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Teucrium marum

Teucrium marum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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No description added yet. Help us by writing one.

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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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
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 characters of Teucrium marum from Sardinia: an endemic plant. Bianco A, Ramunno A, Serrilli AM, Lo Castro M, Ballero M, Serafini M Nat Prod Res 01-Dec-2004
doi:10.1080/14786410310001630564
PMID:15595614
Triterpene acids from Salvia and Teucrium species Salvatore Passannanti, Mariapia Paternostro, Franco Piozzi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)85059-6

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 CC1CCC2C1C(OC=C2COC(=O)C)OC(=O)C 268.30 unknown https://doi.org/10.1016/S0031-9422(00)80146-6
Teucrein 590662 Click to see CC1CCC2C1C(OC=C2COC(=O)C)OC(=O)C 268.30 unknown https://doi.org/10.1016/S0031-9422(00)80146-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Anisomorphal, (+)- 76970747 Click to see CC1CCC(C1C=O)C(=C)C=O 166.22 unknown https://doi.org/10.1071/CH9761375
Cyclopentaneacetaldehyde, 2-formyl-3-methyl-alpha-methylene- 534263 Click to see CC1CCC(C1C=O)C(=C)C=O 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
> 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 CC1CCC2C1C(=O)OCC2=C 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/10.1016/S0031-9422(00)80146-6
https://doi.org/10.1071/CH9761375
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Micromeric acid 73242194 Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)O)C)C)(C)C)O)C 454.70 unknown https://doi.org/10.1016/0031-9422(83)85059-6
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(83)85059-6
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 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 CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CC(CC25CO5)O)COC(=O)C)O 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 CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C(C=C4)OC)O)O)C 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
3,4',5,7-Tetrahydroxy-3',5'-dimethoxy-6-beta-D-glucopyranosylflavone 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 C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzin 107971 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown via CMAUP database
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database

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