Aconitum kongboense

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Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

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Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

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

Description 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

Asia-temperate click to expand
- China
  - China South-central
  - Tibet

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!
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 / 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 COC1=CC(=C(C=C1)C(=O)O)O	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 CC1=CC(=C(C=C1)C(CO)(CO)O)O	198.22	unknown	https://doi.org/10.1007/S10600-011-0084-1
8,9-Dihydroxy-10-isobutyryloxythymol	14427472	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
> 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 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
> 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,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
[(1S,2R,3S,4S,5R,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-4,8-dihydroxy-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl]-phenylmethanone	102095557	Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6(C(=O)C7=CC=CC=C7)O)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 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
Chasmaconitine	101600179	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)COC	613.70	unknown	https://doi.org/10.1016/0031-9422(90)83085-F
> 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 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
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 CCN1C2C3CC4C2(C5CCC4(C1O5)C)C6C37CC(C(C6)O)C(=C)C7O	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 CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(C6O)C)O)O)C	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 CCN1CC2(CCC(C34C2CC(C31)C56C4CC(C(C5)C(=C)C6OC(=O)C)O)O)C	401.50	unknown	https://doi.org/10.1007/S10600-011-0084-1
Napellonine	120706	Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(=O)C(C5)C(=C)C6O)O)C	357.50	unknown	https://doi.org/10.1007/S10600-011-0084-1
Songorine	71456946	Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(=O)C(C5)C(=C)C6O)O)C	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
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester	66883	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O	208.21	unknown	https://doi.org/10.1007/S10600-011-0084-1
Ethyl caffeate	5317238	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O	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 COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1007/S10600-011-0084-1
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Wedelolactone	5281813	Click to see COC1=CC(=C2C(=C1)OC(=O)C3=C2OC4=CC(=C(C=C43)O)O)O	314.25	unknown	https://doi.org/10.1007/S10600-011-0084-1

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Aconitum kongboense

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top