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Aconitum laeve

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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 UUID644007042b2df354061564
Scientific name Aconitum laeve
Authority Royle
First published in Ill. Bot. Himal. Mts. : 56 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum vitifolium Royle ex Stapf Ann. Roy. Bot. Gard. (Calcutta) 10: 136 (1905)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Aconitum laeve var. curvipilosum Tamura & Lauener Notes Roy. Bot. Gard. Edinburgh 37: 433 (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
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000517510
Tropicos 27103047
KEW urn:lsid:ipni.org:names:707510-1
The Plant List kew-2618947
Open Tree Of Life 5737831
Observations.org 504624
NCBI Taxonomy 1960954
IPNI 707510-1
GBIF 7277118
Elurikkus 581709

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
The known, unknown, and the intriguing about members of a critically endangered traditional medicinal plant genus Aconitum Kakkar RA, Haneen MA, Parida AC, Sharma G Front Plant Sci 28-Jul-2023
PMCID:PMC10421671
doi:10.3389/fpls.2023.1139215
PMID:37575934
Neuropharmacological Potential of Diterpenoid Alkaloids Salehi A, Ghanadian M, Zolfaghari B, Jassbi AR, Fattahian M, Reisi P, Csupor D, Khan IA, Ali Z Pharmaceuticals (Basel) 14-May-2023
PMCID:PMC10223254
doi:10.3390/ph16050747
PMID:37242531
Natural Inhibitors of Cholinesterases: Chemistry, Structure–Activity and Methods of Their Analysis Smyrska-Wieleba N, Mroczek T Int J Mol Sci 01-Feb-2023
PMCID:PMC9916849
doi:10.3390/ijms24032722
PMID:36769043
Poisonous Plants of the Indian Himalaya: An Overview Jamloki A, Trivedi VL, Nautiyal MC, Semwal P, Cruz-Martins N Metabolites 13-Jun-2022
PMCID:PMC9229149
doi:10.3390/metabo12060540
PMID:35736473
Isoquinoline Alkaloid Contents in Macleaya cordata Extracts and Their Acetylcholinesterase and Butyrylcholinesterase Inhibition Tuzimski T, Petruczynik A, Szultka-Młyńska M, Sugajski M, Buszewski B Molecules 03-Jun-2022
PMCID:PMC9182188
doi:10.3390/molecules27113606
PMID:35684539
Phytochemical Screening, Antioxidant and Antifungal Activities of Aconitum chasmanthum Stapf ex Holmes Wild Rhizome Extracts Rafiq S, Wagay NA, Elansary HO, Malik MA, Bhat IA, Kaloo ZA, Hadi A, Alataway A, Dewidar AZ, El-Sabrout AM, Yessoufou K, Mahmoud EA Antioxidants (Basel) 26-May-2022
PMCID:PMC9220206
doi:10.3390/antiox11061052
PMID:35739952
Natural Products from Medicinal Plants against Phytopathogenic Fusarium Species: Current Research Endeavours, Challenges and Prospects Seepe HA, Nxumalo W, Amoo SO Molecules 29-Oct-2021
PMCID:PMC8587185
doi:10.3390/molecules26216539
PMID:34770948
Nesting behaviour and foraging characteristics of Andrena cineraria (Hymenoptera: Andrenidae) Dar SA, Sofi MA, El-Sharnouby M, Hassan M, Rashid R, Mir SH, Naggar YA, Salah M, Gajger IT, Sayed S Saudi J Biol Sci 01-May-2021
PMCID:PMC8324941
doi:10.1016/j.sjbs.2021.04.063
PMID:34354394
Medicinal plants resources of Western Himalayan Palas Valley, Indus Kohistan, Pakistan: Their uses and degrees of risk of extinction Islam M, Inamullah, Ahmad I, Akhtar N, Alam J, Razzaq A, Mohammad K, Mahmood T, Khan FU, Muhammad Khan W, Ahmad I, Ullah I, Shafaqat N, Qamar S Saudi J Biol Sci 22-Feb-2021
PMCID:PMC8117167
doi:10.1016/j.sjbs.2021.02.051
PMID:34025183
Phylogeny and reclassification of Aconitum subgenus Lycoctonum (Ranunculaceae) Hong Y, Luo Y, Gao Q, Ren C, Yuan Q, Yang QE PLoS One 31-Jan-2017
PMCID:PMC5334035
doi:10.1371/journal.pone.0171038
PMID:28141851
LAPPACONITINE FROM ACONITUM LAEVE ROYLE K. Handa Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1100166
Alkaloids of Aconitum laeve and their anti-inflammatory antioxidant and tyrosinase inhibition activities. Shaheen F, Ahmad M, Khan MT, Jalil S, Ejaz A, Sultankhodjaev MN, Arfan M, Choudhary MI, Atta-ur-Rahman Phytochemistry 01-Apr-2005
doi:10.1016/J.PHYTOCHEM.2005.02.010
PMID:15934134
Norditerpenoid alkaloids from roots of Aconitum finetianum Gong Wu, Shanhao Jiang, Dayuan Zhu Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00918-3

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
4-[2-(Methoxycarbonyl)anilino]-4-oxobutanoic acid 693074 Click to see COC(=O)C1=CC=CC=C1NC(=O)CCC(=O)O 251.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1R,2S,3S,4R,5R,6R,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,8,9-triol 162948175 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6OC)O)OC)O)O)OC)OC)CO 483.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
(1R,2S,3S,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,8,9-triol 102400121 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4(C5C6OC)O)OC)O)O)OC)OC)CO 483.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 97960151 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
(1S,2S,3S,4R,5S,6R,8S,9S,10S,13S,16S,17R,18R)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 162942620 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
(1S,5R,6S,8R,9S,13S,16S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 145994515 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(95)00918-3
(6S,8R,9R,13S,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 5316490 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
[(1S,5R,6S,8R,9S,13S,16S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-(2,5-dioxopyrrolidin-1-yl)benzoate 145994500 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CCC8=O 668.80 unknown https://doi.org/10.1016/0031-9422(95)00918-3
Delphatine 185591 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(1R,2S,3S,4S,5R,6S,8S,9S,10R,13S,16S,17S)-11-ethyl-4,6-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-3,8,13,16-tetrol 101324719 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5(C6OC)O)OC)O)O)O 409.50 unknown https://doi.org/10.1016/0031-9422(95)00918-3
[(1S,2R,3S,4S,5R,6S,8S,9R,10S,13S,16S,17S)-11-ethyl-2,3,8-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 162830909 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4(C5(C6OC)O)O)OC)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 600.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
[(1S,2R,3S,4S,5R,6S,8S,9R,10S,13S,16S)-11-ethyl-2,3,8-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 163190302 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4(C5(C6OC)O)O)OC)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 600.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
[(1S,2S,3S,4S,5R,6S,8S,9R,10S,13S,16R,17S)-11-ethyl-3,8,9-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 102400122 Click to see CCN1CC2(CCC(C34C2CC(C31)(C5(CC(C6CC4C5(C6OC)O)OC)O)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 600.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
[(1S,2S,3S,4S,5R,6S,8S,9R,10S,13S,16S,17S)-11-ethyl-3,8,9-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 98055304 Click to see CCN1CC2(CCC(C34C2CC(C31)(C5(CC(C6CC4C5(C6OC)O)OC)O)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 600.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
[(1S,2S,3S,4S,5S,6S,8S,9S,10S,13R,16S,17S)-11-ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 134688676 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5(C6OC)O)OC)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 584.70 unknown https://doi.org/10.1016/0031-9422(95)00918-3
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
[(1S,2S,3S,4S,6S,8S,9R,10S,13S,16S,17S)-11-ethyl-3,8,9-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 102004661 Click to see CCN1CC2(CCC(C34C2CC(C31)(C5(CC(C6CC4C5(C6OC)O)OC)O)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 600.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
Acetyl-10-deoxysepaconitine 90479327 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5(C6OC)O)OC)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 584.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
https://doi.org/10.1055/S-0028-1100166
CID 494475 494475 Click to see CCN1CC2(CCC(C34C2CC(C31)(C5(CC(C6CC4C5(C6OC)O)OC)O)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 600.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
Lannaconitine 3886 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5(C6OC)O)OC)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 584.70 unknown https://doi.org/10.1055/S-0028-1100166
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010
Lappaconitine 441743 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5(C6OC)O)OC)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 584.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.010

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