Details Top

Internal ID UUID643feef37dcf8031068099
Scientific name Teucrium marum
Authority L.
First published in Sp. Pl. : 564 (1753)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Essential oil – hydrodistilled from the aerial parts (stems, leaves, inflorescences) of Teucrium marum. The oil is typically a pale‑yellow to yellowish liquid with a characteristic camphoraceous aroma. Reported yields from fresh material are low, usually below 0.5 % (v/w), reflecting the herbaceous habit of the plant.

Industrial and craft applications:
- The essential oil is incorporated into fragrance formulations for soaps, detergents, air‑fresheners and related consumer products, where its strong, fresh scent functions as a top‑note component.

Fragrance and cosmetics:
- In perfumery the oil is employed as a fragrance material in eau de Cologne, body lotions, shampoos and bath products. Its principal constituents—camphor (≈20–30 % of the oil), 1,8‑cineole (≈8–12 %), α‑pinene, β‑pinene and limonene—impart a sharp, aromatic profile that blends well with citrus, herbaceous and woody accords.

Properties relevant to use:
- The oil’s high camphor and 1,8‑cineole content confers pronounced volatility and a pungent scent, while the mixture of monoterpene hydrocarbons provides stability in fragrance blends. Typical physicochemical parameters reported for camphor‑rich essential oils and consistent with ISO 11016 (general requirements) and ISO 3515 (determination of specific gravity, refractive index and optical rotation) include a specific gravity of 0.900–0.920 at 20 °C and a refractive index of 1.470–1.480.

Standards and regulation:
- Fragrance applications of the oil are governed by the International Fragrance Association (IFRA) standards, which restrict the use of camphor‑rich essential oils in certain product categories. Cosmetics containing the oil must comply with the European Union Cosmetics Regulation (EC No 1223/2009), mandating safety assessments and labeling for fragrance constituents.

Sustainability and sourcing:
- Teucrium marum occurs in Mediterranean scrub, rocky slopes and phrygana habitats. Commercial supply relies primarily on wild‑collection, which can lead to local depletion if harvesting is unmanaged. The species is not listed as threatened by the IUCN Red List (assessed as Not Evaluated/ Data Deficient), but population monitoring and sustainable collection practices are recommended.

Scientific/model‑organism use:
- The species serves as a reference in chemotaxonomic and metabolomic investigations of the Lamiaceae. Its essential‑oil composition has been documented in peer‑reviewed journals and entered into phytochemical databases (e.g., the Lamiaceae Phytochemical Database), supporting phylogenetic and comparative‑metabolite research. Herbarium vouchers of T. marum are frequently used to verify taxonomic identity in botanical studies.

Synonyms Top

Scientific name Authority First published in
Chamaedrys marum Moench Methodus : 384 (1794)
Chamaedrys quadratula (Schreb.) Raf. Fl. Tellur. 3: 85. 1837 (1837)

Common names Top

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Language Common/alternative name
Spanish tomillo de gato
Arabic طوقريون جبلي
Arabic مارون
Arabic صعتر الهر
Azerbaijani dərman məryəmnoxudu
Catalan eixorba-rates blanc
Czech ožanka kočičí
Dutch amberkruid

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Teucrium marum subsp. marum Unknown

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
  • Europe
    • Southeastern Europe
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Sardegna

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000322309
UNII 10464S0TAA
Tropicos 17600397
INPN 126006
Flora of Italy 4442
KEW urn:lsid:ipni.org:names:460544-1
The Plant List kew-203094
Open Tree Of Life 355036
Observations.org 133663
NCBI Taxonomy 711380
IPNI 460544-1
iNaturalist 451208
GBIF 7308317
Freebase /m/0h5sx4
EPPO TEUMR
Elurikkus 586400
USDA GRIN 456453
Wikipedia Teucrium_marum
CMAUP NPO453

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
Ethnomedicinal evaluation of medicinal plants used for therapies by men and women in rural and urban communities in Makkah district Qari SH, Alqethami A, Qumsani AT Saudi Pharm J 02-Dec-2023
PMCID:PMC10733703
doi:10.1016/j.jsps.2023.101881
PMID:38130903
Comparative analysis of sorghum (C4) and rice (C3) plant headspace volatiles induced by artificial herbivory Osinde C, Sobhy IS, Wari D, Dinh ST, Hojo Y, Osibe DA, Shinya T, Tugume AK, Nsubuga AM, Galis I Plant Signal Behav 10-Aug-2023
PMCID:PMC10730142
doi:10.1080/15592324.2023.2243064
PMID:37585707
Phytochemical diversity within and among Sardinian populations of the endemic Teucrium marum L. (Lamiaceae) is determined by ecological factors Maccioni A, Macis S, Gibernau M, Farris E Heliyon 29-Jun-2023
PMCID:PMC10395143
doi:10.1016/j.heliyon.2023.e17728
PMID:37539184
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Ethnopharmacobotany and Diversity of Mediterranean Endemic Plants in Marmilla Subregion, Sardinia, Italy Cocco E, Maccioni D, Sanjust E, Falconieri D, Farris E, Maxia A Plants (Basel) 18-Nov-2022
PMCID:PMC9695302
doi:10.3390/plants11223165
PMID:36432894
Formulation and In Vitro Efficacy Assessment of Teucrium marum Extract Loading Hyalurosomes Enriched with Tween 80 and Glycerol Firoznezhad M, Castangia I, Tuberoso CI, Cottiglia F, Marongiu F, Porceddu M, Usach I, Escribano-Ferrer E, Manca ML, Manconi M Nanomaterials (Basel) 26-Mar-2022
PMCID:PMC9000414
doi:10.3390/nano12071096
PMID:35407213
The Endemic Vascular Flora of Sardinia: A Dynamic Checklist with an Overview of Biogeography and Conservation Status Fois M, Farris E, Calvia G, Campus G, Fenu G, Porceddu M, Bacchetta G Plants (Basel) 23-Feb-2022
PMCID:PMC8912449
doi:10.3390/plants11050601
PMID:35270071
Characterization of Essential Oils from Different Taxa Belonging to the Genus Teucrium in Sardinia Island, Italy Maccioni A, Falconieri D, Sanna C, Porcedda S, Piras A, Maxia A Plants (Basel) 02-Jul-2021
PMCID:PMC8309330
doi:10.3390/plants10071359
PMID:34371562
Study of a more than a hundred years old theriac jar’ content: A famous thousand-year-old counter-poison Ricordel I, Milan N, Sibille P, Boillot M, de Vaugelade S, Pirnay S Toxicol Rep 17-Jun-2021
PMCID:PMC8258787
doi:10.1016/j.toxrep.2021.06.009
PMID:34307055
Biochemistry of Terpenes and Recent Advances in Plant Protection Ninkuu V, Zhang L, Yan J, Fu Z, Yang T, Zeng H Int J Mol Sci 27-May-2021
PMCID:PMC8199371
doi:10.3390/ijms22115710
PMID:34071919
Chemical Constituents, Antioxidant, Cyclooxygenase Inhibitor, and Cytotoxic Activities of Teucrium pruinosum Boiss. Essential Oil Jaradat N, Al-lahham S, Abualhasan MN, Bakri A, Zaide H, Hammad J, Hussein F, Issa L, Mousa A, Speih R Biomed Res Int 30-Jul-2018
PMCID:PMC6091332
doi:10.1155/2018/4034689
PMID:30151381
Beyond food and medicine, but necessary for life, too: other folk plant uses in several territories of Catalonia and the Balearic Islands Gras A, Garnatje T, Bonet MÀ, Carrió E, Mayans M, Parada M, Rigat M, Vallès J J Ethnobiol Ethnomed 17-Jun-2016
PMCID:PMC4912702
doi:10.1186/s13002-016-0097-8
PMID:27316670
Monoterpenes of Teucrium marum UM Pagnoni, A Pinetti, R Trave, L Garanti CSIRO Publishing 20-Dec-2006
doi:10.1071/CH9761375
Essential oil of Actinidia macrosperma, a catnip response kiwi endemic to China Zhao YP, Wang XY, Wang ZC, Lu Y, Fu CX, Chen SY J Zhejiang Univ Sci B 15-Aug-2006
PMCID:PMC1559795
doi:10.1631/jzus.2006.B0708
PMID:16909471
Chemical composition, antimicrobial and antioxidant activity of the essential oil of Teucrium marum (Lamiaceae). Ricci D, Fraternale D, Giamperi L, Bucchini A, Epifano F, Burini G, Curini M J Ethnopharmacol 08-Apr-2005
doi:10.1016/J.JEP.2005.01.022
PMID:15763383

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
[(1R,4aR,7R,7aS)-1-acetyloxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-yl]methyl acetate 162950363 Click to see 268.30 unknown https://doi.org/10.1016/S0031-9422(00)80146-6
Teucrein 590662 Click to see 268.30 unknown https://doi.org/10.1016/S0031-9422(00)80146-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
2-Formyl-3-methyl-alpha-methylidenecyclopentaneacetaldehyde 534263 Click to see 166.22 unknown https://doi.org/10.1016/J.JEP.2005.01.022
https://doi.org/10.1016/S0031-9422(00)80146-6
https://doi.org/10.1071/CH9761375
https://doi.org/10.1016/J.JEP.2005.01.022
https://doi.org/10.1071/CH9761375
Anisomorphal, (+)- 76970747 Click to see 166.22 unknown https://doi.org/10.1071/CH9761375
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4aS,7S,7aR)-7-methyl-4-methylidene-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-3-one 11805123 Click to see CC1CCC2C1COC(=O)C2=C 166.22 unknown https://doi.org/10.1071/CH9761375
(4aS,7S,7aR)-7-methyl-4-methylidene-5,6,7,7a-tetrahydro-4aH-cyclopenta[c]pyran-1-one 90442131 Click to see 166.22 unknown https://doi.org/10.1071/CH9761375
7-methyl-4-methylidene-5,6,7,7a-tetrahydro-4aH-cyclopenta[c]pyran-1-one 101410495 Click to see CC1CCC2C1C(=O)OCC2=C 166.22 unknown https://doi.org/10.1071/CH9761375
https://doi.org/10.1016/S0031-9422(00)80146-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(83)85059-6
CID 73242194 73242194 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(83)85059-6
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(83)85059-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 85503171 85503171 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(00)80392-1
NCGC00384925-01_C22H28O8_[(2'R,3R,4'R,4a'R,5S,5'R,7'S,8a'S)-5-(3-Furyl)-4',7'-dihydroxy-2'-methyl-2-oxooctahydrodispiro[furan-3,1'-naphthalene-5',2''-oxiran]-4a'(2'H)-yl]methyl acetate 38361768 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CC(CC25CO5)O)COC(=O)C)O 420.50 unknown https://doi.org/10.1080/14786410310001630564
https://doi.org/10.1016/S0031-9422(00)80392-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-5-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 101326868 Click to see 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
ent-Gallocatechin 4'-methyl ether 10087345 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 320.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
3,5,7-trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 101713180 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 508.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown via CMAUP database
6-(1,1-Dimethylallyl)genistein 44257285 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 338.40 unknown via CMAUP database
Genistein 5280961 Click to see 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzin 107971 Click to see 416.40 unknown via CMAUP database
Genistin 5281377 Click to see 432.40 unknown via CMAUP database

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