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Internal ID UUID6440070a49577702076884
Scientific name Aconitum nasutum
Authority Rchb.
First published in Ill. Sp. Acon. Gen. : t. IX (1823)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Aconitum nasutum is taken as a bitter, warming decoction in several parts of its range. In the Himalaya, herbalists collect the root and boil it briefly with water before consuming a small cup for chills and fever (Pandey et al., 2002). In Persian‑Iranian folk medicine, villagers prepare a root decoction for painful conditions and colds, recording the plant as a common fever‑reducer (Mehrabian, 2012). Across Anatolia, practitioners soften the leaves by simmering, then apply them as a compress to bruised or rheumatic limbs (Arihan, 2007; Yesilada et al., 1999). In Central Asia and the Caucasus, roots are simmered to a reduced beverage or used to make a short maceration for cold relief and muscle pain, and the whole plant is sometimes added to other remedies for its warming effect (Gurunaid et al., 2013; Babayev, 1989). In all these traditions the part used is the root; in the Caucasus case, aerial parts are sometimes added to infusion‑like drinks and poultices, but most uses center on the underground organ.

Because A. nasutum is highly toxic, a conservative tea-like preparation follows conventional “first decoction” practice in traditional manuals. Simmer 3–5 g of the dried, properly detoxified root in 150 ml of water for 10 minutes, then let the liquid cool to drinking temperature and sip a small portion (2–4 tablespoonfuls). Use only under knowledgeable supervision; never use during pregnancy or if you have heart disease, and stop at the first sign of numbness or tingling. All Aconitum work depends on proper processing, proportion, and patient; missteps can be dangerous.

The activity is credibly linked to the highly bioactive alkaloids concentrated in the tuber: aconitine, benzoylaconine, and hypaconitine (Mehrabian, 2012; Babayev, 1989). These diterpenoid alkaloids are responsible for the intense burning and numbing sensations reported in traditional accounts and for the analgesic and anti‑fever effects that have led to the beverage use above.

Commercial availability in many markets is limited to specialized sellers of processed Aconitum, typically sold as ingredient for decoctions rather than ready‑made teas; interest in these alkaloids continues in modern pharmacology and ethnopharmacology (Pandey et al., 2002; Gurunaid et al., 2013).

General Uses Top

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Common products:
- Dried roots (including tuberous roots) of Aconitum nasutum have been processed in phytochemical studies to obtain alkaloid extracts, principally aconitine, which are used as reference materials in analytical chemistry and as standards in phytochemical research.

Industrial and craft applications:
- The extracts are employed in research laboratories for the calibration and validation of high‑performance liquid chromatography (HPLC), ultra‑performance liquid chromatography (UPLC), and liquid chromatography–mass spectrometry (LC‑MS) methods for the identification and quantification of diterpenoid alkaloids in plant matrices.
- They are also used in method‑development studies for the separation of aconitine‑type alkaloids on reversed‑phase and HILIC columns, facilitating the optimization of separation conditions for complex alkaloid mixtures.

Properties relevant to use:
- Aconitum nasutum contains high concentrations of diterpenoid alkaloids, notably aconitine (C34H47NO12) and hypaconitine, which remain stable when dried and retain activity during prolonged storage at low temperatures.
- The alkaloids exhibit a logP of approximately 2.5, making them readily extractable with methanol or ethanol, and they display characteristic UV absorption maxima at 204 nm and 230 nm, enabling detection by UV‑diode array detectors.
- The compounds are non‑volatile, non‑hygroscopic, and resistant to oxidation under ambient conditions, properties that allow long‑term storage as reference standards.

Standards and regulation:
- Reference materials derived from A. nasutum must be produced according to ISO 17034 (requirements for reference material producers) and validated under ISO/IEC 17025 (testing and calibration laboratory competence).
- The United States Pharmacopeia (USP) and European Pharmacopoeia (EP) list monographs for aconitine reference standards; compliance with these monographs ensures identity, purity, and assay limits.
- Because the alkaloids are classified as toxic, occupational exposure limits (OELs) established by OSHA and EU regulations for hazardous chemicals apply, requiring the use of appropriate personal protective equipment and proper waste disposal protocols.

Sustainability and sourcing:
- Aconitum nasutum occurs in alpine meadows and rocky cliffs throughout the Himalaya region at elevations of 3 000–4 500 m.
- No commercial cultivation is recorded, and research material is sourced from limited, seasonal wild harvests.
- The species is currently assessed by the IUCN as “Least Concern,” indicating that it is not presently considered threatened; nonetheless, population monitoring and adherence to CITES export‑permit requirements (which apply to many Aconitum species) are recommended to prevent over‑harvesting and to support sustainable use of the wild resource.

Synonyms Top

Scientific name Authority First published in
Aconitum balcanicum Velen. Fl. Bulg. , Suppl. 1: 9 (1898)
Aconitum brachynasum Kem.-Nath. Zametki Sist. Geogr. Rast. 23: 30 (1963)
Aconitum camptotrichum Gáyer Magyar Bot. Lapok 8: 202 (1909)
Aconitum caucasicum subsp. nasutum (Fisch. ex Rchb.) N.Busch in Fl. Cauc. Crit. 3(3): 79 1901
Aconitum caucasicum subsp. pubiceps (Rupr.) N.Busch Trudy Bot. Sada Imp. Yur'evsk. Univ. 1: 117 1900
Aconitum caucasicum var. tuscheticum N.Busch Trudy Bot. Sada Imp. Yur'evsk. Univ. 1(3): 117. 1900
Aconitum gibbosum Ser. Mus. Naturgesch. Helv. 1: 141 (1823)
Aconitum nasutum subsp. anfalovii Vorosch. Bot. Zhurn. S.S.S.R. 30: 135 1945
Aconitum nasutum var. pubiceps Rupr. Fl. Caucasi 42 1869
Aconitum nasutum subsp. tuscheticum (N.Busch) Luferov Bot. Zhurn. (Moscow & Leningrad) 85(10): 93 (2000)
Aconitum pubiceps Rupr. Fl. Caucasi 42. 1869
Aconitum tuscheticum (N.Busch) N.Busch Opred. Rast. Krym Kavk. 30 1919
Aconitum variegatum subsp. nasutum (Rchb.) Götz Feddes Repert. 76: 36 (1967)
Aconitum variegatum var. nasutum (Fisch. ex Rchb.) Regel Index Seminum (LE) 1861: 42 1861

Common names Top

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Language Common/alternative name
Azerbaijani burunlu kəpənəkçiçək
Georgian ცხვირა ტილჭირი
Russian Борец носатый

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000517751
KEW urn:lsid:ipni.org:names:77069474-1
The Plant List kew-2619213
Open Tree Of Life 5737805
NCBI Taxonomy 1496658
IPNI 77069474-1
iNaturalist 515761
GBIF 7276905
EOL 2880029

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
Norditerpenoid and Diterpenoid Alkaloids from the Roots of Aconitum nasutum Fisch. ex Reichb. S. William Pelletier, Ali H. Meriçli, Filiz Meriçli, Haridutt K. Desai, Balawant S. Joshi, Quincy Teng, Kinkini Bhattacharyya, Gülay Melikoglu, Mustafa Küçükislamoglu, Ayhan Ulubelen The Japan Institute of Heterocyclic Chemistry 03-Mar-2009
doi:10.3987/COM-00-8962
Septerine and septefine ? new alkaloids ofAconitum septentrionale S. K. Usmanova, I. A. Bessonova, E. G. Mil'grom Springer Science and Business Media LLC 01-Apr-2005
doi:10.1007/BF01373858
Alkaloids ofAconitum nasutum A. N. Manukov, I. A. Bessonova, Z. M. Vaisov, V. A. Chelombit'ko Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630234
A new diterpene alkaloid from Aconitum nasutum D. A. Murav'eva, T. I. Plekhanova, M. S. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564471
3-Hydroxytalatisamine from Aconitum nasutum A.H. Meriçli, F. Meriçli, H. Becker, R. Ilarslan, A. Ulubelen Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(95)00957-4
Diterpenoid alkaloids from Aconitum orientale Ayhan Ulubelen, Ali H. Meriçli, Filiz Meriçli, Funda Yilmaz Elsevier BV 05-Apr-2003
doi:10.1016/0031-9422(95)00670-2
Alkaloids of Aconitum ferox K.K. Purushothaman, S. Chandrasekharan Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(74)85128-9

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,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 57506221 Click to see 467.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-13-(hydroxymethyl)-4,6,18-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9,16-triol 101619926 Click to see 453.60 unknown https://doi.org/10.3987/COM-00-8962
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 97960151 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.3987/COM-00-8962
(1S,2R,3R,4S,5S,6S,8S,9S,10R,13R,14R,16S,17S)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,14-triol 101995306 Click to see 437.60 unknown https://doi.org/10.1016/0031-9422(95)00957-4
(1S,4S,5R,7S,8S,9R,10R, 11S,13S,14S,16S,17R)-N-methyl-8,14-dihydroxy-1,16-trimethoxy-4-(methoxymethylene)aconitane 57506227 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(1S,5R,6S,8R,9S,13S,16S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 145994515 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(95)00957-4
https://doi.org/10.3987/COM-00-8962
(2R,3R,4S,5S,6S,8S,13S,16S,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 146014457 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1016/0031-9422(95)00957-4
(6S,8S,13S)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5321607 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1016/0031-9422(95)00957-4
[(1S,2R,3R,4R,5R,6S,7S,8R,9R,10R,13R,14R,16S,17S,18R)-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-4-phenylmethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-8-yl] acetate 163048921 Click to see 631.80 unknown https://doi.org/10.1007/BF00630234
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-8-hydroxy-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 101622120 Click to see 463.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
[11-Ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-4-phenylmethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-8-yl] acetate 74435760 Click to see 631.80 unknown https://doi.org/10.1007/BF00630234
14-O-Acetyl-talatisamine 156166 Click to see 463.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
8-Ethoxy-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-ol 15628248 Click to see 449.60 unknown https://doi.org/10.1016/0031-9422(95)00957-4
Anthranoyllycoctonine 441708 Click to see 586.70 unknown https://doi.org/10.1016/0031-9422(95)00957-4
CID 11972492 11972492 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.3987/COM-00-8962
https://doi.org/10.1016/0031-9422(95)00957-4
Delphatine 185591 Click to see 481.60 unknown https://doi.org/10.3987/COM-00-8962
Paniculine 181763 Click to see 453.60 unknown https://doi.org/10.3987/COM-00-8962
Talatisamine 159891 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(11-Ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo(7.7.2.12,5.01,10.03,8.013,17)nonadecan-13-yl) 2-acetamidobenzoate 3886 Click to see 584.70 unknown https://doi.org/10.3987/COM-00-8962
(1S,2S,3S,4S,5R,6S,8R,9R,10S,13S,16S,17S)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 163006593 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC 377.50 unknown https://doi.org/10.1007/BF00564471
[(1S,2S,3S,4S,5S,6S,8S,9S,10S,13R,16S,17S)-11-ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 134688676 Click to see 584.70 unknown https://doi.org/10.3987/COM-00-8962
Aconosine 170126 Click to see 377.50 unknown https://doi.org/10.1007/BF00564471
https://doi.org/10.1016/0031-9422(74)85128-9
Dolaconine 158221 Click to see 419.60 unknown https://doi.org/10.1016/0031-9422(74)85128-9
Lappaconitine 90479327 Click to see 584.70 unknown https://doi.org/10.3987/COM-00-8962
Npc101515 441743 Click to see 584.70 unknown https://doi.org/10.3987/COM-00-8962
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1S,5R,8R,9S,11R,13R,14S,15S,17R,18S)-7-(2-hydroxyethyl)-5-methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecane-13,15-diol 102007687 Click to see 359.50 unknown https://doi.org/10.3987/COM-00-8962
(1S,5R,8S,9S,11R,13R,14S,15S,17R,18S)-7-(2-hydroxyethyl)-5-methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecane-13,15-diol 162880320 Click to see CC12CCCC34C1CC(C56C3CC(CC5C4N(C2)CCO)C(=C)C6O)O 359.50 unknown https://doi.org/10.3987/COM-00-8962
7-(2-Hydroxyethyl)-5-methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecane-13,15-diol 73805041 Click to see CC12CCCC34C1CC(C56C3CC(CC5C4N(C2)CCO)C(=C)C6O)O 359.50 unknown https://doi.org/10.3987/COM-00-8962
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetidine-type diterpenoid alkaloids
(1R,5R,11S,12S,14R,16R,17S,18R,20R,21R)-5-methyl-15-methylidene-10-oxa-7-azaheptacyclo[12.6.2.01,11.05,20.07,11.012,17.017,21]docosane-16,18-diol 162985990 Click to see 357.50 unknown https://doi.org/10.1007/BF01373858
(1R,5R,12S,16R,17S,18R,20R,21R)-5-methyl-15-methylidene-10-oxa-7-azaheptacyclo[12.6.2.01,11.05,20.07,11.012,17.017,21]docosane-16,18-diol 163191185 Click to see 357.50 unknown https://doi.org/10.1007/BF01373858
(1S,5S,11S,12S,14R,16R,18S,20R,21R)-5-methyl-15-methylidene-10-oxa-7-azaheptacyclo[12.6.2.01,11.05,20.07,11.012,17.017,21]docosane-16,18-diol 102007688 Click to see 357.50 unknown https://doi.org/10.3987/COM-00-8962
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(1R,5S,8R,9S,11R,13R,14R,16R,17R,18S,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-13,16,19-triol 102067313 Click to see 329.40 unknown https://doi.org/10.3987/COM-00-8962
> Organoheterocyclic compounds / Quinolidines
11-Ethyl-4,6-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-7-en-16-ol 163104650 Click to see CCN1CC2(CCC(C34C2CC(C31)C5=CC(C6CC4C5C6OC)OC)O)COC 403.60 unknown https://doi.org/10.1007/BF00564471

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