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Aconitum talassicum

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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 UUID6440071827960931642478
Scientific name Aconitum talassicum
Authority Popov
First published in Rast. Zapovedn. Guralash i Zaaminsk. Lesnich. : 8 (1936)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Kazakh Талас уқорғасыны
Russian Борец таласский
Uzbek oq parpi
Chinese 塔拉斯乌头

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Aconitum talassicum var. villosulum W.T.Wang Fl. Reipubl. Popularis Sin. 27: 611 (1979)

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
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000518152
Tropicos 27102200
KEW urn:lsid:ipni.org:names:707867-1
The Plant List kew-2619592
Open Tree Of Life 5737809
Observations.org 146984
NCBI Taxonomy 1496662
IPNI 707867-1
GBIF 7278307
Elurikkus 581940

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
Investigation of the potential anticancer effects of napelline and talatisamine dirterpenes on experimental brain tumor models Demirbağ Karaali M, Aydın Karataş E Cytotechnology 11-Jun-2020
PMCID:PMC7450011
doi:10.1007/s10616-020-00405-8
PMID:32529352
UPLC-Q-TOF-HDMS analysis of constituents in the root of two kinds of Aconitum using a metabolomics approach. Sun H, Wang M, Zhang A, Ni B, Dong H, Wang X Phytochem Anal 01-May-2013
doi:10.1002/PCA.2407
PMID:23225552
Diterpene alkaloids from Aconitum anthora and assessment of the hERG-inhibiting ability of Aconitum alkaloids. Forgo P, Borcsa B, Csupor D, Fodor L, Berkecz R, Molnár V A, Hohmann J Planta Med 01-Mar-2011
doi:10.1055/S-0030-1250362
PMID:20862641
11-Dehydrokobusine — A new alkaloid from Aconitum thalassicum A. A. Nishanov, M. N. Sultankhodzhaev, M. S. Yunusov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00598284
Alkaloids of the epigeal part of Aconitum talassicum. Structure of actaline A. A. Nishanov, B. Tashkhodzhaev, M. I. Sultankhodzhaev, B. T. Ibragimov, M. S. Yunusov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00596691
Diterpenoid alkaloids from Aconitum talassicum Jianmin Yue, Jun Xu, Yaozu Chen, Shaonong Chen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90435-7

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
[(1R,2R,3S,5S,9S,10S,13S,17S)-11-ethyl-9-methoxy-4-oxo-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-7-en-13-yl]methyl 2-acetamidobenzoate 101677519 Click to see CCN1CC2(CCCC34C2CC(C31)(C5=CCC6CC4C5C6=O)OC)COC(=O)C7=CC=CC=C7NC(=O)C 518.60 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(11-Ethyl-4,8-dihydroxy-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl)methyl 2-acetamidobenzoate 73834227 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC(=O)C7=CC=CC=C7NC(=O)C 568.70 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
(1S,2R,3R,4S,5S,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-13-(hydroxymethyl)-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 101600197 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)CO 407.50 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
(1S,2R,3R,5S,8R,9S,10R,13R,17R)-11-ethyl-8-hydroxy-13-methyl-4-methylidene-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-16-one 162904014 Click to see CCN1CC2(CCC(=O)C34C2CC(C31)C5(CCC6CC4C5C6=C)O)C 341.50 unknown https://doi.org/10.1007/BF00596691
(1S,2S,3S,5R,8S,9S,10R,13R,17R)-11-ethyl-8-hydroxy-13-methyl-4-methylidene-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-16-one 162904015 Click to see CCN1CC2(CCC(=O)C34C2CC(C31)C5(CCC6CC4C5C6=C)O)C 341.50 unknown https://doi.org/10.1007/BF00598284
(2R,3R,4S,5S,6S,8S,13S,16S,17R)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 146014457 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1007/BF00596691
(6S,8S,13S)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5321607 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1007/BF00596691
(8-Ethoxy-11-ethyl-4-hydroxy-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl)methyl 2-acetamidobenzoate 163083536 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)OCC)OC)COC(=O)C7=CC=CC=C7NC(=O)C 596.80 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
[(1S,2R,3R,4S,5R,8R,9R,10R,13S,16S,17R)-11-ethyl-4-hydroxy-16-methoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-6-en-13-yl]methyl 2-acetamidobenzoate 101677520 Click to see CCN1CC2(CCC(C34C2CC(C31)C5C=CC6CC4C5C6O)OC)COC(=O)C7=CC=CC=C7NC(=O)C 520.70 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
[(1S,2R,3R,4S,5S,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-4,8-dihydroxy-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-acetamidobenzoate 101596811 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC(=O)C7=CC=CC=C7NC(=O)C 568.70 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
[(1S,2R,3R,4S,5S,6S,8S,9S,10R,13S,16S,17R)-8-ethoxy-11-ethyl-4-hydroxy-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-acetamidobenzoate 101677518 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)OCC)OC)COC(=O)C7=CC=CC=C7NC(=O)C 596.80 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
11-Ethyl-8-hydroxy-13-methyl-4-methylidene-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-16-one 14285810 Click to see CCN1CC2(CCC(=O)C34C2CC(C31)C5(CCC6CC4C5C6=C)O)C 341.50 unknown https://doi.org/10.1007/BF00596691
20-Ethyl-16-methoxy-4-(methoxymethyl)aconitane-1,8,14-triol 3084020 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.1002/PCA.2407
https://doi.org/10.1055/S-0030-1250362
Cammaconine 441715 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)CO 407.50 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
CID 161735 161735 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)CO 407.50 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
Isotalatisidine 12304578 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.1007/BF00596691
Talatisidine 139066658 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.1007/BF00596691
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
(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 CCN1CC2(CCC(C34C2CC(C31)C56C4CC(=O)C(C5)C(=C)C6O)O)C 357.50 unknown https://doi.org/10.1016/S0031-9422(00)90435-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(1R,5S,8R,9S,11R,13R,14R,16R,17R,18S,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-13,16,19-triol 102067313 Click to see CC12CCCC34C1C5(CC67C3C(C(CC6C4N5C2)C(=C)C7O)O)O 329.40 unknown https://doi.org/10.1007/BF00596691
(1S,5S,8R,9S,11R,13R,14R,16S,17R,18S)-13-hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-19-one 101526427 Click to see CC12CCCC34C1C5CC67C3C(=O)C(CC6C4N5C2)C(=C)C7O 311.40 unknown https://doi.org/10.1007/BF00598284

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