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Teucrium creticum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643feee6c3733735889050
Scientific name Teucrium creticum
Authority L.
First published in Sp. Pl. : 563 (1753)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Teucrium charamoniense Cav. Descr. Pl. : 82 (1801)
Teucrium hyssopifolium Schreb. Pl. Verticill. Unilab. Gen. Sp. : xxviii (1773)
Teucrium rosmarinifolium Lam. Encycl. 2: 693 (1788)
Chamaedrys cretica Raf. Fl. Tellur. 3: 85 (1837)

Common names Top

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Language Common/alternative name
Arabic بقلة الغزال
French germandree a feuilles de romarins
French germandrée à feuilles de romarins
French germandrée à feuilles de romarin
Hebrew געדה כרתית
Georgian isolepis

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
  • Asia-temperate
    • Western Asia
      • Cyprus
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000322039
Tropicos 100265940
Flora of Italy 4423
KEW urn:lsid:ipni.org:names:460351-1
The Plant List kew-202838
Open Tree Of Life 5232684
Observations.org 122898
NCBI Taxonomy 1209849
IPNI 460351-1
iNaturalist 555902
GBIF 3897353
EPPO TEUCR
EOL 5365686
USDA GRIN 50073

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
Earlier Morning Arrival to Pollen-Rewarding Flowers May Enable Feral Bumble Bees to Successfully Compete with Local Bee Species and Expand Their Distribution Range in a Mediterranean Habitat Bar-Shai N, Motro U, Shmida A, Bloch G Insects 07-Sep-2022
PMCID:PMC9503872
doi:10.3390/insects13090816
PMID:36135517
Characterization and Botanical Differentiation of Monofloral and Multifloral Honeys Produced in Cyprus, Greece, and Egypt Using Physicochemical Parameter Analysis and Mineral Content in Conjunction with Supervised Statistical Techniques Karabagias IK, Louppis AP, Kontakos S, Drouza C, Papastephanou C J Anal Methods Chem 05-Jun-2018
PMCID:PMC6008861
doi:10.1155/2018/7698251
PMID:29967713
Effects of selected Palestinian plants on the in vitro exsheathment of the third stage larvae of gastrointestinal nematodes Jamous RM, Ali-Shtayeh MS, Abu-Zaitoun SY, Markovics A, Azaizeh H BMC Vet Res 03-Nov-2017
PMCID:PMC5670504
doi:10.1186/s12917-017-1237-7
PMID:29100544
Teucretol, a neo-clerodane diterpenoid from Teucrium creticum Giuseppe Savona, Franco Piozzi, Maurizio Bruno, Gema Domínguez, Benjamín Rodríguez, Orietta Servettaz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82488-7

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 / Prenol lipids / Terpene lactones / Diterpene lactones
19-Acetylgnaphalin 330709 Click to see 402.40 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
19-Acetylgnaphalin(terpene) 182444 Click to see CC1CC(=O)C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C 402.40 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
CID 5138525 5138525 Click to see CC1CC(=O)C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C 402.40 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(4R,4aR,5S,7R,8R,8aR)-5-acetyloxy-8-[(2S)-2-(furan-3-yl)-2-hydroxyethyl]-8-(hydroxymethyl)-7-methylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 163038778 Click to see 450.50 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
[5-acetyloxy-8-[2-(furan-3-yl)-2-hydroxyethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 13967137 Click to see CC1CC(C2(C(C1(C)CC(C3=COC=C3)O)CCCC24CO4)COC(=O)C)OC(=O)C 434.50 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
[5-acetyloxy-8-[2-(furan-3-yl)-2-hydroxyethyl]-8-(hydroxymethyl)-7-methylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 13967139 Click to see 450.50 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
6,19-Diacetylteumassilin 13967138 Click to see 434.50 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
Teucretol 13967140 Click to see CC1CC(C2(C(C1(CC(C3=COC=C3)O)CO)CCCC24CO4)COC(=O)C)OC(=O)C 450.50 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 13855360 13855360 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)82488-7
Teupolin I 156030 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)82488-7

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