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Prunus × yedoensis

Prunus × yedoensis - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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Prunus × yedoensis, also known as Yoshino cherry, is a hybrid cherry tree that originated in Japan. It is a cross between Prunus speciosa (Oshima cherry) and Prunus pendula f. ascendens (Edo higan). One of its most popular cultivars is 'Somei-yoshino', which is widely planted in temperate regions around the world. This cultivar has inherited the early blooming and large size of Edo higan, as well as the rapid growth and white flowers of Oshima cherry. The oldest known 'Somei-yoshino' tree was planted in Japan in 1775, and it has since been propagated through grafting. In 2019, the genetic information of 'Somei-yoshino' was decoded, revealing that it was a hybrid created over 100 years ago. Yoshino cherry is often used as an ornamental tree for its fragrant, light pink flowers and manageable size. It has many other cultivars, such as 'Mikado-yoshino' and 'America', and has been mistakenly claimed to have originated in South Korea.

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 tokyo cherry
Basque yoshino gereziondo
Persian پرونوس یدوانسیس
Persian سومی-یوشینو
French cerisier yoshino
Upper Sorbian yoshinowa wišnja
Japanese 染井吉野
Japanese 吉野桜
Japanese ソメイヨシノ
Korean 왕벚나무
Dutch yoshino-kers
Dutch yushinokers
Dutch yushino-kers
Dutch yoshinosierkers
Dutch yoshinokers
Dutch yoshino-sierkers
Dutch yoshino sierkers
Slovenian tokijska češnja
Ukrainian Йосіноська вишня
Ukrainian Сакура Йосіно
Ukrainian Сомей йосіно
Ukrainian Сомейська вишня Йосіно
Ukrainian Вишня Йосіно
Vietnamese anh đào yoshino
Chinese 染井吉野樱
Chinese 染井吉野櫻
Chinese 吉野櫻
Chinese 东京樱
Chinese 染井吉野
Chinese 东京樱花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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

Suggest others/fix!
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
Open Tree Of Life 3902817

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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos 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, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Overexpression of a Fragaria vesca NAM, ATAF, and CUC (NAC) Transcription Factor Gene (FvNAC29) Increases Salt and Cold Tolerance in Arabidopsis thaliana Li W, Li H, Wei Y, Han J, Wang Y, Li X, Zhang L, Han D Int J Mol Sci 06-Apr-2024
PMCID:PMC11012600
doi:10.3390/ijms25074088
PMID:38612898
TiO2 Nanocomposite Coatings and Inactivation of Carbapenemase-Producing Klebsiella Pneumoniae Biofilm—Opportunities and Challenges Bereanu AS, Vintilă BI, Bereanu R, Codru IR, Hașegan A, Olteanu C, Săceleanu V, Sava M Microorganisms 28-Mar-2024
PMCID:PMC11051735
doi:10.3390/microorganisms12040684
PMID:38674628
Miyalachnus—A New Lachninae Aphid Genus from Japan (Insecta, Hemiptera, Aphididae) Kanturski M, Lee Y Insects 18-Mar-2024
PMCID:PMC10970859
doi:10.3390/insects15030203
PMID:38535398
Chemometric evaluation of inorganic and organic parameters found in Rosaceae plants proposed as food supplements Zeiner M, Juranović Cindrić I, Nemet I, Šola I, Fiedler H Food Chem X 28-Feb-2024
PMCID:PMC10912348
doi:10.1016/j.fochx.2024.101248
PMID:38444555
The draft genome of Spiraea crenata L. (Rosaceae) – the first complete genome in tribe Spiraeeae Laczkó L, Jordán S, Póliska S, Rácz HV, Nagy NA, Molnár V. A, Sramkó G Sci Data 17-Feb-2024
PMCID:PMC10874383
doi:10.1038/s41597-024-03046-0
PMID:38368431
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
The structure of the tetraploid sour cherry ‘Schattenmorelle’ (Prunus cerasus L.) genome reveals insights into its segmental allopolyploid nature Wöhner TW, Emeriewen OF, Wittenberg AH, Nijbroek K, Wang RP, Blom EJ, Schneiders H, Keilwagen J, Berner T, Hoff KJ, Gabriel L, Thierfeldt H, Almolla O, Barchi L, Schuster M, Lempe J, Peil A, Flachowsky H Front Plant Sci 01-Dec-2023
PMCID:PMC10722297
doi:10.3389/fpls.2023.1284478
PMID:38107002

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
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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