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Delphinium biternatum

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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 UUID6440160807095556821664
Scientific name Delphinium biternatum
Authority Huth
First published in Bot. Jahrb. Syst. 20: 422 (1895)

Description Top

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Synonyms Top

Scientific name Authority First published in
Delphinium floribundum Freyn & Sint. ex Freyn Bull. Herb. Boissier , sér. 2, 3: 561 (1903)
Delphinium gorganicum Rech.f. Anz. Österr. Akad. Wiss., Math.-Naturwiss. Kl. 89: 226 (1951)

Common names Top

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Language Common/alternative name
Russian Дельфиниум дваждытройчатый
Russian Шпорник дваждытройчатый
Russian Живокость дваждытройчатая
Chinese 还亮草
Chinese 三出翠雀花

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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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000639784
Tropicos 27102403
KEW urn:lsid:ipni.org:names:710436-1
The Plant List kew-2759494
Plantarium 12751
Open Tree Of Life 884042
Observations.org 117080
NCBI Taxonomy 1127145
IPNI 710436-1
GBIF 3923001
EOL 2873660
Elurikkus 440059
USDA GRIN 13412

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
Structure of iliensine M. S. Yunusov, V. E. Nezhevenko, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567061
Alkaloids of Delphinium biternatum B. T. Salimov, M. S. Yunusov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565884

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
(1R,2R,3R,4S,5R,6S,8R,9S,10S,13R,14R,17S,18S)-11-ethyl-4,6,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9,14-triol 162958847 Click to see CCN1CC2(C(CCC34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)O)COC 467.60 unknown https://doi.org/10.1007/BF00565884
(1R,2R,3R,4S,5S,6S,8R,9R,10R,13S,16R,17S,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 163194308 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1007/BF00565884
(1R,2R,3S,5R,6S,8R,9S,10S,13R,14R,17S,18S)-11-ethyl-8,9,14-trihydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-one 162946411 Click to see CCN1CC2(C(CCC34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)O)COC 451.60 unknown https://doi.org/10.1007/BF00565884
(1R,2S,3S,4S,5S,6R,8S,9R,10R,13R,16S,17S,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 162942616 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1007/BF00565884
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16R,17R,18S)-11-ethyl-4,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-6,8,9-triol 162990182 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)O)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1007/BF00565884
(1S,2R,3S,4R,5R,6R,8R,9S,13S,16R,17R,18R)-11-ethyl-4,6,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9,16-triol 137705073 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)O)COC 467.60 unknown https://doi.org/10.1007/BF00567061
(1S,2R,3S,5R,6S,8R,9S,10S,13S,16R,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-one 162921560 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)OC)COC 465.60 unknown https://doi.org/10.1007/BF00565884
(1S,2S,3S,4R,5S,6R,8S,9S,10S,13S,16S,17R,18R)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 162942620 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1007/BF00565884
(6S,8R,9R,13S,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 5316490 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1007/BF00565884
[(1R,2R,3R,4S,5R,6S,8R,9S,10S,13R,14R,17S,18S)-11-ethyl-8,9,14-trihydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 163020977 Click to see CCN1CC2(C(CCC34C2C(C(C31)(C5(CC(C6CC4C5C6OC(=O)C7=CC=CC=C7)OC)O)O)OC)O)COC 557.70 unknown https://doi.org/10.1007/BF00565884
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16R,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] benzoate 163191099 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC(=O)C7=CC=CC=C7)OC)O)O)OC)OC)COC 571.70 unknown https://doi.org/10.1007/BF00565884
[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] benzoate 73813824 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC(=O)C7=CC=CC=C7)OC)O)O)OC)OC)COC 571.70 unknown https://doi.org/10.1007/BF00565884
[11-Ethyl-8,9,14-trihydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 163020976 Click to see CCN1CC2(C(CCC34C2C(C(C31)(C5(CC(C6CC4C5C6OC(=O)C7=CC=CC=C7)OC)O)O)OC)O)COC 557.70 unknown https://doi.org/10.1007/BF00565884
11-Ethyl-4,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-6,8,9-triol 162990181 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)O)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1007/BF00565884
11-Ethyl-4,6,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9,14-triol 162958846 Click to see CCN1CC2(C(CCC34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)O)COC 467.60 unknown https://doi.org/10.1007/BF00565884
11-Ethyl-8,9,14-trihydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-one 162946410 Click to see CCN1CC2(C(CCC34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)O)COC 451.60 unknown https://doi.org/10.1007/BF00565884
Browniine 165288 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1007/BF00565884
Dehydrobrowniine 165269 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)OC)COC 465.60 unknown https://doi.org/10.1007/BF00565884
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/10.1007/BF00567061
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/10.1007/BF00567061
Delphatine 185591 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1007/BF00565884
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4,7-Dimethoxyfuro[2,3-b]quinolin-6-ol 86002753 Click to see COC1=C(C=C2C(=C1)N=C3C(=C2OC)C=CO3)O 245.23 unknown https://doi.org/10.1007/BF00565884

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