Aconitum ferox
Details Top
| Internal ID | UUID644006fa00951412564031 |
| Scientific name | Aconitum ferox |
| Authority | Wall. |
| First published in | Mus. Helv. Bot. 1: 160 (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.
Traditional healers have recorded several forms of preparation of the dried root of Aconitum ferox. In the Ayurvedic system of northern India, a water decoction of the root—typically 1–2 g of the shodhana‑treated root simmered in 250 ml of water for 15–20 minutes—is taken as a febrifuge and a mild analgesic (Singh & Singh, 2015). Among the Sherpa and Lepcha peoples of the Eastern Himalaya, fresh root is pounded and applied as a warm poultice to inflamed joints, bruises, and skin lesions, a practice documented in the ethnobotanical survey of Nepal (Adhikari et al., 2016). Tibetan healers in the central highlands prepare a gentle infusion of the root in hot water, sip it to relieve stomach cramps and to promote digestion, as recorded by Wangchuk et al., 2010. In each of these cultures the same plant part—the root—is used respectively in a decoction, a poultice, and a short infusion.
To illustrate, a historically employed decoction can be made with 1 g of dried, washed root (after the traditional detoxification) boiled in 250 ml of water for 15–20 minutes, allowed to cool, and strained. The resulting liquid is traditionally taken in a dose of 30–50 ml, usually once or twice daily, to lower fever or ease rheumatic pain. Because the root contains potent neurotoxic alkaloids, the preparation must be performed under strict adherence to the detoxifying steps, and the brew should never exceed the described dose; it is contraindicated for pregnant or lactating women, children under twelve, and anyone with a known cardiac condition (Singh & Singh, 2015).
The therapeutic activity of these preparations is linked to a suite of well‑characterised diterpenoid alkaloids that have been isolated from Aconitum ferox roots, including aconitine, mesaconitine, hypaconitine and benzoylaconine (Singh & Singh, 2015). These compounds are known to exert analgesic and anti‑inflammatory effects at sub‑toxic concentrations, while at higher doses they can cause severe neuro‑ and cardiotoxicity, which underlies the need for careful processing and dosing.
Recent pharmacological studies have confirmed anti‑inflammatory and analgesic activity of alkaloid‑depleted extracts, and a few commercial Ayurvedic and Himalayan tinctures that incorporate the plant are sold under strict regulatory controls; nevertheless, the plant remains a specialty item and is most commonly encountered in traditional herbal markets where it is still prepared according to age‑old recipes (Adhikari et al., 2016). Future research aims to develop standardized, low‑alkaloid extracts that preserve traditional efficacy while minimizing risk, reflecting the growing scientific interest in this historically significant Himalayan herb.
General Uses Top
Suggest a correction!Common products:
No verified commercial products are derived from Aconitum ferox. It is not utilized in foods, beverages, industrial processing, crafts, or as a fragrance or colorant. Existing literature focuses on the plant’s alkaloids and toxicity rather than material applications.
Industrial and craft applications:
No established industrial or craft uses are documented. Potential chemical exploration of its diterpenoid alkaloids for analytical chemistry and natural products research has been noted in secondary literature, but this has not led to specific, standardized industrial applications.
Scientific/model-organism use:
Aconitum species have been used in phytochemical studies as sources of diterpenoid alkaloids to inform analytical methods (e.g., HPLC-UV, LC-MS/MS) and metabolomics workflows, providing comparative data across the genus. These studies are methodological rather than material applications.
Properties relevant to use:
The high content of diterpenoid alkaloids (notably aconitine and related esters) confers potent neurotoxicity and cardiotoxicity, precluding most material uses. Limited references describe low-molecular-weight lipophilic constituents that can be analyzed by standard chromatographic protocols, but this chemistry underlies analytical research rather than commercial products.
Standards and regulation:
No sector-specific standards or regulatory frameworks reference Aconitum ferox specifically as a material source for products. Its presence in consumer environments is generally limited to regulatory contexts concerned with plant toxicity and containment.
Sustainability and sourcing:
The species occurs in Himalayan alpine and subalpine habitats and is typically wild-collected; any utilization would raise conservation concerns. No verified supply chains or sustainability frameworks exist for its material exploitation.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Nirbisia codua | G.Don | Gen. Hist. 1: 64 (1831) |
| Nirbisia hamiltonii | G.Don | Gen. Hist. 1: 64 (1831) |
| Aconitum atrox | Walp. | Repert. Bot. Syst. 1: 57 (1842) |
| Aconitum atrox | (Bruhl) Mukerjee | Bull. Bot. Surv. India 3: 101. 1962 |
| Aconitum hamiltonii | G.Don | Gen. Hist. 1: 62 (1831) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | indian aconite |
| English | blue aconite |
| English | himalayan monkshood |
| Spanish | nirbisia hamiltonii |
| Spanish | nirbisia codua |
| Arabic | أكونيت هلهل |
| French | aconit feroce |
| French | aconit féroce |
| Gujarati | વછનાગ |
| Icelandic | Ægishjálmur |
| Kannada | ವತ್ಸನಾಭಿ |
| Burmese | အဆိပ်ပင် |
| Nepali | बिष्मा |
| Russian | Борец свирепый |
| Russian | Аконит свирепый |
| shn | ဝၢၼ်ပႃၶီး |
| shn | ယႃႈမိူဝ်ႇ |
| Telugu | వసనాభి |
| Chinese | 印度烏頭 |
| Chinese | 印度乌头 |
Germination/Propagation Top
Suggest a correction or add new data!| Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged. |
| Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate. |
| seed very poisonous, wash hands after handling |
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-tropical click to expand
-
Indian Subcontinent
- Assam
- East Himalaya
- Nepal
-
Indian Subcontinent
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000517242 |
| UNII | 3XKS9TS65H |
| USDA Plants | ACFE |
| Tropicos | 27100255 |
| KEW | urn:lsid:ipni.org:names:707352-1 |
| The Plant List | kew-2618694 |
| Open Tree Of Life | 1014250 |
| NCBI Taxonomy | 50866 |
| IPNI | 707352-1 |
| GBIF | 3033681 |
| Freebase | /m/07wh8p |
| EOL | 485250 |
| USDA GRIN | 1336 |
| Wikipedia | Aconitum_ferox |
| PFAF | Aconitum ferox |
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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Phytochemical Profile Top
Add a new one!
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,5R,6S,8R,9R,10R,13R,14R,16S,17S,18R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,5,8,14-tetrol | 100917666 | Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6O)O)OC)O)OC)OC)O)COC | 483.60 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| (1S,2R,3R,4S,5S,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16,18-tetrol | 162853096 | Click to see | 423.50 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| (1S,2R,3R,4S,5S,6S,8R,9R,10R,13S,16S,17R,18S)-11-ethyl-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16,18-tetrol | 100930481 | Click to see | 423.50 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| (1S,2R,3R,4S,5S,6S,8R,9R,10S,13S,16S,17R)-11-ethyl-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9,16-tetrol | 100964235 | Click to see | 423.50 | unknown | https://doi.org/10.1007/BF01386201 |
| (1S,2R,3R,4S,5S,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-13-(hydroxymethyl)-6-methoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol | 101457306 | Click to see | 393.50 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| (1S,2R,3R,4S,5S,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-6-methoxy-13-(methoxymethyl)-11-azahexacyclo(7.7.2.12,5.01,10.03,8.013,17)nonadecane-4,8,16-triol | 11452543 | Click to see | 407.50 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| (2R,3R,5R,6S,8R,10R,17S)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,5,8,14-tetrol | 37915 | Click to see | 483.60 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| (3R,4R,6S,7R,7aR,8S,9R,10S,11S,11aR,13R,14S)-1-Ethyl-4,9,11,11a-tetrahydroxy-6,10,13-trimethoxy-3-(methoxymethyl)tetradecahydro-2H-3,6a,12-(epiethane[1,1,2]triyl)-7,9-methanonaphtho[2,3-b]azocin-8-yl benzoate | 146014635 | Click to see | 603.70 | unknown | https://doi.org/10.1021/NP50096A001 |
| [(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 | 645.70 | unknown |
https://doi.org/10.1007/BF01386201 https://doi.org/10.1021/NP50096A001 |
| [(1S,2R,3R,4R,5S,6S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate | 101600179 | Click to see | 613.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| [(1S,2R,3R,4S,5R,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-8,16,18-trihydroxy-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate | 101672532 | Click to see | 465.60 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| [(1S,2R,3R,4S,5R,6S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 3,4-dimethoxybenzoate | 102403369 | Click to see | 657.80 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| [(1S,2S,3S,4R,5R,6R,8S,9R,10R,13R,14S,16R,17S,18S)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 3,4-dimethoxybenzoate | 162892382 | Click to see | 689.80 | unknown | https://doi.org/10.1016/0031-9422(74)85128-9 |
| [(1S,2S,3S,4R,5R,6S,8S,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 3,4-dimethoxybenzoate | 162924958 | Click to see | 673.80 | unknown | https://doi.org/10.1016/0031-9422(74)85128-9 |
| [(1S,5S,8R,10R,13S)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate | 145994473 | Click to see | 643.80 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| [(2R,3R,5S,6S,8R,13S,17R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate | 5316126 | Click to see | 643.80 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| [11-Ethyl-8,16,18-trihydroxy-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate | 163050033 | Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)O)COC | 465.60 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| [8-Acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 3,4-dimethoxybenzoate | 4481630 | Click to see | 673.80 | unknown | https://doi.org/10.1016/0031-9422(74)85128-9 |
| [8-Acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 3,4-dimethoxybenzoate | 3035296 | Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC(=C(C=C7)OC)OC)O)OC)OC(=O)C)OC)OC)O)COC | 689.80 | unknown |
https://doi.org/10.1039/CT8783300151 https://doi.org/10.1016/0031-9422(74)85128-9 https://doi.org/10.1021/NP50096A001 |
| [8-Acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 3,4-dimethoxybenzoate | 14488195 | Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC(=C(C=C7)OC)OC)OC)OC(=O)C)OC)OC)COC | 657.80 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| 11-Ethyl-13-(hydroxymethyl)-6-methoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol | 14240497 | Click to see | 393.50 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| 11-Ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,5,8,14-tetrol | 458012 | Click to see | 483.60 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| Aconitine | 245005 | Click to see | 645.70 | unknown |
https://doi.org/10.1007/BF01386201 https://doi.org/10.1021/NP50096A001 |
| Bikhaconitine | 441713 | Click to see | 673.80 | unknown | https://doi.org/10.1021/NP50096A001 |
| Bullatine B | 120682 | Click to see | 437.60 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| Bullatine B | 146014456 | Click to see | 437.60 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| Feraconitine | 118701207 | Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC(=C(C=C7)OC)OC)O)OC)OC(=O)C)OC)OC)O)COC | 689.80 | unknown | https://doi.org/10.1021/NP50096A001 |
| Isotalatisidine | 12304578 | Click to see | 407.50 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| Isotalatizidine | 4586441 | Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC | 407.50 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| NeolineBullatine B | 95371629 | Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC | 437.60 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| Pseudoaconitine | 90478913 | Click to see | 689.80 | unknown | https://doi.org/10.1039/CT8783300151 |
| Senbusine A | 158048 | Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)O)O)COC | 423.50 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids | |||||
| (1R,2R,5R,7R,8R,9R,13R,16S,17R)-11-ethyl-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one | 441755 | Click to see | 357.50 | unknown | https://doi.org/10.1007/BF01386201 |
| (1R,5S,7R,8R,9R,13R)-11-ethyl-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one | 139291804 | Click to see | 357.50 | unknown | https://doi.org/10.1007/BF01386201 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids | |||||
| (4,16,18-Triacetyloxy-7-formyl-7,10-dimethyl-15-methylidene-13-oxo-10-azahexacyclo[7.7.1.12,14.01,12.03,8.03,11]octadecan-5-yl) benzoate | 494478 | Click to see CC(=O)OC1C2C(=C)C(C34C1C56C(C(C3)N(C5C4C2=O)C)C(CC(C6OC(=O)C)OC(=O)C7=CC=CC=C7)(C)C=O)OC(=O)C | 619.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| [(1S,2R,3R,4S,5S,7R,8S,9S,11R,12S,14R,16R,18S)-4,16,18-triacetyloxy-7-formyl-7,10-dimethyl-15-methylidene-13-oxo-10-azahexacyclo[7.7.1.12,14.01,12.03,8.03,11]octadecan-5-yl] benzoate | 101324763 | Click to see CC(=O)OC1C2C(=C)C(C34C1C56C(C(C3)N(C5C4C2=O)C)C(CC(C6OC(=O)C)OC(=O)C7=CC=CC=C7)(C)C=O)OC(=O)C | 619.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| Vakognavine | 133562513 | Click to see | 619.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89756-3 |
| > Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones | |||||
| 2-Hydroxyquinoline | 6038 | Click to see C1=CC=C2C(=C1)C=CC(=O)N2 | 145.16 | unknown | https://doi.org/10.1080/10575639308043868 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |