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Delphinium pictum

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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 UUID6440162c6ccba992448925
Scientific name Delphinium pictum
Authority Willd.
First published in Enum. Pl. : 574 (1809)

Description Top

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Synonyms Top

Scientific name Authority First published in
Delphinium staphisagria subsp. pictum (Willd.) Romo Fl. Silvestres Baleares : 104 (1994)
Staphisagria picta (Willd.) Jabbour PhytoKeys 7: 25 (2011)

Common names Top

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Language Common/alternative name
Catalan esperó baleàric
Italian speronella variopinta

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000640575
Tropicos 50005676
KEW urn:lsid:ipni.org:names:710908-1
The Plant List kew-2760244
Observations.org 138598
IPNI 710908-1
iNaturalist 515807
GBIF 7277813
EPPO DELPI
Elurikkus 581840

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)!
Title Authors Publication Released IDs
Diterpenoid Alkaloids from Delphinium pictum Willd. The Structure of Pictumine Gabriel de la Fuente, Rafael D誕z Acosta, Tom� Orribo The Japan Institute of Heterocyclic Chemistry 02-Mar-2009
doi:10.3987/COM-89-4506

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 / Diterpenoids / Aconitane-type diterpenoid alkaloids
(2R,3R,4S,5S,6S,8R,13S,16S,17R,18R)-11-ethyl-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 146014456 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.3987/COM-89-4506
[(1S,2R,3R,4R,5S,6S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] (E)-3-phenylprop-2-enoate 101600178 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C=CC7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)COC 639.80 unknown https://doi.org/10.3987/COM-89-4506
[(1S,2R,3R,4S,5R,6S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-16-hydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 97032085 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OC(=O)C)OC)O)COC 521.60 unknown https://doi.org/10.3987/COM-89-4506
Aconitane-8,13,14-triol, 1,6,16-trimethoxy-4-(methoxymethyl)-20-methyl-, 8-acetate 14-benzoate, (1alpha,6alpha,14alpha,16beta)- 97909 Click to see CC(=O)OC12CC(C3(CC(C1C3OC(=O)C4=CC=CC=C4)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC)O)OC 599.70 unknown https://doi.org/10.3987/COM-89-4506
Chasmaconitine 101600179 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)COC 613.70 unknown https://doi.org/10.3987/COM-89-4506
Einecs 209-214-0 118701199 Click to see CC(=O)OC12CC(C3(CC(C1C3OC(=O)C4=CC=CC=C4)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC)O)OC 599.70 unknown https://doi.org/10.3987/COM-89-4506
Neoline 120682 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.3987/COM-89-4506

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