Delphinium occidentale

Details Top

Internal ID UUID64401627ebf4e872333482
Scientific name Delphinium occidentale
Authority S.Watson ex J.M.Coult.
First published in Man. Bot. Rocky Mt. : 11 (1885)

Ethnobotanical Use Top

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General Uses Top

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Common products:
No commercial, industrial, or craft applications are documented for *Delphinium occidentale*.

Industrial and craft applications:
No industrial or craft uses are documented.

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

Colorants and tanning:
No use as a colorant or source of tannins is documented.

Wood and fiber:
No timber or fiber uses are documented.

Fragrance and cosmetics:
No fragrance or cosmetic applications are documented.

Properties relevant to use:
No documented non-medicinal properties relevant to use are reported.

Standards and regulation:
No applicable standards or regulatory frameworks are documented.

Sustainability and sourcing:
No sustainability or sourcing information related to non-medicinal uses is documented.

Synonyms Top

Scientific name Authority First published in
Delphinastrum occidentale Nieuwl. Amer. Midl. Naturalist 3: 172 (1914)
Delphinium abietorum Tidestr. Proc. Biol. Soc. Washington 27: 61 (1914)
Delphinium cucullatum A.Nelson Bull. Torrey Bot. Club 27: 262 (1900)
Delphinium elatum var. occidentale S.Watson Botany [Fortieth Parallel] : 11 (1871)
Delphinium multiflorum Rydb. Bull. Torrey Bot. Club 29: 147 (1902)
Delphinium occidentale subsp. cucullatum (A.Nelson) Ewan Univ. Colorado Stud., Ser. D, Phys. Sci. 2: 138 (1945)
Delphinium occidentale var. cucullatum (A.Nelson) R.J.Davis Madroño 11: 144 (1951)
Delphinium occidentale var. reticulatum A.Nelson Bull. Torrey Bot. Club 27: 261 (1900)
Delphinium reticulatum Rydb. Bull. Torrey Bot. Club 33: 140 (1906)
Delphinium scopulorum subsp. occidentale (S.Watson) Abrams Ill. Fl. Pacific States 2: 187 (1944)

Common names Top

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Language Common/alternative name
Chinese 美西翠雀花

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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No forms added yet.

Germination/Propagation Top

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Alternate between 4°C and 20°C for 3 months each, over several cycles, with an extended germination period.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Nevada
      • Utah

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000640469
USDA Plants DEOC
KEW urn:lsid:ipni.org:names:710851-1
The Plant List kew-2760142
Open Tree Of Life 3944974
IPNI 710851-1
iNaturalist 170669
GBIF 3033783
Freebase /m/0120xmvr
EPPO DELOC
USDA GRIN 13456
Wikipedia Delphinium_occidentale

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
Three New C19-Diterpenoid Alkaloids from Delphinium occidentale S. Wats. S. William Pelletier, Palaniappan Kulanthaivel, John D. Olsen The Japan Institute of Heterocyclic Chemistry 23-Feb-2009
doi:10.3987/COM-87-4386
Deltaline, A New Alkaloid from Delphinium Occidentale S. Wats James Fitton Couch American Chemical Society (ACS) 19-Mar-2005
doi:10.1021/JA01295A048
Delbidine, an alkaloid from a hybrid population of delphinium occidentale and delphinium barbeyi Balawant S. Joshi, Haridutt K. Desai, El-Sayeda A. El-kashoury, S.William Pelletier, John D. Olsent Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97796-3
Taxonomic implications of diterpene alkaloids in three toxic tall larkspur species (Delphinium spp.) D.R Gardner, M.H Ralphs, D.L Turner, S.L Welsh Elsevier BV 25-Jul-2002
doi:10.1016/S0305-1978(01)00120-X

Phytochemical Profile Top

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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
Pemoline 4723 Click to see 176.17 unknown https://doi.org/10.3987/COM-87-4386
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1S,2R,3R,4S,5S,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9-triol 92854545 Click to see 467.60 unknown https://doi.org/10.3987/COM-87-4386
(1S,2R,3S,5R,6S,8R,10S,13S,16S,17R,18S)-11-ethyl-8,9,16-trihydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-one 134715256 Click to see 451.60 unknown https://doi.org/10.3987/COM-87-4386
[(1R,2S,3S,4S,5R,6S,8R,12S,13S,16R,19S,20R,21S)-21-acetyloxy-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-4-yl] (2S)-2-methylbutanoate 101665413 Click to see 577.70 unknown https://doi.org/10.3987/COM-87-4386
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] (2S)-2-methylbutanoate 101190667 Click to see 551.70 unknown https://doi.org/10.3987/COM-87-4386
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 2-methylpropanoate 101341143 Click to see 537.70 unknown https://doi.org/10.3987/COM-87-4386
[(2S,5R,6S,8R,13S,16R)-14-ethyl-2-hydroxy-4,6,19-trimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-21-yl] acetate 145994496 Click to see 507.60 unknown https://doi.org/10.3987/COM-87-4386
14-Ethyl-4,6,19-trimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-21-ol 14108117 Click to see 449.60 unknown https://doi.org/10.3987/COM-87-4386
Browniine 441714 Click to see 467.60 unknown https://doi.org/10.3987/COM-87-4386
Dehydrobrowniine 165269 Click to see 465.60 unknown https://doi.org/10.3987/COM-87-4386
Delcosin 145925533 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)COC 453.60 unknown https://doi.org/10.3987/COM-87-4386
Delcosine 120726 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)COC 453.60 unknown https://doi.org/10.3987/COM-87-4386
Delpheline 3083605 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)O)OC)C 449.60 unknown https://doi.org/10.3987/COM-87-4386
Deltaline 441728 Click to see 507.60 unknown https://doi.org/10.3987/COM-87-4386
Deltamine 6-acetate 165537 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4(C6C7OC)O)OC)OCO5)OC(=O)C)OC)C 507.60 unknown https://doi.org/10.1021/JA01295A048
Dictyocarpinine 6-acetate 185280 Click to see 493.60 unknown https://doi.org/10.3987/COM-87-4386
Eldeline 92854547 Click to see 507.60 unknown https://doi.org/10.1021/JA01295A048
Glaucerine 157146 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4(C6C7OC(=O)C(C)C)O)OC)OCO5)OC(=O)C)OC)C 563.70 unknown https://doi.org/10.3987/COM-87-4386
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(13R,21xi)-Hetisan-2alpha,11alpha,13-triol 86567874 Click to see 329.40 unknown https://doi.org/10.3987/COM-87-4386
(1S,3S,5S,8R,9S,11R,14R,16S,17R,18R,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,10,19-triol 101930091 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O 329.40 unknown https://doi.org/10.3987/COM-87-4386
(1S,5R,8R,9S,10R,11R,14R,16S,17R,18R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 131879709 Click to see 327.40 unknown https://doi.org/10.3987/COM-87-4386
(1S,5S,8R,9S,11R,14R,16S,17R,18R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 101930090 Click to see 327.40 unknown https://doi.org/10.3987/COM-87-4386
(5R,10R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 5318032 Click to see 327.40 unknown https://doi.org/10.3987/COM-87-4386
10,19-Dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 73657226 Click to see 327.40 unknown https://doi.org/10.3987/COM-87-4386
Hetisine 431673 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O 329.40 unknown https://doi.org/10.3987/COM-87-4386
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(10,16-Dihydroxy-5-methyl-12-methylidene-3-oxo-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-19-yl) 2-methylbutanoate 73657594 Click to see 427.50 unknown https://doi.org/10.1016/S0305-1978(01)00120-X
(1R,5S,8R,9S,10S,11R,14R,16R,17R,18R,19R)-10,16,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 163105535 Click to see 343.40 unknown https://doi.org/10.1016/S0031-9422(00)97796-3
10,16,19-Trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 163105534 Click to see 343.40 unknown https://doi.org/10.1016/S0031-9422(00)97796-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(11R,12S)-6,13-dimethyl-16-oxo-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-5,14,17-trien-11-yl] acetate 101681249 Click to see CC1=C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)OC(=O)C)CN1 367.50 unknown https://doi.org/10.1016/S0305-1978(01)00120-X

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