Aconitum coreanum - Unknown
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Internal ID UUID644006f62c573664233863
Scientific name Aconitum coreanum
Authority (H.Lév.) Rapaics
First published in Növényt. Közlem. 6: 154 1907

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum delavayi var. coreanum H.Lév. Bull. Acad. Int. Géogr. Bot. 11: 300 1902
Aconitum komarovii Steinb. Fl. URSS 7: 191 (1937)

Common names Top

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Language Common/alternative name
Chinese 白附子
Chinese 关白附
Chinese 关白附子
Chinese 黄花乌头
Chinese 竹节白附
Chinese 黄乌拉花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000517121
UNII A8Y25HFH77
Tropicos 27102122
KEW urn:lsid:ipni.org:names:707279-1
The Plant List kew-2618577
Open Tree Of Life 377294
Observations.org 113911
NCBI Taxonomy 662772
IUCN Red List 13188365
IPNI 707279-1
GBIF 3921701
Freebase /m/0y7tvxb
EOL 2873264
Elurikkus 644111
Elurikkus 613175
USDA GRIN 410029
Wikipedia Aconitum_coreanum

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
Comparative and phylogenetic analysis of Asparagus meioclados Levl. and Asparagus munitus Wang et S. C. Chen plastomes and utility of plastomes mutational hotspots Tian Y, Liu X, Xu Y, Yu B, Wang L, Qu X Sci Rep 20-Sep-2023
PMCID:PMC10511529
doi:10.1038/s41598-023-42945-x
PMID:37730791
Antitumor effects and potential mechanisms of aconitine based on preclinical studies: an updated systematic review and meta-analysis Xiang G, Xing N, Wang S, Zhang Y Front Pharmacol 27-Apr-2023
PMCID:PMC10174313
doi:10.3389/fphar.2023.1172939
PMID:37180714
Efficacy and Safety of Zhenwu Decoction in the Treatment of Diabetic Nephropathy: A Systematic Review and Meta-Analysis Lv X, Zhou M, Liu X, Xiang Q, Yu R Evid Based Complement Alternat Med 01-Nov-2022
PMCID:PMC9643062
doi:10.1155/2022/2133705
PMID:36387355
The Regulatory Roles of Polysaccharides and Ferroptosis-Related Phytochemicals in Liver Diseases Ren Y, Li S, Song Z, Luo Q, Zhang Y, Wang H Nutrients 30-May-2022
PMCID:PMC9182636
doi:10.3390/nu14112303
PMID:35684103
Hematological and Histopathological Effects of Subacute Aconitine Poisoning in Mouse Lu H, Mei L, Guo Z, Wu K, Zhang Y, Tang S, Zhu Y, Zhao B Front Vet Sci 05-Apr-2022
PMCID:PMC9020262
doi:10.3389/fvets.2022.874660
PMID:35464374
Research Progress on Natural Products' Therapeutic Effects on Atrial Fibrillation by Regulating Ion Channels He J, Li S, Ding Y, Tong Y, Li X Cardiovasc Ther 22-Mar-2022
PMCID:PMC8964196
doi:10.1155/2022/4559809
PMID:35387267
East Asian Herbal Medicine to Reduce Primary Pain and Adverse Events in Cancer Patients : A Systematic Review and Meta-Analysis With Association Rule Mining to Identify Core Herb Combination Jo HG, Seo J, Choi S, Lee D Front Pharmacol 17-Jan-2022
PMCID:PMC8802093
doi:10.3389/fphar.2021.800571
PMID:35111066
The Positive Role and Mechanism of Herbal Medicine in Parkinson's Disease Yin R, Xue J, Tan Y, Fang C, Hu C, Yang Q, Mei X, Qi D Oxid Med Cell Longev 03-Sep-2021
PMCID:PMC8457986
doi:10.1155/2021/9923331
PMID:34567415
Plastid Phylogenomic Data Offers Novel Insights Into the Taxonomic Status of the Trichosanthes kirilowii Complex (Cucurbitaceae) in South Korea Park I, Song JH, Yang S, Chae S, Moon BC Front Plant Sci 27-Jul-2021
PMCID:PMC8353159
doi:10.3389/fpls.2021.559511
PMID:34386020
The toxicology and detoxification of Aconitum: traditional and modern views Chan YT, Wang N, Feng Y Chin Med 27-Jul-2021
PMCID:PMC8314510
doi:10.1186/s13020-021-00472-9
PMID:34315520
Green giant—a tiny chloroplast genome with mighty power to produce high‐value proteins: history and phylogeny Daniell H, Jin S, Zhu X, Gitzendanner MA, Soltis DE, Soltis PS Plant Biotechnol J 22-Feb-2021
PMCID:PMC7955891
doi:10.1111/pbi.13556
PMID:33484606
Potential Molecular Target Prediction and Docking Verification of Hua-Feng-Dan in Stroke Based on Network Pharmacology Yang P, He H, Xu S, Liu P, Bai X Evid Based Complement Alternat Med 28-Oct-2020
PMCID:PMC7641700
doi:10.1155/2020/8872593
PMID:33193801
Effects of alkaloids on peripheral neuropathic pain: a review Zhu C, Liu N, Tian M, Ma L, Yang J, Lan X, Ma H, Niu J, Yu J Chin Med 02-Oct-2020
PMCID:PMC7532100
doi:10.1186/s13020-020-00387-x
PMID:33024448
The Complete Chloroplast Genome of Arabidopsis thaliana Isolated in Korea (Brassicaceae): An Investigation of Intraspecific Variations of the Chloroplast Genome of Korean A. thaliana Park J, Xi H, Kim Y Int J Genomics 05-Sep-2020
PMCID:PMC7492873
doi:10.1155/2020/3236461
PMID:32964010
Modulation of Apoptosis by Plant Polysaccharides for Exerting Anti-Cancer Effects: A Review Gan QX, Wang J, Hu J, Lou GH, Xiong HJ, Peng CY, Huang QW Front Pharmacol 27-May-2020
PMCID:PMC7267062
doi:10.3389/fphar.2020.00792
PMID:32536869

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
Codelphine 92854546 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 unknown https://doi.org/10.3184/030823409X393673
Kondelfin 93054 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)COC 449.60 unknown https://doi.org/10.3184/030823409X393673
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(19-Acetyloxy-9,10-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl) acetate 25097891 Click to see CC(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)OC(=O)C)O)O)C 429.50 unknown https://doi.org/10.3184/030823409X393673
(1R,2S,4S,7R,10R,11R)-5-[[(3aR,6S,7aS)-6-hydroxy-1-methyl-3,6,7,7a-tetrahydro-2H-indol-3a-yl]methyl]-13-acetyl-11-methyl-13-azapentacyclo[9.3.3.24,7.01,10.02,7]nonadec-5-en-14-one 162845969 Click to see CC(=O)N1CC2(CCCC3(C2CCC45C3CC(CC4)C(=C5)CC67CCN(C6CC(C=C7)O)C)C1=O)C 492.70 unknown https://doi.org/10.1007/BF00630178
(3aR,7aS)-1-methyl-3a-[[(1R,5R,11R,12S,14R,17S,20R,21R)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.01,11.05,20.07,11.012,17.017,21]docos-15-en-15-yl]methyl]-2,3,7,7a-tetrahydroindol-6-one 163022223 Click to see CC12CCCC34C1CCC56C3CC(CC5C47N(C2)CCO7)C(=C6)CC89CCN(C8CC(=O)C=C9)C 474.70 unknown https://doi.org/10.1007/BF00630323
(9,10,19-Trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl) 2-methylpropanoate 13918230 Click to see CC(C)C(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)O)O)C 415.50 unknown https://doi.org/10.3184/030823409X393673
(9,10,19-Trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl) acetate 3101182 Click to see CC(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)O)O)C 387.50 unknown https://doi.org/10.3184/030823409X393673
[(1S,3S,5R,8S,9R,10S,11R,14R,16S,17R,18S,19S)-10,19-diacetyloxy-9-hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] acetate 162975185 Click to see CC(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)OC(=O)C)OC(=O)C)O)C 471.50 unknown https://doi.org/10.3184/030823409X393673
[(1S,3S,5R,8S,9R,10S,11R,14R,16S,17R,18S,19S)-9,10,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] 2-methylpropanoate 163005101 Click to see CC(C)C(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)O)O)C 415.50 unknown https://doi.org/10.3184/030823409X393673
[(1S,3S,5R,8S,9R,10S,11R,14R,16S,17R,18S,19S)-9,10,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] acetate 97046305 Click to see CC(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)O)O)C 387.50 unknown https://doi.org/10.3184/030823409X393673
[(1S,3S,5R,8S,9R,10S,11S,14R,16S,17R,18S,19S)-19-acetyloxy-9,10-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] acetate 163192921 Click to see CC(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)OC(=O)C)O)O)C 429.50 unknown https://doi.org/10.3184/030823409X393673
[(1S,3S,5S,7S,8S,9R,10R,11R,14R,16S,17R,18S,19S)-10-acetyloxy-9,19-dihydroxy-5-methyl-12-methylidene-7-oxido-7-azoniaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] 2-methylpropanoate 163186906 Click to see CC(C)C(=O)OC1CC2(C[N+]3(C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)OC(=O)C)O)[O-])C 473.60 unknown https://doi.org/10.1007/BF00597858
[(1S,3S,5S,8S,9R,10R,11R,14R,16S,17R,18S,19S)-10-acetyloxy-9,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] 2-methylpropanoate 162872185 Click to see CC(C)C(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)OC(=O)C)O)C 457.60 unknown https://doi.org/10.1007/BF00597859
[(1S,3S,5S,8S,9R,10S,11R,14R,16S,17R,18S,19R)-9,10,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] 2-methylpropanoate 163005103 Click to see CC(C)C(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)O)O)C 415.50 unknown https://doi.org/10.3987/R-1986-01-0049
1-Methyl-3a-[(5-methyl-10-oxa-7-azaheptacyclo[12.6.2.01,11.05,20.07,11.012,17.017,21]docos-15-en-15-yl)methyl]-2,3,7,7a-tetrahydroindol-6-one 73657592 Click to see CC12CCCC34C1CCC56C3CC(CC5C47N(C2)CCO7)C(=C6)CC89CCN(C8CC(=O)C=C9)C 474.70 unknown https://doi.org/10.1007/BF00630323
13-acetyl-5-[(6-hydroxy-1-methyl-3,6,7,7a-tetrahydro-2H-indol-3a-yl)methyl]-11-methyl-13-azapentacyclo[9.3.3.24,7.01,10.02,7]nonadec-5-en-14-one 73816185 Click to see CC(=O)N1CC2(CCCC3(C2CCC45C3CC(CC4)C(=C5)CC67CCN(C6CC(C=C7)O)C)C1=O)C 492.70 unknown https://doi.org/10.1007/BF00630178
Guan-fu base G 85096678 Click to see CC(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)OC(=O)C)OC(=O)C)O)C 471.50 unknown https://doi.org/10.3184/030823409X393673
Guan-fu-base F N-oxide 163184427 Click to see CC(C)C(=O)OC1CC2(C[N+]3(C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)OC(=O)C)O)[O-])C 473.60 unknown https://doi.org/10.1007/BF00597858
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(3,16-Dihydroxy-5-methyl-12-methylidene-10-oxo-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-2-yl) acetate 162986341 Click to see CC(=O)OC1C(CC2(CN3C4C15C2C3(CC67C5CC(C(=C)C6)C(=O)C74)O)C)O 385.50 unknown https://doi.org/10.3184/030823409X393673
[(1S,2S,3S,5R,8R,9S,11S,14R,16R,17R,18R)-3,16-dihydroxy-5-methyl-12-methylidene-10-oxo-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-2-yl] acetate 162986342 Click to see CC(=O)OC1C(CC2(CN3C4C15C2C3(CC67C5CC(C(=C)C6)C(=O)C74)O)C)O 385.50 unknown https://doi.org/10.3184/030823409X393673

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