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Delphinium glaucescens

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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 UUID644016165d328132389602
Scientific name Delphinium glaucescens
Authority Rydb.
First published in Mem. New York Bot. Gard. 1: 155 (1900)

Description Top

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Synonyms Top

Scientific name Authority First published in
Delphinium glaucescens var. multicaule Rydb. Mem. New York Bot. Gard. 1: 156 (1900)

Common names Top

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Language Common/alternative name
English smooth larkspur
Chinese 小粉茎翠雀花

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000640124
USDA Plants DEGL2
Tropicos 27100937
KEW urn:lsid:ipni.org:names:77377-2
The Plant List kew-2759818
Open Tree Of Life 70143
NCBI Taxonomy 136323
Nature Serve 2.146907
IPNI 77377-2
iNaturalist 161667
GBIF 3033716
EOL 487963
USDA GRIN 417504

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
The effect of alkaloid composition of larkspur (Delphinium) species on the intoxication of Angus heifers Green BT, Gardner DR, Pfister JA, Welch KD, Bennett GL, Cook D J Anim Sci 17-Feb-2019
PMCID:PMC6396257
doi:10.1093/jas/skz004
PMID:30772897
Isolation and structure elucidation of the alkaloids of Delphinium glaucescens Rybd S. William Pelletier, Oliver D. Dailey, Naresh V. Mody, John D. Olsen American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00329A028

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
(11-Ethyl-2,8,9-trihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl)methyl 2-aminobenzoate 162882746 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6OC)O)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N 602.70 unknown https://doi.org/10.1021/JO00329A028
(11-Ethyl-8,9,18-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl)methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 162919325 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)O)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 668.80 unknown https://doi.org/10.1021/JO00329A028
(1S,2R,3R,4S,5S,6S,8R,9S,10S,13S,16S,17R,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 92854545 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1021/JO00329A028
(1S,2R,3R,4S,5S,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9,16-tetrol 57525180 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)COC 453.60 unknown https://doi.org/10.1021/JO00329A028
(1S,2R,3S,5R,6S,8R,9S,10S,13S,16S,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 101289627 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)OC)COC 465.60 unknown https://doi.org/10.1021/JO00329A028
[(1R,2S,3S,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-2,8,9-trihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-aminobenzoate 162882747 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6OC)O)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N 602.70 unknown https://doi.org/10.1021/JO00329A028
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,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] (2R)-2-methylbutanoate 162951910 Click to see CCC(C)C(=O)OC1C2CC3C1C(CC2OC)(C4(C(C5C36C4N(CC5(CCC6OC)COC)CC)OC)O)O 551.70 unknown https://doi.org/10.1021/JO00329A028
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-8,9,18-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[(3S)-3-methyl-2,5-dioxopyrrolidin-1-yl]benzoate 162919326 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)O)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 668.80 unknown https://doi.org/10.1021/JO00329A028
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/10.1021/JO00329A028
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/10.1021/JO00329A028
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/10.1021/JO00329A028
Glaucedine 157147 Click to see CCC(C)C(=O)OC1C2CC3C1C(CC2OC)(C4(C(C5C36C4N(CC5(CCC6OC)COC)CC)OC)O)O 551.70 unknown https://doi.org/10.1021/JO00329A028
Lycoctonine 99924 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1021/JO00329A028
Methyllycaconitine Perchlorate, Delphinium sp. 494471 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 682.80 unknown https://doi.org/10.1021/JO00329A028
Royline 57506221 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1021/JO00329A028
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
trans-Ocimenone 6428431 Click to see CC(=CC(=O)C=C(C)C=C)C 150.22 unknown https://doi.org/10.1021/JO00329A028

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