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Taraxacum udum

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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 UUID643fc67b3823c945266188
Scientific name Taraxacum udum
Authority Jord.
First published in Pugill. Pl. Nov. 114. 1852

Description Top

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Synonyms Top

Scientific name Authority First published in
Taraxacum laeticolorifrons Soest Acta Bot. Neerl. xiv. 36 (1965).
Taraxacum hagendijkii Soest Acta Bot. Neerl. 20(1): 141 (1971)

Common names Top

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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
  • Europe
    • Middle Europe
      • Germany
      • Netherlands
      • Poland
      • Switzerland
    • Southwestern Europe
      • France

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000005473
Tropicos 2703359
INPN 125782
KEW urn:lsid:ipni.org:names:255029-1
The Plant List gcc-105270
Open Tree Of Life 3895468
Observations.org 148962
IPNI 255029-1
iNaturalist 967528
GBIF 5694743

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)!
Title Authors Publication Released IDs
Sesquiterpenoids and phenolics from roots of Taraxacum udum. Michalska K, Marciniuk J, Kisiel W Fitoterapia 01-Jul-2010
doi:10.1016/J.FITOTE.2009.12.004
PMID:20006977
Structural analysis of 1L-chiro-inositol diester from Taraxacum udum. Michalska K, Zylewski M, Marciniuk J, Kisiel W Carbohydr Res 11-Jan-2010
doi:10.1016/J.CARRES.2009.10.019
PMID:19926080

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 / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Methyl 4-hydroxyphenylacetate 518900 Click to see COC(=O)CC1=CC=C(C=C1)O 166.17 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
https://doi.org/10.1016/J.CARRES.2009.10.019
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
Episyringaresinol 4'-O-beta-D-glncopyranoside 45482321 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (3aS,5Z,10Z,11aR)-10-methyl-3-methylidene-2-oxo-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylate 162852856 Click to see CC1=CC2C(CC=C(CCC1)C(=O)OC3C(C(C(C(O3)CO)O)O)O)C(=C)C(=O)O2 424.40 unknown https://doi.org/10.1016/J.CARRES.2009.10.019
[(2S,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl] (3aS,6Z,10E,11aR)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylate 162857992 Click to see CC1=CC2C(CCC(=CCC1)C(=O)OC3C(C(C(C(O3)COC(=O)C)O)O)O)C(=C)C(=O)O2 466.50 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylate 76401242 Click to see CC1=CC2C(CCC(=CCC1)C(=O)OC3C(C(C(C(O3)CO)O)O)O)C(=C)C(=O)O2 424.40 unknown https://doi.org/10.1016/J.CARRES.2009.10.019
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-methyl-3-methylidene-2-oxo-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylate 162852854 Click to see CC1=CC2C(CC=C(CCC1)C(=O)OC3C(C(C(C(O3)CO)O)O)O)C(=C)C(=O)O2 424.40 unknown https://doi.org/10.1016/J.CARRES.2009.10.019
[6-(Acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl] 10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylate 162857991 Click to see CC1=CC2C(CCC(=CCC1)C(=O)OC3C(C(C(C(O3)COC(=O)C)O)O)O)C(=C)C(=O)O2 466.50 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
CID 56776213 56776213 Click to see CC1=CC2C(CCC(=CCC1)C(=O)OC3C(C(C(C(O3)CO)O)O)O)C(=C)C(=O)O2 424.40 unknown https://doi.org/10.1016/J.CARRES.2009.10.019
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
5-Hydroxy-3,6,9-trimethylidene-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 13855723 Click to see C=C1C2CC(C(=C)C2C3C(CC1O)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
Macrocliniside A 10455028 Click to see C=C1C2CC(C(=C)C2C3C(CC1O)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
[2,3,4,6-Tetrahydroxy-5-[2-(4-hydroxyphenyl)acetyl]oxycyclohexyl] 2-(4-hydroxyphenyl)acetate 162874543 Click to see C1=CC(=CC=C1CC(=O)OC2C(C(C(C(C2O)OC(=O)CC3=CC=C(C=C3)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.CARRES.2009.10.019
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/J.CARRES.2009.10.019
https://doi.org/10.1016/J.FITOTE.2009.12.004
2-(Hydroxymethyl)-6-[4-(3-hydroxypropyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 69086672 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CCCO 374.40 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
https://doi.org/10.1016/J.CARRES.2009.10.019
Dihydrosyringin 71720642 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CCCO 374.40 unknown https://doi.org/10.1016/J.CARRES.2009.10.019
https://doi.org/10.1016/J.FITOTE.2009.12.004
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
https://doi.org/10.1016/J.CARRES.2009.10.019
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(7'R,8'R)-4,7'-Epoxy-3',5-dimethoxy-4',9,9'-lignanetriol 9'-glucoside 14558383 Click to see COC1=CC(=CC2=C1OC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)CCCO 522.50 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
3-(beta-d-Glucopyranosyloxymethyl)-2-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-(2r,3s)-dihydrobenzofuran 10098244 Click to see COC1=CC(=CC2=C1OC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)CCCO 522.50 unknown https://doi.org/10.1016/J.FITOTE.2009.12.004
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.CARRES.2009.10.019
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(2,4-Dihydroxyphenyl)-3-[8-hydroxy-2-methyl-2-(3,4-epoxy-4-methyl-1-pentenyl)-2h-1-benzopyran-5-yl]-1-propanone 73307005 Click to see CC1(C(O1)C=CC2(C=CC3=C(C=CC(=C3O2)O)CCC(=O)C4=C(C=C(C=C4)O)O)C)C 422.50 unknown https://doi.org/10.1016/J.CARRES.2009.10.019

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