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Delphinium roylei

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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 UUID64401631e1119101900314
Scientific name Delphinium roylei
Authority Munz
First published in J. Arnold Arbor. 48: 292 (1967)

Description Top

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Synonyms Top

Scientific name Authority First published in
Delphinium incanum Royle Ill. Bot. Himal. Mts. [Royle] 55. 1834 [Mar 1834]

Common names Top

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Language Common/alternative name
English royle's larkspur

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-0000640667
Tropicos 50320874
KEW urn:lsid:ipni.org:names:710974-1
The Plant List kew-2760330
Open Tree Of Life 6131791
IPNI 710974-1
GBIF 3927928

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
Royleinine, a New Norditerpenoid Alkaloid from Delphinium roylei Ayhan Ulubelen, Ali H. Meriçli, Filiz Meriçli, Ufuk Kolak, Muhammed Arfan, Manzoor Ahmad, Habib Ahmad The Japan Institute of Heterocyclic Chemistry 03-Mar-2009
doi:10.3987/COM-00-9010

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,18R)-11-ethyl-6,16,18-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 101076550 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)C 421.60 unknown https://doi.org/10.3987/COM-00-9010
[(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/10.3987/COM-00-9010
11-Ethyl-6,16,18-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 73657337 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)C 421.60 unknown https://doi.org/10.3987/COM-00-9010
CID 11452543 11452543 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.3987/COM-00-9010
Codelphine 92854546 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 unknown https://doi.org/10.3987/COM-00-9010
Condelphine 441720 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 unknown https://doi.org/10.3987/COM-00-9010
Fuziline 157773 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6O)C(C5O)OC)O)OC)O)COC 453.60 unknown https://doi.org/10.3987/COM-00-9010
Isotalatizidine 4586441 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.3987/COM-00-9010
Kondelfin 93054 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 unknown https://doi.org/10.3987/COM-00-9010

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