Common products:
Ornamental plants and cut flowers for floristry (whole aerial parts, dried flower stems and seed pods).

Industrial and craft applications:
No industrial-scale products are reported for this species.

Food and beverages (non-medicinal):
No food or beverage uses are reported for this species.

Colorants and tanning:
No dye or tannin applications are reported for this species.

Wood and fiber:
No timber or fiber uses are reported for this species.

Fragrance and cosmetics:
No fragrance or cosmetic uses are reported for this species.

Properties relevant to use:
Tall, erect habit with branched inflorescences and persistent seed pods enables ornamental and craft presentation (textural contrast and form).

Standards and regulation:
Ornamental horticulture and cut-flower trade are subject to general phytosanitary and labeling regulations (e.g., national plant health and consumer protection rules).

Sustainability and sourcing:
Wild collection for ornamental use should follow regional conservation guidance to prevent depletion of local populations; cultivated propagation is preferred.

Synonyms Top

Scientific name	Authority	First published in
Delphinium anthriscifolium var. calleryi	(Franch.) Finet & Gagnep.	Bull. Soc. Bot. France 51: 471 1904
Delphinium callerii	Franch.	Bull. Mens. Soc. Linn. Paris 1: 229 (1882)
Delphinium cavaleriense	H.Lév. & Vaniot	Bull. Acad. Int. Géogr. Bot. 11: 49 (1902)
Delphinium cerefolium	H.Lév. & Vaniot	Bull. Acad. Int. Géogr. Bot. 11: 49 (1902)
Delphinium exiguum	E.Pritz. ex Diels	Bot. Jahrb. Syst. 29: 327 (1900)
Delphinium anthriscifolium f. latilobulatum	W.T.Wang	Acta Bot. Sin. 10: 279 1962
Delphinium anthriscifolium var. ramosum	Pamp.	Nuovo Giorn. Bot. Ital. n.s., 22: 288 1915

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	还亮草
Chinese	车子野芫荽
Chinese	鱼灯苏
Chinese	牛疔草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Delphinium anthriscifolium var. savatieri	(Franch.) Munz	J. Arnold Arbor. 48: 261. 1967 (1967)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000639715
Tropicos	27104728
KEW	urn:lsid:ipni.org:names:710404-1
The Plant List	kew-2759426
Open Tree Of Life	511671
NCBI Taxonomy	215072
IPNI	710404-1
iNaturalist	510233
GBIF	3923581

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

Delphinieae flowers originated from the rewiring of interactions between duplicated and diversified floral organ identity and symmetry genes

Zhao H, Liao H, Li S, Zhang R, Dai J, Ma P, Wang T, Wang M, Yuan Y, Fu X, Cheng J, Duan X, Xie Y, Zhang P, Kong H, Shan H

Plant Cell

23-Dec-2022

PMCID:	PMC10015166
doi:	10.1093/plcell/koac368
PMID:	36560915

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

Comparative Analysis of the Chloroplast Genome for Aconitum Species: Genome Structure and Phylogenetic Relationships

Xia C, Wang M, Guan Y, Li J

Front Genet

31-May-2022

PMCID:	PMC9194378
doi:	10.3389/fgene.2022.878182
PMID:	35711937

Chemistry and biological activities of hetisine-type diterpenoid alkaloids

Yin T, Zhang H, Zhang W, Jiang Z

RSC Adv

08-Nov-2021

PMCID:	PMC9043348
doi:	10.1039/d1ra07173d
PMID:	35492752

Classification, Toxicity and Bioactivity of Natural Diterpenoid Alkaloids

Thawabteh AM, Thawabteh A, Lelario F, Bufo SA, Scrano L

Molecules

05-Jul-2021

PMCID:	PMC8271992
doi:	10.3390/molecules26134103
PMID:	34279443

Comparative chloroplast genomes and phylogenetic analysis of Aquilegia

Zhang W, Wang H, Dong J, Zhang T, Xiao H

Appl Plant Sci

16-Mar-2021

PMCID:	PMC8027367
doi:	10.1002/aps3.11412
PMID:	33854846

Dichocarpum hagiangense—a new species and an updated checklist of Ranunculaceae in Vietnam

Nguyen MT, Trinh NB, Tran TT, Thanh TD, Phan LK, Pham VT

PeerJ

22-Sep-2020

PMCID:	PMC7518158
doi:	10.7717/peerj.9874
PMID:	33024628

Characterization of the complete chloroplast genome of Aconitum flavum (Ranunculaceae)

Liu Y, Yu S, You F

Mitochondrial DNA B Resour

25-Jul-2020

PMCID:	PMC7781867
doi:	10.1080/23802359.2020.1787894
PMID:	33458024

Characterization of the complete chloroplast genome of the Musk Larkspur Delphinium brunonianum (Ranunculales: Ranunculaceae)

Li Q, Guo X, Yuan F, Nima C, Dongzhi D, Duojie, Li X

Mitochondrial DNA B Resour

08-Jun-2020

PMCID:	PMC7782922
doi:	10.1080/23802359.2020.1775522
PMID:	33503075

Structural variation of the complete chloroplast genome and plastid phylogenomics of the genus Asteropyrum (Ranunculaceae)

He J, Yao M, Lyu RD, Lin LL, Liu HJ, Pei LY, Yan SX, Xie L, Cheng J

Sci Rep

25-Oct-2019

PMCID:	PMC6814708
doi:	10.1038/s41598-019-51601-2
PMID:	31653891

Pharmacokinetics and UPLC-MS/MS of Delsoline in Mouse Whole Blood

Shao L, Jin Y, Fu H, Ma J, Wang X, Jin Y, Wen C

J Anal Methods Chem

11-Oct-2018

PMCID:	PMC6201488
doi:	10.1155/2018/9412708
PMID:	30405933

Diterpenoid Alkaloids from Delphinium anthriscifolium var. majus

Shan LH, Zhang JF, Gao F, Huang S, Zhou XL

Sci Rep

20-Jul-2017

PMCID:	PMC5519776
doi:	10.1038/s41598-017-05372-3
PMID:	28729705

Anthriscifolcine A, a C18-diterpenoid alkaloid

Song ZJ, Chen WQ, Du XY, Yuan YF, Xu HH

Acta Crystallogr Sect E Struct Rep Online

15-Jan-2011

PMCID:	PMC3051775
doi:	10.1107/S1600536811001346
PMID:	21523068

New C(19)- and C(18)-diterpenoid alkaloids from Delphinium anthriscifolium var. savatieri.

Song L, Liu XY, Chen QH, Wang FP

Chem Pharm Bull (Tokyo)

01-Feb-2009

doi:	10.1248/CPB.57.158
PMID:	19182405

New C18-diterpenoid alkaloids from Delphinium anthriscifolium var. savatieri.

Song L, Liang XX, Chen DL, Jian XX, Wang FP

Chem Pharm Bull (Tokyo)

01-Jun-2007

doi:	10.1248/CPB.55.918
PMID:	17541195

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(11-Ethyl-9,16,18-trihydroxy-6,8-dimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl) acetate	74429958	Click to see	463.60	unknown	https://doi.org/10.1248/CPB.57.158
(1S,2R,3R,4S,5R,6S,8R,12S,13S,16S,19S,20R,21S)-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-21-ol	101630689	Click to see	479.60	unknown	https://doi.org/10.1248/CPB.55.918
(1S,2R,3R,4S,5S,6S,8R,12R,13S,16S,19S,20R)-14-ethyl-6-methoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19-diol	163027050	Click to see	435.60	unknown	https://doi.org/10.1248/CPB.57.158
(1S,2R,3R,4S,5S,6S,8R,12R,13S,16S,19S,20R)-14-ethyl-6,19-dimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-4-ol	101036271	Click to see CCN1CC2(CCC(C34C2CC5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)OC)COC	449.60	unknown	https://doi.org/10.1248/CPB.57.158
(1S,2R,3R,4S,5S,6S,8R,12S,13S,16R,19S,20R,21S)-14-ethyl-6-methoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19,21-triol	101917137	Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)O)O)C	421.50	unknown	https://doi.org/10.1248/CPB.57.158
(1S,2R,3R,4S,5S,6S,8R,12S,13S,16S,19S,20R,21S)-14-ethyl-6-methoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19,21-triol	101036270	Click to see	451.60	unknown	https://doi.org/10.1248/CPB.57.158
[(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/10.1248/CPB.57.158
[14-Ethyl-6,19-dimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-4-yl] acetate	74429959	Click to see	491.60	unknown	https://doi.org/10.1248/CPB.57.158
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-21-ol	4359763	Click to see	479.60	unknown	https://doi.org/10.1248/CPB.55.918
14-Ethyl-6-methoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19-diol	14527203	Click to see	435.60	unknown	https://doi.org/10.1248/CPB.57.158
14-Ethyl-6-methoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19,21-triol	73812382	Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)O)O)COC	451.60	unknown	https://doi.org/10.1248/CPB.57.158
14-Ethyl-6-methoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19,21-triol	73657141	Click to see	421.50	unknown	https://doi.org/10.1248/CPB.57.158
14-Ethyl-6,19-dimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-4-ol	162869540	Click to see	449.60	unknown	https://doi.org/10.1248/CPB.57.158
14-Ethyl-6,19-dimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-2,4-diol	74429961	Click to see CCN1CC2(CCC(C34C2CC5(C31)C6(CC(C7CC4(C6C7O)O)OC)OCO5)OC)COC	465.60	unknown	https://doi.org/10.1248/CPB.57.158
Anthriscifoldine A	102032664	Click to see	463.60	unknown	https://doi.org/10.1248/CPB.57.158
Anthriscifoldine B	102032665	Click to see	465.60	unknown	https://doi.org/10.1248/CPB.57.158
Anthriscifoldine C	102032666	Click to see	491.60	unknown	https://doi.org/10.1248/CPB.57.158
Deltaline	441728	Click to see	507.60	unknown	https://doi.org/10.1248/CPB.57.158
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/10.1248/CPB.57.158
Eldeline	92854547	Click to see	507.60	unknown	https://doi.org/10.1248/CPB.57.158
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(14-Ethyl-2,6-dihydroxy-4,19-dimethoxy-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-21-yl) acetate	74429962	Click to see CCN1CC2CCC(C34C2C(C5(C31)C6(CC(C7CC4(C6C7OC)O)O)OCO5)OC(=O)C)OC	479.60	unknown	https://doi.org/10.1248/CPB.57.158
(14-Ethyl-6-hydroxy-4,19-dimethoxy-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-21-yl) acetate	74429960	Click to see CCN1CC2CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)O)OCO5)OC(=O)C)OC	463.60	unknown	https://doi.org/10.1248/CPB.57.158
[(1R,2S,3S,4S,5R,6S,8R,12S,13S,16R,19S,20R,21S)-14-ethyl-2,6-dihydroxy-4,19-dimethoxy-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-21-yl] acetate	102032667	Click to see	479.60	unknown	https://doi.org/10.1248/CPB.57.158
[(1S,2R,3R,4S,5R,6S,8R,12S,13S,16R,19S,20R,21S)-14-ethyl-6-hydroxy-4,19-dimethoxy-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-21-yl] acetate	102032668	Click to see	463.60	unknown	https://doi.org/10.1248/CPB.57.158

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Delphinium anthriscifolium

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top