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Aconitum flavum

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644006fb23c48398095335
Scientific name Aconitum flavum
Authority Hand.-Mazz.
First published in Acta Horti Gothob. 13: 86 (1939)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum anthora var. gilvum Maxim. Fl. Tangut. 25 1889
Aconitum gilvum (Maxim.) Hand.-Mazz. Acta Horti Gothob. 13: 86 (1939)

Common names Top

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Language Common/alternative name
Chinese 铁棒锤
Chinese 铁棒锤茎叶
Chinese 伏毛铁棒锤
Chinese 一支篙
Chinese 磨三转
Chinese 断肠草
Chinese 乌药
Chinese 两头尖
Chinese 破叶莲
Chinese 雪上一枝蒿
Chinese 雪上一支蒿
Chinese 小草乌

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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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Inner Mongolia
      • Qinghai
      • Tibet

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000517263
Tropicos 27103906
KEW urn:lsid:ipni.org:names:707359-1
The Plant List kew-2618716
Open Tree Of Life 44348
NCBI Taxonomy 286045
IPNI 707359-1
GBIF 7277341
EOL 2873285
Wikipedia Aconitum_flavum

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
Species Identification and Genetic Diversity Analysis of Medicinal Plants Aconitum pendulum Busch and Aconitum flavum Hand.-Mazz. Sun J, Sun Q, Li X, Li W, Li Y, Zhou Y, Hu Y Plants (Basel) 19-Mar-2024
PMCID:PMC10976075
doi:10.3390/plants13060885
PMID:38592876
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
Pyrrole-2-carboxaldehydes: Origins and Physiological Activities Matsugo S, Nakamura Y Molecules 13-Mar-2023
PMCID:PMC10058459
doi:10.3390/molecules28062599
PMID:36985566
Traditional Tibetan medicine to fight against COVID-19: Basic theory and therapeutic drugs Zhang K, Wang L, Peng J, Sangji K, Luo Y, Zeng Y, Zeweng Y, Fan G Front Pharmacol 16-Feb-2023
PMCID:PMC9978713
doi:10.3389/fphar.2023.1098253
PMID:36874035
Tandem mass tag labeled quantitative proteomic analysis of differential protein expression on total alkaloid of Aconitum flavum Hand.-Mazz. against melophagus ovinus Wang X, Yang Z, Zhang Y, Cheng F, Xing X, Wen F, Hu Y, Chen C, Wei B, Bai P, Wang X, Liu Y, Zhang H, Hao B, Wang S Front Vet Sci 27-Jul-2022
PMCID:PMC9365070
doi:10.3389/fvets.2022.951058
PMID:35968012
Effects of Nitrogen Addition on Soil Carbon-Fixing Microbial Diversity on Different Slopes in a Degraded Alpine Meadow Li C, Li X, Shi Y, Yang Y, Li H Front Plant Sci 24-Jun-2022
PMCID:PMC9263980
doi:10.3389/fpls.2022.921278
PMID:35812957
An Updated Meta-Analysis Based on the Preclinical Evidence of Mechanism of Aconitine-Induced Cardiotoxicity Jiang H, Zhang Y, Zhang Y, Wang X, Meng X Front Pharmacol 08-Jun-2022
PMCID:PMC9213726
doi:10.3389/fphar.2022.900842
PMID:35754486
The Plant Interspecific Association in the Revegetated Alpine Grasslands Determines the Productivity Stability of Plant Community Across Restoration Time on Qinghai–Tibetan Plateau Wu S, Wen L, Dong S, Gao X, Xu Y, Li S, Dong Q, Wessell K Front Plant Sci 21-Mar-2022
PMCID:PMC8978524
doi:10.3389/fpls.2022.850854
PMID:35386668
Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species Hao DC, Zhang Y, He CN, Xiao PG Evid Based Complement Alternat Med 12-Jan-2022
PMCID:PMC8769838
doi:10.1155/2022/9027727
PMID:35069772
Diterpenoid Alkaloids from the Aerial Parts of Aconitum flavum Hand.-Mazz Zhang N, Xia F, Li SY, Nian Y, Wei LX, Xu G Nat Prod Bioprospect 16-Apr-2021
PMCID:PMC8275754
doi:10.1007/s13659-021-00302-3
PMID:33861417
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
Traditional Tibetan Medicine in Cancer Therapy by Targeting Apoptosis Pathways Tang C, Zhao CC, Yi H, Geng ZJ, Wu XY, Zhang Y, Liu Y, Fan G Front Pharmacol 07-Jul-2020
PMCID:PMC7381342
doi:10.3389/fphar.2020.00976
PMID:32774302
Anticancer Activities of C18-, C19-, C20-, and Bis-Diterpenoid Alkaloids Derived from Genus Aconitum Ren MY, Yu QT, Shi CY, Luo JB Molecules 13-Feb-2017
PMCID:PMC6155828
doi:10.3390/molecules22020267
PMID:28208826
Study on the Alkaloids in Tibetan Medicine Aconitum pendulum Busch by HPLC–MSn Combined with Column Chromatography Wang B, Dong J, Ji J, Yuan J, Wang J, Wu J, Tan P, Liu Y J Chromatogr Sci 18-Feb-2016
PMCID:PMC4890449
doi:10.1093/chromsci/bmw002
PMID:26896350

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,4R,5S,6S,7S,8R,9R,13R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 139593379 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)O)COC 645.70 unknown https://doi.org/10.3987/R-1987-06-1455
[(2R,3R,4R,5R,6S,8R,10S,17S,18R)-8,14-diacetyloxy-11-ethyl-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 138404394 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)OC(=O)C)COC 687.80 unknown https://doi.org/10.3987/R-1987-06-1455
[(2R,3R,5R,6S,7S,8R,13R,14R,16S,17S,18R)-11-ethyl-5,7,8,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 146014635 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)O)COC 603.70 unknown https://doi.org/10.3987/R-1987-06-1455
3-Deoxyaconitine 78358503 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)COC 629.70 unknown https://doi.org/10.3987/R-1987-06-1455
Aconitine 245005 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)O)COC 645.70 unknown https://doi.org/10.3987/R-1987-06-1455
CID 146014456 146014456 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.3987/R-1987-06-1455
Neoline 120682 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.3987/R-1987-06-1455
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(11-Ethyl-4,16-dihydroxy-13-methyl-6-methylidene-11-oxido-11-azoniahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-7-yl) acetate 14558194 Click to see CC[N+]1(CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6OC(=O)C)O)O)C)[O-] 417.50 unknown https://doi.org/10.1055/S-2006-962444
(1R,2R,4S,5R,7R,8R,9R,10R,11R,13S,16S,17R)-11-ethyl-13-methyl-6-methylidene-11-oxido-11-azoniahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 163187355 Click to see CC[N+]1(CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6O)O)O)C)[O-] 375.50 unknown https://doi.org/10.3987/COM-89-5139
(1R,2R,4S,5R,7R,8R,9R,10R,13S,16S,17R)-11-ethyl-13-methyl-6-methylidene-11-oxido-11-azoniahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 163187352 Click to see CC[N+]1(CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6O)O)O)C)[O-] 375.50 unknown https://doi.org/10.3987/COM-89-5139
[(2R,4S,7R,8S,11R,13S,16S,17R)-11-ethyl-4,16-dihydroxy-13-methyl-6-methylidene-11-oxido-11-azoniahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-7-yl] acetate 163185005 Click to see CC[N+]1(CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6OC(=O)C)O)O)C)[O-] 417.50 unknown https://doi.org/10.3987/COM-89-5139
11-Ethyl-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosane-16,19-diol 14106919 Click to see CCN1C2C3CC4C2(C5CCC4(C1O5)C)C6C37CC(C(C6)O)C(=C)C7O 357.50 unknown https://doi.org/10.3987/R-1987-06-1455
Flavadine 163184428 Click to see CC[N+]1(CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6OC(=O)C)O)O)C)[O-] 417.50 unknown https://doi.org/10.3987/COM-89-5139
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
(1R,4S,5S,7R,8R,9R,10R,13R,16S)-11-ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 139291788 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6O)O)O)C 359.50 unknown https://doi.org/10.3987/R-1987-06-1455
(2R,4R,5R,7R,8R,13R,16S,17R)-11-ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 138857787 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6O)O)O)C 359.50 unknown https://doi.org/10.3987/R-1987-06-1455
12-Acetyllucidusculine 44445647 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6OC(=O)C)OC(=O)C)O)C 443.60 unknown https://doi.org/10.3987/R-1987-06-1455
Luciculine 17749282 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6O)O)O)C 359.50 unknown https://doi.org/10.3987/R-1987-06-1455
Lucidusculine 138756681 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6OC(=O)C)O)O)C 401.50 unknown https://doi.org/10.3987/R-1987-06-1455
Napelline 441749 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6O)O)O)C 359.50 unknown https://doi.org/10.3987/R-1987-06-1455
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Latifoloside I 10843495 Click to see CC1C(C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1OC6C(C(C(C(O6)CO)O)O)O)CO)C)C)(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C 929.10 unknown https://doi.org/10.3987/R-1987-06-1455
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavamine 27443 Click to see CCN(CC)CC1=CC2=C(C=C1)OC(=C(C2=O)C)C3=CC=CC=C3 321.40 unknown https://doi.org/10.1055/S-2006-962444

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