Aconitum palmatum
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Table of Contents
Details Top
Internal ID | UUID6440070cae9be343976456 |
Scientific name | Aconitum palmatum |
Authority | D.Don |
First published in | Prodr. Fl. Nepal. : 196 (1825) |
Description Top
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Synonyms Top
Scientific name | Authority | First published in |
---|---|---|
Nirbisia bisma | G.Don | Gen. Hist. 1: 63 (1831) |
Aconitum bisma | Rapaics | Növényt. Közlem. 6: 164 (1907) |
Caltha bisma | Buch.-Ham. | Edinburgh J. Sci. 1: 251 (1824) |
Aconitum ferox subsp. palmatum | (D.Don) Brühl | Ann. Roy. Bot. Gard. (Calcutta) 5: 111 1896 |
Germination/Propagation Top
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No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
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Asia-temperate click to expand
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China
- Tibet
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China
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Asia-tropical click to expand
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Indian Subcontinent
- Assam
- East Himalaya
- Nepal
- West Himalaya
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Indo-China
- Myanmar
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Indian Subcontinent
Links to other databases Top
Suggest others/fix!Database | ID/link to page |
---|---|
World Flora Online | wfo-0000517831 |
UNII | 2OPL2F65JB |
Tropicos | 27103072 |
KEW | urn:lsid:ipni.org:names:707673-1 |
The Plant List | kew-2619289 |
Open Tree Of Life | 698584 |
NCBI Taxonomy | 279772 |
IPNI | 707673-1 |
GBIF | 3922197 |
USDA GRIN | 402457 |
CMAUP | NPO23318 |
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.
If you wish to see all the related articles click here.
Title | Authors | Publication | Released | IDs | ||||||
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Herbal Decoction Divya-Peedantak-Kwath Alleviates Allodynia and Hyperalgesia in Mice Model of Chemotherapy-Induced Peripheral Neuropathy via Modulation in Cytokine Response | Balkrishna A, Sakat SS, Karumuri S, Singh H, Tomer M, Kumar A, Sharma N, Nain P, Haldar S, Varshney A | Front Pharmacol | 30-Oct-2020 |
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Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods | Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP | J Ethnobiol Ethnomed | 03-May-2016 |
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Two New Diterpenoid Alkaloids from Aconitum palmatum | Qingping Jiang, S. William Pelletier | American Chemical Society (ACS) | 17-Mar-2005 |
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Alkaloids of aconitum palmatum: carbon skeleton of vakognavine. | Singh N, Jaswal SS | Tetrahedron Lett | 01-Jan-1970 |
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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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives | |||||
Syringic acid | 10742 | Click to see COC1=CC(=CC(=C1O)OC)C(=O)O | 198.17 | unknown | via CMAUP database |
> Benzenoids / Phenols / Methoxyphenols | |||||
Syringaldehyde | 8655 | Click to see COC1=CC(=CC(=C1O)OC)C=O | 182.17 | unknown | via CMAUP database |
> Lignans, neolignans and related compounds / Furanoid lignans | |||||
Sesamin | 72307 | Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 | 354.40 | unknown | via CMAUP database |
Yangambin | 443028 | Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC | 446.50 | unknown | via CMAUP database |
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives | |||||
Linoleic Acid | 5280450 | Click to see CCCCCC=CCC=CCCCCCCCC(=O)O | 280.40 | unknown | via CMAUP database |
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids | |||||
(1R,2S,4S,6R,7S,10S)-11-methyl-5-methylidene-13-oxa-16-azahexacyclo[9.6.3.24,7.01,10.02,7.012,16]docosan-6-ol | 122212724 | Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)CN6C2OCC6 | 343.50 | unknown | https://doi.org/10.1021/NP50074A027 |
(1S,3S,5S,8R,9S,11R,14R,16S,17R,18R,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,10,19-triol | 101930091 | Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O | 329.40 | unknown | https://doi.org/10.1021/NP50074A027 |
(3,19-Dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-10-yl) 3-phenylprop-2-enoate | 162891602 | Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)OC(=O)C=CC8=CC=CC=C8)C(=C)C7)O)O | 459.60 | unknown | https://doi.org/10.1021/NP50074A027 |
(4,18-Diacetyloxy-7-formyl-16-hydroxy-7,10-dimethyl-15-methylidene-13-oxo-10-azahexacyclo[7.7.1.12,14.01,12.03,8.03,11]octadecan-5-yl) benzoate | 14039732 | Click to see CC(=O)OC1C2C(=C)C(C34C1C56C(C(C3)N(C5C4C2=O)C)C(CC(C6OC(=O)C)OC(=O)C7=CC=CC=C7)(C)C=O)O | 577.60 | unknown | https://doi.org/10.1021/NP50074A027 |
[(1S,2R,3R,4S,5S,7R,8R,9S,11R,12S,14R,16R,18S)-4,16,18-triacetyloxy-7-formyl-7,10-dimethyl-15-methylidene-13-oxo-10-azahexacyclo[7.7.1.12,14.01,12.03,8.03,11]octadecan-5-yl] benzoate | 162874266 | Click to see CC(=O)OC1C2C(=C)C(C34C1C56C(C(C3)N(C5C4C2=O)C)C(CC(C6OC(=O)C)OC(=O)C7=CC=CC=C7)(C)C=O)OC(=O)C | 619.70 | unknown | https://doi.org/10.1016/S0040-4039(00)89724-5 |
5,7-Dimethyl-12-methylidene-7-azoniaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,4,10,16-tetrol | 163194570 | Click to see CC12C[N+]3(C4C5C(C6CC7C4(C1C3(CC75CC6=C)O)CC(C2O)O)O)C | 360.50 | unknown | https://doi.org/10.1021/NP50074A027 |
Anthorine | 441709 | Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 | 343.50 | unknown | https://doi.org/10.1021/NP50074A027 |
Hetisine | 431673 | Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O | 329.40 | unknown | https://doi.org/10.1021/NP50074A027 |
Unii-V81K1mmx3X | 135897293 | Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 | 343.50 | unknown | https://doi.org/10.1021/NP50074A027 |
Vakhmadine | 163184425 | Click to see CC12C[N+]3(C4C5C(C6CC7C4(C1C3(CC75CC6=C)O)CC(C2O)O)O)C | 360.50 | unknown | https://doi.org/10.1021/NP50074A027 |
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids | |||||
(19-Acetyloxy-3-hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-10-yl) 3-phenylprop-2-enoate | 162855530 | Click to see CC(=O)OC1C2C(C3C4C56C1C3(CC7C5C(CC(C6)O)(CN74)C)CC2=C)OC(=O)C=CC8=CC=CC=C8 | 501.60 | unknown | https://doi.org/10.1021/NP50074A027 |
5-Methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,6,10,19-tetrol | 163104528 | Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2O)O)C(=C)C7)O)O | 345.40 | unknown | https://doi.org/10.1021/NP50074A027 |
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
(-)-Citronellol | 7793 | Click to see CC(CCC=C(C)C)CCO | 156.26 | unknown | via CMAUP database |
(R)-(+)-Citronellal | 75427 | Click to see CC(CCC=C(C)C)CC=O | 154.25 | unknown | via CMAUP database |
D-Citronellol | 101977 | Click to see CC(CCC=C(C)C)CCO | 156.26 | unknown | via CMAUP database |
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids | |||||
(-)-Isopulegol | 170833 | Click to see CC1CCC(C(C1)O)C(=C)C | 154.25 | unknown | via CMAUP database |
1alpha,3beta,4beta-p-Menthane-3,8-diol | 22214620 | Click to see CC1CCC(C(C1)O)C(C)(C)O | 172.26 | unknown | via CMAUP database |
Menthoglycol | 19100 | Click to see CC1CCC(C(C1)O)C(C)(C)O | 172.26 | unknown | via CMAUP database |
Neomenthoglycol | 9920491 | Click to see CC1CCC(C(C1)O)C(C)(C)O | 172.26 | unknown | via CMAUP database |
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols | |||||
Alpha-Tocopherol | 14985 | Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C | 430.70 | unknown | via CMAUP database |
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
alpha-Cadinol | 10398656 | Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C | 222.37 | unknown | via CMAUP database |
T-Muurolol | 3084331 | Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C | 222.37 | unknown | via CMAUP database |
trans-Calamenene | 6429022 | Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C | 202.33 | unknown | via CMAUP database |
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
Betulinic Acid | 64971 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O | 456.70 | unknown | via CMAUP database |
Betulonic acid | 122844 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O | 454.70 | unknown | via CMAUP database |
Erythrodiol | 101761 | Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C | 442.70 | unknown | via CMAUP database |
Morolic acid | 489944 | Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C | 456.70 | unknown | via CMAUP database |
Squalene | 638072 | Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C | 410.70 | unknown | via CMAUP database |
Ursolic Acid | 64945 | Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O | 456.70 | unknown | via CMAUP database |
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives | |||||
Cycloeucalenol | 101690 | Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C | 426.70 | unknown | via CMAUP database |
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
Beta-Sitosterol | 222284 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C | 414.70 | unknown | via CMAUP database |
Sitogluside | 5742590 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C | 576.80 | unknown | via CMAUP database |
Stigmast-4-en-3-one | 5484202 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C | 412.70 | unknown | via CMAUP database |
Tetraacetyldaucosterol | 12895763 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C | 745.00 | unknown | via CMAUP database |
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives | |||||
Glutaric acid | 743 | Click to see C(CC(=O)O)CC(=O)O | 132.11 | unknown | via CMAUP database |
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves | |||||
Shikimic acid | 8742 | Click to see C1C(C(C(C=C1C(=O)O)O)O)O | 174.15 | unknown | via CMAUP database |
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols | |||||
Aromadendrin | 122850 | Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O | 288.25 | unknown | via CMAUP database |
Fustin | 5317435 | Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O | 288.25 | unknown | via CMAUP database |
Garbanzol | 442410 | Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O | 272.25 | unknown | via CMAUP database |
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols | |||||
Rhamnocitrin | 5320946 | Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O | 300.26 | unknown | via CMAUP database |
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
(2R,3R)-3,4'-Dihydroxy-5,7-dimethoxyflavone | 10403456 | Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(C(O2)C3=CC=C(C=C3)O)O | 316.30 | unknown | via CMAUP database |
Aromadendrin 7-methyl ether | 181132 | Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O | 302.28 | unknown | via CMAUP database |
Eucalyptin | 76573 | Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC=C(C=C3)OC)O | 326.30 | unknown | via CMAUP database |
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins | |||||
Ellagic Acid | 5281855 | Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O | 302.19 | unknown | via CMAUP database |
Collections Top
In private collections | 0 |
In public collections | 0 |