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Teucrium leucocladum

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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 UUID643feef14b0e1105999020
Scientific name Teucrium leucocladum
Authority Boiss.
First published in Diagn. Pl. Orient. 5: 44 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Teucrium cuneifolium Schimp. ex Boiss. Diagn. Pl. Orient. 5: 44 (1844)
Teucrium schimperi C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 530 (1845)

Common names Top

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Language Common/alternative name
Arabic غريقة
Hebrew געדה מלבינה

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Teucrium leucocladum var. glandulosum Danin Willdenowia 27: 169 (1997)

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
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • Western Asia
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000322259
Tropicos 100266077
KEW urn:lsid:ipni.org:names:460512-1
The Plant List kew-203047
Open Tree Of Life 5336818
Observations.org 455943
NCBI Taxonomy 1423403
IPNI 460512-1
iNaturalist 961350
GBIF 7308359
Elurikkus 586408
CMAUP NPO11593

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 analysis, antioxidant, and antihyperlipidemic activities of Teucriumtakoumitense El-Guourrami O, Elbouny H, Ait Benlabchir A, Drioua S, Ouahzizi B, Alem C, Doukkali A, Benzeid H J Taibah Univ Med Sci 31-Jul-2023
PMCID:PMC10492209
doi:10.1016/j.jtumed.2023.07.011
PMID:37693822
Teucrium leucocladum: An Effective Tool for the Treatment of Hyperglycemia, Hyperlipidemia, and Oxidative Stress in Streptozotocin-Induced Diabetic Rats Bassalat N, Taş S, Jaradat N Evid Based Complement Alternat Med 12-Nov-2020
PMCID:PMC7718044
doi:10.1155/2020/3272103
PMID:33293988
In Vitro Characterization and Mosquito (Aedes aegypti) Repellent Activity of Essential-Oils-Loaded Nanoemulsions Nuchuchua O, Sakulku U, Uawongyart N, Puttipipatkhachorn S, Soottitantawat A, Ruktanonchai U AAPS PharmSciTech 28-Oct-2009
PMCID:PMC2799589
doi:10.1208/s12249-009-9323-1
PMID:19862624
Germacrene D Cyclization: An Ab Initio Investigation Setzer WN Int J Mol Sci 25-Jan-2008
PMCID:PMC2635598
doi:10.3390/ijms9010089
PMID:19325722
Chemical analysis and biological activities of the essential oil of Teucrium leucocladum Boiss. (Lamiaceae) Assem M El-Shazly, Karam T Hussein Elsevier BV 01-May-2004
doi:10.1016/J.BSE.2003.12.009
Guaiane sesquiterpenes from Teucrium leucocladum Maurizio Bruno, Maria C. de la Torre, Benjamín Rodríguez, Abdallah A. Omar Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90812-4

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
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
Butylated Hydroxytoluene 31404 Click to see CC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C 220.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(-)-alpha-Alaskene 524815 Click to see CC1CCC(=C(C)C)C12CCC(=CC2)C 204.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> 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/J.BSE.2003.12.009
Dendrolasin 5316534 Click to see CC(=CCCC(=CCCC1=COC=C1)C)C 218.33 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Thujene 637518 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/J.BSE.2003.12.009
(1r,3s,5r)-6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-ol 88302 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/J.BSE.2003.12.009
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1016/J.BSE.2003.12.009
5-Propan-2-ylbicyclo[3.1.0]hex-3-ene-2-carbaldehyde 6429043 Click to see CC(C)C12CC1C(C=C2)C=O 150.22 unknown https://doi.org/10.1016/J.BSE.2003.12.009
6,6-Dimethylbicyclo[3.1.1]heptan-2-one 32735 Click to see CC1(C2CCC(=O)C1C2)C 138.21 unknown https://doi.org/10.1016/J.BSE.2003.12.009
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Bornyl angelate 6428437 Click to see CC=C(C)C(=O)OC1CC2CCC1(C2(C)C)C 236.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/J.BSE.2003.12.009
trans-Thujone 6432452 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Verbenone, (+)- 65724 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
(+)-gamma-Gurjunene 50986224 Click to see CC1CCC(C=C2C1CCC2C)C(=C)C 204.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
[(1S,3aR,4R,7S,7aS)-1-acetyl-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-4-yl] acetate 21679492 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)OC(=O)C 280.40 unknown https://doi.org/10.1016/J.BSE.2003.12.009
alpha-Cadinene, (+)- 12306048 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
alpha-Muurolol 91753440 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Cadina-1,4-diene 6427091 Click to see CC1CCC(C2C1=CCC(=C2)C)C(C)C 204.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
cis-Muurol-5-en-4-alpha-ol 6430793 Click to see CC1CCC(C2=CC(CCC12)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
cis-Muurol-5-en-4-beta-ol 6428412 Click to see CC1CCC2C(CCC(C2=C1)(C(C)C)O)C 222.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
cis-Muurola-4(14),5-diene 51351709 Click to see CC1CCC(C2=CC(=C)CCC12)C(C)C 204.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Cubebol 11276107 Click to see CC1CCC(C2C13C2C(CC3)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledol 92812 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
alpha-Cedr-8(15)ene-9-ol 6430532 Click to see CC1CCC2C13CC(C2(C)C)C(=C)C(C3)O 220.35 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol acetate 6427486 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)OC(=O)C)C 264.40 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1S,3aS,4R,8aR)-1,4-dimethyl-7-propan-2-yl-2,3,3a,5,6,7,8,8a-octahydroazulene-1,4,8-triol 129316632 Click to see CC(C)C1CCC(C2CCC(C2C1O)(C)O)(C)O 256.38 unknown https://doi.org/10.1016/S0031-9422(00)90812-4
1-Methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,7,8,8a-octahydroazulene-1,8-diol 73226242 Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(00)90812-4
1,4-Dimethyl-7-propan-2-yl-2,3,3a,5,6,7,8,8a-octahydroazulene-1,4,8-triol 92001737 Click to see CC(C)C1CCC(C2CCC(C2C1O)(C)O)(C)O 256.38 unknown https://doi.org/10.1016/S0031-9422(00)90812-4
10-Epiteuclatriol 101447991 Click to see CC(C)C1CCC(C2CCC(C2C1O)(C)O)(C)O 256.38 unknown https://doi.org/10.1016/S0031-9422(00)90812-4
Teucladiol 16046185 Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(00)90812-4
Teuclatriol 91884970 Click to see CC(C)C1CCC(C2CCC(C2C1O)(C)O)(C)O 256.38 unknown https://doi.org/10.1016/S0031-9422(00)90812-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
CID 13944860 13944860 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)OC(=O)C 446.50 unknown https://doi.org/10.1016/S0031-9422(00)90812-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Patchouli alcohol 10955174 Click to see CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O 222.37 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Heptanal 8130 Click to see CCCCCCC=O 114.19 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetyl-3-ethylpyrazine 61918 Click to see CCC1=NC=CN=C1C(=O)C 150.18 unknown https://doi.org/10.1016/J.BSE.2003.12.009
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1016/J.BSE.2003.12.009

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