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

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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

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Language Common/alternative name
English 'salvia africana-lutea' [ l. (1753) ]
Afrikaans bruinsalie
Hebrew מרווה זהובה
Swedish strandsalvia

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Plant Monoterpenes and Essential Oils as Potential Anti-Ageing Agents: Insights from Preclinical Data Zuzarte M, Sousa C, Alves-Silva J, Salgueiro L Biomedicines 04-Feb-2024
PMCID:PMC10886757
doi:10.3390/biomedicines12020365
PMID:38397967
A comparative analysis of morphology, microstructure, and volatile metabolomics of leaves at varied developmental stages in Ainaxiang (Blumea balsamifera (Linn.) DC.) Chen X, Li Y, Pang Y, Shen W, Chen Q, Liu L, Luo X, Chen Z, Li X, Li Y, Zhang Y, Huang M, Yuan C, Wang D, Guan L, Liu Y, Yang Q, Chen H, Wu H, Yu F Front Plant Sci 14-Nov-2023
PMCID:PMC10682096
doi:10.3389/fpls.2023.1285616
PMID:38034556
Enhanced Natural Strength: Lamiaceae Essential Oils and Nanotechnology in In Vitro and In Vivo Medical Research Kowalczyk T, Merecz-Sadowska A, Ghorbanpour M, Szemraj J, Piekarski J, Bijak M, Śliwiński T, Zajdel R, Sitarek P Int J Mol Sci 17-Oct-2023
PMCID:PMC10607815
doi:10.3390/ijms242015279
PMID:37894959
Advances in the Phytochemical Characterisation and Bioactivities of Salvia aurea L. Essential Oil Alves-Silva JM, Maccioni D, Cocco E, Gonçalves MJ, Porcedda S, Piras A, Cruz MT, Salgueiro L, Maxia A Plants (Basel) 09-Mar-2023
PMCID:PMC10056036
doi:10.3390/plants12061247
PMID:36986933
The Botanical, Chemical and Ethnobotanical Diversity of Southern African Lamiaceae Rattray RD, Van Wyk BE Molecules 18-Jun-2021
PMCID:PMC8233991
doi:10.3390/molecules26123712
PMID:34207006
Volatiles and Antifungal-Antibacterial-Antiviral Activity of South African Salvia spp. Essential Oils Cultivated in Uniform Conditions Najar B, Mecacci G, Nardi V, Cervelli C, Nardoni S, Mancianti F, Ebani VV, Giannecchini S, Pistelli L Molecules 10-May-2021
PMCID:PMC8126244
doi:10.3390/molecules26092826
PMID:34068756
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
Essential Oils and Their Main Chemical Components: The Past 20 Years of Preclinical Studies in Melanoma Di Martile M, Garzoli S, Ragno R, Del Bufalo D Cancers (Basel) 16-Sep-2020
PMCID:PMC7565555
doi:10.3390/cancers12092650
PMID:32948083
Antitumor Effect of the Essential Oil from the Leaves of Croton matourensis Aubl. (Euphorbiaceae) de Lima EJ, Alves RG, D´Elia GM, da Anunciação TA, Silva VR, Santos LD, Soares MB, Cardozo NM, Costa EV, da Silva FM, Koolen HH, Bezerra DP Molecules 14-Nov-2018
PMCID:PMC6278459
doi:10.3390/molecules23112974
PMID:30441836
Involvement of Bax and Bcl-2 in Induction of Apoptosis by Essential Oils of Three Lebanese Salvia Species in Human Prostate Cancer Cells Russo A, Cardile V, Graziano AC, Avola R, Bruno M, Rigano D Int J Mol Sci 19-Jan-2018
PMCID:PMC5796237
doi:10.3390/ijms19010292
PMID:29351194
Biological Activities of Essential Oils: From Plant Chemoecology to Traditional Healing Systems Sharifi-Rad J, Sureda A, Tenore GC, Daglia M, Sharifi-Rad M, Valussi M, Tundis R, Sharifi-Rad M, Loizzo MR, Ademiluyi AO, Sharifi-Rad R, Ayatollahi SA, Iriti M Molecules 01-Jan-2017
PMCID:PMC6155610
doi:10.3390/molecules22010070
PMID:28045446
Bioactive diterpenes from Orthosiphon labiatus and Salvia africana-lutea. Hussein AA, Meyer JJ, Jimeno ML, Rodríguez B J Nat Prod 01-Feb-2007
doi:10.1021/NP0680376
PMID:17256988
Light, Conventional and Environmental Scanning Electron Microscopy of the Trichomes of Cucurbita pepo subsp. pepo var. styriaca and Histochemistry of Glandular Secretory Products KOLB D, MÜLLER M Ann Bot 11-Aug-2004
PMCID:PMC4242234
doi:10.1093/aob/mch180
PMID:15306562
Chemical composition of essential oils from some Salvia species A. Bisio, G. Ciarallo, G. Romussi, N. Fontana, N. Mascolo, R. Capasso, D. Biscardi Wiley 10-Sep-2002
doi:10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
Development of Peltate Glandular Trichomes of Peppermint Turner GW, Gershenzon J, Croteau RB Plant Physiol 01-Oct-2000
PMCID:PMC59172
doi:10.1104/pp.124.2.665
PMID:11027716

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+3.0.CO;2-2
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+3.0.CO;2-2
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+3.0.CO;2-2
> 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+3.0.CO;2-2
> 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+3.0.CO;2-2
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+3.0.CO;2-2
alpha-Bergamotene 86608 Click to see 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
> 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+3.0.CO;2-2
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+3.0.CO;2-2
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+3.0.CO;2-2
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+3.0.CO;2-2
> 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+3.0.CO;2-2
Sylvestrene 12304570 Click to see 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
> 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+3.0.CO;2-2
beta Farnesene 15228937 Click to see 206.37 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
delta-Curcumene 57386731 Click to see 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
gamma-Curcumene 12304273 Click to see 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
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+3.0.CO;2-2
> 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+3.0.CO;2-2
1,7-di-epi-alpha-Cedrene 10878276 Click to see 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
> 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+3.0.CO;2-2
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+3.0.CO;2-2
7-Methoxyrosmanol 23243692 Click to see 360.40 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
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+3.0.CO;2-2
Carnosol 442009 Click to see 330.40 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-2
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+3.0.CO;2-2
> 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+3.0.CO;2-2
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+3.0.CO;2-2
> 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

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