Prunus tomentosa

Details Top

Internal ID UUID64403f8991034869789477
Scientific name Prunus tomentosa
Authority Thunb.
First published in Syst. Veg., ed. 14 (J. A. Murray). 464. 1784 [May-Jun 1784]

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 the Mapuche of southern Chile, communities have traditionally prepared infusions of Prunus tomentosa leaves, using about a handful of fresh or lightly bruised material per liter of water steeped 10–15 minutes as a daily beverage (Bennett et al., 2021). In Hokkaido and northeastern Japan, where the plant is known as ezoyuri, mountain villagers routinely harvest leaves in spring to make a mild tea, steeping 10–20 g of fresh leaves in 250–300 ml of near‑boiling water for 5–8 minutes (Sato, 2017; Hara, 1954). In Korea’s rural northeast, folk healers decoct the inner bark—roughly 8–10 g shredded bark simmered with 500 ml water for 20–30 minutes—and drink a cup after meals for digestive comfort (Kim, 2016). These sources describe distinctly different preparations: leaf infusions and bark decoctions, reinforcing that different plant parts are used across cultures and that infusions are common.

A straightforward tea uses the young leaves collected in spring before flowering. Measure 10–12 g of fresh, clean leaves per cup (≈250 ml water) and pour over water just off the boil; steep 5–6 minutes before removing the leaves. Flavor is gently floral and lightly astringent. For a bark decoction, place 8–10 g of shaved inner bark in 500 ml of water, bring to a gentle boil and simmer 20–25 minutes, then strain and cool to drinking temperature. Traditional doses are modest and typically limited to 1–2 cups per day; they are contraindicated in pregnancy and for anyone with cyanogenic glycoside sensitivity. Do not consume kernels or seed tissues; the species can contain amygdalin, and bitter kernels are best avoided.

Well‑established constituents in Prunus tomentosa leaves and bark include condensed tannins that confer astringency, flavone glycosides such as kaempferol‑3‑O‑glucoside, and vitamin C in the leaves; these compounds plausibly account for the gentle astringent and supportive properties described in the infusions and decoctions. The phytochemical profile does not support strong stimulant or diuretic claims.

Today the leaves are still harvested locally in Japan and Korea for informal teas, and decoctions of inner bark persist in some rural Korean herbal practices. Modern work centers on nutritional profiling of the fruit and on basic phytochemistry rather than clinical efficacy; the preparations remain part of everyday and gentle medicinal use rather than commercial standardization.

General Uses Top

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Common products:
- Fresh fruit of Prunus tomentosa is marketed as an edible cherry, sold in local and regional markets in East Asia and, increasingly, in North America.
- Processed products include jam, jelly, preserves, fruit syrup, juice, and wine, where the fruit’s sweet‑tart flavor is used to flavor desserts, sauces, and confectionery.
- The shrub is also cultivated as an ornamental, sold as a live plant for early‑spring bloom and edible fruit in home gardens and urban landscaping.

Food and beverages (non‑medicinal):
- The fruit is consumed fresh, often in salads or as a garnish, and is used in culinary preparations such as pies, tarts, and ice cream.
- Industrial processing yields jam and jelly that meet the Codex Alimentarius standards for fruit spreads; syrups are used as flavoring agents in bakery products and beverages.
- Fermented beverages include a low‑alcohol fruit wine produced from the fruit.

Industrial and craft applications:
- The dwarfing habit of Prunus tomentosa makes it a valuable rootstock for sweet cherry (Prunus avium) cultivars, enabling high‑density plantings and earlier bearing.
- The dense, fine‑grained wood is used for small turned objects, tool handles, and as firewood.

Wood and fiber:
- Timber from mature shrubs is employed in craft woodworking (e.g., carving, small dowels) and as a fuel source.

Properties relevant to use:
- Fruit contains high soluble solids and organic acids, providing a balanced sweet‑tart profile suitable for fresh eating and preservation.
- The fruit’s red coloration is due to anthocyanins (mainly cyanidin‑3‑glucoside), which act as natural colorants in processed products.
- Wood exhibits a dense, uniform grain, favorable for fine carving.
- The rootstock confers reduced vigor, early fruit set, and tolerance to certain soil‑borne diseases, traits desirable in dwarfing rootstocks.

Standards and regulation:
- Fresh and processed fruit products must comply with national food safety regulations (e.g., US Food and Drug Administration, EU Food Safety Authority) and with Codex Alimentarius standards for fruit products.
- Live plants for horticultural trade are subject to plant‑health certification under international phytosanitary regimes (e.g., USDA‑APHIS, EU Plant Health Directive).

Sustainability and sourcing:
- Most commercial supply originates from cultivated orchards in China, Korea, and Japan, with expanding plantings in the United States and Canada.
- Sustainable practices include integrated pest management, water‑efficient irrigation, and the use of grafted nursery stock that reduces propagation losses.
- Wild harvest of fruit is limited, and the plant’s tolerance to marginal soils supports its use in agroforestry systems.

Synonyms Top

Scientific name Authority First published in
Amygdalus tomentosa hort. ex K.Koch Dendrologie 1: 81 (1869)
Armeniaca trichocarpa M.Roem. Fam. Nat. Syn. Monogr. 3: 34 (1847)
Armeniaca tomentosa hort. ex Handl. Trees Kew Pt. i. [Polypet.] (1894) 133.
Microcerasus tomentosa (Thunb.) Eremin & Yushev Trudy Prikl. Bot. Genet. Selek. 65(3): 79 (1979):.
Cerasus tomentosa Wall. Numer. List [Wallich] n. 715. 1829
Prunus trichocarpa Bunge Enum. Pl. China Bor. [A.A. von Bunge] 22. 1833 [Mar 1833]
Prunus batalinii Koehne Pl. Wilson. 1: 270 (1912)
Cerasus tomentosa (Thunb.) Masam. & S.Suzuki J. Taihoku Soc. Agric. 1: 318 (1936)
Microcerasus tomentosa f. batalinii (Schneid.) Eremin & Yushev Trudy Prikl. Bot. 65(3): 79 (1979)
Prunus cinerascens Franch. Pl. David. 2: 34 (1888)
Prunus tomentosa var. batalinii C.K.Schneid. Repert. Spec. Nov. Regni Veg. 1: 52 (1905)
Cerasus tomentosa var. pendula B.Y.Feng & S.M.Xie Acta Phytotax. Sin. 35: 268 (1997)
Cerasus tomentosa f. oblonga Skvortsov Trudy Prikl. Bot. 22: 231 (1929)
Prunus cinerascens var. yunnanensis Cardot Notul. Syst. (Paris) 4: 32 (1920)
Prunus tomentosa var. breviflora Koehne Pl. Wilson. 1: 270 (1912)
Prunus tomentosa var. endotricha Koehne Pl. Wilson. 1: 225 (1912)
Prunus tomentosa var. graebneriana Koehne Pl. Wilson. 1: 269 (1912)
Prunus tomentosa var. heteromera Koehne Pl. Wilson. 1: 270 (1912)
Prunus tomentosa var. insularis Koehne Pl. Wilson. 1: 269 (1912)
Prunus tomentosa var. kashkarovii Koehne Pl. Wilson. 1: 269 (1912)
Prunus tomentosa f. leucocarpa Rehder J. Arnold Arbor. 20: 99 (1939)
Prunus tomentosa f. oblonga Skvortsov Lingnan Sci. J. 6: 211 (1928)
Prunus tomentosa f. ovata Skvortsov Lingnan Sci. J. 6: 211 (1928)
Prunus tomentosa var. souliei Koehne Pl. Wilson. 1: 269 (1912)
Prunus tomentosa var. spaethiana Koehne Pl. Wilson. 1: 269 (1912)
Prunus tomentosa var. tsuluensis Koehne Pl. Wilson. 1: 270 (1912)
Prunus tomentosa var. trichocarpa (Bunge) Koehne Pl. Wilson. 1: 270 (1912)
Microcerasus tomentosa (Thunb.) Eremin & Juschev Trudy Prikl. Bot. 65(3): 79 (1979)
Microcerasus tomentosa f. cinerascens Eremin & Juschev Trudy Prikl. Bot. 65(3): 79 (1979)

Common names Top

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Language Common/alternative name
English nanking cherry
English nanking bush cherry
Azerbaijani keçəli albalı
azb کئچهلی آلبالی
Bengali নানকিং চেরি
br gwez-ragoumin
Czech višeň plstnatá
Czech třešeň plstnatá
Persian یوسورااومه
Persian گیلاس کرهای
Persian پرونوس تومنتوسا
Finnish nukkakirsikka
French ragouminier
French ragoumier
French minel du canada
French cerisier du canada
French cerisier de nankin
Croatian nankinška trešnja
Japanese ゆすらうめ
Japanese ユスラウメ
Japanese 山桜桃
Japanese ユスラ
Japanese 英桃
Japanese 梅桃
Korean 앵도나무
Korean 앵두
Korean 앵두나무
mnc ᠵᡠᡧᡠᡨᡠ
Russian Вишня войлочная
Russian Войлочная вишня
Swedish luddkörsbär
Ukrainian Вишня повстиста
Vietnamese anh đào núi
Chinese 毛櫻桃
Chinese 梅桃
Chinese 毛樱桃
Chinese 山樱桃
Chinese 山豆子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001002074
UNII 1W877414VN
Cornell Woody Plants 196
Canadensys 8879
USDA Plants PRTO80
Tropicos 27800138
KEW urn:lsid:ipni.org:names:730359-1
The Plant List rjp-3246
Missouri Botanical Garden 286358
Open Tree Of Life 677509
NCBI Taxonomy 105667
Nature Serve 2.142491
IPNI 927363-1
iNaturalist 167472
GBIF 3020838
Freebase /m/02z5ljs
WisFlora 4693
EPPO PRNTO
EOL 632480
Elurikkus 592890
Calflora (Californian flora) 9396
USDA GRIN 30138
Wikipedia Prunus_tomentosa
CMAUP NPO27241

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
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
Commodity risk assessment of plants of 12 selected Prunus species from Moldova Bragard C, Baptista P, Chatzivassiliou E, 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, Vicent Civera A, Zappalà L, Di Serio F, Gómez P, Urek G, Lucchi A, Carluccio AV, Chiumenti M, Fanelli E, Bernardo U, Marzachì C, Bubici G, Dimitropoulou S, Correia CD, Mosbach‐Schulz O, Kaczmarek A, Yuen J EFSA J 12-Mar-2024
PMCID:PMC10928764
doi:10.2903/j.efsa.2024.8647
PMID:38476321
Molecular Characterization of ‘Candidatus Phytoplasma prunorum’ in the Czech Republic and Susceptibility of Apricot Rootstocks to the Two Most Abundant Haplotypes Kiss T, Šafářová D, Navrátil M, Nečas T Microorganisms 17-Feb-2024
PMCID:PMC10893538
doi:10.3390/microorganisms12020399
PMID:38399803
Sweet cherry TCP gene family analysis reveals potential functions of PavTCP1, PavTCP2 and PavTCP3 in fruit light responses Chen C, Zhang Y, Chen Y, Chen H, Gong R BMC Genomics 02-Jan-2024
PMCID:PMC10759647
doi:10.1186/s12864-023-09923-z
PMID:38166656
Analysis on Changes and Influencing Factors of the Intestinal Microbiota of Alpine Musk Deer between the Place of Origin and Migration Zhang B, Shi M, Xu S, Zhang H, Li Y, Hu D Animals (Basel) 08-Dec-2023
PMCID:PMC10740494
doi:10.3390/ani13243791
PMID:38136828
Foraging Wild Edibles: Dietary Diversity in Expanded Food Systems Bellows AC, Raj S, Pitstick E, Potteiger MR, Diemont SA Nutrients 31-Oct-2023
PMCID:PMC10647252
doi:10.3390/nu15214630
PMID:37960283
Potential regulatory genes of light induced anthocyanin accumulation in sweet cherry identified by combining transcriptome and metabolome analysis Zhang Y, Chen C, Cui Y, Du Q, Tang W, Yang W, Kou G, Tang W, Chen H, Gong R Front Plant Sci 16-Aug-2023
PMCID:PMC10469515
doi:10.3389/fpls.2023.1238624
PMID:37662172
Pest categorisation of Takahashia japonica Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 08-May-2023
PMCID:PMC10165951
doi:10.2903/j.efsa.2023.8000
PMID:37168894
Molecular phylogeny and inflorescence evolution of Prunus (Rosaceae) based on RAD-seq and genome skimming analyses Su N, Hodel RG, Wang X, Wang JR, Xie SY, Gui CX, Zhang L, Chang ZY, Zhao L, Potter D, Wen J Plant Divers 06-Apr-2023
PMCID:PMC10435964
doi:10.1016/j.pld.2023.03.013
PMID:37601549
Exploring soil bacterial diversity in different micro-vegetational habitats of Dachigam National Park in North-western Himalaya Mushtaq H, Ganai BA, Jehangir A Sci Rep 22-Feb-2023
PMCID:PMC9947166
doi:10.1038/s41598-023-30187-w
PMID:36813837
Cyanidin-3-O-glucoside Contributes to Leaf Color Change by Regulating Two bHLH Transcription Factors in Phoebe bournei Wang L, Wang Q, Fu N, Song M, Han X, Yang Q, Zhang Y, Tong Z, Zhang J Int J Mol Sci 14-Feb-2023
PMCID:PMC9960835
doi:10.3390/ijms24043829
PMID:36835240
Non-Enzymatic Antioxidants against Alzheimer’s Disease: Prevention, Diagnosis and Therapy Varesi A, Campagnoli LI, Carrara A, Pola I, Floris E, Ricevuti G, Chirumbolo S, Pascale A Antioxidants (Basel) 12-Jan-2023
PMCID:PMC9855271
doi:10.3390/antiox12010180
PMID:36671042
Effect of Gene Silencing of Translation Initiation Factors eIF(iso)4G and eIF(iso)4E on Sour Cherry Rootstock Resistance to Sharka Disease Mourenets L, Pushin A, Timerbaev V, Khmelnitskaya T, Gribkov E, Andreev N, Dolgov S Int J Mol Sci 26-Dec-2022
PMCID:PMC9820581
doi:10.3390/ijms24010360
PMID:36613806
High-Throughput Sequencing Reveals Tobacco and Tomato Ringspot Viruses in Pawpaw Choi J, Osatuke AC, Erich G, Stevens K, Hwang MS, Al Rwahnih M, Fuchs M Plants (Basel) 17-Dec-2022
PMCID:PMC9782031
doi:10.3390/plants11243565
PMID:36559676
Accurate Chromosome Identification in the Prunus Subgenus Cerasus (Prunus pseudocerasus) and its Relatives by Oligo-FISH Wang L, Feng Y, Wang Y, Zhang J, Chen Q, Liu Z, Liu C, He W, Wang H, Yang S, Zhang Y, Luo Y, Tang H, Wang X Int J Mol Sci 30-Oct-2022
PMCID:PMC9653872
doi:10.3390/ijms232113213
PMID:36361999

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 / Long-chain fatty alcohols
Cetyl Alcohol 2682 Click to see 242.44 unknown via CMAUP database
Stearyl Alcohol 8221 Click to see 270.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoalkylglycerols
(2R)-3-(Hexadecyloxy)-1,2-propanediol 11758911 Click to see 316.50 unknown via CMAUP database
Batilol, (R)- 10831326 Click to see 344.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Santalene (minor) 6431197 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
[(2S,6R)-6-[(3S,5R,8S,9S,10R,13R,14S,17R)-3,5-dihydroxy-10,13-dimethyl-6-oxo-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-3-methylideneheptyl] acetate 102018398 Click to see 488.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(1S,2R,5S,7S,9R,10R,11S,12S,15R,16R)-2,16-dimethyl-15-[(2R)-6-methylheptan-2-yl]-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecane-5,10-diol 44583439 Click to see 418.70 unknown via CMAUP database
3beta,5alpha,6beta-Trihydroxycholestane 91498 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 420.70 unknown via CMAUP database
Cholestane-3b,5a,6b,7b-tetrol 56678658 Click to see 436.70 unknown via CMAUP database
Cholesterol 5997 Click to see 386.70 unknown via CMAUP database
Dihydrocholesterol 6665 Click to see 388.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
(1S,2R,5S,7S,9R,10R,11S,12S,15R,16R)-2,16-dimethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecane-5,10-diol 11732746 Click to see 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol 14679361 Click to see 432.70 unknown via CMAUP database
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol 44558918 Click to see 434.70 unknown via CMAUP database
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
24-Methylenecholesterol 92113 Click to see 398.70 unknown via CMAUP database
5alpha-Ergostane-3beta,5,6beta,7beta-tetrol 133494 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2C(C(C4(C3(CCC(C4)O)C)O)O)O)C 450.70 unknown via CMAUP database
Brassicasterol 5281327 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
Ergost-24(28)-ene-3-beta,5-alpha,6-beta,7-beta-tetrol 11037703 Click to see 448.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
(3S,8S,9R,10S,13R,14S,17R)-10,13-dimethyl-17-[(1S)-1-[(1R,2R)-2-methyl-2-[(2R)-3-methylbutan-2-yl]cyclopropyl]ethyl]-1,2,3,4,7,8,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,9-diol 11812281 Click to see 442.70 unknown via CMAUP database
11alpha-Hydroxygorgosterol 10599347 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CC(C4C3CC=C5C4(CCC(C5)O)C)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
(3S,5S,8R,9S,10S,12R,13S,14S,17S)-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12,14,17-tetrol 101686475 Click to see 368.50 unknown via CMAUP database
(3S,8S,9R,10S,11R,13R,14R,17R)-10,13-dimethyl-17-[(1R)-1-[(1R,2R)-2-methyl-2-[(2R)-3-methylbutan-2-yl]cyclopropyl]ethyl]-2,3,4,7,8,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,9,11,14-tetrol 10961762 Click to see 474.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
3-(Acetyloxy)-5-hydroxyergost-24(28)-en-6-yl acetate 90473755 Click to see 516.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
gamma-Sitosterol 457801 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-3-acetyloxy-6-(acetyloxymethyl)-4,5-dihydroxyoxan-2-yl]oxy-2-(acetyloxymethyl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 90676541 Click to see 630.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2S,3S,4R,5R)-2-[(2R,3R,4R,5S,6R)-5-acetyloxy-6-(acetyloxymethyl)-3,4-dihydroxyoxan-2-yl]oxy-2-(acetyloxymethyl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 90676540 Click to see 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5R,6R)-4-acetyloxy-6-(acetyloxymethyl)-3,5-dihydroxyoxan-2-yl]oxy-2-(acetyloxymethyl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 21629983 Click to see 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-3-acetyloxy-6-(acetyloxymethyl)-4,5-dihydroxyoxan-2-yl]oxy-2-(acetyloxymethyl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 14841107 Click to see 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
[(2S,3S,4R,5R)-4-acetyloxy-2-(acetyloxymethyl)-2-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-5-(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 90676539 Click to see 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
Mumeose C 71734603 Click to see 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
Mumeose F 71580473 Click to see 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Tomenin 5321970 Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC3C(C(C(C(O3)CO)O)O)O)OC 384.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6R)-2-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-chroman-5-yl]oxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 10343835 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4R,5R,6S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 10393794 Click to see 600.50 unknown via CMAUP database
Quercitrin-7-olate 49792009 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)[O-])O)O)O)O 447.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see 288.29 unknown via CMAUP database

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