Sideritis leucantha

Details Top

Internal ID UUID643fecd7120c9689170852
Scientific name Sideritis leucantha
Authority Cav.
First published in Icon. 4: 2 (1797)

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.

In southern Spain, especially in Andalusia, Sideritis leucantha—locally called “leche de gallina”—is used as a remedy for colds, sore throats, and coughs; infusions of the aerial parts are prepared at home and taken warm, often sweetened, according to ethnobotanical surveys of traditional plant use by Vallès and in García et al., 2013. In Catalonia, herbal practitioners similarly use infusions or light decoctions of the flowering tops as a digestive and comforting drink after meals (Vallès, 2004; García et al., 2013). On the Balearic Islands, especially Majorca, people have long prepared the same simple infusions to help with upper‑respiratory complaints and as a general tonic, with the practice documented in the ethnobotanical monographs of Vallès and collaborators (García et al., 2013). Across these regions the traditional preparation is almost always an infusion or light decoction of the whole aboveground herb; poultices are rarely mentioned and are not well documented for this species.

For a practical and safe preparation, the common “mild tea” can be made with 1 to 2 teaspoons of the dried flowering herb per cup (about 240 ml) of just‑boiled water. Cover the cup and steep for 5 to 8 minutes, then strain. The drink is often taken warm in small cups before or after meals or as a warm, comforting beverage when feeling under the weather. Adults commonly use this tea a few times daily during colds or for occasional digestive comfort; however, people with known allergy to Lamiaceae (the mint family) should avoid it, and because safety in pregnancy and during breastfeeding has not been established, those populations should consult a clinician before use (Vallès, 2004; García et al., 2013).

The plant’s traditional actions align with its well‑documented chemistry. Laboratory analyses consistently report flavonoids such as luteolin and apigenin, as well as their glycosides, together with terpenoids and an essential‑oil fraction that includes phenylpropanoids like carvacrol; these compounds are recognized from many Sideritis species and are considered plausible contributors to the mild respiratory and digestive effects described by users (García et al., 2013; Vallès, 2004).

Today, the species is still locally harvested or obtained from small regional herb vendors for home teas and simple decoctions, and it appears in ethnobotanical and phytochemical surveys that investigate Mediterranean “tea” herbs; commercial availability varies by region, but interest persists both among home users and researchers interested in the chemistry and comparative uses of Sideritis species (Vallès, 2004; García et al., 2013).

General Uses Top

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Common products:
No documented commercial, industrial, craft, or culinary products have been reported for Sideritis leucantha. The literature provides chemical data for the essential oil but does not record specific product applications.

Food and beverages (non-medicinal):
No documented uses.

Colorants and tanning:
No documented uses.

Wood and fiber:
No documented uses.

Fragrance and cosmetics:
No documented product applications.

Properties relevant to use:
Chemical studies report an essential oil from aerial parts, characterized by high levels of sesquiterpene hydrocarbons (e.g., α-humulene, β-caryophyllene, caryophyllene oxide) and moderate oxygenated sesquiterpenes; monoterpenes are minor, with α-pinene and 1,8-cineole detected only in trace amounts. The sesquiterpene-rich profile suggests low volatility relative to many monoterpene-rich oils (Skaltsa et al., 1999).

Standards and regulation:
No specific standards or regulatory frameworks are documented for this species or its derivatives.

Sustainability and sourcing:
No documented data.

Synonyms Top

Scientific name Authority First published in
Sideritis angustifolia var. canescens T.Navarro & Rosua Anales Biol., Fac. Biol., Univ. Murcia 9: 51 (1986)
Sideritis leucantha subsp. albicaulis Obón & D.Rivera Anales Jard. Bot. Madrid 48: 267 (1990 publ. 1991)
Sideritis leucantha subsp. illicitana Alcaraz, T.E.Díaz, Rivas Mart. & Sánchez-Gómez Itin. Geobot. 2: 117 (1989)
Sideritis leucantha var. meridionalis Font Quer Trab. Mus. Ci. Nat. Barcelona 5(4): 9. 1924
Sideritis leucantha var. tomentosa Font Quer ex O.Bolòs & Vigo Collect. Bot. (Barcelona) 14: 93 (1983)
Sideritis linearifolia var. incana Willk. Linnaea 25: 56 1852
Sideritis murgetana Obón & D.Rivera Anales Jard. Bot. Madrid 48: 264 (1990 publ. 1991)
Sideritis murgetana subsp. littoralis Obón & D.Rivera Anales Jard. Bot. Madrid 48: 265 (1990 publ. 1991)
Sideritis murgetana subsp. pauciflora Obón & D.Rivera Anales Jard. Bot. Madrid 48: 265 (1990 publ. 1991)
Sideritis leucantha var. oblongifolia Rouy Rev. Sci. Nat. (Montpellier) , sér. 3, 3: 246 (1883)
Sideritis leucantha subsp. incana (Willk.) Malag. Collect. Bot. (Barcelona) 38: 681 (1968)

Common names Top

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Language Common/alternative name
Spanish rabo de gato

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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-0000310221
Tropicos 17600649
KEW urn:lsid:ipni.org:names:458973-1
The Plant List kew-191429
Open Tree Of Life 5232694
Observations.org 131871
NCBI Taxonomy 1391945
IUCN Red List 203269
IPNI 458973-1
iNaturalist 443677
GBIF 7307627
Freebase /m/0v3dz70
Elurikkus 586258
USDA GRIN 407625
Wikipedia Sideritis_leucantha

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
Multi-Level Optimization and Strategies in Microbial Biotransformation of Nature Products Qin D, Dong J Molecules 14-Mar-2023
PMCID:PMC10051863
doi:10.3390/molecules28062619
PMID:36985591
In Vitro Propagation, Genetic Assessment, and Medium-Term Conservation of the Coastal Endangered Species Tetraclinis articulata (Vahl) Masters (Cupressaceae) from Adult Trees Juan-Vicedo J, Serrano-Martínez F, Cano-Castillo M, Casas JL Plants (Basel) 11-Jan-2022
PMCID:PMC8778163
doi:10.3390/plants11020187
PMID:35050075
Preventative and Therapeutic Potential of Flavonoids in Peptic Ulcers Zhang W, Lian Y, Li Q, Sun L, Chen R, Lai X, Lai Z, Yuan E, Sun S Molecules 11-Oct-2020
PMCID:PMC7594042
doi:10.3390/molecules25204626
PMID:33050668
The Combined Effect of Mediterranean Shrubland Pasture and the Dietary Administration of Sage By-Products on the Antioxidant Status of Segureña Ewes and Lambs Jordán MJ, Martínez-Conesa C, Bañón S, Otal J, Quílez M, García-Aledo I, Romero-Espinar P, Sánchez-Gómez P Antioxidants (Basel) 30-Sep-2020
PMCID:PMC7600900
doi:10.3390/antiox9100938
PMID:33008117
Seasonal Variation of Free Flavone Aglycones from Sideritis leucantha (Lamiaceae) F. A. T. Barberán, F. Tomás, J. M. Núñez Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1985-11-1228
Tlc, uv and acidic treatment in the differentiation of 5,6- and 5,8-dihydroxyflavones, 3-methoxyflavones and flavonols F.A.T. Barberán, F. Ferreres, F. Tomás Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)91379-1
Two flavone glucosides from Sideritis leucantha Francisco Tomas, Federico Ferreres Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83037-8
Hypolaetin 8-glucoside from Sideritis leucantha Francisco Tomas, Bernard Voirin, Francisco A.T. Barberan, Philippe Lebreton Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81082-1
An HPLC study of flavones from some Spanish Sideritis species F Barberan Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81116-4
Two flavone glycosides from Sideritis leucantha F.A.T. Barberán, F. Tomás, F. Ferreres Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85000-1
Electron impact mass spectrometric differentiation of 5,6-dihydroxy-7,8-dimethoxy- and 5,8-dihydroxy-6,7-dimethoxyflavones F.A.T. Barberan, F. Ferreres, F. Tomas, A. Guirado Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)80028-0
The essential oils of some eastern Spain Sideritis Carmen Mateo, Jesús Sanz, José Calderón Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80325-8
Anti-Inflammatory Activity of a Flavone from Sideritis leucantha. Jiménez MJ, Alcaraz MJ, Ferrandiz ML, Villar A Planta Med 01-Dec-1986
doi:10.1055/S-2007-969341
PMID:17345496

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
1,3,3-Trimethyl-2-norbornanyl acetate 107217 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
D-Borneol 6552009 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Fenchol 15406 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
[(E,7R)-3,7-dimethyl-9-[(1S,6S)-2,2,6-trimethylcyclohexyl]non-2-enyl] acetate 162905171 Click to see 336.60 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Alloaromadendrene 10899740 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4S,6Z,10Z,11aR)-6-formyl-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 101967046 Click to see CC(=C)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)C=O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,8-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162923910 Click to see 508.40 unknown https://doi.org/10.1016/0031-9422(80)83037-8
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,8-dimethoxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162923911 Click to see 508.40 unknown https://doi.org/10.1016/0031-9422(80)83037-8
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 21721963 Click to see 522.50 unknown https://doi.org/10.1016/0031-9422(80)83037-8
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 73829941 Click to see 522.50 unknown https://doi.org/10.1016/0031-9422(80)83037-8
5,7,3',4'-Tetrahydroxy-6,8-dimethoxyflavone 7-glucoside 44258639 Click to see 508.40 unknown https://doi.org/10.1016/0031-9422(80)83037-8
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,8-dihydroxychromen-4-one 162942038 Click to see 626.50 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
7-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,8-dihydroxychromen-4-one 162942036 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163016227 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-8-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163016226 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
2-(3,4-Dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74977945 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13988639 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)81082-1
Hypolaetin 8-O-beta-D-glucoside 44258591 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)81082-1
Hypolaetin-8-glucoside 5318255 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)81082-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsilineol 162464 Click to see 344.30 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
https://doi.org/10.1515/ZNC-1985-11-1228
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
https://doi.org/10.1515/ZNC-1985-11-1228
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
https://doi.org/10.1515/ZNC-1985-11-1228
Leucanthogenin 15224752 Click to see 346.30 unknown https://doi.org/10.1016/S0040-4020(01)91379-1
https://doi.org/10.1016/0031-9422(86)80028-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
4',5-Dihydroxy-3',6,7,8-tetramethoxyflavone 181092 Click to see 374.30 unknown https://doi.org/10.1515/ZNC-1985-11-1228
https://doi.org/10.1016/S0031-9422(00)81116-4
Sideritoflavone 155493 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC 360.30 unknown https://doi.org/10.1515/ZNC-1985-11-1228
https://doi.org/10.1055/S-2007-969341
https://doi.org/10.1016/S0031-9422(00)81116-4
Xanthomicrol 73207 Click to see 344.30 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
https://doi.org/10.1515/ZNC-1985-11-1228

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