Scientific name	Authority	First published in
Taraxacum kansaiense	Koidz. ex Kitam.	Acta Phytotax. Geobot. 2: 125 (1933)
Taraxacum liukiuense	H.Koidz.	J. Jap. Bot. ix. 350 (1933).
Taraxacum bitchuense	H.Koidz.	J. Jap. Bot. ix. 352 (1933).

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	طرخشقون ياباني
Japanese	カンサイタンポポ

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

Asia-temperate click to expand
- Eastern Asia
  - Japan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000002100
Tropicos	2735305
KEW	urn:lsid:ipni.org:names:253647-1
The Plant List	gcc-102019
PFAF	Taraxacum japonicum
Open Tree Of Life	207572
NCBI Taxonomy	131536
IPNI	253647-1
iNaturalist	701907
GBIF	5394322
Freebase	/m/07s5k7s
EPPO	TARJA
Wikipedia	Taraxacum_japonicum

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 phytochemical and pharmacological profile of taraxasterol

Jiao F, Tan Z, Yu Z, Zhou B, Meng L, Shi X

Front Pharmacol

04-Aug-2022

PMCID:	PMC9386448
doi:	10.3389/fphar.2022.927365
PMID:	35991893

Frequency-dependent fitness and reproductive dynamics contribute to habitat segregation in sympatric jewelflowers

Christie K, Strauss SY

Proc Biol Sci

13-May-2020

PMCID:	PMC7287356
doi:	10.1098/rspb.2020.0559
PMID:	32396796

Comparison of mechanisms of reproductive interference in Taraxacum

Takemori A, Naiki A, Takakura KI, Kanaoka MM, Nishida S

Ann Bot

02-Feb-2019

PMCID:	PMC6589510
doi:	10.1093/aob/mcz007
PMID:	30715137

Co-occurrence of related asexual, but not sexual, lineages suggests that reproductive interference limits coexistence

Whitton J, Sears CJ, Maddison WP

Proc Biol Sci

06-Dec-2017

PMCID:	PMC5740271
doi:	10.1098/rspb.2017.1579
PMID:	29212720

The Efficacy of Dandelion Root Extract in Inducing Apoptosis in Drug-Resistant Human Melanoma Cells

Chatterjee SJ, Ovadje P, Mousa M, Hamm C, Pandey S

Evid Based Complement Alternat Med

30-Dec-2010

PMCID:	PMC3018636
doi:	10.1155/2011/129045
PMID:	21234313

Composite constituents: four new triterpenoids, neolupenol, tarolupenol and their acetates isolated from roots of a japanese dandelion, taraxacum japonicum

H. Ageta, K. Shiojima, K. Masuda, T. Lin

Elsevier BV

25-Jul-2002

doi:	10.1016/S0040-4039(01)92912-0

Anti-carcinogenic activity of Taraxacum plant. II.

Takasaki M, Konoshima T, Tokuda H, Masuda K, Arai Y, Shiojima K, Ageta H

Biol Pharm Bull

01-Jun-1999

doi:	10.1248/BPB.22.606
PMID:	10408235

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 / Benzoic acid esters
Monohexyl Phthalate	90532	Click to see CCCCCCOC(=O)C1=CC=CC=C1C(=O)O	250.29	unknown	https://doi.org/10.1016/S0040-4039(01)92912-0
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(1R,3aR,5bR,7aS,9S,11aR,11bR,13aS,13bR)-3a,5b,8,8,11a,13a-hexamethyl-1-propan-2-yl-1,2,3,4,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol	162962326	Click to see CC(C)C1CCC2(C1C3(CCC4C5(CCC(C(C5CCC4(C3=CC2)C)(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1016/S0040-4039(01)92912-0
[(1R,3aR,5bR,7aS,9S,11aR,11bR,13aS,13bR)-3a,5b,8,8,11a,13a-hexamethyl-1-propan-2-yl-1,2,3,4,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-yl] acetate	162861748	Click to see CC(C)C1CCC2(C1C3(CCC4C5(CCC(C(C5CCC4(C3=CC2)C)(C)C)OC(=O)C)C)C)C	468.80	unknown	https://doi.org/10.1016/S0040-4039(01)92912-0
[(3S,4aR,6aR,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate	5458941	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
3a,5b,8,8,11a,13a-Hexamethyl-1-propan-2-yl-1,2,3,4,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol	162962324	Click to see CC(C)C1CCC2(C1C3(CCC4C5(CCC(C(C5CCC4(C3=CC2)C)(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1016/S0040-4039(01)92912-0
Epitaraxerol	344467	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
Taraxerol	92097	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
Taraxerol acetate	94225	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
Taraxeryl acetate	5205968	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(18R,19R)-Lup-12-en-3beta-ol	78178079	Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0040-4039(01)92912-0
(1R,3aR,5aS,5bR,7aS,9S,11aR,11bR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysen-9-ol	162976445	Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0040-4039(01)92912-0
(3a,5a,5b,8,8,11a-Hexamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysen-9-yl) acetate	14105802	Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1016/S0040-4039(01)92912-0
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate	345510	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol	145706026	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
[(1R,3aR,5aS,5bR,7aS,9S,11aR,11bR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysen-9-yl] acetate	163020648	Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1016/S0040-4039(01)92912-0
[(4aR,6aS,6aR,6bR,8aR,12aS,14aS,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl] acetate	137704689	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
alpha-Amyrenyl acetate	92842	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
alpha-Amyrin acetate	293754	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
beta-Amyrin acetate	92156	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
Lup-20(29)-en-3-one	323075	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	424.70	unknown	https://doi.org/10.1248/BPB.22.606
Lup-20(29)-en-3beta-ol, acetate	323074	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
Lupenone	92158	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	424.70	unknown	https://doi.org/10.1248/BPB.22.606
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
Lupeol acetate	92157	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
Olean-12-en-3beta-ol	225689	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
Psi-taraxasterol acetate	13970054	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
psi-Taraxasteryl acetate	13970053	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
Taraxasterol	115250	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1248/BPB.22.606
Taraxasterol acetate	13889352	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606
Taraxasterol, acetate	344468	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	https://doi.org/10.1248/BPB.22.606

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Taraxacum japonicum

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