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Delphinium davisii

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 UUID6440160fc99bb669055160
Scientific name Delphinium davisii
Authority Munz
First published in J. Arnold Arbor. 48: 256 (1967)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Delphinium bithynicum P.H.Davis Notes Roy. Bot. Gard. Edinburgh 26: 172. 1965
Delphinium sintenisii Freyn Oesterr. Bot. Z. 43: 374. 1893

Common names Top

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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-0000639957
Tropicos 100321160
KEW urn:lsid:ipni.org:names:710547-1
The Plant List kew-2759656
Open Tree Of Life 6131635
IPNI 710547-1
GBIF 3921762

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 uncinatum Ayhan Ulubelen, Muhammad Arfan, Ufuk Sönmez, Ali H. Meriçli, Filiz Meriçli Elsevier BV 03-Aug-2011
doi:10.1016/S0031-9422(98)80087-3
Diterpenoid alkaloids from Delphinium caeruleum Yan Wang, Shao Nong Chen, Yuanjiang Pan, Jiaming Zhang, Yaozu Chen Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)85421-5
Diterpenoid alkaloids from Delphinium davisii. Ulubelen A, Desai HK, Srivastava SK, Hart BP, Park JC, Joshi BS, Pelletier SW, Meriçli AH, Meriçli F, Ilarslan R J Nat Prod 01-Apr-1996
doi:10.1021/NP960215F
PMID:8699181

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,6S,8R,9R,10R,13R,16S,17R,18S)-11-ethyl-6,8,16-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,18-diol 101714011 Click to see 421.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
(1S,2R,3R,4S,5S,6S,8S,13R,16S,17R)-11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 137706265 Click to see 377.50 unknown https://doi.org/10.1016/0031-9422(96)85421-5
Carmicheline 441742 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)C 377.50 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(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/10.1016/0031-9422(96)85421-5
(1S,5R,8R,9S,11R,14S,16S,17S,18R,19S)-5-(hydroxymethyl)-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-19-ol 163034893 Click to see C=C1CC23CC4C5C6(CCCC57C2C(C1CC3C7N4C6)O)CO 313.40 unknown https://doi.org/10.1021/NP960215F
(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/10.1016/0031-9422(96)85421-5
(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/10.1016/S0031-9422(98)80087-3
Davisinol 101714437 Click to see 313.40 unknown https://doi.org/10.1016/0031-9422(96)85421-5
Hetisine 431673 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O 329.40 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(1S,2R,5S,8R,9S,11R,13R,14S,16S,17R,18R)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-2,13-diol 101712457 Click to see 313.40 unknown https://doi.org/10.1016/0031-9422(96)85421-5
[(1S,5R,8R,9S,11R,14S,16S,17S,18R,19S)-19-hydroxy-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-5-yl]methyl benzoate 163104974 Click to see C=C1CC23CC4C5C6(CCCC57C2C(C1CC3C7N4C6)O)COC(=O)C8=CC=CC=C8 417.50 unknown https://doi.org/10.1021/NP960215F
[(1S,5S,8R,9S,11R,14S,16S,17S,18R,19S)-19-hydroxy-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-5-yl]methyl benzoate 101714438 Click to see C=C1CC23CC4C5C6(CCCC57C2C(C1CC3C7N4C6)O)COC(=O)C8=CC=CC=C8 417.50 unknown https://doi.org/10.1016/0031-9422(96)85421-5

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