Fagus grandifolia

Details Top

Internal ID UUID64403be704308428258632
Scientific name Fagus grandifolia
Authority Ehrh.
First published in Beitr. Naturk. 1: 22 (1787)

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.

Among Algonquin, Iroquois, and Wabanaki-speaking peoples of the northeastern woodlands, Fagus grandifolia was employed mainly as an external medicine. Fresh or lightly crushed bark, sometimes with a thin layer of inner bark, was applied to fresh cuts, abrasions, and sores as a poultice or direct compress; the same bark decoction was used as a wash to dress and cleanse wounds (Moerman, 1998). The Jesuits recorded that the Canadian Huron boiled the twigs of American beech for fevers and bathed patients with the decoction (Rousseau, 1945), and the Cherokee reportedly used a bark infusion or decoction for “bad blood,” a broad local term for systemic or blood-related illness (Merrill, 1928). Historically, foresters in New England, Vermont, and Ontario prepared bark decoctions for fevers and wound care and sometimes rubbed bruised leaves over insect bites, though leaf use is comparatively lesser known (Peattie, 1948; Odel, 1908).

A simple, practical preparation is a bark decoction used as an external wash: finely chop or bruise 1 to 2 tablespoons of fresh inner bark and outer bark, cover with 1 cup of water, bring to a boil, then simmer 10 to 15 minutes; cool to lukewarm and rinse the affected area 2–3 times daily. For a compress, soak a clean cloth in the cooled decoction and apply for 15–20 minutes. Do not drink this preparation; for external use only. Avoid applying to deep or contaminated wounds without medical supervision, and discontinue if irritation develops. Pregnant or breastfeeding individuals should avoid using any Fagus preparation unless advised by a qualified practitioner.

The bark and leaves of American beech contain abundant tannins, notably gallotannins, which are astringent and protein‑precipitating; these constituents plausibly explain the traditional styptic and wound‑dressing actions (Oates, 1986). Small phenolic acids and triterpenoids have also been identified in beech bark and leaves (Jones and Dickson, 1976), but the astringent tannin fraction is the most biochemically consistent with topical hemostasis and mucosal tightening in wound care.

Today, American beech remains mostly a timber and ornamental tree, with interest in its dark brown bark and persistence in the forest understory. Decoctions for external use persist locally, and minor research continues on beech leaf and bark phenolics for astringency and antioxidant properties (Schulz and Hamar, 1988), though commercial therapeutic products are uncommon in herbal trade.

General Uses Top

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Common products:
American beech (Fagus grandifolia) yields utility-grade lumber and dimension stock. Small, clean pieces are converted into wood flour for fillers and abrasives. Lath and turnery blanks are produced for handles, dowels, and turnery.

Industrial and craft applications:
Dimension lumber and sawn products are used for flooring, interior trim, furniture parts, kitchenware, butcher blocks, and turnery (e.g., spools, brush backs, tool handles). Beech steam-bends well and takes fasteners and screws, which supports architectural moldings and chair components. Cross-sections are used as disk blanks. Wood flour (often from offcuts) serves as a filler in phenolic and other adhesive systems.

Food and beverages (non-medicinal):
The seed (beechnut) is edible and can be processed for oil; culinary references describe roasting or cooking to reduce tannins and using the meal to fortify flour blends. No health claims or traditional-remedy uses are included.

Wood and fiber:
The species produces hardwood logs with a typical specific gravity of about 0.65–0.70 and high shrinkage from green to oven-dry (radial ~4.5%; tangential ~8–10%; volumetric ~13–14%; T/R ratio ~2.2). The Janka hardness is about 1,300 lbf, and air-dry density roughly 700–720 kg/m³. These properties underpin flooring performance and the selection of steam-bending and high-strength turnery applications. Lumber is graded and traded under standards such as NHLA rules and applicable ASTM/EN hardwood specifications.

Properties relevant to use:
American beech is dense, close-grained, and light-colored; it sands and machines well and takes a clear finish. Dimensional stability and bending strength are adequate for flooring and furniture parts; the species steam-bends effectively.

Sustainability and sourcing:
Trees often occur in mature hardwood forests; adoption of sustainable forestry practices and chain-of-custody certification (e.g., FSC) reduces impacts on mixed northern-hardwood ecosystems. Sawn-lumber yields vary due to rot and insect damage, making grading efficiency variable.

Synonyms Top

Scientific name Authority First published in
Fagus grandifolia f. mollis Fernald & Rehder Rhodora 9: 114 1907
Fagus sylvatica var. atropunicea Marshall Arbust. Amer. : 46 (1785)
Fagus sylvatica var. americana Pers. Syn. Pl. 2: 571. 1807
Fagus atropunicea (Marshall) Sudw. Bull. Torrey Bot. Club 20(2): 43. 1893 [15 Feb 1893]
Fagus grandifolia subsp. heterophylla Camp Unknown
Fagus latifolia L'Hér. ex Steud. Nomencl. Bot. , ed. 2, 1: 624 (1840)
Fagus purpurea Desf. Tabl. École Bot. : 214 (1804)
Fagus ferruginea Aiton Hort. Kew. [W. Aiton] 3: 362. 1789
Fagus grandifolia var. typica Rehder Mitt. Deutsch. Dendrol. Ges. 16: 70 (1907)

Common names Top

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Language Common/alternative name
English american beech
Spanish fagus sylvatica var. atropunicea
Spanish fagus sylvatica var. americana
Spanish fagus purpurea
Spanish fagus atropunicea
Spanish fagus latifolia
Spanish haya americana
Arabic زان أمريكي
Bulgarian едролистен бук
Czech buk velkolistý
Danish amerikansk bøg
German fagus ferruginea
German amerikanische buche
German mexikanische buche
Esperanto grandfolia fago
Persian راش آمریکایی
Finnish amerikanpyökki
French hêtre à grandes feuilles
French hêtre américain
French hetre d'amerique
French hêtre d'amérique
French hêtre rouge
Hebrew אשור אמריקאי
Upper Sorbian ameriski buk
Hungarian amerikai bükk
Japanese アメリカブナ
Cornish fow amerika gledh
Lithuanian amerikinis bukas
Latvian amerikas dižskābardis
Norwegian Bokmål amerikabøk
Polish buk amerykański
Polish buk wielkolistny
Russian Бук крупнолистный
Slovenian ameriška bukev
Turkish amerika kayını
Ukrainian Бук великолистковий
Ukrainian Бук американський
Ukrainian Американський бук
Chinese 北美山毛櫸
Chinese 美国水青冈
Chinese 紫叶水青冈
Chinese 紫叶欧洲水青冈
Chinese 北美水青冈

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Fagus grandifolia subsp. grandifolia Unknown
Fagus grandifolia subsp. mexicana (Martinez) A.E.Murray Kalmia 13: 6 (1983):.

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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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
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
    • North-central U.S.A.
      • Illinois
      • Missouri
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000966434
UNII TVM295J64J
Florida Plant Atlas 982
Flora of Alabama 2147
Cornell Woody Plants 93
Canadensys 5957
USDA Plants FAGR
UConn 175
Tropicos 13100023
KEW urn:lsid:ipni.org:names:295597-1
The Plant List kew-83824
Missouri Botanical Garden 280709
PFAF Fagus grandifolia
Open Tree Of Life 422459
NCBI Taxonomy 60423
Nature Serve 2.140235
IUCN Red List 62004694
IPNI 295597-1
iNaturalist 49202
GBIF 2882274
Freebase /m/02h6vp
WisFlora 3616
FEIS plants/tree/faggra
EPPO FAUGR
EOL 1143553
Elurikkus 4734
USDA GRIN 100831
Wikipedia Fagus_grandifolia
CMAUP NPO9017
PaleoBotany 100617

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
Biosecurity risks to human food supply associated with plant-parasitic nematodes Kantor C, Eisenback JD, Kantor M Front Plant Sci 30-Apr-2024
PMCID:PMC11091314
doi:10.3389/fpls.2024.1404335
PMID:38745921
Pollen identification through convolutional neural networks: First application on a full fossil pollen sequence Durand M, Paillard J, Ménard MP, Suranyi T, Grondin P, Blarquez O PLoS One 30-Apr-2024
PMCID:PMC11060525
doi:10.1371/journal.pone.0302424
PMID:38687746
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
The risk of contact between visitors and Borrelia burgdorferi-infected ticks is associated with fine-scale landscape features in a southeastern Canadian nature park Dumas A, Bouchard C, Drapeau P, Lindsay LR, Ogden NH, Leighton PA BMC Public Health 26-Apr-2024
PMCID:PMC11055428
doi:10.1186/s12889-024-18673-w
PMID:38671429
An inexpensive moist chamber culture technique for finding microbiota on live tree bark Bordelon AP, Keller HW, Scarborough AR Appl Plant Sci 16-Apr-2024
PMCID:PMC11022227
doi:10.1002/aps3.11578
Leaf gene expression trajectories during the growing season are consistent between sites and years in American beech Sezen UU, Shue JE, Worthy SJ, Davies SJ, McMahon SM, Swenson NG Proc Biol Sci 10-Apr-2024
PMCID:PMC11003779
doi:10.1098/rspb.2023.2338
PMID:38593851
Frequent and strong cold‐air pooling drives temperate forest composition Pastore MA, Classen AT, D'Amato AW, English ME, Rand K, Foster JR, Adair EC Ecol Evol 01-Apr-2024
PMCID:PMC10985370
doi:10.1002/ece3.11126
PMID:38571787
Bichromatic tetraphasic full-field optical coherence microscopy Iyer RR, Žurauskas M, Rao Y, Chaney EJ, Boppart SA J Biomed Opt 25-Mar-2024
PMCID:PMC10996847
doi:10.1117/1.JBO.29.S2.S22704
PMID:38584966
Interplay of biotic and abiotic factors shapes tree seedling growth and root-associated microbial communities Chamard J, Faticov M, Blanchet FG, Chagnon PL, Laforest-Lapointe I Commun Biol 22-Mar-2024
PMCID:PMC10960049
doi:10.1038/s42003-024-06042-7
PMID:38519711
Nitrogen acquisition strategy shifts with tree age depending on root functional traits and soil properties in Larix principis-rupprechtii plantations Liu Q, Chen Y, Chen Y Front Plant Sci 12-Mar-2024
PMCID:PMC10964345
doi:10.3389/fpls.2024.1358367
PMID:38533407
Long‐term effects of a tornado: Impacts on woody native vegetation and invasive Amur honeysuckle (Lonicera maackii) in an urban forest Culley TM, Bécus MS, Cameron GN Ecol Evol 11-Mar-2024
PMCID:PMC10927907
doi:10.1002/ece3.10890
PMID:38476700
Phytopathogenic Curtobacterium flaccumfaciens Strains Circulating on Leguminous Plants, Alternative Hosts and Weeds in Russia Tokmakova AD, Tarakanov RI, Lukianova AA, Evseev PV, Dorofeeva LV, Ignatov AN, Dzhalilov FS, Subbotin SA, Miroshnikov KA Plants (Basel) 28-Feb-2024
PMCID:PMC10934172
doi:10.3390/plants13050667
PMID:38475514
Exploring risk factors for insect borer attack in Georgia’s (USA) urban landscapes Williamson ZV, Blaauw BR, Joseph SV PLoS One 26-Feb-2024
PMCID:PMC10896510
doi:10.1371/journal.pone.0299368
PMID:38408102
American marten occupancy and activity patterns at the southern extent of their range in the eastern United States Ashbrook S, Hapeman P Ecol Evol 05-Feb-2024
PMCID:PMC10844684
doi:10.1002/ece3.10904
PMID:38322003
Flavonoids influence key rhizocompetence traits for early root colonization and PCB degradation potential of Paraburkholderia xenovorans LB400 Ghitti E, Rolli E, Vergani L, Borin S Front Plant Sci 02-Feb-2024
PMCID:PMC10869545
doi:10.3389/fpls.2024.1325048
PMID:38371405

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
(Z)-Sinapyl alcohol 10130521 Click to see 210.23 unknown https://doi.org/10.1016/S0031-9422(00)81239-X
4-Hydroxy-3-methoxycinnamylic alcohol 1549094 Click to see 180.20 unknown https://doi.org/10.1016/S0031-9422(00)83580-3
https://doi.org/10.1016/S0031-9422(00)81239-X
4-Hydroxy-3,5-dimethoxy-cinnamyl alcohol 439703 Click to see COC1=CC(=CC(=C1O)OC)C=CCO 210.23 unknown https://doi.org/10.1016/S0031-9422(00)81239-X
Coniferyl Alcohol 1549095 Click to see 180.20 unknown https://doi.org/10.1016/S0031-9422(00)81239-X
Phenol, 4-(3-hydroxy-1-propenyl)-2-methoxy- 9983 Click to see 180.20 unknown https://doi.org/10.1016/S0031-9422(00)81239-X
Sinapyl alcohol 5280507 Click to see COC1=CC(=CC(=C1O)OC)C=CCO 210.23 unknown https://doi.org/10.1016/S0031-9422(00)81239-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2Z)-3-(4-Hydroxy-3-methoxyphenyl)prop-2-en-1-yl beta-D-glucopyranoside 14330981 Click to see 342.34 unknown https://doi.org/10.1016/0031-9422(88)80107-9
2-[3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85313722 Click to see 342.34 unknown https://doi.org/10.1016/0031-9422(88)80107-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(Z)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 9799599 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/0031-9422(88)80107-9
(Z)-Coniferin 91895380 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1016/0031-9422(88)80107-9
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4,5-triol 3496897 Click to see 342.34 unknown https://doi.org/10.1016/0031-9422(88)80107-9
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(88)80107-9
Di-O-Methylcrenatin 10736338 Click to see 346.33 unknown via CMAUP database
Isotachioside 15098566 Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown via CMAUP database
Multifidol glucoside 14412552 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Urolithin C 60198001 Click to see 244.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 102115501 Click to see 562.50 unknown via CMAUP database
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 101297694 Click to see 562.50 unknown via CMAUP database
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 102115500 Click to see 562.50 unknown via CMAUP database
(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 102400061 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
(2R,3S)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 102400062 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 594.50 unknown via CMAUP database
Epirobinetinidol-(4beta,8)-catechin 51042196 Click to see 578.50 unknown via CMAUP database
Fisetinidol-(4A8)-catechin 14332862 Click to see 562.50 unknown via CMAUP database
Fisetinidol-(4alpha,6)-gallocatechin 51041987 Click to see 578.50 unknown via CMAUP database
Fisetinidol-(4alpha,8)-catechin 11731408 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 562.50 unknown via CMAUP database
Robinetinidol-(4alpha->8)-catechin-(6->4alpha)-robinetinidol 442689 Click to see 866.80 unknown via CMAUP database
Robinetinidol-(4alpha,8)-catechin 70697937 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Robinetinidol-(4alpha,8)-gallocatechin 70697956 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
5-[(2R,3R)-3,7-dihydroxy-3,4-dihydro-2H-chromen-2-yl]benzene-1,2,3-triol 101846310 Click to see 290.27 unknown via CMAUP database
Robinetinidol 12314983 Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC(=C(C(=C3)O)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Butin 92775 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
ent-Epifisetinidol-4beta-ol 44257142 Click to see 290.27 unknown via CMAUP database
Fisetinidol-4alpha-ol 164762 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)O)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see 286.24 unknown via CMAUP database
Robinetin 5281692 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
4'-O-methylrobinetinidol 3'-O-beta-D-glucopyranoside 51041986 Click to see COC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)C3C(CC4=C(O3)C=C(C=C4)O)O)O 466.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Fisetin 3-methyl ether 9839293 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Fisetin tetramethyl ether 631171 Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(C=C3)OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database

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