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Aconitum japonicum subsp. ibukiense

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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
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Details Top

Internal ID UUID64400700763eb602454444
Scientific name Aconitum japonicum subsp. ibukiense
Authority (Nakai) Kadota
First published in Rev. Aconitum E. Asia : 170 (1987)

Description Top

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Common names Top

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Language Common/alternative name
English aconitum japonicum ibukiense
Spanish aconitum japonicum ibukiense
Bulgarian aconitum japonicum ibukiense
French aconitum japonicum ibukiense
Italian aconitum japonicum ibukiense
Russian aconitum japonicum ibukiense

Varieties (abbr. var.) 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-0000517433
Tropicos 100282778
KEW urn:lsid:ipni.org:names:954033-1
The Plant List kew-2618874
Open Tree Of Life 7049050
NCBI Taxonomy 1977834
IPNI 954033-1
GBIF 3924296

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)!
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Title Authors Publication Released IDs
On the Alkaloids of Aconitum ibukiense NAKAI Collected at Mt. Ryosen (Shiga Pref.) SHINICHIRO SAKAI, ICHIRO YAMAMOTO, KATSUMI HOTODA, KEIICHI YAMAGUCHI, NORIO AIMI, ETSUJI YAMANAKA, JOJU HAGINIWA, TOSHIHIKO OKAMOTO Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.104.3_222
Three new alkaloids, ryosenamine, ryosenaminol, and ibukinamine from Aconitum ibukiense Nakai. Shinichiro Sakai, Keiichi Yamaguchi, Ichiro Yamamoto, Katsumi Hotoda, Toshio Okazaki, Norio Aimi, Joju Haginiwa, Toshihiko Okamoto Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.31.3338

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,18S)-11-ethyl-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16,18-tetrol 100930481 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)O)O)COC 423.50 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
(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 CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)O)COC 451.60 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
[(1S,2R,3R,4R,5R,6S,7S,8S,9R,10R,13S,16S,17R,18S)-8-acetyloxy-5,7-dihydroxy-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 163074000 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC 615.70 unknown https://doi.org/10.1248/CPB.31.3338
[(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/10.1248/YAKUSHI1947.104.3_222
[(1S,5R,6S,7S,8R,9R,10R,13R,14R,16S)-8-acetyloxy-5,7,14-trihydroxy-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 145994469 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CC(C7(C5C(C2C6N(C7)C)OC)COC)O)OC 631.70 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
[(2S,3S,5R,8R,13S,17S)-8-acetyloxy-5,7-dihydroxy-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 138115321 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC 615.70 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
3-Deoxyaconitine 78358503 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)COC 629.70 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
Aconitane-3,8,13,14,15-pentol, 4-(methoxymethyl)-20-methyl-1,6,16-trimethoxy-, 14-benzoate, (1-alpha,3-alpha,6-alpha,14-alpha,15-alpha,16-beta)- 145925535 Click to see CN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)O)COC 589.70 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
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/10.1248/YAKUSHI1947.104.3_222
CID 146014456 146014456 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
Dehydrobrowniine 165269 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6=O)OC)O)O)OC)OC)COC 465.60 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
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/10.1248/YAKUSHI1947.104.3_222
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/10.1248/YAKUSHI1947.104.3_222
Hypaconitine 441737 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC 615.70 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
Mesaconitine 441747 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CC(C7(C5C(C2C6N(C7)C)OC)COC)O)OC 631.70 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
https://doi.org/10.1248/CPB.31.3338
Neoline 120682 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(13,18-Dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl) benzoate 73657338 Click to see CC12CC(CC34C1C5CC67C3(CC(CC6C4N5C2)C(=C)C7O)O)OC(=O)C8=CC=CC=C8 433.50 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
https://doi.org/10.1248/CPB.31.3338
[(1R,3R,4R,5S,8R,9S,11S,13R,14S,16S,17R,18R)-4,13,18-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] benzoate 101603143 Click to see CC12CN3C4C1C5(C3C6CC7CC5(C6(C4)C(C7=C)O)O)CC(C2O)OC(=O)C8=CC=CC=C8 449.50 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222
Ignavine 3035320 Click to see CC12CN3C4C1C5(C3C6CC7CC5(C6(C4)C(C7=C)O)O)CC(C2O)OC(=O)C8=CC=CC=C8 449.50 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_222

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