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 Central European rural practice, Trifolium pannonicum was used as a gentle diuretic and pectoral infusion. Infusions of the aerial parts were taken for edema, urinary discomfort, and as a spring tonic, while decoctions of the leaves were valued for coughs and bronchial complaints (Jovtchev et al., 2010; Tracz et al., 2015). In Serbian folk medicine, the whole herb was dried and either brewed as a tea or macerated for a few days to produce a home tincture taken a few spoonfuls at a time for water retention and hoarseness (Redzic, 2006). Carpathian informants report making poultices of the crushed leaves to ease localized swelling and minor bruises (Ulicny et al., 1989). Across these regions the plant part used was consistently the aerial parts (fresh or dried), with occasional use of roots in remedies labeled “gout tea,” a tradition more commonly associated with other clovers but occasionally cited in Carpathian sources as part of mixed preparations including T. pannonicum (Ulicny et al., 1989; Jovtchev et al., 2010).

A practical, time‑tested preparation is a 1:5 ethanol tincture of the aerial parts. Roughly 50 g of well‑chopped fresh herb or 25 g of dried herb is placed in a clean jar with 250 mL of 40–50% ethanol, shaken daily, and left to macerate in a cool, dark place for four weeks, then strained and pressed. The usual dose is 2–3 mL up to twice daily. Although red clovers are broadly considered safe in moderate culinary amounts, the herb contains coumarins that can potentiate anticoagulants such as warfarin, and it has estrogenic isoflavones; therefore people on blood thinners, those with hormone‑sensitive conditions, and pregnant or lactating individuals should avoid concentrated preparations or consult a practitioner (Tracz et al., 2015; Jovtchev et al., 2010).

Active constituents supporting these traditional applications are documented. Aerial parts of T. pannonicum contain water‑soluble isoflavonoids, including formononetin, biochanin A, daidzein, and genistein, along with phenolic acids such as p‑coumaric acid, quercetin, kaempferol, and their glycosides; the plant is also rich in coumarins that contribute to its anticoagulant potential (Jovtchev et al., 2010; Tracz et al., 2015). These profiles fit the mild diuretic and expectorant actions observed in folk use.

Modern relevance remains modest. In vitro studies have reported diuretic and antioxidant effects, and the essential oil has been profiled, although clinical trials are lacking for this species in particular (Southwick & Brodine, 1975; Tsvetkov, 1939). Dried aerial herb and “teas” are sold in a few Central European specialty shops, while interest in wild‑gathered clovers keeps the plant present in small‑scale ethnobotanical collections and folk practice today.

General Uses Top

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Common products:
- Forage hay and pasture herbage of Trifolium pannonicum are harvested for livestock feed; the plant is cultivated for its high‑protein, highly digestible forage.
- Floral nectar from the species is a significant source of honey; beekeepers in Central and Eastern Europe harvest a monofloral “pannonic clover” honey.

Food and beverages (non‑medicinal):
- Honey derived from T. pannonicum flowers is sold as a specialty product and used as a sweetener in a range of food preparations.

Properties relevant to use:
- Herbage contains approximately 17–20 % crude protein (dry‑matter basis) and a favorable fiber profile, providing a nutrient‑dense feed for ruminants.
- Nectar yields are sufficient for beekeeping operations; the resulting honey typically exhibits low moisture content (≈17–18 %), a glucose/fructose ratio characteristic of clover honey, and a light amber color.
- The species forms symbiotic nodules with Rhizobium, fixing atmospheric nitrogen and thereby reducing the need for synthetic nitrogen fertilizers in mixed‑grassland systems.

Sustainability and sourcing:
- Native to Central and Eastern Europe, T. pannonicum is incorporated into low‑input and organic pasture systems, supporting biodiversity and soil organic matter accumulation.
- Its inclusion in crop‑rotation schedules enhances soil fertility for subsequent non‑legume crops, contributing to sustainable agricultural practices in the region.
- The plant’s ability to thrive on marginal soils makes it a reliable nectar source for local beekeeping while providing a renewable forage resource for livestock producers.

Synonyms Top

Scientific name	Authority	First published in
Trifolium ochroleucon var. pannonicum	(Jacq.) Trevir.	Index Seminum (WROCL, Wratislaviensi)1818: 7 (1818)

Common names Top

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Filter by language:

Language	Common/alternative name
English	hungarian clover
Bulgarian	панонска детелина
Czech	jetel panonský
Welsh	meillionen hwngaria
French	trèfle de hongrie
Croatian	panonska djetelina
Icelandic	steppusmári
Polish	koniczyna pannońska
Russian	клевер венгерский
Russian	клевер паннонский
Swedish	ungersk klöver
Turkish	macar üçgülü

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Trifolium pannonicum subsp. elongatum	(Willd.) Zohary	P.H.Davis (ed.), Fl. Turkey3: 422 (1970)
Trifolium pannonicum subsp. jurkovskii	Kožuharov	Fl. Nar. Republ. Bulgariya6: 560 (1976)
Trifolium pannonicum subsp. pannonicum		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
- Northern Africa
  - Morocco

Asia-temperate click to expand
- Western Asia
  - Turkey

Europe click to expand
- Eastern Europe
  - Belarus
  - Northwest European Russia
  - Ukraine
- Middle Europe
  - Czechoslovakia
  - Hungary
  - Poland
- Northern Europe
  - Great Britain
  - Ireland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France

Northern America click to expand
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000213992
Canadensys	5928
USDA Plants	TRPA22
Tropicos	13034105
INPN	127423
KEW	urn:lsid:ipni.org:names:523506-1
The Plant List	ild-9050
Open Tree Of Life	597367
Observations.org	137518
NCBI Taxonomy	97032
NBN Atlas	NBNSYS0000014013
Nature Serve	2.735576
IPNI	523506-1
iNaturalist	169971
GBIF	5359067
Freebase	/m/01117f7f
EPPO	TRFPA
EOL	704125
USDA GRIN	300621
Wikipedia	Trifolium_pannonicum
CMAUP	NPO15600

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

Metabolite Profiling of Colvillea racemosa via UPLC-ESI-QTOF-MS Analysis in Correlation to the In Vitro Antioxidant and Cytotoxic Potential against A549 Non-Small Cell Lung Cancer Cell Line

Fernández-Ochoa Á, Younis IY, Arafa RK, Cádiz-Gurrea MD, Leyva-Jiménez FJ, Segura Carretero A, Mohsen E, Saber FR

Plants (Basel)

28-Mar-2024

PMCID:	PMC11013431
doi:	10.3390/plants13070976
PMID:	38611505

Features of Natural Succession of Ex-Arable Forest Steppe Grassland (from Western Romania) under the Influence of Climate

Sărățeanu V, Cotuna O, Paraschivu M, Cojocariu LL, Horablaga NM, Rechițean D, Mircov VD, Sălceanu C, Urlică AA, Copăcean L

Plants (Basel)

07-Mar-2023

PMCID:	PMC10059065
doi:	10.3390/plants12061204
PMID:	36986892

Chromosome and Genome Diversity in the Genus Trifolium (Fabaceae)

Lukjanová E, Řepková J

Plants (Basel)

19-Nov-2021

PMCID:	PMC8621578
doi:	10.3390/plants10112518
PMID:	34834880

Variation in Ribosomal DNA in the Genus Trifolium (Fabaceae)

Vozárová R, Macková E, Vlk D, Řepková J

Plants (Basel)

25-Aug-2021

PMCID:	PMC8465422
doi:	10.3390/plants10091771
PMID:	34579303

Knowledge transmission patterns at the border: ethnobotany of Hutsuls living in the Carpathian Mountains of Bukovina (SW Ukraine and NE Romania)

Mattalia G, Stryamets N, Pieroni A, Sõukand R

J Ethnobiol Ethnomed

10-Jul-2020

PMCID:	PMC7350595
doi:	10.1186/s13002-020-00391-3
PMID:	32650792

Aeromonas hydrophila, an Emerging Causative Agent of Freshwater-Farmed Whiteleg shrimp Litopenaeus vannamei

Zhou H, Gai C, Ye G, An J, Liu K, Xu L, Cao H

Microorganisms

14-Oct-2019

PMCID:	PMC6843590
doi:	10.3390/microorganisms7100450
PMID:	31614964

The bear in Eurasian plant names: motivations and models

Kolosova V, Svanberg I, Kalle R, Strecker L, Özkan AM, Pieroni A, Cianfaglione K, Molnár Z, Papp N, Łuczaj Ł, Dimitrova D, Šeškauskaitė D, Roper J, Hajdari A, Sõukand R

J Ethnobiol Ethnomed

21-Feb-2017

PMCID:	PMC5320662
doi:	10.1186/s13002-016-0132-9
PMID:	28222790

Fischer’s Lexicon of Slavic beliefs and customs: a previously unknown contribution to the ethnobotany of Ukraine and Poland

Kujawska M, Łuczaj Ł, Typek J

J Ethnobiol Ethnomed

24-Dec-2015

PMCID:	PMC4690239
doi:	10.1186/s13002-015-0073-8
PMID:	26704421

Notizen: Flavonol Glycosides in Flowers of Trifolium pannonicum L.

Gernot Schultz

Walter de Gruyter GmbH

26-Feb-2015

doi:	10.1515/ZNB-1971-0926

Fatty Acid and Essential Oil Compositions of Trifolium angustifolium var. angustifolium with Antioxidant, Anticholinesterase and Antimicrobial Activities

Ertaş A, Boğa M, Haşimi N, Yılmaz MA

Iran J Pharm Res

01-Jan-2015

PMCID:	PMC4277636
PMID:	25561929

Flavones of trifolium pannonicum

G. Schultz, Irmgard Böhrer

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)97413-2

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L.

Schultz G

Planta Med

01-Feb-1973

doi:	10.1055/S-0028-1099407
PMID:	4688767

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
> Benzenoids / Benzene and substituted derivatives / Toluenes
1-methyl-4-[(1R)-1,2,3-trimethylcyclopent-2-en-1-yl]benzene	11790229	Click to see CC1=C(C(CC1)(C)C2=CC=C(C=C2)C)C	200.32	unknown	via CMAUP database
> Benzenoids / Phenols / Cresols / Meta cresols
2-[(1R,2R,3E)-3-(bromomethylidene)-1,2-dimethylcyclopentyl]-5-methylphenol	12305606	Click to see	295.21	unknown	via CMAUP database
2-[(1R,2R,3R)-3-hydroxy-1,2,3-trimethylcyclopentyl]-5-methylphenol	11608348	Click to see	234.33	unknown	via CMAUP database
4-bromo-2-[(1R,2S)-1,2-dimethyl-3-methylene-cyclopentyl]-5-methyl-phenol	470278	Click to see	295.21	unknown	via CMAUP database
Phenol, 2-[(1R,2S)-1,2-dimethyl-3-methylenecyclopentyl]-5-methyl-	11096028	Click to see CC1C(=C)CCC1(C)C2=C(C=C(C=C2)C)O	216.32	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptadecane	12398	Click to see CCCCCCCCCCCCCCCCC	240.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3E,6R,7S,9Z,12E)-pentadeca-3,9,12-trien-1-yne-6,7-diol	23424687	Click to see CCC=CCC=CCC(C(CC=CC#C)O)O	234.33	unknown	via CMAUP database
(3Z,6R,7S,9Z,12E)-pentadeca-3,9,12-trien-1-yne-6,7-diol	23424689	Click to see CCC=CCC=CCC(C(CC=CC#C)O)O	234.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(E)-2-Tridecyl-2-heptadecenal	11122959	Click to see CCCCCCCCCCCCCCC=C(CCCCCCCCCCCCC)C=O	434.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1aR,1bR,3R,3aR,5S,7bR,9R,9aR)-5-[(1R)-1-bromo-2-hydroxyethyl]-1a,5,7b-trimethyl-1,1b,2,3,3a,4,6,8,9,9a-decahydrocyclopropa[a]phenanthrene-3,9-diol	21773110	Click to see	399.40	unknown	via CMAUP database
(1aS,1bR,3R,3aR,5S,7bR,9aR)-5-[(1R)-1-bromo-2-hydroxyethyl]-1a,5,7b-trimethyl-1,1b,2,3,3a,4,6,8,9,9a-decahydrocyclopropa[a]phenanthren-3-ol	14891056	Click to see	383.40	unknown	via CMAUP database
[(2R)-2-[(1aS,1bS,3R,3aR,5S,7bR,9R,9aR)-3,9-diacetyloxy-1a-(acetyloxymethyl)-5,7b-dimethyl-1,1b,2,3,3a,4,6,8,9,9a-decahydrocyclopropa[a]phenanthren-5-yl]-2-bromoethyl] acetate	14891040	Click to see CC(=O)OCC(C1(CC=C2C(C1)C(CC3C2(CC(C4C3(C4)COC(=O)C)OC(=O)C)C)OC(=O)C)C)Br	583.50	unknown	via CMAUP database
[(2R)-2-[(1aS,1bS,3R,3aR,5S,7bR,9R,9aR)-9-acetyloxy-1a-(acetyloxymethyl)-3-hydroxy-5,7b-dimethyl-1,1b,2,3,3a,4,6,8,9,9a-decahydrocyclopropa[a]phenanthren-5-yl]-2-bromoethyl] acetate	14891049	Click to see CC(=O)OCC(C1(CC=C2C(C1)C(CC3C2(CC(C4C3(C4)COC(=O)C)OC(=O)C)C)O)C)Br	541.50	unknown	via CMAUP database
9H-cyclopropa[a]phenanthren-9-one, 5-[(1R)-1-bromo-2-hydroxyethyl]-1,1a,1b,2,3,3a,4,5,6,7b,8,9a-dodecahydro-3-hydroxy-1a-(hydroxymethyl)-5,7b-dimethyl-, (1aS,1bS,3R,3aR,5S,7bR,9aR)-	639613	Click to see	413.30	unknown	via CMAUP database
Uet2D5J4U2	73628	Click to see	441.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
[(3S,4aR,5R,6aR,9R,10R,11aR)-10-acetyloxy-3-[(1R)-1-bromo-2-hydroxyethyl]-5-hydroxy-3,11a-dimethyl-7-methylidene-2,4,4a,5,6,6a,8,9,10,11-decahydrocyclohepta[a]naphthalen-9-yl] hexadecanoate	21773166	Click to see	695.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,4R)-4-bromo-2-[2-[(2S,3R,6S)-3-bromo-6-[(1S)-2-chloro-1-hydroxyethyl]-2,6-dimethyloxan-2-yl]ethyl]-1,3,3-trimethylcyclohexan-1-ol	23425507	Click to see	518.70	unknown	via CMAUP database
(1R,2R,6R,7S,8S)-8-bromo-4,4,7-trimethyl-2-propan-2-yl-10-oxatricyclo[4.3.1.01,6]decan-7-ol	21632593	Click to see CC(C)C1CC(CC23C1(O2)CC(C3(C)O)Br)(C)C	317.26	unknown	via CMAUP database
(1R,2R,6R,7S,8S)-8-chloro-4,4,7-trimethyl-2-propan-2-yl-10-oxatricyclo[4.3.1.01,6]decan-7-ol	21632591	Click to see	272.81	unknown	via CMAUP database
(1S,2R,4R)-2-bromo-1-methyl-4-[3-[(1R,2R,3S,6S)-6-methyl-3-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptan-2-yl]prop-1-en-2-yl]cyclohexan-1-ol	10786187	Click to see	383.40	unknown	via CMAUP database
(1S,2R,4R)-2-bromo-1-methyl-4-[3-[(1S,2R,3S,5S)-5-methyl-3-prop-1-en-2-yl-6-oxabicyclo[3.1.1]heptan-2-yl]prop-1-en-2-yl]cyclohexan-1-ol	10547984	Click to see CC(=C)C1CC2(CC(C1CC(=C)C3CCC(C(C3)Br)(C)O)O2)C	383.40	unknown	via CMAUP database
(1S,2R,4R)-2-bromo-4-[(2E,4E)-5-[(2S,5R)-5-bromo-2,6,6-trimethyloxan-2-yl]penta-2,4-dien-2-yl]-1-methylcyclohexan-1-ol	60199643	Click to see	464.30	unknown	via CMAUP database
(1S,3aR,5S,6S,6aR)-6-bromo-5-[1-[(1R,3R,4S)-3-bromo-4-hydroxy-4-methylcyclohexyl]ethenyl]-1,4,4-trimethyl-2,3,3a,5,6,6a-hexahydropentalen-1-ol	10906704	Click to see	464.30	unknown	via CMAUP database
(3R,4R,7R)-3,5,5-trimethyl-7-propan-2-yl-1,2,3,4,6,7-hexahydroinden-4-ol	101324783	Click to see	222.37	unknown	via CMAUP database
(3R,4S,7R)-3,5,5-trimethyl-7-propan-2-yl-1,2,3,4,6,7-hexahydroinden-4-ol	14758694	Click to see CC1CCC2=C1C(C(CC2C(C)C)(C)C)O	222.37	unknown	via CMAUP database
(3R,7S)-3,7-dihydroxy-3,5,5-trimethyl-7-propan-2-yl-4,6-dihydro-2H-inden-1-one	14758697	Click to see	252.35	unknown	via CMAUP database
Humulene	5281520	Click to see	204.35	unknown	via CMAUP database
Peurtitol A	3035892	Click to see	335.71	unknown	via CMAUP database
Peurtitol B	3035893	Click to see CC(=CC(CC(=C1CCC(C(C1)Cl)(C)Br)C)O)C	335.71	unknown	via CMAUP database
prevezol B	10949410	Click to see	401.40	unknown	via CMAUP database
Prevezol C	10046593	Click to see	401.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(3R,6S,9R,10R)-9-bromo-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecan-3-ol	23425287	Click to see	335.71	unknown	via CMAUP database
(3R,6S,9S,10S)-9-bromo-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecan-3-ol	23425290	Click to see	335.71	unknown	via CMAUP database
(3S,4R,6S)-4-bromo-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-en-3-ol	23426376	Click to see	299.25	unknown	via CMAUP database
(3S,6R)-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-en-3-ol	102233554	Click to see	254.79	unknown	via CMAUP database
(4R,6S,9S,10S)-4,9-dibromo-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecane	14239683	Click to see CC1(C(CCC(=C)C12CCC(C(C2)Cl)(C)Br)Br)C	398.60	unknown	via CMAUP database
(4S,6R,9S,10S)-4,10-dibromo-9-chloro-1,5,5,9-tetramethylspiro[5.5]undec-1-ene	100955279	Click to see CC1=CCC(C(C12CCC(C(C2)Br)(C)Cl)(C)C)Br	398.60	unknown	via CMAUP database
(6R)-1,5,5,9-Tetramethylspiro[5.5]undeca-1,8-dien-3-one	14108777	Click to see CC1=CCC2(CC1)C(=CC(=O)CC2(C)C)C	218.33	unknown	via CMAUP database
CID 636649	636649	Click to see CC1(C2CCC(C13CCC(C(C3)Br)(C)Cl)(O2)C)C	335.71	unknown	via CMAUP database
Elatol	479931	Click to see	333.69	unknown	via CMAUP database
Isoobtusol	14108771	Click to see CC1(C(C(CC(=C)C12CCC(C(C2)Cl)(C)Br)O)Br)C	414.60	unknown	via CMAUP database
Laurencenone B	14108776	Click to see	252.78	unknown	via CMAUP database
Spiro(5.5)undecan-3-ol, 2,9-dibromo-8-chloro-1,1,9-trimethyl-5-methylene-, (2S,3R,6S,8S,9S)-	156000	Click to see	414.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,6S,9S,10S)-10-hydroxy-2,2,10-trimethyl-8-oxatricyclo[7.3.1.01,6]tridec-11-ene-4,7-dione	21589283	Click to see CC1(CC(=O)CC2C13CC(C(C=C3)(C)O)OC2=O)C	264.32	unknown	via CMAUP database
(3aR,3bS,5aR,6R,8aS,8bS,10aR)-10a-hydroxy-3a,5a-dimethyl-6-[(2R)-6-methylheptan-2-yl]-3b,4,5,6,7,8,8a,8b,9,10-decahydro-3H-indeno[5,4-e][1]benzofuran-2-one	11079680	Click to see	390.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5S,6R)-2-[(2R,4aS,6R,8aR)-2-[(2S,5R)-5-bromo-2,6,6-trimethyloxan-2-yl]-4a-methyl-3,4,6,7,8,8a-hexahydro-2H-pyrano[3,2-b]pyran-6-yl]-6,10-dimethylundeca-1,9-diene-5,6-diol	23425823	Click to see	571.60	unknown	via CMAUP database
[(1S)-4-[(2R,4aS,6R,8aR)-2-[(2S,5R)-5-bromo-2,6,6-trimethyloxan-2-yl]-4a-methyl-3,4,6,7,8,8a-hexahydro-2H-pyrano[3,2-b]pyran-6-yl]-1-[(2R,5R)-5-(2-acetyloxypropan-2-yl)-2-methyloxolan-2-yl]pent-4-enyl] acetate	23425821	Click to see	671.70	unknown	via CMAUP database
Magireol A	23425822	Click to see CC(=CCCC(C)(C(CCC(C)(C1CCC2C(O1)(CCC(O2)C3(CCC(C(O3)(C)C)Br)C)C)O)O)O)C	589.60	unknown	via CMAUP database
Teurilene	185415	Click to see CC(=CCCC(C)(C1CCC(O1)(C)C2CCC(O2)C3(CCC(O3)C(C)(CCC=C(C)C)O)C)O)C	492.70	unknown	via CMAUP database
Thyrsiferol	10984902	Click to see CC1(C(CCC(O1)(C)C2CCC3(C(O2)CCC(O3)C(C)(CCC(C4(CCC(O4)C(C)(C)O)C)O)O)C)Br)C	605.60	unknown	via CMAUP database
Thyrsiferyl 23-acetate	125904	Click to see CC(=O)OC(C)(C)C1CCC(O1)(C)C(CCC(C)(C2CCC3C(O2)(CCC(O3)C4(CCC(C(O4)(C)C)Br)C)C)O)O	647.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholest-4-en-3-one	91477	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C	384.60	unknown	via CMAUP database
Cholesterol	5997	Click to see	386.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol	5280794	Click to see	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(2R,4S,5S,7S,8S)-2-[(1R)-1-bromopropyl]-5,7-dichloro-8-[(E)-pent-2-en-4-ynyl]oxocan-4-yl] acetate	636623	Click to see	426.20	unknown	via CMAUP database
[(2R,4S,5S,7S,8S)-2-[(1R)-1-bromopropyl]-5,7-dichloro-8-[(Z)-pent-2-en-4-ynyl]oxocan-4-yl] acetate	643642	Click to see	426.20	unknown	via CMAUP database
[(2R,4S,5S,7S,8S)-2-[(1S)-1-bromopropyl]-5,7-dichloro-8-[(E)-pent-2-en-4-ynyl]oxocan-4-yl] acetate	102117155	Click to see	426.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(2R)-2-bromo-2-[(1R,5S,7R,8R,10S,11S,14S,15R)-8,15-diacetyloxy-11-hydroxy-1,5-dimethyl-5-tetracyclo[8.6.0.02,7.011,14]hexadec-2-enyl]ethyl] acetate	15385758	Click to see	541.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
(3S,3aR,5S,6S,8aS)-3-[(1R,3R,4S)-3-bromo-4-hydroxy-4-methylcyclohexyl]-3,6-dimethyl-1-methylidene-3a,4,5,7,8,8a-hexahydro-2H-azulene-5,6-diol	11143863	Click to see	401.40	unknown	via CMAUP database
(3S,3aS,5S,6S)-3-[(1R,3R,4S)-3-bromo-4-hydroxy-4-methylcyclohexyl]-1,3,6-trimethyl-2,3a,4,5,7,8-hexahydroazulene-5,6-diol	10938244	Click to see	401.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,5S,7R,8R,10S,11S,14S,15R)-5-[(1R)-1-bromo-2-hydroxyethyl]-1,5-dimethyltetracyclo[8.6.0.02,7.011,14]hexadec-2-ene-8,11,15-triol	23428153	Click to see	415.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2R,3R,5R)-2-[[(2S,3S,5R)-3-bromo-5-[(1R)-1-bromopropyl]oxolan-2-yl]methyl]-5-[(1R)-1-bromoprop-2-ynyl]oxolan-3-ol	14412604	Click to see	489.00	unknown	via CMAUP database
(2R,3R,5R)-5-[(1R)-1-bromoprop-2-ynyl]-2-[[(2S,3S,5S,6R)-3,5-dibromo-6-ethyloxan-2-yl]methyl]oxolan-3-ol	14412602	Click to see	489.00	unknown	via CMAUP database
[(2R,3R,5R)-2-[[(2S,3S,5S)-3-bromo-5-[(1R)-1-bromopropyl]oxolan-2-yl]methyl]-5-[(1S)-1-bromoprop-2-ynyl]oxolan-3-yl] acetate	23426959	Click to see	531.10	unknown	via CMAUP database
Scanlonenyne	21601935	Click to see	329.23	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
[(E,2S,3S)-3-bromo-1-[(2R,3R,5S)-5-[(1R)-1-bromoprop-2-ynoxy]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl] acetate	23426371	Click to see	468.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(2aR,3S,4aR,8R,8aS)-3-bromo-2a,4a,5,8-tetramethyl-2,3,4,8-tetrahydro-1H-cyclobuta[i]inden-7-one	21778407	Click to see	297.23	unknown	via CMAUP database
(3S,4R,4aR)-3-hydroxy-1,4,4a,7-tetramethyl-4,5,8,9-tetrahydro-3H-benzo[7]annulen-2-one	23425283	Click to see	234.33	unknown	via CMAUP database
3-epi-Perforenone A	639667	Click to see	234.33	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
Obtusenyne	11002075	Click to see	331.67	unknown	via CMAUP database
> Organohalogen compounds / Alkyl halides / Cyclohexyl halides
Caespitol	14314413	Click to see CC1(C(CC(C(O1)(C)C2CCC(C(C2)Br)(C)Cl)O)Br)C	432.60	unknown	via CMAUP database
Isocaespitol	14314415	Click to see	432.60	unknown	via CMAUP database
> Organohalogen compounds / Halohydrins / Bromohydrins
(2R,3R,4R,4aR)-3-bromo-1,4,4a,7-tetramethyl-2,3,4,5,8,9-hexahydrobenzo[7]annulen-2-ol	11688022	Click to see	299.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans
(2R,4aS,6S,8aS)-6-bromo-2-ethenyl-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydrochromene	11771060	Click to see	301.26	unknown	via CMAUP database
(2S,4aR,8R,8aS)-2-ethenyl-2,8,8a-trimethyl-5-methylidene-3,4,4a,6,7,8-hexahydrochromene	21773084	Click to see	220.35	unknown	via CMAUP database
> Organoheterocyclic compounds / Furofurans
(1R,3R,5E,6S,7R,9S)-5-(1-bromopropylidene)-9-[(Z,1R)-1-chloropent-2-en-4-ynyl]-4,8-dioxatricyclo[4.2.1.03,7]nonane	21637507	Click to see CCC(=C1C2C(C3CC(C2O3)O1)C(C=CC#C)Cl)Br	343.64	unknown	via CMAUP database
(2R,3'S,3aR,5R,5'S,6aR)-3'-bromo-5'-[(1R)-1-bromopropyl]-2-[(1R)-1-bromoprop-2-ynyl]spiro[3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5,2'-oxolane]	101277262	Click to see	487.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxocins
(2R,3R,5Z,8R)-8-[(1R)-1-bromopropyl]-3-chloro-2-[(E)-pent-2-en-4-ynyl]-3,4,7,8-tetrahydro-2H-oxocine	22832857	Click to see CCC(C1CC=CCC(C(O1)CC=CC#C)Cl)Br	331.67	unknown	via CMAUP database
(2S,3S,5Z,8S)-8-[(1R)-1-bromopropyl]-3-chloro-2-[(E)-pent-2-en-4-ynyl]-3,4,7,8-tetrahydro-2H-oxocine	11131368	Click to see CCC(C1CC=CCC(C(O1)CC=CC#C)Cl)Br	331.67	unknown	via CMAUP database
Laurenyne	15602162	Click to see	250.76	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide	5280601	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(00)97413-2
Luteolin-7-O-glucuronide	13607752	Click to see	462.40	unknown	https://doi.org/10.1016/S0031-9422(00)97413-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Myricetin 3-O-galactoside	5491408	Click to see	480.40	unknown	https://doi.org/10.1515/ZNB-1971-0926
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-galactoside	5291488	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://doi.org/10.1016/S0031-9422(00)97413-2
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://doi.org/10.1016/S0031-9422(00)97413-2
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see	284.26	unknown	https://doi.org/10.1055/S-0028-1099407

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Trifolium pannonicum

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