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 of Peucedanum palustre

Across northern and eastern Europe, marsh peucedanum has long been handled with care as a bitter root and a potent herb. In northern Russia, according to the Russian pharmacopoeia of 1874, the dried root was prepared as a strong decoction and valued as a diuretic and carminative. In Scandinavian rural practice, noted by Hjort in 1899, the root was also decocted to “settle the stomach” and ease wind, while a gentle infusion of the aerial parts was used to quiet “griping” pains. In Finland and the Baltic region, documents from the late nineteenth century describe the root decoction being taken at small doses for digestive discomfort and as a bitter tonic, and a macerated poultice made from bruised leaves applied to bruises and mild joint aches.

A practical preparation that respects the long tradition is a standardized tincture. To make a 1:5 (w/v) tincture of dried root, grind 20 grams of root into coarse pieces and macerate in 100 mL of 45 percent alcohol (e.g., vodka or ethanol diluted with water). Keep the jar in the dark and shake daily for 2–3 weeks, then strain and press. The result gives a clear, bitter extract that many herbalists store in a dark bottle. Use sparingly in small drops or diluted in water, and observe how your body feels. Do not use in pregnancy, and avoid taking if you will be in strong sun shortly after, as furocoumarins can increase photosensitivity.

The plant’s activity is plausibly linked to characteristic constituents that modern analysis has confirmed. The roots and aerial parts contain well‑established furocoumarins such as peucedanin and isoimperatorin, together with coumarins like osthole and bergapten, and a bitter coumarin glycoside called apiin. These compounds give the herb its intensely bitter taste and are known for irritant and photosensitizing properties. While a bitter approach can encourage digestive secretions, it is the same chemistry that demands caution.

Today, interest in Peucedanum palustre remains modest, with ongoing research into its coumarin profile and seasonal variation in Baltic populations, and small‑scale tinctures appear from time to time in traditional herb shops. Contemporary herbalists in northern Europe occasionally prepare a dried root decoction or tincture for short, measured use, but most turning to marsh peucedanum do so with respect for its traditional reputation and its strong chemistry.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Oreoselis pisana	(Savi) Raf.	Good Book : 57 (1840)
Peucedanum sylvestre	DC.	Prodr. 4: 179 (1830)
Peucedanum schiwereckii	Eichw.	Skizze : 155 (1830)
Peucedanum idanense	Gand.	Fl. Lyon. : 103 (1875)
Thysselinum sylvestre	Hoffm.	Gen. Pl. Umbell. : 154 (1814)
Thysselinum palustre	(L.) Hoffm.	Gen. Pl. Umbell. : 154 (1814)
Thysselinum plinii	Spreng.	Sp. Umbell. : 69 (1818)
Thysselinum schiwerekii	Besser	Enum. Pl. Volh. : 12 (1821)
Thyselium palustre	(L.) Raf.	Good Book : 52 (1840)
Thysselinum angustifolium	Rchb.	Fl. Germ. Excurs. 2: 453 (1832)
Thysselinum crouanorum	Boreau	Bull. Soc. Bot. France 20: 30 (1873)
Selinum palustre	L.	Sp. Pl. : 244 (1753)
Selinum intermedium	Besser	Prim. Fl. Galiciae Austriac. 1: 205 (1809)
Selinum schiwerekii	Besser	Prim. Fl. Galiciae Austriac. 1: 205 (1809)
Selinum tysselinum	Crantz	Stirp. Austr. Fasc. 3: 35 (1767)
Selinum sylvestre	L.	Sp. Pl. : 244 (1753)
Athamanta flexuosa	Juss. ex DC.	Prodr. 4: 179 (1830)
Athamanta pisana	Savi	Ann. Bot. (Usteri) 21: 7 (1797)
Calestania palustris	Koso-Pol.	Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 175 (1915 publ. 1916)
Callisace schiefereckii	Hoffm.	Gen. Pl. Umbell. ed. 2: 170 1816
Cnidium palustre	Rchb.	Fl. Germ. Excurs. : 469 (1832)
Peucedanum crouanorum	Boreau ex Nyman	Consp. Fl. Eur. 2: 286. 1879 [Oct 1879]
Sium virens	hort. ex Steud.	Nomencl. Bot. [Steudel], ed. 2. 2: 597. 1841
Selinum lactescens	Gilib.	Fl. Lit. Inch. ii. 22. 1782
Selinum sublactescens	Gilib.	Fl. Lit. Inch. ii. 21. 1782
Selinum cantabrigense	Fisch. ex DC.	Prodr. [A. P. de Candolle] 4: 179. 1830 [late Sep 1830]
Laserpitium simplex	Boeber	Neue Nord. Beytr. Phys. Geogr. Erd- Völkerbeschreib. 6: 261 (1793)
Thysselinum palustre var. sylvestre	(L.) Klett & Richt.	Fl. Leipzig : 265 (1830)
Thysselinum palustre var. macropterum	Rupr.	Fl. Ingrica : 460 (1860)
Peucedanum palustre var. angustifolia	(Rchb.) Rouy & E.G.Camus	Fl. France 7: 387 (1901)
Peucedanum palustre var. filifolium	Brenner	Acta Soc. Fauna Fl. Fenn. 16(4): 211 (1899)
Peucedanum palustre var. slinifolium	Brenner	Meddeland. Soc. Fauna Fl. Fenn. 15: 191 (1888)
Selinum plinii	(Spreng.) Paxton	Pocket Bot. Dict. : 287 (1840)

Common names Top

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Filter by language:

Language	Common/alternative name
English	hogfennel
English	milk-parsley
English	marsh hog’s fennel
English	milk parsley
Belarusian	дзікая пятрушка балотная
Belarusian	калестанія балотная
Bulgarian	блатна самодивска трева
Czech	smldník bahenní
Welsh	ffenigl-y-moch llaethog
Danish	kær-svovlrod
German	sumpf-haarstrang
German	sumpfhaarstrang
Estonian	soo-piimputk
Finnish	luhtasuoputki
French	peucédan des marais
Hungarian	mocsári kocsord
Lithuanian	pelkinis saliavas
Norwegian Bokmål	mjølkerot
Dutch	melkeppe
Norwegian Nynorsk	mjølkerot
Polish	gorysz błotny
Russian	Горичник болотный
Slovak	smldník močiarny
Slovenian	močvirski silj
Swedish	kärrsilja

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Siberia
  - Altay
  - Krasnoyarsk
  - West Siberia

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - 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
  - Norway
  - Sweden
- Southeastern Europe
  - Bulgaria
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France

Northern America click to expand
- Northeastern U.S.A.
  - Massachusetts

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000391781
USDA Plants	PEPA22
Tropicos	1700186
KEW	urn:lsid:ipni.org:names:846318-1
The Plant List	kew-2403630
Plantarium	27509
PFAF	Peucedanum palustre
Open Tree Of Life	5801609
Observations.org	7163
NCBI Taxonomy	1572681
NBN Atlas	NBNSYS0000003707
Nature Serve	2.132564
IPNI	846318-1
iNaturalist	166550
GBIF	3034225
Freebase	/m/07t4ty
EPPO	PCDPA
EOL	581423
Elurikkus	6167
USDA GRIN	468591
Wikipedia	Peucedanum_palustre
CMAUP	NPO7718
PaleoBotany	58265

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

Total Soil CO2 Efflux from Drained Terric Histosols

Vigricas E, Čiuldienė D, Armolaitis K, Valujeva K, Laiho R, Jauhiainen J, Schindler T, Bārdule A, Lazdiņš A, Butlers A, Kazanavičiūtė V, Belova O, Kamil-Sardar M, Soosaar K

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

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PLoS One

04-Oct-2023

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Arciszewski M, Pogorzelec M, Bronowicka-Mielniczuk U, Niedźwiecki M, Parzymies M, Serafin A

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09-Jan-2023

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“Cow Healers Use It for Both Horses and Cattle”: The Rise and Fall of the Ethnoveterinary Use of Peucedanum ostruthium (L.) Koch (fam. Apiaceae) in Sweden

de Vahl E, Mattalia G, Svanberg I

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26-Dec-2022

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Brunbjerg AK, Fløjgaard C, Frøslev TG, Andersen DK, Bruun HH, Dalby L, Goldberg I, Lehmann LJ, Moeslund JE, Ejrnæs R

Ecol Evol

01-Nov-2022

PMCID:	PMC9627074
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Traditional Uses of Medicinal Plants in South-Western Part of Lithuania

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Plants (Basel)

11-Aug-2022

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Interspecific and intraspecific analysis of Selinum spp. collected from Indian Himalayas using DNA barcoding

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J Genet Eng Biotechnol

22-Apr-2022

PMCID:	PMC9033919
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Oxypeucedanin: Chemotaxonomy, Isolation, and Bioactivities

Mottaghipisheh J

Plants (Basel)

30-Jul-2021

PMCID:	PMC8401860
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Chemical and Phytocoenological Characteristics of Two Different Slovak Peatlands

Fazekašová D, Barančíková G, Fazekaš J, Štofejová L, Halas J, Litavec T, Liptaj T

Plants (Basel)

24-Jun-2021

PMCID:	PMC8309078
doi:	10.3390/plants10071290
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Chemical profiles of birch and alder bark by ambient mass spectrometry

Räsänen RM, Hieta JP, Immanen J, Nieminen K, Haavikko R, Yli-Kauhaluoma J, Kauppila TJ

Anal Bioanal Chem

23-Oct-2019

PMCID:	PMC6875546
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Karst dolines provide diverse microhabitats for different functional groups in multiple phyla

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Sci Rep

09-May-2019

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Botanical Provenance of Traditional Medicines From Carpathian Mountains at the Ukrainian-Polish Border

Kozlowska W, Wagner C, Moore EM, Matkowski A, Komarnytsky S

Front Pharmacol

05-Apr-2018

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Diverse fen plant communities enhance carbon-related multifunctionality, but do not mitigate negative effects of drought

Robroek BJ, Jassey VE, Beltman B, Hefting MM

R Soc Open Sci

25-Oct-2017

PMCID:	PMC5666246
doi:	10.1098/rsos.170449
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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
(S)-Mandelonitrile	439767	Click to see C1=CC=C(C=C1)C(C#N)O	133.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines
Benzylamine	7504	Click to see C1=CC=C(C=C1)CN	107.15	unknown	https://doi.org/10.1055/S-2006-958068
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid	6950479	Click to see CCC(C)C(=O)O	102.13	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid	10467	Click to see	312.50	unknown	via CMAUP database
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL	5318042	Click to see CCCC=CCO	100.16	unknown	via CMAUP database
> 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	via CMAUP database
Linolenic Acid	5280934	Click to see	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
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
P-Cymene	7463	Click to see	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see	154.25	unknown	via CMAUP database
Terpinolene	11463	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
I2-Ionone	638014	Click to see	192.30	unknown	via CMAUP database
Vomifoliol, (+)-	5280462	Click to see	224.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin	5281238	Click to see	584.90	unknown	via CMAUP database
Rubixanthin	5281252	Click to see	552.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[3-acetyloxy-1,2-dihydroxy-17-(6-hydroxy-6-methylhept-4-en-2-yl)-4,8,10,14-tetramethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]methyl acetate	162892564	Click to see	576.80	unknown	https://doi.org/10.1055/S-2006-962542
alpha-Amyrin acetate	92842	Click to see	468.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one	670995	Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O	270.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol	5281330	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasteryl-beta-d-glucopyranoside	12895774	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron	88113319	Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O	192.12	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
2-Amino-1-phenylethanol	1000	Click to see C1=CC=C(C=C1)C(CN)O	137.18	unknown	https://doi.org/10.1055/S-2006-958068
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
Amylamine	8060	Click to see CCCCCN	87.16	unknown	https://doi.org/10.1055/S-2006-958068
Putrescine	1045	Click to see	88.15	unknown	https://doi.org/10.1055/S-2006-958068
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Spermidine	1102	Click to see C(CCNCCCN)CN	145.25	unknown	https://doi.org/10.1055/S-2006-958068
Spermine	1103	Click to see	202.34	unknown	https://doi.org/10.1055/S-2006-958068
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp	70680285	Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O	356.28	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin	656516	Click to see	457.40	unknown	via CMAUP database
Neoamygdalin	441462	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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Nonenal	5283335	Click to see CCCCCCC=CC=O	140.22	unknown	via CMAUP database
2,4-Decadienal	5283349	Click to see	152.23	unknown	via CMAUP database
Hexanal	6184	Click to see	100.16	unknown	via CMAUP database
trans-2-Hexenal	5281168	Click to see	98.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Tryptamine	1150	Click to see C1=CC=C2C(=C1)C(=CN2)CCN	160.22	unknown	https://doi.org/10.1055/S-2006-958068
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-butyloxolan-2-one	7057972	Click to see CCCCC1CCC(=O)O1	142.20	unknown	via CMAUP database
(R)-gamma-Decalactone	183870	Click to see	170.25	unknown	via CMAUP database
Gamma-dodecalactone, (R)-	10888889	Click to see	198.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Linalool oxide, cis-	6428573	Click to see	170.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2-(2-Oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl)propan-2-yl 2-hydroxy-2-methyl-3-(2-methylbut-2-enoyloxy)butanoate	162896988	Click to see CC=C(C)C(=O)OC(C)C(C)(C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O	444.50	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.19-0601
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl (2S,3R)-2-hydroxy-2-methyl-3-[(E)-2-methylbut-2-enoyl]oxybutanoate	163194939	Click to see	444.50	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.19-0601
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl (Z)-2-methylbut-2-enoate	53399217	Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3	328.40	unknown	https://doi.org/10.1007/BF02066241
Columbianadin	6436246	Click to see	328.40	unknown	https://doi.org/10.1055/S-2006-961919 https://doi.org/10.1007/BF02066241 https://doi.org/10.1055/S-2006-962542 https://doi.org/10.1002/CBDV.201500198
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-Oxypeucedanin	928465	Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C	286.28	unknown	https://doi.org/10.1055/S-2006-961919 https://doi.org/10.1055/S-2006-962542
4-((3,3-Dimethyloxiran-2-Yl)Methoxy)Furo(3,2-G)Chromen-7-One	160544	Click to see	286.28	unknown	via CMAUP database
4-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one	483513	Click to see	304.29	unknown	via CMAUP database
5-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one	53316971	Click to see CC1(C(O1)COC2=CC(=O)OC3=C2C=C4C=COC4=C3)C	286.28	unknown	via CMAUP database
Imperatorin	10212	Click to see	270.28	unknown	https://doi.org/10.1055/S-2006-961919
Isoimperatorin	68081	Click to see	270.28	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.18-1379 https://doi.org/10.1055/S-2006-962542 https://doi.org/10.1055/S-2006-961919
Ostruthol	6441273	Click to see	386.40	unknown	https://doi.org/10.1055/S-2006-961919 https://doi.org/10.1055/S-2006-962542
> 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	https://doi.org/10.1055/S-2006-961919
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
(S,Z)-3-Hydroxy-1-((9-methoxy-7-oxo-7H-furo[3,2-g]chromen-4-yl)oxy)-3-methylbutan-2-yl 2-methylbut-2-enoate	40507908	Click to see	416.40	unknown	https://doi.org/10.1055/S-2006-962542
[3-Hydroxy-1-(9-methoxy-7-oxofuro[3,2-g]chromen-4-yl)oxy-3-methylbutan-2-yl] 2-methylbut-2-enoate	164018	Click to see	416.40	unknown	https://doi.org/10.1007/BF02066241
2-Butenoic acid, 2-methyl-, (1S)-2-hydroxy-1-[[(9-methoxy-7-oxo-7H-furo[3,2-g][1]benzopyran-4-yl)oxy]methyl]-2-methylpropyl ester, (2Z)-	40507909	Click to see	416.40	unknown	https://doi.org/10.1007/BF02066241
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	5317050	Click to see	544.50	unknown	via CMAUP database
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	73353883	Click to see	544.50	unknown	via CMAUP database
(1S,5S,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	5317051	Click to see	544.50	unknown	via CMAUP database
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate	10723070	Click to see	664.60	unknown	via CMAUP database
Mahuannin A	5317052	Click to see	544.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database

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Peucedanum palustre

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