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Aconitum nagarum

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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 UUID64400708e3aaf644382836
Scientific name Aconitum nagarum
Authority Stapf
First published in Ann. Roy. Bot. Gard. (Calcutta) 10: 176 (1905)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum nagarum var. ecalcaratum (Airy Shaw) Airy Shaw Bull. Misc. Inform. Kew 1935: 579 1935
Aconitum nagarum f. ecalcaratum (Airy Shaw) W.T.Wang Fl. Reipubl. Popularis Sin. 27: 194 (1979)
Aconitum venatorium Diels Notes Roy. Bot. Gard. Edinburgh 5: 268 (1912)
Aconitum venatorium var. ecalcaratum Airy Shaw Bull. Misc. Inform. Kew 1932: 245 1932
Aconitum bullatifolium var. homotrichum W.T.Wang ex Y.L.Zeng Acta Pharm. Sin. 10: 111 1963

Common names Top

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Language Common/alternative name
Chinese 保山附片
Chinese 保山乌头
Chinese 山乌头
Chinese 草乌
Chinese 小黑牛
Chinese 水乌头
Chinese 七星草乌
Chinese 小白撑
Chinese 雪上一枝蒿
Chinese 撒发
Chinese 雪上一支蒿
Chinese 保山烏頭

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Aconitum nagarum var. lasiandrum W.T.Wang Fl. Reipubl. Popularis Sin. 27: 605 (1979)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000517671
Tropicos 27102953
KEW urn:lsid:ipni.org:names:707608-1
The Plant List kew-2619096
Open Tree Of Life 488235
NCBI Taxonomy 50874
IPNI 707608-1
GBIF 7276938
EOL 2873341
USDA GRIN 410028

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
Exploring the Biomedical Potential of Terpenoid Alkaloids: Sources, Structures, and Activities Wang X, Xin J, Sun L, Sun Y, Xu Y, Zhao F, Niu C, Liu S Molecules 25-Apr-2024
PMCID:PMC11085545
doi:10.3390/molecules29091968
PMID:38731459
Discussion on evolution of Mongolian medicinal material names and countermeasures for standardization Long B, Aodungerile, Bai L Chin Herb Med 22-Jul-2022
PMCID:PMC9476683
doi:10.1016/j.chmed.2022.06.005
PMID:36118000
Two decades of advances in diterpenoid alkaloids with cytotoxicity activities Liang X, Gao Y, Luan S RSC Adv 02-Jul-2018
PMCID:PMC9081856
doi:10.1039/c8ra03911a
PMID:35540251
Liquid chromatography coupled with time-of-flight and ion trap mass spectrometry for qualitative analysis of herbal medicines Chen XF, Wu HT, Tan GG, Zhu ZY, Chai YF J Pharm Anal 21-Oct-2011
PMCID:PMC5760787
doi:10.1016/j.jpha.2011.09.008
PMID:29403704
8β-Acet-oxy-14α-benzo-yloxy-N-ethyl-3α,10β,13β,15α-tetra-hydr-oxy-1α,6α,16β-trimeth-oxy-4β-(methoxy-methyl-ene)aconitane: aconifine from Aconitum karakolicum Rapaics. Tashkhodjaev B, Sultankhodjaev MN Acta Crystallogr Sect E Struct Rep Online 10-Jun-2009
PMCID:PMC2969206
doi:10.1107/S1600536809021436
PMID:21582830
Fuziline, a New Alkaloid from the Chinese Drug “Fuzi” (Aconitum carmichae Debx.) S. William Pelletier, S. W. Pelletier, Naresh V. Mody, KottayilI. Varughese, Chen Szu-Ying The Japan Institute of Heterocyclic Chemistry 13-Apr-2009
doi:10.3987/S(B)-1982-01-0047
Two New C19-Diterpenoid Alkaloids from Aconitum racemulosum Franch var. Pengzhouense Feng-Peng Wang, Chong-Sheng Peng, Qiao-Hong Chen, Dong-Lin Chen, Xi-Xian Jian The Japan Institute of Heterocyclic Chemistry 08-Mar-2009
doi:10.3987/COM-02-9455
Three new diterpene alkaloids from the roots of Aconitum nagarum var. lasiandrum. Zhang F, Peng SL, Liao X, Yu KB, Ding LS Planta Med 01-Nov-2005
doi:10.1055/S-2005-873135
PMID:16320214
A QSAR analysis of toxicity of Aconitum alkaloids. Bello-Ramírez AM, Nava-Ocampo AA Fundam Clin Pharmacol 01-Dec-2004
doi:10.1111/J.1472-8206.2004.00280.X
PMID:15548242

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,18R)-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 162853096 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)O)O)COC 423.50 unknown https://doi.org/10.1055/S-2005-873135
(1S,4S,5R,7S,8S,9R,10R, 11S,13S,14S,16S,17R)-N-methyl-8,14-dihydroxy-1,16-trimethoxy-4-(methoxymethylene)aconitane 57506227 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1055/S-2005-873135
[(1S,2R,3R,4R,5R,6S,7S,8R,9R,10R,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,7,14,16-tetrahydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 162974904 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)O)O)COC 631.70 unknown https://doi.org/10.3987/S(B)-1982-01-0047
[(1S,2R,3R,4R,5R,6S,7S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 60155415 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/10.1055/S-2005-873135
[8-Acetyloxy-11-ethyl-2,5,7,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 3748601 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4(CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC(=O)C)OC)OC)O)COC 661.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969206/
[8-Acetyloxy-11-ethyl-5,7,14,16-tetrahydroxy-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 162974903 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)O)O)COC 631.70 unknown https://doi.org/10.3987/S(B)-1982-01-0047
Aconifine 441705 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4(CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC(=O)C)OC)OC)O)COC 661.70 unknown https://doi.org/10.1111/J.1472-8206.2004.00280.X
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969206/
CID 11250863 11250863 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown https://doi.org/10.1055/S-2005-873135
CID 11452543 11452543 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.1055/S-2005-873135
CID 14108159 14108159 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/10.1055/S-2005-873135
CID 155569 155569 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown https://doi.org/10.1055/S-2005-873135
Isotalatizidine 4586441 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.1055/S-2005-873135
Neoline 120682 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.1055/S-2005-873135
NeolineBullatine B 95371629 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)O)COC 437.60 unknown https://doi.org/10.1055/S-2005-873135
Senbusine A 158048 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)O)O)COC 423.50 unknown https://doi.org/10.1055/S-2005-873135
Talatisamine 159891 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1055/S-2005-873135
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1S,5R,8R,9R,10S,11R,13R,14S,15S,16R)-7-ethyl-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecane-11,14-diol 92854548 Click to see CCN1CC2(CCCC34C2CC(C31)C56C4C(C(CC5)C(=C)C6O)O)C 343.50 unknown https://doi.org/10.1055/S-2005-873135
https://doi.org/10.3987/COM-02-9455
CID 4481785 4481785 Click to see CCN1CC2(CCCC34C2CC(C31)C56C4C(C(CC5)C(=C)C6O)O)C 343.50 unknown https://doi.org/10.1055/S-2005-873135
https://doi.org/10.3987/COM-02-9455

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