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Aconitum kirinense

Aconitum kirinense - 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 UUID6440070233726040220253
Scientific name Aconitum kirinense
Authority Nakai
First published in Rep. Exped. Manchoukuo Sect. IV 2: 147 (1935)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lycoctonum kirinense (Nakai) Nakai J. Jap. Bot. 13: 406 (1937)
Lycoctonum kirinense var. villipes Nakai

Common names Top

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Language Common/alternative name
Russian Борец гиринский
Chinese 吉林乌头
Chinese 藤乌头

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Aconitum kirinense var. heterophyllum W.T.Wang Acta Bot. Yunnan. 15: 349 (1993)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
seed very poisonous, wash hands after handling, 20°C x 4 weeks, then -7°C x 6 weeks, then 10°C; germinates well from seed stored dry 5 months and with GA3 if stored longer than 5 months

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Manchuria
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000517466
Tropicos 27102143
KEW urn:lsid:ipni.org:names:707484-1
The Plant List kew-2618905
Open Tree Of Life 5737821
NCBI Taxonomy 1961225
IPNI 707484-1
iNaturalist 853738
GBIF 7277161
EOL 2873312

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
Exploring the Biomedical Potential of Terpenoid Alkaloids: Sources, Structures, and Activities Wang X, Xin J, Sun L, Sun Y, Xu Y, Zhao F, Niu C, Liu S Molecules 25-Apr-2024
PMCID:PMC11085545
doi:10.3390/molecules29091968
PMID:38731459
Neuropharmacological Potential of Diterpenoid Alkaloids Salehi A, Ghanadian M, Zolfaghari B, Jassbi AR, Fattahian M, Reisi P, Csupor D, Khan IA, Ali Z Pharmaceuticals (Basel) 14-May-2023
PMCID:PMC10223254
doi:10.3390/ph16050747
PMID:37242531
Alkaloids ofAconitum kirinense the structure of akiramine U. T. Teshebaeva, M. N. Sultankhodzhaev, A. A. Nishanov Springer Science and Business Media LLC 25-Jan-2006
doi:10.1007/BF02282515
Akiranine — A new alkaloid fromAconitum kirinense M. N. Sultankhodzhaev, Z. S. Boronova, A. A. Nishanov Springer Science and Business Media LLC 15-Nov-2005
doi:10.1007/BF02249649
Alkaloids ofAconitum kirinense. Structure of akiramidine U. T. Teshebaeva, A. N. Sultankhodzhaev, A. A. Nishanov Springer Science and Business Media LLC 21-Oct-2005
doi:10.1007/BF02236297
Alkaloids of Aconitum kirinense. Structure of akirine A. A. Nishanov, B. Tashkhodzhaev, I. M. Usupova, M. N. Sultankhodzhaev Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630652
Alkaloids of the epigeal part ofAconitum kirinense A. A. Nishanov, M. N. Sultankhodzhaev, V. G. Kondrat'ev Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630217
8-Acetylexcelsine ? A new alkaloid form Aconitum kirinense A. A. Nishanov, M. N. Sultankhodzhaev, M. S. Yunusov, B. G. Kondrat'ev Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00629765
Diterpene alkaloids from Aconitum kirinense Feng Feng, Jing-Han Liu, Shou-Xun Zhao Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00230-1

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 / Lappaconitine-type diterpenoid alkaloids
(1R,2S,3S,7R,8R,9S,11S,12S,13R,16S,18S,20S,21S)-14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.12,8.01,13.03,7.03,11.016,18.016,21]tricosane-11,20-diol 163072308 Click to see CCN1CC23C4CC5C1C4(C6CC7C(CC5(C68C7OCO8)O)OC)C(CC2O3)O 405.50 unknown https://doi.org/10.1007/BF00630652
(1S,2R,3R,4S,5R,6S,8R,9R,10R,13S,16S,17R,18S)-11-ethyl-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,13-diol 162935887 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC)OC)O)OC)OC)O 437.60 unknown https://doi.org/10.1007/BF02249649
(8-Ethyl-2,16-dihydroxy-13,15-dimethoxy-5-oxa-8-azaheptacyclo[8.7.2.114,17.01,9.04,6.06,18.011,16]icosan-11-yl) acetate 14832019 Click to see CCN1CC23C4CC5C1C4(C6CC7C(CC5(C6(C7OC)O)OC(=O)C)OC)C(CC2O3)O 449.50 unknown https://doi.org/10.1007/BF00629765
[(1S,2S,4S,6S,9R,10S,11S,13S,14R,15S,16S,17S,18S)-8-ethyl-2,16-dihydroxy-13,15-dimethoxy-5-oxa-8-azaheptacyclo[8.7.2.114,17.01,9.04,6.06,18.011,16]icosan-11-yl] acetate 101608292 Click to see CCN1CC23C4CC5C1C4(C6CC7C(CC5(C6(C7OC)O)OC(=O)C)OC)C(CC2O3)O 449.50 unknown https://doi.org/10.1007/BF00629765
11-Ethyl-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,13-diol 162935886 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC)OC)O)OC)OC)O 437.60 unknown https://doi.org/10.1007/BF02249649
13-Ethyl-23-methoxy-7,9,16-trioxa-13-azaoctacyclo[9.8.2.24,10.01,12.02,6.06,10.015,17.015,20]tricosane-5,19-diol 163192340 Click to see CCN1CC23C4CC5C1C4(C6CC7C(CC58C6(C7O)OCO8)OC)C(CC2O3)O 405.50 unknown https://doi.org/10.1016/S0031-9422(98)00230-1
14-Ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.12,8.01,13.03,7.03,11.016,18.016,21]tricosane-11,20-diol 73834226 Click to see CCN1CC23C4CC5C1C4(C6CC7C(CC5(C68C7OCO8)O)OC)C(CC2O3)O 405.50 unknown https://doi.org/10.1007/BF00630652
Akiramidine 15867697 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC)OC)O)OC)O)O 423.50 unknown https://doi.org/10.1007/BF02236297
Akiramine 15867700 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC)OC)O)OC)O)OC(=O)C 465.60 unknown https://doi.org/10.1007/BF02282515
> 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/BF00630652
https://doi.org/10.1016/S0031-9422(98)00230-1
(1S,2R,4S,5R,8S,10R,12R,13R,14R,15S,16R,18R)-11-ethyl-5-methyl-17-methylidene-9-oxa-11-azaheptacyclo[14.2.2.01,14.02,12.04,13.05,10.08,13]icosane-15,18-diol 163104863 Click to see CCN1C2C3CC4C2(C5CCC4(C1O5)C)C6C37CCC(C6O)C(=C)C7O 357.50 unknown https://doi.org/10.1016/S0031-9422(98)00230-1
(1S,2S,5R,7S,10S,11R,13R,14S,15R,16R)-7-ethyl-5-methyl-12-methylidene-7-oxido-7-azoniahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecane-2,11,14-triol 163186730 Click to see CC[N+]1(CC2(CCC(C34C2CC(C31)C56C4C(C(CC5)C(=C)C6O)O)O)C)[O-] 375.50 unknown https://doi.org/10.1007/BF00630217
(1S,4S,5R,8S,13R,14R,15S,16R,18R)-11-ethyl-5-methyl-17-methylidene-9-oxa-11-azaheptacyclo[14.2.2.01,14.02,12.04,13.05,10.08,13]icosane-15,18-diol 100956104 Click to see CCN1C2C3CC4C2(C5CCC4(C1O5)C)C6C37CCC(C6O)C(=C)C7O 357.50 unknown https://doi.org/10.1016/S0031-9422(98)00230-1
[(1R,2S,5R,10S,11R,13R,14S,15R,16R)-7-ethyl-2,14-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecan-11-yl] acetate 100956106 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4C(C(CC5)C(=C)C6OC(=O)C)O)O)C 401.50 unknown https://doi.org/10.1016/S0031-9422(98)00230-1
[(1R,2S,5R,8R,9R,10S,11R,13R,14S,15R,16R)-11,14-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadec-6-en-2-yl] acetate 162844513 Click to see CC(=O)OC1CCC2(C=NC3C14C2CC3C56C4C(C(CC5)C(=C)C6O)O)C 371.50 unknown https://doi.org/10.1016/S0031-9422(98)00230-1
7-Ethyl-5-methyl-12-methylidene-7-oxido-7-azoniahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecane-2,11,14-triol 73813840 Click to see CC[N+]1(CC2(CCC(C34C2CC(C31)C56C4C(C(CC5)C(=C)C6O)O)O)C)[O-] 375.50 unknown https://doi.org/10.1007/BF00630217
Lepenine N-oxide 163184426 Click to see CC[N+]1(CC2(CCC(C34C2CC(C31)C56C4C(C(CC5)C(=C)C6O)O)O)C)[O-] 375.50 unknown https://doi.org/10.1007/BF00630217
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Danudatine-type diterpenoid alkaloids
(1R,2S,5R,8R,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 162848245 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4C(C(CC5)C(=C)C6O)O)O)C 359.50 unknown https://doi.org/10.1016/S0031-9422(98)00230-1
[(1R,2S,5S,11S,12R,14R,15S,16R,17R)-12,15-dihydroxy-5-methyl-13-methylidene-8-azaheptacyclo[8.6.2.211,14.01,9.05,17.06,8.011,16]icosan-2-yl] acetate 100956105 Click to see CC(=O)OC1CCC2(C3C14C5C(C6CCC5(C(C3)C4N7C2C7)C(C6=C)O)O)C 385.50 unknown https://doi.org/10.1016/S0031-9422(98)00230-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
Excelsin 49866283 Click to see CCC(C)C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C 480.50 unknown https://doi.org/10.1007/BF02249649
https://doi.org/10.1016/S0031-9422(98)00230-1

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