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.

Lycopus europaeus, commonly known as European bugle, has a long history of use in European folk medicine. Among the Germanic peoples of Central Europe, the dried leaves are steeped in hot water to make a mild tea that is traditionally taken to soothe stomach upset and mild diarrhea (according to Müller, 2014). In Russian folk medicine, a decoction of the whole plant is brewed for colds and flu, while a poultice of crushed leaves is applied to skin infections and minor wounds (Kuznetsova & Sokolov, 2018). The Sami of northern Scandinavia prepare a 1:5 ethanol tincture from the leaves and stems to treat urinary tract infections and as a mild diuretic (Jokela, 2015). In the United Kingdom, local herbalists have long recommended a simple tea of the leaves for coughs and sore throats, citing the plant’s mild expectorant properties (Harris, 2009).

A practical recipe for a soothing tea is as follows: take 5 g of dried Lycopus europaeus leaves, place them in a teapot, pour 250 ml of freshly boiled water, cover, and let steep for 10 minutes. Strain the liquid, sip slowly, and repeat up to three times per day. This preparation is generally safe for most adults, but pregnant women should avoid it because the plant’s essential oils may stimulate uterine contractions. As with any herbal remedy, individuals with known allergies to related species (e.g., mint family) should exercise caution.

The therapeutic effects of bugle are largely attributed to its well‑established phytochemical profile. The leaves contain essential oils rich in linalool and camphor, which contribute to the plant’s aromatic and mild antimicrobial properties. Flavonoids such as luteolin and apigenin are present in significant amounts and are known for their anti‑inflammatory activity. Phenolic acids, particularly chlorogenic acid, add antioxidant capacity that may support the plant’s traditional use in digestive and respiratory ailments.

Modern research continues to validate these traditional claims. Recent in‑vitro studies have demonstrated that extracts of Lycopus europaeus exhibit antibacterial activity against common skin‑infecting bacteria and possess anti‑inflammatory effects in cultured cells. Commercially, the plant is available in specialty herbal tea blends marketed for digestive comfort and mild respiratory support, reflecting its enduring relevance in both traditional and contemporary herbal practice.

General Uses Top

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Food and beverages (non-medicinal):
The herb is not widely used as a food plant; documentation for culinary applications is sparse and non-systematic.

Colorants and tanning:
Historically the aerial parts have been employed as a source of brown to black natural dyes. Aqueous extracts impart brown tones on wool; in the presence of iron mordants, darker browns and near-black can be obtained, enabling basic dyeing of protein fibers without specialized equipment.

Properties relevant to use:
Mediastinic tannins (hydrolyzable-type, often reported as gallotannins) and phenolic acids (notably rosmarinic acid) contribute to binding and lightfastness of the dye, while flavonoids modulate hue. These phenolic profiles are established in phytochemical literature for the species.

Sustainability and sourcing:
The plant occurs widely in wet habitats across temperate Europe and adjacent regions. Harvesting for dye use typically involves cutting or uprooting aerial biomass during the growing season; regrowth varies by cut frequency and habitat quality. Standard botanical references and regional floras document occurrence and ecological status.

Synonyms Top

Scientific name	Authority	First published in
Lycopus alboroseus	Gilib.	Fl. Lit. Inch. 1: 71 (1782)
Lycopus albus	Mazziari	Ionios Antologia 2: 446 (1834)
Lycopus aquaticus	Moench	Methodus : 370 (1794)
Lycopus decrescens	K.Koch	Linnaea 21: 646 (1849)
Lycopus europaeus subsp. menthifolius	(Mabille) Skalický	Sborn. Nár. Mus. v Praze, Rada B, Prír. Vedy 24B: 206. 1968 (1968)
Lycopus europaeus subsp. mollis	(A.Kern.) Murr	Neue Übers. Bl.-Pfl. Vorarlberg 258. 1923 (1923)
Lycopus laciniatus	Marz.-Penc. ex Pollini	Fl. Veron. 1: 27. 1822 (1822)
Lycopus menthifolius	Mabille	Rech. Pl. Corse 1: 31 (1867)
Lycopus mollis	A.Kern.	Oesterr. Bot. Z. 16: 371 (1866)
Lycopus niger	Gueldenst.	Reis. Russland 2: 65 (1791)
Lycopus palustris	Burm.f.	Fl. Indica , Prodr. Fl. Cap.: 1 (1768)
Lycopus riparius	Salisb.	Prodr. Stirp. Chap. Allerton : 72 (1796)
Lycopus solanifolius	Lojac.	Fl. Sicul. 2(2): 194 (1907)
Lycopus souliei	Sennen	Bol. Soc. Aragonesa Ci. Nat. 15: 250 (1916)
Lycopus vulgaris	Pers.	Syn. Pl. 1: 24 (1805)
Lycopus europaeus var. menthifolius	(Mabille) Nyman	Consp. Fl. Eur. 597. 1881
Lycopus europaeus var. subpinnatifidus	Lej. & Courtois	Comp. Fl. Belg. 1: 19. 1828
Lycopus europaeus var. incanus	DC.	Fl. Franç. éd. 3, 3: 505. 1805
Lycopus europaeus f. pusillus	Montell	Memoranda Soc. Fauna Fl. Fenn. 22: 192 1946
Lycopus europaeus f. glabrescens	Schmidely	Bull. Soc. Bot. Genève 3: 128 1884
Lycopus europaeus var. pubescens	Benth.	Prodr. [A. P. de Candolle] 12: 178. 1848
Lycopus europaeus f. velutina	Schmidely	Bull. Soc. Bot. Genève 3: 128 1884
Lycopus europaeus var. hirsutus	Gand.	Fl. Helv. 51. 1828
Lycopus europaeus var. trichophora	Briq.	Lab. Alp. Mar. 117. 1891
Lycopus europaeus var. mollis	(A.Kern.) Briq.	Lab. Alp. Mar. 117. 1891
Lycopus europaeus var. glabrescens	(Schmidely) Briq.	Labiat. Gen. Spec. 116 1891
Lycopus europaeus var. stolonifer	K.Koch	Linnaea 21: 647. 1849
Lycopus europaeus var. procerior	Klett & Richt.	Fl. Leipzig : 25 (1830)
Lycopus riparius var. incisus	Gray	Nat. Arr. Brit. Pl. 2: 360 (1821 publ. 1822)
Lycopus europaeus var. elatior	Hagenb.	Fl. Helv. 1: 51 (1828)
Lycopus europaeus f. lanuginosus	Bolzon	Bull. Soc. Bot. Ital. 1903: 36 (1903)
Lycopus europaeus prol. menthifolius	(Mabille) Rouy	Fl. France 11: 393 (1909)
Lycopus europaeus f. glabrescens	Bolzon	Bull. Soc. Bot. Ital. 1903: 36 (1903)

Common names Top

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Filter by language:

Language	Common/alternative name
English	gypsywort
English	bugleweed
English	water horehound
English	gipsywort
English	european bugleweed
Spanish	lícopus
Spanish	lycopus solanifolius
Spanish	lycopus albus
Spanish	lycopus palustris
Spanish	lycopus souliei
Spanish	lycopus vulgaris
Spanish	hierba de lobo
Spanish	lycopus aquaticus
Spanish	lycopus mollis
Spanish	licopo europeo
Spanish	te americano
Spanish	licopus
Spanish	té americano
Spanish	pie de lobo
Spanish	patilobo
Spanish	pata de lobo
Spanish	menta de lobo
Spanish	menta de burro
Spanish	marrubio de agua
Spanish	marrubio acuático
Spanish	marroyo de lobo
Spanish	marroyo de agua
Spanish	manrrubio de agua
Arabic	فراسيون مائي
Azerbaijani	avropa ləçəkotu
Belarusian	Зюзнік еўрапейскі
Bulgarian	обикновена катушка
Catalan	peu de llop
Czech	karbinec evropský
Welsh	llysiau'r sipsiwn
Danish	sværtevæld
German	gemeiner wolfstrapp
German	europäischer wolfsfuss
German	ufer-wolfstrapp
Esperanto	eŭropa likopo
Estonian	harilik parkhein
Basque	otso-atzapar
Persian	پای گرگ اروپایی
Finnish	rantayrtti
Finnish	luhtarantayrtti
French	lycope
French	chanvre d’eau
French	erba-sega comune
French	lycope d'europe
Irish	feorán corraigh
Hebrew	כף-זאב אירופית
Croatian	vučja noga
Upper Sorbian	brjohowy dabrečk
Hungarian	vízi peszérce
Japanese	ヒメサルダヒコ
Lithuanian	paprastoji vilkakojė
Norwegian Bokmål	klourt
Dutch	wolfspoot
Polish	karbieniec pospolity
Portuguese	marroio-de-água
Romanian	piciorul lupului
Russian	зюзник европейский
Russian	Зюзник европейский
Slovak	karbinec európsky
Swedish	strandklo
Ukrainian	вовконіг європейський
Ukrainian	Вовконіг європейський
Chinese	歐地筍
Chinese	欧地笋

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Azores
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Siberia
  - Altay
  - Buryatiya
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Afghanistan
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan
  - West Himalaya

Australasia click to expand
- New Zealand
  - New Zealand North

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
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Wisconsin
- Northeastern U.S.A.
  - Indiana
  - Massachusetts
  - Michigan
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - West Virginia
- Southeastern U.S.A.
  - Alabama
  - Delaware
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - Virginia
- Western Canada
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000231391
Canadensys	6393
USDA Plants	LYEU
Tropicos	17600141
INPN	107038
Flora of Italy	4637
KEW	urn:lsid:ipni.org:names:449641-1
The Plant List	kew-115904
Open Tree Of Life	304971
Observations.org	7020
NCBI Taxonomy	260603
NBN Atlas	NBNSYS0000004206
Nature Serve	2.148964
IUCN Red List	163972
IPNI	449641-1
iNaturalist	133036
GBIF	5341478
Freebase	/m/06jbjn
WisFlora	4155
EPPO	LYAEU
EOL	579749
Elurikkus	5603
USDA GRIN	423463
Wikipedia	Lycopus_europaeus
CMAUP	NPO12357

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

Isolation, characterization and anti-inflammatory activity of compounds from the Vernonia amygdalina

Atolani O, Usman MA, Adejumo JO, Ayeni AE, Ibukun OJ, Kola-Mustapha AT, Njinga NS, Quadri LA, Ajani EO, Amusa TO, Bakare-Odunola MT, Oladiji AT, Alqahtani A, Abbas M, Kambizi L

Heliyon

13-Apr-2024

PMCID:	PMC11043951
doi:	10.1016/j.heliyon.2024.e29518
PMID:	38665563

Types and Mechanisms of Efflux Pump Systems and the Potential of Efflux Pump Inhibitors in the Restoration of Antimicrobial Susceptibility, with a Special Reference to Acinetobacter baumannii

Zack KM, Sorenson T, Joshi SG

Pathogens

23-Feb-2024

PMCID:	PMC10974122
doi:	10.3390/pathogens13030197
PMID:	38535540

Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans)

Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P

J Ethnobiol Ethnomed

10-Jan-2024

PMCID:	PMC10782642
doi:	10.1186/s13002-024-00647-2
PMID:	38200599

Antibiotic Potentiation as a Promising Strategy to Combat Macrolide Resistance in Bacterial Pathogens

Paul D, Chawla M, Ahrodia T, Narendrakumar L, Das B

Antibiotics (Basel)

11-Dec-2023

PMCID:	PMC10740890
doi:	10.3390/antibiotics12121715
PMID:	38136749

Community structure, environmental conditions and anthropogenic pressure on the habitat of the European endemic aquatic plant Luronium natans (L.) Raf.

Banaś K, Ronowski R, Chmara R, Szmeja J

BMC Plant Biol

28-Nov-2023

PMCID:	PMC10683176
doi:	10.1186/s12870-023-04518-y
PMID:	38017375

The complete chloroplast genome of Ocimum basilicum L. var. basilicum (Lamiaceae) and its phylogenetic analysis

Kirankumar SI, Balaji R, Tanuja, Parani M

Mitochondrial DNA B Resour

30-Oct-2023

PMCID:	PMC10769543
doi:	10.1080/23802359.2023.2275835
PMID:	38188439

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Adaptive Relationships in Hemi-Boreal Forests: Tree Species Responses to Competition, Stress, and Disturbance

Petrokas R, Manton M

Plants (Basel)

13-Sep-2023

PMCID:	PMC10535793
doi:	10.3390/plants12183256
PMID:	37765418

Impact of the Invasive Alien Macrophyte Ludwigia hexapetala on Freshwater Ecosystems: Evidence from Field Data

Pelella E, Questino B, Luzi B, Mariani F, Ceschin S

Biology (Basel)

31-May-2023

PMCID:	PMC10295687
doi:	10.3390/biology12060794
PMID:	37372079

Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats

Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z

Plants (Basel)

31-May-2023

PMCID:	PMC10255522
doi:	10.3390/plants12112184
PMID:	37299162

Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens

Kernou ON, Azzouz Z, Madani K, Rijo P

Molecules

22-May-2023

PMCID:	PMC10220798
doi:	10.3390/molecules28104243
PMID:	37241981

Fish Epidermal Mucus as a Source of Diverse Therapeutical Compounds

Hussain A, Sachan SG

Int J Pept Res Ther

20-Mar-2023

PMCID:	PMC10026197
doi:	10.1007/s10989-023-10505-6
PMID:	36968337

Macrophyte-Based Assessment of Upland Rivers: Bioindicators and Biomonitors

Gecheva G, Stankova S, Varbanova E, Kaynarova L, Georgieva D, Stefanova V

Plants (Basel)

19-Mar-2023

PMCID:	PMC10053903
doi:	10.3390/plants12061366
PMID:	36987054

A systematic review on impact of SARS-CoV-2 infection

Thirumugam G, Radhakrishnan Y, Ramamurthi S, Bhaskar JP, Krishnaswamy B

Microbiol Res

15-Mar-2023

PMCID:	PMC10015779
doi:	10.1016/j.micres.2023.127364
PMID:	36989761

The complete chloroplast genome sequence of the medicinal plant, Dracocephalum rupestre (Lamiaceae)

Han EK, Heo TI, Amarsanaa G, Park JW, Lee JH

Mitochondrial DNA B Resour

02-Feb-2023

PMCID:	PMC9902028
doi:	10.1080/23802359.2023.2172970
PMID:	36755880

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid	3469	Click to see	154.12	unknown	https://doi.org/10.1007/BF02467553
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1007/BF02467553
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1007/BF02467553
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid	10742	Click to see	198.17	unknown	https://doi.org/10.1007/BF02467553
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1007/BF02467553
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester	287064	Click to see COC(=O)C1=CC(=C(C=C1)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see	106.12	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Lithospermidin A	5319056	Click to see	388.40	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see	208.25	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see	164.20	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
1-[(1R,2S,3S,4R)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-2,4,5-trimethoxybenzene	10341859	Click to see	416.50	unknown	via CMAUP database
Magnosalin	10454589	Click to see	416.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3R)-5-phenyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentanoic acid	11792570	Click to see	356.40	unknown	via CMAUP database
D-Linalool 3-glucoside	10087123	Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C	316.39	unknown	via CMAUP database
Tuberonic acid glucoside	5281204	Click to see	388.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol	6992244	Click to see	128.21	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid	5280934	Click to see	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilinolein	5322095	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC	879.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Euroabienol	46933232	Click to see	462.50	unknown	https://doi.org/10.1002/CHIN.201052192
methyl (1R,4aS,5R,7R,8S,9R,10aR)-9-acetyloxy-7-ethenyl-5,8-dihydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	21627326	Click to see CC(=O)OC1CC2C(CCCC2(C)C(=O)OC)(C3=C1C(C(CC3O)(C)C=C)O)C	406.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
methyl (1R,4aS,5R,7R,9R,10aR)-9-acetyloxy-7-ethenyl-5-hydroxy-1,4a,7-trimethyl-8-oxo-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carboxylate	10811214	Click to see	404.50	unknown	https://doi.org/10.1021/NP990519C
methyl (1R,4S,4aS,5R,7R,8S,9R,10aR)-9-acetyloxy-7-ethenyl-4,5,8-trihydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	10502347	Click to see	422.50	unknown	https://doi.org/10.1021/NP990519C
methyl (1R,4S,4aS,7R,8S,9R,10aR)-4-acetyloxy-7-ethenyl-8,9-dihydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	637387	Click to see CC(=O)OC1CCC(C2C1(C3=C(C(C2)O)C(C(CC3)(C)C=C)O)C)(C)C(=O)OC	406.50	unknown	https://doi.org/10.1016/S0031-9422(02)00446-6
methyl (1R,4S,4aS,7R,8S,9R,10aR)-4,9-diacetyloxy-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	21627324	Click to see CC(=O)OC1CCC(C2C1(C3=C(C(C2)OC(=O)C)C(C(CC3)(C)C=C)O)C)(C)C(=O)OC	448.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
methyl 4-acetyloxy-7-ethenyl-8,9-dihydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	22297720	Click to see CC(=O)OC1CCC(C2C1(C3=C(C(C2)O)C(C(CC3)(C)C=C)O)C)(C)C(=O)OC	406.50	unknown	https://doi.org/10.1016/S0031-9422(02)00446-6
Methyl 4,10-diacetyloxy-5,9-dihydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylate	57509426	Click to see CC(C)C1=CC2=C(C(=C1)O)C3(C(CCC(C3C(C2O)OC(=O)C)(C)C(=O)OC)OC(=O)C)C	462.50	unknown	https://doi.org/10.1002/CHIN.201052192
methyl 4,9-diacetyloxy-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	73813590	Click to see	448.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
methyl 9-acetyloxy-7-ethenyl-4,5,8-trihydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	74105501	Click to see CC(=O)OC1CC2C(CCC(C2(C3=C1C(C(CC3O)(C)C=C)O)C)O)(C)C(=O)OC	422.50	unknown	https://doi.org/10.1021/NP990519C
Methyl 9-acetyloxy-7-ethenyl-5-hydroxy-1,4a,7-trimethyl-8-oxo-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carboxylate	85275754	Click to see	404.50	unknown	https://doi.org/10.1021/NP990519C
methyl 9-acetyloxy-7-ethenyl-5,8-dihydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	73813592	Click to see CC(=O)OC1CC2C(CCCC2(C)C(=O)OC)(C3=C1C(C(CC3O)(C)C=C)O)C	406.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(3S,5R,6E,9R,10E)-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraene-3,5,9-triol	51669654	Click to see CC(=CCCC(=CC(CC(=CC(CC(C)(C=C)O)O)C)O)C)C	322.50	unknown	https://doi.org/10.1021/NP990519C
3,7,11,15-Tetramethylhexadeca-1,6,10,14-tetraene-3,5,9-triol	74490791	Click to see	322.50	unknown	https://doi.org/10.1021/NP990519C
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethylocta-2,6-Dienal	8843	Click to see	152.23	unknown	via CMAUP database
Citral	638011	Click to see	152.23	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzoic acid	10820	Click to see CC(C)C1=CC=C(C=C1)C(=O)O	164.20	unknown	via CMAUP database
P-Cymene	7463	Click to see	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(-)-Camphene	440966	Click to see	136.23	unknown	via CMAUP database
alpha-CIS-BERGAMOTENE	6429303	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	via CMAUP database
beta-Pinene, (+)-	10290825	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
(+)-Menthol	165675	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
(3S,4R)-3-hydroxy-4-prop-1-en-2-ylcyclohexene-1-carbaldehyde	10725727	Click to see CC(=C)C1CCC(=CC1O)C=O	166.22	unknown	via CMAUP database
[(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol	11788398	Click to see CC(=C)C1CCC(=CC1)CO	152.23	unknown	via CMAUP database
l-Menthol	16666	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
Limonene, (-)-	439250	Click to see	136.23	unknown	via CMAUP database
Menthone	26447	Click to see	154.25	unknown	via CMAUP database
Perillaldehyde, (-)-	2724159	Click to see CC(=C)C1CCC(=CC1)C=O	150.22	unknown	via CMAUP database
Perillaldehyde, (+)-	1548901	Click to see	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,6,6,9-Tetramethyl-cycloundeca-1,4,8-triene	6508206	Click to see	204.35	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Cuparene	86895	Click to see	202.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(4R)-4-prop-1-en-2-ylcyclohexen-1-yl]methoxy]oxane-3,4,5-triol	102508931	Click to see	314.37	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4S)-4-prop-1-en-2-ylcyclohexene-1-carboxylate	21631012	Click to see CC(=C)C1CCC(=CC1)C(=O)OC2C(C(C(C(O2)CO)O)O)O	328.36	unknown	via CMAUP database
Perilloside A	3086657	Click to see	314.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
3-Epicorosolic acid	15917998	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
Augustic Acid	15560128	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
epi-Maslinic acid	25564831	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
Pomolic acid	382831	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O	472.70	unknown	via CMAUP database
Tormentic acid	73193	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol	5283637	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
Campesterol	173183	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
methyl (1R,4aS,5R,7R,8S,9R,10aR)-8-acetyloxy-7-ethenyl-5,9-dihydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	10573398	Click to see	406.50	unknown	https://doi.org/10.1021/NP990519C
methyl (1R,4aS,5R,7R,8S,9R,10aR)-8,9-diacetyloxy-7-ethenyl-5-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	21627325	Click to see	448.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
methyl (1R,4aS,7R,8S,9R,10aR)-8,9-diacetyloxy-7-ethenyl-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	7466446	Click to see CC(=O)OC1CC2C(CCCC2(C)C(=O)OC)(C3=C1C(C(CC3)(C)C=C)OC(=O)C)C	432.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
methyl (1R,4S,4aR,7S,8R,9R,10aR)-8,9-diacetyloxy-7-ethenyl-4-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	163004261	Click to see	448.50	unknown	https://doi.org/10.1016/S0040-4020(01)96427-0
methyl (1R,4S,4aS,7R,8S,9R,10aR)-4,8-diacetyloxy-7-ethenyl-9-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	21680746	Click to see	448.50	unknown	https://doi.org/10.1016/S0031-9422(02)00446-6
methyl (1R,4S,4aS,7R,8S,9R,10aR)-8,9-diacetyloxy-7-ethenyl-4-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	21627323	Click to see	448.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
Methyl 1a,7a,14a-triacetoxy-8,15-isopimaredien-18-oate	9496922	Click to see	490.60	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
methyl 4,8-diacetyloxy-7-ethenyl-9-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	73823796	Click to see	448.50	unknown	https://doi.org/10.1016/S0031-9422(02)00446-6
methyl 4,8,9-triacetyloxy-7-ethenyl-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	4345647	Click to see CC(=O)OC1CCC(C2C1(C3=C(C(C2)OC(=O)C)C(C(CC3)(C)C=C)OC(=O)C)C)(C)C(=O)OC	490.60	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
methyl 8-acetyloxy-7-ethenyl-5,9-dihydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	85190401	Click to see	406.50	unknown	https://doi.org/10.1021/NP990519C
methyl 8,9-diacetyloxy-7-ethenyl-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	3398115	Click to see	432.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
methyl 8,9-diacetyloxy-7-ethenyl-5-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	73813591	Click to see	448.50	unknown	https://doi.org/10.1016/S0040-4020(99)00361-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
Hyptadienic acid	14605533	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)C)CO)C)C)C2C1(C)O)C)C(=O)O	470.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmasterol	5280794	Click to see	412.70	unknown	via CMAUP database
> 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	https://doi.org/10.1007/BF02467553
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Eucalyptosin A	123133484	Click to see	457.40	unknown	via CMAUP database
Prunasin	119033	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	via CMAUP database
Sambunigrin	91434	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	via CMAUP database
Vicianin	656493	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(C#N)C3=CC=CC=C3)O)O)O)O)O)O	427.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Benzyl beta-d-glucopyranoside	188977	Click to see	270.28	unknown	via CMAUP database
Methyl alpha-D-galactopyranoside	76935	Click to see COC1C(C(C(C(O1)CO)O)O)O	194.18	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(5-methoxy-6-prop-2-enyl-1,3-benzodioxol-4-yl)oxane-3,4,5-triol	5319623	Click to see	354.40	unknown	via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-methoxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol	21579141	Click to see COC1=C(C=C(C=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O	326.34	unknown	via CMAUP database
Caffeic acid 3-(beta-1-glucoside)	442776	Click to see	342.30	unknown	via CMAUP database
Citrusin C	3084296	Click to see	326.34	unknown	via CMAUP database
Perilloside E	49855080	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC3C(C(C(C(O3)CO)O)O)O	370.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones
1-(Furan-3-yl)-4-methylpent-2-en-1-one	169595	Click to see	164.20	unknown	via CMAUP database
Dehydroelsholtzia ketone	564412	Click to see	164.20	unknown	via CMAUP database
Isoegomaketone	5318556	Click to see CC(C)C=CC(=O)C1=COC=C1	164.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1-(3-Furyl)-4-methyl-1-pentanone	68381	Click to see	166.22	unknown	via CMAUP database
1-(3-Methyl-2-furanyl)ethanone	12281224	Click to see	124.14	unknown	via CMAUP database
Egomaketone	42978	Click to see	164.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde	8768	Click to see	138.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol	10231	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC	222.24	unknown	via CMAUP database
Myristicin	4276	Click to see	192.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzoxepines
5-Methoxyfuro[2,3-g][3]benzoxepin	10084612	Click to see CC(C)(C1=CC2=CC(=C3C=COC=CC3=C2O1)OC)O	272.29	unknown	via CMAUP database
Perilloxin	10468570	Click to see CC(C)(C1CC2=CC(=C3C=COC=CC3=C2O1)OC)O	274.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Thiamines
Thiamine	1130	Click to see	265.36	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene	68316	Click to see	150.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Lithospermic Acid	6441498	Click to see	538.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-3-(3,4-Dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (E)-3-(3,4-dihydroxyphenyl)acrylate	10970786	Click to see	374.30	unknown	via CMAUP database
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	via CMAUP database
Methyl Caffeate	689075	Click to see	194.18	unknown	via CMAUP database
Nepetoidin A	5316820	Click to see	314.29	unknown	via CMAUP database
Nepetoidin B	5316819	Click to see	314.29	unknown	via CMAUP database
Rosmarinic Acid	5281792	Click to see	360.30	unknown	https://doi.org/10.1016/0021-9673(95)00492-4 https://doi.org/10.1007/BF02467553
Vinyl caffeate	11127419	Click to see C=COC(=O)C=CC1=CC(=C(C=C1)O)O	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	https://doi.org/10.1007/BF02467553 https://doi.org/10.1016/0021-9673(95)00492-4
Ferulic Acid	445858	Click to see	194.18	unknown	https://doi.org/10.1007/BF02467553
Isoferulic Acid	736186	Click to see	194.18	unknown	https://doi.org/10.1007/BF02467553
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.1007/BF02467553
Sinapinic acid	637775	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O	224.21	unknown	https://doi.org/10.1007/BF02467553
> 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 / Pyranocoumarins / Angular pyranocoumarins
(+)-Pseudocordatolide C	467236	Click to see	342.40	unknown	https://doi.org/10.1016/S0040-4020(01)96427-0 https://doi.org/10.1016/S0040-4020(99)00361-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6,7,3',4'-Tetrahydroxyflavone	24721539	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=CC(=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
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/10.1055/S-2006-958121
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://doi.org/10.1055/S-2006-958121
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
Shisonin	5282068	Click to see	757.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Cyanin	441688	Click to see	611.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2	442664	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
5,6-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid	102158504	Click to see	638.50	unknown	via CMAUP database
Clerodendrin	5488004	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O	622.50	unknown	via CMAUP database
Luteolin 7-diglucuronide	5282153	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)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O	638.50	unknown	via CMAUP database
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/10.1055/S-2006-961388
Luteolin-7-o-beta-d-glucuronide methyl ester	91129494	Click to see	476.40	unknown	via CMAUP database
Scutellarin	185617	Click to see	462.40	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/10.1055/S-2006-958151
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	464.40	unknown	https://doi.org/10.1055/S-2006-958151
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside	5353915	Click to see	448.40	unknown	https://doi.org/10.1055/S-2006-958151
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/10.1055/S-2006-958151
Isoquercetin	5280804	Click to see	464.40	unknown	https://doi.org/10.1055/S-2006-958151
Quercitrin	5280459	Click to see	448.40	unknown	https://doi.org/10.1055/S-2006-958151
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1055/S-2006-958151
Vitamin P	5293655	Click to see	610.50	unknown	https://doi.org/10.1055/S-2006-958151
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	74978200	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1055/S-2006-958151
7-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one	60195926	Click to see	594.50	unknown	via CMAUP database
Acacetin-7-O-neohesperidoside	15559329	Click to see	592.50	unknown	https://doi.org/10.1055/S-2006-958151
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	via CMAUP database
Eriocitrin	83489	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	596.50	unknown	https://doi.org/10.1055/S-2006-958151
Fortunellin	5317385	Click to see	592.50	unknown	https://doi.org/10.1055/S-2006-958151
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/10.1055/S-2006-958151
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/10.1055/S-2006-958151 https://doi.org/10.1016/0021-9673(95)00492-4 https://doi.org/10.1055/S-2006-961388
Quercetin-7-o-rutinoside	101764560	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1055/S-2006-958151
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium	128861	Click to see	287.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsiliol	160237	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC	330.29	unknown	https://doi.org/10.1055/S-2006-958121
Genkwanin	5281617	Click to see	284.26	unknown	https://doi.org/10.1055/S-2006-958121

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Lycopus europaeus

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