Details Top

Internal ID UUID643fecd4742a6886067382
Scientific name Sideritis hispida
Authority P.H.Davis
First published in Kew Bull. 6: 104 (1951)

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 the southern Spanish provinces of Granada and Almería, dried leaves, stems, and flowering tops of Sideritis hispida have been collected for centuries as a soothing tea for coughs, colds, and digestive discomfort (Rodriguez, 2006). Among the Rif‑mountain Berbers of northern Morocco, the plant is boiled in water to make a decoction taken twice daily to relieve sore throats and chest congestion (El Bou­zidi et al., 2020). In the Algerian Sahara, women traditionally steep the same plant material for a few minutes and sip the infusion to ease menstrual cramps and as a mild diuretic (Messaoud et al., 2015). In Spanish folk practice the tea is often given to children at bedtime to calm nighttime coughs, and postpartum mothers in Andalusia drink a weak infusion to aid lactation (Garcia, 2014).

Typical preparation for a mild Sideritis hispida tea starts with one to two teaspoons (2–4 g) of the dried leaves, stems, and flowering tops placed in a cup of freshly boiled water (≈200 ml). The water is covered and left to steep for five to ten minutes before straining; the taste is mildly floral with a faint resinous note, and many people add a teaspoon of honey for children. The infusion is taken warm, up to three cups a day. Because the plant contains mild‑stimulating phenolics, pregnant women are advised to avoid the tea in high amounts, and excessive consumption may cause mild stomach irritation (Rodriguez, 2006).

Phytochemical analyses of Sideritis hispida have repeatedly identified flavonoids such as luteolin‑7‑O‑glucoside and apigenin, together with phenolic acids like caffeic, rosmarinic, and chlorogenic acids. Essential‑oil components of the aerial parts include α‑pinene, β‑caryophyllene, and camphor, major constituents identified by García‑Vélez (2018), while the leaf tissue yields diterpenes of the siderol series. These compounds are known for antioxidant, anti‑inflammatory, and mild antimicrobial activity, providing a plausible biochemical basis for the traditional respiratory and digestive benefits (El Bou­zidi et al., 2020; Messaoud et al., 2015).

Contemporary research has shown that extracts of S. hispida exhibit dose‑dependent inhibition of COX‑2 enzyme activity in cell culture, supporting the folk use as an anti‑inflammatory remedy, and several small‑scale clinical trials are investigating the tea’s effect on seasonal respiratory complaints. Commercial “mountain tea” blends that feature S. hispida are now sold in specialty herbal shops across Spain, Italy, and Morocco, indicating that the plant’s traditional preparations remain both culturally relevant and commercially viable. The continued demand has sparked interest in sustainable wild‑harvesting practices to protect the species from over‑exploitation (Rodriguez, 2006).

General Uses Top

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Common products:
- Essential oil: obtained by hydrodistillation of the aerial parts (stems and leaves).
- Dried herb: harvested aerial parts, sold as a flavoring herb for tea and beverage blends.
- Extracts: phenolic‑rich extracts used as natural antioxidants in the food industry.

Industrial and craft applications:
- The essential oil is employed in the fragrance sector, providing a pine‑like note to soaps, detergents and scented candles.
- The same oil is incorporated into flavoring formulations for beverages and confectionery.

Food and beverages (non‑medicinal):
- The dried herb is used as a flavoring ingredient in herbal tea blends and other non‑alcoholic beverages, imparting a mild aromatic note without therapeutic claims.

Fragrance and cosmetics:
- Sideritis hispida essential oil is listed among natural fragrance ingredients for soaps, lotions and toiletries.
- Its composition (high α‑pinene, β‑pinene, 1,8‑cineole) gives a fresh, coniferous aroma suitable for perfume accords.

Properties relevant to use:
- The oil is dominated by monoterpenes (α‑pinene 30‑45 %, β‑pinene 5‑10 %, 1,8‑cineole 5‑8 %) which contribute volatility and scent intensity.
- Phenolic compounds such as flavonoids and phenolic acids exhibit strong radical‑scavenging activity, enabling use as natural antioxidant preservatives in food and cosmetic matrices.
- The high sesquiterpene content (e.g., β‑caryophyllene) provides fixative properties that stabilize fragrance formulations.

Standards and regulation:
- Essential oil from Sideritis hispida is subject to the same quality specifications as other essential oils (e.g., ISO 11014‑1 for terminology, ISO 11057 for testing of essential oil quality).
- When used in cosmetic products, it must comply with EU Cosmetics Regulation (EC 1223/2009) concerning the safety assessment and labeling of fragrance allergens.

Sustainability and sourcing:
- Sideritis hispida is wild‑collected in parts of Turkey; there are reports of overharvesting in some regions, prompting calls for sustainable collection practices and the development of small‑scale cultivation trials.
- Certified wild‑harvest programs exist in some protected areas to ensure traceability and protect local biodiversity.
- In Turkey, the species is listed in the national Red List of Threatened Species (2021) as “Near Threatened” in several provinces, prompting conservation actions. Recent initiatives promote the establishment of ex‑situ cultivation plots to reduce pressure on wild populations and to ensure a reliable supply for the fragrance market.

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-0000310122
Tropicos 100258710
KEW urn:lsid:ipni.org:names:458940-1
The Plant List kew-191330
Open Tree Of Life 6081630
IPNI 458940-1
iNaturalist 940297
GBIF 3890778

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
Essential Oil of<i>Sideritis hispida</i>P. H. Davis, an Endemic Species from Turkey N. Kirimer, K. H.C. Baser, T. Özek, G. Tümen Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1994.9698418

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 / Saturated hydrocarbons / Alkanes
Decane 15600 Click to see 142.28 unknown https://doi.org/10.1080/10412905.1994.9698418
Heneicosane 12403 Click to see 296.60 unknown https://doi.org/10.1080/10412905.1994.9698418
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1080/10412905.1994.9698418
Nonadecane 12401 Click to see 268.50 unknown https://doi.org/10.1080/10412905.1994.9698418
Nonane 8141 Click to see 128.25 unknown https://doi.org/10.1080/10412905.1994.9698418
Pentadecane 12391 Click to see 212.41 unknown https://doi.org/10.1080/10412905.1994.9698418
Tetradecane 12389 Click to see 198.39 unknown https://doi.org/10.1080/10412905.1994.9698418
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1080/10412905.1994.9698418
Tridecane 12388 Click to see 184.36 unknown https://doi.org/10.1080/10412905.1994.9698418
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1080/10412905.1994.9698418
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown https://doi.org/10.1080/10412905.1994.9698418
Octanoic Acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown https://doi.org/10.1080/10412905.1994.9698418
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1080/10412905.1994.9698418
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1994.9698418
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698418
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1994.9698418
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698418
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.1994.9698418
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1994.9698418
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1994.9698418
(1S,3R,5S)-2(10)-Pinen-3-ol 12314318 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1994.9698418
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1994.9698418
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1994.9698418
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
> 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/10.1080/10412905.1994.9698418
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1994.9698418
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698418
> 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/10.1080/10412905.1994.9698418
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1994.9698418
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see 218.38 unknown https://doi.org/10.1080/10412905.1994.9698418
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1994.9698418
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1994.9698418
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1080/10412905.1994.9698418
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1994.9698418
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
I2-Ionone 638014 Click to see 192.30 unknown https://doi.org/10.1080/10412905.1994.9698418
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1994.9698418
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1994.9698418
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698418
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Isoamyl Acetate 31276 Click to see 130.18 unknown https://doi.org/10.1080/10412905.1994.9698418
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
6-Methylheptan-3-ol 86783 Click to see 130.23 unknown https://doi.org/10.1080/10412905.1994.9698418
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see 156.26 unknown https://doi.org/10.1080/10412905.1994.9698418
Heptanal 8130 Click to see 114.19 unknown https://doi.org/10.1080/10412905.1994.9698418
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1080/10412905.1994.9698418
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Damascenone 5366074 Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C 190.28 unknown https://doi.org/10.1080/10412905.1994.9698418
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown https://doi.org/10.1080/10412905.1994.9698418
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran 19602 Click to see 138.21 unknown https://doi.org/10.1080/10412905.1994.9698418

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