Aconitum tanguticum - Unknown
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Internal ID UUID6440071871b7a358977744
Scientific name Aconitum tanguticum
Authority (Maxim.) Stapf
First published in Ann. Roy. Bot. Gard. (Calcutta) 10: 151 (1905)

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Synonyms Top

Scientific name Authority First published in
Aconitum iochanicum var. robustum F.H.Chen & Y.Liu Bull. Fan Mem. Inst. Biol. 11: 46 1941
Aconitum qinghaiense Kadota J. Jap. Bot. 76: 185 (2001)
Aconitum rotundifolium var. tanguticum Maxim. Fl. Tangut. 26 1899
Aconitum tanguticum f. robustum (F.H.Chen & Y.Liu) W.T.Wang Acta Phytotax. Sin., Addit. 1: 96 1965
Aconitum tanguticum var. trichocarpum Hand.-Mazz. Acta Horti Gothob. 13: 91 1931
Aconitum tanguticum f. viridulum W.T.Wang Acta Phytotax. Sin., Addit. 1: 96 1965
Aconitum wolongense W.T.Wang Bull. Bot. Res., Harbin 9(2): 1 (1989)

Common names Top

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Language Common/alternative name
Icelandic hulduhjálmur
Russian Борец тангутский
Chinese 甘青乌头
Chinese 翁阿鲁
Chinese 金牛七
Chinese 雪乌
Chinese 辣辣草
Chinese 查干泵嘎
Chinese 船盔乌头
Chinese 榜嘎
Chinese 甘青乌头(唐古特乌头)
Chinese 山附子

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Varieties (abbr. var.) 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
      • China South-central
      • Qinghai
      • Tibet

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000518155
Tropicos 27102201
KEW urn:lsid:ipni.org:names:707870-1
The Plant List kew-2619596
Plantarium 605
Open Tree Of Life 1088652
Observations.org 147050
NCBI Taxonomy 215068
IPNI 707870-1
GBIF 3931303
CMAUP NPO17479

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
Phytochemical Elucidation and Effect of Maesa indica (Roxb.) Sweet on Alleviation of Potassium Dichromate-Induced Pulmonary Damage in Rats Abdelgawad FA, El-Hawary SS, El-Kader EM, Alshehri SA, Rabeh MA, El-Mosallamy AE, Salama A, El Gedaily RA Plants (Basel) 23-Jan-2024
PMCID:PMC10857331
doi:10.3390/plants13030338
PMID:38337870
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
Standardised Sonneratia apetala Buch.-Ham. fruit extract inhibits human neutrophil elastase and attenuates elastase-induced lung injury in mice Sengupta S, Abhinav N, Singh S, Dutta J, Mabalirajan U, Kaliyamurthy K, Mukherjee PK, Jaisankar P, Bandyopadhyay A Front Pharmacol 07-Dec-2022
PMCID:PMC9768866
doi:10.3389/fphar.2022.1011216
PMID:36569308
Progress in ICP-MS Analysis of Minerals and Heavy Metals in Traditional Medicine Chen W, Yang Y, Fu K, Zhang D, Wang Z Front Pharmacol 28-Jun-2022
PMCID:PMC9274010
doi:10.3389/fphar.2022.891273
PMID:35837276
Unravelling the Therapeutic Potential of Botanicals Against Chronic Obstructive Pulmonary Disease (COPD): Molecular Insights and Future Perspectives Mitra S, Anand U, Ghorai M, Vellingiri B, Jha NK, Behl T, Kumar M, Radha, Shekhawat MS, Proćków J, Dey A Front Pharmacol 11-May-2022
PMCID:PMC9130824
doi:10.3389/fphar.2022.824132
PMID:35645819
The Treatment of Cholecystitis and Cholelithiasis by Tibetan Medicine Pan L, Gao J, Han Y, Shi Y, Tang X, Pu L, Lai X, Dongzhu R, Zhang J, Xiangmao Q, Pengcuo J Evid Based Complement Alternat Med 30-Sep-2021
PMCID:PMC8497101
doi:10.1155/2021/9502609
PMID:34630620
Tangutidines A–C, Three Amphoteric Diterpene Alkaloids from Aconitum tanguticum Li HY, Yan BC, Wei LX, Sun HD, Puno PT Nat Prod Bioprospect 12-May-2021
PMCID:PMC8275809
doi:10.1007/s13659-021-00310-3
PMID:33978930
Characterization of the complete chloroplast genome of the Tangut monkshood Aconitum tanguticum (Ranunculales: Ranunculaceae) Li Q, Li X, Qieyang R, Nima C, Dongzhi D, Duojie, Guo X Mitochondrial DNA B Resour 02-Jun-2020
PMCID:PMC7782905
doi:10.1080/23802359.2020.1773338
PMID:33457769
Pharmaceutical resource discovery from traditional medicinal plants: Pharmacophylogeny and pharmacophylogenomics Hao DC, Xiao PG Chin Herb Med 12-Mar-2020
PMCID:PMC9476761
doi:10.1016/j.chmed.2020.03.002
PMID:36119793
Nephrotoxicity and Chinese Herbal Medicine Yang B, Xie Y, Guo M, Rosner MH, Yang H, Ronco C Clin J Am Soc Nephrol 03-Apr-2018
PMCID:PMC6218812
doi:10.2215/CJN.11571017
PMID:29615394
Therapeutic Potential of Medicinal Plants and Their Constituents on Lung Inflammatory Disorders Kim HP, Lim H, Kwon YS Biomol Ther (Seoul) 16-Dec-2016
PMCID:PMC5340533
doi:10.4062/biomolther.2016.187
PMID:27956716
Important Poisonous Plants in Tibetan Ethnomedicine Ma L, Gu R, Tang L, Chen ZE, Di R, Long C Toxins (Basel) 14-Jan-2015
PMCID:PMC4303819
doi:10.3390/toxins7010138
PMID:25594733
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315
Diterpenoid alkaloids from Aconitum tanguticum Shi-Jin Qu, Chang-Heng Tan, Zu-Long Liu, Shan-Hao Jiang, Long Yu, Da-Yuan Zhu Elsevier BV 07-Mar-2011
doi:10.1016/J.PHYTOL.2011.02.003
Tangutisine, a New Diterpenoid Alkaloid from Aconitum tanguticum (Maxim.) Stapf, W. T. Wang S. William Pelletier, Balawant S. Joshi, Di Hua Chen, Xiaolin Zhang, John K. Snyder The Japan Institute of Heterocyclic Chemistry 03-Mar-2009
doi:10.3987/COM-91-5809

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 / Benzoic acid esters
[(1S,6S,9S,10R,14R,17S,19S)-12-ethyl-9-hydroxy-17-methoxy-14-methyl-4-oxo-5-oxa-12-azahexacyclo[8.7.2.12,6.01,11.03,9.014,18]icosan-19-yl] benzoate 139292156 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CCC6CC4C5C(=O)O6)O)OC(=O)C7=CC=CC=C7)OC)C 495.60 unknown https://doi.org/10.1016/S0944-7113(97)80053-0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Hordenine 68313 Click to see CN(C)CCC1=CC=C(C=C1)O 165.23 unknown https://doi.org/10.1002/CHIN.200541200
Hydrogen sulfate;2-(4-hydroxyphenyl)ethyl-dimethylazanium 44655713 Click to see C[NH+](C)CCC1=CC=C(C=C1)O.OS(=O)(=O)[O-] 263.31 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1S,2R,3R,4S,5R,6S,8R,12S,13S,16R,19S,20R,21S)-14-ethyl-4,6-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-19,21-diol 101630687 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)O)O)C 435.60 unknown https://doi.org/10.1002/HLCA.200590079
(2R,3R,5S,8S,9S,10S,13S,17R)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 11969798 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown via CMAUP database
[(1S,2R,3R,4S,5S,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-4,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-acetamidobenzoate 101670652 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)C 614.70 unknown https://doi.org/10.1002/HLCA.200590079
14-Ethyl-4,6-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-19,21-diol 162943735 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)O)O)C 435.60 unknown https://doi.org/10.1002/HLCA.200590079
CID 14312978 14312978 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)C 614.70 unknown https://doi.org/10.1002/HLCA.200590079
Stock1N-53305 118701209 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1002/CHIN.200541200
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,5R,8R,9S,11R,14R,16S,17R,18R)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 162926558 Click to see CC12CC(=O)CC34C1C5CC67C3CC(CC6C4N5C2)C(=C)C7 295.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.003
(1S,2R,4R,6R,7R,10R,11S,17R)-11-methyl-5-methylidene-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-6-ol 162923620 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.003
(1S,3S,5R,8R,9S,10R,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 86567874 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O 329.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.003
(1S,3S,5R,8S,9R,10S,11R,14R,16S,17R,18S,19R)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,9,10,19-tetrol 162956976 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6(C4N5C2)O)O)C(=C)C7)O)O 345.40 unknown https://doi.org/10.3987/COM-91-5809
(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 CC12CC(=O)CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O 327.40 unknown https://doi.org/10.1002/CHIN.200541200
(3,19-Dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-10-yl) acetate 14039745 Click to see CC(=O)OC1C2C(C3C4(C1C5C36CC(CC7(C6C(C4)N5C7)C)O)CC2=C)O 371.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.003
(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 CC12CC(=O)CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O 327.40 unknown via CMAUP database
(5R,13R,18R)-5-methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadec-6-ene-13,18-diol 5321616 Click to see CC12CCCC34C1CCC56C3(CC(CC5C4N=C2)C(=C)C6O)O 313.40 unknown via CMAUP database
[(1R,2S,3S,5R,7R,8S,9R,11R,12S,14R,16S,17R,18S)-16,17,18-triacetyloxy-13-benzoyloxy-7-formyl-7,10-dimethyl-15-methylidene-10-azahexacyclo[7.7.1.12,14.01,12.03,8.03,11]octadecan-5-yl] benzoate 101733186 Click to see CC(=O)OC1C2C(C3C4C56C1C3(C(C(C5C(CC(C6)OC(=O)C7=CC=CC=C7)(C)C=O)N4C)OC(=O)C)C(C2=C)OC(=O)C)OC(=O)C8=CC=CC=C8 725.80 unknown https://doi.org/10.1002/CHIN.200435196
[(1S,3S,5R,8R,9S,10R,11R,14R,16S,17R,18R,19S)-3,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-10-yl] acetate 162910537 Click to see CC(=O)OC1C2C(C3C4(C1C5C36CC(CC7(C6C(C4)N5C7)C)O)CC2=C)O 371.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.003
11-Methyl-5-methylidene-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-6-ol 4481626 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.003
5-Methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadec-6-ene-13,18-diol 78385507 Click to see CC12CCCC34C1CCC56C3(CC(CC5C4N=C2)C(=C)C6O)O 313.40 unknown https://doi.org/10.1002/CHIN.200541200
Hetisine 431673 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O 329.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.003
Unii-V81K1mmx3X 135897293 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown https://doi.org/10.1002/CHIN.200541200
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(1S,5R,8R,9S,10R,11R,13R,14S,16S,17R,18S,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-10,13,19-triol 162930398 Click to see CC12CCCC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7O)O 329.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.003
(3S,5R,11R,13R,16R,17R,18S,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,13,19-triol 75124250 Click to see CC12CC(CC34C1C5CC67C3C(C(CC6C4N5C2)C(=C)C7O)O)O 329.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
7beta-Hydroxysitosterol 12309569 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Ikshusterol 161816 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 86311182 Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)O 242.22 unknown via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 54353627 Click to see COC1=CC(=CC(=C1O)OC)C(=O)CCO 226.23 unknown via CMAUP database
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolidines
CID 25084349 25084349 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CCC6CC4C5C(=O)O6)O)O)OC)C 391.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C=C3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(2S,3R)-3-Ethoxy-2,3-bis(3-methoxy-4-hydroxyphenyl)propane-1-ol 11759831 Click to see CCOC(C1=CC(=C(C=C1)O)OC)C(CO)C2=CC(=C(C=C2)O)OC 348.40 unknown via CMAUP database
[4-[(4R,5R)-4-(4-acetyloxy-3-methoxyphenyl)-1,3-dioxan-5-yl]-2-methoxyphenyl] acetate 21591953 Click to see CC(=O)OC1=C(C=C(C=C1)C2COCOC2C3=CC(=C(C=C3)OC(=O)C)OC)OC 416.40 unknown via CMAUP database
4-[(4S,5S)-4-(4-hydroxy-3-methoxyphenyl)-1,3-dioxan-5-yl]-2-methoxyphenol 10871293 Click to see COC1=C(C=CC(=C1)C2COCOC2C3=CC(=C(C=C3)O)OC)O 332.30 unknown via CMAUP database

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