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Delphinium grandiflorum

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 UUID64401616e5c50249874774
Scientific name Delphinium grandiflorum
Authority L.
First published in Sp. Pl. : 531 (1753)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Chienia honanensis W.T.Wang Acta Phytotax. Sin. 9: 104 (1964)
Delphinastrum grandiflorum Spach Hist. Nat. Vég. 7: 338 (1838)
Delphinium bonatii H.Lév. Repert. Spec. Nov. Regni Veg. 7: 99 (1909)
Delphinium chinense Fisch. ex DC. Prodr. 1: 53 (1824)
Delphinium grandiflorum f. album T.J.Feng & J.X.Huang Bull. Bot. Res., Harbin 14(1): 75. 1994
Delphinium grandiflorum var. pilosum Y.Z.Zhao Acta Sci. Nat. Univ. Intramongol. 19: 677 (1988)
Delphinium grandiflorum f. roseolum Y.Z.Zhao Acta Sci. Nat. Univ. Intramongol. 19: 677 (1988)
Delphinium grandiflorum var. tigridum Kitag. Rep. Exped. Manchoukou Sect. IV 4: 17 1936
Delphinium sinense Fisch. ex Link Enum. Hort. Berol. Alt. 2: 80 (1822)
Delphinium virgatum J.Jacq. ex Spreng. Syst. Veg., ed. 16 [Sprengel] 2: 617. 1825 [Jan-May 1825]
Delphinium grandiflorum f. glanduliferum W.T.Wang Acta Phytotax. Sin., Addit. 1: 103 1965
Delphinium grandiflorum f. heterotrichum W.T.Wang Acta Phytotax. Sin., Addit. 1: 103 1965
Delphinium grandiflorum var. chinense Fisch. ex DC. Syst. Nat. 1: 351 1817

Common names Top

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Language Common/alternative name
English siberian larkspur
Arabic عائق كبير الأزهار
Azerbaijani İriçiçək mahmızçiçək
Azerbaijani İriyarpaq mahmızçiçək
Bulgarian едроцветна ралица
Estonian suureõiene kukekannus
Finnish kiinanritarinkannus
Icelandic greifaspori
Korean 제비고깔
mn Том гэзэг цэцэг
Slovenian grmasti ostrožnik
Swedish kinesisk riddarsporre
Chinese 崔雀
Chinese 翠雀
Chinese 翠雀花
Chinese 百部草
Chinese 鸡爪连图
Chinese 鸽子花
Chinese 小草乌

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Delphinium grandiflorum var. deinocarpum W.T.Wang Acta Phytotax. Sin. 32: 469 (1994)
Delphinium grandiflorum var. fangshanense (W.T.Wang) W.T.Wang Fl. Reipubl. Popularis Sin. 27: 447 (1979)
Delphinium grandiflorum var. gilgianum (Pilg. ex Gilg) Finet & Gagnep. Bull. Soc. Bot. France 51: 483 1904
Delphinium grandiflorum var. mosoynense (Franch.) Huth Bot. Jahrb. Syst. 20: 461. 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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Sow at 4°C for 3 weeks, then increase to 20°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
    • Eastern Asia
      • Korea
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
    • Siberia
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000640138
USDA Plants DEGR80
KEW urn:lsid:ipni.org:names:710650-1
The Plant List kew-2759830
Missouri Botanical Garden 286134
Open Tree Of Life 1004833
Observations.org 127132
NCBI Taxonomy 85439
Nature Serve 2.153249
IPNI 710650-1
iNaturalist 161668
GBIF 3033699
Freebase /m/047p7tt
EPPO DELGR
EOL 487965
Elurikkus 4266
USDA GRIN 13443
Wikipedia Delphinium_grandiflorum

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
Exploring the Biomedical Potential of Terpenoid Alkaloids: Sources, Structures, and Activities Wang X, Xin J, Sun L, Sun Y, Xu Y, Zhao F, Niu C, Liu S Molecules 25-Apr-2024
PMCID:PMC11085545
doi:10.3390/molecules29091968
PMID:38731459
Chemical Constituents and Bioactivities of the Plant-Derived Fungus Aspergillus fumigatus Sang Z, Zhang Y, Qiu K, Zheng Y, Chen C, Xu L, Lai J, Zou Z, Tan H Molecules 30-Jan-2024
PMCID:PMC10856792
doi:10.3390/molecules29030649
PMID:38338395
Assessing the win–win situation of forage production and soil organic carbon through a short-term active restoration strategy in alpine grasslands Wang Y, Wang Z, Kang Y, Zhang Z, Bao D, Sun X, Su J Front Plant Sci 11-Jan-2024
PMCID:PMC10808524
doi:10.3389/fpls.2023.1290808
PMID:38273956
The Impact and Determinants of Mountainous Topographical Factors on Soil Microbial Community Characteristics Yu J, Li S, Sun X, Zhou W, He L, Zhao G, Chen Z, Bai X, Zhang J Microorganisms 28-Nov-2023
PMCID:PMC10746091
doi:10.3390/microorganisms11122878
PMID:38138022
Isolation of endophytic fungi from Cotoneaster multiflorus and screening of drought-tolerant fungi and evaluation of their growth-promoting effects Lü ZW, Liu HY, Wang CL, Chen X, Huang YX, Zhang MM, Huang QL, Zhang GF Front Microbiol 02-Nov-2023
PMCID:PMC10653309
doi:10.3389/fmicb.2023.1267404
PMID:38029186
Assessment of residual plant DNA in bulk milk for Grana Padano PDO production by a metabarcoding approach Pozzi A, Nazzicari N, Capoferri R, Radovic S, Bongioni G PLoS One 25-Jul-2023
PMCID:PMC10368264
doi:10.1371/journal.pone.0289108
PMID:37490502
Editorial: Advances in natural product chemistry: Yunnan University 100th anniversary Chen W, Dong J, Panda SS Front Chem 13-Jun-2023
PMCID:PMC10299917
doi:10.3389/fchem.2023.1234211
PMID:37388946
The complete chloroplast genome sequence of Aconitum tschangbaischanense (Ranunculaceae) Liu X, Zhu J, Jiang M, Guan S, Zhang L, Zhao H Mitochondrial DNA B Resour 08-Jun-2023
PMCID:PMC10251779
doi:10.1080/23802359.2023.2220435
PMID:37303611
Economically viable flower drying techniques to sustain flower industry amid COVID-19 pandemic Kumar M, Chaudhary V, Sirohi U, Srivastav AL Environ Dev Sustain 29-May-2023
PMCID:PMC10225293
doi:10.1007/s10668-023-03376-w
PMID:37363010
Comparative analysis of codon usage patterns in chloroplast genomes of ten Epimedium species Wang Y, Jiang D, Guo K, Zhao L, Meng F, Xiao J, Niu Y, Sun Y BMC Genom Data 09-Jan-2023
PMCID:PMC9830715
doi:10.1186/s12863-023-01104-x
PMID:36624369
Chloroplast gene expression level is negatively correlated with evolutionary rates and selective pressure while positively with codon usage bias in Ophioglossum vulgatum L Hao J, Liang Y, Ping J, Li J, Shi W, Su Y, Wang T BMC Plant Biol 13-Dec-2022
PMCID:PMC9746204
doi:10.1186/s12870-022-03960-8
PMID:36510137
Grandiflolines A–F, new anti-inflammatory diterpenoid alkaloids isolated from Delphinium grandiflorum Yan Y, Jiang H, Yang X, Ding Z, Yin T Front Chem 19-Sep-2022
PMCID:PMC9527285
doi:10.3389/fchem.2022.1012874
PMID:36199660
Genome-wide identification and characterization of active ingredients related β-Glucosidases in Dendrobium catenatum Wang Z, Zhao M, Zhang X, Deng X, Li J, Wang M BMC Genomics 23-Aug-2022
PMCID:PMC9400273
doi:10.1186/s12864-022-08840-x
PMID:35999493
Anthocyanic Vacuolar Inclusions: From Biosynthesis to Storage and Possible Applications Buhrman K, Aravena-Calvo J, Ross Zaulich C, Hinz K, Laursen T Front Chem 28-Jun-2022
PMCID:PMC9273883
doi:10.3389/fchem.2022.913324
PMID:35836677
Comparative analysis of complete chloroplast genome of ethnodrug Aconitum episcopale and insight into its phylogenetic relationships Xia C, Wang M, Guan Y, Li Y, Li J Sci Rep 08-Jun-2022
PMCID:PMC9178047
doi:10.1038/s41598-022-13524-3
PMID:35676401

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,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 97960151 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1021/NP0401922
(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/10.1016/S0031-9422(02)00514-9
(1S,2S,3S,4S,5R,6R,8S,9S,10S,13S,16S,17R,18R)-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 163013302 Click to see 467.60 unknown https://doi.org/10.1016/S0031-9422(02)00514-9
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[[(3R)-4-amino-3-methyl-4-oxobutanoyl]amino]benzoate 101341025 Click to see 699.80 unknown https://doi.org/10.1021/NP0401922
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-8,9,16-trihydroxy-4,6,18-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 100915311 Click to see 668.80 unknown https://doi.org/10.1016/S0031-9422(02)00514-9
[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[(4-amino-2-methyl-4-oxobutanoyl)amino]benzoate 145994478 Click to see 699.80 unknown https://doi.org/10.1021/NP0401922
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/S0031-9422(02)00514-9
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/S0031-9422(02)00514-9
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/S0031-9422(02)00514-9
Deoxylycoctonine 12309209 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)C 451.60 unknown https://doi.org/10.1021/NP0401922
> Organoheterocyclic compounds / Benzazepines
13-Methyl-12,12a,13,14-tetrahydro-2H,6H,9H-6a,14-epoxy(1,3)dioxolo(4,5-i)(1,3)dioxolo(5,6)indeno(2,1-c)(2)benzazepine 494334 Click to see 351.40 unknown https://doi.org/10.1016/S0031-9422(02)00514-9

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