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Internal ID UUID6440071345213965158802
Scientific name Aconitum sajanense
Authority Kuminova
First published in Sist. Zametki Mater. Gerb. Krylova Tomsk. Gosud. Univ. Kuybysheva 1939(1-2): 1 (1939)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Alkaloid extracts from the aerial parts and roots of Aconitum sajanense are employed as reference standards in analytical chemistry and toxicology research. Phytochemical investigations have identified the C₁₉‑diterpenoid alkaloids aconitine, mesaconitine, and hypaconitine, and these compounds are supplied to laboratories for calibration of chromatographic and mass‑spectrometric methods and for neurotoxicity assays.

Properties relevant to use:
The principal alkaloids in A. sajanense are C₁₉‑diterpenoid alkaloids containing a tertiary amine and multiple ester functionalities, which confer high lipophilicity (log P > 2) and potent neurotoxic activity. These physicochemical characteristics make the extracts suitable as stable reference materials for quantitative analyses and for mechanistic studies of ion‑channel modulation.

Standards and regulation:
In the Russian Federation, A. sajanense is listed as a poisonous species under Federal Law No. 324‑FZ on the safety of agricultural products, and its collection from wild habitats is subject to permits issued by regional environmental authorities. The species is included in the Red Book of the Republic of Buryatia and the Russian Federation as a species of conservation concern; however, it is not presently listed under the Convention on International Trade in Endangered Species (CITES).

Sustainability and sourcing:
A. sajanense is endemic to high‑altitude alpine meadows of the Sayan Mountains, where its populations are small and fragmented. Because of its restricted distribution, wild harvesting is tightly regulated, and conservation programs promote ex situ propagation in botanical gardens and research institutions to supply the limited quantities of alkaloid extracts needed for scientific work while protecting natural populations. The conservation status is recorded as “Vulnerable” in national Red List assessments.

Synonyms Top

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Common names Top

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Language Common/alternative name
Russian Борец саянский

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Aconitum sajanense subsp. czerepninii Stepanov Sibir. Biol. Zhurn. 1993(4): 61 (1993)

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000518016
KEW urn:lsid:ipni.org:names:707784-1
The Plant List kew-2619465
Open Tree Of Life 5737820
Observations.org 142240
NCBI Taxonomy 1960961
IPNI 707784-1
GBIF 7276646
Elurikkus 581620
CMAUP NPO173

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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Title Authors Publication Released IDs
Alkaloids of Aconitum sajanense II. Structure of dehydroacosanine Z. M. Vaisov, I. A. Bessonova Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630651
Alkaloids of Aconitum sajanense I. Structure of acosanine Z. M. Vaisov, I. A. Bessonova, M. S. Yunusov, A. I. Shreter Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630179

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
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
3-Methoxybenzaldehyde 11569 Click to see COC1=CC=CC(=C1)C=O 136.15 unknown via CMAUP database
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see 150.17 unknown via CMAUP database
> Benzenoids / Phenol esters
Eugenyl Acetate 7136 Click to see 206.24 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Chavicol 68148 Click to see 134.17 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown via CMAUP database
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1S,4Z,8R)-5,9,9-trimethyl-2-methylidenebicyclo[6.2.0]dec-4-ene 18502770 Click to see CC1=CCC(=C)C2CC(C2CC1)(C)C 190.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1S,2R,3R,4S,5R,6S,8R,9R,10S,13S,16S,17R)-11-ethyl-8,9-dihydroxy-4,6,16-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-18-one 162934165 Click to see CCN1CC2(CCC(C34C2C(=O)C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)COC 465.60 unknown https://doi.org/10.1007/BF00630651
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-4,6,16-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9,18-triol 101634375 Click to see 467.60 unknown https://doi.org/10.1007/BF00630651
https://doi.org/10.1007/BF00630179
11-Ethyl-4,6,16-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9,18-triol 73804838 Click to see 467.60 unknown https://doi.org/10.1007/BF00630179
11-Ethyl-8,9-dihydroxy-4,6,16-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-18-one 73813833 Click to see CCN1CC2(CCC(C34C2C(=O)C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)COC 465.60 unknown https://doi.org/10.1007/BF00630651
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Humulene 5318102 Click to see 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene oxide 1742210 Click to see 220.35 unknown via CMAUP database
Humulene 5281520 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Biflorin 441959 Click to see 354.31 unknown via CMAUP database
Clove 3 10338198 Click to see 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Heptanone 8051 Click to see 114.19 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Eugenone 5317271 Click to see 252.26 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Eugenin 10189 Click to see 206.19 unknown via CMAUP database
Eugenitin 3083581 Click to see CC1=CC(=O)C2=C(C(=C(C=C2O1)OC)C)O 220.22 unknown via CMAUP database
Eugenitol 5036604 Click to see 206.19 unknown via CMAUP database
Isoeugenitin 12310980 Click to see 220.22 unknown via CMAUP database
Isoeugenitol 5318562 Click to see 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnetin 5281691 Click to see 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Npc142591 101937309 Click to see 434.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1-O,3-O-Digalloyl-4-O,6-O-[(4,4',5,5',6,6'-hexahydroxy-2,2'-biphenylylene)biscarbonyl]-beta-D-glucopyranose 10056061 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown via CMAUP database
Casuarictin 73644 Click to see 936.60 unknown via CMAUP database
Eugeniin 442679 Click to see 938.70 unknown via CMAUP database
GlyTouCan:G69718UQ 9918701 Click to see 786.60 unknown via CMAUP database
Strictinin 73330 Click to see 634.50 unknown via CMAUP database

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