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Delphinium leroyi

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 UUID6440161ef25ea419902135
Scientific name Delphinium leroyi
Authority Franch. ex Huth
First published in Helios 11: 73 (1873)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Delphinium candidum Hemsl. Bot. Mag. 133: t. 8170 (1907)
Delphinium goetzeanum Engl. Bot. Jahrb. Syst. 30: 308 (1901)
Delphinium gommengingeri Volkens ex Engl. Bot. Jahrb. Syst. 45: 266 (1910)
Delphinium gomminggeri Volkens ex Engl. Bot. Jahrb. Syst. 45: 266 (1910)
Delphinium macrosepalum Engl. Bot. Jahrb. Syst. 45: 267 1910
Delphinium van-der-weyeri auct. Gard. Chron. III, 54: 55 1913

Common names Top

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Language Common/alternative name
Chinese 晚香翠雀花

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Malawi
      • Zambia
    • West-central Tropical Africa
      • Rwanda
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000640301
Tropicos 27102970
KEW urn:lsid:ipni.org:names:710747-1
The Plant List kew-2759988
Open Tree Of Life 259373
NCBI Taxonomy 1127171
IPNI 710747-1
GBIF 3930376
EPPO DELLE
USDA GRIN 105355

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
Norditerpenoid alkaloids of Delphinium leroyi Yili Bai, Michael Benn Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83484-G

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-8,9,16-trihydroxy-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl) acetate 163106218 Click to see 435.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
(1S,2R,3R,4S,5S,6R,8R,9R,10S,13R,16S,17R)-11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9,16-tetrol 101631697 Click to see 393.50 unknown https://doi.org/10.1016/0031-9422(92)83484-G
(1S,2R,3R,4S,5S,6S,8R,10S,13S,16S,17R,18S)-11-ethyl-6,8,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,9,16-triol 134715261 Click to see 467.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
(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 467.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
Browniine 441714 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
Delcosin 145925533 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)COC 453.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
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/10.1016/0031-9422(92)83484-G
Deltatsine 185185 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)OC)O)OC)O)COC 467.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
> Organoheterocyclic compounds / Azepanes
(1S,2R,4S,5R,6R,8R,9S,10S,13S,16S,17R,18S,20S)-11-ethyl-16,18,20-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.24,8.01,10.02,6.013,17]icosane-5,8,9-triol 162986046 Click to see 481.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
(1S,2R,4S,5R,6R,8R,9S,10S,13S,16S,17R,18S,20S)-11-ethyl-18,20-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.24,8.01,10.02,6.013,17]icosane-5,8,9,16-tetrol 163026350 Click to see 467.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
(1S,2R,4S,5R,6R,8R,9S,10S,13S,16S,17R,18S,20S)-11-ethyl-8,18,20-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.24,8.01,10.02,6.013,17]icosane-5,9,16-triol 162847583 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC6C4CC(C6O)C(C5)OC)OC)O)OC)O)COC 481.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
[(1S,2R,4R,5R,6R,8S,9S,10S,13S,16S,17R,18S,20S)-11-ethyl-8,9,16-trihydroxy-18,20-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.24,8.01,10.02,6.013,17]icosan-5-yl] acetate 162880795 Click to see 509.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
[11-Ethyl-8,9,16-trihydroxy-18,20-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.24,8.01,10.02,6.013,17]icosan-5-yl] acetate 162880794 Click to see 509.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
11-Ethyl-16,18,20-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.24,8.01,10.02,6.013,17]icosane-5,8,9-triol 162986045 Click to see 481.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
11-Ethyl-18,20-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.24,8.01,10.02,6.013,17]icosane-5,8,9,16-tetrol 163026349 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC6C4CC(C6O)C(C5)OC)O)O)OC)O)COC 467.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G
11-Ethyl-8,18,20-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.24,8.01,10.02,6.013,17]icosane-5,9,16-triol 162847582 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC6C4CC(C6O)C(C5)OC)OC)O)OC)O)COC 481.60 unknown https://doi.org/10.1016/0031-9422(92)83484-G

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