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Aconitum monticola

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64400708c7275049699006
Scientific name Aconitum monticola
Authority Steinb.
First published in Fl. URSS 7: 730 (1937)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Aconitum wangyedianense Y.Z.Zhao Bull. Bot. Res., Harbin 3(1): 159 (1983)

Common names Top

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Language Common/alternative name
Bulgarian планинска самакитка
Russian Борец горный
Chinese 雪乌
Chinese 山地乌头
Chinese 山地烏頭

Subspecies (abbr. subsp./ssp.) Top

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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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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-0000517665
Tropicos 27102155
KEW urn:lsid:ipni.org:names:707602-1
The Plant List kew-2619090
Open Tree Of Life 625485
Observations.org 504645
NCBI Taxonomy 1045225
IPNI 707602-1
GBIF 3922885
Elurikkus 440019

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
Structure, property, biogenesis, and activity of diterpenoid alkaloids containing a sulfonic acid group from Aconitum carmichaelii Guo Q, Xia H, Wu Y, Shao S, Xu C, Zhang T, Shi J Acta Pharm Sin B 27-Jan-2020
PMCID:PMC7606178
doi:10.1016/j.apsb.2020.01.013
PMID:33163346
The Diterpenoid Alkaloids from Aconitum napellus Gabriel de la Fuente, Mat誕s Reina, Emir Valencia, Antonio Rodr暖uez-Ojeda The Japan Institute of Heterocyclic Chemistry 24-Feb-2009
doi:10.3987/COM-87-4445
Structures of montticamine and monticoline �. F. Ametova, M. S. Yunusov, V. E. Bannikova, N. D. Abdullaev, V. A. Tel'nov Springer Science and Business Media LLC 11-Feb-2005
doi:10.1007/BF01185263
Deoxydelsoline and dihydromonticamine fromAconitum monticola É. F. Ametova, M. S. Yunusov, V. A. Tel'nov Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579646
Alkaloids of Aconitum monticola structure of acomonine V. Nezhevenko, M. S. Yunusov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00571219
Alkaloids of Aconitum monticola V. E. Nezhevenko, M. S. Yunusov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563921
Songorine N-oxide fromAconitum monticola É. F. Ametova, M. S. Yunusov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565543

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,3S,4R,5R,6R,8R,9S,13S,16R,17R,18R)-11-ethyl-4,6,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9,16-triol 137705073 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)O)COC 467.60 unknown https://doi.org/10.1007/BF00579646
https://doi.org/10.1007/BF00571219
https://doi.org/10.1007/BF00565543
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2R,7R,9R,10R,13R,16S,17R)-11-ethyl-7,16-dihydroxy-13-methyl-6-methylidene-11-oxido-11-azoniahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one 100930479 Click to see 373.50 unknown https://doi.org/10.1007/BF00565543
(1R,2S,4R,5S,8R,10S,12S,13R,14R,17R,19S)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosan-16-one 162944214 Click to see CCN1C2C3CC4C2(C5CCC4(C1O5)C)C6C37CC(C(=C)C7O)C(=O)C6 355.50 unknown https://doi.org/10.3987/COM-87-4445
(1R,4S,5R,8S,10S,12R,13S,14R,17S,19R)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosan-16-one 134715137 Click to see 355.50 unknown https://doi.org/10.1007/BF00579646
https://doi.org/10.1007/BF00571219
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
(1R,2R,5R,7R,8R,9R,10S,13R,16S,17R)-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one 101683076 Click to see 329.40 unknown https://doi.org/10.1007/BF00565543
https://doi.org/10.1007/BF00571219
https://doi.org/10.1007/BF00579646
https://doi.org/10.1007/BF00563921
(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/BF00563921
https://doi.org/10.1007/BF00571219
https://doi.org/10.1007/BF00565543
https://doi.org/10.1007/BF00579646
(1R,2S,5R,7R,8R,9R,10S,13R,16S,17R)-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one 163195041 Click to see 329.40 unknown https://doi.org/10.1007/BF00563921
(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/BF00579646
https://doi.org/10.1007/BF00565543
https://doi.org/10.1007/BF00571219
https://doi.org/10.1007/BF00563921
7,16-Dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one 4376120 Click to see 329.40 unknown https://doi.org/10.1007/BF00563921
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(1R,2S,3S,4S,5S,6R,8R,9R,10S,13R,16R,17R)-11-ethyl-4,6-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,13,16-triol 162882215 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC)OC)O)O)O 393.50 unknown https://doi.org/10.1007/BF00579646
(1S,2S,3S,4S,5S,6R,8S,9R,10R,13R,17S,18S)-11-ethyl-4,6,13,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 162971106 Click to see 437.60 unknown https://doi.org/10.1007/BF00579646
(1S,2S,4S,6S,10R,11R,13S,14R)-8-ethyl-13,15-dimethoxy-5-oxa-8-azaheptacyclo[8.7.2.114,17.01,9.04,6.06,18.011,16]icosane-2,10,11-triol 145994505 Click to see CCN1CC23C(O2)CC(C45C3CC(C41)(C6(CC(C7CC5C6C7OC)OC)O)O)O 407.50 unknown https://doi.org/10.1007/BF00579646
https://doi.org/10.1007/BF01185263
(1S,2S,4S,6S,9R,10S,11S,13S,14R,15S,16R,17R,18S)-8-ethyl-13,15-dimethoxy-5-oxa-8-azaheptacyclo[8.7.2.114,17.01,9.04,6.06,18.011,16]icosane-2,11-diol 101600647 Click to see 391.50 unknown https://doi.org/10.1007/BF01185263
https://doi.org/10.1007/BF00579646
11-Ethyl-4,6-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,13,16-triol 5235752 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC)OC)O)O)O 393.50 unknown https://doi.org/10.1007/BF00579646
11-Ethyl-4,6,13,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 162971105 Click to see 437.60 unknown https://doi.org/10.1007/BF00579646
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[1-[4-[4-[4-(4,5-Dihydroxy-3-methoxy-6-methyloxan-2-yl)oxy-5-hydroxy-3-methoxy-6-methyloxan-2-yl]oxy-3,5-dimethoxy-6-methyloxan-2-yl]oxyphenyl]-10-methoxy-9-methyl-2-(2-methylpentanoyloxy)dodecan-4-yl] 2-methylpentanoate 163062555 Click to see 1029.30 unknown https://doi.org/10.1007/BF00571219
https://doi.org/10.1007/BF00579646

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