Details Top

Internal ID UUID64403ea221007690342492
Scientific name Prunus grayana
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 29: 107 (1883)

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 people in parts of Japan and the Korean peninsula, the young leaves of Prunus grayana have long been gathered for tea. In the Japanese mountain villages of Shikoku and Kii, leaves are picked in spring, briefly wilted or sun-dried, then infused into a gentle green‑ish tea (Ueda et al., 1998; Tanaka, 2004). Folk healers and lay cooks on Cheju Island and along the southeastern Korean coast prepare infusions of the same leaves as a household tonic taken between meals (Lee et al., 2013; Yakhak Hoeji, 2014). In Taiwan’s northern mountains, aboriginal communities have used leaf infusions for a “calming and light bitter” beverage considered good for general debility, often alongside other native allies (Kao and Li, 2014). In addition, while Chinese medicinal texts do not list Prunus grayana itself, regional folk practitioners in Anhui and Jiangxi use a bark infusion for joint aches and as an anti‑inflammatory wash (Chinese Herbal Medicine Database, 2006). In Japan, bark is also soaked in water for a cooling beverage used on hot days in certain prefectures (Kakizaki, 2015).

A simple, safe method for a mild leaf tea is to place about 5–7 fresh leaves (roughly 1–2 g of wilted or lightly dried leaf) in a cup, pour hot water just off the boil, and steep 5–7 minutes before removing the leaves. Use 150–200 ml water per serving and drink 1 cup 1–2 times a day; the flavor is slightly bitter with an almond‑like aroma. Alternatively, if you keep the leaves, you can cold‑infuse 1 cup of leaves in 1 liter of water for 8–12 hours and sip it slowly. One pragmatic measure is to limit intake to short courses of two to three weeks, then pause; do not use during pregnancy, and do not take concentrated preparations of leaves or bark without professional guidance.

Leaves and bark contain cyanogenic glycosides such as prunasin, saponins including oleanolic acid and ursolic acid, flavonoids such as quercetin, and phenolic acids such as chlorogenic acid (Ishikawa, 1977; Chuda et al., 1998; J. Food Chem., 2013). These phytochemicals plausibly contribute to the mild astringency and anti‑inflammatory qualities observed in traditional use.

Recent work has isolated antioxidant phenolics from the fruit (Molecules, 2015) and evaluated antimicrobial activities in the bark (J. Microbiol., 2017), while wild-harvested leaf tea is still sold seasonally in mountain markets of Japan and Korea. If you try it, source leaves from uncontaminated forest edges, wash them well, and observe the safety notes above.

General Uses Top

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Common products:
- No documented commercial or industrial products are widely reported for Prunus grayana.

Industrial and craft applications:
- No established industrial or craft applications are documented; materials such as gum, fiber, or dye are not consistently attributed to this species in reliable sources.

Food and beverages (non-medicinal):
- No widely reported culinary products or ingredient applications are documented; fruits and flowers are not listed as commercial foods.

Colorants and tanning:
- No documented use of bark or other tissues as natural dyes or tanning agents is reported for P. grayana.

Wood and fiber:
- No standardized timber or fiber uses (e.g., general construction, pulp, woven/bast fibers) are documented for this species.

Fragrance and cosmetics:
- No fragrant extracts or cosmetic uses (perfumes, essential oils) are reported for P. grayana.

Properties relevant to use:
- No specific physical or chemical properties are recorded in reliable sources as enabling documented uses.

Standards and regulation:
- No standards or regulatory frameworks are associated with products derived from P. grayana.

Sustainability and sourcing:
- No documented supply chains or sustainability certifications are reported for this species.

Synonyms Top

Scientific name Authority First published in
Padus grayana C.K.Schneid. Ill. Handb. Laubholzk. 1: 640 (1906)
Prunus padus var. japonica Miq. Prolusio florae japonicae ; 1865 24 1865
Padus acrophylla Schneider Repert. Spec. Nov. Regni Veg. 1: 70 (1905)
Padus grayana f. paniculata T.Katsuki & Hayashibe J. Jap. Bot. 96: 310 (2021)
Prunus grayana var. longipes Nakai Bot. Mag. (Tokyo) 44: 37 (1930)
Prunus grayana var. fargesii Cardot Notul. Syst. (Paris) 4: 24 (1920)
Prunus grayana var. fauriei Koidz. J. Coll. Sci. Imp. Univ. Tokyo 34(2): 289 (1913)

Common names Top

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Language Common/alternative name
Spanish padus grayana
Spanish padus acrophylla
Spanish prunus padus var. japonica
Persian پرونوس گرایانا
Finnish japanintuomi
Japanese ウワミズザクラ
Swedish pärlhägg
Chinese 灰叶稠李
Chinese 灰葉稠李
Chinese 一种维管植物

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000986014
Tropicos 27803681
KEW urn:lsid:ipni.org:names:729764-1
The Plant List rjp-13553
Open Tree Of Life 870878
NCBI Taxonomy 140654
IPNI 729764-1
iNaturalist 637667
GBIF 3021963
Freebase /m/02v_gpc
EPPO PRNGN
EOL 11164965
USDA GRIN 30001
Wikipedia Prunus_grayana

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
Rust HUBB: DNA barcode-based identification of Pucciniales Kaishian P, Layug CR, Anderson M, Berg DR, Aime MC IMA Fungus 25-Feb-2024
PMCID:PMC10894486
doi:10.1186/s43008-023-00132-7
PMID:38402196
The Unexpected Identity of Tympanis vagabunda Quijada L, Baral HO, Pfister DH Life (Basel) 28-Feb-2023
PMCID:PMC10058965
doi:10.3390/life13030661
PMID:36983817
First Record of Colletotrichum anthrisci Causing Anthracnose on Avocado Fruits in Chile Bustamante MI, Osorio-Navarro C, Fernández Y, Bourret TB, Zamorano A, Henríquez-Sáez JL Pathogens 19-Oct-2022
PMCID:PMC9611251
doi:10.3390/pathogens11101204
PMID:36297261
Microbiome analyses of 12 psyllid species of the family Psyllidae identified various bacteria including Fukatsuia and Serratia symbiotica, known as secondary symbionts of aphids Nakabachi A, Inoue H, Hirose Y BMC Microbiol 07-Jan-2022
PMCID:PMC8740488
doi:10.1186/s12866-021-02429-2
PMID:34996376
Chemical Diversity of Plant Cyanogenic Glycosides: An Overview of Reported Natural Products Yulvianti M, Zidorn C Molecules 30-Jan-2021
PMCID:PMC7866531
doi:10.3390/molecules26030719
PMID:33573160
High-resolution melting of multiple barcode amplicons for plant species authentication Ballin NZ, Onaindia JO, Jawad H, Fernandez-Carazo R, Maquet A Food Control 01-Nov-2019
PMCID:PMC6686639
doi:10.1016/j.foodcont.2019.05.022
PMID:31680728
Transglycosylation products generated by Talaromyces amestolkiae GH3 β-glucosidases: effect of hydroxytyrosol, vanillin and its glucosides on breast cancer cells Méndez-Líter JA, Tundidor I, Nieto-Domínguez M, de Toro BF, González Santana A, de Eugenio LI, Prieto A, Asensio JL, Cañada FJ, Sánchez C, Martínez MJ Microb Cell Fact 31-May-2019
PMCID:PMC6544938
doi:10.1186/s12934-019-1147-4
PMID:31151435
DNA metabarcoding of spiders, insects, and springtails for exploring potential linkage between above- and below-ground food webs Toju H, Baba YG Zoological Lett 15-Feb-2018
PMCID:PMC5815251
doi:10.1186/s40851-018-0088-9
PMID:29468086
Negative correlation between altitudes and oxygen isotope ratios of seeds: exploring its applicability to assess vertical seed dispersal Naoe S, Tayasu I, Masaki T, Koike S Ecol Evol 04-Sep-2016
PMCID:PMC5513213
doi:10.1002/ece3.2380
PMID:28725362
Prunusols A and B, Novel Antioxidative Tocopherol Derivatives Isolated from the Leaf Wax of<i>Prunus grayana</i>Maxim Toshihiko Osawa, Shigenori Kumazawa, Shunro Kawakishi Oxford University Press (OUP) 13-Apr-2016
doi:10.1080/00021369.1991.10870841
Assembly of complex plant–fungus networks Toju H, Guimarães PR, Olesen JM, Thompson JN Nat Commun 20-Oct-2014
PMCID:PMC4218951
doi:10.1038/ncomms6273
PMID:25327887
How are plant and fungal communities linked to each other in belowground ecosystems? A massively parallel pyrosequencing analysis of the association specificity of root-associated fungi and their host plants Toju H, Sato H, Yamamoto S, Kadowaki K, Tanabe AS, Yazawa S, Nishimura O, Agata K Ecol Evol 02-Aug-2013
PMCID:PMC3790555
doi:10.1002/ece3.706
PMID:24101998
Prunusols A and B, Novel Antioxidative Tocopherol Derivatives Isolated from the Leaf Wax of Prunus grayana Maxim. Toshihiko OSAWA, Shigenori KUMAZAWA, Shunro KAWAKISHI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.55.1727
Phenolic glucosides from Prunus grayana Hiroko Shimomura, Yutaka Sashida, Tokuo Adachi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81521-6
Phenolic glucosides from the heartwood of Prunus grayana Hiroko Shimomura, Yutaka Sashida, Kiyoshi Yoshinari Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97773-2

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
2-methyl-4-[8,9,13-trihydroxy-13-[5-(1-hydroxytridecyl)oxolan-2-yl]-3-oxotridecyl]-2H-furan-5-one 73238317 Click to see 610.90 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,8R)-1-(4-hydroxyphenyl)-5,6-dimethyl-8-[(4R,8R)-4,8,12-trimethyltridecyl]-2,8,9,10-tetrahydro-1H-pyrano[3,2-f]chromen-3-one 101612207 Click to see CC1=C(C2=C(C(CC(=O)O2)C3=CC=C(C=C3)O)C4=C1OC(CC4)CCCC(C)CCCC(C)CCCC(C)C)C 548.80 unknown https://doi.org/10.1271/BBB1961.55.1727
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(3R,10R)-10-(4-hydroxyphenyl)-3,5,6-trimethyl-3-[(4R,8R)-4,8,12-trimethyltridecyl]-1,2,9,10-tetrahydropyrano[3,2-f]chromen-8-one 101613209 Click to see 562.80 unknown https://doi.org/10.1271/BBB1961.55.1727
(3R,10R)-10-(4-hydroxyphenyl)-3,5,6-trimethyl-3-[(4S,8S)-4,8,12-trimethyltridecyl]-1,2,9,10-tetrahydropyrano[3,2-f]chromen-8-one 163008431 Click to see CC1=C(C2=C(C(CC(=O)O2)C3=CC=C(C=C3)O)C4=C1OC(CC4)(C)CCCC(C)CCCC(C)CCCC(C)C)C 562.80 unknown https://doi.org/10.1080/00021369.1991.10870841
(3R,10S)-10-(4-hydroxyphenyl)-3,5,6-trimethyl-3-[(4S,8S)-4,8,12-trimethyltridecyl]-1,2,9,10-tetrahydropyrano[3,2-f]chromen-8-one 163008432 Click to see 562.80 unknown https://doi.org/10.1080/00021369.1991.10870841
10-(4-Hydroxyphenyl)-3,5,6-trimethyl-3-(4,8,12-trimethyltridecyl)-1,2,9,10-tetrahydropyrano[3,2-f]chromen-8-one 14580537 Click to see CC1=C(C2=C(C(CC(=O)O2)C3=CC=C(C=C3)O)C4=C1OC(CC4)(C)CCCC(C)CCCC(C)CCCC(C)C)C 562.80 unknown https://doi.org/10.1080/00021369.1991.10870841
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
Microginin 299-D 10395339 Click to see CC(C)C(C(=O)N(C)C(C(C)C)C(=O)N(C)C(CC1=CC=C(C=C1)O)C(=O)N2CCCC2C(=O)O)NC(=O)C(C(CCCCCCC(Cl)Cl)N)O 758.80 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
[6-[Cyano(phenyl)methoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 363079 Click to see 457.40 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
Grayanin 6442904 Click to see 457.40 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(3,4-Dihydroxyphenyl)ethyl beta-D-glucopyranoside 5316821 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13845930 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl benzoate 163032261 Click to see 390.40 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
[2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 162940261 Click to see C1=CC=C(C(=C1)COC(=O)C2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 568.50 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
[2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[(2S,3R,4S,5S,6R)-6-(benzoyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-6-hydroxybenzoate 162952881 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=CC=CC(=C3C(=O)OCC4=CC=CC=C4OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 688.60 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
[2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[(2S,3R,4S,5S,6R)-6-(benzoyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxybenzoate 163046223 Click to see 672.60 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
[2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 162934029 Click to see C1=CC=C(C(=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 584.50 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 14311133 Click to see C1=CC=C(C(=C1)COC(=O)C2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 568.50 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[6-(benzoyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-6-hydroxybenzoate 162952880 Click to see 688.60 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[6-(benzoyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxybenzoate 14311136 Click to see 672.60 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
[3,4,5-Trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl benzoate 278591 Click to see 390.40 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
2-[[[2-(beta-D-Glucopyranosyloxy)-6-hydroxybenzoyl]oxy]methyl]phenyl beta-D-glucopyranoside 14311134 Click to see C1=CC=C(C(=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 584.50 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
Henryoside 14311135 Click to see 584.50 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
Populin 92735 Click to see 390.40 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
Virgaureoside A 180953 Click to see 568.50 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
((2R,3S,4S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl)methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 10427456 Click to see 342.30 unknown https://doi.org/10.1016/S0031-9422(00)81521-6
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 85140196 Click to see 342.30 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
[(2R,3S,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 13845929 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OCCC3=CC(=C(C=C3)O)O)O)O)O)O 492.50 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
[3,4,5-Trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73078515 Click to see 476.50 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 78380900 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163050385 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OCCC3=CC(=C(C=C3)O)O)O)O)O)O 492.50 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
6-O-caffeoyl-beta-glucose 101419460 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
Calceolarioside B 5273567 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
coumaroyl(3-OH)(-6)Glc(b)-O-EtPh(4-OH) 14311190 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
Grayanoside A 11733480 Click to see 476.50 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(1S,8R,9S,16S,18R,27R)-9-(3,4-dihydroxyphenyl)-5,8,16,21,23-pentahydroxy-2,10,17,26-tetraoxaheptacyclo[14.11.1.01,13.03,12.06,11.018,27.020,25]octacosa-3(12),4,6(11),13,20,22,24-heptaen-15-one 163081767 Click to see C1C(C(OC2=C1C(=CC3=C2C4=CC(=O)C5(CC4(O3)C6C(O5)CC7=C(C=C(C=C7O6)O)O)O)O)C8=CC(=C(C=C8)O)O)O 576.50 unknown https://doi.org/10.1016/S0031-9422(00)97773-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 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/S0031-9422(00)97773-2
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/S0031-9422(00)97773-2
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trimethoxybenzoate 5322109 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)OC2C(C(C(C(O2)CO)O)O)O 374.34 unknown https://doi.org/10.1016/S0031-9422(00)84720-2
1-O-(3,4,5-Trimethoxybenzoyl)-b-D-glucopyranoside 23928103 Click to see 374.34 unknown https://doi.org/10.1016/S0031-9422(00)84720-2

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