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

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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)

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 třešeň plstnatá
Czech višeň plstnatá
Persian پرونوس تومنتوسا
Persian یوسورااومه
Persian گیلاس کرهای
French ragouminier
French ragoumier
French minel du canada
French cerisier du canada
French cerisier de nankin
Croatian nankinška trešnja
Japanese 英桃
Japanese ユスラ
Japanese ユスラウメ
Japanese 山桜桃
Japanese ゆすらうめ
Japanese 梅桃
Korean 앵도나무
Korean 앵두나무
Korean 앵두
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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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
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
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
Ecological Niche and Interspecific Association of Plant Communities in Alpine Desertification Grasslands: A Case Study of Qinghai Lake Basin Hu Y, Wang H, Jia H, Pen M, Liu N, Wei J, Zhou B Plants (Basel) 15-Oct-2022
PMCID:PMC9609917
doi:10.3390/plants11202724
PMID:36297752
Advances in the roles and mechanisms of lignans against Alzheimer’s disease Han N, Wen Y, Liu Z, Zhai J, Li S, Yin J Front Pharmacol 12-Oct-2022
PMCID:PMC9596774
doi:10.3389/fphar.2022.960112
PMID:36313287
Metabolome and Transcriptome Analyses of Anthocyanin Accumulation Mechanisms Reveal Metabolite Variations and Key Candidate Genes Involved in the Pigmentation of Prunus tomentosa Thunb. Cherry Fruit Zhang A, Yang H, Ji S, Tian C, Chen N, Gong H, Li J Front Plant Sci 29-Jun-2022
PMCID:PMC9277446
doi:10.3389/fpls.2022.938908
PMID:35845695

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 CCCCCCCCCCCCCCCCO 242.44 unknown via CMAUP database
Stearyl Alcohol 8221 Click to see CCCCCCCCCCCCCCCCCCO 270.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoalkylglycerols
(R)-3-(Hexadecyloxy)propane-1,2-diol 11758911 Click to see CCCCCCCCCCCCCCCCOCC(CO)O 316.50 unknown via CMAUP database
Batilol, (R)- 10831326 Click to see CCCCCCCCCCCCCCCCCCOCC(CO)O 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
(25S)-26-Acetoxy-3beta,5alpha-dihydroxyergosta-24(28)-ene-6-one 102018398 Click to see CC(CCC(=C)C(C)COC(=O)C)C1CCC2C1(CCC3C2CC(=O)C4(C3(CCC(C4)O)C)O)C 488.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
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
5beta,6beta-Epoxycholestane-3beta,7beta-diol 44583439 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C(C4C5(C3(CCC(C5)O)C)O4)O)C 418.70 unknown via CMAUP database
Cholestane-3b,5a,6b,7b-tetrol 56678658 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C(C(C4(C3(CCC(C4)O)C)O)O)O)C 436.70 unknown via CMAUP database
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown via CMAUP database
Dihydrocholesterol 6665 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C 388.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
5beta,6beta-Epoxyergosta-24(28)-ene-3beta,7beta-diol 11732746 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2C(C4C5(C3(CCC(C5)O)C)O4)O)C 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
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 CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
5alpha-Ergostane-3beta,5,6beta-triol 44558918 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 434.70 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-3beta,5alpha,6beta,7beta-tetrol 11037703 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2C(C(C4(C3(CCC(C4)O)C)O)O)O)C 448.70 unknown via CMAUP database
Ergosta-24(28)-ene-3beta,5alpha,6beta-triol 14679361 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 432.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
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
9-Hydroxygorgosterol 11812281 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CCC4(C3CC=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
9,11alpha,14-Trihydroxygorgosterol 10961762 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3(C2(CC(C4(C3CC=C5C4(CCC(C5)O)C)O)O)C)O)C 474.70 unknown via CMAUP database
Tomentogenin 101686475 Click to see CC(C1(CCC2(C1(C(CC3C2CCC4C3(CCC(C4)O)C)O)C)O)O)O 368.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
24-Methylene-5alpha-cholestane-3beta,5,6beta-triol 3,6-diacetate 90473755 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)OC(=O)C)C)O)OC(=O)C)C 516.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Clionasterol 457801 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)COC(=O)C)OC(=O)C)O)O 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 CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)OC(=O)C=CC3=CC=C(C=C3)O)COC(=O)C)O)O)OC(=O)C 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 CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)OC(=O)C)OC(=O)C=CC3=CC=C(C=C3)O)COC(=O)C)O)O)O 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
2-O-(2-O,6-O-Diacetyl-alpha-D-glucopyranosyl)-1-O-acetyl-3-O-[(E)-3-(4-hydroxyphenyl)acryloyl]-beta-D-fructofuranose 14841107 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)OC(=O)C=CC3=CC=C(C=C3)O)COC(=O)C)OC(=O)C)O)O 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
3-O-[4-Hydroxy-trans-cinnamoyl]-1-O-acetyl-beta-D-fructofuranosyl 3-O,6-O-diacetyl alpha-D-glucopyranoside 21629983 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)OC(=O)C=CC3=CC=C(C=C3)O)COC(=O)C)O)OC(=O)C)O 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
Mumeose C 71734603 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)OC(=O)C=CC3=CC=C(C=C3)O)CO)OC(=O)C)OC(=O)C)O 614.50 unknown https://doi.org/10.1016/J.BMCL.2014.04.018
Mumeose F 71580473 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)OC(=O)C=CC3=CC=C(C=C3)O)CO)O)OC(=O)C)OC(=O)C 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 CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 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 CC1CC2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O 288.29 unknown via CMAUP database

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