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Teucrium montbretii

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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 UUID643feef54d88d166779185
Scientific name Teucrium montbretii
Authority Benth.
First published in Ann. Sci. Nat., Bot. , sér. 2, 6: 56 (1836)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Hebrew געדת הסלעים

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Teucrium montbretii subsp. heliotropiifolium (Barbey) P.H.Davis Notes Roy. Bot. Gard. Edinburgh 21: 138 (1953)
Teucrium montbretii subsp. montbretii Unknown
Teucrium montbretii subsp. yildirimlii Dinç & Doğu Biologia (Bratislava) 67(4): 669 (2012)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000322346
Tropicos 100266131
KEW urn:lsid:ipni.org:names:460564-1
The Plant List kew-203127
Open Tree Of Life 5232634
Observations.org 134860
NCBI Taxonomy 1209874
IPNI 460564-1
iNaturalist 887104
GBIF 3895175
Elurikkus 435535

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
Phytotoxic Effects of Plant Essential Oils: A Systematic Review and Structure-Activity Relationship Based on Chemometric Analyses Abd-ElGawad AM, El Gendy AE, Assaeed AM, Al-Rowaily SL, Alharthi AS, Mohamed TA, Nassar MI, Dewir YH, Elshamy AI Plants (Basel) 25-Dec-2020
PMCID:PMC7823517
doi:10.3390/plants10010036
PMID:33375618
Anticancer Activity of Essential Oils and Other Extracts from Aromatic Plants Grown in Greece Fitsiou E, Pappa A Antioxidants (Basel) 07-Aug-2019
PMCID:PMC6720353
doi:10.3390/antiox8080290
PMID:31394842
Checklist of Wadi Hassan flora, Northeastern Badia, Jordan Kherissat F, Al-Esawi D Plant Divers 11-May-2019
PMCID:PMC6702440
doi:10.1016/j.pld.2019.05.001
PMID:31453416
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
Effects of Flower and Fruit Extracts of Melastoma malabathricum Linn. on Growth of Pathogenic Bacteria: Listeria monocytogenes, Staphylococcus aureus, Escherichia coli, and Salmonella typhimurium Che Omar SN, Ong Abdullah J, Khairoji KA, Chin Chin S, Hamid M Evid Based Complement Alternat Med 10-Apr-2013
PMCID:PMC3638579
doi:10.1155/2013/459089
PMID:23662136
Antioxidant and Anti-Inflammatory Activities of Essential Oils: A Short Review Miguel MG Molecules 15-Dec-2010
PMCID:PMC6259136
doi:10.3390/molecules15129252
PMID:21160452
Neo-clerodane diterpenoids from three species of Teucrium Roberto Alcázar, Maria C. De la Torre, Benjamin Rodríguez, Maurizio Bruno, Franco Piozzi, Giuseppe Savona, Nelly A. Arnold Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97562-9
Neo-clerodane diterpenes from Teucrium species Maurizio Bruno, Franco Piozzi, Benjamín Rodríguez, Giuseppe Savona, María C. de la Torre, Orietta Servettaz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80480-3
Neoclerodane diterpenoids from Teucrium montbretii subsp. libanoticum and their absolute configuration. Bruno M, Bondì ML, Rosselli S, Maggio A, Piozzi F, Arnold NA J Nat Prod 01-Feb-2002
doi:10.1021/NP010303M
PMID:11858745

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
(3R,5S,3'aR,10'aR)-5-(3-Furyl)-8'alpha-methyl-4,5,4',5',6',6'abeta-hexahydrospiro[furan-3(2H),7'(8'H)-naphtho[1,8a-c]furan]-2,3',10'(3a'H,9'H)-trione 45033628 Click to see CC1CC(=O)C23COC(=O)C2CCCC3C14CC(OC4=O)C5=COC=C5 358.40 unknown https://doi.org/10.1021/NP010303M
[(1S,7S,12S,13S,14S)-14-acetyloxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-3,8,16-trien-12-yl] benzoate 162877670 Click to see CC1=CC2C(=C(C(=O)O2)C)CC3C(=CCC(C3(C(CC1)OC(=O)C4=CC=CC=C4)C)OC(=O)C)C 478.60 unknown https://doi.org/10.1021/NP010303M
5'-(furan-3-yl)-10-hydroxy-8-methylspiro[5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-7,3'-oxolane]-2',3-dione 74105486 Click to see CC1CC(C23COC(=O)C2=CCCC3C14CC(OC4=O)C5=COC=C5)O 358.40 unknown https://doi.org/10.1021/NP010303M
5'-(Furan-3-yl)-8-methylspiro[1,3a,4,5,6,6a,8,9-octahydrobenzo[d][2]benzofuran-7,3'-oxolane]-2',3,10-trione 14396806 Click to see CC1CC(=O)C23COC(=O)C2CCCC3C14CC(OC4=O)C5=COC=C5 358.40 unknown https://doi.org/10.1021/NP010303M
5'-(Furan-3-yl)-9-hydroxy-2a-(hydroxymethyl)-7-methylspiro[1,3,4,5,5a,7,8,9-octahydronaphtho[1,8a-b]oxete-6,3'-oxolane]-2'-one 15627942 Click to see CC1CC(C23COC2(CCCC3C14CC(OC4=O)C5=COC=C5)CO)O 362.40 unknown https://doi.org/10.1021/NP010303M
6beta-Hydroxyteuscordin 76319628 Click to see CC1CC(C23COC(=O)C2=CCCC3C14CC(OC4=O)C5=COC=C5)O 358.40 unknown https://doi.org/10.1021/NP010303M
Montanin D 21634412 Click to see CC1CC(C23COC2(CCCC3C14CC(OC4=O)C5=COC=C5)CO)O 362.40 unknown https://doi.org/10.1021/NP010303M
https://doi.org/10.1016/0031-9422(92)80480-3
https://doi.org/10.1016/S0031-9422(00)97562-9
Teucrin H-2 13120894 Click to see CC1CC(C23COC(=O)C2CCCC3C14CC(OC4=O)C5=COC=C5)O 360.40 unknown https://doi.org/10.1016/0031-9422(92)80480-3
https://doi.org/10.1016/S0031-9422(00)97562-9
Teugin 76312390 Click to see CC1CC(C23COC(=O)C2=CC(CC3C14CC(OC4=O)C5=COC=C5)O)O 374.40 unknown https://doi.org/10.1016/0031-9422(92)80480-3
https://doi.org/10.1016/S0031-9422(00)97562-9
Teuscordinon 21123660 Click to see CC1CC(=O)C23COC(=O)C2=CCCC3C14CC(OC4=O)C5=COC=C5 356.40 unknown https://doi.org/10.1021/NP010303M
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 11762362 11762362 Click to see CC1CC(C2(C(C13CC(OC3O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)OC(=O)C 464.50 unknown https://doi.org/10.1021/NP010303M
CID 21635657 21635657 Click to see CC1CC(C2(C(C13CC(OC3O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)OC(=O)C 464.50 unknown https://doi.org/10.1021/NP010303M
CID 73090254 73090254 Click to see CC1CC(C2(C(C13CC(OC3O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)OC(=O)C 464.50 unknown https://doi.org/10.1021/NP010303M
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
CID 11812587 11812587 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)OC(=O)C 462.50 unknown https://doi.org/10.1021/NP010303M
CID 21635658 21635658 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)OC(=O)C 462.50 unknown https://doi.org/10.1021/NP010303M
CID 3036767 3036767 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/10.1016/0031-9422(92)80480-3
CID 495980 495980 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)OC(=O)C 462.50 unknown https://doi.org/10.1021/NP010303M
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Sterostrein R 139584475 Click to see CC1(CC2C(C1O)C(=O)C3=C(C2(C)O)CC(OC3)O)C 282.33 unknown https://doi.org/10.1021/NP010303M
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
5'-(Furan-3-yl)-7-methylspiro[12,14-dioxatetracyclo[7.4.1.01,10.05,10]tetradecane-6,3'-oxolane]-2',13-dione 13918564 Click to see CC1CC2C34COC(=O)C3(O2)CCCC4C15CC(OC5=O)C6=COC=C6 358.40 unknown https://doi.org/10.1016/0031-9422(92)80480-3
> Organoheterocyclic compounds / Furopyrans
[(1R,4S,6S,8R,9S,12S,13R,14S,16R)-6-(furan-3-yl)-12-hydroxy-16-methylspiro[3,5-dioxatetracyclo[6.5.3.01,9.04,8]hexadecane-13,2'-oxirane]-14-yl] acetate 11014960 Click to see CC1CC(C23COC4C1(C2CCC(C35CO5)O)CC(O4)C6=COC=C6)OC(=O)C 404.50 unknown https://doi.org/10.1021/NP010303M
[6-(Furan-3-yl)-12-hydroxy-16-methylspiro[3,5-dioxatetracyclo[6.5.3.01,9.04,8]hexadecane-13,2'-oxirane]-14-yl] acetate 85367257 Click to see CC1CC(C23COC4C1(C2CCC(C35CO5)O)CC(O4)C6=COC=C6)OC(=O)C 404.50 unknown https://doi.org/10.1021/NP010303M
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 101617533 101617533 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)O 420.50 unknown https://doi.org/10.1021/NP010303M
CID 162873277 162873277 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)O 420.50 unknown https://doi.org/10.1021/NP010303M
Teuflin 13071598 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown https://doi.org/10.1016/0031-9422(92)80480-3

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