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Aconitum sajanense

Aconitum sajanense - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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)

Description Top

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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)

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

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)!
If you wish to see all the related articles click here.
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 C1=CC=C(C=C1)C=O 106.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see CC(=O)OCC1=CC=CC=C1 150.17 unknown via CMAUP database
> Benzenoids / Phenol esters
Eugenol acetate 7136 Click to see CC(=O)OC1=C(C=C(C=C1)CC=C)OC 206.24 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown via CMAUP database
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 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 CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)O)OC)COC 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 CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)O)OC)COC 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-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
beta-Humulene 5318102 Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Biflorin 441959 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown via CMAUP database
Clove-3 10338198 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Heptanone 8051 Click to see CCCCCC(=O)C 114.19 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Eugenone 5317271 Click to see CC(=O)CC(=O)C1=C(C=C(C=C1OC)OC)OC 252.26 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Eugenin 10189 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC)O 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 CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C)O 206.19 unknown via CMAUP database
Isoeugenitin 12310980 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)OC)C 220.22 unknown via CMAUP database
Isoeugenitol 5318562 Click to see CC1=CC(=O)C2=C(C=C(C(=C2O1)C)O)O 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnetin 5281691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoengeletin 101937309 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1-Desgalloyleugeniin 9918701 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)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
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 C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown via CMAUP database
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown via CMAUP database
Strictinin 73330 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 634.50 unknown via CMAUP database

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