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

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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

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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

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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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

Links to other databases Top

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Mercuric-sulphide based metallopharmaceutical formulation as an alternative therapeutic to combat viral and multidrug-resistant (MDR) bacterial infections Malarvizhi K, Ramyadevi D, Vedha Hari BN, Sarveswari HB, Solomon AP, Fang H, Luo RH, Zheng YT Sci Rep 04-Oct-2023
PMCID:PMC10550948
doi:10.1038/s41598-023-43103-z
PMID:37794044
Rabies control in Nepal: a missed opportunity Acharya KP, Kwon R, Cho SH, Yon DK Front Vet Sci 20-Sep-2023
PMCID:PMC10548377
doi:10.3389/fvets.2023.1184371
PMID:37799411
Triose Phosphate Isomerase Structure-Based Virtual Screening and In Vitro Biological Activity of Natural Products as Leishmania mexicana Inhibitors González-Morales LD, Moreno-Rodríguez A, Vázquez-Jiménez LK, Delgado-Maldonado T, Juárez-Saldivar A, Ortiz-Pérez E, Paz-Gonzalez AD, Lara-Ramírez EE, Yépez-Mulia L, Meza P, Rivera G Pharmaceutics 29-Jul-2023
PMCID:PMC10458937
doi:10.3390/pharmaceutics15082046
PMID:37631260
The known, unknown, and the intriguing about members of a critically endangered traditional medicinal plant genus Aconitum Kakkar RA, Haneen MA, Parida AC, Sharma G Front Plant Sci 28-Jul-2023
PMCID:PMC10421671
doi:10.3389/fpls.2023.1139215
PMID:37575934
Analytical insights into the detoxification process and characterization of a traditional metallopharmaceutical formulation K. M, B. N. VH, P. R, S. D, Durai R RSC Med Chem 01-May-2023
PMCID:PMC10285764
doi:10.1039/d3md00123g
PMID:37360396
In vitro propagation of Codonopsis pilosula (Franch.) Nannf. using apical shoot segments and phytochemical assessments of the maternal and regenerated plants Gang R, Komakech R, Chung Y, Okello D, Kim WJ, Moon BC, Yim NH, Kang Y BMC Plant Biol 16-Jan-2023
PMCID:PMC9841653
doi:10.1186/s12870-022-03950-w
PMID:36642714
No ambiguity: Chemosensory-based ayurvedic classification of medicinal plants can be fingerprinted using E-tongue coupled with multivariate statistical analysis Jayasundar R, Ghatak S, Kumar D, Singh A, Bhosle P Front Pharmacol 02-Dec-2022
PMCID:PMC9755338
doi:10.3389/fphar.2022.1025591
PMID:36532778
Climate change‐induced distributional change of medicinal and aromatic plants in the Nepal Himalaya Shrestha UB, Lamsal P, Ghimire SK, Shrestha BB, Dhakal S, Shrestha S, Atreya K Ecol Evol 15-Aug-2022
PMCID:PMC9379350
doi:10.1002/ece3.9204
PMID:35991283
A Contemporary Exploration of Traditional Indian Snake Envenomation Therapies Deshpande AM, Sastry KV, Bhise SB Trop Med Infect Dis 16-Jun-2022
PMCID:PMC9227218
doi:10.3390/tropicalmed7060108
PMID:35736986
Poisonous Plants of the Indian Himalaya: An Overview Jamloki A, Trivedi VL, Nautiyal MC, Semwal P, Cruz-Martins N Metabolites 13-Jun-2022
PMCID:PMC9229149
doi:10.3390/metabo12060540
PMID:35736473
Anti-cancer activities of Schedule E1 drugs used in ayurvedic formulations Vikram EN, Ilavarasan R, Kamaraj R J Ayurveda Integr Med 31-May-2022
PMCID:PMC9163510
doi:10.1016/j.jaim.2022.100545
PMID:35661925
Animal models - Mimicking the pain of trigeminal neuralgia Gupta S, Bansal RN, Sodhi SP, Brar GK Indian J Pharmacol 10-May-2022
PMCID:PMC9249160
doi:10.4103/ijp.ijp_296_19
PMID:35546466
Effect of Siddha medicine Poorna chandirodayam and Gorojanai mathirai among Covid 19 patients suffering from hypoxia – A case series Jeyavenkatesh J, Saravanapandian P, Amali JancyMargaret M, Shanmuga Priya R J Ayurveda Integr Med 02-Feb-2022
PMCID:PMC8808716
doi:10.1016/j.jaim.2022.100553
PMID:35125807
Management of Psoriatic Erythroderma (PsE) with Ayurvedic herbomineral preparations: A case report Girhepunje KS, Gupta V, Srivastava VK, Pandey AK, Prasad R, Singh OP J Ayurveda Integr Med 03-Jan-2022
PMCID:PMC8814395
doi:10.1016/j.jaim.2021.11.001
PMID:34991934
Assessment of the systemic toxicity of Laghu vishagarbha taila, an Ayurvedic medicated oil formulation after dermal exposure Wanjari MM, Yadav M, Dey YN, Sharma D, Srivastava B, Jamdagni SB, Gaidhani SN, Jadhav AD, Gautam M Toxicol Res (Camb) 07-Dec-2021
PMCID:PMC8882792
doi:10.1093/toxres/tfab104
PMID:35237409

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,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

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