Aconitum ferox, also known as Indian Aconite, is a highly toxic plant found in the Himalayas. It is commonly used in Ayurvedic medicine and has various Hindi names, including vatsanabha and mahavisha. The plant contains a toxic alkaloid called pseudaconitine and is considered one of the most poisonous plants in the world. It grows at high altitudes and is known to cause symptoms such as numbness, vomiting, and slowed heart rate. Despite its toxicity, it has been used in traditional medicine for various ailments. However, it has also been used as a dangerous ingredient in alcoholic drinks and as an entheogen by Aghori tantrics. In recent years, it gained notoriety in the UK when a woman was found guilty of using it to murder her ex-lover and attempt to murder his fiancée.

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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Filter by language:

Language	Common/alternative name
English	indian aconite
English	himalayan monkshood
English	blue aconite
French	aconit feroce
French	aconit féroce
Gujarati	વછનાગ
Icelandic	Ægishjálmur
Kannada	ವತ್ಸನಾಭಿ
Nepali	बिष्मा
Russian	Аконит свирепый
Russian	Борец свирепый
Telugu	వసనాభి
Chinese	印度乌头
Chinese	印度烏頭

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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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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - Nepal

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)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

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

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

Standard operating procedure of Purification of Chitraka (Plumbago zeylanica Linn.) along with pharmacognostical and analytical profiles of Plumbagin

Bhinde SS, Ravi AK, Patgiri BJ, Harisha CR, Shukla VJ

Ayu

23-Oct-2021

PMCID:	PMC8614202
doi:	10.4103/ayu.AYU_299_20
PMID:	34908796

Pharmacologic Activities of Plant-Derived Natural Products on Respiratory Diseases and Inflammations

Timalsina D, Pokhrel KP, Bhusal D

Biomed Res Int

04-Oct-2021

PMCID:	PMC8505070
doi:	10.1155/2021/1636816
PMID:	34646882

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

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 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
(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 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
(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 CCN1CC2(CCC(C34C2CC(C31)(C5(CC(C6CC4C5C6O)OC)O)O)O)COC	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 CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)CO	393.50	unknown	https://doi.org/10.1016/S0031-9422(00)89756-3
(2R,3R,4S,5S,6S,8R,13S,16S,17R,18R)-11-ethyl-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol	146014456	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
[(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/10.1021/NP50096A001 https://doi.org/10.1007/BF01386201
[(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 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
[(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 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
[(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 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/10.1016/0031-9422(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 CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC(=C(C=C7)OC)OC)O)OC)OC(=O)C)OC)OC)COC	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 CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)COC	643.80	unknown	https://doi.org/10.1016/S0031-9422(00)89756-3
[(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/10.1021/NP50096A001
[(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 CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)COC	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 CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC(=C(C=C7)OC)OC)O)OC)OC(=O)C)OC)OC)COC	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/10.1021/NP50096A001 https://doi.org/10.1016/0031-9422(74)85128-9 https://doi.org/10.1039/CT8783300151
[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 CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)CO	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 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
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/10.1007/BF01386201 https://doi.org/10.1021/NP50096A001
Bikhaconitine	441713	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC(=C(C=C7)OC)OC)O)OC)OC(=O)C)OC)OC)COC	673.80	unknown	https://doi.org/10.1021/NP50096A001
Chasmaconitine	101600179	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)COC	613.70	unknown	https://doi.org/10.1016/S0031-9422(00)89756-3
CID 11452543	11452543	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
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 CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC	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
Neoline	120682	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC	437.60	unknown	https://doi.org/10.1016/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
Pseudaconine	37915	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
Pseudaconitine	90478913	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
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 CCN1CC2(CCC(C34C2CC(C31)C56C4CC(=O)C(C5)C(=C)C6O)O)C	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 CCN1CC2(CCC(C34C2CC(C31)C56C4CC(=O)C(C5)C(=C)C6O)O)C	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 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
> 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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Aconitum ferox

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