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Pedicularis palustris

Pedicularis palustris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID6440008e118e6582964585
Scientific name Pedicularis palustris
Authority L.
First published in Sp. Pl. : 607 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pedicularis insubrica Rota Prosp. Fl. Bergamo : 102 (1853)
Pedicularis erecta Gilib. Exerc. Phyt. 1: 135. 1792

Common names Top

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Language Common/alternative name
English european purple lousewort
English marsh lousewort
Belarusian гніднік
Belarusian сітовіца
Belarusian прорва
Belarusian насаднік
Belarusian надсаднік
Belarusian кукушкіна была
Belarusian завушніца
Belarusian елачка
Belarusian тваражаўнік
Belarusian увярэднік
Belarusian ушывая трава
Belarusian увярэднік балотны
Belarusian ваўчкі
Bulgarian блатно пропадниче
Catalan pédiculaire des marais
Czech všivec bahenní
Welsh melog y waun
Welsh blodyn y llyffant
Danish eng-troldurt
German sumpf-läusekraut
German sumpfläusekraut
German pédiculaire des marais
Estonian soo-kuuskjalg
Finnish luhtakuusio
French pédiculaire des marais
Upper Sorbian wulka wšowica
Hungarian posvány kakastaréj
Cornish lowles an lefans
Lithuanian pédiculaire des marais
Lithuanian pelkinė glindė
Norwegian Bokmål myrklegg
Dutch moeraskartelblad
Polish gnidosz błotny
Russian Мытник болотный
Slovak všivec močiarny
Swedish pédiculaire des marais
Swedish kärrspira
Ukrainian Шолудивник болотний
Ukrainian Шолудивник
Chinese 沼地马先蒿
Chinese 沼生馬先蒿
Chinese 沼生马先蒿卡氏亚种
Chinese 沼生马先蒿沼生亚种
Chinese 沼生馬先蒿沼生
Chinese 沼生马先蒿沼生
Chinese 沼生马先蒿

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Pedicularis palustris subsp. borealis (J.W.Zetterst.) Hyl. Uppsala Univ. Årsskr. 1845(7): 293. 1945 (1945)
Pedicularis palustris subsp. opsiantha (Ekman) Almq. Acta Phytogeogr. Suec. 1: 592 1929

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
  • Europe
    • Eastern Europe
      • Baltic States
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Føroyar
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France
  • Northern America
    • Eastern Canada
      • Newfoundland
      • Nova Scotia
      • Québec

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000470843
Canadensys 7062
USDA Plants PEPA38
Tropicos 29200365
INPN 112590
KEW urn:lsid:ipni.org:names:807439-1
The Plant List kew-2542534
Plantarium 27216
Open Tree Of Life 541020
Observations.org 2668
NCBI Taxonomy 462877
NBN Atlas NBNSYS0000004130
Nature Serve 2.135174
IUCN Red List 19620542
IPNI 807439-1
iNaturalist 118803
GBIF 3171734
EPPO PEAPA
EOL 486609
Elurikkus 6135
USDA GRIN 27084
Wikipedia Pedicularis_palustris

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 most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Scrub encroachment promotes biodiversity in temperate European wetlands under eutrophic conditions Brunbjerg AK, Fløjgaard C, Frøslev TG, Andersen DK, Bruun HH, Dalby L, Goldberg I, Lehmann LJ, Moeslund JE, Ejrnæs R Ecol Evol 01-Nov-2022
PMCID:PMC9627074
doi:10.1002/ece3.9445
PMID:36340817
The bright side of parasitic plants: what are they good for? Těšitel J, Li AR, Knotková K, McLellan R, Bandaranayake PC, Watson DM Plant Physiol 29-Dec-2020
PMCID:PMC8133642
doi:10.1093/plphys/kiaa069
PMID:33793868
Deceptive strategy in Dactylorhiza orchids: multidirectional evolution of floral chemistry Wróblewska A, Szczepaniak L, Bajguz A, Jędrzejczyk I, Tałałaj I, Ostrowiecka B, Brzosko E, Jermakowicz E, Mirski P Ann Bot 11-Feb-2019
PMCID:PMC6589506
doi:10.1093/aob/mcz003
PMID:30753414
The bear in Eurasian plant names: motivations and models Kolosova V, Svanberg I, Kalle R, Strecker L, Özkan AM, Pieroni A, Cianfaglione K, Molnár Z, Papp N, Łuczaj Ł, Dimitrova D, Šeškauskaitė D, Roper J, Hajdari A, Sõukand R J Ethnobiol Ethnomed 21-Feb-2017
PMCID:PMC5320662
doi:10.1186/s13002-016-0132-9
PMID:28222790
Using Eddy Covariance Sensors to Quantify Carbon Metabolism of Peatlands: A Case Study in Turkey Evrendilek F, Karakaya N, Aslan G, Ertekin C Sensors (Basel) 06-Jan-2011
PMCID:PMC3274076
doi:10.3390/s110100522
PMID:22346588
Adaptive plasticity of floral display size in animal-pollinated plants Harder LD, Johnson SD Proc Biol Sci 04-Oct-2005
PMCID:PMC1559982
doi:10.1098/rspb.2005.3268
PMID:16321788
Iridoid glucosides from Pedicularis Thomas Berg, Søren Damtoft, Søren Rosendal Jensen, Bent Juhl Nielsen, Lars Fledelius Rickelt Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80754-2

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,7S,7aR)-4a,7-dihydroxy-7-methyl-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carbaldehyde 162971989 Click to see CC1(CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
(1S,4aR,7S,7aS)-4a,7-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carbaldehyde 163188963 Click to see CC1(CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
(1S,4aS,7R,7aS)-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbaldehyde 162977549 Click to see CC1CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O 344.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
(1S,4aS,7S,7aR)-7-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carbaldehyde 163028016 Click to see CC1(CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
(1S)-1-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydro-7alpha-hydroxy-7-methylcyclopenta[c]pyran-4-carbaldehyde 72746025 Click to see CC1(CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
(1S)-1-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydro-7beta-methylcyclopenta[c]pyran-4-carbaldehyde 4490432 Click to see CC1CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O 344.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
(2S,3R,4S,5R,6R)-2-[[(1S,4aS,5R,7aS)-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 12358434 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
(2S,3R,4S,5R,6R)-2-[[(1S,4aS,5R)-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163194563 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
(2S,3R,4S,5S,6R)-2-[[(1S,4aS,5S,7aR)-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 7160346 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
2-[[5-Hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 348157 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
4a,7-Dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carbaldehyde 14589172 Click to see CC1(CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
5-chloro-2-(4-(2-(2-hydroxyethoxy)ethyl)piperazin-1-yl)-N-(6-(3-methoxybenzamido)pyridin-3-yl)isonicotinamide 13848072 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
8-Epiiridotrial glucoside 155942 Click to see CC1CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O 344.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Deacetyl asperulosidic acid methyl ester 6325021 Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Euphroside 14589173 Click to see CC1(CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
methyl (1S,4aS,5R,7R,7aR)-5-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101643005 Click to see CC1CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
methyl 4a,5-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 53462289 Click to see CC1CC(C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Methyl 5-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 14193886 Click to see CC1CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
methyl 5,7-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 13892721 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Methyl 6-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 601562 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Mussaenoside 182423 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Penstemonoside 133626 Click to see CC1CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Penstemoside 101637370 Click to see CC1CC(C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Plantarenaloside 155882 Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Shanzhiside methyl ester 13892722 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Shanzhiside-methylester 3085296 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
Yuheinoside 13890717 Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Gardoside methyl ester 51692952 Click to see COC(=O)C1=COC(C2C1CC(C2=C)O)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2
methyl 6-hydroxy-7-methylidene-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 14313744 Click to see COC(=O)C1=COC(C2C1CC(C2=C)O)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(00)80754-2

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