Euphorbia palustris - Unknown
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Details Top

Internal ID UUID64403b71d8441506988687
Scientific name Euphorbia palustris
Authority L.
First published in Sp. Pl. : 462 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tithymalus fruticosus Gilib. Fl. Lit. Inch. 2: 206 (1782)
Tithymalus palustris Garsault Fig. Pl. Méd. : 592 (1764)
Galarhoeus palustris Haw. Syn. Pl. Succ. : 145 (1812)
Euphorbia palustris var. angustifolia Pers. Syn. Pl. 2: 18. 1806
Euphorbia brachiata Jan Elench. Pl. : 7 (1831)
Euphorbia sauliana Boreau ex Boiss. Prodr. 15(2): 1266 (1866)
Euphorbia palustris var. brinonense N.Cezard Bull. Acad. Soc. Lorraines Sci. 16: 34 (1977)

Common names Top

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Language Common/alternative name
English marsh spurge
Spanish tithymalus nudus
Spanish tithymalus velenovskyi
Spanish galarhoeus nudus
Azerbaijani bataqlıq südləyəni
Belarusian Малачай балотны
Bulgarian блатна млечка
Catalan euphorbe des marais
Czech pryšec bahenní
German sumpf-wolfsmilch
German sumpfwolfsmilch
German euphorbe des marais
Estonian soo-piimalill
Persian یوفوربیا باتلاقی
Finnish rantatyräkki
French euphorbe des marais
Upper Sorbian Žabjaca mlóčeń
Hungarian mocsári kutyatej
Lithuanian euphorbe des marais
Norwegian Bokmål strandvortemelk
Dutch moeraswolfsmelk
Polish wilczomlecz błotny
Romanian alior de baltă
Russian молочай болотный
Russian Молочай болотный
Slovak mliečnik močiarny
Swedish kärrtörel
Swedish euphorbe des marais

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
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000963795
USDA Plants EUPA25
Tropicos 12805622
INPN 97601
Flora of Italy 2904
KEW urn:lsid:ipni.org:names:347635-1
The Plant List kew-81302
Missouri Botanical Garden 280237
Open Tree Of Life 315806
Observations.org 2504
NCBI Taxonomy 492572
IUCN Red List 19618301
IPNI 347635-1
iNaturalist 438839
GBIF 3064056
Freebase /m/0bbylwy
EPPO EPHPB
EOL 1144255
Elurikkus 4702
USDA GRIN 412028
Wikipedia Euphorbia_palustris
CMAUP NPO17166
Plantarium 15619

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
Lutein Isomers: Preparation, Separation, Structure Elucidation, and Occurrence in 20 Medicinal Plants Nagy V, Agócs A, Balázs VL, Purger D, Filep R, Sándor V, Turcsi E, Gulyás-Fekete G, Deli J Molecules 25-Jan-2023
PMCID:PMC9921531
doi:10.3390/molecules28031187
PMID:36770852
Metabolomics as a Potential Chemotaxonomical Tool: Application on the Selected Euphorbia Species Growing Wild in Serbia Sofrenić I, Anđelković B, Gođevac D, Ivanović S, Simić K, Ljujić J, Tešević V, Milosavljević S Plants (Basel) 06-Jan-2023
PMCID:PMC9864624
doi:10.3390/plants12020262
PMID:36678975
Extensive archaeobotanical data estimate carrying capacity, duration, and land use of the Late Bronze Age settlement site Březnice (Czech Republic) Šálková T, Vobejda L, Chvojka O, Beneš J, Vondrovský V, Kuna M, Křivánek R, Menšík P, Novák J Sci Rep 25-Nov-2022
PMCID:PMC9700714
doi:10.1038/s41598-022-24753-x
PMID:36434129
Insight into the Way the Content of Biologically Active Compounds in Meadowsweet Inflorescences (Filipendula ulmaria (L.) Maxim.) Is Shaped by Phytosociological Habitats Stawarczyk K, Chrupek A, Sękara A, Gostkowski M, Karbarz M Molecules 26-Aug-2021
PMCID:PMC8433760
doi:10.3390/molecules26175172
PMID:34500608
Comparative Analysis of Machine Learning Methods to Predict Growth of F. sporotrichioides and Production of T-2 and HT-2 Toxins in Treatments with Ethylene-Vinyl Alcohol Films Containing Pure Components of Essential Oils Mateo EM, Gómez JV, Tarazona A, García-Esparza MÁ, Mateo F Toxins (Basel) 05-Aug-2021
PMCID:PMC8402422
doi:10.3390/toxins13080545
PMID:34437416
Latex Metabolome of Euphorbia Species: Geographical and Inter-Species Variation and its Proposed Role in Plant Defense against Herbivores and Pathogens Salomé-Abarca LF, Gođevac D, Kim MS, Hwang GS, Park SC, Jang YP, Van Den Hondel CA, Verpoorte R, Klinkhamer PG, Choi YH J Chem Ecol 21-Apr-2021
PMCID:PMC8217033
doi:10.1007/s10886-021-01274-x
PMID:33881708
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
Families and genera of diaporthalean fungi associated with canker and dieback of tree hosts Fan XL, Bezerra JD, Tian CM, Crous PW Persoonia 06-Feb-2018
PMCID:PMC6146645
doi:10.3767/persoonia.2018.40.05
PMID:30504998
Plant Secondary Metabolites as Anticancer Agents: Successes in Clinical Trials and Therapeutic Application Seca AM, Pinto DC Int J Mol Sci 16-Jan-2018
PMCID:PMC5796209
doi:10.3390/ijms19010263
PMID:29337925
Juglanconis gen. nov. on Juglandaceae, and the new family Juglanconidaceae (Diaporthales) Voglmayr H, Castlebury LA, Jaklitsch WM Persoonia 19-Jan-2017
PMCID:PMC5645181
doi:10.3767/003158517X694768
PMID:29151630
Ethnoveterinary practices of Covasna County, Transylvania, Romania Bartha SG, Quave CL, Balogh L, Papp N J Ethnobiol Ethnomed 06-May-2015
PMCID:PMC4449595
doi:10.1186/s13002-015-0020-8
PMID:25943542
Conservation Potential of Abandoned Military Areas Matches That of Established Reserves: Plants and Butterflies in the Czech Republic Cizek O, Vrba P, Benes J, Hrazsky Z, Koptik J, Kucera T, Marhoul P, Zamecnik J, Konvicka M PLoS One 09-Jan-2013
PMCID:PMC3541396
doi:10.1371/journal.pone.0053124
PMID:23326388
The genus Cladosporium Bensch K, Braun U, Groenewald JZ, Crous PW Stud Mycol 06-Jun-2012
PMCID:PMC3390897
doi:10.3114/sim0003
PMID:22815589
A systematic account of the genus Plagiostoma (Gnomoniaceae, Diaporthales) based on morphology, host-associations, and a four-gene phylogeny Mejía LC, Castlebury LA, Rossman AY, Sogonov MV, White JF Jr Stud Mycol 01-Jan-2011
PMCID:PMC3065992
doi:10.3114/sim.2011.68.10
PMID:21523196
Leaf-inhabiting genera of the Gnomoniaceae, Diaporthales Sogonov MV, Castlebury LA, Rossman AY, Mejía LC, White JF Stud Mycol 01-Jan-2008
PMCID:PMC2621335
doi:10.3114/sim.2008.62.01
PMID:19287541

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
> Alkaloids and derivatives / Aporphines
(+)-1,2-Methylenedioxy-5,6,6aalpha,7-tetrahydro-4H-dibenzo[de,g]quinoline 26202781 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline 1078819 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown via CMAUP database
1-[(12R)-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone 10246449 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)OC)OCO3 337.40 unknown via CMAUP database
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)- 158516 Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O 293.30 unknown via CMAUP database
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
N-acetylanonaine 6453733 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 307.30 unknown via CMAUP database
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol 15560530 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[1,1'-Biphenyl]-4-ol, 2'-methoxy-3,5'-di-2-propenyl- 11857938 Click to see COC1=C(C=C(C=C1)CC=C)C2=CC(=C(C=C2)O)CC=C 280.40 unknown via CMAUP database
4-O-Methylhonokiol 155160 Click to see COC1=C(C=C(C=C1)C2=C(C=CC(=C2)CC=C)O)CC=C 280.40 unknown via CMAUP database
Caryolanemagnolol 21726647 Click to see CC1(CC2C1CCC3(CC2(CCC3O)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C)C 486.70 unknown via CMAUP database
Honokiol 72303 Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=C(C=C2)O)CC=C 266.30 unknown via CMAUP database
Magnaldehyde E 5319190 Click to see C=CCC1=C(C=CC(=C1)C2=C(C=CC(=C2)C=O)O)O 254.28 unknown via CMAUP database
Magnolol 72300 Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O 266.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2,3,4-Trihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde 71812224 Click to see C=CCC1=CC=C(C=C1)OC2=C(C(=C(C(=C2)C=O)O)O)O 286.28 unknown via CMAUP database
3-[3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)phenyl]prop-2-enal 134367 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O 296.30 unknown via CMAUP database
3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde 23259953 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=O 270.28 unknown via CMAUP database
5-[(E)-3-methoxyprop-1-enyl]-3-(4-prop-2-enylphenoxy)benzene-1,2-diol 71812222 Click to see COCC=CC1=CC(=C(C(=C1)OC2=CC=C(C=C2)CC=C)O)O 312.40 unknown via CMAUP database
Obovatal 6439677 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O 296.30 unknown via CMAUP database
Obovatol 100771 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)CC=C 282.30 unknown via CMAUP database
Phenol, 2-[3-hydroxy-4-(2-propenyl)phenoxy]-5-(2-propenyl)- 10016628 Click to see C=CCC1=CC(=C(C=C1)OC2=CC(=C(C=C2)CC=C)O)O 282.30 unknown via CMAUP database
Phenol, 4-(2-propenyl)-2-(4-(2-propenyl)phenoxy)- 159137 Click to see C=CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)CC=C)O 266.30 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Cadalene 10225 Click to see CC1=CC2=C(C=CC(=C2C=C1)C)C(C)C 198.30 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Clovanemagnolol 10323149 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[2R-cis]-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol 91730386 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol 118976561 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown via CMAUP database
Eudeshonokiol A 14587421 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)C4=C(C=CC(=C4)CC=C)O)CC=C 488.70 unknown via CMAUP database
Eudeshonokiol B 21726646 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=CC(=C(C=C4)O)CC=C 488.70 unknown via CMAUP database
Eudesmagnolol 14587417 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)CC=C)O 488.70 unknown via CMAUP database
Eudesobovatol A 442837 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=CC(=CC(=C3O)OC4=CC=C(C=C4)CC=C)CC=C 504.70 unknown via CMAUP database
Eudesobovatol B 10346031 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3OC4=CC=C(C=C4)CC=C)CC=C)O 504.70 unknown via CMAUP database
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
Proximadiol 165258 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O 240.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Magnolianin 9918938 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC3=C2OC(C(O3)C4=CC(=C(C(=C4)OC5=CC=C(C=C5)CC=C)O)O)COC6=C(C=C(C=C6)CC=C)C7=C(C=CC(=C7)CC=C)O)CC=C 827.00 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol 6093330 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
Magnocurarine 53266 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 21629882 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumanolignan 24796112 Click to see C=CCC1=CC(=C(C=C1)O)C2=C3C(=CC(=C2)CC=C)C=CC(=O)O3 318.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Myricetin(1-) 25201643 Click to see C1=C(C=C(C(=C1O)[O-])O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 317.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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