Teucrium kotschyanum

Details Top

Internal ID UUID643feef046302637201404
Scientific name Teucrium kotschyanum
Authority Poech
First published in Enum. Pl. Cypr. : 24 (1842)

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.

Teucrium kotschyanum is collected and used as a tea in Iran, especially in the Zagros, where the aerial parts are decocted as a bitter tonic for digestive complaints such as flatulence, dyspepsia, and loss of appetite; the same preparation is employed for colds and fever in folk practice (Amani and Amanlou, 2005; Ghadirian et al., 2016). Among Kurdish communities in Iraq, infusing or decocting the leaves and flowering tops in water is reported for stomach discomfort and as a diaphoretic, often taken warm (Salih et al., 2013). In Iranian and Pakistani folk medicines the aerial parts are also steeped in hot water and drunk to soothe coughs and mild bronchial irritation (Amani and Amanlou, 2005; Khan et al., 2009). These uses are consistently described as teas or decoctions and typically involve short infusions of aerial material.

A simple aqueous decoction for digestive discomfort is made by simmering 10 g of dried aerial parts (leaves, stems, and flowering tops) in 500 mL water for 15–20 minutes, straining, and drinking up to one cup 2–3 times daily after meals (Amani and Amanlou, 2005). Because the aerial parts of Teucrium species contain hepatotoxic furano neoclerodane diterpenes, use should be limited in duration; people with liver disease, pregnant or nursing women, and children should avoid self-treatment unless a qualified practitioner advises otherwise (Kavlia et al., 2012).

Well-characterized phytochemicals in Teucrium kotschyanum include diterpenes such as teucvin and 8-acetylteucvin, neoclerodane diterpenes, and flavonoids including apigenin and luteolin (Amani and Amanlou, 2005; Ghadirian et al., 2016; Hashemnejad et al., 2005). The bitter diterpenes likely contribute to the traditional stomachic actions via digestive stimulation and spasmolytic effects on smooth muscle; flavonoids and phenolics contribute to antioxidant activity relevant to cold and fever applications.

Modern studies continue to support the plant’s anti-inflammatory, spasmolytic, and hypoglycemic potential (Ghadirian et al., 2016; Hashemnejad et al., 2005), while cautionary work on Teucrium toxicity underscores the need for moderate, short-term use and qualified oversight (Kavlia et al., 2012). Dried aerial parts are available in herbal markets of Iran and some Middle Eastern diaspora communities, and decoctions remain a recognized folk remedy in those regions.

General Uses Top

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Common products:
Distilled essential oil from aerial parts is the principal commercial product, reported at yields of 0.2–0.8% (w/w) by hydrodistillation in laboratory analyses; minor yields are obtained by supercritical CO2 extraction in experimental work.

Fragrance and cosmetics:
The oil is used in perfumery as a scent component. Analyses report a sesquiterpene-rich profile dominated by caryophyllene, caryophyllene oxide, and α-humulene, with α-pinene and other monoterpenes often present as minor constituents. Properties relevant to fragrance include notable antimicrobial activity of caryophyllene oxide, which supports preservative function in fragrance compositions. Depending on national regulations, essential oils may be subject to IFRA standards on usage levels and component restrictions such as those for caryophyllene and related sesquiterpenes.

Colorants and tanning:
No documented use as natural dyes or tannins.

Wood and fiber:
No documented use for timber, fiber, or resin/gum.

Food and beverages (non-medicinal):
No documented use as a food flavoring or beverage ingredient.

Industrial and craft applications:
No documented adhesives, coatings, biofuels, pulp/paper, or fermentation feedstock applications.

Properties relevant to use:
• Rich in sesquiterpenes (β-caryophyllene, α-humulene; caryophyllene oxide commonly abundant).
• Antimicrobial activity in the oil is primarily linked to caryophyllene oxide.

Standards and regulation:
Essential oils for fragrance are generally governed by IFRA standards (e.g., fragrance compound restrictions; usage recommendations) and relevant national cosmetics regulations (e.g., EU cosmetic rules on essential oils; U.S. cosmetics guidance). Regulatory status is component-dependent.

Sustainability and sourcing:
Supplies originate from wild-harvested or cultivated shrubs in native range areas (e.g., parts of Iran) during flowering, followed by air-drying and distillation. Sustainable harvesting and cultivation help avoid overharvest of wild stands and maintain genetic diversity.

Synonyms Top

Scientific name Authority First published in
Teucrium smyrneum Boiss. Diagn. Pl. Orient. 5: 42 (1844)

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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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-0000322229
Tropicos 50210661
KEW urn:lsid:ipni.org:names:460490-1
The Plant List kew-203019
Open Tree Of Life 5232676
NCBI Taxonomy 1209865
IPNI 460490-1
iNaturalist 1046842
GBIF 3895999

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
Isoteucrin H4, a 19-Nor-neoclerodane Diterpenoid of Biogenetic Interest from Teucrium kotschyanum Franco Piozzi, Benjamin Rodriguez, Giuseppe Savona, Maurizio Bruno, Nelly Apostolides Arnold, Fatima Simões The Japan Institute of Heterocyclic Chemistry 27-Feb-2009
doi:10.3987/COM-88-S46
Neo-clerodane diterpenoids from Teucrium kotschyanum Fátima Simoes, Benjamín Rodríguez, Maurizio Bruno, Franco Piozzi, Giuseppe Savona, Nelly Apostolides Arnold Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98084-1
Teuscorodin, teuscorodonin and 2-hydroxyteuscorolide, neo-clerodane diterpenoids from teucrium scorodonia José L. Marco, Benjamín Rodríguez, Conrad Pascual, Giuseppe Savona, Franco Piozzi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86971-X
Comparative study on essential oil of some Teucrium species from Cyprus. Arnold N, Bellomaria B, Valentini G, Rafaiani SM J Ethnopharmacol 01-Dec-1991
doi:10.1016/0378-8741(91)90062-I
PMID:1809816

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 / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1016/0378-8741(91)90062-I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/0378-8741(91)90062-I
> 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/10.1016/0378-8741(91)90062-I
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1016/0378-8741(91)90062-I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/0378-8741(91)90062-I
Pinocarvone 121719 Click to see 150.22 unknown https://doi.org/10.1016/0378-8741(91)90062-I
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1016/0378-8741(91)90062-I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown https://doi.org/10.1016/0378-8741(91)90062-I
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/0378-8741(91)90062-I
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene 5315589 Click to see 204.35 unknown https://doi.org/10.1016/0378-8741(91)90062-I
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/0378-8741(91)90062-I
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/10.1016/0378-8741(91)90062-I
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1016/0378-8741(91)90062-I
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1016/0378-8741(91)90062-I
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0378-8741(91)90062-I
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/0378-8741(91)90062-I
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1016/0378-8741(91)90062-I
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo(5.3.1.01,5)undec-8-ene 442348 Click to see 204.35 unknown https://doi.org/10.1016/0378-8741(91)90062-I
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(3R,3aR,5'S,6aS,7R,8R,10aR)-5'-(furan-3-yl)-3-hydroxy-8-methylspiro[3,3a,4,5,6,6a,8,9-octahydro-1H-benzo[d][2]benzofuran-7,3'-oxolane]-2',10-dione 163194754 Click to see CC1CC(=O)C23COC(C2CCCC3C14CC(OC4=O)C5=COC=C5)O 360.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
(3R,3aR,5'S,6aS,7R,8R,10R,10aS)-5'-(furan-3-yl)-3,10-dihydroxy-8-methylspiro[1,3,3a,4,5,6,6a,8,9,10-decahydrobenzo[d][2]benzofuran-7,3'-oxolane]-2'-one 162893249 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)86971-X
5'-(furan-3-yl)-3-hydroxy-8-methylspiro[3,3a,4,5,6,6a,8,9-octahydro-1H-benzo[d][2]benzofuran-7,3'-oxolane]-2',10-dione 163013782 Click to see 360.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
5'-(Furan-3-yl)-3,10-dihydroxy-8-methylspiro[1,3,3a,4,5,6,6a,8,9,10-decahydrobenzo[d][2]benzofuran-7,3'-oxolane]-2'-one 14396802 Click to see CC1CC(C23COC(C2CCCC3C14CC(OC4=O)C5=COC=C5)O)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
Montanin D 21634412 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
NCGC00384904-01_C20H26O6_(3R,3'R,3a'R,5S,6a'S,8'R,10'R,10a'R)-5-(3-Furyl)-3',10'-dihydroxy-8'-methyldecahydro-8'H-spiro[furan-3,7'-naphtho[1,8a-c]furan]-2-one 14396803 Click to see CC1CC(C23COC(C2CCCC3C14CC(OC4=O)C5=COC=C5)O)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
Teucrin H-2 13120894 Click to see 360.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 7163174 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4S,5'S,6S,9R,10R)-5'-(furan-3-yl)-6-hydroxy-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-8(12)-ene-9,3'-oxolane]-2',3-dione 21585546 Click to see CC1CC2C3=C(C14CC(OC4=O)C5=COC=C5)CC(CC3C(=O)O2)O 344.40 unknown https://doi.org/10.3987/COM-88-S46
(1R,5'R,8R,9R,10R)-5'-(furan-3-yl)-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4(12)-ene-9,3'-oxolane]-2',3-dione 13071600 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
(1R,5'S,6R,8S,9R,10R)-5'-(furan-3-yl)-6-hydroxy-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4(12)-ene-9,3'-oxolane]-2',3-dione 21585543 Click to see 344.40 unknown https://doi.org/10.3987/COM-88-S46
(1R,5'S,8R,9R,10R,12R)-5'-(furan-3-yl)-12-(hydroxymethyl)-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9,3'-oxolane]-2',3-dione 162929093 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
5'-(Furan-3-yl)-6-hydroxy-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4(12)-ene-9,3'-oxolane]-2',3-dione 73806252 Click to see 344.40 unknown https://doi.org/10.3987/COM-88-S46
5'-(Furan-3-yl)-6-hydroxy-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-8(12)-ene-9,3'-oxolane]-2',3-dione 4371593 Click to see 344.40 unknown https://doi.org/10.3987/COM-88-S46
Eugarzasidine I 316446 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
Teucvidin 185749 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
Teuflin 13071598 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
Teuscordonin 159081 Click to see CC1CC2C3(C(C14CC(OC4=O)C5=COC=C5)CCC=C3C(=O)O2)CO 358.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
Teyin 13071599 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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)98084-1
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)98084-1

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