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Teucrium abutiloides

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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 UUID643feedb9634d567529146
Scientific name Teucrium abutiloides
Authority L'Hér.
First published in Stirp. Nov. : 84 (1788)

Description Top

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Synonyms Top

Scientific name Authority First published in
Teucrium globuliferum Salisb. Prodr. Stirp. Chap. Allerton : 77 (1796)
Teucrium macrophyllum Lam. Encycl. 2: 692 (1788)

Common names Top

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Language Common/alternative name
Portuguese erva-branca
Portuguese abrotona

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000321814
Tropicos 17603690
KEW urn:lsid:ipni.org:names:460199-1
The Plant List kew-202620
Open Tree Of Life 5232665
Observations.org 122876
NCBI Taxonomy 1209833
NBN Atlas NBNSYS0000163628
IUCN Red List 161815
IPNI 460199-1
iNaturalist 57435
GBIF 3901655
EPPO TEUAB
Elurikkus 436730

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
Pollinator shifts drive petal epidermal evolution on the Macaronesian Islands bird-flowered species Ojeda DI, Valido A, Fernández de Castro AG, Ortega-Olivencia A, Fuertes-Aguilar J, Carvalho JA, Santos-Guerra A Biol Lett 01-Apr-2016
PMCID:PMC4881347
doi:10.1098/rsbl.2016.0022
PMID:27122008
Sterols from Teucrium abutiloides and T. betonicum Helena Gaspar, Fernando M.S. Brito Palma, María C. de la Torre, Benjamín Rodríguez Elsevier BV 01-May-2003
doi:10.1016/0031-9422(96)00337-8
Neo-clerodane diterpenoids from Teucrium abutiloides María C. de la Torre, Benjamín Rodríguez, Franco Piozzi, Giuseppe Savona, Maurizio Bruno, María C. Carreiras Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85120-5

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 / Triterpenoids
[(3S,8R,9S,10R,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 163004234 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(=C)C 454.70 unknown https://doi.org/10.1016/0031-9422(96)00337-8
[(3S,8R,9S,10R,13R,14S,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 12945162 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 454.70 unknown https://doi.org/10.1016/0031-9422(96)00337-8
[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 15921 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 454.70 unknown https://doi.org/10.1016/0031-9422(96)00337-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9S,10R,13R,14S,17R)-17-[(2R,3E,5S)-5-ethyl-6-methylhepta-3,6-dien-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 102003014 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown https://doi.org/10.1016/0031-9422(96)00337-8
17-(5-ethyl-6-methylhepta-3,6-dien-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 73200193 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown https://doi.org/10.1016/0031-9422(96)00337-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
CID 101526594 101526594 Click to see CC1CC(C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCCC25CO5)COC(=O)C)OC(=O)C 490.50 unknown https://doi.org/10.1016/0031-9422(90)85120-5
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/10.1016/0031-9422(90)85120-5
CID 14488594 14488594 Click to see CC1CC(C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCCC25CO5)COC(=O)C)OC(=O)C 490.50 unknown https://doi.org/10.1016/0031-9422(90)85120-5
> Organoheterocyclic compounds / Furopyrans
[(1R,4R,6S,8R,9S,13R,14S,16R)-6-(furan-3-yl)-16-methylspiro[3,5-dioxatetracyclo[6.5.3.01,9.04,8]hexadecane-13,2'-oxirane]-14-yl] acetate 162899499 Click to see CC1CC(C23COC4C1(C2CCCC35CO5)CC(O4)C6=COC=C6)OC(=O)C 388.50 unknown https://doi.org/10.1016/0031-9422(90)85120-5
[(1R,4S,6S,8S,9S,13R,14S,16R)-6-(furan-3-yl)-16-methylspiro[3,5-dioxatetracyclo[6.5.3.01,9.04,8]hexadecane-13,2'-oxirane]-14-yl] acetate 101526941 Click to see CC1CC(C23COC4C1(C2CCCC35CO5)CC(O4)C6=COC=C6)OC(=O)C 388.50 unknown https://doi.org/10.1016/0031-9422(90)85120-5
[6-(Furan-3-yl)-16-methylspiro[3,5-dioxatetracyclo[6.5.3.01,9.04,8]hexadecane-13,2'-oxirane]-14-yl] acetate 14488592 Click to see CC1CC(C23COC4C1(C2CCCC35CO5)CC(O4)C6=COC=C6)OC(=O)C 388.50 unknown https://doi.org/10.1016/0031-9422(90)85120-5
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 14163581 14163581 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)CO)OC(=O)C 404.50 unknown https://doi.org/10.1016/0031-9422(90)85120-5

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