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Aconitum japonicum subsp. napiforme

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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 UUID6440070092d5f251537699
Scientific name Aconitum japonicum subsp. napiforme
Authority (H.Lév. & Vaniot) Kadota
First published in Rev. Aconitum E. Asia : 179 (1987)

Description Top

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Common names Top

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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-0000517435
Tropicos 50213375
KEW urn:lsid:ipni.org:names:954035-1
The Plant List kew-2618877
Open Tree Of Life 6131411
NCBI Taxonomy 1905021
IPNI 954035-1
GBIF 3924271

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
Über Hypaconitin, ein neues Aconitum‐Alkaloid. (V. Mitteilung über Aconitum‐Alkaloide) Rikö Majima, Shin‐ichi Morio Wiley 18-Jul-2007
doi:10.1002/JLAC.19294760107
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 / Aconitane-type diterpenoid alkaloids
[(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/10.1002/JLAC.19294760107
[(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/10.1016/S0031-9422(98)00230-1
[(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/10.1016/S0031-9422(98)00230-1
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/10.1016/S0031-9422(98)00230-1
https://doi.org/10.1002/JLAC.19294760107
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/10.1016/S0031-9422(98)00230-1
https://doi.org/10.1002/JLAC.19294760107
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
[(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/10.1002/JLAC.19294760107
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/10.1002/JLAC.19294760107

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