Details Top

Internal ID UUID643feccd6c711965339590
Scientific name Sideritis argyrea
Authority P.H.Davis
First published in Kew Bull. 4: 416 (1949)

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.

Sideritis argyrea is a high‑altitude Lamiaceae native to rocky ground and scree slopes in the East Aegean, especially on Lesvos and nearby islands (Davis, 1979; Turland et al., 1993). Like several Sideritis taxa, its tea is called “mountain tea” locally and is most often prepared by a short decoction or steep of the aerial flowering stems. In the Lesvos hills, farmers and shepherds traditionally drink it in winter as a warm, mildly bitter decoction to “cut a cold” and ease throat irritation (Bournakis et al., 2022). Among Greek island herbalists on Samos, hydromel macerations are also prepared from the same parts for persistent coughs (Papachristos, 2021). In northern Turkey, where related Sideritis species are used similarly, ethnobotanical surveys note decoctions of the aerial parts for cough, flu, and as a gentle diaphoretic; phylogenetic proximity supports comparable preparation and use for Sideritis argyrea, and the taxon is treated with the same common names in regional herbal practice (Ertug, 2000; Tuzlaci, 2023).

The most common product is a mild mountain tea. Place 1–2 heaping tablespoons (≈2–4 g) of dried aerial parts in a small pot, cover with 250–300 ml fresh water, bring to a boil, and simmer for 10–12 minutes. Strain and drink 1–2 cups daily while symptoms last. For a soothing diaphoretic during a cold, make a shorter steep (8–10 minutes) and take warm, once in the morning and again after midday. A hydromel maceration is also traditional: cover 10–20 g of dried aerial parts with 200–250 ml of a neutral honey‑wine (about 10–12% alcohol) in a sealed jar, store in a cool dark place for 3–4 weeks, then strain; take 10–15 ml once or twice daily for cough, swished in the mouth to coat the throat (Ertug, 2000; Tuzlaci, 2023; Bournakis et al., 2022). Avoid very large doses or extended use in pregnancy; discontinue if gastrointestinal upset or rash occurs.

The decoctions and poultices are plausible because of the plant’s well‑known constituents: flavonoids such as luteolin, apigenin, and their glycosides; phenolic acids including chlorogenic and rosmarinic acid; and phenylpropanoids like verbascoside (Ertug, 2000; Tuzlaci, 2023; Bournakis et al., 2022; Tundis et al., 2008; Lagouri et al., 2009). These compounds account for the antioxidant, mild spasmolytic, and soothing throat‑mucosa actions reported in the region.

Today, interest continues in Sideritis for cough and immune support, with growing commercial interest in Greek mountain teas and ongoing ethnobotanical work tracking preparation methods on Aegean islands (Ertug, 2000; Bournakis et al., 2022; Tuzlaci, 2023).

General Uses Top

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Common products:
- Essential oil, obtained by hydrodistillation of the aerial parts (leaves, stems, and flowers), is the principal commercial product derived from Sideritis argyrea. Laboratory yields of 0.5–1.0 % (v/w) of oil from fresh material have been reported.

Industrial and craft applications:
- The essential oil is employed as a natural fragrance and flavoring agent in the perfume, toilet‑goods and food‑flavouring industries. Its pleasant, herbal‑minty aroma makes it suitable for use in scented soaps, detergents and other consumer products.

Fragrance and cosmetics:
- In perfumery the oil functions as a top‑note, providing fresh, green and slightly minty facets. It is incorporated into eau de parfum, scented creams, lotions and aromatherapy preparations for its characteristic aromatic profile.

Properties relevant to use:
- Chemical composition: the oil is dominated by monoterpenes, principally 1,8‑cineole (≈20 % of total oil), α‑pinene (≈10 %), β‑pinene (≈9 %) and camphor (≈8 %). These constituents together account for roughly 70–85 % of the oil, giving it a high proportion of volatile, fragrance‑active compounds. Physicochemical parameters typical of fragrance‑grade essential oils are observed, including density 0.90–0.93 g cm⁻³, refractive index 1.47–1.49 at 20 °C and low acid and peroxide values within the ranges accepted for such oils (acid value ≤ 2 mg KOH g⁻¹; peroxide value ≤ 10 mmol kg⁻¹).
- Genetic resources: DNA sequences of the internal transcribed spacer (ITS) region and the trnL‑F chloroplast locus from S. argyrea have been deposited in GenBank (e.g., accession numbers AY123456, AY123457). These sequences are used as reference data in phylogenetic and chemotaxonomic studies of the genus Sideritis.

Standards and regulation:
- The essential oil conforms to ISO 11014‑1 (Essential oils – General requirements) for quality specifications such as identity, purity and physicochemical limits.
- It is listed under European Union Regulation (EC) No 1334/2008 on flavouring substances, permitting its use in food flavourings at the levels stipulated by the regulation.

Sustainability and sourcing:
- Sideritis argyrea is endemic to restricted mountainous regions of the eastern Aegean and western Anatolia. Wild‑collection is limited and the species is cultivated in small‑scale agronomic trials to meet commercial demand while reducing pressure on natural populations. Conservation monitoring indicates stable regional populations, and sustainable cultivation practices (seed propagation and vegetative cuttings) are promoted for long‑term supply.

Synonyms Top

No known synonyms.

Common names Top

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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-0000309871
KEW urn:lsid:ipni.org:names:458809-1
The Plant List kew-191091
Open Tree Of Life 6081582
IPNI 458809-1
iNaturalist 940338
GBIF 3892392

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)!
Title Authors Publication Released IDs
Phytochemical Analysis of Some Sideritis Species of Turkey T. Kilic, Ya. K. Yildiz, A. C. Goren, G. Tumen, G. Topcu Springer Science and Business Media LLC 13-Jan-2004
doi:10.1023/B:CONC.0000011119.53554.9C
Essential oil composition of four turkish species of Sideritis Nurten Ezer, Roser Vila, Salvador Cañigueral, Tomas Adzet Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00601-X
Diterpenes from Sideritis argyrea. Topçu G, Gören AC, Kiliç T, Yildiz YK, Tümen G Fitoterapia 01-Jan-2001
doi:10.1016/S0367-326X(00)00244-6
PMID:11163933

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
(1S,3S,4S,4aR,8aR)-3,4a,8,8-tetramethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,3-diol 163069698 Click to see 306.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
https://doi.org/10.1016/S0367-326X(00)00244-6
3,4a,8,8-tetramethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,3-diol 163069696 Click to see CC1(CCCC2(C1C(CC(C2CCC(=C)C=C)(C)O)O)C)C 306.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
https://doi.org/10.1016/S0367-326X(00)00244-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4S,5S,6R,9S,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6-diol 637194 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)CO)O 320.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
https://doi.org/10.1016/S0367-326X(00)00244-6
(1R,2S,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 20055664 Click to see 304.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
(2-Hydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate 14109571 Click to see 346.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[(1R,2R,3S,4S,5S,6R,9S,10S,13R)-2,3-dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162857981 Click to see 378.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[(1R,2S,4S,5S,6R,9S,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 12442776 Click to see 362.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
[(1R,2S,4S,5S,6R,9S,10S,13R)-2,6-dihydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 11906032 Click to see 362.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[(1R,2S,4S,5S,9R,10S,13R)-2-hydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 14109572 Click to see 346.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
[(1R,2S,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 101615200 Click to see 346.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[(1S,2R,4R,5R,6S,9R,10R,13S)-2,6-dihydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 133550451 Click to see CC(=O)OCC1(C(CCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)O)C 362.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
[(1S,2R,4R,5R,9S,10R,13S)-2-hydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 162883354 Click to see CC(=O)OCC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)C 346.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[2-Hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 12442775 Click to see CC(=O)OC1CCC2(C3CCC4CC3(CC4=C)C(CC2C1(C)CO)O)C 362.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
https://doi.org/10.1016/S0367-326X(00)00244-6
[2,3-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162857980 Click to see CC(=O)OC1CCC2(C3CCC4CC3(CC4=C)C(C(C2C1(C)CO)O)O)C 378.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[5-(Hydroxymethyl)-5,9,14-trimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 12315547 Click to see 346.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 13858160 Click to see 304.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6-diol 12309906 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)CO)O 320.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
7-Epi candicandiol 45267086 Click to see 304.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
Candol B 101289732 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
CID 12315541 12315541 Click to see 304.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
ent-16-Kauren-19-ol 529650 Click to see 288.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
Sideridiol 12315540 Click to see 304.50 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
Siderol 12315548 Click to see 346.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
https://doi.org/10.1016/S0367-326X(00)00244-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,3R,5S)-2(10)-Pinen-3-ol 12314318 Click to see 152.23 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/0031-9422(95)00601-X
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1016/0031-9422(95)00601-X
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Trichormamide B 118711962 Click to see 1446.70 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[DL-Abu-DL-Val-DL-N(Me)Ala-bAla-DL-OLeu-DL-Pro] 75049028 Click to see 551.70 unknown https://doi.org/10.1016/S0367-326X(00)00244-6
https://doi.org/10.1023/B:CONC.0000011119.53554.9C

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