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Aconitum sachalinense subsp. yezoense

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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
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Details Top

Internal ID UUID644007132c9aa699374170
Scientific name Aconitum sachalinense subsp. yezoense
Authority (Nakai) Kadota
First published in Rev. Aconitum E. Asia : 119 (1987)

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000518014
Tropicos 100283047
KEW urn:lsid:ipni.org:names:954031-1
The Plant List kew-2619463
Open Tree Of Life 395972
NCBI Taxonomy 246712
IPNI 954031-1
iNaturalist 361897
GBIF 3921189
USDA GRIN 403538

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
On the Alkaloids of Aconitum yesoense NAKAI HIROMITSU TAKAYAMA, AKIKO(nee NAKADA) TOKITA, MIYUKI ITO, SHINICHIRO SAKAI, FUMIYA KUROSAKI, TOSHIHIKO OKAMOTO Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.102.3_245
Studies on Aconitum Species. XIII. Two New Diterpenoid Alkaloids from Aconitum yesonese var. Macroyesoense (Nakai) Tamura. VI. Koji Wada, Hideo Bando, Norio Kawahara The Japan Institute of Heterocyclic Chemistry 16-Apr-2009
doi:10.3987/COM-90-5360
Studies on Aconitum Species VI1. Yesoline, a new C20-Diterpenoid Alkaloid from Aconitum Yesoense Var. Macroyesoense (Nakai) Tamura Takashi Amiya, Koji Wada, Hideo Bando The Japan Institute of Heterocyclic Chemistry 24-Feb-2009
doi:10.3987/COM-88-4502
Studies on Aconitum Species V. Constituents of Aconitum yesoense var. macroyesoense (Nakai) Tamura Takashi Amiya, Hideo Bando, Koji Wada, Kimiko Kobayashi, Yasuo Fujimoto, Toshio Sakurai The Japan Institute of Heterocyclic Chemistry 23-Feb-2009
doi:10.3987/R-1987-10-2623
Two New C20-Diterpenoid Alkaloids from Aconitum yesoense var. macroyesoense (Nakai) Tamura, Structures of Dehydrolucidusculine and N-Deethyldehydrolucidusculine Takashi Amiya, Koji Wada, Hideo Bando The Japan Institute of Heterocyclic Chemistry 19-Feb-2009
doi:10.3987/R-1985-10-2473
Studies on Aconitum Species. XI. Two New Diterpenoid Alkaloids from Aconitum yesoense var. Macroyesoense (Nakai) Tamura V Hideo Bando, Koji Wada, Takashi Amiya, Norio Kawahara The Japan Institute of Heterocyclic Chemistry 18-Feb-2009
doi:10.3987/COM-89-5139
Determination and quantitative analysis of Aconitum alkaloids in plants by liquid chromatography—atmospheric pressure chemical ionization mass spectrometry Koji Wada, Hideo Bando, Norio Kawahara Elsevier BV 25-Jul-2002
doi:10.1016/0021-9673(93)80118-R

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,10S,13S,16S,17R)-11-ethyl-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9,16-tetrol 100964235 Click to see 423.50 unknown https://doi.org/10.3987/R-1987-10-2623
(1S,2R,3R,4S,5S,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9-triol 92854545 Click to see 467.60 unknown https://doi.org/10.3987/R-1987-10-2623
(1S,2R,3R,4S,5S,6S,8S,13R,16S,17R)-11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 137706265 Click to see 377.50 unknown https://doi.org/10.3987/R-1987-10-2623
(1S,2R,3S,5R,6S,8R,10S,13S,16S,17R,18S)-11-ethyl-8,9,16-trihydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-one 134715256 Click to see 451.60 unknown https://doi.org/10.3987/COM-88-4502
(1S,5S,6S,8R,9R,13S,16S)-11-ethyl-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 145994513 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.3987/COM-90-5360
[(1S,2R,3R,4S,6S,8R,9R,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 49767730 Click to see 509.60 unknown https://doi.org/10.3987/R-1987-10-2623
11-Ethyl-18-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,6,8,9,16-pentol 14239970 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)O)O)O)OC)O)COC 439.50 unknown https://doi.org/10.3987/COM-90-5360
4-Ethyl-12,16-dimethoxy-10-(methoxymethyl)-6-oxa-4-azaheptacyclo[15.2.1.02,7.02,11.03,13.05,10.014,19]icosane-13,14,18-triol 14558197 Click to see 451.60 unknown https://doi.org/10.3987/COM-89-5139
Browniine 441714 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.3987/R-1987-10-2623
Carmicheline 441742 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)C 377.50 unknown https://doi.org/10.3987/R-1987-10-2623
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/10.3987/R-1985-10-2473
https://doi.org/10.1016/0021-9673(93)80118-R
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/10.1016/0021-9673(93)80118-R
https://doi.org/10.3987/R-1985-10-2473
Delcosine 14-acetate 137332012 Click to see 495.60 unknown https://doi.org/10.1016/0021-9673(93)80118-R
https://doi.org/10.3987/R-1985-10-2473
Isotalatisidine 12304578 Click to see 407.50 unknown https://doi.org/10.3987/R-1987-10-2623
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(11-Ethyl-4,16-dihydroxy-13-methyl-6-methylidene-11-oxido-11-azoniahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-7-yl) acetate 14558194 Click to see 417.50 unknown https://doi.org/10.3987/COM-89-5139
CID 102585909 102585909 Click to see 399.50 unknown https://doi.org/10.3987/R-1985-10-2473
https://doi.org/10.1016/0021-9673(93)80118-R
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
(1R,4S,5S,7R,8R,9R,10R,13R,16S)-11-ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 139291788 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6O)O)O)C 359.50 unknown https://doi.org/10.3987/R-1987-10-2623
12-Acetyllucidusculine 44445647 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6OC(=O)C)OC(=O)C)O)C 443.60 unknown https://doi.org/10.3987/R-1987-10-2623
Lucidusculine 138756681 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6OC(=O)C)O)O)C 401.50 unknown https://doi.org/10.3987/R-1987-10-2623
https://doi.org/10.1016/0021-9673(93)80118-R
> 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 329.40 unknown https://doi.org/10.3987/R-1985-10-2473
https://doi.org/10.1016/0021-9673(93)80118-R
https://doi.org/10.1248/YAKUSHI1947.102.3_245
(1S,5S,8R,9S,11R,13R,14R,16S,17R,18S,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-13,19-diol 101306750 Click to see 313.40 unknown https://doi.org/10.3987/R-1985-10-2473
https://doi.org/10.1016/0021-9673(93)80118-R
5-Methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-13,19-diol 494479 Click to see 313.40 unknown https://doi.org/10.3987/R-1985-10-2473
https://doi.org/10.1016/0021-9673(93)80118-R
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Latifoloside I 10843495 Click to see 929.10 unknown https://doi.org/10.3987/R-1987-10-2623
https://doi.org/10.1016/0021-9673(93)80118-R
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavamine 27443 Click to see CCN(CC)CC1=CC2=C(C=C1)OC(=C(C2=O)C)C3=CC=CC=C3 321.40 unknown https://doi.org/10.3987/COM-89-5139
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.3987/COM-89-5139

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