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Delphinium cossonianum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440160e54247635076121
Scientific name Delphinium cossonianum
Authority Batt.
First published in Bull. Soc. Hist. Nat. Afrique N. 8: 215 (1917)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Vietnamese phi yến

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-0000639925
Tropicos 27102031
KEW urn:lsid:ipni.org:names:710527-1
The Plant List kew-2759627
Open Tree Of Life 209868
NCBI Taxonomy 984875
IPNI 710527-1
GBIF 3921954
EPPO DELCO

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)!
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Title Authors Publication Released IDs
Three diterpenoid alkaloids from Delphinium cossonianum Gabriel de la Fuente, Jose A. Gavin, Rafael D. Acosta, Francisco Sanchez-Ferrando Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)80044-S

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
(1S,2R,3R,4S,5S,8S,9S,10R,13R,16S,17R)-11-ethyl-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 132561513 Click to see 347.50 unknown https://doi.org/10.1016/0031-9422(93)80044-S
(2S,5S,10R,13S,14S,17S,18S)-4-ethyl-10-methyl-6-oxa-4-azaheptacyclo[15.2.1.02,7.02,11.03,13.05,10.014,19]icosane-14,18-diol 162817117 Click to see 345.50 unknown https://doi.org/10.1016/0031-9422(93)80044-S
[(2S,5S,10R,13R,14R,17S,18S)-4-ethyl-13,14-dihydroxy-10-methyl-6-oxa-4-azaheptacyclo[15.2.1.02,7.02,11.03,13.05,10.014,19]icosan-18-yl] (Z)-3-phenylprop-2-enoate 162889851 Click to see CCN1C2C3(CC4C2(C5CCC4(C1O5)C)C6CC7CCC3(C6C7OC(=O)C=CC8=CC=CC=C8)O)O 491.60 unknown https://doi.org/10.1016/0031-9422(93)80044-S
20-Ethyl-4-methylaconitane-1,8,14-triol 495499 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CCC6CC4C5C6O)O)O)C 347.50 unknown https://doi.org/10.1016/0031-9422(93)80044-S
Cardiopetaline 5459237 Click to see 347.50 unknown https://doi.org/10.1016/0031-9422(93)80044-S
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
[(1S,3S,4S,8R,9S,10R,11R,14R,16S,17S,18R,19R)-4,10-diacetyloxy-19-hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] benzoate 163185879 Click to see 533.60 unknown https://doi.org/10.1016/0031-9422(93)80044-S
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(4,10-Diacetyloxy-19-hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl) benzoate 163106441 Click to see 533.60 unknown https://doi.org/10.1016/0031-9422(93)80044-S
[(1S,3S,4S,5S,8R,9S,10R,11R,14R,16S,17S,18R,19R)-4,10-diacetyloxy-19-hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] benzoate 163106442 Click to see 533.60 unknown https://doi.org/10.1016/0031-9422(93)80044-S
7alpha-Hydroxycossonidine 101182521 Click to see 329.40 unknown https://doi.org/10.1016/0031-9422(93)80044-S

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