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.

Red clover (Trifolium pratense) has long been brewed as a soothing tea in several folk traditions. Among the British, Bennett et al. (2021) report that dried flowers are steeped to relieve menopausal hot flashes, a practice still common in contemporary herbal shops. In German folk medicine, the same flowers are boiled into a decoction to treat urinary tract infections, as documented in the 2010 edition of *Deutsche Volksmedizin*. Australian Aboriginal communities have used a tea made from the leaves and young stems to soothe sore throats, a use noted in the 2018 ethnobotanical survey *Ethnobotany of the Australian Aboriginals*. In each case the preparation is an infusion or decoction, and the plant part is typically the aerial portion (flowers, leaves, or stems).

A simple, safe recipe for a mild red clover tea is as follows: combine 5 g of dried flowers with 250 ml of freshly boiled water. Let the mixture steep for 10 minutes, then strain and sip. Drink two to three cups per day, limiting intake to 10 g of dried material per day to avoid excessive estrogenic effects. Pregnant or breastfeeding women should consult a healthcare professional before use, as the isoflavones can act as weak estrogen mimics.

The therapeutic effects of red clover are largely attributed to its isoflavone content, particularly genistein and daidzein, which are phytoestrogens. These compounds, along with flavonoids such as kaempferol and phenolic acids like chlorogenic acid, have been isolated from the flowers and are believed to underlie the plant’s traditional use for hormonal balance and anti‑inflammatory purposes. The presence of these well‑established phytochemicals provides a biochemical basis for the observed benefits in menopausal symptom relief and urinary tract health.

Modern research continues to explore red clover’s isoflavones for menopausal symptom management, and the plant is widely available as a standardized supplement in health food stores. Its enduring use in both traditional and contemporary settings underscores its relevance as a natural remedy with a solid phytochemical foundation.

General Uses Top

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Common products:
Red clover is used primarily as a forage legume in agriculture. The principal products are hay, haylage, and silage; it is also managed as pasture and green manure. Its use in pastures is favored by its ability to fix atmospheric nitrogen and to regrow after cutting or grazing.

Food and beverages (non-medicinal):
Red clover is a major nectar source for honey production, contributing distinctive light-amber honey that is marketed under varietal names in apiculture. Forage and hay from red clover provide feed for ruminant livestock and horses; the crop is also used for grazing systems where it supplies digestible fiber and protein.

Properties relevant to use:
Forage quality is typically assessed by crude protein, fiber (acid and neutral detergent fiber), digestibility, and voluntary intake. Red clover’s relatively high protein and digestible fiber support rapid animal growth and milk production; its nitrogen fixation contributes to yield without synthetic nitrogen inputs.

Standards and regulation:
Forage quality and hay grading commonly follow USDA forage testing standards (e.g., NDF/ADF, crude protein), with moisture content and bale standards governed by national agricultural extension and regulatory bodies.

Sustainability and sourcing:
Red clover enhances soil fertility through biological nitrogen fixation and improves sward productivity in rotations, supporting regenerative and low-input forage systems. It is cultivated widely in temperate regions as a pasture and hay crop and is valued in sustainable agriculture for reducing synthetic fertilizer needs.

Synonyms Top

Scientific name	Authority	First published in
Trifolium ukrainicum	Opperman
Trifolium pratense var. pratense	L.
Lagopus pratensis	(L.) Bernh.	Syst. Verz. Erf.: 230 (1800)

Common names Top

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Filter by language:

Language	Common/alternative name
English	red clover
Spanish	carretón
Spanish	teble
Spanish	trébol
Spanish	caramelos
Spanish	chupamieles
Spanish	berrillo
Spanish	chupador
Spanish	chupetes
Spanish	chupetitos
Spanish	chupón
Spanish	chupones
Spanish	farucha
Spanish	farusa
Spanish	hierba de las cataratas
Spanish	hirusta gorria
Spanish	hoja la nube
Spanish	mamatetas
Spanish	media luna
Spanish	melga
Spanish	meliguel
Spanish	meriguel
Spanish	motas encarnadas
Spanish	quínola
Spanish	tefla
Spanish	trábol de la media luna
Spanish	trebalejo
Spanish	trebo
Spanish	trebo silvestre
Spanish	trébol arvense
Spanish	trébol común
Spanish	trébol de la luna
Spanish	trébol de la media luna
Spanish	trébol de los prados
Spanish	trébol de los prados colorado
Spanish	trébol de media luna
Spanish	trébol de prado
Spanish	trébol de prados
Spanish	trébol de prados de flores encarnadas
Spanish	trébol de prados purpúreas
Spanish	trébol del príncipe
Spanish	trébol enano
Spanish	trébol encarnado
Spanish	trébol ladino
Spanish	trébol pratense
Spanish	trébol pratense que hace las flores purpúreas
Spanish	trébol productivo
Spanish	trébol rojo
Spanish	trébol rojo de los prados
Spanish	trébol silvestre
Spanish	trébol sopaenvino
Spanish	trébol sopavino
Spanish	trébol violeta
Spanish	trébole
Spanish	trébul
Spanish	trebulo
Spanish	tres en rama
Spanish	trevol
Spanish	trifolio
Spanish	yerba chupelera
Spanish	trebol rojo
Arabic	نفل أحمر
Arabic	نفل احمر
Arabic	نفل المروج
Arabic	برسيم احمر
Arabic	رطبه
Azerbaijani	Çəmənlik üçyarpaq yoncası
ba	Туҡранбаш
Belarusian	Канюшына лугавая
Bulgarian	Червена детелина
Catalan	trèvol comú
Catalan	trèvol de prat
Catalan	trèvol vermell
Czech	jetel luční
Welsh	meillion coch
Welsh	meillionen goch
Danish	rød kløver
Danish	rød-kløver
Danish	rødkløver
German	wiesenklee
German	rot-klee
German	rotklee
German	saatklee
German	wiesen-klee
Esperanto	ruĝa trifolio
Estonian	aasristik
Estonian	punane ristik
Estonian	punane ristikhein
Basque	hirusta gorri
Persian	شبدر قرمز
Finnish	puna-apila
French	trefle des pres
French	trèfle des prés
French	trèfle violet
Irish	seamair dhearg
Galician	trevo rubio
Upper Sorbian	Čerwjeny dźećel
Hungarian	réti here
Armenian	Երեքնուկ մարգագետնային
Igbo	red clover
Icelandic	rauðsmári
Italian	trifoglio dei prati
Italian	trifoglio rosso
Italian	trifoglio violetto
Japanese	アカツメクサ
Japanese	アカツメグサ
Japanese	ムラサキツメクサ
Japanese	ムラサキツメグサ
Japanese	紫詰草
Georgian	წითელი სამყურა
Korean	붉은토끼풀
Cornish	mellyonen rudh
lb	wisekléi
Lithuanian	raudonasis dobilas
Latvian	pļavas āboliņš
Macedonian	црвена детелина
mn	Нугын хошоонгор
myv	Вараканьбал
myv	Лугалангонь вараканьпря тикше
myv	Лугань вараканьпал
Norwegian Bokmål	rød kløver
Norwegian Bokmål	rødkløver
Norwegian Bokmål	sukkertopp
Dutch	rode klaver
Norwegian Nynorsk	raudkløver
os	Уыгæрдæны æртæсыфон
Polish	koniczyna czerwona
Polish	koniczyna łąkowa
Portuguese	trevo vermelho
Romanian	trifoi de luncă
Romanian	trifoi roșu
Russian	Клевер луговой
Russian	Клевер красный
Russian	Дятлина красная
Serbo-Croatian	crvena detelina
Slovak	ďatelina lúčna
Slovenian	Črna detelja
Serbian	Црвена детелина
Swedish	rödklöver
Turkish	Çayır üçgülü
Turkish	kırmızı yonca
Ukrainian	Конюшина лучна
vec	strafòjo
vep	imičaine
Chinese	紅菽草
Chinese	红车轴草
Chinese	三叶草
Chinese	红三叶
Chinese	红三叶草
Chinese	红菽草
Chinese	一种维管植物

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Trifolium pratense subsp. baeticum	(Boiss.) Vicioso	Anales Inst. Bot. Cavanilles11: 317 (1953)
Trifolium pratense subsp. kotulae	(Pawl.) Soják	Novit. Bot. Delect. Seminum Horti Bot. Univ. Carol. Prag.1963: 49 (1963)
Trifolium pratense subsp. pratense		Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia
- Southern Africa
  - Cape Provinces
  - Kwazulu-Natal
  - Northern Provinces

Antarctica click to expand
- Subantarctic Islands
  - Falkland Islands

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Kamchatka
  - Khabarovsk
  - Kuril Islands
  - Magadan
  - Primorye
  - Sakhalin
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Afghanistan
  - Iran
  - Iraq
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Malesia
  - Jawa

Australasia click to expand
- Australia
  - New South Wales
  - Queensland
  - 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
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Føroyar
  - Great Britain
  - Iceland
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - Labrador
  - Newfoundland
- Mexico
  - Mexico Southwest
- North-central U.S.A.
  - Illinois
  - Minnesota
  - Wisconsin
- Northeastern U.S.A.
  - New York
  - Vermont
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Oregon
  - Washington
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - Alabama
  - Kentucky
  - Maryland
  - Tennessee
- Southwestern U.S.A.
  - California
  - Nevada
- Subarctic America
  - Aleutian Islands

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Brazil
  - Brazil South
- Caribbean
  - Bahamas
  - Bermuda
  - Cuba
  - Dominican Republic
  - Puerto Rico
- Central America
  - Costa Rica
  - Guatemala
- Northern South America
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Argentina South
  - Chile Central
  - Chile South
  - Uruguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000213053
UNII	FG30UR681Y
Florida Plant Atlas	1857
Flora of Alabama	2086
Canadensys	5929
USDA Plants	TRPR2
Tropicos	13034154
INPN	127439
Flora of Italy	2657
KEW	urn:lsid:ipni.org:names:523575-1
The Plant List	ild-8127
Plantarium	39025
PFAF	Trifolium pratense
Open Tree Of Life	839027
Observations.org	7573
NCBI Taxonomy	57577
NBN Atlas	NBNSYS0000003231
Nature Serve	2.140855
IUCN Red List	174713
IPNI	523575-1
iNaturalist	51875
GBIF	8324121
Freebase	/m/064tx6
WisFlora	5272
EPPO	TRFPR
EOL	703430
Elurikkus	8006
Calflora (Californian flora)	8104
USDA GRIN	300623
Wikipedia	Trifolium_pratense
CMAUP	NPO22104

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCF_020283565.1	ARS_RC_1.1	Chromosome	USDA ARS	2021-10-13	55	394.42 Mb

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

Effects of experimental drought and plant diversity on multifunctionality of a model system for crop rotation

Grange G, Brophy C, Vishwakarma R, Finn JA

Sci Rep

04-May-2024

PMCID:	PMC11069507
doi:	10.1038/s41598-024-60233-0
PMID:	38704461

Strategies, Achievements, and Potential Challenges of Plant and Microbial Chassis in the Biosynthesis of Plant Secondary Metabolites

Han T, Miao G

Molecules

02-May-2024

PMCID:	PMC11085123
doi:	10.3390/molecules29092106
PMID:	38731602

Unveiling the Potential of Natural Compounds: A Comprehensive Review on Adipose Thermogenesis Modulation

Shin J, Lee Y, Ju SH, Jung YJ, Sim D, Lee SJ

Int J Mol Sci

30-Apr-2024

PMCID:	PMC11084502
doi:	10.3390/ijms25094915
PMID:	38732127

Analysis of small-scale soil CO2 fluxes in an orange orchard under irrigation and soil conservative practices

Guarrera S, Vanella D, Consoli S, Giudice G, Toscano S, Ramírez-Cuesta JM, Milani M, Ferlito F, Longo D

Heliyon

30-Apr-2024

PMCID:	PMC11079320
doi:	10.1016/j.heliyon.2024.e30543
PMID:	38726109

A Cluster of Peronospora parasitica 13-like (NBS-LRR) Genes Is Associated with Powdery Mildew (Erysiphe polygoni) Resistance in Mungbean (Vigna radiata)

Waengwan P, Laosatit K, Lin Y, Yimram T, Yuan X, Chen X, Somta P

Plants (Basel)

29-Apr-2024

PMCID:	PMC11085486
doi:	10.3390/plants13091230
PMID:	38732445

Growth Performance of Buffalo Calves in Response to Different Diets with and without Saccharomyces cerevisiae Supplementation

Zicarelli F, Iommelli P, Musco N, Wanapat M, Lotito D, Lombardi P, Infascelli F, Tudisco R

Animals (Basel)

22-Apr-2024

PMCID:	PMC11047708
doi:	10.3390/ani14081245
PMID:	38672393

Comparative Genomics of Lotus japonicus Reveals Insights into Proanthocyanidin Accumulation and Abiotic Stress Response

Sun Z, Liu Z, Zhi M, Ran Q, Xue W, Tang Y, Wu Y

Plants (Basel)

20-Apr-2024

PMCID:	PMC11054356
doi:	10.3390/plants13081151
PMID:	38674560

Changes in Growth and Heavy Metal and Phenolic Compound Accumulation in Buddleja cordata Cell Suspension Culture under Cu, Fe, Mn, and Zn Enrichment

Vazquez-Marquez AM, Bernabé-Antonio A, Correa-Basurto J, Burrola-Aguilar C, Zepeda-Gómez C, Cruz-Sosa F, Nieto-Trujillo A, Estrada-Zúñiga ME

Plants (Basel)

19-Apr-2024

PMCID:	PMC11054087
doi:	10.3390/plants13081147
PMID:	38674556

2-oxoglutarate-dependent dioxygenases and BAHD acyltransferases drive the structural diversification of orobanchol in Fabaceae plants

Homma M, Uchida K, Wakabayashi T, Mizutani M, Takikawa H, Sugimoto Y

Front Plant Sci

18-Apr-2024

PMCID:	PMC11063326
doi:	10.3389/fpls.2024.1392212
PMID:	38699535

What are the drivers of female success in food‐deceptive orchids?

Wróblewska A, Ostrowiecka B, Kotowicz J, Jermakowicz E, Tałałaj I, Szefer P

Ecol Evol

18-Apr-2024

PMCID:	PMC11026981
doi:	10.1002/ece3.11233
PMID:	38646005

Polyphenols and Health Benefits: Volume I

Trujillo J, Ramírez V

Foods

17-Apr-2024

PMCID:	PMC11048924
doi:	10.3390/foods13081221
PMID:	38672893

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

Global changes in gene expression during compatible and incompatible interactions of faba bean (Vicia faba L.) during Orobanche foetida parasitism

Boukteb A, Sato K, Gan P, Kharrat M, Sakouhi H, Shibata A, Shirasu K, Ichihashi Y, Bouhadida M

PLoS One

16-Apr-2024

PMCID:	PMC11020376
doi:	10.1371/journal.pone.0301981
PMID:	38626155

A bird’s-eye view: exploration of the flavin-containing monooxygenase superfamily in common wheat

Sun S, Bakkeren G

Front Plant Sci

12-Apr-2024

PMCID:	PMC11046709
doi:	10.3389/fpls.2024.1369299
PMID:	38681221

Technological Functionalisation of Microencapsulated Genistein and Daidzein Delivery Systems Soluble in the Stomach and Intestines

Kazlauskaite JA, Matulyte I, Marksa M, Bernatoniene J

Pharmaceutics

12-Apr-2024

PMCID:	PMC11054921
doi:	10.3390/pharmaceutics16040530
PMID:	38675191

Phytochemical Profile Top

Add a new one!

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 / Betalains / Betacyanins and derivatives
Prebetanin	6325833	Click to see C1C(NC(=CC1=CC=[N+]2C(CC3=CC(=C(C=C32)O)OC4C(C(C(C(O4)COS(=O)(=O)[O-])O)O)O)C(=O)O)C(=O)O)C(=O)O	630.50	unknown	via CMAUP database
> Alkaloids and derivatives / Corynanthean-type alkaloids
Methyl (2R)-2-[(2S,12bS)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate	5321352	Click to see	354.40	unknown	https://doi.org/10.1080/00021369.1974.10861294
> Benzenoids / Benzene and substituted derivatives
1-Phenylethanol	7409	Click to see	122.16	unknown	https://doi.org/10.1021/JF00122A019
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1021/JF00122A019
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate	4133	Click to see COC(=O)C1=CC=CC=C1O	152.15	unknown	https://doi.org/10.1021/JF00122A019
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,4-Dimethoxybenzoic acid	7121	Click to see COC1=C(C=C(C=C1)C(=O)O)OC	182.17	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see	164.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Hexadecenoic acid	5282743	Click to see CCCCCCCCCCCCCC=CC(=O)O	254.41	unknown	https://doi.org/10.1007/BF00579976
2-Hexadecenoic acid	152802	Click to see	254.41	unknown	https://doi.org/10.1007/BF00579976
Heneicosanoic Acid	16898	Click to see	326.60	unknown	https://doi.org/10.1007/BF00579976
Heptadecaenoic acid	117769	Click to see	268.40	unknown	https://doi.org/10.1007/BF00579976
Heptadecanoic Acid	10465	Click to see	270.50	unknown	https://doi.org/10.1007/BF00579976
Hexadecadienoic Acid	5312421	Click to see	252.39	unknown	https://doi.org/10.1007/BF00579976
Myristoleic Acid	5281119	Click to see	226.35	unknown	https://doi.org/10.1007/BF00579976
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Dodeca-2,4,6-trienoic acid	54225634	Click to see	194.27	unknown	https://doi.org/10.1007/BF00579976
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Docosaenoic acid	3032811	Click to see CCCCCCCCCCCCCCCCCCCC=CC(=O)O	338.60	unknown	https://doi.org/10.1007/BF00579976
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-((Z)-hex-3-enoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	5318045	Click to see	262.30	unknown	via CMAUP database
methyl 4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoate	10564679	Click to see	280.27	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Decyl acetate	8167	Click to see	200.32	unknown	https://doi.org/10.1021/JF00122A019
Dodecyl acetate	8205	Click to see CCCCCCCCCCCCOC(=O)C	228.37	unknown	https://doi.org/10.1021/JF00122A019
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1021/JF00122A019
1-Octen-3-Ol	18827	Click to see	128.21	unknown	https://doi.org/10.1021/JF00122A019
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1007/BF00579976
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1021/JF00122A019
beta-Ocimene, (3Z)-	5320250	Click to see	136.23	unknown	https://doi.org/10.1021/JF00122A019
Menthiafolic acid, (S)-	10845194	Click to see	184.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(+)-alpha-Phellandrene	443160	Click to see	136.23	unknown	via CMAUP database
(1R,4R)-Dihydrocarvone	22227	Click to see	152.23	unknown	via CMAUP database
(1S,2S,4R)-iso-dihydrocarveol	443165	Click to see CC1CCC(CC1O)C(=C)C	154.25	unknown	via CMAUP database
(1S,4S)-Dihydrocarvone	443183	Click to see	152.23	unknown	via CMAUP database
(5S)-5-[(1R)-1,2-Dihydroxy-1-methylethyl]-2-methyl-2-cyclohexen-1-one	11830092	Click to see	184.23	unknown	via CMAUP database
(5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohex-2-en-1-one	10877793	Click to see	184.23	unknown	via CMAUP database
Alpha-Terpinene	7462	Click to see	136.23	unknown	via CMAUP database
Carvone, (-)-	439570	Click to see	150.22	unknown	via CMAUP database
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	via CMAUP database
trans-(2S,5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohexan-1-one	10867057	Click to see	186.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R)-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-ol	101338767	Click to see	210.31	unknown	via CMAUP database
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene	289151	Click to see	204.35	unknown	https://doi.org/10.1021/JF00122A019
alpha-Irone	5371002	Click to see	206.32	unknown	via CMAUP database
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1021/JF00122A019
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF00122A019
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	https://doi.org/10.1021/JF00122A019
CID 16396350	16396350	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1021/JF00122A019
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1S,2R,4R,8S)-2-(beta-D-Glucopyranosyloxy)-p-menthane-8,9-diol	11727818	Click to see CC1CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(CO)O	350.40	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1R,2S,5R)-5-[(2R)-1,2-dihydroxypropan-2-yl]-2-methylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	102021736	Click to see	350.40	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	14729929	Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC=C(C)CO	332.39	unknown	via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S,5R)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol	11823766	Click to see CC(=C)C1CCC(C(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)O	332.39	unknown	via CMAUP database
(2R,3S,4S,5R,6S)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(1S,2S,5R)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol	10885097	Click to see	464.50	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(1S,2S,5R)-2-hydroxy-5-(2-hydroxypropan-2-yl)-2-methylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11810246	Click to see	350.40	unknown	via CMAUP database
(2S,5S)-5-[(2S)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2-methylcyclohexan-1-one	11089348	Click to see CC1CCC(CC1=O)C(C)(COC2C(C(C(C(O2)CO)O)O)O)O	348.39	unknown	via CMAUP database
(5S)-5-[(2S)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2-methylcyclohex-2-en-1-one	11024434	Click to see	346.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(4S,6aR,8aR,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)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	6325919	Click to see	913.10	unknown	https://doi.org/10.1016/S0031-9422(02)00230-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
4abeta,7alpha,7abeta-Nepetalactone	6431022	Click to see	166.22	unknown	via CMAUP database
Umbelliprenin	1781413	Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C	366.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(10-Acetyloxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-5-yl) acetate	163018569	Click to see	366.40	unknown	https://doi.org/10.1271/BBB.56.1955
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Strigolactones
Orobanchol	10665247	Click to see	346.40	unknown	https://doi.org/10.1016/S0031-9422(98)00419-1
Strigol	5281396	Click to see	346.40	unknown	https://doi.org/10.1016/S0031-9422(98)00419-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4S,6aR,8aS,12aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,12,12a,14,14a-dodecahydropicen-3-ol	5321408	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C=C1)C)C)C)(C)CO)O)C)C	440.70	unknown	https://doi.org/10.5586/ASBP.1986.025
(4aS,6bR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,2,4a,6a,6b,9,12a-heptamethyl-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picen-3-one	5321410	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C)C)C)(C)CO)O)C)C	456.70	unknown	https://doi.org/10.5586/ASBP.1986.025
Soyasapogenol B	115012	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C	458.70	unknown	https://doi.org/10.5586/ASBP.1986.025
Soyasapogenol C	3083637	Click to see	440.70	unknown	https://doi.org/10.5586/ASBP.1986.025
Soyasapogenol D	46173903	Click to see CC1(CC(C2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C)C)OC)C	472.70	unknown	https://doi.org/10.5586/ASBP.1986.025
Soyasapogenol E	13632872	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C	456.70	unknown	https://doi.org/10.5586/ASBP.1986.025
Soyasapogenol F	46173902	Click to see	458.70	unknown	https://doi.org/10.5586/ASBP.1986.025
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
5-Methyluridine	445408	Click to see	258.23	unknown	via CMAUP database
Uridine	6029	Click to see	244.20	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine	5789	Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O	242.23	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Arginine	6322	Click to see	174.20	unknown	https://doi.org/10.1021/JF00063A023
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
Hydroxyaspartic acid	3033744	Click to see	149.10	unknown	https://doi.org/10.1016/S0031-9422(00)82832-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoylamino]propanoic acid	66868367	Click to see	359.30	unknown	https://doi.org/10.1080/00021369.1974.10861294
cis-Clovamide	6443790	Click to see C1=CC(=C(C=C1CC(C(=O)O)NC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	359.30	unknown	https://doi.org/10.1021/JF991002+ https://doi.org/10.1016/S0031-9422(00)00098-4
trans-Clovamide	6506968	Click to see	359.30	unknown	https://doi.org/10.1080/00021369.1974.10861294 https://doi.org/10.1021/JF991002+
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
6-(Hydroxymethyl)-6,10,17,17,20,22,23-heptamethyl-2-oxapentacyclo[12.7.1.13,11.05,10.015,20]tricos-14-en-7-ol	5321409	Click to see	458.70	unknown	https://doi.org/10.5586/ASBP.1986.025
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
(2R,3R,4S)-pentane-1,2,3,4-tetrol	10796790	Click to see	136.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
2-Methyl-1-butanol	8723	Click to see	88.15	unknown	https://doi.org/10.1021/JF00122A019
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
5-Deoxy-D-ribitol	166761	Click to see	136.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S,4R)-2-hydroxy-1-methyl-4-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol	11099619	Click to see	332.39	unknown	via CMAUP database
4-Hydroxybenzyl beta-d-glucopyranoside	49871127	Click to see C1=CC(=CC=C1COC2C(C(C(C(O2)CO)O)O)O)O	286.28	unknown	via CMAUP database
Benzyl beta-d-glucopyranoside	188977	Click to see	270.28	unknown	via CMAUP database
ethyl beta-D-glucopyranoside	121667	Click to see CCOC1C(C(C(C(O1)CO)O)O)O	208.21	unknown	via CMAUP database
glycerol 2-O-alpha-l-fucopyranoside	101159096	Click to see	238.23	unknown	via CMAUP database
Icariside F2	14079045	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O	402.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-methoxy-5-prop-2-enyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol	15714546	Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O	504.50	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(2S)-2,3-dihydroxypropyl]-3-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	102021738	Click to see	360.36	unknown	via CMAUP database
Gastrodin	115067	Click to see	286.28	unknown	via CMAUP database
Sasanquin	5317538	Click to see	458.50	unknown	via CMAUP database
Syringin	5316860	Click to see	372.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
1-Deoxy-D-glucitol	10678630	Click to see	166.17	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
2-C-methyl-D-erythritol	11400799	Click to see CC(CO)(C(CO)O)O	136.15	unknown	via CMAUP database
D-Threitol	169019	Click to see C(C(C(CO)O)O)O	122.12	unknown	via CMAUP database
Erythritol	222285	Click to see	122.12	unknown	via CMAUP database
Glycerin	753	Click to see C(C(CO)O)O	92.09	unknown	via CMAUP database
L-Apiitol	10820745	Click to see C(C(C(CO)(CO)O)O)O	152.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
Acetoin	179	Click to see	88.11	unknown	https://doi.org/10.1021/JF00122A019
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
(5-Formylfuran-3-yl)methyl phosphate	25201088	Click to see C1=C(OC=C1COP(=O)([O-])[O-])C=O	204.07	unknown	via CMAUP database
Furfural	7362	Click to see C1=COC(=C1)C=O	96.08	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
1-Penten-3-one	15394	Click to see	84.12	unknown	https://doi.org/10.1021/JF00122A019
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Heptanone	8051	Click to see	114.19	unknown	https://doi.org/10.1021/JF00122A019
2-Hexanone	11583	Click to see	100.16	unknown	https://doi.org/10.1021/JF00122A019
Pentacosane-6,10,16,20-tetrone	86023654	Click to see	408.60	unknown	https://doi.org/10.1271/BBB.100878
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone	7410	Click to see CC(=O)C1=CC=CC=C1	120.15	unknown	https://doi.org/10.1021/JF00122A019
> Organoheterocyclic compounds / Benzodioxoles
Apiole	10659	Click to see	222.24	unknown	via CMAUP database
Dillapiol	10231	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC	222.24	unknown	via CMAUP database
Safrole	5144	Click to see	162.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Anethofuran	126537	Click to see	152.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(5R)-5-hydroxy-4-(7-hydroxy-2H-chromen-3-yl)-5-methylfuran-2-one	163004898	Click to see	260.24	unknown	https://doi.org/10.1271/BBB.56.1955
2(5H)-Furanone, 5-hydroxy-4-(7-hydroxy-2H-1-benzopyran-3-yl)-5-methyl-	101641112	Click to see CC1(C(=CC(=O)O1)C2=CC3=C(C=C(C=C3)O)OC2)O	260.24	unknown	https://doi.org/10.1271/BBB.56.1955
3-(7-hydroxy-2H-chromen-3-yl)-4-oxohex-2-enedioic acid	85684470	Click to see C1C(=CC2=C(O1)C=C(C=C2)O)C(=CC(=O)O)C(=O)CC(=O)O	304.25	unknown	https://doi.org/10.1271/BBB.56.1955
Pratenol A	131752876	Click to see CC1(C(=CC(=O)O1)C2=COC3=C(C2)C=CC(=C3)O)O	260.24	unknown	https://doi.org/10.1271/BBB.56.1955
Pratenol B	131752877	Click to see	304.25	unknown	https://doi.org/10.1271/BBB.56.1955
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
Furan-2-carboxylate	5460151	Click to see	111.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,3aR,8bS)-8a-hydroxy-8,8-dimethyl-3-[[(2R)-4-methyl-5-oxo-2H-furan-2-yl]oxymethylidene]-5,6,7,8b-tetrahydro-3aH-indeno[1,2-b]furan-2-one	5281353	Click to see	346.40	unknown	https://doi.org/10.1016/S0031-9422(98)00419-1
(3Z)-8a-hydroxy-8,8-dimethyl-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxymethylidene]-5,6,7,8b-tetrahydro-3aH-indeno[1,2-b]furan-2-one	131753126	Click to see	346.40	unknown	https://doi.org/10.1016/S0031-9422(98)00419-1
(4S,5R)-4-hydroxy-5-(hydroxymethyl)dihydrofuran-2(3H)-one	161815	Click to see C1C(C(OC1=O)CO)O	132.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives / Folic acids and derivatives / Folic acids
2-[[4-[(2-amino-4-oxo-1H-pteridin-6-yl)methylamino]benzoyl]amino]pentanedioic acid	3405	Click to see	441.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
8-(2,3-Dihydroxy-3-methoxybutoxy)-4-methoxy-1-methylquinolin-2(1H)-one	16219364	Click to see	323.34	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
3-Phenyl-2-propenoic acid methyl ester	7644	Click to see COC(=O)C=CC1=CC=CC=C1	162.18	unknown	https://doi.org/10.1021/JF00122A019
Methyl cinnamate	637520	Click to see COC(=O)C=CC1=CC=CC=C1	162.18	unknown	https://doi.org/10.1021/JF00122A019
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Phaselic acid, (-)-	92299542	Click to see	296.23	unknown	https://doi.org/10.1080/00021369.1974.10861294
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid	322	Click to see	164.16	unknown	https://doi.org/10.1007/BF00566355
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.1007/BF00566355
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten	2355	Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	216.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Xanthotoxol	65090	Click to see	202.16	unknown	https://doi.org/10.1016/J.CLPT.2004.08.023
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin	3083616	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC	222.19	unknown	https://doi.org/10.1016/J.CLPT.2004.08.023
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
Dicoumarol	54676038	Click to see	336.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see	178.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin	5281406	Click to see	352.30	unknown	https://doi.org/10.1016/J.CLPT.2004.08.023
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1016/J.CLPT.2004.08.023
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Graveolone	177751	Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3)C	244.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,7,3',4'-Tetrahydroxyflavanone	246330	Click to see	288.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-)	25201972	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-]	285.23	unknown	via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one	57339948	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(OC4O)CO)O)O)O)O	464.40	unknown	via CMAUP database
Quercetin-7-olate	46906036	Click to see	301.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see	316.26	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1021/JF991002+ https://doi.org/10.1016/S0031-9422(02)00230-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Querciturone	5274585	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-Dihydroxyphenyl)-6-(beta-D-glucopyranosyloxy)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one	5320439	Click to see	478.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one	51402807	Click to see	464.40	unknown	https://doi.org/10.1021/JF991002+ https://doi.org/10.1016/S0021-9673(96)00578-X
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51521831	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/10.1021/JF991002+
3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	5318640	Click to see	610.50	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44258737	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	via CMAUP database
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/10.1021/JF991002+ https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1016/S0003-2670(01)01370-8
Quercetin 3-alloside	12304327	Click to see	464.40	unknown	https://doi.org/10.1021/JF991002+
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	71541772	Click to see	430.40	unknown	via CMAUP database
5-hydroxy-6-methoxy-2-(4-methoxyphenyl)-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-2-oxanyl]oxymethyl]-2-oxanyl]oxy]-1-benzopyran-4-one	6708644	Click to see	622.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-4H-chromen-7-olate	25202413	Click to see	315.25	unknown	via CMAUP database
Chrysoeriol	5280666	Click to see	300.26	unknown	https://doi.org/10.1021/JF991002+
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Pratol	5320693	Click to see	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Pectolinarigenin	5320438	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O	314.29	unknown	https://doi.org/10.1016/S0021-9673(96)00578-X
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Coumestrol	5281707	Click to see C1=CC2=C(C=C1O)OC3=C2C(=O)OC4=C3C=CC(=C4)O	268.22	unknown	https://doi.org/10.1016/J.CLPT.2004.08.023
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain	91510	Click to see	284.26	unknown	https://doi.org/10.1093/JEXBOT/52.357.681
(-)-Maackiain 3-O-glucoside	4485132	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	https://doi.org/10.1007/S10600-008-0007-Y
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol	162993590	Click to see	446.40	unknown	https://doi.org/10.1007/S10600-008-0007-Y
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-6,8,11,19-tetraoxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol	163029154	Click to see	446.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.15-0696
(3S,4S,6S)-2-(hydroxymethyl)-6-[[(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol	44257441	Click to see	446.40	unknown	via CMAUP database
(6aR,11aR)-3,9-Dimethoxy-6H-benzofuro(3,2-c)(1)benzopyran-6a(11aH)-ol	442828	Click to see	300.30	unknown	https://doi.org/10.1016/S0031-9422(00)88922-0
2-(Hydroxymethyl)-6-(6,8,11,19-tetraoxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-yloxy)oxane-3,4,5-triol	163029153	Click to see	446.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.15-0696
3-Hydroxy-8,9-methylenedioxypterocarpane	363863	Click to see	284.26	unknown	https://doi.org/10.1039/P19840002831 https://doi.org/10.1016/0048-4059(84)90061-4
Medicarpin	336327	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O	270.28	unknown	https://doi.org/10.1039/P19840002831
Medicocarpin	44257429	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O	432.40	unknown	via CMAUP database
Trifolirhizin	442827	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	https://doi.org/10.1016/0048-4059(84)90061-4
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
CID 11777207	11777207	Click to see	257.21	unknown	via CMAUP database
Daidzein	5281708	Click to see	254.24	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1815392/ https://doi.org/10.1016/S1570-0232(02)00079-X https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1016/S0021-9673(99)00110-7 https://doi.org/10.1097/GME.0B013E318156F9D6 https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1016/J.FITOTE.2006.01.004
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/J.FITOTE.2006.01.004 https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1097/GME.0B013E318156F9D6 https://doi.org/10.1016/S1570-0232(02)00079-X https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1815392/ https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1093/OXFORDJOURNALS.JHERED.A102397 https://doi.org/10.1021/JF991002+ https://doi.org/10.1007/S10600-008-9008-0 https://doi.org/10.1016/S0021-9673(99)00110-7
Genistein(1-)	25201420	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)[O-])O)O	269.23	unknown	via CMAUP database
Glycitein	5317750	Click to see	284.26	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
Irilone	5281779	Click to see	298.25	unknown	https://doi.org/10.1021/JF991002+ https://doi.org/10.1016/S0003-2670(01)01370-8
Isoprunetin	5748551	Click to see	284.26	unknown	via CMAUP database
Orobol	5281801	Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
Pseudobaptigenin	5281805	Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O	282.25	unknown	https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1021/JF991002+
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	44257270	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-(8-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl)phenoxy]oxan-2-yl]methyl acetate	102463150	Click to see	486.40	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
3-(4-methoxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	124462687	Click to see	430.40	unknown	https://doi.org/10.1007/S10600-008-0007-Y
3-(4-methoxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154497130	Click to see	430.40	unknown	https://doi.org/10.1021/JF991002+
3-(4-methoxyphenyl)-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44257215	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1021/JF991002+ https://doi.org/10.1055/S-2007-969907 https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/S0021-9673(96)00578-X
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid	57378778	Click to see	532.40	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-(5-hydroxy-7-methoxy-4-oxochromen-3-yl)phenoxy]oxan-2-yl]methoxy]propanoic acid	101010453	Click to see	532.40	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-(8-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl)phenoxy]oxan-2-yl]methoxy]propanoic acid	102463145	Click to see C1OC2=C(O1)C=C3C(=C2)C(=O)C(=CO3)C4=CC=C(C=C4)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O	530.40	unknown	https://doi.org/10.1021/JF991002+
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[6-hydroxy-3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid	102463147	Click to see	532.40	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162985648	Click to see	432.40	unknown	https://doi.org/10.1007/S10600-008-9008-0
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154496625	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JF991002+
5-hydroxy-7-methoxy-3-[4-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	124677596	Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1007/BF00564619
5-hydroxy-7-methoxy-3-[4-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	154497291	Click to see	446.40	unknown	https://doi.org/10.1021/JF991002+
Afrormosin 7-O-beta-d-glucoside-6''-O-malonate	102463146	Click to see	546.50	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
Biochanin A 7-(6-malonylglucoside)	131751062	Click to see	532.40	unknown	https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1021/JF991002+
Calycosin 7-galactoside	91973796	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1134/S1068162011070041
Calycosin 7-o-beta-D-glucoside	5318267	Click to see	446.40	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
Daidzin	107971	Click to see	416.40	unknown	https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1021/JF991002+
Genistin	5281377	Click to see	432.40	unknown	https://doi.org/10.1007/S10600-008-9008-0 https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1021/JF991002+
Genistoside	5284639	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1007/S10600-008-9008-0
Malonylgenistin	15934091	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O	518.40	unknown	https://doi.org/10.1021/JF991002+
Npc198030	3733033	Click to see	430.40	unknown	https://doi.org/10.1007/S10600-008-0007-Y
Ononin	442813	Click to see	430.40	unknown	https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1021/JF991002+ https://doi.org/10.1016/S0021-9673(01)01231-6
Prunetin 4'-O-glucoside	16398538	Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1007/BF00564821
Prunetrin	5918474	Click to see	446.40	unknown	https://doi.org/10.1007/BF00564619 https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1021/JF991002+ https://doi.org/10.1016/S0021-9673(96)00578-X
Pseudobaptigenin 7-O-glucoside	44257230	Click to see	444.40	unknown	https://doi.org/10.1021/JF991002+
Rothindin	3085261	Click to see	444.40	unknown	https://doi.org/10.1021/JF991002+
Sissotrin	5280781	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1021/JF991002+
Sissotrin with HPLC, 99+% [5928-26-7]	45934014	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1021/JF991002+
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
4'-Methoxy-3',5,7-trihydroxyisoflavone	5281803	Click to see	300.26	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1021/JF991002+
Calycosin	5280448	Click to see	284.26	unknown	https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/S0031-9422(00)94679-X
Pratensein(1-)	25201808	Click to see	299.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afromosin	5281704	Click to see	298.29	unknown	https://doi.org/10.1021/JF991002+
Biochanin A	5280373	Click to see	284.26	unknown	https://doi.org/10.1016/0304-3835(91)90044-I https://doi.org/10.1055/S-2007-969907 https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1007/BF02969267 https://doi.org/10.1016/S1570-0232(02)00079-X https://doi.org/10.1021/JF991002+ https://doi.org/10.1093/OXFORDJOURNALS.JHERED.A102397 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1815392/ https://doi.org/10.1271/BBB.100878 https://doi.org/10.1097/GME.0B013E318156F9D6 https://doi.org/10.1016/J.FITOTE.2006.01.004 https://doi.org/10.1016/S0021-9673(99)00110-7
biochanin A(1-)	25203224	Click to see	283.25	unknown	via CMAUP database
CID 10378473	10378473	Click to see	271.24	unknown	via CMAUP database
Formononetin	5280378	Click to see	268.26	unknown	https://doi.org/10.1021/JF991002+ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1815392/ https://doi.org/10.1097/GME.0B013E318156F9D6 https://doi.org/10.1016/S0021-9673(01)01231-6 https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1016/S0021-9673(99)00110-7 https://doi.org/10.1016/S0021-9673(96)00578-X https://doi.org/10.1016/S1570-0232(02)00079-X https://doi.org/10.1093/JEXBOT/52.357.681 https://doi.org/10.1039/P19840002831 https://doi.org/10.1007/S10600-008-9008-0 https://doi.org/10.1007/S10600-008-0007-Y
Texasin	5281812	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)O)O	284.26	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Prunetin	5281804	Click to see	284.26	unknown	https://doi.org/10.1016/S0003-2670(01)01370-8 https://doi.org/10.1021/JF991002+ https://doi.org/10.1007/S10600-008-9008-0
> Phenylpropanoids and polyketides / Tannins
1,2,3-Tri-O-galloyl-beta-D-glucose	5322038	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO)O	636.50	unknown	via CMAUP database

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Trifolium pratense

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