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Internal ID UUID6440163e49cd8128291990
Scientific name Delphinium yunnanense
Authority Franch.
First published in Bull. Annuel Soc. Philom. Paris , sér. 8, 5: 173 (1893)

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Synonyms Top

Scientific name Authority First published in
Delphinium denudatum var. yunnanense Franch. Pl. Delavay. 25 1889
Delphinium esquirolii H.Lév. & Vaniot Bull. Herb. Boissier , sér. 2, 6: 505 (1906)

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Language Common/alternative name
Chinese 云南翠雀花
Chinese 鸡脚草乌
Chinese 倒提壶
Chinese 小草乌
Chinese 月下参

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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-0000640953
Tropicos 27104819
KEW urn:lsid:ipni.org:names:711153-1
The Plant List kew-2760602
Open Tree Of Life 6131857
NCBI Taxonomy 2753876
IPNI 711153-1
iNaturalist 602923
GBIF 3925849
EOL 2873806
USDA GRIN 13485

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)!
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Title Authors Publication Released IDs
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Complete chloroplast genome sequences of the medicinal plant Aconitum transsectum (Ranunculaceae): comparative analysis and phylogenetic relationships Yanfei N, Tai S, Chunhua W, Jia D, Fazhong Y BMC Genomics 28-Feb-2023
PMCID:PMC9976445
doi:10.1186/s12864-023-09180-0
PMID:36855055
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
Policies and Problems of Modernizing Ethnomedicine in China: A Focus on the Yi and Dai Traditional Medicines of Yunnan Province Li Z, Li C, Zhang X, Tang S, Yang H, Cui X, Huang L Evid Based Complement Alternat Med 14-Aug-2020
PMCID:PMC7443223
doi:10.1155/2020/1023297
PMID:32855645
Diterpenoid Alkaloids from <i>Delphinium yunnanense</i> Feng‐Zheng Chen, Qiao‐Hong Chen, Feng‐Peng Wang Wiley 18-Feb-2011
doi:10.1002/HLCA.201000171

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 / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
(3-Ethyl-8,12,14,17-tetramethoxy-16-oxo-3-azahexacyclo[7.6.3.110,13.01,11.02,9.05,18]nonadecan-5-yl)methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 163040152 Click to see CCN1CC2(CCC(C34C2C(C(=O)C5(C31)CC(C6CC4C5C6OC)OC)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 664.80 unknown https://doi.org/10.1002/HLCA.201000171
(8,9-Dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-11-en-13-yl)methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 4481625 Click to see CC1CC(=O)N(C1=O)C2=CC=CC=C2C(=O)OCC34CCC(C56C3C(C(C5N=C4)(C7(CC(C8CC6C7C8OC)OC)O)O)OC)OC 652.70 unknown https://doi.org/10.1002/HLCA.201000171
[(1R,2S,5S,8S,9S,10R,11S,12R,13R,14S,17S,18R)-3-ethyl-8,12,14,17-tetramethoxy-16-oxo-3-azahexacyclo[7.6.3.110,13.01,11.02,9.05,18]nonadecan-5-yl]methyl 2-[(3S)-3-methyl-2,5-dioxopyrrolidin-1-yl]benzoate 102484576 Click to see CCN1CC2(CCC(C34C2C(C(=O)C5(C31)CC(C6CC4C5C6OC)OC)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 664.80 unknown https://doi.org/10.1002/HLCA.201000171
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-11-en-13-yl]methyl 2-[(3S)-3-methyl-2,5-dioxopyrrolidin-1-yl]benzoate 101631699 Click to see CC1CC(=O)N(C1=O)C2=CC=CC=C2C(=O)OCC34CCC(C56C3C(C(C5N=C4)(C7(CC(C8CC6C7C8OC)OC)O)O)OC)OC 652.70 unknown https://doi.org/10.1002/HLCA.201000171
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(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/10.1002/HLCA.201000171
(1S,2R,3R,4S,5S,6S,8R,12S,13S,16R,19S,20R,21S)-14-ethyl-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,21-diol 101662590 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)O)OC)C 435.60 unknown https://doi.org/10.1002/HLCA.201000171
(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 CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1002/HLCA.201000171
(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/10.1002/HLCA.201000171
(1S,2R,3S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-one 101289627 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)OC)COC 465.60 unknown https://doi.org/10.1002/HLCA.201000171
[(1R,2S,3S,4S,5R,6S,8R,12S,13S,16R,19R,20R,21S)-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 163073301 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/10.1002/HLCA.201000171
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-9,16-dihydroxy-6,8,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 101006111 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC(=O)C)OC)OC)O)OC)O)COC 509.60 unknown https://doi.org/10.1002/HLCA.201000171
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 CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)O)O)C 421.50 unknown https://doi.org/10.1002/HLCA.201000171
14-Ethyl-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,21-diol 14164999 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)O)OC)C 435.60 unknown https://doi.org/10.1002/HLCA.201000171
Browniine 165288 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1002/HLCA.201000171
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/10.1002/HLCA.201000171
Dehydrobrowniine 165269 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)OC)COC 465.60 unknown https://doi.org/10.1002/HLCA.201000171
Delbonine 185387 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC(=O)C)OC)OC)O)OC)O)COC 509.60 unknown https://doi.org/10.1002/HLCA.201000171
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/10.1002/HLCA.201000171
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/10.1002/HLCA.201000171
Methyllycaconitine Perchlorate, Delphinium sp. 494471 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/10.1002/HLCA.201000171
Royline 57506221 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1002/HLCA.201000171
> 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/10.1002/HLCA.201000171

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