Thymus kotschyanus
Details Top
| Internal ID | UUID643fef435c5d8312057494 |
| Scientific name | Thymus kotschyanus |
| Authority | Boiss. & Hohen. |
| First published in | Diagn. Pl. Orient. 5: 16 (1844) |
Ethnobotanical Use Top
Suggest a correction!
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.
Thymus kotschyanus Boiss. & Hohen., known locally as “kotschy thyme” in Iran and “yavuz çay” in Turkey, is a small, aromatic shrub of the Lamiaceae that thrives on rocky, high‑altitude slopes of the Zagros, Caucasus and Anatolian ranges. Across these regions, its foliage has a long history of being prepared as a simple water infusion or decoction, and the fresh or dried herb is also mashed into a poultice for topical applications. The plant’s use is documented in three independent ethnobotanical surveys – among the Kurdish peoples of western Iran (Zare & Maleki, 2018), among shepherds and village healers in Eastern Anatolia (Gülçin, Ayhan & Ünlü, 2010) and among Turkmen tribal healers in north‑western Iran (Mikaili, Shayegan & Sufi, 2013).
In the Kurdish villages of Kermanshah Province, a tea made from a handful of fresh, finely chopped leaves of Thymus kotschyanus is taken two to three times a day to calm cough and to reduce the fever that often accompanies respiratory infections (Zare & Maleki, 2018). In Eastern Anatolia, a decoction of the aerial parts – roughly 15 g of dried stems and leaves boiled in 500 ml of water for 15 minutes – is strained and drunk warm to relieve sore throat irritation, indigestion and menstrual cramps (Gülçin, Ayhan & Ünlü, 2010). Among Turkmen communities, fresh leaves are bruised, mixed with a little cold water and applied as a compress (a macerated poultice) to cuts, abrasions and slow‑healing wounds, a practice that has been linked to accelerated tissue repair in local ethnomedical reports (Mikaili, Shayegan & Sufi, 2013). A related infusion is also mentioned by Barseghyan (2010) as a remedy for colds among Armenian highlanders, underscoring the plant’s pan‑regional therapeutic role.
To prepare a mild, soothing tea, measure 1 g of dried Thymus kotschyanus leaves (about one loosely packed teaspoon) and place them in a cup. Bring 200 ml of fresh water to a rolling boil, pour it over the herb, cover the cup and let the infusion steep for 5–10 minutes. The resulting tea can be strained and drunk warm, 1 cup two to three times a day. The same amount can be used in a decoction: boil the leaves in water for 15 minutes, cool, and drink the liquid. In all cases, avoid exceeding three cups per day, and pregnant women should limit intake to one cup daily because high concentrations of thymol may stimulate uterine activity (Yilmaz, Uyanik & Sevim, 2020).
The therapeutic actions of Thymus kotschyanus are linked to its well‑documented phytochemicals. Its essential oil, reported by Özgüven, Şener & Çolakoğlu (2009), is rich in the monoterpenes thymol (≈30 % of the oil), carvacrol (≈20 %) and p‑cymene, compounds noted for strong antimicrobial and expectorant activity. The plant also contains significant amounts of phenolic acids such as rosmarinic acid and caffeic acid, as well as flavonoids like apigenin and luteolin, both identified in detailed phenolic profiling by Yilmaz, Uyanik & Sevim (2020). These constituents plausibly underlie the anti‑inflammatory, antioxidant and spasmolytic effects reported in the ethnobotanical literature. Today, the dried herb is sold in specialty herbal shops across Iran and Turkey, and the essential oil is under investigation for its broad‑spectrum antibacterial properties in clinical settings (Khosravi et al., 2015). While modern science confirms many traditional actions, the tea and poultice remain a living part of rural health practices, bridging folk memory with contemporary research.
General Uses Top
Suggest a correction!Common products:
- Steam‑distilled essential oil (hydrodistillation or water‑distillation) obtained from the aerial parts (leaves, stems, and flowering tops) of Thymus kotschyanus; yields typically range from 0.3 % to 1.2 % (v/w) of fresh plant material.
- Dried aerial parts (leaf‑stem mixture) marketed as a culinary herb, usually milled to a coarse powder or retained in leaf form.
Industrial and craft applications:
- The essential oil is employed as a natural flavoring agent in the food‑processing industry for sauces, marinades, baked goods, confectionery, and functional beverages; typical inclusion rates are 0.01 %–0.1 % (w/w) to provide a characteristic thyme aroma without conferring health claims.
- Because of its antimicrobial activity, the oil functions as a non‑thermal preservative in packaged foods, extending shelf‑life by inhibiting bacterial growth; this use is documented in food‑technology literature for thyme‑derived essential oils.
- In perfumery, the oil supplies spicy‑herbaceous top‑note accents in men’s and women’s fragrances and is used in specialty aromatic blends.
Food and beverages (non‑medicinal):
- The dried herb is used as a spice in regional cuisines of Iran, Turkey, and the Caucasus, imparting a warm, slightly minty flavor to meat dishes, soups, stews, and rice preparations.
- The oil is incorporated as a flavoring in alcoholic beverages (e.g., flavored vodkas and herbal liqueurs) and in non‑alcoholic functional drinks, where it contributes aromatic depth without any medicinal purpose.
Fragrance and cosmetics:
- Essential oil is a component of soaps, shampoos, shower gels, and body lotions for its persistent herbaceous scent and stabilising effect on the perfume base.
- It is also listed as an aroma‑active ingredient in toothpaste and oral‑care rinses, where it adds a fresh, clean note.
- Leaf extracts are used in fragrance formulations for perfumes, scented candles, and air‑fresheners.
Properties relevant to use:
- Chemical composition: the oil is dominated by thymol (≈20 %–55 % of the total volatiles) and carvacrol (≈10 %–30 %); minor constituents include p‑cymene, γ‑terpinene, linalool, and borneol.
- Physical characteristics: specific gravity 0.92‑0.98 (20 °C), refractive index 1.49‑1.51 (20 °C), optical rotation –2° to +2°, acid value
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Thymus arthooclades | Stapf | Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 50: 36 (1885) |
| Thymus eriophorus | Ronniger | Fl. Kavkaza 3: 336 (1932) |
| Thymus hyrcanus | Czerniak. ex Klokov | Rassobrazov. Thymus Sov. Soyuza : 66 (1973) |
| Thymus kotschyanus var. eriophorus | (Ronniger) Jalas | Ann. Bot. Fenn. 17: 321 (1980) |
| Thymus lamprophyllus | Borbás | Math. Term. Közlem. 24: 108. 1890 (1890) |
| Thymus kotschyanus var. elbursensis | Rech.f. | Phyton (Horn) 5: 294 (1954) |
| Thymus kotschyanus var. behboudianus | Rech.f. | Phyton (Horn) 5: 295 (1954) |
| Thymus kotschyanus var. pseuderiophorus | Rech.f. | Phyton (Horn) 5: 292 (1954) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Arabic | زعتر كوتشي |
| Azerbaijani | koçi kəklikotu |
| Azerbaijani | koçi kəklikotusu |
| Persian | آویشن آزوربه |
| Armenian | Ուրց Կոչիի |
| Russian | Тимьян Кочиев |
| Russian | Тимьян Кочи |
Germination/Propagation Top
Suggest a correction or add new data!
No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000324234 |
| Tropicos | 17604707 |
| KEW | urn:lsid:ipni.org:names:461322-1 |
| The Plant List | kew-204954 |
| Open Tree Of Life | 5801250 |
| Observations.org | 130706 |
| NCBI Taxonomy | 2019954 |
| IPNI | 461323-1 |
| iNaturalist | 1091350 |
| GBIF | 7307181 |
| Elurikkus | 586176 |
| USDA GRIN | 419466 |
| EOL | 5372156 |
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.
If you wish to see all the related articles click here.
Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
You can also contribute to this by clicking here.
| 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/10.1002/(SICI)1099-1026(199911/12)14:6<405::AID-FFJ853>3.0.CO;2-M https://doi.org/10.1080/10412905.1999.9701184 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
| Linalool | 6549 | Click to see | 154.25 | unknown | https://doi.org/10.1021/NP50047A039 |
| > 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/10.1080/10412905.1999.9701184 https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<405::AID-FFJ853>3.0.CO;2-M https://doi.org/10.1021/NP50047A039 |
| P-Cymene | 7463 | Click to see | 134.22 | unknown |
https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<405::AID-FFJ853>3.0.CO;2-M https://doi.org/10.1021/NP50047A039 https://doi.org/10.1080/10412905.1999.9701184 https://doi.org/10.1055/S-0029-1243136 |
| Thymol | 6989 | Click to see | 150.22 | unknown |
https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<405::AID-FFJ853>3.0.CO;2-M https://doi.org/10.1080/10412905.1999.9701184 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (+-)-alpha-Pinene | 6654 | Click to see | 136.23 | unknown |
https://doi.org/10.1080/10412905.1999.9701184 https://doi.org/10.1021/NP50047A039 |
| 3-Carene | 26049 | Click to see CC1=CCC2C(C1)C2(C)C | 136.23 | unknown | https://doi.org/10.1080/10412905.1999.9701184 |
| alpha Thujene | 6451618 | Click to see | 136.23 | unknown | https://doi.org/10.1080/10412905.1999.9701184 |
| alpha-Thujene | 17868 | Click to see | 136.23 | unknown | https://doi.org/10.1080/10412905.1999.9701184 |
| Beta-Pinene | 14896 | Click to see | 136.23 | unknown |
https://doi.org/10.1055/S-0029-1243136 https://doi.org/10.1080/10412905.1999.9701184 |
| Borneol | 64685 | Click to see | 154.25 | unknown |
https://doi.org/10.1021/NP50047A039 https://doi.org/10.1080/10412905.1999.9701184 https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<405::AID-FFJ853>3.0.CO;2-M |
| Camphene | 6616 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50047A039 |
| CID 44630107 | 44630107 | Click to see CC1(C2CCC1(C(C2)O)C)C | 154.25 | unknown |
https://doi.org/10.1080/10412905.1999.9701184 https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<405::AID-FFJ853>3.0.CO;2-M |
| Tricyclene | 79035 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50047A039 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids | |||||
| Alpha-Terpinene | 7462 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50047A039 |
| Terpinolene | 11463 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50047A039 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| (R)-beta-bisabolene | 68128 | Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C | 204.35 | unknown | https://doi.org/10.1080/10412905.1999.9701184 |
| Beta-Bisabolene | 10104370 | Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C | 204.35 | unknown | https://doi.org/10.1080/10412905.1999.9701184 |
| Caryophyllene | 5281515 | Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C | 204.35 | unknown |
https://doi.org/10.1021/NP50047A039 https://doi.org/10.1080/10412905.1999.9701184 |
| > 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/10.1055/S-0029-1243136 https://doi.org/10.1080/10412905.1999.9701184 |
| Germacrene D | 5317570 | Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C | 204.35 | unknown |
https://doi.org/10.1080/10412905.1999.9701184 https://doi.org/10.1055/S-0029-1243136 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |