Details Top

Internal ID UUID6440161006c83404852852
Scientific name Delphinium delavayi
Authority Franch.
First published in Bull. Soc. Bot. France 33: 379 (1886)

Ethnobotanical Use Top

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General Uses Top

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Scientific/model-organism use:
Delphinium delavayi is employed in genetic and molecular studies of plant secondary metabolism. Researchers have generated transcriptomic data for D. delavayi, which are publicly accessible to support gene discovery and functional analysis. The species has been used to investigate the evolution of the delphinine biosynthetic pathway and to compare alkaloid profiles across Ranunculaceae, with results published in peer‑reviewed journals. In addition, D. delavayi is included in broader phylogenetic analyses of the family, helping to resolve relationships among genera and to map the distribution of alkaloid‑related genes. Seed and DNA voucher specimens of D. delavayi are preserved in national and international gene banks, providing permanent access for future genomic studies and comparative analyses within the family.

Properties relevant to use:
The aerial parts of D. delavayi contain high levels of the diterpenoid alkaloid delphinine, which can constitute up to several percent of dry weight in mature leaves and flowers. Delphinine is a C19‑diterpenoid alkaloid with a toxic, nitrogenous structure that makes the plant unsuitable for food or medicinal use without extensive processing. The flowers also accumulate anthocyanins, principally delphinidin‑based glycosides, which give the characteristic blue‑violet coloration and display good stability under acidic conditions, a property of interest for natural dye research. The plant’s vegetative tissue is fibrous, with a bast‑fiber component similar to that of other Ranunculaceae, but it is not exploited commercially for fiber, oil, gum, or resin production.

Sustainability and sourcing:
In its native range in southwestern China, D. delavayi grows in forest margins and alpine meadows and is not currently listed as threatened on the IUCN Red List. Local regulations protect wild populations, requiring permits for collection of seeds or plant material. Commercial production is limited; most ornamental and scientific material originates from cultivated stock propagated by seed or vegetative division in botanical gardens and private collections. Cultivation reduces harvest pressure on wild populations, and the species is subject to the same plant‑trade regulations as other non‑CITES‑listed ornamental perennials. Export of plant material requires phytosanitary certification under China’s Plant Quarantine Regulations, ensuring compliance with international trade standards.

Synonyms Top

Scientific name Authority First published in
Delphinium trichophorum f. brevungue H.Lév. Repert. Spec. Nov. Regni Veg. 7: 102 1909
Delphinium delavayi f. aureum W.T.Wang Acta Bot. Sin. 10: 144 1962
Delphinium delavayi var. acuminatum Franch. Bull. Soc. Bot. France 33: 380 1886

Common names Top

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Language Common/alternative name
Chinese 小草乌
Chinese 鸡脚草乌
Chinese 滇川翠雀花
Chinese 细草乌
Chinese 鸡足草乌

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Delphinium delavayi var. baoshanense (W.T.Wang) W.T.Wang Phytologia 79: 384 (1995 publ. 1996)
Delphinium delavayi var. lasiandrum W.T.Wang Bull. Bot. Res., Harbin 6(1): 14 (1986)
Delphinium delavayi var. pogonanthum (Hand.-Mazz.) W.T.Wang Fl. Reipubl. Popularis Sin. 27: 401 (1979)

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-0000639973
Tropicos 27104721
KEW urn:lsid:ipni.org:names:710554-1
The Plant List kew-2759673
Open Tree Of Life 70138
NCBI Taxonomy 136321
IPNI 710554-1
GBIF 7276715
USDA GRIN 13429

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
New amide and diterpene alkaloids with anticholinesterase activity from Delphinium cyphoplectrum roots Salehi A, Zolfaghari B, Aghaei M, Sirous H, Sadeghi M, Gholami MR, Reisi P, Ghanadian M Daru 18-Mar-2024
PMCID:PMC11087438
doi:10.1007/s40199-024-00509-y
PMID:38498253
An ethnobiological study on traditional knowledge associated  with black-boned sheep (Ovis aries) in Northwest Yunnan, China Fan Y, Cheng Z, Liu B, Hu X, Ali M, Long C J Ethnobiol Ethnomed 17-May-2022
PMCID:PMC9112469
doi:10.1186/s13002-022-00537-5
PMID:35581643
Pollen sensitivity to ultraviolet-B (UV-B) suggests floral structure evolution in alpine plants Zhang C, Yang YP, Duan YW Sci Rep 31-Mar-2014
PMCID:PMC3970119
doi:10.1038/srep04520
PMID:24682234
Deltaline from Delphinium delavayi Franch Wang XQ, Song Q, Guo XQ, Yan J Acta Crystallogr Sect E Struct Rep Online 22-Jan-2011
PMCID:PMC3051497
doi:10.1107/S1600536811001681
PMID:21523103
The Diterpenoid Alkaloids of Delphinium delavayi Franch var. pogonanthum (H. -M.) Wang S. William Pelletier, Fathalla M. Harraz, Mohamed M. Badawi, Sirirat Tantiraksachai, Feng-peng Wang, Szu-ying Chen The Japan Institute of Heterocyclic Chemistry 17-Feb-2009
doi:10.3987/R-1986-07-1853

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
> Benzenoids / Benzene and substituted derivatives
Pemoline 4723 Click to see 176.17 unknown https://doi.org/10.3987/R-1986-07-1853
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides / Anthranilamides
N-methyl-2-(methylamino)-N-(2-phenylethyl)benzamide 10858497 Click to see 268.35 unknown https://doi.org/10.3987/R-1986-07-1853
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(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-methoxy-2-methyl-4-oxobutanoyl)amino]benzoate 4481784 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)C(C)CC(=O)OC 714.80 unknown https://doi.org/10.3987/R-1986-07-1853
(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-methoxy-3-methyl-4-oxobutanoyl)amino]benzoate 162873552 Click to see 714.80 unknown https://doi.org/10.3987/R-1986-07-1853
(1R,2S,3S,4S,5R,6S,8R,12S,13S,16R,19S,20R,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]docosane-2,21-diol 101289626 Click to see 465.60 unknown https://doi.org/10.3987/R-1986-07-1853
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-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 57506221 Click to see 467.60 unknown https://doi.org/10.3987/R-1986-07-1853
(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/10.3987/R-1986-07-1853
[(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-[[(2R)-4-amino-2-methyl-4-oxobutanoyl]amino]benzoate 163088578 Click to see 699.80 unknown https://doi.org/10.3987/R-1986-07-1853
[(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-[[(2R)-4-methoxy-2-methyl-4-oxobutanoyl]amino]benzoate 162849282 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)C(C)CC(=O)OC 714.80 unknown https://doi.org/10.3987/R-1986-07-1853
[(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/10.3987/R-1986-07-1853
[(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-methoxy-3-methyl-4-oxobutanoyl]amino]benzoate 162873554 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)CC(C)C(=O)OC 714.80 unknown https://doi.org/10.3987/R-1986-07-1853
[(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-aminobenzoate 57519466 Click to see 586.70 unknown https://doi.org/10.3987/R-1986-07-1853
[(1S,4S,5R,6S,8R,9S,13S,16S)-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-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 139292146 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/10.3987/R-1986-07-1853
[(2S,5R,6S,8R,13S,16R)-14-ethyl-2-hydroxy-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-yl] acetate 145994496 Click to see 507.60 unknown https://doi.org/10.3987/R-1986-07-1853
CID 11972492 11972492 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.3987/R-1986-07-1853
CID 99924 99924 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.3987/R-1986-07-1853
Delavaine A 441723 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)C(C)CC(=O)OC 714.80 unknown https://doi.org/10.3987/R-1986-07-1853
Delavaine B 133065623 Click to see 714.80 unknown https://doi.org/10.3987/R-1986-07-1853
Deltaline 441728 Click to see 507.60 unknown https://doi.org/10.3987/R-1986-07-1853
Deltamine 6-acetate 165537 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4(C6C7OC)O)OC)OCO5)OC(=O)C)OC)C 507.60 unknown https://doi.org/10.3987/R-1986-07-1853
Eldeline 92854547 Click to see 507.60 unknown https://doi.org/10.3987/R-1986-07-1853
Inuline 3800367 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N 586.70 unknown https://doi.org/10.3987/R-1986-07-1853
Methyllycaconitine Perchlorate, Delphinium sp. 494471 Click to see 682.80 unknown https://doi.org/10.3987/R-1986-07-1853
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(13R,21xi)-Hetisan-2alpha,11alpha,13-triol 86567874 Click to see 329.40 unknown https://doi.org/10.3987/R-1986-07-1853
(1S,3S,5S,8R,9S,11R,14R,16S,17R,18R,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,10,19-triol 101930091 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O 329.40 unknown https://doi.org/10.3987/R-1986-07-1853
(1S,5R,8R,10R,11S,14S,16R,17R)-7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.211,14.01,8.05,17.011,16]icosan-12-ol 133562510 Click to see 359.50 unknown https://doi.org/10.3987/R-1986-07-1853
(1S,5R,8R,9S,10R,11R,14R,16S,17R,18R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 131879709 Click to see 327.40 unknown https://doi.org/10.3987/R-1986-07-1853
(1S,5S,8R,9S,11R,14R,16S,17R,18R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 101930090 Click to see 327.40 unknown https://doi.org/10.3987/R-1986-07-1853
(5R,10R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 5318032 Click to see 327.40 unknown https://doi.org/10.3987/R-1986-07-1853
10,19-Dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 73657226 Click to see 327.40 unknown https://doi.org/10.3987/R-1986-07-1853
Ajaconine 441706 Click to see 359.50 unknown https://doi.org/10.3987/R-1986-07-1853
Hetisine 431673 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O 329.40 unknown https://doi.org/10.3987/R-1986-07-1853
> 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/10.3987/R-1986-07-1853
> Organoheterocyclic compounds / Imidazopyridines / Imidazopyridinones
(3R,8aR)-3-(2-methylpropyl)-1,3,6,7,8,8a-hexahydroimidazo[1,2-a]pyridine-2,5-dione 162987928 Click to see CC(C)CC1C(=O)NC2N1C(=O)CCC2 210.27 unknown https://doi.org/10.3987/R-1986-07-1853
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
CID 75167685 75167685 Click to see 494.50 unknown https://doi.org/10.3987/R-1986-07-1853

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