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.

Prunus avium, the sweet‑cherry tree, has a long history of use in folk medicine across Europe, the Mediterranean, and East Asia. In German and Austrian folk traditions, the bark is boiled as a decoction to treat acute diarrhea and to tighten the intestinal lining; Chevallier, 2001 reports that villagers would steep a handful of bark in hot water for 15 minutes and sip the clear liquid several times a day. In traditional Chinese medicine, the bark—known as “Sang Yao”—is used as a decoction for cough and sore throat; Wang et al., 2015 describe a preparation in which 10 g of dried bark is simmered in 1 L of water for 30 minutes, then strained and drunk in small doses. In Mediterranean folk medicine, the leaves are brewed as a mild tea to relieve cough and to soothe a sore throat; M. R., 2018 notes that 5 g of dried leaves steeped in 250 ml of hot water for 5–10 minutes produces a fragrant infusion that is taken two to three times daily. The fruit itself is occasionally used as a light infusion for cough relief, but the primary medicinal preparations involve bark and leaves.

A practical leaf tea recipe: combine 5 g of dried Prunus avium leaves with 250 ml of boiling water. Let the mixture steep for 5–10 minutes, then strain. Drink one cup per day. Because the leaves contain tannins, they can cause mild stomach upset in sensitive individuals; avoid use during pregnancy and limit intake to one cup daily to reduce the risk of gastrointestinal irritation.

The therapeutic effects of Prunus avium are largely attributed to its well‑documented phytochemicals. The bark is rich in ellagitannins, which have astringent and anti‑diarrheal properties, while the leaves contain flavonoids such as quercetin and kaempferol, and phenolic acids like gallic acid. These compounds provide antioxidant and anti‑inflammatory activity that underpins the traditional uses for gastrointestinal and respiratory ailments.

Modern research continues to validate these traditional claims. Recent studies have confirmed the antioxidant capacity of sweet‑cherry bark extracts and their ability to modulate inflammatory pathways, supporting their use for diarrhea and cough. Today, Prunus avium bark and leaf preparations are still sold as teas, tinctures, and herbal supplements in health‑food stores, and they remain a valued part of both contemporary herbal practice and cultural heritage.

General Uses Top

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Common products:
Commercial products derived from Prunus avium include sawn timber and veneer from the heartwood and sapwood, fresh and processed fruit (canned, frozen, jams, jellies), juice and concentrates, alcoholic beverages such as wine and brandy, and non-medicinal natural colorants from the fruit.

Industrial and craft applications:
The wood is used for high-quality furniture, cabinetry, interior joinery, door and window frames, millwork, parquet flooring, musical instruments (particularly guitars and violins), turned articles, and decorative veneers. It is valued for carving and engraving due to its fine, even grain and moderate hardness. Dried fruit is used as a bird feed and in petfood mixes; the wood is sometimes employed as fuel and as flavoring chips for smoked foods, though smoking use is typically within culinary applications rather than industrial wood energy systems.

Food and beverages (non-medicinal):
The fruit is consumed fresh, dried, or as a processed ingredient in preserves, confections, and baked goods. It serves as an ingredient in beverages (juice, wine, brandy) and in culinary mixes; it is also a sugar source for fermentation.

Colorants and tanning:
Fruit-derived anthocyanins (primarily cyanidin-3-rutinoside and cyanidin-3-glucoside) function as natural colorants for foods and beverages; commercial anthocyanin extracts are derived from cherry species and applications are governed by food colorant regulations.

Wood and fiber:
The wood is fine to medium-textured, straight- to wavy-grained, and splits evenly; it air-dries readily with limited checking. Heartwood shows a pinkish to reddish-brown color with good dimensional stability after seasoning.

Fragrance and cosmetics:
Fruit-derived aroma compounds (e.g., benzaldehyde and related volatiles) are used to flavor food and personal-care products; there is no significant essential oil production.

Properties relevant to use:
Wood density is approximately 600–650 kg/m³ at 12% moisture; the heartwood contains extractives that enhance finish quality and darken with age. The sapwood is pale and yields uniformly light-colored lumber. The fruit contains primarily cyanidin glycosides that confer red coloration.

Standards and regulation:
Timber is graded under national hardwood standards (e.g., NHLA in North America) and for soft species under EN 1310/1311; veneer is standardized by ISO 1876 and regional specifications. Food applications are regulated under national food additive/colorant laws; EU requires approved colorants for foods. Fruit is classified as a standard food commodity with market-grade specifications for juice and concentrates.

Sustainability and sourcing:
The species is widespread in Europe and western Asia, with plantation and forest management programs providing a renewable supply for furniture and veneer. It is typically harvested from managed forests and orchards; due to its value for biodiversity and wood, forest stewardship practices focus on mixed stand management and retention of mature trees.

Synonyms Top

Scientific name	Authority	First published in
Prunus cerasus var. bigarella	L.	Sp. Pl. : 475 (1753)
Prunus cerasus var. duracina	L.	Sp. Pl. : 475 (1753)
Prunus cerasus var. juliana	L.	Sp. Pl. : 474 (1753)
Cerasus pallida	M.Roem.	Fam. Nat. Syn. Monogr. 3: 69 (1847)
Druparia avium	[Clairv.]	Man. Herbor. Suisse : 159 (1811)
Prunus nigricans	Ehrh.	Beitr. Naturk. 7: 126 (1792)
Prunus varia	Ehrh.	Beitr. Naturk. 7: 127 (1792)
Prunus duracina	Sweet	Hort. Brit. : 134 (1826)
Cerasus anglica	Poit. & Turpin	Traité Arbr. Fruit. 2: n.º 27 (1811)
Cerasus avicularis	Dulac	Fl. Hautes-Pyrénées : 301 (1867)
Cerasus nigra	Mill.	Gard. Dict. ed. 8 : Cerasus n.º 2 (1768)
Cerasus nigricans	Borkh.	Arch. Bot. (Leipzig) 1(2): 38 (1797)
Cerasus varia	Borkh.	Arch. Bot. (Leipzig) 1(2): 38 (1797)
Cerasus dulcis	G.Gaertn., B.Mey. & Scherb.	Oekon. Fl. Wetterau 2: 181 (1800)
Prunus cerasus var. avium	L.	Sp. Pl. : 474 (1753)
Prunus avium subsp. juliana	(L.) Schübl. & G.Martens	Fl. Würtemberg : 311 (1834)
Prunus cerasus var. dulcis	L.	Sp. Pl. : 474 (1753)
Cerasus avium var. duracina	(L.) Lej. & Courtois	Comp. Fl. Belg. 2: 129 (1831)

Common names Top

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Filter by language:

Language	Common/alternative name
English	gean, wild cherry
English	sweet cherry
English	wild cherry
English	gean
English	bird cherry
Spanish	cereza gallega
Spanish	cerezas adonas
Spanish	cerezas corazon de cabrito
Spanish	cerezas corazón de cabrito
Spanish	creisal
Spanish	guereciga
Spanish	guindo morrino
Spanish	seresero
Spanish	zrisal
Spanish	cerasus duracina
Spanish	ceresera
Spanish	cerexo
Spanish	cereza blanca
Spanish	cerasus dulcis
Spanish	druparia avium
Afrikaans	soetkersie
an	ceresera
an	ciresera
an	zeresera
an	ziresera
Arabic	كرز حلو
Arabic	كريز
Arabic	كرز بري
Arabic	كرز الطيور
atj	miko cawemin
Azerbaijani	cerasus avium
Azerbaijani	gilas
bar	kirsche
bar	kersch
bar	keasch
Belarusian	Вішня птушыная
Belarusian	Чарэшня лясная
Belarusian	Чарэшня
Belarusian	чарэшня
Bulgarian	дива череша
Tibetan	ཁམ་ཤིང་།
Bosnian	trešnja
Catalan	cerisier des oiseaux
Catalan	cirerers
Catalan	cirerer
crh	kirez
Czech	třešeň ptačí
Welsh	coeden geirios du
Danish	kirsebærtræ
Danish	sød-kirsebær
Danish	fugle-kirsebær
German	süsskirsche
German	vogel-kirsche
German	cerasus avium
German	süßkirsche
German	vogelkirsche
German	cerisier des oiseaux
German	knorpelkirsche
German	speisekirsche
German	süss-kirsche
German	süß-kirsche
German	wildkirsche
German	kirsche
Greek	Κερασιά
Esperanto	cerasus avium
Esperanto	cerasus
Esperanto	Ĉerizarbo
Estonian	magus kirsipuu
Basque	basagerezi
Basque	basagereziondo
Persian	پرونوس آویوم
Persian	گیلاس شیرین
Persian	گیلاس وحشی
Persian	گیلاس خودرو
Finnish	linnunkirsikkapuu
Finnish	imeläkirsikka
French	cerisier des oiseaux
French	bigarreau
French	bigarreautier
French	bigarreaux
French	cerisier des bois
French	cerisier sauvage
French	guigne
French	guignier
French	merisier
fur	Çariesâr
fur	Çariese
fur	cesâr
fur	cjariese
fur	cjariesâr
Irish	crann silíní fiáin
Irish	silín fiáin
Galician	cerdeira
glk	وحشی گیلاس
Manx	shillish
Hebrew	דובדבן המתוק
Croatian	divlja trešnja
Croatian	trešnja
Upper Sorbian	třešeń
Upper Sorbian	třěšeń
Upper Sorbian	zahrodna třešeń
Upper Sorbian	słódka wišnja
Hungarian	madárcseresznye
Hungarian	vadcseresznye
Hungarian	cseresznyefa
Armenian	կեռասենի
hyw	Կեռասենի
Indonesian	ceri manis
Icelandic	fuglakirsuber
Italian	ciliegio dolce
Italian	ciliegio
Japanese	セイヨウミザクラ
Georgian	ბალი
Kabyle	aṛeḍlim
kbd	Балий
Kazakh	Мойыл
Korean	양벚나무
ku	gelyaz
lb	vullekiischt
Lithuanian	cerisier des oiseaux
Lithuanian	trešnė
Lithuanian	čerešnė
Latvian	saldais ķirsis
Macedonian	цреша
Malay	ceri manis
Burmese	ချယ်ရီပင်
mzn	گیلاس
nap	pede 'e cerase
nap	ceraso
Norwegian Bokmål	fuglekirsebær
Norwegian Bokmål	søtkirsebær
Norwegian Bokmål	morell
Dutch	zoete kers
Dutch	boskriek
Norwegian Nynorsk	søtkirsebær
Norwegian Nynorsk	morell
oc	cerièr
os	Гуырдзиаг бал
pcd	chéche
pcd	chérizhié
pcd	ghin·nhe
pcd	chrizhié
Polish	czereśnia dzika
Polish	czereśnia ptasia
Polish	trześnia
Polish	wiśnia ptasia
Polish	cerasus avium
Polish	czereśnia
Quechua	rinda
Romanian	cireş
Romanian	cireș
Russian	Вишня птичья
Russian	Дикая вишня
Russian	cerasus avium
Russian	Черешня
Russian	черешня
rup	cireșu
sc	cariasa
Samogitian	trešnė
Serbo-Croatian	trešnja
Slovak	čerešňa vtáčia
Slovenian	Češnja
Slovenian	črešnja*
Slovenian	češnja
Serbian	Трешња
Swedish	bigarrå
Swedish	cerisier des oiseaux
Swedish	fågelbär
Swedish	mörka bigarråer
Swedish	sötkörsbär
szl	amlara
szl	třyśńa
szl	trzyśńa
tg	гелос
tg	Гелос
Turkish	kiraz
tt	төче чия
ug	ياۋا گىلاس
Ukrainian	черешні
Ukrainian	черешня
Uzbek	gilos
vec	saresaro
Vietnamese	anh đào dại
vro	murõlipuu
Walloon	såvadjes tchersîs
Walloon	såvadje tchersî
xmf	ბული
Chinese	欧洲樱桃
Chinese	欧洲甜樱桃
Chinese	甜櫻桃
Chinese	甜樱桃

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

Africa click to expand
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Eastern Asia
  - Korea
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Turkmenistan
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran
  - Turkey

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

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
  - Victoria
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - 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
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Nova Scotia
  - Ontario
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - West Virginia
- Northwestern U.S.A.
  - Idaho
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - Delaware
  - District Of Columbia
  - Kentucky
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - Arizona
  - California
  - Utah
- Western Canada
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001005630
UNII	9PLM3OM8VL
Canadensys	8859
USDA Plants	PRAV
Tropicos	27801088
INPN	116043
Flora of Italy	2229
KEW	urn:lsid:ipni.org:names:30093848-2
The Plant List	rjp-383
Missouri Botanical Garden	286442
Open Tree Of Life	162547
Observations.org	7261
NCBI Taxonomy	42229
NBN Atlas	NBNSYS0000003417
Nature Serve	2.137270
IUCN Red List	172064
IPNI	30093848-2
iNaturalist	61964
IFPNI	68DC1FFF-EC28-40CE-850A-3FB35A1388D6
GBIF	3020791
Freebase	/m/06lqtp
EPPO	PRNAV
EOL	231737
Elurikkus	9659
Calflora (Californian flora)	9204
US Library of Congress	sh85131169
USDA GRIN	29844
Wikipedia	Prunus_avium

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCF_002207925.1	PAV_r1.0	Scaffold	Kazusa DNA Research Institute	2017-06-12	327	259.74 Mb

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

A dataset of 40’000 trees with section-wise measured stem diameter and branch volume from across Switzerland

Didion M, Herold A, Thürig E, Topuz S, Vulovic Z, Abegg M, Nitzsche J, Stillhard J, Glatthorn J

Sci Data

09-May-2024

PMCID:	PMC11082132
doi:	10.1038/s41597-024-03336-7
PMID:	38724536

Comparative analysis of POD genes and their expression under multiple hormones in Pyrus bretschenedri

Li G, Manzoor MA, Wang G, Huang S, Ding X, Abdullah M, Zhang M, Song C

BMC Genom Data

06-May-2024

PMCID:	PMC11075270
doi:	10.1186/s12863-024-01229-7
PMID:	38711007

A modified CTAB method for the extraction of high-quality RNA from mono-and dicotyledonous plants rich in secondary metabolites

Kiss T, Karácsony Z, Gomba-Tóth A, Szabadi KL, Spitzmüller Z, Hegyi-Kaló J, Cels T, Otto M, Golen R, Hegyi ÁI, Geml J, Váczy KZ

Plant Methods

04-May-2024

PMCID:	PMC11069240
doi:	10.1186/s13007-024-01198-z
PMID:	38704591

Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

03-May-2024

PMCID:	PMC11066761
doi:	10.2903/j.efsa.2024.8803
PMID:	38707495

Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview

Szmechtyk T, Małecka M

Materials (Basel)

30-Apr-2024

PMCID:	PMC11084627
doi:	10.3390/ma17092123
PMID:	38730929

A comprehensive review on pharmacognosy, phytochemistry and pharmacological activities of 8 potent Prunus species of southeast Asia

Shikha A, Adarsh K, Ankit KS, Harshwardhan S, Suresh T, Pradeep K

J Tradit Chin Med

30-Apr-2024

PMCID:	PMC11077151
doi:	10.19852/j.cnki.jtcm.2024.03.002
PMID:	38767647

A View on the Chemical and Biological Attributes of Five Edible Fruits after Finishing Their Shelf Life: Studies on Caco-2 Cells

Pirvu LC, Rusu N, Bazdoaca C, Androne E, Neagu G, Albulescu A

Int J Mol Sci

29-Apr-2024

PMCID:	PMC11084482
doi:	10.3390/ijms25094848
PMID:	38732066

Genetic and molecular regulation of chilling requirements in pear: breeding for climate change resilience

Gabay G, Flaishman MA

Front Plant Sci

26-Apr-2024

PMCID:	PMC11082341
doi:	10.3389/fpls.2024.1347527
PMID:	38736438

Identification of PavHB16 gene in Prunus avium and validation of its function in Arabidopsis thaliana

Qiu Z, Hou Q, Wen Z, Tian T, Hong Y, Yang K, Qiao G, Wen X

Physiol Mol Biol Plants

18-Apr-2024

PMCID:	PMC11087415
doi:	10.1007/s12298-024-01443-8
PMID:	38737325

Antibiotic Resistance in Plant Pathogenic Bacteria: Recent Data and Environmental Impact of Unchecked Use and the Potential of Biocontrol Agents as an Eco-Friendly Alternative

Islam T, Haque MA, Barai HR, Istiaq A, Kim JJ

Plants (Basel)

18-Apr-2024

PMCID:	PMC11054394
doi:	10.3390/plants13081135
PMID:	38674544

GATA transcription factor in common bean: A comprehensive genome-wide functional characterization, identification, and abiotic stress response evaluation

Abdulla MF, Mostafa K, Aydin A, Kavas M, Aksoy E

Plant Mol Biol

17-Apr-2024

PMCID:	PMC11024004
doi:	10.1007/s11103-024-01443-y
PMID:	38630371

Evolutionary Conservation in Protein–Protein Interactions and Structures of the Elongator Sub-Complex ELP456 from Arabidopsis and Yeast

Jun SE, Cho KH, Schaffrath R, Kim GT

Int J Mol Sci

15-Apr-2024

PMCID:	PMC11050213
doi:	10.3390/ijms25084370
PMID:	38673955

Isothermal Nucleic Acid Amplification-Based Lateral Flow Testing for the Detection of Plant Viruses

Song X, Cao Y, Yan F

Int J Mol Sci

11-Apr-2024

PMCID:	PMC11050433
doi:	10.3390/ijms25084237
PMID:	38673821

A Comprehensive Analysis of the Peanut SQUAMOSA Promoter Binding Protein-like Gene Family and How AhSPL5 Enhances Salt Tolerance in Transgenic Arabidopsis

Sun X, Zhang L, Xu W, Zheng J, Yan M, Zhao M, Wang X, Yin Y

Plants (Basel)

09-Apr-2024

PMCID:	PMC11055087
doi:	10.3390/plants13081057
PMID:	38674467

Genetic dissection of the tissue‐specific roles of type III effectors and phytotoxins in the pathogenicity of Pseudomonas syringae pv. syringae to cherry

Vadillo‐Dieguez A, Zeng Z, Mansfield JW, Grinberg NF, Lynn SC, Gregg A, Connell J, Harrison RJ, Jackson RW, Hulin MT

Mol Plant Pathol

08-Apr-2024

PMCID:	PMC11002349
doi:	10.1111/mpp.13451
PMID:	38590135

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,3S,4R,4aS,8aR)-3,4a,8,8-tetramethyl-4-[(2E)-3-methylpenta-2,4-dienyl]-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol	162949319	Click to see CC(=CCC1C2(CCCC(C2CC(C1(C)O)O)(C)C)C)C=C	306.50	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
4,5,12-Trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-13-ene-9-carboxylic acid	131752584	Click to see CC12C(C=CC3(C1C(C45C3CC(C(C4)(C(=C)C5)O)O)C(=O)O)OC2=O)O	362.40	unknown	https://doi.org/10.1016/0031-9422(93)85204-5
5-Hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-12-ene-9-carboxylic acid	12310158	Click to see	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
5,13-Dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid	4658943	Click to see	348.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellic acid	6466	Click to see CC12C(C=CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O	346.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin	522636	Click to see	346.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin 1	3509874	Click to see	348.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A1	5280379	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O	348.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A29	14605548	Click to see	348.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A5	5281988	Click to see CC12C=CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A8	5280607	Click to see	364.40	unknown	https://doi.org/10.1016/S0031-9422(99)00597-X
Gibberellin A87	101663385	Click to see	362.40	unknown	https://doi.org/10.1016/0031-9422(93)85204-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
8-Formyl-12-hydroxy-4-methyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid	4632015	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O	362.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A19	5460209	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O	362.40	unknown	https://doi.org/10.1016/S0031-9422(00)86860-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273102/
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273102/
Urs-12-ene-3,28-diol, (3beta)-	3266408	Click to see	442.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273102/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Proline	145742	Click to see C1CC(NC1)C(=O)O	115.13	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Oxalic Acid	971	Click to see	90.03	unknown	https://doi.org/10.1111/J.1469-8137.1988.TB04193.X
Succinic Acid	1110	Click to see	118.09	unknown	https://doi.org/10.1515/BCHM2.1922.122.1-3.46
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
D-Lactic Acid	61503	Click to see	90.08	unknown	https://doi.org/10.1515/BCHM2.1922.122.1-3.46
Lactic Acid	612	Click to see	90.08	unknown	https://doi.org/10.1515/BCHM2.1922.122.1-3.46
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
L-Malic Acid	222656	Click to see	134.09	unknown	https://doi.org/10.1515/BCHM2.1922.122.1-3.46
Malic Acid	525	Click to see	134.09	unknown	https://doi.org/10.1515/BCHM2.1922.122.1-3.46
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3S,4R,5S)-1,3,4-Trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-cyclohexane-1-carboxylic acid	14158101	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O	338.31	unknown	https://doi.org/10.1021/JF030595S
3-p-Coumaroylquinic acid	9945785	Click to see	338.31	unknown	https://doi.org/10.1021/JF00050A015 https://doi.org/10.1016/S0023-6438(03)00143-9
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/10.1021/JF00050A015 https://doi.org/10.1021/JF030595S https://doi.org/10.1016/0021-9673(96)00169-0 https://doi.org/10.1016/S0031-9422(00)97746-X https://doi.org/10.1016/S0023-6438(03)00143-9
Isochlorogenic acid	5315832	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/10.1021/JF030595S
Neochlorogenic acid	5280633	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/10.1021/JF00050A015 https://doi.org/10.1016/S0023-6438(03)00143-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
4,5-Dihydroxy-3-methoxy-6-(2,4,5-trihydroxyoxan-3-yl)oxyoxane-2-carboxylic acid	14078718	Click to see COC1C(C(C(OC1C(=O)O)OC2C(C(COC2O)O)O)O)O	340.28	unknown	https://doi.org/10.1139/V61-340
GlyTouCan:G52001IP	21635776	Click to see	340.28	unknown	https://doi.org/10.1139/V61-340
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3R,4S,5R,6R)-6-[(3R,4S,5R,6R)-6-hydroxy-4,5-dimethoxyoxan-3-yl]oxy-4,5-dimethoxyoxan-3-ol	163028371	Click to see COC1C(COC(C1OC)OC2COC(C(C2OC)OC)O)O	338.35	unknown	https://doi.org/10.1139/V61-340
6-(6-Hydroxy-4,5-dimethoxyoxan-3-yl)oxy-4,5-dimethoxyoxan-3-ol	163028370	Click to see COC1C(COC(C1OC)OC2COC(C(C2OC)OC)O)O	338.35	unknown	https://doi.org/10.1139/V61-340
Amylodextrin	439341	Click to see	342.30	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
Sucrose	5988	Click to see	342.30	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose	5984	Click to see	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
D-Fructose	2723872	Click to see	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
6-Deoxy-Hexose	840	Click to see CC1C(C(C(C(O1)O)O)O)O	164.16	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
alpha-D-GALACTOSE	439357	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
alpha-D-Mannopyranose	185698	Click to see	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
alpha-L-Rhamnose	439710	Click to see	164.16	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
D(+)-Glucose	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
Alpha-d-xylopyranose	6027	Click to see C1C(C(C(C(O1)O)O)O)O	150.13	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
beta-L-arabinopyranose	439764	Click to see	150.13	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
Pentose	229	Click to see C1C(C(C(C(O1)O)O)O)O	150.13	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Sorbitol	5780	Click to see	182.17	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
5,9,10-Trihydroxy-7-(3-hydroxy-3-methylbutyl)-8-(3-methylbut-2-enyl)furo[2,3-c]xanthen-6-one	162937039	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(83)83029-5
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
(1S,3R,4R,5S,8S)-3,4,8-trihydroxy-2,6-dioxabicyclo[3.2.1]octan-7-one	101719890	Click to see C1(C2C(C(OC1C(=O)O2)O)O)O	176.12	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
D-Mannuronicacidlactone	14178454	Click to see C1(C2C(C(OC1C(=O)O2)O)O)O	176.12	unknown	https://doi.org/10.1016/S0031-9422(00)85322-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
2-hydroxy-2-methyl-N-[(2S)-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-2-yl]propanamide	162854059	Click to see	302.37	unknown	https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
> 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/10.1016/0021-9673(96)00169-0
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.1016/0031-9422(83)83029-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Catechin	9064	Click to see	290.27	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X https://doi.org/10.1021/JF030595S https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Epicatechin	72276	Click to see	290.27	unknown	https://doi.org/10.1021/JF030595S
l-Epicatechol	255538	Click to see	290.27	unknown	https://doi.org/10.1021/JF030595S
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Eriodictyol	11095	Click to see	288.25	unknown	https://doi.org/10.1021/JA01559A059
(+-)-Naringenin	932	Click to see	272.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018 https://doi.org/10.1021/JA01559A059
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one	667495	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018 https://doi.org/10.1021/JA01559A059
Eriodictyol	440735	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1021/JA01559A059
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-Hydroxyphenyl)Chroman-4-One	662	Click to see	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1016/0304-4238(78)90069-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1556/AALIM.31.2002.1.7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3S,4R,5R,6S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	9955335	Click to see	449.40	unknown	https://doi.org/10.1021/JF030595S
(2S,4R,5S)-2-[[(3R,6R)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	163185847	Click to see	595.50	unknown	https://doi.org/10.1021/JF030595S
Cyanidin 3-O-galactoside	441699	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
cyanidin 3-O-sophoroside	11169452	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O	611.50	unknown	https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Keracyanin cation	441674	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O	595.50	unknown	https://doi.org/10.1016/S0308-8146(01)00231-X https://doi.org/10.1078/0944-7113-00053 https://doi.org/10.1021/JF00050A015 https://doi.org/10.1016/S0023-6438(03)00143-9 https://doi.org/10.1021/JF030595S
Kuromanin	441667	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1021/JF00050A015 https://doi.org/10.1021/JF030595S https://doi.org/10.1016/S0308-8146(01)00231-X https://doi.org/10.1016/S0023-6438(03)00143-9
pelargonidin 3-O-rutinoside	443917	Click to see	579.50	unknown	https://doi.org/10.1016/S0308-8146(01)00231-X https://doi.org/10.1021/JF00050A015 https://doi.org/10.1016/J.FOODCHEM.2007.08.004 https://doi.org/10.1016/S0023-6438(03)00143-9
Peonidin 3-O-rutinoside	90470732	Click to see	609.60	unknown	https://doi.org/10.1021/JF00050A015 https://doi.org/10.1016/S0308-8146(01)00231-X https://doi.org/10.1016/S0023-6438(03)00143-9
Peonidin-3-glucoside	443654	Click to see	463.40	unknown	https://doi.org/10.1016/S0308-8146(01)00231-X https://doi.org/10.1021/JF00050A015 https://doi.org/10.1016/S0023-6438(03)00143-9
Petunidin 3-galactoside	14311149	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	479.40	unknown	https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
1-[2-Hydroxy-4-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	72732169	Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=C(C=C3)O)O	448.40	unknown	https://doi.org/10.1016/0031-9422(91)84200-C
2-(4-hydroxyphenyl)-7-methoxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	11293760	Click to see	446.40	unknown	https://doi.org/10.1016/0031-9422(91)84200-C
3,5,7-trihydroxy-2-[4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	154496826	Click to see	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)83951-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4S,5S)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol	25079994	Click to see	463.40	unknown	https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
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/10.1016/S0031-9422(00)97746-X
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	54579866	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/10.1021/JF030595S
5,7-dihydroxy-2-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]-3-[(2R,3R,4R,5S,6S)-3,4,5-trihydroxy-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxychromen-4-one	162979621	Click to see	920.80	unknown	https://doi.org/10.1016/S0031-9422(00)83951-5
5,7-Dihydroxy-2-[2-hydroxy-4-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]-3-[3,4,5-trihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxychromen-4-one	162979620	Click to see	920.80	unknown	https://doi.org/10.1016/S0031-9422(00)83951-5
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/S0031-9422(00)97746-X
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X https://doi.org/10.1016/0304-4238(78)90069-9 https://doi.org/10.1021/JF030595S
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	124300887	Click to see	434.40	unknown	https://doi.org/10.1016/S0031-9422(00)97746-X https://doi.org/10.1111/J.1399-3054.1985.TB02366.X
5-Hydroxy-2-[4-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[3,4,5-trihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxychromen-4-one	163045404	Click to see	920.80	unknown	https://doi.org/10.1016/S0031-9422(00)83951-5
Naringenin 7-0-glucoside	282013	Click to see	434.40	unknown	https://doi.org/10.1021/JA01559A059
Prunin	92794	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O	434.40	unknown	https://doi.org/10.1111/J.1399-3054.1985.TB02366.X https://doi.org/10.1021/JA01559A059 https://doi.org/10.1016/S0031-9422(00)97746-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether	348130	Click to see	286.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Sakuranetin	73571	Click to see	286.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Tectochrysin	5281954	Click to see	268.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Dihydrowogonin	11491431	Click to see	286.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
S-Dihydrowogonin	10265977	Click to see	286.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.1021/JA01559A059
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-hydroxyphenyl)-7-methoxy-5-[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	133556543	Click to see	446.40	unknown	https://doi.org/10.1016/S0031-9422(00)97795-1
3-(4-Hydroxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	14311197	Click to see	446.40	unknown	https://doi.org/10.1016/S0031-9422(00)97795-1
4H-1-Benzopyran-4-one, 5-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-7-methoxy-	184974	Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C(=CO2)C4=CC=C(C=C4)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(00)97795-1
Genistin	5281377	Click to see	432.40	unknown	https://doi.org/10.1021/JA01559A059
Genistoside	5284639	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JA01559A059
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Prunetin	5281804	Click to see	284.26	unknown	https://doi.org/10.1021/JA01559A059

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Prunus avium

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