Pyrola rotundifolia, also known as the round-leaved wintergreen, is a type of plant belonging to the Pyrola genus. It can be found in various regions including Europe, Japan, Mongolia, Myanmar, and Russia. This plant has round-shaped leaves and is commonly used for medicinal purposes. It is a popular species among gardeners and is known for its attractive appearance.

Synonyms Top

Scientific name	Authority	First published in
Pyrola tianschanica	Poljakov	Byull. Glavn. Bot. Sada 6: 55 (1950)
Pyrola major	Lam.	Fl. Franç. 2: 530 (1779)
Pyrola magna	Gueldenst. ex Ledeb.	Fl. Ross. 2: 928 (1846)
Pyrola serotina	La Fons	Ann. Pas-de-Calais 1848-1849: 223 (1849)
Pyrola ovalifolia	Schur	Enum. Pl. Transsilv. : 449 (1866)
Pyrola declinata	Moench	Methodus : 71 (1794)
Pyrola groenlandica	Hornem.	Fl. Dan. 11: t. 1817 (1825)
Thelaia intermedia	Alef.	Linnaea 28: 65 (1856)
Thelaia rotundifolia	(L.) Alef.	Linnaea 28: 60 (1856)
Thelaia arenaria	Alef.	Bot. Zeitung (Berlin) 20: 220 (1862)
Thelaia bracteosa	Alef.	Linnaea 28: 57 (1856)
Pyrola pumila	(Hornem.) Hornem. ex Cham. & Schltdl.	Linnaea 1: 514 (1826)

Common names Top

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Filter by language:

Language	Common/alternative name
English	round-leaved wintergreen
Arabic	نعنع مستدير الورق
Arabic	قوقاع
Arabic	بيرولا
Azerbaijani	dəyirmiyarpaq pirola
Belarusian	Грушанка круглалістая
Bulgarian	кръглолистна мурава
Czech	hruštička okrouhlolistá
Welsh	glesyn-y-gaeaf deilgrwn
Danish	mose-vintergrøn
German	rundblättriges wintergrün
Persian	پیرولا روتندیفولیا
Finnish	isotalvikki
French	pyrole à feuilles rondes
Irish	glasluibh chruinn
Hungarian	kereklevelű körtike
Kazakh	Дөңгелек жапырақты алмұртшөп
Lithuanian	apskritalapė kriaušlapė
Latvian	apaļlapu ziemciete
Dutch	rond wintergroen
Polish	gruszyczka okrągłolistna
Russian	Грушанка круглолистная
Slovak	hruštička okrúhlolistá
Swedish	vitpyrola
Ukrainian	Грушанка круглолиста
Chinese	鹿蹄草
Chinese	圆叶鹿蹄草
Chinese	鹿衔草

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Pyrola rotundifolia subsp. maritima	(Kenyon) E.F.Warb	Fl. Brit. Isles [Clapham et al.] 789. 1952
Pyrola rotundifolia subsp. rotundifolia

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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difficult; plant in soil from established plant, or pour boiling water over milled sphagnum moss, sow seeds, enclose in plastic bag

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

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

Asia-tropical click to expand
- Indo-China
  - Myanmar
  - Vietnam

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
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000396288
Tropicos	26800027
INPN	116547
KEW	urn:lsid:ipni.org:names:331846-1
The Plant List	kew-2410818
Open Tree Of Life	18686
Observations.org	2705
NCBI Taxonomy	13651
NBN Atlas	NBNSYS0000004592
IPNI	331846-1
iNaturalist	60374
GBIF	2888269
Freebase	/m/0d7d6v
EPPO	PYWRO
Elurikkus	6663
USDA GRIN	430229
Wikipedia	Pyrola_rotundifolia
CMAUP	NPO2236

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

Chryseobacterium herbae Isolated from the Rhizospheric Soil of Pyrola calliantha H. Andres in Segrila Mountain on the Tibetan Plateau

Zhang L, Wang Y, Kong D, Ma Q, Li Y, Xing Z, Ruan Z

Microorganisms

05-Aug-2023

PMCID:	PMC10459008
doi:	10.3390/microorganisms11082017
PMID:	37630577

Long-Term Vegetation Changes and Socioeconomic Effects of River Engineering in Industrialized Areas (Southern Poland)

Rahmonov O, Dragan W, Cabała J, Krzysztofik R

Int J Environ Res Public Health

27-Jan-2023

PMCID:	PMC9915360
doi:	10.3390/ijerph20032255
PMID:	36767623

Phytogeographic Characteristics of Montane Coniferous Forests of the Central Balkan Peninsula (SE Europe)

Ilić T, Kuzmanović N, Vukojičić S, Lakušić D

Plants (Basel)

22-Nov-2022

PMCID:	PMC9741231
doi:	10.3390/plants11233194
PMID:	36501234

Scrub encroachment promotes biodiversity in temperate European wetlands under eutrophic conditions

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
doi:	10.1002/ece3.9445
PMID:	36340817

Diverse in Local, Overlapping in Official Medical Botany: Critical Analysis of Medicinal Plant Records from the Historic Regions of Livonia and Courland in Northeast Europe, 1829–1895

Prakofjewa J, Anegg M, Kalle R, Simanova A, Prūse B, Pieroni A, Sõukand R

Plants (Basel)

13-Apr-2022

PMCID:	PMC9032843
doi:	10.3390/plants11081065
PMID:	35448792

Vascular Plants Flora of Mire Ecosystem of the Bolshoy Shantar Island (the Far East of Russia)

Kuptsova VA, Antonova LA, Chakov VV

Plants (Basel)

08-Mar-2022

PMCID:	PMC8948750
doi:	10.3390/plants11060723
PMID:	35336605

Interaction Between Chinese Medicine and Warfarin: Clinical and Research Update

Zhuang W, Liu S, Zhao X, Sun N, He T, Wang Y, Jia B, Lin X, Chu Y, Xi S

Front Pharmacol

20-Sep-2021

PMCID:	PMC8489681
doi:	10.3389/fphar.2021.751107
PMID:	34616303

Phthalic Acid Esters: Natural Sources and Biological Activities

Huang L, Zhu X, Zhou S, Cheng Z, Shi K, Zhang C, Shao H

Toxins (Basel)

16-Jul-2021

PMCID:	PMC8310026
doi:	10.3390/toxins13070495
PMID:	34357967

Plant CSR types in the north: comparing the morphological and morpho-physiological approaches

Novakovskiy AB, Dubrovskiy YA, Dalke IV, Maslova SP

Physiol Mol Biol Plants

22-Mar-2021

PMCID:	PMC8055743
doi:	10.1007/s12298-021-00973-9
PMID:	33967455

How to Protect Natural Habitats of Rare Terrestrial Orchids Effectively: A Comparative Case Study of Cypripedium calceolus in Different Geographical Regions of Europe

Jakubska-Busse A, Tsiftsis S, Śliwiński M, Křenová Z, Djordjević V, Steiu C, Kolanowska M, Efimov P, Hennigs S, Lustyk P, Kreutz K(

Plants (Basel)

20-Feb-2021

PMCID:	PMC7923770
doi:	10.3390/plants10020404
PMID:	33672509

Long-reads reveal that Rhododendron delavayi plastid genome contains extensive repeat sequences, and recombination exists among plastid genomes of photosynthetic Ericaceae

Li H, Guo Q, Li Q, Yang L

PeerJ

22-Apr-2020

PMCID:	PMC7183307
doi:	10.7717/peerj.9048
PMID:	32351791

Phenolic Composition of the Leaves of Pyrola rotundifolia L. and Their Antioxidant and Cytotoxic Activity

Szewczyk K, Bogucka-Kocka A, Vorobets N, Grzywa-Celińska A, Granica S

Molecules

10-Apr-2020

PMCID:	PMC7180938
doi:	10.3390/molecules25071749
PMID:	32290223

“A herder’s duty is to think”: landscape partitioning and folk habitats of Mongolian herders in a mountain forest steppe (Khuvsugul-Murun region)

Gantuya B, Avar Á, Babai D, Molnár Á, Molnár Z

J Ethnobiol Ethnomed

20-Nov-2019

PMCID:	PMC6868869
doi:	10.1186/s13002-019-0328-x
PMID:	31747913

In vitro axenic germination and cultivation of mixotrophic Pyroloideae (Ericaceae) and their post-germination ontogenetic development

Figura T, Tylová E, Šoch J, Selosse MA, Ponert J

Ann Bot

07-Nov-2018

PMCID:	PMC6417480
doi:	10.1093/aob/mcy195
PMID:	30403767

Contrasting spatial, temporal and environmental patterns in observation and specimen based species occurrence data

Speed JD, Bendiksby M, Finstad AG, Hassel K, Kolstad AL, Prestø T

PLoS One

26-Apr-2018

PMCID:	PMC5919666
doi:	10.1371/journal.pone.0196417
PMID:	29698441

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
> Alkaloids and derivatives
Ethyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate	34167	Click to see CCOC(=O)C1=CCCN(C1)C	169.22	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
7-(Hydroxymethyl)-2-methylnaphthalene-1,4-dione	11820154	Click to see CC1=CC(=O)C2=C(C1=O)C=C(C=C2)CO	202.21	unknown	https://doi.org/10.1248/CPB.40.2083
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Methylhydroquinone	7253	Click to see CC1=C(C=CC(=C1)O)O	124.14	unknown	https://doi.org/10.1248/CPB.40.2083
> Benzenoids / Tetralins
(2R,4R)-4-hydroxy-2,7-dimethyl-3,4-dihydro-2H-naphthalen-1-one	10397654	Click to see CC1CC(C2=C(C1=O)C=C(C=C2)C)O	190.24	unknown	https://doi.org/10.1248/CPB.40.2083
(2R,4S)-4-hydroxy-2,7-dimethyl-3,4-dihydro-2H-naphthalen-1-one	10261926	Click to see CC1CC(C2=C(C1=O)C=C(C=C2)C)O	190.24	unknown	https://doi.org/10.1248/CPB.40.2083
(3S,4R)-4-hydroxy-3,6-dimethyl-3,4-dihydro-2H-naphthalen-1-one	10352512	Click to see CC1CC(=O)C2=C(C1O)C=C(C=C2)C	190.24	unknown	https://doi.org/10.1248/CPB.40.2083
1(2H)-Naphthalenone, 3,4-dihydro-4-hydroxy-3,6-dimethyl-, (3S,4S)-	10352511	Click to see CC1CC(=O)C2=C(C1O)C=C(C=C2)C	190.24	unknown	https://doi.org/10.1248/CPB.40.2083
4-hydroxy-2,7-dimethyl-3,4-dihydro-2H-naphthalen-1-one	85670900	Click to see CC1CC(C2=C(C1=O)C=C(C=C2)C)O	190.24	unknown	https://doi.org/10.1248/CPB.40.2083
4-hydroxy-3,6-dimethyl-3,4-dihydro-2H-naphthalen-1-one	85119147	Click to see CC1CC(=O)C2=C(C1O)C=C(C=C2)C	190.24	unknown	https://doi.org/10.1248/CPB.40.2083
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate	6999980	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	via CMAUP database
(R)-(+)-Citronellal	75427	Click to see CC(CCC=C(C)C)CC=O	154.25	unknown	via CMAUP database
beta-Ocimene	18756	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	via CMAUP database
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	via CMAUP database
Neral	643779	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene	443160	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	via CMAUP database
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
(+)-beta-Phellandrene	442484	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
(1R)-1-Isopropenyl-4-methyl-3-cyclohexene-1beta-ol	16059268	Click to see CC1=CCC(CC1)(C(=C)C)O	152.23	unknown	via CMAUP database
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4E,9S)-	6887	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(+)-abscisic acid beta-D-glucopyranosyl ester	46173811	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)C)O)(C)C	426.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1Z,4E)-germacrene B	5371080	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	via CMAUP database
(6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	49796490	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	via CMAUP database
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	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	https://doi.org/10.1248/CPB.33.5355
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione	92966492	Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C	470.50	unknown	via CMAUP database
Nomilin	72320	Click to see CC(=O)OC1CC(=O)OC(C2C1(C3CCC4(C(OC(=O)C5C4(C3(C(=O)C2)C)O5)C6=COC=C6)C)C)(C)C	514.60	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-(4-hydroxy-3-methylphenoxy)oxane-3,4,5-triol	22524271	Click to see CC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O	286.28	unknown	https://doi.org/10.1248/CPB.40.2083 https://doi.org/10.1248/CPB.53.1051
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol	7576924	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O	272.25	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(4-hydroxy-3,6-dimethyl-5,8-dihydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	5320926	Click to see CC1=CCC2=C(C=C(C(=C2C1)O)C)OC3C(C(C(C(O3)CO)O)O)O	352.40	unknown	via CMAUP database
2-[4-Hydroxy-3-[2-[2-hydroxy-3-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]-3-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5-methylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85427100	Click to see CC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C)OC4=C(C(=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O	854.80	unknown	https://doi.org/10.1248/CPB.53.1051
2-[4-Hydroxy-3-[2-hydroxy-3-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5-methylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	72764087	Click to see CC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C)O)OC4C(C(C(C(O4)CO)O)O)O	570.50	unknown	https://doi.org/10.1248/CPB.53.1051
CID 5318079	5318079	Click to see CC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O	286.28	unknown	https://doi.org/10.1248/CPB.53.1051 https://doi.org/10.1248/CPB.40.2083
Homoarbutin	324796	Click to see CC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O	286.28	unknown	https://doi.org/10.1248/CPB.40.2083 https://doi.org/10.1248/CPB.53.1051
Isohomoarbutin	5318573	Click to see CC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O	286.28	unknown	https://doi.org/10.1248/CPB.53.1051
Pyrolaside A	11238460	Click to see CC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C)O)OC4C(C(C(C(O4)CO)O)O)O	570.50	unknown	https://doi.org/10.1248/CPB.53.1051
Pyrolaside B	11182040	Click to see CC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C)OC4=C(C(=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O	854.80	unknown	https://doi.org/10.1248/CPB.53.1051
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal	8175	Click to see CCCCCCCCCC=O	156.26	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone	7469	Click to see CC(=O)C1=CC=C(C=C1)O	136.15	unknown	https://doi.org/10.1248/CPB.40.2083
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
3-Hydroxy-4H-pyran-4-one	68129	Click to see C1=COC=C(C1=O)O	112.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
5-Methoxynoracronycine	14463134	Click to see CC1(C=CC2=C(O1)C=C(C3=C2N(C4=C(C3=O)C=CC=C4OC)C)O)C	337.40	unknown	via CMAUP database
Junosidine	11660079	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(N3C)C(=CC=C4)OC)C	337.40	unknown	via CMAUP database
Junosine	15286413	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(N2C)C(=CC=C3)O)O)C	325.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one	13917410	Click to see CC(=O)C=CC1=C(C=CC2=C1OC(=O)C=C2)OC	244.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
6,8-Diprenyl-7-hydroxy-2H-1-benzopyran-2-one	14769401	Click to see CC(=CCC1=C(C(=C2C(=C1)C=CC(=O)O2)CC=C(C)C)O)C	298.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Butanoic acid, 3-methyl-, 9,10-dihydro-10-hydroxy-8,8-dimethyl-2-oxo-2H,8H-benzo(1,2-b:3,4-b')dipyran-9-yl ester, (9R-trans)-	14055879	Click to see CC(C)CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O	346.40	unknown	via CMAUP database
Seselin	68229	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C=C3)C	228.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Clausarin	5315945	Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=C(C(=O)O3)C(C)(C)C=C)C(C)(C)C=C)C	380.50	unknown	via CMAUP database
Dentatin	342801	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC(=O)C=C3)OC)C	326.40	unknown	via CMAUP database
nor-Dentatin	5495613	Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=CC(=O)O3)C(C)(C)C=C)C	312.40	unknown	via CMAUP database
Ponfolin	174673	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC(=O)C=C3)OC(C)(C)C=C)C	380.50	unknown	via CMAUP database
Xanthoxyletin	66548	Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C	258.27	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-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12304330	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/10.1248/CPB.40.2083
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/10.1248/CPB.40.2083
3-[(2S,3S,4R,5S)-5-(1,2-dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	10226724	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O	464.40	unknown	via CMAUP database
4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[[2-O-(3,4,5-trihydroxybenzoyl)-b-D-galactopyranosyl]oxy]-	133568497	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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O	616.50	unknown	https://doi.org/10.1248/CPB.40.2083
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/10.1248/CPB.40.2083
Quercetin 3-(2-galloylglucoside)	13889202	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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O	616.50	unknown	https://doi.org/10.1248/CPB.40.2083
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(S)-3',5-Dihydroxy-4'-methoxy-7-[2-O,6-O-di(alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyloxy]flavanone	102316658	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)OC)O)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O	756.70	unknown	via CMAUP database
Hesperidin	10621	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)OC)O)O)O)O)O)O)O)O	610.60	unknown	via CMAUP database
Naringenin 7-O-(2'',6''-di-O-alpha-rhamnopyranosyl)-beta-glucopyranoside	5278403	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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O	726.70	unknown	via CMAUP database
Narirutin	442431	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	580.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
beta-D-Glucopyranose, cyclic-3,6-(4,4',5,5',6,6'-hexahydroxy(1,1'-biphenyl)-2,2'-dicarboxylate) 4-(4-hydrogen-2-(3-carboxy-3,4-dihydro-5,6,7-trihydroxy-1-oxo-1H-2-benzopyran-4-yl)-2-butenedioate)-1-(3,4,5-trihydroxybenzoate)	6475760	Click to see C=C1C2=CC(=C(C(=C2C(C(O1)C(=O)O)C(=CC(=O)O)C(=O)OC3C4COC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)OC3C(C(O4)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)O)O)O)O)O)O)O)O	968.70	unknown	via CMAUP database

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Pyrola rotundifolia

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