Lotus pedunculatus, also known as big trefoil or marsh bird's-foot trefoil, is a perennial plant in the pea family that can be found throughout Europe in wet, open areas. It is larger than other Lotus species, growing up to 80cm tall with yellow flowers in an umbel at the top of its stem. Its stem is hollow and its sepals form a distinctive "green star" at the end of the flower bud. This plant blooms in June and July in the UK and is often found in neutral, damp habitats such as fen-meadows. It is also a host plant for the wood white butterfly.

Synonyms Top

Scientific name	Authority	First published in
Lotus uluginosus	Schkuhr
Lotus granadensis	Zertova
Lotus corniculatus subsp. decumbens	(Poir.) Merino	Fl. Galicia3: 540 (1909)
Lotus corniculatus prol. pedunculatus	(Cav.) Rouy	G.Rouy & J.Foucaud, Fl. France5: 149 (1899)
Lotus uliginosus var. brachycarpus	Willk.	Oesterr. Bot. Z.41: 84 (1891)
Lotus corniculatus var. pedunculatus	(Cav.) Willk.	M.Willkomm & J.M.C.Lange, Prodr. Fl. Hispan.3: 343 (1877)

Common names Top

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Filter by language:

Language	Common/alternative name
English	big trefoil
English	greater bird's-foot-trefoil
English	greater birdsfoot-trefoil
English	marsh bird's-foot trefoil,
English	greater bird's-foot trefoil
English	marsh bird's-foot trefoil
Spanish	cuernecillo grande
Spanish	lotera
Spanish	alfalfa chilota
Arabic	قرن الغزال السبخي
Arabic	لوطس سبخي
Czech	štírovník bažinný
Welsh	pysen-y-ceirw fawr
Danish	sump-kællingetand
German	sumpfhornklee
German	sumpf-hornklee
Estonian	soo-nõiahammas
Finnish	isomaite
French	lotier des marais
French	lotier pédonculé
French	lotier des fanges
Irish	crobh éin corraigh
Upper Sorbian	bahnowy ledźbjenc
Japanese	ネビキミヤコグサ
Cornish	pys an gath bras
Lithuanian	pelkinis garždenis
Latvian	dūkstu vanagnadziņš
Norwegian Bokmål	fôrtiriltunge
Dutch	moerasrolklaver
Polish	komonica błotna
Slovak	ľadenec barinný
Swedish	stor käringtand
Chinese	欧洲百脉根

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Lotus pedunculatus subsp. granadensis	(Chrtková) Molero Mesa & Pérez Raya	Fl. Sierra Nevada: 152 (1987)
Lotus pedunculatus subsp. pedunculatus		Unknown

Varieties (abbr. var.) Top

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No variety added yet.

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

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
- Western Indian Ocean
  - Réunion

Antarctica click to expand
- Subantarctic Islands
  - Falkland Islands

Asia-temperate click to expand
- Eastern Asia
  - Japan
  - Korea
- Western Asia
  - Turkey

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
  - Tasmania
  - Victoria
  - Western Australia
- New Zealand
  - Antipodean Islands
  - Chatham Islands
  - Kermadec Islands
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Føroyar
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Northwestern U.S.A.
  - Oregon
  - Washington
- Southwestern U.S.A.
  - California

Pacific click to expand
- North-central Pacific
  - Hawaii
- South-central Pacific
  - Easter Island

Southern America click to expand
- Southern South America
  - Argentina South
  - Chile Central
  - Chile South

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000212230
Florida Plant Atlas	476
Canadensys	16301
USDA Plants	LOPE80
Tropicos	13022320
INPN	106698
Flora of Italy	2704
KEW	urn:lsid:ipni.org:names:503822-1
The Plant List	ild-7307
Open Tree Of Life	484501
NCBI Taxonomy	347994
NBN Atlas	NBNSYS0000003260
Nature Serve	2.144590
IPNI	503822-1
iNaturalist	164834
GBIF	5356854
Freebase	/m/06fw9h
EPPO	LOTUL
EOL	702919
Elurikkus	5572
USDA GRIN	22733
Wikipedia	Lotus_pedunculatus

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

Effect of plant edges strips on the conservation soil properties in modern farming field

Šarūnaitė L, Arlauskienė A, Jablonskytė-Raščė D

PLoS One

16-Apr-2024

PMCID:	PMC11020931
doi:	10.1371/journal.pone.0299104
PMID:	38625970

Extreme environments simplify reassembly of communities of arbuscular mycorrhizal fungi

Šibanc N, Clark DR, Helgason T, Dumbrell AJ, Maček I

mSystems

20-Feb-2024

PMCID:	PMC10949450
doi:	10.1128/msystems.01331-23
PMID:	38376262

Artificial light at night reduces earthworm activity but increases growth of invasive ragweed

Mittmannsgruber M, Kavassilas Z, Spangl B, Gruber E, Jagg E, Zaller JG

BMC Ecol Evol

19-Jan-2024

PMCID:	PMC10797752
doi:	10.1186/s12862-024-02200-x
PMID:	38243160

The Lotus angustissumus Group (Fabaceae): Can Phylogenetic Patterns Be Accommodated by a Taxonomic Concept?

Kramina TE, Hadziev TR, Samigullin TH

Plants (Basel)

28-Dec-2023

PMCID:	PMC10780816
doi:	10.3390/plants13010101
PMID:	38202409

The nutritional dimension of facultative bacterial symbiosis in aphids: Current status and methodological considerations for future research

Renoz F

Curr Res Insect Sci

20-Dec-2023

PMCID:	PMC10787254
doi:	10.1016/j.cris.2023.100070
PMID:	38222793

Receptor-Independent Therapies for Forensic Detainees with Schizophrenia–Dementia Comorbidity

Sfera A, Andronescu L, Britt WG, Himsl K, Klein C, Rahman L, Kozlakidis Z

Int J Mol Sci

31-Oct-2023

PMCID:	PMC10647468
doi:	10.3390/ijms242115797
PMID:	37958780

Part-night exposure to artificial light at night has more detrimental effects on aphid colonies than fully lit nights

Heinen R, Sanchez-Mahecha O, Martijn Bezemer T, Dominoni DM, Knappe C, Kollmann J, Kopatsch A, Pfeiffer ZA, Schloter M, Sturm S, Schnitzler JP, Corina Vlot A, Weisser WW

Philos Trans R Soc Lond B Biol Sci

30-Oct-2023

PMCID:	PMC10613545
doi:	10.1098/rstb.2022.0357
PMID:	37899021

A framework for untangling the consequences of artificial light at night on species interactions

Seymoure B, Dell A, Hölker F, Kalinkat G

Philos Trans R Soc Lond B Biol Sci

30-Oct-2023

PMCID:	PMC10613547
doi:	10.1098/rstb.2022.0356
PMID:	37899016

Sulla (Hedysarum coronarium L.) Response to Drought Stress during Early Vegetative Stage

Rossi R, Amato M, Claps S

Plants (Basel)

26-Sep-2023

PMCID:	PMC10574800
doi:	10.3390/plants12193396
PMID:	37836136

Antimicrobial, Antioxidant, and Anti-Inflammatory Properties of Monofloral Honeys from Chile

Poulsen-Silva E, Gordillo-Fuenzalida F, Velásquez P, Llancalahuen FM, Carvajal R, Cabaña-Brunod M, Otero MC

Antioxidants (Basel)

21-Sep-2023

PMCID:	PMC10526086
doi:	10.3390/antiox12091785
PMID:	37760088

Seasonal Effect of Grass Nutritional Value on Enteric Methane Emission in Islands Pasture Systems

Nunes HP, Maduro Dias CS, Vouzela CM, Borba AE

Animals (Basel)

30-Aug-2023

PMCID:	PMC10486569
doi:	10.3390/ani13172766
PMID:	37685031

Embryo Rescue in Plant Breeding

Rogo U, Fambrini M, Pugliesi C

Plants (Basel)

29-Aug-2023

PMCID:	PMC10489947
doi:	10.3390/plants12173106
PMID:	37687352

Facultative symbiont virulence determines horizontal transmission rate without host strain specificity

Noh S, Larson ER, Covitz RM, Chen A, Mazumder PR, Peck RF, Hamilton MC, Dettmann RA

bioRxiv

31-Jul-2023

PMCID:	PMC9949114
doi:	10.1101/2023.02.16.528903
PMID:	36824889

Potential of Halophytes as Sustainable Fodder Production by Using Saline Resources: A Review of Current Knowledge and Future Directions

Hasnain M, Abideen Z, Ali F, Hasanuzzaman M, El-Keblawy A

Plants (Basel)

29-May-2023

PMCID:	PMC10255648
doi:	10.3390/plants12112150
PMID:	37299129

Antibacterial and wound-healing action of Ulmo honey (Eucryphia cordifolia) of differing degrees of purity

Muñoz M, del Sol M, Vásquez B

Front Vet Sci

12-May-2023

PMCID:	PMC10213365
doi:	10.3389/fvets.2023.1172025
PMID:	37252390

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 / Fatty Acyls / Fatty alcohols
1-Octacosanol	68406	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO	410.80	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4S,6aR,8aR,9R,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	6326067	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C	959.10	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Soyasaponin Ba	91973815	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C	959.10	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
cyclo[Gly-Thr-Phe-Leu-Tyr-Val]	10101075	Click to see CC(C)CC1C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N1)CC2=CC=CC=C2)C(C)O)C(C)C)CC3=CC=C(C=C3)O	680.80	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Karakin	100274	Click to see C(C[N+](=O)[O-])C(=O)OCC1C(C(C(C(O1)OC(=O)CC[N+](=O)[O-])OC(=O)CC[N+](=O)[O-])O)O	483.34	unknown	https://doi.org/10.1007/BF00987645 https://doi.org/10.1016/S0031-9422(00)85490-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(4-Hydroxyphenoxy)-6-[3-(4-hydroxyphenyl)prop-2-enoxymethyl]oxane-3,4,5-triol	162890773	Click to see C1=CC(=CC=C1C=CCOCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O	404.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(3-nitropropanoyloxy)oxan-2-yl]methyl 3-nitropropanoate	163195482	Click to see C(C[N+](=O)[O-])C(=O)OCC1C(C(C(C(O1)OC(=O)CC[N+](=O)[O-])O)O)O	382.28	unknown	https://doi.org/10.1016/S0031-9422(00)85490-4
[(2S,3S,4S,5S,6S)-3,4,6-trihydroxy-5-(3-nitropropanoyloxy)oxan-2-yl]methyl 3-nitropropanoate	163193768	Click to see C(C[N+](=O)[O-])C(=O)OCC1C(C(C(C(O1)O)OC(=O)CC[N+](=O)[O-])O)O	382.28	unknown	https://doi.org/10.1016/S0031-9422(00)85490-4
Cibarian	100275	Click to see C(C[N+](=O)[O-])C(=O)OCC1C(C(C(C(O1)OC(=O)CC[N+](=O)[O-])O)O)O	382.28	unknown	https://doi.org/10.1007/BF00987645 https://doi.org/10.1016/S0031-9422(00)85490-4
Coronarian	441560	Click to see C(C[N+](=O)[O-])C(=O)OCC1C(C(C(C(O1)O)OC(=O)CC[N+](=O)[O-])O)O	382.28	unknown	https://doi.org/10.1007/BF00987645 https://doi.org/10.1016/S0031-9422(00)85490-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Dehydrokaempferol	137176164	Click to see C1=C(C#CC(=C1)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	284.22	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
> Phenylpropanoids and polyketides / Depsides and depsidones
Chloroatranorin	68065	Click to see CC1=CC(=C(C(=C1C(=O)OC)O)C)OC(=O)C2=C(C(=C(C(=C2O)C=O)O)Cl)C	408.80	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R)-2alpha-(3,4,5-Trihydroxyphenyl)-2'alpha-(3,4-dihydroxyphenyl)-4beta,8'-bichroman-3alpha,3'beta,5,5',7,7'-hexol	13831060	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	130556	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Epigallocatechin-(4beta->8)-catechin	13831061	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Gallocatechin-(4alpha->8)-epigallocatechin	442682	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Proanthocyandin der.	467304	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Procyanidin B1	11250133	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Procyanidin B2, (+)-	122738	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Procyanidin B3	146798	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Procyanidin B4	147299	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Prodelphinidin B	5089687	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Prodelphinidin B1	13831065	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-(2,4,6-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	14009029	Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C=C4O)O)O)O)O)O	414.40	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
2-(3,4-dihydroxyphenyl)-4-(2,4,6-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	14009025	Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C=C4O)O)O)O)O)O	414.40	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2 https://doi.org/10.1034/J.1399-3054.1999.100301.X https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Procyanidin	107876	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4(C(C(C5=C(C=C(C=C5O4)O)O)O)O)C6=CC(=C(C=C6)O)O	594.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
Prodelphinidin B6	14009028	Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C=C4O)O)O)O)O)O	414.40	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2R,3R,4S)-4-(2,4,6-trihydroxyphenyl)-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	15299157	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C=C4O)O)O)O	430.40	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
(2R,3S,4R)-4-(2,4,6-trihydroxyphenyl)-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	21626721	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C=C4O)O)O)O	430.40	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
4-(2,4,6-trihydroxyphenyl)-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	73191354	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C=C4O)O)O)O	430.40	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Flavan-3,3',4',5,5',7-hexol	1249	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Gallocatechin	65084	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1016/S0031-9422(97)00198-2
Prodelphiniline	285704	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4(C(C(C5=C(C=C(C=C5O4)O)O)O)O)C6=CC(=C(C(=C6)O)O)O	610.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one	667495	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1034/J.1399-3054.1999.100301.X
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1034/J.1399-3054.1999.100301.X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1034/J.1399-3054.1999.100301.X https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1034/J.1399-3054.1999.100301.X https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/ https://doi.org/10.1034/J.1399-3054.1999.100301.X
Rhamnetin	5281691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 5-glucoside	5317471	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol-7-rhamnoside	25079965	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Flavylium, 3,3',4',5,5',7-hexahydroxy-	128853	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O	303.24	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075570/

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Lotus pedunculatus

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