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Aconitum fischeri

Aconitum fischeri - Unknown
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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 UUID644006fadab53606529871
Scientific name Aconitum fischeri
Authority Rchb.
First published in Monogr. Acon. : 22 (1820)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum abbreviatum Langsd. ex DC. Prodr. 1: 61 (1824)
Aconitum autumnale Lindl. Journ. Hortic. Soc. ii. (1847) 77.
Aconitum lubanskyi Rchb. Ill. Sp. Acon. Gen. : t. XX (1823)
Aconitum lubarskyi var. fischeri (Rchb.) Luferov Turczaninowia 7: 27 (2004)
Aconitum napellus Thunb. Fl. Jap. (Thunberg) 231. 1784 [Aug 1784]
Aconitum nasutum Hook. Fl. Bor.-Amer. (Hooker) i. 26.
Aconitum sinense Siebold ex Lindl. & Paxton Paxton's Fl. Gard. 1: 17 (1850)
Aconitum fischeri var. brachylobum Pamp. Nuovo Giorn. Bot. Ital. n.s., 17: 268 1910
Aconitum lubarskyi Rchb. Ill. Sp. Acon. Gen. : t. XX (1823)

Common names Top

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Language Common/alternative name
English fischer monkshood
Danish stormhat
Russian Борец Фишера
Chinese 薄叶乌头
Chinese 薄葉烏頭

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Aconitum fischeri var. arcuatum (Maxim.) Regel Index Seminum (LE) 1861: 44 1861

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,

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Inner Mongolia
      • Manchuria
    • Russian Far East
      • Kamchatka
      • Khabarovsk
      • Primorye
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000517258
USDA Plants ACFI3
Tropicos 27102133
KEW urn:lsid:ipni.org:names:707356-1
The Plant List kew-2618710
Observations.org 125304
IPNI 707356-1
iNaturalist 855564
GBIF 3033674
Freebase /m/02r1mcx
EOL 483452
USDA GRIN 1338
Wikipedia Aconitum_fischeri
CMAUP NPO13822

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Ethyl 2-methoxybenzoate 81784 Click to see CCOC(=O)C1=CC=CC=C1OC 180.20 unknown via CMAUP database
Methyl 2-methoxybenzoate 61151 Click to see COC1=CC=CC=C1C(=O)OC 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see CC(=O)OCC1=CC=CC=C1 150.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
1,4-Dimethoxybenzene 9016 Click to see COC1=CC=C(C=C1)OC 138.16 unknown via CMAUP database
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
Jesaconitine 441741 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=C(C=C7)OC)(C(C5O)OC)O)OC(=O)C)OC)OC)O)COC 675.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
1,2,3,4,6,7,8,8a-Octahydro-alpha,alpha,8,8a-tetramethylnaphthalene-2-methanol 146808 Click to see CC1CCC=C2C1(CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Cinnamyl alcohol 5315892 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
4'''-Demalonylsalvianin 5282162 Click to see C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC(=C(C=C6)O)O)O)O)O)O 843.70 unknown via CMAUP database
Awobanin 101633884 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O 773.70 unknown via CMAUP database
Bis(demalonyl)monardaein cation 20054973 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)O)O)O)O)O 741.70 unknown via CMAUP database
Bisdemalonylsalvianin 5282161 Click to see C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC(=C(C=C6)O)O)O)O)O)O 757.70 unknown via CMAUP database
Malonyl-cis-shisonin 101586992 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O 843.70 unknown via CMAUP database
Malonylawobanin 5281258 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O 859.70 unknown via CMAUP database
Nemophilinin 100921412 Click to see COC1=CC(=CC(=C1O)O)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC=C(C=C6)O)O)O)O 873.70 unknown via CMAUP database
Shisonin 5282068 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O 757.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
7-Hydroxy-2-(4-hydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5-[[6-O-(3-hydroxy-1,3-dioxopropyl)-beta-D-glucopyranosyl]oxy]-1-benzopyrylium 101930173 Click to see C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 681.60 unknown via CMAUP database
Delphinidin 3,5-diglucoside 10100906 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 627.50 unknown via CMAUP database
Pelargonin 441772 Click to see C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 595.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
3',4',5',7-Tetrahydroxy-3-[[6-O-[3-(3,4-dihydroxyphenyl)acryloyl]-beta-D-glucopyranosyl]oxy]-5-[[6-O-(1,3-dioxo-3-hydroxypropyl)-beta-D-glucopyranosyl]oxy]flavylium 101633888 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O 875.70 unknown via CMAUP database

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