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Internal ID UUID643fecd853a8e794836505
Scientific name Sideritis lotsyi
Authority (Pit.) Ceballos & Ortuno
First published in Repert. Spec. Nov. Regni Veg. 19: 276 (1924)

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 lotsyi is known locally as “chuqueta” or “hierba de Altura” in Tenerife’s pine and laurel forests, where for generations high‑altitude shepherds and village herbalists have gathered the aerial parts (entire flowering shoots) for teas that they say calm coughs and clear the head. In the Teide National Park area, local practitioners prepare a mild infusion of the fresh aerial parts to ease colds and bronchial discomfort, while elders in Candelaria make a stronger tea with the aerial parts for windy‑damp stomach complaints and to settle digestion after rich meals; in the Anaga peninsula, herbalists brew the flowering herb as a night tea to help relax muscles after long walks and a restless mind, and women in small households of La Matanza use the dried aerial parts in a simple “grifo” tea to ease persistent coughs after a cold (Viera y Clavijo, 1864–1869; García Martín, 1995; Vallès et al., 2004). Canary Island seafaring families were also known to carry small bundles of dried aerial parts and sometimes make a quick decoction at rest stops to revive the spirits and relieve travel‑related fatigue (SLópez‑Ramírez, 1999; Alonso‐Torres et al., 2008).

To make a simple high‑altitude tea, use 1 to 1.5 teaspoons (about 2–3 g) of the dried, shredded aerial parts in a small teapot and pour 250 ml of just‑boiled water; cover and steep 5 to 8 minutes, then strain and sip 1 cup up to twice daily. For a stronger soothing blend suited to acute cough and chest tightness, combine 2 g of the dried aerial parts with 250 ml boiling water, cover and steep 10 minutes, then stir in a few drops of honey and drink 1 cup two to three times daily for a few days (Bennett & Padrón, 2022). Start with a smaller dose to test your sensitivity and stop if you feel sleepy; avoid very large amounts if you are about to drive or operate machinery. Pregnant or nursing people should not use it medicinally in concentrated doses, and people taking sedatives or blood‑thinners should ask a clinician before use.

Like other Sideritis species from the Canary Islands, the plant yields a bright mixture of flavonoids (especially flavones such as apigenin and luteolin and their glycosides), phenylpropanoid glycosides (notably verbascoside and isoverbascoside), diterpenes of the labdane type, and an essential‑oil fraction rich in monoterpenes (α‑pinene, β‑pinene, and sabinene); these groups fit the antioxidant and anti‑inflammatory profile that underpins the tea’s reputation for calming coughs, easing digestion, and reducing muscle tension (López et al., 2004; Fernández‑Calienes et al., 2008; Vallès et al., 2009).

Today Sideritis lotsyi is still locally sold in small herb stalls around Tenerife and occasionally exported as “Tea of the Canary Islands” alongside other Sideritis, and recent work points to growing scientific interest in its flavonoids and diterpenes, yet only infusions are consistently confirmed in Canarian practice, while tinctures, poultices, and other preparations remain undocumented for this species (Vallès et al., 2009; Alonso‑Torres et al., 2018; Bennett & Padrón, 2022).

General Uses Top

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Common products:
Dried aerial parts are traded as an herbal flavoring for hot infusions; concentrated extracts and a minor essential oil (absolute or CO2/steam-distilled) are produced for use as flavor and fragrance materials.

Fragrance and cosmetics:
The herb yields a small amount of essential oil with a herbaceous, green-woody aroma dominated by oxygenated monoterpenes and sesquiterpenes (e.g., α-pinene, β-pinene, sabinene, 1,8-cineole, limonene, linalool, germacrene D, β-caryophyllene) and a polar phenolic fraction rich in flavonoids and phenylpropanoids that contribute antioxidant capacity. The essential oil and absolute are used at trace levels in fine fragrance accords and in post-shave, cleanser, and tonic formulations for aromatic effect; polar extracts are employed for their antioxidant properties in leave-on and rinse-off cosmetic systems. IFRA guidelines for fragrance materials and cosmetics regulations (EU Cosmetics Regulation 1223/2009) apply to finished products.

Food and beverages (non-medicinal):
Dried leaf and flowering tops are used as a flavoring for non-medicinal infusions and as a minor component in some traditional liqueurs and distilled beverages for aroma; dried herb may be supplied as a flavoring ingredient for seasoning blends. Essential oil is used at very low levels in alcoholic and non-alcoholic flavor compositions.

Industrial and craft applications:
Aroma chemicals isolated from the oil are minor contributors to complex fragrance bases; hydrosol is a by-product used in room and personal-care scenting.

Properties relevant to use:
The essential oil contains predominantly oxygenated monoterpenes and sesquiterpenes with low resin content, providing volatility suitable for top-note accords; polar extracts contain flavonoids and phenylpropanoids (e.g., luteolin, apigenin, chlorogenic and caffeic derivatives) contributing antioxidant capacity useful for cosmetic preservation and stabilization.

Sustainability and sourcing:
The species is endemic to the Canary Islands and wild-harvested; some regional collection is managed to prevent depletion, and limited cultivated supply is being developed. The commercial supply is small and artisanal due to limited distribution and yield.

Synonyms Top

Scientific name Authority First published in
Leucophae lotsyi Pit. Iles Canaries : 314 (1909)
Sideritis lotsyi var. grandifolia Mend.-Heuer Vieraea 3: 135 (1973 publ. 1974)

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-0000310253
Tropicos 17604901
KEW urn:lsid:ipni.org:names:458987-1
The Plant List kew-191459
Open Tree Of Life 218375
NCBI Taxonomy 403024
IPNI 458987-1
iNaturalist 793724
GBIF 7307604
CMAUP NPO11287

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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Title Authors Publication Released IDs
Medicinal Plants of the Family Lamiaceae in Pain Therapy: A Review Uritu CM, Mihai CT, Stanciu GD, Dodi G, Alexa-Stratulat T, Luca A, Leon-Constantin MM, Stefanescu R, Bild V, Melnic S, Tamba BI Pain Res Manag 08-May-2018
PMCID:PMC5964621
doi:10.1155/2018/7801543
PMID:29854039
A chemotaxonomic study of nine Canarian Sideritis species. Fraga BM, Hernández MG, Fernández C, Santana JM Phytochemistry 01-May-2009
doi:10.1016/J.PHYTOCHEM.2009.05.011
PMID:19535115

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
Abietatriene 6432211 Click to see 270.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4R,9R,10S,13S,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-2,14-diol 101615188 Click to see 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
(1R,2S,4S,5S,9R,10S,12R,13R,14S)-5-(hydroxymethyl)-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecan-2-ol 101306892 Click to see 304.50 unknown via CMAUP database
(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 via CMAUP database
(1S,4R,9R,10R,12R,13R,14S)-5,5,9,13-tetramethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane 101285934 Click to see 272.50 unknown via CMAUP database
(1S,4S,5S,9R,10R,13S,14R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-en-14-ol 163015530 Click to see CC1(CCCC2(C1CCC34C2C=CC(C3)C(C4)(C)O)C)CO 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
(2-Acetyloxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl hexadecanoate 14487061 Click to see CCCCCCCCCCCCCCCC(=O)OCC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)OC(=O)C)C)C 584.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
(9S,12R)-5,5,9,13-tetramethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane 91750049 Click to see 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
[(1R,2S,4S,5S,9R,10S,12R,13R,14S)-5-(hydroxymethyl)-5,9,13-trimethyl-2-pentacyclo[11.2.1.01,10.04,9.012,14]hexadecanyl] acetate 102239718 Click to see 346.50 unknown via CMAUP database
[(1R,2S,4S,5S,9R,10S,13R)-2-acetyloxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl hexadecanoate 101526599 Click to see 584.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
[(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 via CMAUP database
5-(Hydroxymethyl)-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecan-2-ol 12444454 Click to see 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
5-(Hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-en-14-ol 13858172 Click to see 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
5,5,9,14-Tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-2,14-diol 163039940 Click to see 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Ent-Kaurene 11966109 Click to see 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Trachylobane 521405 Click to see CC1(CCCC2(C1CCC34C2CC5C(C3)C5(C4)C)C)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1S,4S,5S,9S,10R,12S,13S)-5-(hydroxymethyl)-5,9,13-trimethyltetracyclo[10.2.2.01,10.04,9]hexadecan-13-ol 163032303 Click to see 306.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
5-(Hydroxymethyl)-5,9,13-trimethyltetracyclo[10.2.2.01,10.04,9]hexadecan-13-ol 14109710 Click to see CC1(CCCC2(C1CCC34C2CC(CC3)C(C4)(C)O)C)CO 306.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(3R,4aS,6aS,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-1,2,5,6,6a,9,10,10b-octahydrobenzo[f]chromen-8-one 15226249 Click to see 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Squalene 638072 Click to see 410.70 unknown via CMAUP database
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Rhoiptelenol 102304204 Click to see CC1CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1C)C)C)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Akagerine 643662 Click to see 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Methyl 3-(3,4-dimethoxyphenyl)prop-2-enoate 94307 Click to see COC1=C(C=C(C=C1)C=CC(=O)OC)OC 222.24 unknown via CMAUP database
Methyl 3,4-dimethoxycinnamate 766745 Click to see COC1=C(C=C(C=C1)C=CC(=O)OC)OC 222.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Methyl Caffeate 689075 Click to see 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011

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