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Aconitum toxicum

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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
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Details Top

Internal ID UUID64400719e0f20407936461
Scientific name Aconitum toxicum
Authority Rchb.
First published in Uebers. Aconitum : 43 (1819)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum bosniacum Beck Ann. K. K. Naturhist. Hofmus. 6: 342 (1891)
Aconitum toxicum subsp. bosniacum (Beck) Niketić Fl. Serbia 1: 316 (1992)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Aconitum toxicum subsp. bucegiense (Nyár.) Mucher Phyton (Horn) 33: 68 (1993)
Aconitum toxicum subsp. crispulum (Nyár.) Mucher Phyton (Horn) 33: 70 (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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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-0000518199
Tropicos 100283105
KEW urn:lsid:ipni.org:names:707898-1
The Plant List kew-2619640
Open Tree Of Life 5737811
Observations.org 148032
NCBI Taxonomy 1496663
IPNI 707898-1
iNaturalist 515783
GBIF 7277059
EPPO AAOTX
Elurikkus 581699

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
Bioinformatics Tools for the Analysis of Active Compounds Identified in Ranunculaceae Species Mareş C, Udrea AM, Şuţan NA, Avram S Pharmaceuticals (Basel) 05-Jun-2023
PMCID:PMC10303079
doi:10.3390/ph16060842
PMID:37375790
Grapevine Plants Management Using Natural Extracts and Phytosynthesized Silver Nanoparticles Vizitiu DE, Sardarescu DI, Fierascu I, Fierascu RC, Soare LC, Ungureanu C, Buciumeanu EC, Guta IC, Pandelea LM Materials (Basel) 18-Nov-2022
PMCID:PMC9697161
doi:10.3390/ma15228188
PMID:36431673
Phytosynthesis of Biological Active Silver Nanoparticles Using Echinacea purpurea L. Extracts Fierascu IC, Fierascu I, Baroi AM, Ungureanu C, Ortan A, Avramescu SM, Somoghi R, Fierascu RC, Dinu-Parvu CE Materials (Basel) 20-Oct-2022
PMCID:PMC9609611
doi:10.3390/ma15207327
PMID:36295404
Aconitum Alkaloid Songorine Exerts Potent Gamma-Aminobutyric Acid-A Receptor Agonist Action In Vivo and Effectively Decreases Anxiety without Adverse Sedative or Psychomotor Effects in the Rat Bali ZK, Bruszt N, Kőszegi Z, Nagy LV, Atlasz T, Kovács P, Csupor D, Csupor-Löffler B, Hernádi I Pharmaceutics 28-Sep-2022
PMCID:PMC9610616
doi:10.3390/pharmaceutics14102067
PMID:36297502
Metallic and Metal Oxides Nanoparticles for Sensing Food Pathogens—An Overview of Recent Findings and Future Prospects Ungureanu C, Tihan GT, Zgârian RG, Fierascu I, Baroi AM, Răileanu S, Fierăscu RC Materials (Basel) 04-Aug-2022
PMCID:PMC9370041
doi:10.3390/ma15155374
PMID:35955309
Gold Nanoparticles: Biosynthesis and Potential of Biomedical Application Mikhailova EO J Funct Biomater 03-Dec-2021
PMCID:PMC8708476
doi:10.3390/jfb12040070
PMID:34940549
Phytosynthesized Metallic Nanoparticles—between Nanomedicine and Toxicology. A Brief Review of 2019′s Findings Fierascu I, Fierascu IC, Brazdis RI, Baroi AM, Fistos T, Fierascu RC Materials (Basel) 25-Jan-2020
PMCID:PMC7040630
doi:10.3390/ma13030574
PMID:31991830
Rare tradition of the folk medicinal use of Aconitum spp. is kept alive in Solčavsko, Slovenia Povšnar M, Koželj G, Kreft S, Lumpert M J Ethnobiol Ethnomed 08-Aug-2017
PMCID:PMC5549329
doi:10.1186/s13002-017-0171-x
PMID:28789666
Bisnorditerpene, norditerpene, and lipo-alkaloids from Aconitum toxicum. Csupor D, Forgo P, Wenzig EM, Bauer R, Hohmann J J Nat Prod 01-Oct-2008
doi:10.1021/NP800322Q
PMID:18841905

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,4S,5S,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-13-(hydroxymethyl)-6,18-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 124928671 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)CO 423.50 unknown https://doi.org/10.1021/NP800322Q
(1S,2R,3R,4S,5S,6S,8S,9R,10R,13S,16S,17R,18S)-11-ethyl-13-(hydroxymethyl)-6,18-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 162931234 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)CO 423.50 unknown https://doi.org/10.1021/NP800322Q
(1S,4S,6S,8S,9R,10R,13S,16S,17R,18S)-11-ethyl-13-(hydroxymethyl)-6,18-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 163185704 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)CO 423.50 unknown https://doi.org/10.1021/NP800322Q
(2R,3R,4S,5S,6S,8R,13S,17R)-11-ethyl-13-(hydroxymethyl)-6,18-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 137706241 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)CO 423.50 unknown https://doi.org/10.1021/NP800322Q
Neolinine 14060211 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)CO 423.50 unknown https://doi.org/10.1021/NP800322Q
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(1R,2R,3R,4S,5R,6R,8S,9S,10R,13R,16S,17R)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,5,8-triol 163104245 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6(CC4C5C6O)O)OC)O)OC 393.50 unknown https://doi.org/10.1021/NP800322Q
(1R,2R,3R,4S,5S,6S,8S,9S,10R,13R,14R,16S,17R)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,14-triol 102590023 Click to see CCN1CC2C3CC4C1C3(C5CC6C(CC4(C5C6O)O)OC)C(CC2O)OC 393.50 unknown https://doi.org/10.1021/NP800322Q
(1R,2R,3R,4S,5S,6S,8S,9S,10R,13R,16S,17R)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 95796295 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC 377.50 unknown https://doi.org/10.1021/NP800322Q
(1S,2R,3R,4R,5S,6R,8S,9R,10S,13S,14S,16R,17S)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,14-triol 163070110 Click to see CCN1CC2C3CC4C1C3(C5CC6C(CC4(C5C6O)O)OC)C(CC2O)OC 393.50 unknown https://doi.org/10.1021/NP800322Q
(1S,2R,3R,4R,5S,6S,8S,9R,10S,13S,16R,17S)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 163006592 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC 377.50 unknown https://doi.org/10.1021/NP800322Q
(1S,2S,3S,4R,5R,6R,8R,9R,10S,13S,14S,16R,17S)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,14-triol 163070109 Click to see CCN1CC2C3CC4C1C3(C5CC6C(CC4(C5C6O)O)OC)C(CC2O)OC 393.50 unknown https://doi.org/10.1021/NP800322Q
[(1R,2R,3R,4S,5R,6S,8S,9S,10R,13R,16S,17R)-11-ethyl-8-hydroxy-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 162950448 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)OC 419.60 unknown https://doi.org/10.1021/NP800322Q
[(1R,2S,3S,4S,5S,6R,8R,9S,10R,13R,16S,17R)-11-ethyl-8-hydroxy-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 162950447 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)OC 419.60 unknown https://doi.org/10.1021/NP800322Q
[(2R,3R,5S,6S,8S,17R)-11-ethyl-5,8-dihydroxy-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 5316477 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)O)OC 497.60 unknown https://doi.org/10.1021/NP800322Q
11-Ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,14-triol 74392446 Click to see CCN1CC2C3CC4C1C3(C5CC6C(CC4(C5C6O)O)OC)C(CC2O)OC 393.50 unknown https://doi.org/10.1021/NP800322Q
Aconosine 170126 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC 377.50 unknown https://doi.org/10.1021/NP800322Q
Delavaconine 5748533 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6(CC4C5C6O)O)OC)O)OC 393.50 unknown https://doi.org/10.1021/NP800322Q
Delavaconitine 121441 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)O)OC 497.60 unknown https://doi.org/10.1021/NP800322Q
Dolaconine 158221 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)OC 419.60 unknown https://doi.org/10.1021/NP800322Q

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