Details Top

Internal ID UUID643ff8b3ca189484194143
Scientific name Rumex acetosa
Authority L.
First published in Sp. Pl. : 337 (1753)

Ethnobotanical Use Top

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Important notice
  • 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.

In traditional European and Himalayan folk medicine, the young leaves of garden sorrel are prepared as an infusion for internal soothing. Among the Andean communities of southern Bolivia and northern Chile, a tea made by steeping 2–3 g of fresh leaves in hot water is drunk after meals to ease mild stomach cramps and to act as a gentle diuretic (Bennett et al., 2021). In the Swiss Alps, rural herbalists recorded a similar leaf decoction, simmered for 10 minutes, used as a diuretic tonic and to relieve urinary discomfort (Müller, 2018). In the high‑altitude valleys of Ladakh, India, villagers boil the leaves for 15 minutes to make a decoction taken after the evening meal for indigestion and as a prophylaxis against scurvy (Tashi & Singh, 2020). The same leaf poultice, crushed and applied directly to insect bites, is cited in alpine folk practice for its cooling and astringent effect (Müller, 2018).

One practical preparation widely described in these records is a simple leaf tea. Place 1–2 teaspoons (≈1 g) of dried young leaves in a cup, pour 250 ml of freshly boiled water, cover and let steep for 5–10 minutes, then strain. The resulting beverage can be taken 1–2 times daily. Because the leaves contain oxalic acid, people prone to kidney‑stone formation or with a history of hyperoxaluria should limit consumption to one cup per day; pregnant women are advised to avoid large or repeated doses (Müller, 2018).

The therapeutic actions of garden sorrel are linked to a suite of well‑documented phytochemicals. The high content of vitamin C (ascorbic acid) explains its historical use against scurvy and as an antioxidant in the tea (Van Wyk & Wink, 2012). Flavonoids such as quercetin‑3‑O‑glucoside and rutin have been isolated from the leaves and possess anti‑inflammatory and capillary‑protective activities that may underpin the astringent relief reported for digestive upset (Khan et al., 2017). Oxalic acid, while responsible for the tart flavor, also provides a mild astringent quality (Müller, 2018).

Contemporary interest remains strong: recent phytochemical studies confirm the antioxidant capacity of Rumex acetosa leaf extracts, and the plant is commercially cultivated for its culinary greens and sold in specialty tea blends in Europe and North America (Van Wyk & Wink, 2012). In addition, some herbal manufacturers are exploring standardized extracts for dietary supplements aimed at supporting urinary health, while communities in the Alps and Ladakh continue to brew the same traditional tea as part of everyday home remedies.

General Uses Top

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Common products:
Fresh or cooked mature leaves are sold as leafy culinary herb; shoots may be blanched for milder flavor.

Food and beverages (non-medicinal):
Leaves are used as an acidic leafy green in salads, soups, sauces, and omelettes; high oxalic acid content provides sour taste. Shoots/flower stems may be blanched; leaves may be blanched or cooked to reduce harshness. Preparation details vary by local tradition; no health claims are made.

Properties relevant to use:
Oxalic acid content accounts for acidity and tartness, enabling use as an acidulant; mature leaves contain higher oxalic acid and are often cooked, whereas young leaves are eaten raw; blanching reduces bitterness.

Fragrance and cosmetics:
No documented non-medicinal applications.

Standards and regulation:
No specific ISO/ASTM/EN standards identified for this species.

Sustainability and sourcing:
No specific sustainability or provenance standards identified for this species.

References:
Plants of the World Online. Kew Royal Botanic Gardens. https://powo.science.kew.org (accessed 2023-10).
Flora of Britain and Northern Europe. Blamey, M., Fitter, R., Fitter, A. London: A&C Black, 2003.

Synonyms Top

Scientific name Authority First published in
Rumex fontanopaludosus Kalela Ann. Bot. Soc. Zool.-Bot. Fenn. "Vanamo" 14(2): 10 (1940)
Rumex acetosa subsp. biformis (Lange) Valdés Berm. & Castrov. Anales Inst. Bot. Cavanilles 34: 326 (1977)
Rumex biformis Lange Index Seminum (C, Hauniensi) 1857: 26 (1857)
Acetosa agrestis Raf. New Fl. 4: 52 (1838)
Acetosa amplexicaulis Raf. New Fl. 4: 53 (1838)
Acetosa angustata Raf. New Fl. 4: 53 (1838)
Acetosa bidentula Raf. New Fl. 4: 52 (1838)
Acetosa fontanopaludosa (Kalela) Holub Folia Geobot. Phytotax. 11: 80 (1976)
Acetosa hastifolia Schur Enum. Pl. Transsilv. : 581 (1866)
Acetosa hastulata Raf. New Fl. 4: 52 (1838)
Acetosa magna Gilib. Exerc. Phyt. 2: 445. 1792
Acetosa officinalis Gueldenst. ex Ledeb. Fl. Ross. 3: 510 (1850)
Acetosa olitoria Raf. New Fl. 4: 53 (1838)
Acetosa pratensis Garsault Fig. Pl. Med. 2: t. 124 a. 1764, nom. inval., opus utique oppressum; Descr. Pl. Anim. 91. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 786.
Acetosa pratensis Mill. Gard. Dict. ed. 8 : n.º 1 (1768)
Acetosa pratensis subsp. fontanopaludosa (Kalela) Tzvelev Novosti Sist. Vyssh. Rast. 32: 183 (2000)
Acetosa subalpina Schur Enum. Pl. Transsilv. : 581 (1866)
Rumex acetosa subsp. fontanopaludosus (Kalela) Hyl. Uppsala Univ. Årsskr. 7: 132 1945
Rumex acetosa var. fontanopaludosus (Kalela) Hyl. Nordisk Kärlväxtflora 2: 388 1966

Common names Top

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Language Common/alternative name
English common sorrel
English sorrel
English garden sorrel
Spanish angrinos
Spanish arceron
Spanish arcerón
Spanish arietes
Spanish atrancon
Spanish atrancón
Spanish azadera
Spanish azaderas
Spanish azedera
Spanish azitota
Spanish benjaminas
Spanish binagrera
Spanish binagreras
Spanish binagreta
Spanish binagretas
Spanish calamines
Spanish carabanes
Spanish chuletes
Spanish chupes
Spanish espigu
Spanish gambones
Spanish gretes
Spanish grietes
Spanish lapathum acetosa
Spanish lapazuala
Spanish linchara
Spanish línchara
Spanish llingua del gue
Spanish llingua del güe
Spanish lluenga de gue
Spanish lluenga de güe
Spanish magretas de prau
Spanish mineta
Spanish oreja de buey
Spanish pan y vinu
Spanish piallo
Spanish piayo
Spanish renabre
Spanish respigo
Spanish romaza medicinal
Spanish sigoletes
Spanish tañaro
Spanish tánaro
Spanish táñaro
Spanish targaros
Spanish tárgaros
Spanish vinagretes
Spanish xerreta
Spanish zargatena
Spanish zargateña
Spanish tarrago
Spanish lapathum pratense
Spanish tanaro
Spanish adera
Spanish acedera
Spanish acidera
Spanish aceas
Spanish aceda
Spanish acedera comestible
Spanish acedera comun
Spanish acedera con hoja de romaza
Spanish acedera de prado
Spanish acedera de secano
Spanish acedera silvestre
Spanish acederas
Spanish acederas coyundas
Spanish acedra de pico de pajaro
Spanish acedra de pico de pájaro
Spanish acerilla
Spanish acetabla
Spanish achitabla
Spanish acicera
Spanish acitabla
Spanish agreta
Spanish agrieta
Spanish agrietas
Spanish agrietes
Spanish agriguella
Spanish agrilla
Spanish agrillas
Spanish agrillo
Spanish alcalamines
Spanish ancera
Spanish angleta
Spanish angreta
Spanish angretas
Spanish angrietes
Spanish angrina
Spanish acedera común
Spanish rumex acetosa subsp. biformis
Spanish acetosa pratensis
Spanish rumex biformis
Afrikaans veldsuring
Arabic حماض أسفاناخي
Arabic حماض بستاني
Arabic حماض
Arabic سلق بري
Arabic الحماض الصغير
Arabic رواند بري
Azerbaijani adi əvəlik
Azerbaijani turş əvəlik
azb عادی اولیک
ba Ҡуҙғалаҡ
Belarusian шчаўе
Belarusian кісляніца
Belarusian шчавей
Belarusian шчавель
Belarusian шчавель праўдзівы
Belarusian шчаўе звычайнае
Belarusian шчаўнік
Belarusian шчаўе кіслае
Bulgarian киселец
Catalan agrella
Czech šťovík kyselý
Czech kyseláč luční
Czech acetosa pratensis
Welsh dail surion bach
Welsh suran y cŵn
Danish almindelig syre
German wiesen-sauer-ampfer
German gartensauerampfer
German großer sauer-ampfer
German großer sauerampfer
German sauerampfer
German sauerlump
German wiesensauerampfer
German wiesen-sauerampfer
diq amênvaş
Greek Λάπατο
Greek Λάπαθο
Esperanto okzalo
Estonian hapuoblikas
Estonian hapu oblikas
Estonian acetosa pratensis
Basque uztao handi
Basque mingarratz handi
Persian سورل، لوئیزیانا
Finnish niittysuolaheinä
French oseille sauvage
French grande oseille
French oseille rouge
French oseille commune
frr ruad jüd
Irish samhadh bó
Irish samhadh
Galician herba acedeira
Galician aceda
Hebrew חומעה מצויה
Hindi खट्टा पालक
Croatian obična kiselica
Upper Sorbian kisały zdźer
Hungarian mezei sóska
Indonesian sijungkot bayam
io oxalo
Icelandic túnsúra
Italian acetosa di pecora
Italian erba brusca
Italian erba soleggiata
Italian acetosa
Japanese スカンボ
Japanese
Japanese ソレル
Japanese スカンポ
Japanese スイバ
Georgian მჟაუნა
Korean 수영
koi Тшöтшкöр
koi Тшӧтшкӧр
ku kerika berxê
ku sêxaşik
ku tirsho
ku tirşo
Cornish trenkan
lb saueramper
lb sauerampel
Lithuanian valgomoji rūgštynė
Latvian pļavas skābene
lzh 酸模
mi horera
Macedonian Киселец
Marathi चुका
mwl azedones
Norwegian Bokmål engsyre
Dutch veldzuring
Dutch zurkel
Norwegian Nynorsk engsyre
nv chaatʼíní
os Тауæг тъаффæ
os Тауæгтъаффæ
os Хуырхæг
Polish szczaw zwyczajny
Portuguese azeda
Portuguese azedões
Romanian măcriș
Russian щавель обыкновенный
Russian щавель болотно-ключевой
Russian щавель луговой
Russian щавель кислый
se gieddejuopmu
se sáltesuoidni
se suvrrarássi
se juopmu
Samogitian rūgštīnė
Serbo-Croatian kiseljak
Slovak Štiav lúčny
Slovenian navadna kislica
smn sälttisyeini
sms säʹlttsueiʹnn
Albanian lëpjeta
Serbian киселица
Serbian кисељак
stq suurke
Swedish Ängsyra
Swedish lappsyra
Swedish smal ängssyra
Swedish vanlig ängssyra
Swedish Ängssyra
Tamil புளியாரைக் கீரை
tg Туршак
Ukrainian щавель звичайний
Ukrainian шавель кислий
Urdu ہوبابل
vec spanavin
vep sol'hein
Vietnamese chút chít
Chinese 酸模
Chinese 酸模叶
Chinese 遏蓝菜
Chinese 酸模(毛脉酸模)
Chinese 酸溜溜
Chinese 毛脉酸模

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Rumex acetosa subsp. hibernicus (Rech.f.) Akeroyd Watsonia 17: 444 (1989)
Rumex acetosa subsp. vinealis (Timb.-Lagr. & Jeanb.) O.Bolòs & Vigo Butl. Inst. Catalana Hist. Nat., Secc. Bot. 38(1): 85 (1974)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
    • Western Asia
      • Afghanistan
      • Iran
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • West Himalaya
  • Europe
    • 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
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Svalbard
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Québec
    • North-central U.S.A.
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New York
      • Pennsylvania
      • Vermont
    • Northwestern U.S.A.
      • Oregon
    • Subarctic America
      • Alaska
      • Aleutian Islands
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan
  • Southern America
    • Caribbean
      • Haiti
    • Southern South America
      • Argentina Northeast
      • Argentina South
      • Chile South

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000403595
UNII IA49H9SY8T
Canadensys 8200
USDA Plants RUAC2
Tropicos 26000095
INPN 119418
KEW urn:lsid:ipni.org:names:332105-2
The Plant List kew-2424198
Missouri Botanical Garden 285455
Open Tree Of Life 134757
Observations.org 7368
NCBI Taxonomy 41241
NBN Atlas NBNSYS0000003778
Nature Serve 2.139185
IPNI 332105-2
iNaturalist 55821
GBIF 2888951
Freebase /m/06rsv
WisFlora 4915
EPPO RUMAC
EOL 485385
Elurikkus 6962
USDA GRIN 32518
Wikipedia Sorrel

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
Name Level Submitter Released Coverage Size
GCA_977966345.1 dcRumAcet1.hap1.1 Chromosome WELLCOME SANGER INSTITUTE 2026-02-01 43 2.75 Gb

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
Co-located ecological data for exploring top- and subsoil carbon dynamics across grassland-woodland contrasts Reinsch S, Lebron I, Brentegani M, Brooks M, Busi SB, Cagnarini C, Cooper D, Day J, Emmett BA, Fitos E, Goodall T, Griffiths R, Jones B, Keenan P, Keith A, Lopes-Mazzetto JM, Mason KE, Pallett D, Pereira MG, Pinder A, Robinson DA, Smart SM, Thomas A, Benham S, Vanguelova E, Cosby BJ Sci Data 09-May-2024
PMCID:PMC11081944
doi:10.1038/s41597-024-03333-w
PMID:38724554
Degradation Rate/Vulnerability Potential and Fertility Status of Luvisols in the Mandara Mountains (Far-North Cameroon) Tamto Mamdem EL, Tsozué D, Matakon E, Apiniel Atourakail MR, Moudjie Noubissie NM, Basga SD, Nzeugang Nzeukou A, Oyono Bitom DL ScientificWorldJournal 06-May-2024
PMCID:PMC11090670
doi:10.1155/2024/6565723
PMID:38741609
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Diet of moulting Swainson's Thrushes (Catharus ustulatus) and Tennessee Warblers (Leiothlypis peregrina) at a stopover site during fall migration measured with fecal DNA metabarcoding Blanc-Benigeri A, Poirier V, Narango D, Elliott KH, Frei B Sci Rep 30-Apr-2024
PMCID:PMC11061280
doi:10.1038/s41598-024-59462-0
PMID:38688969
Expressing banana transcription factor MaERFVII3 in Arabidopsis confers enhanced waterlogging tolerance and root growth Teoh EY, Teo CH, Baharum NA, Tan BC PeerJ 30-Apr-2024
PMCID:PMC11067909
doi:10.7717/peerj.17285
PMID:38708359
Risk assessment of Retithrips syriacus for the EU Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, 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, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
Impacts of Soil Properties on Species Diversity and Structure in Alternanthera philoxeroides-Invaded and Native Plant Communities Wu H, Liu Y, Zhang T, Xu M, Rao B Plants (Basel) 25-Apr-2024
PMCID:PMC11085794
doi:10.3390/plants13091196
PMID:38732411
Nose of dog, eye of elk, and wolf’s liver: exploring the interconnectedness of Indigenous health and foraging among the Dukha reindeer herders of Mongolia Hatcherson J Int J Circumpolar Health 18-Apr-2024
PMCID:PMC11028006
doi:10.1080/22423982.2024.2343454
PMID:38634711
Phased Assembly of Neo-Sex Chromosomes Reveals Extensive Y Degeneration and Rapid Genome Evolution in Rumex hastatulus Sacchi B, Humphries Z, Kružlicová J, Bodláková M, Pyne C, Choudhury BI, Gong Y, Bačovský V, Hobza R, Barrett SC, Wright SI Mol Biol Evol 12-Apr-2024
PMCID:PMC11057207
doi:10.1093/molbev/msae074
PMID:38606901
A chromosome-level genome reveals genome evolution and molecular basis of anthraquinone biosynthesis in Rheum palmatum Zhang T, Zhou L, Pu Y, Tang Y, Liu J, Yang L, Zhou T, Feng L, Wang X BMC Plant Biol 10-Apr-2024
PMCID:PMC11005207
doi:10.1186/s12870-024-04972-2
PMID:38594606
Exploring the effects of habitat management on grassland biodiversity: A case study from northern Serbia Milić D, Rat M, Bokić B, Mudri-Stojnić S, Milošević N, Sukur N, Jakovetić D, Radak B, Tot T, Vujanović D, Anačkov G, Radišić D PLoS One 28-Mar-2024
PMCID:PMC10977728
doi:10.1371/journal.pone.0301391
PMID:38547306
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
The Role of Polyphenols in Modulating PON1 Activity Regarding Endothelial Dysfunction and Atherosclerosis Sirca TB, Mureșan ME, Pallag A, Marian E, Jurca T, Vicaș LG, Tunduc IP, Manole F, Ștefan L Int J Mol Sci 04-Mar-2024
PMCID:PMC10931629
doi:10.3390/ijms25052962
PMID:38474211
Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L Plants (Basel) 24-Feb-2024
PMCID:PMC10934440
doi:10.3390/plants13050621
PMID:38475472

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Anthracenes
1,3,8-Trihydroxy-6-methyl-9(10H)-anthracenone 122635 Click to see 256.25 unknown https://doi.org/10.1080/00021369.1982.10865350
1,8-Dihydroxy-3-methoxy-6-methyl-9(10H)-anthracenone 19132 Click to see 270.28 unknown https://doi.org/10.1080/00021369.1982.10865350
Chrysophanic acid-9-anthrone 68111 Click to see 240.25 unknown https://doi.org/10.1080/00021369.1982.10865350
> Benzenoids / Anthracenes / Anthraquinones
Physcion 10639 Click to see 284.26 unknown https://doi.org/10.1248/BPB.28.2158
https://doi.org/10.1080/00021369.1982.10865350
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see 270.24 unknown https://doi.org/10.1248/BPB.28.2158
https://doi.org/10.1080/00021369.1982.10865350
Emodin-8-glucoside 99649 Click to see 432.40 unknown https://doi.org/10.1248/BPB.28.2158
Glucofrangulin 318730 Click to see 432.40 unknown https://doi.org/10.1248/BPB.28.2158
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
hyperibone K 44575719 Click to see CC(=CCC12CC3C(C(C1=O)(C(=O)C(C2=O)(C3(C)C)CC=C(C)C)C(=O)C4=CC=CC=C4)C=C(C)C)C 500.70 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(-)-Epiafzelechin-(4beta-8)-(-)-epicatechin 10239837 Click to see 562.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
(1R,5R,6R,7S,13S,21R)-13-(3,4-dihydroxyphenyl)-7-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 14586202 Click to see 848.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
(1R,5R,6R,7S,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-(2,4,6-trihydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 162910389 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C4=C(C=C3O)OC5(C(C4C6=C(C=C(C=C6O5)O)O)O)C7=CC(=C(C=C7)O)O)C8=C(C=C(C=C8O)O)O)O)O)O 700.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3R,4R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162891895 Click to see 850.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[(1R,5R,6R,7R,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-6,9,17,19-tetrahydroxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 3,4,5-trihydroxybenzoate 162889257 Click to see 1016.90 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2R,3R,4S)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 162940056 Click to see 714.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R,3R,4R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 163187046 Click to see 714.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 102005056 Click to see 730.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 162940055 Click to see 714.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 162916052 Click to see 714.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 5320714 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 730.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 9897565 Click to see 882.70 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[5,13-bis(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-6,9,17,19-tetrahydroxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 3,4,5-trihydroxybenzoate 162889256 Click to see 1016.90 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
1,1'-((2R,2'R,3R,3'R,4S)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-5,5',7,7'-tetrahydroxy(4,6'-bi-2H-1-benzopyran)-3,3'-diyl) bis(3,4,5-trihydroxybenzoate) 3086518 Click to see 882.70 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
1,1a(2)-[(2R,2a(2)R,3R,3a(2)R,4R)-2a(2)-(3,4-Dihydroxyphenyl)-3,3a(2),4,4a(2)-tetrahydro-5,5a(2),7,7a(2)-tetrahydroxy-2-(4-hydroxyphenyl)[4,8a(2)-bi-2H-1-benzopyran]-3,3a(2)-diyl] bis(3,4,5-trihydroxybenzoate) 102241853 Click to see 866.70 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
13-(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 14586201 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC=C(C=C9)O)O)O)O)C1=CC(=C(C=C1)O)O)O 848.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 73193906 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC=C(C=C7)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 850.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 16163749 Click to see 1155.00 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
2-(3,4-dihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 5089688 Click to see 562.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
5,13-bis(3,4-dihydroxyphenyl)-10-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2,8,10,15,17,19-hexaene-6,9,17,19,21-pentol 163030951 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C5C6C(C(OC7=CC(=CC(=C67)O)O)(OC5=C(C(=C34)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
5,13-Bis(3,4-dihydroxyphenyl)-7-(2,4,6-trihydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 85262587 Click to see 700.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Arecatannin A1 13752000 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Cinnamtannin A2 16130899 Click to see 1155.00 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
ent-Epicatechin-(4alpha->6)-ent-epicatechin 13990892 Click to see 578.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
ent-Epicatechin-(4alpha->8)-ent-epicatechin 3,3'-digallate 12795893 Click to see 882.70 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Epiafzelechin-(4b->8)-epicatechin 3,3'-digallate 131752746 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 866.70 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Parameritannin A-1 16146159 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C5C6C(C(OC7=CC(=CC(=C67)O)O)(OC5=C(C(=C34)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Pavetannin B2 13990886 Click to see 864.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Pavetannin B6 13990885 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin A1 5089889 Click to see 576.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin B2 3'-O-gallate 15593124 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 730.60 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin B4 147299 Click to see 578.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin B7 13990893 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin C1 169853 Click to see 866.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin C1 3,3,3-tri-O-gallate 16152264 Click to see 1323.10 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin C1 3,3',3''-tri-O-gallate 16170075 Click to see 1323.10 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Procyanidin trimer T2 13751990 Click to see 866.80 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
> 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.FITOTE.2009.08.015
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxychroman-3-Yl 3,4,5-Trihydroxybenzoate 367141 Click to see 442.40 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
[(2R,3S,4S,5R,6S)-5-acetyloxy-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-6-yl]-3,4-dihydroxyoxan-2-yl]methyl acetate 14681455 Click to see 532.40 unknown https://doi.org/10.1248/CPB.38.2277
[(2R,3S,4S,5S,6S)-5-acetyloxy-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-6-yl]-3,4-dihydroxyoxan-2-yl]methyl acetate 163028197 Click to see 532.40 unknown https://doi.org/10.1248/CPB.38.2277
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] acetate 14681459 Click to see 490.40 unknown https://doi.org/10.1248/CPB.38.2277
[2-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] acetate 14681458 Click to see 490.40 unknown https://doi.org/10.1248/CPB.38.2277
[5-Acetyloxy-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-6-yl]-3,4-dihydroxyoxan-2-yl]methyl acetate 14681454 Click to see CC(=O)OCC1C(C(C(C(O1)C2=C(C3=C(C=C2O)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)OC(=O)C)O)O 532.40 unknown https://doi.org/10.1248/CPB.38.2277
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)chromen-4-one 6426860 Click to see 448.40 unknown https://doi.org/10.1248/CPB.38.2277
Isoorientin 114776 Click to see 448.40 unknown https://doi.org/10.1248/CPB.38.2277
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] acetate 14681461 Click to see CC(=O)OC1C(C(C(OC1C2=C(C=C(C3=C2OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)O)CO)O)O 490.40 unknown https://doi.org/10.1248/CPB.38.2277
[(2S,3S,4S,5R,6S)-5-acetyloxy-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-3,4-dihydroxyoxan-2-yl]methyl acetate 162903546 Click to see 532.40 unknown https://doi.org/10.1248/CPB.38.2277
2''-Acetylorientin 14681460 Click to see CC(=O)OC1C(C(C(OC1C2=C(C=C(C3=C2OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)O)CO)O)O 490.40 unknown https://doi.org/10.1248/CPB.38.2277
2'',6''-Diacetylorientin 14681456 Click to see 532.40 unknown https://doi.org/10.1248/CPB.38.2277
8-(2,6-Di-O-acetyl-beta-D-glucopyranosyl)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one 14681457 Click to see CC(=O)OCC1C(C(C(C(O1)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)O)OC(=O)C)O)O 532.40 unknown https://doi.org/10.1248/CPB.38.2277
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.38.2277
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.38.2277
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1248/CPB.38.2277
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1248/CPB.38.2277
Avicularine 12308704 Click to see 434.30 unknown https://doi.org/10.1248/CPB.38.2277
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.38.2277
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1080/00021369.1982.10865350
https://doi.org/10.1248/BPB.28.2158
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3S,4S,5R,6S)-6-(2,4-dihydroxy-6-methoxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate 132530686 Click to see 498.40 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015
[6-(2,4-Dihydroxy-6-methoxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate 162866214 Click to see 498.40 unknown https://doi.org/10.1016/J.FITOTE.2009.08.015

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