Scientific name	Authority	First published in
Agrimonia eupatoria var. mollis	Torr. & A.Gray	Fl. N. Amer. 1(3): 431 (1840)
Agrimonia bracteosa	E.Mey.	Zwei Pflanzengeogr. Docum. (Drège) 51, 142, nomen.
Agrimonia adhaerens	Gilib.	Fl. Lit. Inch. ii. 185. 1782
Agrimonia adscendens	Andrz.	Enum. Pl. Podol. : 36 (1860)
Agrimonia canescens	Dumort.	Fl. Belg. : 97 (1827)
Agrimonia humilis	Wallr.	Beitr. Bot. 1: 37 (1842)
Agrimonia elata	Salisb.	Prodr. Stirp. Chap. Allerton 361. 1796 [Nov-Dec 1796]
Agrimonia eupatoria var. rotundifolia	Wallr.	; 1842 46 1842
Agrimonia eupatoria var. longifolia	Wallr.	; 1842 46 1842
Agrimonia minor	Mill.	Gard. Dict. ed. 8 : n.º 2 (1768)
Agrimonia officinarum	Lam.	Fl. Franç. (Lamarck) 3: 477. 1779 [1778 publ. after 21 Mar 1779]
Agrimonia sulcata	Dulac	Fl. Hautes-Pyrénées 303. 1867
Agrimonia vulgaris	Gray	Nat. Arr. Brit. Pl. 2: 577. 1821 [1 Nov 1821]
Agrimonia eupatoria var. fallax	Fiek	; 1889 174 1889
Agrimonia eupatoria var. humilis	(Wallr.) Asch. & Graebn.	Synopsis der mitteleurop„ischen Flora ; 1896 421 1902
Agrimonia eupatoria var. sepium	Bréb.	Flore de la Normandie ; 1859 105 1859
Agrimonia eupatoria subsp. officinalis	(Lam.) Gams	Illustrierte Flora von Mittel-Europa ; 1906 932 1923
Agrimonia officinalis	Gaterau	Descr. Pl. Montauban 87. 1789
Agrimonia alba	hort. ex Gizycki	; 1949 279 1949
Agrimonia eupatoria var. major	Mutel	Fl. Franç. (Mutel) 1: 342. 1834
Agrimonia eupatoria var. major	K.Koch	; 1847 44 1847
Agrimonia eupatoria var. ochroleuca	Ostenf.	; 1924 170 1924
Agrimonia eupatoria var. sylvatica	Čelak.	; 1882 1882
Agrimonia eupatoria var. minor	(Mill.) Sol.	Hortus kewensis ; 1789 130 1789
Agrimonia eupatoria var. canescens	(Dumort.) Wirtg.	Fl. Preuss. Rheinprov. : 165 (1857)

Common names Top

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Filter by language:

Language	Common/alternative name
English	agrimony
English	churchsteeples
English	common agrimony
English	medicinal agrimony
Spanish	hierba de san guillermo
Spanish	algafil
Spanish	arquimonia
Spanish	cabsitiella
Spanish	cafal
Spanish	caphith
Spanish	gafeti
Spanish	gafetí
Spanish	merma sangre
Spanish	yerba de san guilllermo
Spanish	yerba-bacera
Arabic	غافث شائع
Arabic	الغافث
Azerbaijani	aptek gücotu
Belarusian	дзядкі
Belarusian	Дзядкі звычайныя
Belarusian	дзядкі-трава
Belarusian	Дзядок
Belarusian	Рэпік
Belarusian	смятаннік
Belarusian	сучкі
Belarusian	шчэрб
Belarusian	Дзядкі аптэчныя
Bulgarian	Камшик
Bulgarian	Лечебен камшик
Catalan	herba de la sang
Catalan	agrimònia comuna
Catalan	herba de sant antoni
Catalan	herba de sant ramon
Catalan	herba del garrotillo
Catalan	herba ramona
Catalan	herba tossera
Catalan	herberola
Catalan	serverola
Czech	řepík lékařský
Welsh	llysiau'r dryw;
Danish	almindelig agermåne
German	gemeiner odermennig
German	kleiner odermennig
German	odermennig
German	gewöhnlicher odermennig
Greek	Αγριμόνια
Esperanto	eŭpatoria agrimonio
Estonian	harilik maarjalepp
Estonian	krassid
Estonian	maapihelgas
Estonian	maarjakadakas
Estonian	maarjapihlakas
Estonian	maarjatakjas
Estonian	papirohi
Estonian	üheksapäelill
Basque	usu-belar
Persian	غافث
Finnish	maarianverijuuri
French	aigremoine eupatoire
Irish	airgeadán
Irish	marbhdhraighean
Hebrew	אבגר צהוב
Croatian	turica
Upper Sorbian	mały žiłan
Hungarian	közönséges párlófű
Hungarian	apróbojtorján
Armenian	Երեսնակ դեղատու
Icelandic	akurmáni
Italian	agrimonio
Cornish	skawen an wyrghes
Lithuanian	vaistinė dirvuolė
Latvian	Ārstniecības ancītis
Macedonian	Петровец или камшик
Dutch	gewone agrimonie
Polish	rzepik pospolity
Portuguese	agrimônia comum
Romanian	turița mare
Russian	Репешок обыкновенный
Russian	Печёночник
Russian	Приворот обыкновенный
Russian	Репейничек аптечный
Russian	Репейничек обыкновенный
Russian	Репешок лекарственный
Russian	Репешок посконный
Russian	Репяшок обыкновенный
Serbo-Croatian	petrovac
Serbo-Croatian	džigeričnjak
Serbo-Croatian	ruričica
Serbo-Croatian	trava celog sveta
Serbo-Croatian	trava cijelog svijeta
Serbo-Croatian	turica
Slovak	repík lekársky
Slovenian	navadni repik
Serbian	Петровац
Serbian	Рањеник
Serbian	петровац
Swedish	småborre
Swedish	Åkermönja
Turkish	adi kızılyaprak
Ukrainian	Парило звичайне
Ukrainian	парило звичайне
Chinese	仙鹤草
Chinese	广东万年青
Chinese	欧龙芽草
Chinese	欧洲龙牙草
Chinese	欧洲龙芽草
Chinese	歐洲龍芽草
Chinese	歐洲龍牙草

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Agrimonia eupatoria subsp. asiatica	(Juz.) Skalický	Feddes Repert. 79: 35. 1968 (1968)
Agrimonia eupatoria subsp. grandis	(Andrz. ex C.A.Mey.) Bornm.	; 1940 244 1940

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

Suggest a correction or add new data!

Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Siberia
  - Altay
  - West Siberia
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Assam

Australasia click to expand
- Australia
  - New South Wales

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
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- North-central U.S.A.
  - Iowa
  - Minnesota
- Northeastern U.S.A.
  - Connecticut
  - Massachusetts
  - New York
  - Ohio
  - Pennsylvania
- Northwestern U.S.A.
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - North Carolina
  - Tennessee
- Southwestern U.S.A.
  - California

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001006654
Canadensys	8600
USDA Plants	AGEU
Tropicos	27800017
INPN	80410
KEW	urn:lsid:ipni.org:names:316550-2
The Plant List	rjp-408
Open Tree Of Life	852855
Observations.org	2321
NCBI Taxonomy	57912
NBN Atlas	NBNSYS0000003366
Nature Serve	2.130343
IPNI	316550-2
iNaturalist	55893
GBIF	3001956
Freebase	/m/026vqsk
EPPO	AGIEU
EOL	1260720
Elurikkus	2587
USDA GRIN	1786
Wikipedia	Agrimonia_eupatoria
CMAUP	NPO11762
Plantarium	913

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

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

Šarūnaitė L, Arlauskienė A, Jablonskytė-Raščė D

PLoS One

16-Apr-2024

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

A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics

Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B

J Ethnopharmacol

25-Mar-2024

PMCID:	PMC7615571
doi:	10.1016/j.jep.2023.117622
PMID:	38128894

Biosynthesis and characterization of silver nanoparticles synthesized using extracts of Agrimonia eupatoria L. and in vitro and in vivo studies of potential medicinal applications

Marković K, Kesić A, Novaković M, Grujović M, Simijonović D, Avdović EH, Matić S, Paunović M, Milutinović M, Nikodijević D, Stefanović O, Marković Z

RSC Adv

05-Feb-2024

PMCID:	PMC10839552
doi:	10.1039/d3ra07819a
PMID:	38318620

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

Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy

Sulaiman N, Zocchi DM, Borrello MT, Mattalia G, Antoniazzi L, Berlinghof SE, Bewick A, Häfliger I, Schembs M, Torri L, Pieroni A

Plants (Basel)

22-Dec-2023

PMCID:	PMC10780445
doi:	10.3390/plants13010043
PMID:	38202351

Anti-Inflammatory Effects of Alphitolic Acid Isolated from Agrimonia coreana Nakai Extracts Are Mediated via the Inhibition of ICRAC Activity in T Cells

Park SJ, Lee JS, Nam YR, Lee JM, Ki DW, Yun BS, Choi SW, Van NT, Nam JH, Kim HJ, Kim WK

Int J Mol Sci

09-Dec-2023

PMCID:	PMC10743429
doi:	10.3390/ijms242417309
PMID:	38139137

Plant Extracts as Skin Care and Therapeutic Agents

Michalak M

Int J Mol Sci

22-Oct-2023

PMCID:	PMC10607442
doi:	10.3390/ijms242015444
PMID:	37895122

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

Potential use of the Asteraceae family as a cure for diabetes: A review of ethnopharmacology to modern day drug and nutraceuticals developments

Mohanta YK, Mishra AK, Nongbet A, Chakrabartty I, Mahanta S, Sarma B, Panda J, Panda SK

Front Pharmacol

03-Aug-2023

PMCID:	PMC10441548
doi:	10.3389/fphar.2023.1153600
PMID:	37608892

Remnants from the Past: From an 18th Century Manuscript to 21st Century Ethnobotany in Valle Imagna (Bergamo, Italy)

Milani F, Bottoni M, Bardelli L, Colombo L, Colombo PS, Bruschi P, Giuliani C, Fico G

Plants (Basel)

24-Jul-2023

PMCID:	PMC10386062
doi:	10.3390/plants12142748
PMID:	37514363

Environmental toxicants and health adversities: A review on interventions of phytochemicals

Sokan-Adeaga AA, Sokan-Adeaga MA, Sokan-Adeaga ED, Oparaji AN, Edris H, Tella EO, Balogun FA, Aledeh M, Amubieya OE

J Public Health Res

29-Jun-2023

PMCID:	PMC10334012
doi:	10.1177/22799036231181226
PMID:	37440795

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

The Antibacterial and Wound Healing Properties of Natural Products: A Review on Plant Species with Therapeutic Potential against Staphylococcus aureus Wound Infections

Morguette AE, Bartolomeu-Gonçalves G, Andriani GM, Bertoncini GE, de Castro IM, Spoladori LF, Bertão AM, Tavares ER, Yamauchi LM, Yamada-Ogatta SF

Plants (Basel)

29-May-2023

PMCID:	PMC10255540
doi:	10.3390/plants12112147
PMID:	37299127

Weed Species from Tea Gardens as a Source of Novel Aluminum Hyperaccumulators

Hajiboland R, Moradi A, Kahneh E, Poschenrieder C, Nazari F, Pavlovic J, Tolra R, Salehi-Lisar SY, Nikolic M

Plants (Basel)

27-May-2023

PMCID:	PMC10255622
doi:	10.3390/plants12112129
PMID:	37299108

Usage of Fermental Traps for the Study of the Species Diversity of Coleoptera in Open Biotopes

Ruchin AB, Egorov LV, Khapugin AA

Insects

21-Apr-2023

PMCID:	PMC10143697
doi:	10.3390/insects14040404
PMID:	37103219

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 / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
Dehydrodigallic acid	14057208	Click to see C1=C(C=C(C(=C1O)O)OC2=C(C(=C(C=C2C(=O)O)O)O)O)C(=O)O	338.22	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane	11636	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC	380.70	unknown	via CMAUP database
Tetratriacontane	26519	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	478.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(5Z)-9,15-Dioxoprosta-5,8(12)-diene-1-oic acid methyl ester	21609756	Click to see CCCCCC(=O)CCC1=C(C(=O)CC1)CC=CCCCC(=O)OC	348.50	unknown	via CMAUP database
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate	21160888	Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)OC)O	348.50	unknown	via CMAUP database
prostaglandin B2	5280881	Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)O)O	334.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid	444899	Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O	304.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid	3893	Click to see CCCCCCCCCCCC(=O)O	200.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
2-[(1R,4E,6E,10E,14R)-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-7-yl]propan-2-ol	23247586	Click to see CC1=CCCC2(C(O2)CCC(=CC=C(CC1)C(C)(C)O)C)C	304.50	unknown	via CMAUP database
dimethyl (1S,4E,6Z,10Z,14S)-14-methyl-7-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene-4,10-dicarboxylate	16091634	Click to see CC(C)C1=CC=C(CCC2C(O2)(CCC=C(CC1)C(=O)OC)C)C(=O)OC	376.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
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
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	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
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
(+)-Bornyl acetate	6950274	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(+)-Camphene	92221	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
Camphor (synthetic)	159055	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
Limonene, (-)-	439250	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Levomenol	442343	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	via CMAUP database
Secogorgosterol	386853	Click to see CC(C)C(C)C1(CC1C(C)C2CCC(C2(C)CCO)C3CC=C4CC(CCC4(C3=O)C)O)C	458.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
7-Methanoazulen-6-ol-6-acetate	54146524	Click to see CC1CCC23CC1C(C2CCC3(C)OC(=O)C)(C)C	264.40	unknown	via CMAUP database
alpha-Cedrene	6431015	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aS,6bR,10S,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	6325924	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1016/0031-9422(88)80641-1
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,6aR,8aS,12aR,14bR)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	137705657	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1016/0031-9422(88)80641-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,2S,5E,7E)-2-acetyloxy-1-methyl-16-oxo-8-propan-2-yl-15-oxabicyclo[9.3.2]hexadeca-5,7,11-triene-5-carboxylate	16059808	Click to see CC(C)C1=CC=C(CCC(C2(CCC=C(CC1)C(=O)O2)C)OC(=O)C)C(=O)OC	404.50	unknown	via CMAUP database
Sarcrassin E	16091635	Click to see CC(C)C1=CC=C(CCC(=O)C2(CCC=C(CC1)C(=O)O2)C)C(=O)OC	360.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide A	11995173	Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)O)(C)O	392.50	unknown	via CMAUP database
Crassocolide B	11995280	Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)OC(=O)C)(C)O	434.50	unknown	via CMAUP database
Crassocolide C	11995174	Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C)(C)O	376.50	unknown	via CMAUP database
Crassocolide D	11995281	Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)O)(C)O	334.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol	14034721	Click to see CC(CCC(C)C(C)(C)OC(=O)C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C	492.70	unknown	via CMAUP database
5alpha-Ergostane-3beta,5,6beta-triol	44558918	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C	434.70	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 / Furospirostanes and derivatives
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol	101007150	Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C	444.60	unknown	via CMAUP database
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate	101007149	Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C	486.70	unknown	via CMAUP database
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol	54586888	Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C	444.60	unknown	via CMAUP database
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate	101007148	Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C	486.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
11alpha-Hydroxygorgosterol	10599347	Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CC(C4C3CC=C5C4(CCC(C5)O)C)O)C)C	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone	8955	Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	316.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(24E)-24-N-Propylidenecholesterol	5281328	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
24-Propylidenecholest-5-en-3beta-ol	193212	Click to see CCC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	426.70	unknown	via CMAUP database
Fucosterol	5281326	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(R)-3-Hydroxybutyric acid	92135	Click to see CC(CC(=O)O)O	104.10	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Patchouli alcohol	10955174	Click to see CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O	222.37	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Maltotriose	871	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O	504.40	unknown	https://doi.org/10.1007/BF00579983
> Organoheterocyclic compounds / Dihydrofurans
(1R,2E,6R,8S,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-triene	54585297	Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(CO3)C)CC1)C)C	302.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A	70691856	Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C	390.50	unknown	via CMAUP database
Sarcocrassocolide B	70696020	Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C	390.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see C1=CC=C2C(=C1)C=CC(=O)O2	146.14	unknown	via CMAUP database
Osthol	10228	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C	244.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
Agrimol B	194000	Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C(=O)C(C)CC)O)CC3=C(C(=C(C(=C3O)C)OC)C(=O)CCC)O)O)O)C)OC	682.80	unknown	via CMAUP database
Agrimol C	442900	Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C)OC)C(=O)CCC)O)O)CC3=C(C(=C(C(=C3O)C)OC)C(=O)CCC)O)O	668.70	unknown	via CMAUP database
Agrimol F	5316827	Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C)OC)C(=O)CCC)O)O)CC3=C(C(=C(C(=C3O)C)OC)C(=O)C)O)O	640.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferide	5281666	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1007/BF00579983
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2S,3R,4R,5S,6R)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-chromen-3-yl]oxy-3,4,5-trihydroxy-tetrahydropyran-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	6479298	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1271/BBB.100200
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	57369598	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1271/BBB.100200
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	5387370	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)O)O)O	446.40	unknown	https://doi.org/10.1271/BBB.100200
Apigenin 7-glucuronide	5319484	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)O)O)O	446.40	unknown	https://doi.org/10.1271/BBB.100200
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/10.1271/BBB.100200
Luteolin-7-o-glucuronide	13607752	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/10.1271/BBB.100200
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4R,5R,6S)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] acetate	133561907	Click to see CC(=O)OC1C(C(C(OC1OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)CO)O)O	490.40	unknown	https://doi.org/10.1271/BBB.100200
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1271/BBB.100200
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	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/10.1271/BBB.100200
3-[(6-Deoxy-alpha-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one	53317405	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)OC)O)O)O	446.40	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	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	https://doi.org/10.1271/BBB.100200 https://doi.org/10.1016/0031-9422(93)85262-P
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12313332	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
5,7-Dihydroxy-2-(4-methoxyphenyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	74978151	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)OC)O)O)O	446.40	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
5,7-dihydroxy-2-(4-methoxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	154496818	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)OC)O)O)O	446.40	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
Afzelin	5316673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
Astragalin	5282102	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	https://doi.org/10.1016/0031-9422(93)85262-P
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	via CMAUP database
Isoquercetin	5280804	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/10.1271/BBB.100200
kaempferol 3-O-beta-L-glucopyranoside	9911508	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	https://doi.org/10.1271/BBB.100200
Kaempferol-3-O-rhamnoside	5835713	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
Kaempferol-3-O-rutinoside	5318767	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/0031-9422(93)85262-P
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1271/BBB.100200 https://doi.org/10.1016/S0305-1978(02)00170-9
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1271/BBB.100200
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1271/BBB.100200
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/BF00579983
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/10.1271/BBB.100200
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/10.1007/BF00579983 https://doi.org/10.1271/BBB.100200
> Phenylpropanoids and polyketides / Macrolides and analogues
(1aS,4E,8E,10aR,13aR,14aS)-4,8,14a-trimethyl-11-methylene-1a,3,6,7,10,10a,11,13a,14,14a-decahydrooxireno[12,13]cyclotetradeca[1,2-b]furan-12(2H)-one	643720	Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C	316.40	unknown	via CMAUP database
(1R,3R,5R,8E,12E,14S,15R)-14-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one	21574172	Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)O)OC(=O)C3=C)C	332.40	unknown	via CMAUP database
(1R,3R,5R,8E,12E,15S)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one	643718	Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C	316.40	unknown	via CMAUP database
[(1R,3R,5R,8E,12E,14S,15R)-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-14-yl] acetate	21638415	Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C	374.50	unknown	via CMAUP database
13-Acetoxysarcocrassolide	21775908	Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C	374.50	unknown	via CMAUP database
Crassocolide E	11995175	Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C	316.40	unknown	via CMAUP database
Crassocolide F	11995282	Click to see CC1=CCC(C(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C)OC(=O)C	374.50	unknown	via CMAUP database
Crassocolide N	54764414	Click to see CC1=CCCC(=CC2C(CC3C(O3)(C(=O)CC1)C)C(=C)C(=O)O2)C	330.40	unknown	via CMAUP database
ent-Sarcophine	101472593	Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C	316.40	unknown	via CMAUP database
Lobophytolide	23425511	Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C	316.40	unknown	via CMAUP database
Sarcocrassocolide C	46233394	Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C	332.40	unknown	via CMAUP database
Sarcocrassocolide D	46233452	Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C	332.40	unknown	via CMAUP database
Sarcocrassolide	643719	Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C	316.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database
Hexahydroxydiphenic acid	10315050	Click to see C1=C(C(=C(C(=C1O)O)O)C2=C(C(=C(C=C2C(=O)O)O)O)O)C(=O)O	338.22	unknown	via CMAUP database

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Agrimonia eupatoria

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