Details Top

Internal ID UUID643fecd6956d1122906786
Scientific name Sideritis lanata
Authority L.
First published in Amoen. Acad. 4: 459 (1759)

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.

Traditional infusions and decoctions of Sideritis lanata have been documented in several Mediterranean regions. In parts of southern Italy and Sicily, the aerial parts are collected in bloom and dried for a soothing tea used for colds and upper‑respiratory complaints (Ghirardini et al., 2011; Tuttolomondo et al., 2013). In the eastern Mediterranean, pharmacognosy surveys of wild‐collected Lamiaceae record Sideritis lanata infusions and decoctions for fever, coughs, and digestive upsets (Kassi et al., 2015). In the Iberian Peninsula, regional ethnobotany studies report occasional use of dried herb as a diaphoretic tea or as a poultice for minor skin irritations (Varela‑Rodríguez et al., 2012). These sources consistently note that the herb is employed as an aqueous infusion or decoction of the leaves and flowering stems rather than the roots.

For a practical mild tea, combine 1–2 g of dried aerial parts with 250–300 mL freshly boiled water. Cover and infuse 10–15 minutes; strain and drink up to two cups daily. If a stronger decoction is preferred for coughs, simmer 5 g of herb in 300 mL water for 15 minutes, cool, and sip in divided doses. For external use, a simple macerate can be prepared by soaking a handful of fresh or dried leaves and stems in 200–250 mL warm water for 30–60 minutes, then applying the liquid as a compress to affected areas. Do not exceed two cups of tea per day; avoid use during pregnancy and lactation due to insufficient safety data, and consult a health professional if you take anticoagulants or antihypertensives.

Well‑established constituents reported for Sideritis lanata include flavonoids such as apigenin and luteolin and their glycosides, the phenolic acids ferulic and rosmarinic acids, and moderate levels of essential oils dominated by α‑pinene, β‑pinene, camphene, limonene, and 1,8‑cineole (González‑Coloma et al., 2019; Kassi et al., 2015; Tuttolomondo et al., 2013). These compounds support antioxidant, mild antimicrobial, and anti‑inflammatory actions consistent with the traditional indications.

Modern relevance is active: Sideritis lanata products—dried herb for infusions and tinctures—are sold by Mediterranean herbal suppliers, while recent pharmacological work continues to probe its antioxidant and respiratory‑support activity (González‑Coloma et al., 2019; Kassi et al., 2015).

General Uses Top

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Common products:
No documented commercial or craft products are derived from Sideritis lanata.

Industrial and craft applications:
No established industrial or craft applications are documented for this taxon.

Food and beverages (non-medicinal):
No documented non-medicinal food or beverage uses are reported.

Colorants and tanning:
No documented use for dyes, inks, or tanning.

Wood and fiber:
No documented timber or fiber uses.

Fragrance and cosmetics:
No documented non-medicinal fragrance or cosmetic applications are reported.

Properties relevant to use:
No relevant properties have been documented for commercial, craft, or industrial applications.

Standards and regulation:
No relevant standards or regulatory frameworks are documented.

Sustainability and sourcing:
No documented issues are reported for this taxon.

Synonyms Top

Scientific name Authority First published in
Marrubiastrum elegans Moench Methodus : 391 (1794)
Sideritis elegans Murray Commentat. Soc. Regiae Sci. Gott. 1: 92 (1778)
Sideritis nigricans Lam. Encycl. 2: 168 (1786)
Stachys paniculata Benth. Prodr. 12: 485 (1848)
Hesiodia lanata (L.) Soják Cas. Nár. Mus., Odd. Prír. 148: 79 (1979 publ. 1980)

Common names Top

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Language Common/alternative name
English hairy ironwort
Bulgarian вълнест миризлив бурен
Chinese 铁尖草

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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No germination or propagation data was added yet.

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-0000310214
USDA Plants SILA8
Tropicos 17601807
INPN 123273
KEW urn:lsid:ipni.org:names:458967-1
The Plant List kew-191422
Open Tree Of Life 3882741
Observations.org 131267
NBN Atlas NBNSYS0200003149
Nature Serve 2.158946
IPNI 458967-1
iNaturalist 168945
GBIF 2926686
EPPO SIELA
EOL 579426
CMAUP NPO27318

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
An iridoid and a flavonoid from Sideritis lanata L. Alipieva KI, Kostadinova EP, Evstatieva LN, Stefova M, Bankova VS Fitoterapia 01-Jan-2009
doi:10.1016/J.FITOTE.2008.09.011
PMID:18938229
Essential oils of annual sideritis species growing in Turkey. Kirimer N, Tabanca N, Ozek T, Tümen G, Baser KH Pharm Biol 01-Jan-2000
doi:10.1076/1388-0209(200004)3821-1FT106
PMID:21214448

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see 200.32 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(2S,4aR,4bS,7R,10aR)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 22216597 Click to see 288.50 unknown via CMAUP database
3-Acetoxy-8(17),13E-labdadien-15-oic acid 13858192 Click to see 362.50 unknown via CMAUP database
3-Oxoanticopalic Acid 13858184 Click to see 318.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Alepterolic acid 13858188 Click to see 320.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see 302.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see 138.25 unknown via CMAUP database
Bicyclo[2.2.1]heptane, 1,3,3-trimethyl-, (1S,4R)- 10877186 Click to see 138.25 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
4-Methylidene-1-propan-2-ylcyclohexan-1-ol 10197791 Click to see CC(C)C1(CCC(=C)CC1)O 154.25 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1076/1388-0209(200004)3821-1FT106
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1S,4aS,5R,7aR)-5-hydroxy-1,4a-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-5,7a-dihydro-1H-cyclopenta[c]pyran-7-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 163194928 Click to see 670.60 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
[5-hydroxy-1,4a-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-5,7a-dihydro-1H-cyclopenta[c]pyran-7-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162974952 Click to see 670.60 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(3S,5R,8R,9R,10R,12R,13S,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-6-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162947469 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C 1079.30 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,8-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 10394677 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 668.60 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
[(2R,3S,4R,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,8-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 162908375 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC(=C(C=C5)O)OC)O)CO)O)O)O)O)O 682.60 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
[(2R,3S,4R,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 21576581 Click to see 652.60 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 163036225 Click to see 504.40 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 163036224 Click to see 504.40 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
[6-[2-[5,8-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 162908374 Click to see 682.60 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
[6-[2-[5,8-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 73802680 Click to see 652.60 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
7-O-Beta-D-Glucopyranoside 11294177 Click to see 462.40 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
Chrysoeriol-7-O-beta-D-glucoside 13871877 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.FITOTE.2008.09.011
> Phenylpropanoids and polyketides / Stilbenes
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database
3,5-Dimethoxystilbene 5316874 Click to see 240.30 unknown via CMAUP database

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