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Delphinium caeruleum

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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 UUID644016098838b998013346
Scientific name Delphinium caeruleum
Authority Jacquem. ex Cambess.
First published in Voy. Inde 4: 7 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Delphinium beesianum var. malacotrichum Hand.-Mazz. Acta Horti Gothob. 13: 60 1939
Delphinium grandiflorum var. kunawarense Brühl Ann. Roy. Bot. Gard. (Calcutta) 5(2): 98 1896
Delphinium grandiflorum var. tsangense Brühl Ann. Roy. Bot. Gard. (Calcutta) 5(2): 99 1896
Delphinium caeruleum f. album W.T.Wang Acta Bot. Sin. 10: 266 1962

Common names Top

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Language Common/alternative name
Chinese 囊距翠雀
Chinese 蓝翠雀花
Chinese 雀冈

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Delphinium caeruleum var. obtusilobum Brühl ex Huth Bot. Jahrb. Syst. 20: 463. 1895 (1895)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Maintain seeds at a constant 10°C.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
short viability

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Qinghai
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000639822
Tropicos 27104864
KEW urn:lsid:ipni.org:names:710459-1
The Plant List kew-2759529
PFAF Delphinium caeruleum
Open Tree Of Life 884038
NCBI Taxonomy 1127147
IPNI 710459-1
GBIF 7276914

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
Valorization of Quercus suber L. Bark as a Source of Phytochemicals with Antimicrobial Activity against Apple Tree Diseases Sánchez-Hernández E, González-García V, Casanova-Gascón J, Barriuso-Vargas JJ, Balduque-Gil J, Lorenzo-Vidal B, Martín-Gil J, Martín-Ramos P Plants (Basel) 07-Dec-2022
PMCID:PMC9785260
doi:10.3390/plants11243415
PMID:36559527
The Biomechanical Screening Game between Visitor Power and Staminode Operative Strength of Delphinium caeruleum (Ranunculaceae) Hou QZ, Shao WJ, Ehmet N, Yang G, Zhong YQ, Min WR, Xu YF, Gao RC Plants (Basel) 05-Sep-2022
PMCID:PMC9459735
doi:10.3390/plants11172319
PMID:36079701
A Decrease in the Staminode-Mediated Visitor Screening Mechanism in Response to Nectar Robbers Positively Affects Reproduction in Delphinium caeruleum Jacq. ex Camb. (Ranunculaceae) Hou Q, Wang T, Yang G, Shao W, Min W, Zhong Y Biology (Basel) 11-Aug-2022
PMCID:PMC9405158
doi:10.3390/biology11081203
PMID:36009830
Responses of Plant Reproductive Phenology to Winter-Biased Warming in an Alpine Meadow Hu X, Zhou W, Sun S Front Plant Sci 04-Sep-2020
PMCID:PMC7498618
doi:10.3389/fpls.2020.534703
PMID:33013961
Variation in Soil Fungal Composition Associated with the Invasion of Stellera chamaejasme L. in Qinghai–Tibet Plateau Grassland He W, Detheridge A, Liu Y, Wang L, Wei H, Griffith GW, Scullion J, Wei Y Microorganisms 20-Nov-2019
PMCID:PMC6955776
doi:10.3390/microorganisms7120587
PMID:31756979
Plant diversity of the Kangchenjunga Landscape, Eastern Himalayas Kandel P, Chettri N, Chaudhary RP, Badola HK, Gaira KS, Wangchuk S, Bidha N, Uprety Y, Sharma E Plant Divers 26-Apr-2019
PMCID:PMC6702437
doi:10.1016/j.pld.2019.04.006
PMID:31453415
A toxic endophyte-infected grass helps reverse degradation and loss of biodiversity of over-grazed grasslands in northwest China Yao X, Christensen MJ, Bao G, Zhang C, Li X, Li C, Nan Z Sci Rep 18-Dec-2015
PMCID:PMC4683511
doi:10.1038/srep18527
PMID:26679518
Effects of Warming on Chlorophyll Degradation and Carbohydrate Accumulation of Alpine Herbaceous Species during Plant Senescence on the Tibetan Plateau Shi C, Sun G, Zhang H, Xiao B, Ze B, Zhang N, Wu N PLoS One 18-Sep-2014
PMCID:PMC4169446
doi:10.1371/journal.pone.0107874
PMID:25232872
Specific Duplication and Dorsoventrally Asymmetric Expression Patterns of Cycloidea-Like Genes in Zygomorphic Species of Ranunculaceae Jabbour F, Cossard G, Le Guilloux M, Sannier J, Nadot S, Damerval C PLoS One 21-Apr-2014
PMCID:PMC3994137
doi:10.1371/journal.pone.0095727
PMID:24752428
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315
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

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
(1R,2S,3S,4R,5S,6S,8S,12R,13R,16S,19R,20S,21S)-14-ethyl-4,6,19-trimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-21-ol 160563992 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)O)OC)C 449.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
(1S,2R,3R,4S,5S,6S,8S,12S,13R,16R,19S,20S)-14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-3-ol 163103657 Click to see CCN1CC2(CCC(C34C2CC5(C31)C6(CC(C7CC4C6(C7OC)O)OC)OCO5)OC)COC 479.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
(1S,2S,3S,4S,5R,6R,8S,12S,13S,16S,19R,20R,21R)-14-ethyl-6,21-dimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19-diol 163100117 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)OC)O)COC 465.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
(1S,5R,6S,8R,9S,13S,16S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 145994515 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
[(1S,2R,3R,4R,5R,6S,8R,9S,10S,13S,16R,17R,18R)-11-ethyl-8,9,16-trihydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 162908854 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)OC)O)COC 495.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
[(1S,2R,3R,4R,5R,6S,8S,9R,10R,13R,16S,17R,18S)-11-ethyl-16-hydroxy-4,6-dimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-18-yl] acetate 101647997 Click to see CCN1CC2(C=CC(C34C2C(C(C31)C5CC(C6CC4C5C6OC)OC)OC(=O)C)O)C 431.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
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(96)85421-5
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(96)85421-5
Delsine 11972492 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
Tatsiensine 163526 Click to see CCN1CC2(C=CC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)OC(=O)C)OC)C 489.60 unknown https://doi.org/10.1016/0031-9422(96)85421-5
> Organoheterocyclic compounds / Azepines
(1R,2S,3S,4R,5R,6S,8R,12R,13S,16S,19S,20R)-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docos-14-en-3-ol 163103627 Click to see COCC12CCC(C34C1CC5(C3N=C2)C6(CC(C7CC4C6(C7OC)O)OC)OCO5)OC 449.50 unknown https://doi.org/10.1016/0031-9422(96)85421-5
(1R,2S,3S,4S,5R,6S,8R,12R,13S,16S,19S,20R)-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docos-14-en-3-ol 101986488 Click to see COCC12CCC(C34C1CC5(C3N=C2)C6(CC(C7CC4C6(C7OC)O)OC)OCO5)OC 449.50 unknown https://doi.org/10.1016/0031-9422(96)85421-5

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