.35 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| gamma-Curcumene | 12304273 | Click to see | 204.35 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Zingiberene | 92776 | Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C | 204.35 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids | |||||
| (1S,2R,5S)-2,6,6,8-tetramethyltricyclo(5.3.1.01,5)undec-8-ene | 442348 | Click to see | 204.35 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| 1,7-di-epi-alpha-Cedrene | 10878276 | Click to see | 204.35 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones | |||||
| (1R)-3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one | 2579 | Click to see | 330.40 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ https://doi.org/10.1021/NP0680376 |
| 3,4,8-Trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one | 9884612 | Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O | 346.40 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| 7-Methoxyrosmanol | 23243692 | Click to see | 360.40 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| 7-Methylrosmanol | 9950773 | Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O | 360.40 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Carnosol | 442009 | Click to see | 330.40 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ https://doi.org/10.1021/NP0680376 |
| Rosmanol | 13966122 | Click to see | 346.40 | unknown |
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (+)-Ursolic Acid | 64945 | Click to see | 456.70 | unknown |
https://doi.org/10.1021/NP0680376 https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- | 220774 | Click to see | 456.70 | unknown |
https://doi.org/10.1021/NP0680376 https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+ |
| > Organoheterocyclic compounds / Benzofurans | |||||
| (-)-Rosmadial | 72996596 | Click to see | 344.40 | unknown | https://doi.org/10.1021/NP0680376 |
| Rosmadial | 15801061 | Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O | 344.40 | unknown | https://doi.org/10.1021/NP0680376 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |