Details Top

Internal ID UUID64403f88304f6488017190
Scientific name Prunus japonica
Authority Thunb.
First published in Syst. Veg., ed. 14 (J. A. Murray). 463. 1784 [May-Jun 1784]

Ethnobotanical Use Top

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General Uses Top

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Common products:
Edible products made from P. japonica fruits include jams, jellies, preserves, sauces, syrups, and confectionery. The fruit is also processed into the Korean liqueur maesil-ju (maesil-cheong syrup used for fermentation or non-alcoholic mixing) and less commonly into maesil-cha (fruit pieces or sweetened concentrate for non-alcoholic beverages). These products are based on sweet–sour fruit varieties and commercial pectin or acidification strategies rather than medicinal use.

Food and beverages (non-medicinal):
Food uses center on fresh or brined fruit for syrups and jams, and on large-scale production of maesil-cheong, a sugar-fruit conserve or syrup used as a food ingredient and sweetener, leading to alcoholic maesil-ju via controlled fermentation. Large-scale processing typically involves acidification (citric acid), pectin addition for texture, and heat treatment for stability.

Colorants and tanning:
Although not a primary commercial dye plant, P. japonica bark and stones contain tannins (gallotannins and ellagitannins) and phenolics, which have been studied for natural brown dyes on protein fibers and as tanning agents in leather processing. These uses remain niche and are not widely standardized for industrial tannin supply.

Wood and fiber:
The wood is dense and fine-grained, suitable for small turnery and ornamental objects; it does not supply a major commercial timber. The kernel fat (prunus kernel oil) is not a recognized food or cosmetic oil due to cyanogenic glycosides and has no established industrial use.

Fragrance and cosmetics:
No documented fragrance or cosmetic applications are reported for P. japonica.

Properties relevant to use:
Fruits are high in acidity and soluble solids, enabling stable syrups and preserves; they exhibit relatively high pectin content supporting jams. Bark and stones contain tannins (gallotannins/ellagitannins) with potential tanning and dyeing utility. Kernel lipids contain cyanogenic glycosides, precluding culinary or cosmetic use and limiting industrial extraction.

Scientific/model-organism use:
P. japonica serves as a genetic and physiological model within Prunus research for flowering time, cold hardiness, fruit ripening, and breeding of ornamental and edible forms; genetic studies and horticultural research databases list it among the East Asian cherry-plum group for comparative genomics and trait mapping.

Standards and regulation:
Food uses of the fruit comply with national food additive and processing standards (for example, Japan’s Food Sanitation Act and general food sanitation norms for heat treatment and labeling). Kernel materials are controlled under general restrictions on cyanogenic plant products; no dedicated ISO/ASTM standards exist for P. japonica fruit or bark tanning agents.

Sustainability and sourcing:
Cultivation occurs across Korea, Japan, and China on smallholder and semi-commercial orchard systems. Fruit supply is often local or regional for syrups and liqueurs; availability and varietal selection vary by season. Tannin-related bark use, where practiced, is minor and generally opportunistic rather than plantation-driven.

Synonyms Top

Scientific name Authority First published in
Cerasus japonica (Thunb.) Loisel. Trait‚ des arbres et arbustes que l'on cultive en France ; 1800 33 1809
Microcerasus japonica M.Roem. Fam. Nat. Syn. Monogr. 3: 95 (1847)
Prunus ishidoyana Nakai Bot. Mag. (Tokyo) 33: 8 (1919)
Microcerasus glandulosa var. japonica (Thunb.) Eremin & Juschev Trudy Prikl. Bot. 65(3): 77 (1979)

Common names Top

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Language Common/alternative name
English japanese bush cherry
Czech třešeň japonská
Persian بوتهٔ گیلاس شرقی
Persian بوته گیلاس شرقی
French cerisier de corée
Japanese ニワウメ
lzh 郁李
Vietnamese cerasus japonica
Chinese 郁李
Chinese 爵梅
Chinese 秧李

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Prunus japonica var. nakaii (H.Lév.) Rehder J. Arnold Arbor. 3: 29. 1922 (1922)
Prunus japonica var. japonica Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001002027
UNII O948O30Z65
USDA Plants PRJA
Tropicos 27805918
INPN 116084
KEW urn:lsid:ipni.org:names:729847-1
The Plant List rjp-3239
Open Tree Of Life 478349
NCBI Taxonomy 97319
IPNI 927360-1
iNaturalist 452165
GBIF 3020565
Freebase /m/05x70c
EPPO PRNJP
EOL 301174
USDA GRIN 30017
Wikipedia Prunus_japonica
CMAUP NPO18659

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
The complete chloroplast genome sequence of Prunus salicina cultivar ‘Zuili’ (Rosaceae) Yao Z, Miao J, Xu W, Cao L, Lu Q Mitochondrial DNA B Resour 12-Feb-2024
PMCID:PMC10863533
doi:10.1080/23802359.2024.2316068
PMID:38352190
Human Sperm as an In Vitro Model to Assess the Efficacy of Antioxidant Supplements during Sperm Handling: A Narrative Review Moretti E, Signorini C, Corsaro R, Giamalidi M, Collodel G Antioxidants (Basel) 15-May-2023
PMCID:PMC10215929
doi:10.3390/antiox12051098
PMID:37237965
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
Hexane fraction of Prunus japonica thunb. Seed extract enhances boar sperm motility via CatSper ion channel Cooray A, Chae MR, Wijerathne TD, Kim DG, Kim J, Kim CY, Lee SW, Lee KP Heliyon 09-Feb-2023
PMCID:PMC9950932
doi:10.1016/j.heliyon.2023.e13616
PMID:36846677
IBA Delivery Technique and Media Salts Affected In Vitro Rooting and Acclimatization of Eight Prunus Genotypes Lawson JD, Bridges WC, Adelberg JW Plants (Basel) 07-Jan-2023
PMCID:PMC9861824
doi:10.3390/plants12020289
PMID:36679002
‘Food and medicine continuum’ in the East and West: Old tradition and current regulation Yao R, He C, Xiao P Chin Herb Med 17-Dec-2022
PMCID:PMC9975626
doi:10.1016/j.chmed.2022.12.002
PMID:36875443
Evaluation of the chemical profile from four germplasms sources of Pruni Semen using UHPLC-LTQ-Orbitrap-MS and multivariate analyses Zhao Z, Liu Y, Zhang Y, Geng Z, Su R, Zhou L, Han C, Wang Z, Ma S, Li W J Pharm Anal 06-Jul-2022
PMCID:PMC9615524
doi:10.1016/j.jpha.2022.06.007
PMID:36320598
Honeysuckle (Lonicera japonica) and Huangqi (Astragalus membranaceus) Suppress SARS-CoV-2 Entry and COVID-19 Related Cytokine Storm in Vitro Yeh YC, Doan LH, Huang ZY, Chu LW, Shi TH, Lee YR, Wu CT, Lin CH, Chiang ST, Liu HK, Chuang TH, Ping YH, Liu HS, Huang CY Front Pharmacol 25-Mar-2022
PMCID:PMC8990830
doi:10.3389/fphar.2021.765553
PMID:35401158
The Potential Application of Green-Synthesized Metal Nanoparticles in Dentistry: A Comprehensive Review Yazdanian M, Rostamzadeh P, Rahbar M, Alam M, Abbasi K, Tahmasebi E, Tebyaniyan H, Ranjbar R, Seifalian A, Yazdanian A Bioinorg Chem Appl 03-Mar-2022
PMCID:PMC8913069
doi:10.1155/2022/2311910
PMID:35281331
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Role of medicinal plants in inhibiting SARS-CoV-2 and in the management of post-COVID-19 complications Mukherjee PK, Efferth T, Das B, Kar A, Ghosh S, Singha S, Debnath P, Sharma N, Bhardwaj PK, Haldar PK Phytomedicine 05-Jan-2022
PMCID:PMC8730822
doi:10.1016/j.phymed.2022.153930
PMID:35114450
Identification and Molecular Analysis of Putative Self-Incompatibility Ribonuclease Alleles in an Extreme Polyploid Species, Prunus laurocerasus L. Halász J, Molnár AB, Ilhan G, Ercisli S, Hegedűs A Front Plant Sci 23-Sep-2021
PMCID:PMC8495262
doi:10.3389/fpls.2021.715414
PMID:34630463
Systematic Review on Biosynthesis of Silver Nanoparticles and Antibacterial Activities: Application and Theoretical Perspectives Qamer S, Romli MH, Che-Hamzah F, Misni N, Joseph NM, AL-Haj NA, Amin-Nordin S Molecules 20-Aug-2021
PMCID:PMC8398138
doi:10.3390/molecules26165057
PMID:34443644
Fusarium: more than a node or a foot-shaped basal cell Crous PW, Lombard L, Sandoval-Denis M, Seifert KA, Schroers HJ, Chaverri P, Gené J, Guarro J, Hirooka Y, Bensch K, Kema GH, Lamprecht SC, Cai L, Rossman AY, Stadler M, Summerbell RC, Taylor JW, Ploch S, Visagie CM, Yilmaz N, Frisvad JC, Abdel-Azeem AM, Abdollahzadeh J, Abdolrasouli A, Akulov A, Alberts JF, Araújo JP, Ariyawansa HA, Bakhshi M, Bendiksby M, Ben Hadj Amor A, Bezerra JD, Boekhout T, Câmara MP, Carbia M, Cardinali G, Castañeda-Ruiz RF, Celis A, Chaturvedi V, Collemare J, Croll D, Damm U, Decock CA, de Vries RP, Ezekiel CN, Fan XL, Fernández NB, Gaya E, González CD, Gramaje D, Groenewald JZ, Grube M, Guevara-Suarez M, Gupta VK, Guarnaccia V, Haddaji A, Hagen F, Haelewaters D, Hansen K, Hashimoto A, Hernández-Restrepo M, Houbraken J, Hubka V, Hyde KD, Iturriaga T, Jeewon R, Johnston PR, Jurjević Ž, Karalti İ, Korsten L, Kuramae EE, Kušan I, Labuda R, Lawrence DP, Lee HB, Lechat C, Li HY, Litovka YA, Maharachchikumbura SS, Marin-Felix Y, Matio Kemkuignou B, Matočec N, McTaggart AR, Mlčoch P, Mugnai L, Nakashima C, Nilsson RH, Noumeur SR, Pavlov IN, Peralta MP, Phillips AJ, Pitt JI, Polizzi G, Quaedvlieg W, Rajeshkumar KC, Restrepo S, Rhaiem A, Robert J, Robert V, Rodrigues AM, Salgado-Salazar C, Samson RA, Santos AC, Shivas RG, Souza-Motta CM, Sun GY, Swart WJ, Szoke S, Tan YP, Taylor JE, Taylor PW, Tiago PV, Váczy KZ, van de Wiele N, van der Merwe NA, Verkley GJ, Vieira WA, Vizzini A, Weir BS, Wijayawardene NN, Xia JW, Yáñez-Morales MJ, Yurkov A, Zamora JC, Zare R, Zhang CL, Thines M Stud Mycol 17-Aug-2021
PMCID:PMC8379525
doi:10.1016/j.simyco.2021.100116
PMID:34466168
Plant-based green synthesis of silver nanoparticles and its effective role in abiotic stress tolerance in crop plants Alabdallah NM, Hasan MM Saudi J Biol Sci 04-Jun-2021
PMCID:PMC8459083
doi:10.1016/j.sjbs.2021.05.081
PMID:34588874

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
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
15-Amido-3-demethoxy-2alpha,3alpha-methylenedioxyerythroculine 16091679 Click to see 342.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Physcion 10639 Click to see 284.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1248/YAKUSHI1947.99.4_439
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1248/YAKUSHI1947.99.4_439
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Benzoic acid, 2-hydroxy-6-tetradecyl- 5318118 Click to see CCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 334.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Multiradiatin 442284 Click to see CC1C2C=CC(=O)C2(C(C3C(C1=O)OC(=O)C3=C)OC(=O)C=C(C)C)C 358.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 101623260 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1248/YAKUSHI1947.99.4_439
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see 428.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Hennadiol 489919 Click to see 442.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1248/YAKUSHI1947.99.4_439
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6R,7S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 44423591 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown via CMAUP database
[(1S,3R,6R,7S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methyl-5-oxoheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 72708917 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1OC(=O)C)C)C(C)CCC(=O)C(C)C)C 470.70 unknown via CMAUP database
1-Dehydroxy-23-deoxojessic acid 3008861 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C(=O)O)O)C)C 470.70 unknown via CMAUP database
Cycloeucalenone 21594790 Click to see 424.70 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Organic cyanides / Nitriles
Hydrogen Cyanide 768 Click to see 27.03 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2R)-2-phenyl-2-[(2R,4R,5S)-3,4,5-trihydroxy-6-[[(2R,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyacetonitrile 24801909 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
[(6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy](phenyl)acetonitrile 34751 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
2-Phenyl-2-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxyacetonitrile 2180 Click to see 457.40 unknown via CMAUP database
Amygdalin 656516 Click to see 457.40 unknown via CMAUP database
Mandelonitrile-beta-gentiobioside 656495 Click to see 457.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Aryl-phenylketones
methyl 3,5-dimethoxy-2-[4-oxo-6-[(E)-prop-1-enyl]-1H-pyridine-3-carbonyl]benzoate 24761002 Click to see CC=CC1=CC(=O)C(=CN1)C(=O)C2=C(C=C(C=C2OC)OC)C(=O)OC 357.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Penicidone A 24761000 Click to see CC=CC1=CC(=O)C(=CN1)C2C3=C(C=C(C=C3OC)OC)C(=O)O2 327.30 unknown via CMAUP database
Penicidone B 24761001 Click to see 313.30 unknown via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Alloxazines and isoalloxazines / Flavins
Lumichrome 5326566 Click to see CC1=CC2=C(C=C1C)N=C3C(=N2)C(=O)NC(=O)N3 242.23 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolizidines
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-5-en-4-one 10060497 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4 246.35 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol oxoanion 25202062 Click to see 285.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 10304351 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)OC5C(C(C(C(O5)CO)O)O)O 610.50 unknown via CMAUP database
3-[(2S,3S,5R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 44258929 Click to see 594.50 unknown via CMAUP database
CID 44258969 44258969 Click to see 636.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44258935 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown via CMAUP database

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