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Aconitum turczaninowii

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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 UUID6440071ac3676064561683
Scientific name Aconitum turczaninowii
Authority Vorosch.
First published in Byull. Glavn. Bot. Sada 64: 36 (1967)

Description Top

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Synonyms Top

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Common names Top

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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-0000518228
Tropicos 27102205
KEW urn:lsid:ipni.org:names:707917-1
The Plant List kew-2619669
Observations.org 148751
IPNI 707917-1
GBIF 3930943
Elurikkus 442052

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)!
Title Authors Publication Released IDs
Alkaloids of the Monolian flora. IV. Turcosine ? A new alkaloid from Aconitum turczaninowi N. Batbayar, D. Batsur�n, M. N. Sultankhodzhaev Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00631013
Alkaloids of the Mongolian flora II. Alkaloids of Aconitum turczaninowii N. Batbarya, D. Batsurén, M. N. Sultankhodzhaeva Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630679
Alkaloids of the flora of Mongolia V. Turpelline — A new alkaloid fromAconitum turczaninowii N. Batbaryar, D. Batsurén, A. A. Semenov, M. N. Sultankhodzhaev Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630219

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
(1R,2S,3S,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-4,6,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,8,9,16-tetrol 101674024 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6OC)O)OC)O)O)OC)O)COC 483.60 unknown https://doi.org/10.1007/BF00630679
[(1R,2S,3S,4R,5R,6S,7S,8S,13R,14R,16S,17R,18R)-8-acetyloxy-2,5,7,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 118701715 Click to see CC(=O)OC12C3C(C4C5(CN(C3C4(C(CC5O)OC)C6(C1C(C(C6)(C(C2O)OC)O)OC(=O)C7=CC=CC=C7)O)C)COC)OC 647.70 unknown https://doi.org/10.1007/BF00631013
[(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/10.1007/BF00630679
https://doi.org/10.1007/BF00631013
10-Hydroxy mesaconitine 441712 Click to see CC(=O)OC12C3C(C4C5(CN(C3C4(C(CC5O)OC)C6(C1C(C(C6)(C(C2O)OC)O)OC(=O)C7=CC=CC=C7)O)C)COC)O 633.70 unknown https://doi.org/10.1007/BF00631013
11-Ethyl-4,6,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,8,9,16-tetrol 162875514 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6OC)O)OC)O)O)OC)O)COC 483.60 unknown https://doi.org/10.1007/BF00630679
11-Ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,4,8,9-tetrol 73813249 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6O)O)OC)O)O)OC)OC)COC 483.60 unknown https://doi.org/10.1007/BF00631013
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/BF00630679
https://doi.org/10.1007/BF00631013
Delcosin 145925533 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)COC 453.60 unknown https://doi.org/10.1007/BF00630679
https://doi.org/10.1007/BF00631013
Delcosine 120726 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)COC 453.60 unknown https://doi.org/10.1007/BF00630679
https://doi.org/10.1007/BF00631013
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
11-Ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-3,4,7,16-tetrol 73813843 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4C(C(C(C5)C(=C)C6O)O)O)O)C 375.50 unknown https://doi.org/10.1007/BF00630219
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,2S,5R,9R,10S,11R,13R,14S,15R,16R)-7-Ethyl-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecane-2,11,14-triol 15226908 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4C(C(CC5)C(=C)C6O)O)O)C 359.50 unknown https://doi.org/10.1007/BF00630679
https://doi.org/10.1007/BF00631013

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