Prunus × yedoensis - Unknown
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Internal ID UUID64403e6fe7c39166184795
Scientific name Prunus × yedoensis
Authority Matsum.
First published in Bot. Mag. (Tokyo) 15: 100 (1901)

Description Top

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Synonyms Top

Scientific name Authority First published in
Prunus morioka-pendula Miyoshi Bot. Mag. (Tokyo) 34: 169 (1920)
Cerasus yedoensis (Matsum.) A.N.Vassiljeva Trudy Sukhumsk. Bot. Sada 10: 124 (1957)

Common names Top

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Language Common/alternative name
English prunus yedoensis
English tokyo cherry
Azerbaijani prunus × yedoensis
ceb prunus yedoensis
Esperanto prunus × yedoensis
Basque yoshino gereziondo
Persian سومی-یوشینو
Persian پرونوس یدوانسیس
French cerisier yoshino
French prunus yedoensis
French prunus xyedoensis
French prunus × yedoensis
Upper Sorbian prunus × yedoensis
Upper Sorbian yoshinowa wišnja
Japanese ソメイヨシノ
Japanese 染井吉野
Japanese 吉野桜
Korean 왕벚나무
Dutch yushinokers
Dutch yushino-kers
Dutch yoshinosierkers
Dutch yoshinokers
Dutch yoshino-kers
Dutch yoshino sierkers
Dutch prunus yedoensis
Dutch prunus x yedoensis
Dutch yoshino-sierkers
Swedish prunus yedoensis
Ukrainian Вишня Йосіно
Ukrainian Сомейська вишня Йосіно
Ukrainian Сомей йосіно
Ukrainian Сакура Йосіно
Ukrainian Йосіноська вишня
Ukrainian prunus x yedoensis
Ukrainian prunus × yedoensis
Vietnamese prunus × yedoensis
Vietnamese prunus x yedoensis
Vietnamese anh đào yoshino
war prunus yedoensis
Chinese 染井吉野櫻
Chinese 吉野櫻
Chinese 东京樱
Chinese 染井吉野
Chinese 东京樱花
Chinese 染井吉野樱

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
  • Northern America
    • Northwestern U.S.A.
      • Washington
    • Southeastern U.S.A.
      • Alabama
      • District Of Columbia
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000983576
UNII 22A02T0I1S
Cornell Woody Plants 395
USDA Plants PRYE
UConn 364
Tropicos 27805366
KEW urn:lsid:ipni.org:names:30119904-2
The Plant List rjp-10409
Missouri Botanical Garden 286608
Observations.org 764632
NCBI Taxonomy 3759
IPNI 30119904-2
iNaturalist 47352
GBIF 3021335
Freebase /m/02qg1nw
EPPO PRNYE
Elurikkus 351626
US Library of Congress sh85069639
USDA GRIN 30157
Wikipedia Prunus_%C3%97_yedoensis

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_005406145.1 CYE_r3.1 Contig Kazusa DNA Research Institute 2019-03-18 54.0x 658.14 Mb

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
Seed Dormancy Class and Germination Characteristics of Prunus spachiana (Lavallée ex Ed.Otto) Kitam. f. ascendens (Makino) Kitam Native to the Korean Peninsula Kim GM, Ko CH, Chung JM, Kwon HC, Rhie YH, Lee SY Plants (Basel) 11-Feb-2024
PMCID:PMC10891651
doi:10.3390/plants13040502
PMID:38498410
Study of summer microclimate and PM2.5 concentration in campus plant communities Jiang Y, Liu C, Wen C, Long Y Sci Rep 09-Feb-2024
PMCID:PMC10853255
doi:10.1038/s41598-024-52508-3
PMID:38332000
Sakuranetin as a Potential Regulator of Blood Pressure in Spontaneously Hypertensive Rats by Promoting Vasorelaxation through Calcium Channel Blockade Shin S, Park J, Choi HY, Bu Y, Lee K Biomedicines 01-Feb-2024
PMCID:PMC10887318
doi:10.3390/biomedicines12020346
PMID:38397948
Integrated Identification and Genetic Diversity of Potentially Invasive Clearwing Moths (Lepidoptera: Cossoidea: Sesiidae) in Korea Kim S, Jung JK, Park I, Lee BW, Kim YH Insects 22-Jan-2024
PMCID:PMC10816279
doi:10.3390/insects15010079
PMID:38276828
Commodity risk assessment of Corylus avellana plants from the UK 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, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
A chromosome-scale assembly of the early-flowering Prunus campanulata and comparative genomics of cherries Hu Y, Feng C, Wu B, Kang M Sci Data 21-Dec-2023
PMCID:PMC10739980
doi:10.1038/s41597-023-02843-3
PMID:38129445
Functional Analysis of PbbZIP11 Transcription Factor in Response to Cold Stress in Arabidopsis and Pear Zhang Y, Wu L, Liu L, Jia B, Ye Z, Tang X, Heng W, Liu L Plants (Basel) 20-Dec-2023
PMCID:PMC10780769
doi:10.3390/plants13010024
PMID:38202332
Adipose tissue inflammation linked to obesity: A review of current understanding, therapies and relevance of phyto-therapeutics Aruwa CE, Sabiu S Heliyon 02-Dec-2023
PMCID:PMC10755291
doi:10.1016/j.heliyon.2023.e23114
PMID:38163110
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
Erwiniaceae bacteria play defensive and nutritional roles in two widespread ambrosia beetles Cambronero-Heinrichs JC, Battisti A, Biedermann PH, Cavaletto G, Castro-Gutierrez V, Favaro L, Santoiemma G, Rassati D FEMS Microbiol Ecol 10-Nov-2023
PMCID:PMC10664977
doi:10.1093/femsec/fiad144
PMID:37951293
Green Synthesis of Metal and Metal Oxide Nanoparticles: A Review of the Principles and Biomedical Applications Radulescu DM, Surdu VA, Ficai A, Ficai D, Grumezescu AM, Andronescu E Int J Mol Sci 20-Oct-2023
PMCID:PMC10607471
doi:10.3390/ijms242015397
PMID:37895077
Chromosome-level reference genome assembly provides insights into the evolution of Pennisetum alopecuroides Teng K, Guo Q, Liu L, Guo Y, Xu Y, Hou X, Teng W, Zhang H, Zhao C, Yue Y, Wen H, Wu J, Fan X Front Plant Sci 23-Aug-2023
PMCID:PMC10481962
doi:10.3389/fpls.2023.1195479
PMID:37680353
Cryo-attenuated properties of Tilia miqueliana pericarps and seeds Wu Y, Sun XR, Peng CY, Shen YB, Visscher AM, Pritchard HW, Wang MZ, Deng ZY Front Plant Sci 15-Aug-2023
PMCID:PMC10486270
doi:10.3389/fpls.2023.1228069
PMID:37692432
Commodity risk assessment of Fagus sylvatica plants from the UK 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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Involvement of Vacuolar Processing Enzyme CgVPE1 in Vacuole Rupture in the Programmed Cell Death during the Development of the Secretory Cavity in Citrus grandis ‘Tomentosa’ Fruits Huai B, Liang M, Lin J, Tong P, Bai M, He H, Liang X, Chen J, Wu H Int J Mol Sci 20-Jul-2023
PMCID:PMC10380461
doi:10.3390/ijms241411681
PMID:37511439

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
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1271/BBB.59.1944
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1271/BBB.59.1944
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1271/BBB.59.1944
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see CC(=O)OCC1=CC=CC=C1 150.17 unknown https://doi.org/10.1271/BBB.56.1655
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
17-(2-Hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 4220788 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 442.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.11.001
Dipterocarpol 441676 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 442.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.11.001
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Prulaurasin 120639 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown https://doi.org/10.1271/BBB.59.1944
Sambunigrin 91434 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown https://doi.org/10.1271/BBB.59.1944
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1271/BBB.59.1944
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl caffeate 5317238 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown https://doi.org/10.1007/S11418-006-0033-7
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1271/BBB.59.1944
https://doi.org/10.1271/BBB.56.1655
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/JA01143A513
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/JA01143A513
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/JA01143A513
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/JA01143A513
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 282013 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1021/JA01143A513
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1021/JA01143A513
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1021/JA01143A513

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