Details Top

Internal ID UUID644018f28f412587531034
Scientific name Echium pininana
Authority Webb & Berthel.
First published in Hist. Nat. Iles Canaries 3(2; 3): 44 (1844)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Echium pininana is cultivated as an ornamental, with cut stems and fresh inflorescences used in floral arrangements. No other documented non-medicinal products are reported.

Industrial and craft applications:
No documented uses.

Food and beverages (non-medicinal):
No documented uses.

Colorants and tanning:
No documented uses.

Wood and fiber:
No documented uses.

Fragrance and cosmetics:
No documented uses.

Properties relevant to use:
No documented uses.

Standards and regulation:
No documented uses.

Sustainability and sourcing:
Primarily grown as an ornamental; specific horticultural sustainability standards are not reported.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English pine echium
English pininana
Spanish pininana
Arabic زهرة الأفعى الشجرية
Welsh gwiberlys mawr
Russian Синяк сосновый

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-0000662987
USDA Plants ECPI2
Tropicos 100328761
INPN 611198
KEW urn:lsid:ipni.org:names:115832-1
The Plant List kew-2784279
Open Tree Of Life 967604
NCBI Taxonomy 113444
NBN Atlas NHMSYS0000458279
IUCN Red List 165250
IPNI 115832-1
iNaturalist 76763
GBIF 4068166
Freebase /m/04jhlz0
EPPO EHIPI
EOL 5355791
Elurikkus 460229
Calflora (Californian flora) 2889
USDA GRIN 14874
Wikipedia Echium_pininana
CMAUP NPO10017

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
New species of Cladosporium associated with human and animal infections Sandoval-Denis M, Gené J, Sutton DA, Wiederhold NP, Cano-Lira JF, Guarro J Persoonia 24-May-2016
PMCID:PMC4988372
doi:10.3767/003158516X691951
PMID:27616793
The genus Cladosporium Bensch K, Braun U, Groenewald JZ, Crous PW Stud Mycol 06-Jun-2012
PMCID:PMC3390897
doi:10.3114/sim0003
PMID:22815589
Pyrrolizidine alkaloids from Echium pininana E. Roeder, K. Liu, T. Bourauel Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98263-3

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
> Alkaloids and derivatives
[(7R,8R)-7-(3-methylbut-2-enoyloxy)-4-oxido-5,6,7,8-tetrahydro-3H-pyrrolizin-4-ium-1-yl]methyl (2S)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 101609674 Click to see 397.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
[(7R,8R)-7-(3-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 101609251 Click to see 381.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
[(7R,8R)-7-[(E)-2-methylbut-2-enoyl]oxy-4-oxido-5,6,7,8-tetrahydro-3H-pyrrolizin-4-ium-1-yl]methyl (2S)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 101609673 Click to see 397.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
[(7R,8R)-7-[(Z)-2-methylbut-2-enoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2,3-dihydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 91746607 Click to see 397.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
[(7R,8R)-7-[(Z)-2-methylbut-2-enoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2,3-dihydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate 124300747 Click to see 397.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
[(7R)-7-[(E)-2-methylbut-2-enoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate 5319976 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)C)(C(C)O)O 381.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
[7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 4581422 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)C)(C(C)O)O 381.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
[7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 10627 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)O)(C(C)(C)O)O 397.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
[7-(3-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 163025055 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C=C(C)C)O 381.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
3'-Acetyllycopsamine 586647 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C)O 341.40 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
7-Acetylintermedine 3035235 Click to see 341.40 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
Hydroxymyoscorpine 12308839 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)O)(C(C)(C)O)O 397.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
Myoscorpine 6440700 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)C)(C(C)O)O 381.50 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridopyrimidines
Spiroquinazoline 10409484 Click to see CC12C3=NC4=CC=CC=C4C(=O)N3C(CC15C6NCC(=O)N6C7=CC=CC=C57)C(=O)N2 413.40 unknown https://doi.org/10.1016/S0031-9422(00)98263-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Cyanidin 3-O-(6-O-malonyl-beta-D-glucoside) 443915 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O)O)O 535.40 unknown via CMAUP database
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Kaempferol 3-O-glucuronide 5318759 Click to see 462.40 unknown via CMAUP database
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
kaempferol 3-O-beta-D-(6''-O-malonyl)-glucoside 14162699 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O 534.40 unknown via CMAUP database
Quercetin 3-o-beta-D-(6''-o-malonyl)-glucoside 5282159 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O 550.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database

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