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Delphinium uncinatum

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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 UUID6440163ac33c7469795957
Scientific name Delphinium uncinatum
Authority Hook.f. & Thomson
First published in Fl. Brit. India 1: 24 (1872)

Description Top

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Synonyms Top

Scientific name Authority First published in
Delphinium penicillatum Hook.f. & Thomson Fl. Ind. [Hooker f. & Thomson] 48. 1855
Delphinium uncinatum var. glabrum Qureshi & Chaudhri Pakistan Syst. 3: 9 (1987)
Delphinium vestitum Boiss. Diagn. Pl. Orient. ser. 2, 1: 13. 1854 [May-Aug 1854]
Delphinium uncinatum var. aitchisonii Brühl Ann. Roy. Bot. Gard. (Calcutta) 5: 94 1896
Delphinium uncinatum var. pseudovestitum Brühl Ann. Roy. Bot. Gard. (Calcutta) 5: 94 1896
Delphinium uncinatum var. aitchisoni Boiss. Ann. Roy. Bot. Gard. (Calcutta) 5: 94 1896

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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-0000640867
Tropicos 50320864
KEW urn:lsid:ipni.org:names:711109-1
The Plant List kew-2760522
Observations.org 505721
IPNI 711109-1
GBIF 7277500
Elurikkus 581787
USDA GRIN 407311
Open Tree Of Life 5737881

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

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 / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
Undulatin 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(18-Acetyloxy-11-ethyl-6,8,16-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl) acetate 73657010 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OC)OC(=O)C)OC)C 505.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
(1R,2S,3S,4S,5S,6R,8R,12R,13R,16R,19S,20S,21R)-14-ethyl-4,6,19,21-tetramethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane 163098740 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)OC)OC)COC 493.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
(2R,3R,6S,8R,12R,16S,20R,21S)-14-ethyl-4,6,19,21-tetramethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane 5316483 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)OC)OC)COC 493.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
[(1R,2S,3S,4R,5S,6R,8S,9S,10S,13R,16S,17S,18R)-18-acetyloxy-11-ethyl-6,8,16-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 163001406 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OC)OC(=O)C)OC)C 505.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
[(1S,2R,3R,4S,5R,6S,8R,9R,10R,13R,16S,17R,18R)-18-acetyloxy-11-ethyl-6,8,16-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 163001407 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OC)OC(=O)C)OC)C 505.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
[(1S,2R,3R,4S,5S,6S,8R,9R,10S,13R,16S,17R)-11-ethyl-8,16-dihydroxy-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 134688067 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
[(1S,2S,3S,4S,5S,6R,8S,9R,10S,13S,16R,17R)-11-ethyl-8,9,16-trihydroxy-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 163027589 Click to see CCN1CC2(CCC(C34C2CC(C31)(C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)O)COC 465.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
14-Ethyl-4,6,19,21-tetramethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane 14059164 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)OC)OC)COC 493.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
Acetylvirescenine 100964236 Click to see CCN1CC2(CCC(C34C2CC(C31)(C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)O)COC 465.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
Codelphine 92854546 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
Condelphine 441720 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
Kondelfin 93054 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 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,2S,4S,6S,7R,8R,10R,11R)-13-[(E)-2-hydroxyethenyl]-11-methyl-5-methylidene-13-azapentacyclo[9.3.3.24,7.01,10.02,7]nonadecane-6,8-diol 102121479 Click to see CC12CCCC3(C1CC(C45C3CC(CC4)C(=C)C5O)O)CN(C2)C=CO 359.50 unknown https://doi.org/10.1016/S0031-9422(98)80087-3
13-(2-Hydroxyethenyl)-11-methyl-5-methylidene-13-azapentacyclo[9.3.3.24,7.01,10.02,7]nonadecane-6,8-diol 163059489 Click to see CC12CCCC3(C1CC(C45C3CC(CC4)C(=C)C5O)O)CN(C2)C=CO 359.50 unknown https://doi.org/10.1016/S0031-9422(98)80087-3

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