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Aconitum naviculare

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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 UUID6440070ac3da4686031242
Scientific name Aconitum naviculare
Authority Stapf
First published in Ann. Roy. Bot. Gard. (Calcutta) 10: 154 (1905)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum bhutanicum Kadota Himalayan Pl. 1: 211 (1988)
Aconitum creagromorphum Lauener Notes Roy. Bot. Gard. Edinburgh 25: 12 (1963)
Aconitum ferox var. naviculare Brühl Ann. Roy. Bot. Gard. (Calcutta) 5: 111 1896
Aconitum naviculare var. leiocarpum Tamura Acta Phytotax. Geobot. 23: 28 1968

Common names Top

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Language Common/alternative name
Chinese 查干泵嘎
Chinese 船盔乌头
Chinese 船盔乌头人船形乌头）
Chinese 滂噶尔

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000517761
Tropicos 27103900
KEW urn:lsid:ipni.org:names:707621-1
The Plant List kew-2619222
Open Tree Of Life 5737802
NCBI Taxonomy 1551426
IPNI 707621-1
GBIF 3922672
EOL 2873342

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
Traditional Tibetan medicine to fight against COVID-19: Basic theory and therapeutic drugs Zhang K, Wang L, Peng J, Sangji K, Luo Y, Zeng Y, Zeweng Y, Fan G Front Pharmacol 16-Feb-2023
PMCID:PMC9978713
doi:10.3389/fphar.2023.1098253
PMID:36874035
The tibetan medicine Zuozhu-Daxi can prevent Helicobacter pylori induced-gastric mucosa inflammation by inhibiting lipid metabolism Shi Y, Ning J, Norbu K, Hou X, Zheng H, Zhang H, Yu W, Zhou F, Li Y, Ding S, Zhang Q Chin Med 08-Nov-2022
PMCID:PMC9641849
doi:10.1186/s13020-022-00682-9
PMID:36348469
Current advances on the phytochemical composition, pharmacologic effects, toxicology, and product development of Phyllanthi Fructus Yan X, Li Q, Jing L, Wu S, Duan W, Chen Y, Chen D, Pan X Front Pharmacol 19-Oct-2022
PMCID:PMC9626985
doi:10.3389/fphar.2022.1017268
PMID:36339628
Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species Hao DC, Zhang Y, He CN, Xiao PG Evid Based Complement Alternat Med 12-Jan-2022
PMCID:PMC8769838
doi:10.1155/2022/9027727
PMID:35069772
The Treatment of Cholecystitis and Cholelithiasis by Tibetan Medicine Pan L, Gao J, Han Y, Shi Y, Tang X, Pu L, Lai X, Dongzhu R, Zhang J, Xiangmao Q, Pengcuo J Evid Based Complement Alternat Med 30-Sep-2021
PMCID:PMC8497101
doi:10.1155/2021/9502609
PMID:34630620
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
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
PMCID:PMC4855762
doi:10.1186/s13002-016-0089-8
PMID:27142597
Important Poisonous Plants in Tibetan Ethnomedicine Ma L, Gu R, Tang L, Chen ZE, Di R, Long C Toxins (Basel) 14-Jan-2015
PMCID:PMC4303819
doi:10.3390/toxins7010138
PMID:25594733
Studies on C20-Diterpenoid Alkaloids: Synthesis of the Hetidine Framework and Its Application to the Synthesis of Dihydronavirine and the Atisine Skeleton Hamlin AM, Lapointe D, Owens K, Sarpong R J Org Chem 08-Jul-2014
PMCID:PMC4120980
doi:10.1021/jo501214b
PMID:25004408
Phytochemical and Antioxidant-Related Investigations on Bark of Abies spectabilis (D. Don) Spach. from Nepal Dall’Acqua S, Minesso P, Shresta BB, Comai S, Jha PK, Gewali MB, Greco E, Cervellati R, Innocenti G Molecules 08-Feb-2012
PMCID:PMC6268527
doi:10.3390/molecules17021686
PMID:22318324
A new diterpenoid alkaloid from a Tibetan medicinal herb <i>Aconitum naviculare</i> Stapf Liming Gao, Xiaomei Wei, Li Yang SAGE Publications 16-Dec-2009
doi:10.3184/0308234041209220
Two New C<sub>20</sub>‐Diterpenoid Alkaloids from the Tibetan Medicinal Plant <i>Aconitum naviculare</i><scp>Stapf</scp> Jin‐Xin Cao, Liang‐Bo Li, Jie Ren, Si‐Ping Jiang, Ren‐Rong Tian, Xu‐Lin Chen, Shu‐Lin Peng, Jie Zhang, Hua‐Jie Zhu Wiley 29-Oct-2008
doi:10.1002/HLCA.200890209
Ethnomedicinal plants used by the people of Manang district, central Nepal Bhattarai S, Chaudhary RP, Taylor RS J Ethnobiol Ethnomed 04-Oct-2006
PMCID:PMC1618386
doi:10.1186/1746-4269-2-41
PMID:17020612

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 / Phenethylamines
Hordenine 68313 Click to see CN(C)CCC1=CC=C(C=C1)O 165.23 unknown https://doi.org/10.3184/0308234041209220
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1S,2R,4R,6R,7R,10R,11S,17R)-11-methyl-5-methylidene-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-6-ol 162923620 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown https://doi.org/10.3184/0308234041209220
(1S,5R,8R,9R,11R,14S,17S,18S)-12-[[4-[2-(dimethylamino)ethyl]phenoxy]methyl]-5-methyl-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadeca-6,12-dien-9-ol 163188626 Click to see CC12CCCC34C1CCC56C3CC(CC5(C4N=C2)O)C(=C6)COC7=CC=C(C=C7)CCN(C)C 460.60 unknown https://doi.org/10.3184/0308234041209220
(1S,5R,8R,9S,10R,11R,14R,16S,17R,18R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 131879709 Click to see CC12CC(=O)CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O 327.40 unknown https://doi.org/10.3184/0308234041209220
(1S,5S,8R,9S,11R,13S,14S,17R,18R)-5-methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadec-6-ene-13,17-diol 163043512 Click to see CC12CCCC34C1(CCC56C3CC(CC5C4N=C2)C(=C)C6O)O 313.40 unknown https://doi.org/10.1002/HLCA.200890209
10,19-Dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 73657226 Click to see CC12CC(=O)CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O 327.40 unknown https://doi.org/10.3184/0308234041209220
11-Methyl-5-methylidene-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-6-ol 4481626 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown https://doi.org/10.3184/0308234041209220
12-[[4-[2-(Dimethylamino)ethyl]phenoxy]methyl]-5-methyl-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadeca-6,12-dien-9-ol 162956940 Click to see CC12CCCC34C1CCC56C3CC(CC5(C4N=C2)O)C(=C6)COC7=CC=C(C=C7)CCN(C)C 460.60 unknown https://doi.org/10.3184/0308234041209220
5-Methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadec-6-ene-13,17-diol 74396940 Click to see CC12CCCC34C1(CCC56C3CC(CC5C4N=C2)C(=C)C6O)O 313.40 unknown https://doi.org/10.1002/HLCA.200890209

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