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Aconitum kongboense

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64400702c2c59454218635
Scientific name Aconitum kongboense
Authority Lauener
First published in Notes Roy. Bot. Gard. Edinburgh 25: 17 (1963)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Aconitum chienningense W.T.Wang Fl. Reipubl. Popularis Sin. 27: 609 (1979)
Aconitum chienningense var. lasiocarpum W.T.Wang Fl. Reipubl. Popularis Sin. 27: 609 (1979)
Aconitum chuosjiaense W.T.Wang Fl. Reipubl. Popularis Sin. 27: 607 (1979)
Aconitum lhasaense Lauener Notes Roy. Bot. Gard. Edinburgh 25: 15 (1963)
Aconitum tsangpoense Lauener Notes Roy. Bot. Gard. Edinburgh 25: 16 (1963)
Aconitum viridiflorum Lauener Notes Roy. Bot. Gard. Edinburgh 25: 23 (1963)

Common names Top

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Language Common/alternative name
Chinese 藤乌头
Chinese 工布乌头

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Aconitum kongboense var. villosum W.T.Wang Fl. Reipubl. Popularis Sin. 27: 609 (1979)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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-0000517487
Tropicos 27103730
KEW urn:lsid:ipni.org:names:707497-1
The Plant List kew-2618926
Open Tree Of Life 723190
NCBI Taxonomy 632161
IPNI 707497-1
GBIF 7277142
EOL 2873314

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
Wild plants used by the Lhoba people in Douyu Village, characterized by high mountains and valleys, in southeastern Tibet, China Chen WY, Yang T, Yang J, Qiu ZC, Ding XY, Wang YH, Wang YH J Ethnobiol Ethnomed 23-Jul-2021
PMCID:PMC8305498
doi:10.1186/s13002-021-00472-x
PMID:34301287
Ethnobotanical study on wild plants used by Lhoba people in Milin County, Tibet Li F, Zhuo J, Liu B, Jarvis D, Long C J Ethnobiol Ethnomed 24-Mar-2015
PMCID:PMC4374410
doi:10.1186/s13002-015-0009-3
PMID:25879656
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
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315
Qualitative Exploration of the Potential Causes of Serious Reduction in Availability of Medicinal Plants in the Qinghai-Tibetan High Plateau Cuomu M East Asian Sci Technol Soc 01-Mar-2013
PMCID:PMC4250539
doi:10.1215/18752160-2332366
PMID:25478035
Chemical constituents of the aerial parts of Aconitum kongboense Jian-Jun Fu, Jiang-Jiang Qin, Qi Zeng, Hui-Zi Jin, Wei-Dong Zhang Springer Science and Business Media LLC 09-Dec-2011
doi:10.1007/S10600-011-0084-1
C19-diterpenoid alkaloids of Aconitum kongboense Yue Jian-Min, Jun Xu, Chen Yao-Zu Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90619-8
C19-diterpenoid alkaloids of Aconitum kongboense Jian-min Yue, Yao-zu Chen, Yuan-zong Li Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)83085-F

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 / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2,4-Dimethoxybenzoic acid 7052 Click to see COC1=CC(=C(C=C1)C(=O)O)OC 182.17 unknown https://doi.org/10.1007/S10600-011-0084-1
4-Methoxysalicylic Acid 75231 Click to see 168.15 unknown https://doi.org/10.1007/S10600-011-0084-1
> Benzenoids / Phenols / Cresols / Meta cresols
[(2R)-2,3-dihydroxy-2-(2-hydroxy-4-methylphenyl)propyl] 2-methylpropanoate 163033511 Click to see CC1=CC(=C(C=C1)C(CO)(COC(=O)C(C)C)O)O 268.30 unknown https://doi.org/10.1007/S10600-011-0084-1
2-(2-Hydroxy-4-methylphenyl)propane-1,2,3-triol 14543617 Click to see 198.22 unknown https://doi.org/10.1007/S10600-011-0084-1
8,9-Dihydroxy-10-isobutyryloxythymol 14427472 Click to see 268.30 unknown https://doi.org/10.1007/S10600-011-0084-1
> Lignans, neolignans and related compounds / Furanoid lignans
4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 4546425 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1007/S10600-011-0084-1
Medioresinol, (+)- 181681 Click to see 388.40 unknown https://doi.org/10.1007/S10600-011-0084-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,3aR,5E,9R,12aS)-1-(2-hydroxypropan-2-yl)-3a,6-dimethyl-10-methylidene-1,2,3,4,7,8,9,11,12,12a-decahydrocyclopenta[11]annulen-9-ol 101385923 Click to see CC1=CCC2(CCC(C2CCC(=C)C(CC1)O)C(C)(C)O)C 306.50 unknown https://doi.org/10.1007/S10600-011-0084-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(2R,3R,4S,5S,6S,8S,13S,16S,17R)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 146014457 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1016/0031-9422(90)83085-F
(6S,8S,13S)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5321607 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1016/S0031-9422(00)90619-8
[(1S,2R,3R,4R,5S,6S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 101600179 Click to see 613.70 unknown https://doi.org/10.1016/0031-9422(90)83085-F
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-8-hydroxy-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 95371484 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=CC=C7)OC)O)OC)COC 525.70 unknown https://doi.org/10.1016/S0031-9422(00)90619-8
[11-Ethyl-8-hydroxy-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 4555607 Click to see 525.70 unknown https://doi.org/10.1016/S0031-9422(00)90619-8
14-Benzoyltalatisamine 102095557 Click to see 525.70 unknown https://doi.org/10.1016/S0031-9422(00)90619-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(11-Ethyl-16-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosan-19-yl) acetate 162990605 Click to see CCN1C2C3CC4C2(C5CCC4(C1O5)C)C6C37CC(C(C6)O)C(=C)C7OC(=O)C 399.50 unknown https://doi.org/10.1007/S10600-011-0084-1
(1R,2R,4S,5R,8S,10R,12S,13S,14R,16R,17R,19R)-11-ethyl-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosane-16,19-diol 162983525 Click to see CCN1C2C3CC4C2(C5CCC4(C1O5)C)C6C37CC(C(C6)O)C(=C)C7O 357.50 unknown https://doi.org/10.1007/S10600-011-0084-1
[(1R,2R,4S,5R,8S,10R,12S,13S,14R,16R,17R,19R)-11-ethyl-16-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosan-19-yl] acetate 162990607 Click to see 399.50 unknown https://doi.org/10.1007/S10600-011-0084-1
11-Ethyl-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosane-16,19-diol 14106919 Click to see 357.50 unknown https://doi.org/10.1007/S10600-011-0084-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
(1R,2R,4R,5R,6S,7R,8R,9R,10R,13R,16S,17R)-11-ethyl-6,13-dimethyl-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 162943613 Click to see 361.50 unknown https://doi.org/10.1007/S10600-011-0084-1
[(1R,2R,4R,5R,7R,8R,9R,10R,13R,16S,17R)-11-ethyl-4,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-7-yl] acetate 162929460 Click to see 401.50 unknown https://doi.org/10.1007/S10600-011-0084-1
Napellonine 120706 Click to see 357.50 unknown https://doi.org/10.1007/S10600-011-0084-1
Songorine 71456946 Click to see 357.50 unknown https://doi.org/10.1007/S10600-011-0084-1
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 66883 Click to see 208.21 unknown https://doi.org/10.1007/S10600-011-0084-1
Ethyl Caffeate 5317238 Click to see 208.21 unknown https://doi.org/10.1007/S10600-011-0084-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1007/S10600-011-0084-1
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Wedelolactone 5281813 Click to see 314.25 unknown https://doi.org/10.1007/S10600-011-0084-1

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