Common products:
No commercial, industrial, craft, or culinary products are documented for this taxon; the plant has no established non-medicinal use.

Industrial and craft applications:
No applications are documented.

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

Colorants and tanning:
No documented use as a dye or tannin source.

Wood and fiber:
No timber or fiber applications are recorded.

Fragrance and cosmetics:
No fragrance, essential oil, or cosmetic uses are documented for this species.

Properties relevant to use:
No physical/chemical properties relevant to established uses have been reported.

Standards and regulation:
No relevant standards or regulatory frameworks apply.

Sustainability and sourcing:
No documented harvesting, cultivation, or trade exists for non-medicinal uses.

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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Filter by language:

Language	Common/alternative name
Arabic	غريقة
Hebrew	געדה מלבינה

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Teucrium leucocladum subsp. leucocladum		Unknown

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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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

Africa click to expand
- Northern Africa
  - Egypt

Asia-temperate click to expand
- 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

Add a new one!

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
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2,6-Di-tert-butyl-4-methylphenol	31404	Click to see	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	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	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	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
(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	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	136.23	unknown	https://doi.org/10.1016/J.BSE.2003.12.009
Bornyl angelate	6428437	Click to see	236.35	unknown	https://doi.org/10.1016/J.BSE.2003.12.009
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1016/J.BSE.2003.12.009
trans-Pinocarveol	88302	Click to see	152.23	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
(+)-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	280.40	unknown	https://doi.org/10.1016/J.BSE.2003.12.009
alpha-Cadinene, (+)-	12306048	Click to see	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	222.37	unknown	https://doi.org/10.1016/J.BSE.2003.12.009
beta-Cubebene	93081	Click to see	204.35	unknown	https://doi.org/10.1016/J.BSE.2003.12.009
cis-Muurol-5-en-4-alpha-ol	6430793	Click to see	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	204.35	unknown	https://doi.org/10.1016/J.BSE.2003.12.009
Cubebol	11276107	Click to see	222.37	unknown	https://doi.org/10.1016/J.BSE.2003.12.009
delta-Cadinene	441005	Click to see	204.35	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
Npc109838	6427091	Click to see	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
Ledum camphor	92812	Click to see	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	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	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	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	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	426.70	unknown	via CMAUP database
Friedelin	91472	Click to see	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	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	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	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	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	328.30	unknown	https://doi.org/10.1016/J.BSE.2003.12.009

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Teucrium leucocladum

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top