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Delphinium ternatum

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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
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Details Top

Internal ID UUID64401638681ac063464822
Scientific name Delphinium ternatum
Authority Huth
First published in Bot. Jahrb. Syst. 20: 421 (1895)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
  • Asia-temperate
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000640811
Tropicos 27102503
KEW urn:lsid:ipni.org:names:711069-1
The Plant List kew-2760466
Open Tree Of Life 6131820
Observations.org 147496
NCBI Taxonomy 2978106
IPNI 711069-1
GBIF 3926868
Elurikkus 441026

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
Ternatine, a new diterpene alkaloid fromDelphinium ternatum A. S. Narzullaev, N. D. Abdullaev, M. S. Yunusov, V. M. Matveev, S. G. Yunusova Springer Science and Business Media LLC 19-Sep-2006
doi:10.1007/BF02495370
Alkaloids ofDelphinium ternatum V. M. Matveev, A. S. Narzullaev, S. S. Sabirov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00576119
Dehydroeldelidine ? A new alkaloid fromDelphinium ternatum V. M. Matveev, A. S. Narzullaev, S. S. Sabirov, M. S. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574282
Alkaloids from Delphinium fangshanense S Zhang Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00756-0

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 / Aporphines
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1007/BF00574282
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1R,2S,3S,4S,5R,6S,8R,9R,10S,13R,16S,17R,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,8,9-triol 162971938 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6OC)O)OC)O)O)OC)OC)C 467.60 unknown https://doi.org/10.1007/BF00574282
11-Ethyl-4,6,16,18-tetramethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,8,9-triol 15599718 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6OC)O)OC)O)O)OC)OC)C 467.60 unknown https://doi.org/10.1007/BF00574282
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 CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)O)OC)C 449.60 unknown https://doi.org/10.1016/S0031-9422(98)00756-0
Dictyocarpine 185280 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4(C6C7O)O)OC)OCO5)OC(=O)C)OC)C 493.60 unknown https://doi.org/10.1007/BF00574282
SureCN4281363 118701198 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)O)OC)COC 479.60 unknown https://doi.org/10.1016/S0031-9422(98)00756-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(1S,5S,6R,8R,9S,11R,13R,14S,15S,16R,17S,18S,19R)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-6,13,15,19-tetrol 163057505 Click to see CC12CCCC34C1C5C(C67C3C(C(CC6C4N5C2O)C(=C)C7O)O)O 345.40 unknown https://doi.org/10.1007/BF02495370
(6,13,19-Trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-15-yl) 2-methylpropanoate 162952141 Click to see CC(C)C(=O)OC1C2C3C4(CCCC35C6C17C(C5N2C4O)CC(C6O)C(=C)C7O)C 415.50 unknown https://doi.org/10.1007/BF02495370
[(1S,5S,6R,8R,9S,11R,13R,14S,15S,16R,17S,18S,19R)-6,13,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-15-yl] 2-methylpropanoate 162952143 Click to see CC(C)C(=O)OC1C2C3C4(CCCC35C6C17C(C5N2C4O)CC(C6O)C(=C)C7O)C 415.50 unknown https://doi.org/10.1007/BF02495370
5-Methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-6,13,15,19-tetrol 163057504 Click to see CC12CCCC34C1C5C(C67C3C(C(CC6C4N5C2O)C(=C)C7O)O)O 345.40 unknown https://doi.org/10.1007/BF02495370
> Organoheterocyclic compounds / Quinolidines
(1S,2S,4R,5R,7S,8S,12S,13S,16R,19S,20R,21S,22S)-14-ethyl-5,19,22-trimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.14,7.01,13.02,7.08,12.016,20]docosan-21-ol 163002558 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C(C67C4CC(C6OC)C(C7)OC)OCO5)O)OC)C 449.60 unknown https://doi.org/10.1007/BF00576119
14-Ethyl-5,19,22-trimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.14,7.01,13.02,7.08,12.016,20]docosan-21-ol 163002557 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C(C67C4CC(C6OC)C(C7)OC)OCO5)O)OC)C 449.60 unknown https://doi.org/10.1007/BF00576119
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Ternatin 5459184 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)OC)OC)OC)O 374.30 unknown https://doi.org/10.1007/BF02495370

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