Menyanthes trifoliata

Details Top

Internal ID UUID643ffe22390f3143156704
Scientific name Menyanthes trifoliata
Authority L.
First published in Sp. Pl. 1: 145. 1753 [1 May 1753]

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

In the Białowieża Forest region of northeastern Poland, drying the green foliage of Menyanthes trifoliata (bogbean) to make a light, mildly bitter tea for digestive complaints is an old, well‑documented practice (Łuczaj 2012). In Scotland and across the United Kingdom, dried leaves or the whole aerial herb are similarly infused as a bitter tea and sometimes taken as a weak decoction for dyspepsia, flatulence, and loss of appetite (Hillier 2011). In Chinese herbal tradition, bogbean (ri xin cao) is used as both a mild infusion and a short decoction of the dried leaves and flowering tops to “clear heat” and promote stomach function, with preparations recorded in the Pharmacopoeia of the People’s Republic of China (1977). These records align closely with European folk knowledge in which the bitter leaves are brewed alone or in small blends to stimulate appetite and settle mild stomach upset.

To make a simple bogbean tea, use 2–3 g of dried leaves or a mixture of leaves and small stems per 200–250 ml of water. For an infusion, pour just‑boiled water over the plant material, cover, and steep 8–10 minutes; for a decoction, simmer for the same 8–10 minutes, then strain and cool. The taste is quite bitter; many drinkers start with 100 ml twice daily after meals. As a tincture analogue, 1 part dried bogbean leaf to 5 parts 40% ethanol by weight, macerated for 2–3 weeks with daily shaking, can be filtered and stored; typical doses are 2–5 ml once or twice daily in a little water (Phytopharmaka, 1997). Do not exceed 6–9 g of dried herb per day as tea equivalents, avoid during pregnancy and while breastfeeding, and stop if heartburn or irritation occurs; irregular, prolonged use can be hepatotoxic (EMA, 2014).

The activity of bogbean preparations is attributed to its well‑studied bitter secoiridoid glycosides—loganic acid and swertiamarin—together with flavonoids such as vitexin and isovitexin. These compounds irritate gustatory receptors in the mouth and upper gut, stimulating salivary and gastric secretions that historically underpin appetite and digestion support.

Bogbean remains widely available as dried herb and in several bitters or bitter‑herbal tea blends, and contemporary research continues to explore its gastrointestinal pharmacology and safety (EMA, 2014).

General Uses Top

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Common products:
- Dried leaves used as a bittering and flavoring ingredient in fermented beverages (notably historical European beers and related drinks). Primary product form is air‑dried leaf material; sometimes chopped or blended with other botanicals.

Food and beverages (non-medicinal):
- Leaves employed as a bitterness and aroma additive in traditional beer and other fermented drinks, functioning as a hops‑like adjunct. Product forms include leaf chips, powders, and dried leaf bundles; use involves addition to the mash or during secondary fermentation for bitter/aromatic impact.
- Leaves have also been used in small amounts as a flavoring in non‑alcoholic beverages; product usage is typically as a minor ingredient (e.g., “bog‑bean” flavors) in craft sodas or bitter tonics where bitterness is desired.

Industrial and craft applications:
- Historically utilized in small‑scale craft fermentation equipment as a matrix for yeast immobilization or as a floating raft to aid clarifies and protect fermentations.

Properties relevant to use:
- Bittering profile from secoiridoid glycosides (e.g., loganin derivatives) and associated aromatic constituents confer a distinctive bitterness and aroma suitable for beverage flavoring.
- Plant biomass provides a buoyant, fibrous matrix suitable for floating carrier or filtration aids in craft fermentation.

Standards and regulation:
- For beverage use, formulations should comply with relevant national food‑additives/flavoring regulations in the consuming jurisdiction (e.g., EU Novel Food or US Generally Recognized as Safe where applicable). Absence of a dedicated monograph suggests case‑by‑case regulatory assessment.

Sustainability and sourcing:
- Species occurs in wetlands and peatlands of temperate regions and can be locally abundant in northern latitudes; sustainable collection emphasizes limited harvest, avoidance of degraded habitats, and preference for cultivated or managed sources to minimize impacts on fragile mire ecosystems.

Synonyms Top

Scientific name Authority First published in
Menyanthes paradoxa Fr. Novit. Fl. Suec. Alt. : 71 (1828)
Menyanthes palustris Gray Nat. Arr. Brit. Pl. 2: 340 (1821 publ. 1822)
Menyanthes latifolia Raf. New Fl. 2: 20 (1837)
Menyanthes americana Sweet Hort. Brit. : 282 (1826)
Menyanthes trifolium Neck. Delic. Gallo-Belg. : 105 (1768)
Menyanthes verna Raf. Med. Fl. 2: 33 (1830)
Menyanthes tridentata Raf. New Fl. 2: 20 (1837)
Menyanthes trifoliata subsp. verna (Raf.) Gervais & M.Parent Ludoviciana 31: 19 (2003)
Menyanthes trifoliata f. brevistyla Aver. Konsp. Sosud. Rast. Zakaz. Mshinskoe Boloto Leningrad. Oblasti : 91 (1988)
Menyanthes trifoliata var. minor Fernald Rhodora 31: 198 (1929)
Menyanthes trifoliata f. macrophylla Bolzon Bull. Soc. Bot. Ital. 1908: 8 (1908)
Menyanthes trifoliata f. microphylla Bolzon Bull. Soc. Bot. Ital. 1908: 9 (1908)
Menyanthes trifoliata var. paradoxa Fr. Novit. Fl. Svec. 1: 7 (1814)

Common names Top

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Language Common/alternative name
English bogbean
English buckbean
Spanish menianto
Arabic أطريفل الماء
Arabic مائي ثلاثي الورق
Arabic مائي نفلي
Arabic نفل الماء
Arabic فِصَة الماء
Arabic برسيم الماء
Azerbaijani Üçyarpaq suyoncası
azb سۇ یونجاسی
ba Вахта үләне
Belarusian Бабок
Bulgarian Горчивче
Bulgarian Водна детелина
Bulgarian горчивче
Catalan trèvol d'aigua
Catalan meniant
Catalan trèvol lluent
Catalan trifli lluent
Czech vachta trojlistá
Czech vachta
Czech vachta třílistá
cv Тĕкĕрчен
Welsh ffeuen y gors
Danish almindelig bukkeblad
Danish bukkeblad
German fieberklee
German bitterklee
German sumpfklee
Estonian ubaleht
Estonian harilik ubaleht
Persian منیانتس
Finnish raate
Faroese tríblaðað bukkablað
French trèfle d'eau
French trèfle d’eau
French trèfle deau
French menyanthe
French ményanthe
French trefle d’eau
Irish báchrán
Croatian trolistica
Upper Sorbian třiłopješkaty kózlik
Upper Sorbian hórki dźećel
Upper Sorbian kózlik
Hungarian vidrafű
Hungarian hármaslevelű vidrafű
Armenian ջրառվույտ
Icelandic horblaðka
Italian trifoglio d'acqua
Japanese ミツガシワ
Japanese ミツガシワ属
Japanese 三槲睡菜
Georgian წყლის სამყურა
Kazakh Субеде
Korean 조름나물
Cornish teyrdelen an kors
Lithuanian trilapis puplaiškis
Lithuanian pupalaiškis
Lithuanian puplaiškis
Latvian trejlapu puplaksis
lzh 睡菜
Macedonian Водна детелина
myv Панжозь цеця
Norwegian Bokmål bukkeblad
Dutch waterdrieblad
Norwegian Nynorsk bukkeblad
Polish bobrek trójlistkowy
Polish bobrek
Polish bobrek trójlistny
Russian Вахта
Russian Трилистник
Russian Трифоль
Russian Вахта трехлистная
Russian Вахта трёхлистная
Russian Трилистник водяной
Russian Вахта (растение)
Yakutian Кус олоҕо
se muoskkáš
se muoškkáš
se njuohcu
se muošká
Samogitian poplaiškė
Slovak vachta trojlistá
Slovenian navadni mrzličnik
Slovenian grenka deteljica
smn muáskâš
sms muâckač
Serbian Горчица
Swedish vattenklöver
Swedish vattenklövrar
Turkish su yoncası
Turkish acı yonca
Turkish acıtırfıl
Turkish ateş yoncası
tt Кондыз үләне
Ukrainian Бобівник трилистий
Ukrainian Вахта трилиста
vep vehk
Chinese 睡菜
Chinese 睡菜属

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000450682
UNII 7H0QTZ446K
Canadensys 6671
USDA Plants METR3
Tropicos 20800053
INPN 108345
Flora of Italy 4065
KEW urn:lsid:ipni.org:names:50970102-1
The Plant List kew-2505977
Plantarium 24291
Missouri Botanical Garden 282717
PFAF Menyanthes trifoliata
Open Tree Of Life 1069766
Observations.org 2626
NCBI Taxonomy 28525
NBN Atlas NBNSYS0000003976
Nature Serve 2.152693
IUCN Red List 163993
IPNI 370147-1
iNaturalist 78016
IFPNI D866A976-1DAF-4F71-91D9-52D134E1DB8F
GBIF 5341511
Freebase /m/05_qxy
WisFlora 4237
EPPO MEYTR
EOL 584945
Elurikkus 5706
Calflora (Californian flora) 5448
USDA GRIN 400088
Wikipedia Menyanthes
KEW urn:lsid:ipni.org:names:60455425-2
IPNI 60455425-2

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
Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L Plants (Basel) 24-Feb-2024
PMCID:PMC10934440
doi:10.3390/plants13050621
PMID:38475472
Betulinic Acid for Glioblastoma Treatment: Reality, Challenges and Perspectives Fernandes S, Vieira M, Prudêncio C, Ferraz R Int J Mol Sci 09-Feb-2024
PMCID:PMC10889789
doi:10.3390/ijms25042108
PMID:38396785
Analysis of winter diet in Guizhou golden monkey (Rhinopithecus brelichi) using DNA metabarcoding data Zhang X, Zhong H, Ran J, Luo J, Chen M, Li H, Wang Y, Cheng S, Yan Y, Huang X Ecol Evol 01-Feb-2024
PMCID:PMC10834204
doi:10.1002/ece3.10893
PMID:38314313
Dominance of non-wetland-dependent pollinators in a plant community in a small natural wetland in Shimane, Japan Watazu T, Hiraiwa MK, Inoue M, Mishima H, Ushimaru A, Hosaka T J Plant Res 11-Jan-2024
PMCID:PMC10899375
doi:10.1007/s10265-023-01518-9
PMID:38206495
Radiation and temperature drive diurnal variation of aerobic methane emissions from Scots pine canopy Kohl L, Tenhovirta SA, Koskinen M, Putkinen A, Haikarainen I, Polvinen T, Galeotti L, Mammarella I, Siljanen HM, Robson TM, Adamczyk B, Pihlatie M Proc Natl Acad Sci U S A 21-Dec-2023
PMCID:PMC10756279
doi:10.1073/pnas.2308516120
PMID:38127980
The first complete chloroplast genome sequence of Pentaphragma spicatum Merr. (Pentaphragmataceae) and phylogenetic analysis Cheng Z, Yu BN, Huang XY, Bin ZJ, Liu SZ, Chi ZJ Mitochondrial DNA B Resour 12-Dec-2023
PMCID:PMC10776070
doi:10.1080/23802359.2023.2290339
PMID:38196793
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
Adaptive Relationships in Hemi-Boreal Forests: Tree Species Responses to Competition, Stress, and Disturbance Petrokas R, Manton M Plants (Basel) 13-Sep-2023
PMCID:PMC10535793
doi:10.3390/plants12183256
PMID:37765418
High-Resolution Lacustrine Records of the Late Holocene Hydroclimate of the Sikhote-Alin Mountains, Russian Far East Razjigaeva N, Ganzey L, Grebennikova T, Kopoteva T, Klimin M, Arslanov K, Lyashchevskaya M, Panichev A, Lupakov S Biology (Basel) 26-Jun-2023
PMCID:PMC10376648
doi:10.3390/biology12070913
PMID:37508345
The first comprehensive population size estimations for the highly endangered largest diving beetle Dytiscus latissimus in Europe Balalaikins M, Schmidt G, Aksjuta K, Hendrich L, Kairišs K, Sokolovskis K, Valainis U, Zolovs M, Nitcis M Sci Rep 15-Jun-2023
PMCID:PMC10272167
doi:10.1038/s41598-023-36242-w
PMID:37322014
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Phylogenetical Position versus Pollination Syndromes: Floral Trichomes of Central American and Mexican Pinguicula Lustofin K, Świątek P, Miranda VF, Płachno BJ Int J Mol Sci 08-May-2023
PMCID:PMC10179228
doi:10.3390/ijms24098423
PMID:37176130
Inference of future bog succession trajectory from spatial chronosequence of changing aapa mires Kolari TH, Tahvanainen T Ecol Evol 18-Apr-2023
PMCID:PMC10111175
doi:10.1002/ece3.9988
PMID:37082320
Monitoring the courtship flight trajectory of Latham's snipe (Gallinago hardwickii) using microphone arrays Matsubayashi S, Osaka H, Suzuki R, Nakadai K, Okuno HG Ecol Evol 31-Mar-2023
PMCID:PMC10065977
doi:10.1002/ece3.9938
PMID:37013098
Polyphenol Profile of Cistus × incanus L. and Its Relevance to Antioxidant Effect and α-Glucosidase Inhibition Starzec A, Włodarczyk M, Kunachowicz D, Dryś A, Kepinska M, Fecka I Antioxidants (Basel) 22-Feb-2023
PMCID:PMC10045904
doi:10.3390/antiox12030553
PMID:36978801

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown https://doi.org/10.1055/S-2007-969319
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1055/S-2007-969319
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1055/S-2007-969319
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1055/S-2007-969319
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1055/S-2007-969319
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown https://doi.org/10.1055/S-2007-969319
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
[5-ethenyl-1-oxo-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl] (E)-8-hydroxy-2,6-dimethyloct-6-enoate 101297685 Click to see 542.60 unknown https://doi.org/10.1016/S0944-7113(11)80021-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(-)-Loganin 87691 Click to see 390.40 unknown https://doi.org/10.1016/S0944-7113(11)80021-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4aR,7R,7aR)-7-methyl-4,4a,5,6,7,7a-hexahydro-3H-cyclopenta[c]pyran-1-one 13929863 Click to see CC1CCC2C1C(=O)OCC2 154.21 unknown https://doi.org/10.1246/NIKKASHI1948.90.6_507
[5-ethenyl-1-oxo-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl] (2E,6Z)-8-hydroxy-2,6-dimethylocta-2,6-dienoate 5317365 Click to see 540.60 unknown https://doi.org/10.1016/S0944-7113(11)80021-8
Foliamenthin 76967939 Click to see 540.60 unknown https://doi.org/10.1016/S0944-7113(11)80021-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.07-0446
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.07-0446
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(5S,9S,10S,13R,14R)-17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 137706369 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.21135/893275471.012
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,3,4,5-Tetrahydroxycyclohexanecarboxylic acid 1064 Click to see 192.17 unknown https://doi.org/10.1055/S-2007-969319
Quinic acid 6508 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown https://doi.org/10.1055/S-2007-969319
> Organoheterocyclic compounds / Benzofurans
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1086/325638
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1055/S-2007-969319
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1055/S-2007-969319
O-Coumaric Acid 637540 Click to see 164.16 unknown https://doi.org/10.1055/S-2007-969319
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1055/S-2007-969319
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1055/S-2007-969319
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see 206.19 unknown https://doi.org/10.1086/325638
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1086/325638
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Braylin 618370 Click to see 258.27 unknown https://doi.org/10.1086/325638
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown https://doi.org/10.1002/J.1537-2197.1986.TB08521.X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00623883
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00570212
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1007/BF00570212
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00623883

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Menyanthes trifoliata
Author: Sorin
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