Prunus cerasoides - Unknown
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Internal ID UUID64404089cab5b873355842
Scientific name Prunus cerasoides
Authority D.Don
First published in Prodr. Fl. Nepal. : 239 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cerasus cerasoides (Buch.-Ham. ex D.Don) S.Ya.Sokolov Trees & Shrubs USSR iii. 736 (1954).
Cerasus puddum Wall. Pl. Asiat. Rar. (Wallich). 2: 37, t. 143. 1831
Prunus puddum Roxb. ex Wall. Plantae asiaticae rariores ; 1829 37 1831
Cerasus cerasoides (D.Don) S.Ya.Sokolov Derev. Kustarnik. URSS 3: 736 (1954)
Maddenia pedicellata Hook.f. Fl. Brit. India 2: 318 (1878)

Common names Top

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Language Common/alternative name
English wild himalayan cherry
Spanish cerasus cerasoides var. rubea
Persian گیلاس خودروی هیمالیایی
Persian هیمالیا-زاکورا
Persian گیلاس وحشی هیمالیایی
Persian پرونوس سراسوایدس
Japanese ヒマラヤザクラ
Japanese ヒマラヤ桜
Nepali पैयुँ
Russian Вишня вишнеобразная
Thai ชมพูภูพิงค์
Thai นางพญาเสือโคร่ง
Thai ซากุระเมืองไทย
Turkish himalaya yabani kirazı
Chinese 云南欧李
Chinese 高盆櫻桃
Chinese 高盆樱桃
Chinese 箐樱桃

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Prunus cerasoides var. majestica (Koehne) Ingram ; 1947 162 1947

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001017427
Tropicos 27800330
KEW urn:lsid:ipni.org:names:729572-1
The Plant List rjp-8103
Open Tree Of Life 937996
NCBI Taxonomy 378224
IPNI 729572-1
iNaturalist 431494
GBIF 3021409
Freebase /m/02667vn
EPPO PRNCS
EOL 301113
USDA GRIN 29865
Wikipedia Prunus_cerasoides
CMAUP NPO10448

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Ayurvedic and herbal plaque control agents in gingivitis: A systematic review and meta-analysis of randomized controlled trials Javed D, Dixit AK, Anwar S, Rai A, Krishan K J Educ Health Promot 31-Oct-2023
PMCID:PMC10744006
doi:10.4103/jehp.jehp_204_23
PMID:38144032
Ethnobotanical study on edible flowers in Xishuangbanna, China Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C J Ethnobiol Ethnomed 30-Sep-2023
PMCID:PMC10542681
doi:10.1186/s13002-023-00608-1
PMID:37777741
How do root fungi of Alnus nepalensis and Schima wallichii recover during succession of abandoned land? Balami S, Vašutová M, Chaudhary VK, Cudlín P Mycorrhiza 13-Sep-2023
PMCID:PMC10752848
doi:10.1007/s00572-023-01124-6
PMID:37702798
Potential use of barks of woody vascular plants in bone mending: A review Joshi DD, Deb L, Somkuwar BG, Rana VS Saudi Pharm J 27-Jul-2023
PMCID:PMC10406872
doi:10.1016/j.jsps.2023.101714
PMID:37559869
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
Socio-administrative conservation and collection practices of the sacred Thal Kedar forest, Uttarakhand, India Joshi DD, Rana VS, Kharkwal H Heliyon 21-Mar-2023
PMCID:PMC10161254
doi:10.1016/j.heliyon.2023.e14619
PMID:37151682
Current scenario of traditional medicines in management of diabetic foot ulcers: A review Rayate AS, Nagoba BS, Mumbre SS, Mavani HB, Gavkare AM, Deshpande AS World J Diabetes 15-Jan-2023
PMCID:PMC9850800
doi:10.4239/wjd.v14.i1.1
PMID:36684382
Responses of photosystem to long-term light stress in a typically shade-tolerant species Panax notoginseng Cun Z, Xu XZ, Zhang JY, Shuang SP, Wu HM, An TX, Chen JW Front Plant Sci 12-Jan-2023
PMCID:PMC9878349
doi:10.3389/fpls.2022.1095726
PMID:36714733
Rice Phytoalexins: Half a Century of Amazing Discoveries; Part I: Distribution, Biosynthesis, Chemical Synthesis, and Biological Activities Valletta A, Iozia LM, Fattorini L, Leonelli F Plants (Basel) 05-Jan-2023
PMCID:PMC9862927
doi:10.3390/plants12020260
PMID:36678973
The Cytotoxic and Inhibitory Effects of Plant Derivatives on Candida albicans Biofilms: A Scoping Review Loaiza-Oliva M, Arias-Durango L, Martínez-Pabón MC Molecules 23-Dec-2022
PMCID:PMC9822484
doi:10.3390/molecules28010130
PMID:36615324
Diversity, distribution, and sustainability of traditional medicinal plants in Kaski district, western Nepal Khakurel D, Uprety Y, Ahn G, Cha JY, Kim WY, Lee SH, Rajbhandary S Front Pharmacol 20-Dec-2022
PMCID:PMC9807671
doi:10.3389/fphar.2022.1076351
PMID:36605393
Pharmacodynamic appraisal of wound-healing herbs of Sushruta Samhita Kumar V, Nesari TM, Ghildiyal S, Sherkhane R Ayu 07-Dec-2022
PMCID:PMC9893898
doi:10.4103/ayu.AYU_34_20
PMID:36743272
Photoinhibition of Photosystem I Induced by Different Intensities of Fluctuating Light Is Determined by the Kinetics of ∆pH Formation Rather Than Linear Electron Flow Shi Q, Wang XQ, Zeng ZL, Huang W Antioxidants (Basel) 24-Nov-2022
PMCID:PMC9774317
doi:10.3390/antiox11122325
PMID:36552532
The framework species method: harnessing natural regeneration to restore tropical forest ecosystems Elliott S, Tucker NI, Shannon DP, Tiansawat P Philos Trans R Soc Lond B Biol Sci 14-Nov-2022
PMCID:PMC9661958
doi:10.1098/rstb.2021.0073
PMID:36373920

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 / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1S,2S,4R)-Limonene-1,2-diol 441246 Click to see CC(=C)C1CCC(C(C1)O)(C)O 170.25 unknown via CMAUP database
2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enal 92467550 Click to see CC1=CCC(CC1)C(=C)C=O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Ursolic Acid 64945 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/10.1080/0005772X.2004.11099634
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1080/0005772X.2004.11099634
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/0005772X.2004.11099634
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/0040-4020(59)80074-0
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/0040-4020(59)80074-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(4-Hydroxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 348162 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1007/BF03172499
Neosakuranin 14524443 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=C(C=C3)O)O 448.40 unknown https://doi.org/10.1080/0005772X.2004.11099634
Sakuranin 73607 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1007/BF03172499
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2R)-5-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 162898411 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(CO4)O)O)O)O 418.40 unknown https://doi.org/10.1016/0031-9422(82)80175-1
Isosakuranetin 7-xyloside 74819383 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(CO4)O)O)O)O 418.40 unknown https://doi.org/10.1016/0031-9422(82)80175-1
Puddumin A 13871818 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1021/NP50050A020
Puddumin B 42607953 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.3109/13880208909116906
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Blumeatin C; Taxifolin 7-methyl ether 12313900 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC(=C(C=C3)O)O)O 318.28 unknown https://doi.org/10.1016/0040-4020(59)80074-0
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown via CMAUP database
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/10.1007/BF03052797
https://doi.org/10.1007/BF03172499
Padmatin 12313901 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC(=C(C=C3)O)O)O 318.28 unknown https://doi.org/10.1016/0040-4020(59)80074-0
Penduletin 5320462 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Calycopterin 10429470 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)OC 374.30 unknown via CMAUP database
Xanthomicrol 73207 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1021/NP50050A020
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Prunetinoside 133556543 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C(=CO2)C4=CC=C(C=C4)O 446.40 unknown https://doi.org/10.1080/0005772X.2004.11099634
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Prunetin 5281804 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1021/NP50050A020
https://doi.org/10.1007/BF03048800

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