Prunus mandshurica - Unknown
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Details Top

Internal ID UUID6440408768d6e626068751
Scientific name Prunus mandshurica
Authority (Maxim.) Koehne
First published in Deut. Dendrol. : 318 (1893)

Description Top

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Synonyms Top

Scientific name Authority First published in
Armeniaca mandshurica var. glabra (Nakai) T.T.Yu & L.T.Lu Fl. Reipubl. Popularis Sin. 38: 31 (1986)
Prunus mandshurica f. barbinervis (Nakai) W.Lee Lin. Fl. Koreae 1: 503 (1996)

Common names Top

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Language Common/alternative name
English armeniaca mandshurica
English manchurian apricot
English scout apricot
Azerbaijani armeniaca mandshurica
Azerbaijani mancuriya əriyi
azb مانجوری اریی
Belarusian Абрыкос маньчжурскі
Persian زردآلوی منچوری
Korean 개살구나무
Korean 산살구나무
Korean 개살구
Russian armeniaca mandschurica
Russian armeniaca mandshurica
Russian Абрикос манчжурский
Russian Абрикос маньчжурский
Ukrainian Абрикоса манчжурська
Vietnamese armeniaca mandshurica
Chinese 辽杏
Chinese 东北杏

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001017338
Tropicos 27805800
KEW urn:lsid:ipni.org:names:729939-1
The Plant List rjp-7998
Plantarium 3722
Missouri Botanical Garden 286614
Open Tree Of Life 692781
NCBI Taxonomy 122122
IPNI 729939-1
iNaturalist 543506
GBIF 3023411
Freebase /m/0_h1fvz
EPPO PRNMN
EOL 628572
USDA GRIN 30037
Wikipedia Prunus_mandshurica
CMAUP NPO25099

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
Exploring the immune-inflammatory mechanism of Maxing Shigan Decoction in treating influenza virus A-induced pneumonia based on an integrated strategy of single-cell transcriptomics and systems biology Zhang S, Li B, Zeng L, Yang K, Jiang J, Lu F, Li L, Li W Eur J Med Res 15-Apr-2024
PMCID:PMC11017673
doi:10.1186/s40001-024-01777-9
PMID:38622728
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
Armeniacae semen amarum: a review on its botany, phytochemistry, pharmacology, clinical application, toxicology and pharmacokinetics Tang S, Wang M, Peng Y, Liang Y, Lei J, Tao Q, Ming T, Shen Y, Zhang C, Guo J, Xu H Front Pharmacol 23-Jan-2024
PMCID:PMC10844384
doi:10.3389/fphar.2024.1290888
PMID:38323080
Integrative traditional Chinese medicine treatment for children with obstructive sleep apnea Lai WY, Wei CC, Lin CH, Hang LW, Shih YH, Huang FW, Yen HR J Tradit Complement Med 07-Aug-2023
PMCID:PMC10785241
doi:10.1016/j.jtcme.2023.08.002
PMID:38223810
Potential herb–drug interactions between anti-COVID-19 drugs and traditional Chinese medicine Ye L, Fan S, Zhao P, Wu C, Liu M, Hu S, Wang P, Wang H, Bi H Acta Pharm Sin B 05-Jun-2023
PMCID:PMC10239737
doi:10.1016/j.apsb.2023.06.001
PMID:37360014
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
‘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
Spontaneous, Artificial, and Genome Editing-Mediated Mutations in Prunus Prudencio AS, Devin SR, Mahdavi SM, Martínez-García PJ, Salazar JA, Martínez-Gómez P Int J Mol Sci 31-Oct-2022
PMCID:PMC9653787
doi:10.3390/ijms232113273
PMID:36362061
A Real-World Study on Ge Gen Tang in Combination with Herbal Medicines for Relieving Common Cold-Associated Symptoms Chou PY, Tai CJ, Tang YJ, Chen YC, Lin KY, Wang CC Evid Based Complement Alternat Med 22-Jul-2022
PMCID:PMC9337945
doi:10.1155/2022/4790910
PMID:35911138
Exploration on Varying Patterns of Morphological Features and Quality of Armeniacae Semen Amarum in Rancid Process Based on Colorimeter, Electronic Nose, and GC/MS Coupled With Human Panel Shao Y, Chen H, Lin H, Feng H, Gong J, Cao G, Hong W, Yao Y, Zou H, Yan Y Front Pharmacol 03-May-2022
PMCID:PMC9110824
doi:10.3389/fphar.2022.599979
PMID:35592420
Effects of Maren Pills on the Intestinal Microflora and Short-Chain Fatty Acid Profile in Drug-Induced Slow Transit Constipation Model Rats Zhan Y, Wen Y, Du LJ, Wang XX, Tang SY, Kong PF, Huang WG, Tang XG Front Pharmacol 12-Apr-2022
PMCID:PMC9039019
doi:10.3389/fphar.2022.804723
PMID:35496291
Clinical Evidence on the Use of Chinese Herbal Medicine for Acute Infectious Diseases: An Overview of Systematic Reviews Luo X, Zhang Y, Li H, Ren M, Liu Y, Liu Y, Zhang Y, Kuang Z, Cai Y, Chen Y, Ni X Front Pharmacol 25-Feb-2022
PMCID:PMC8914111
doi:10.3389/fphar.2022.752978
PMID:35281902
Novel Mango Ginger Bioactive (2,4,6-Trihydroxy-3,5-diprenyldihydrochalcone) Inhibits Mitochondrial Metabolism in Combination with Avocatin B Jayasankar V, Vrdoljak N, Roma A, Ahmed N, Tcheng M, Minden MD, Spagnuolo PA ACS Omega 07-Jan-2022
PMCID:PMC8771686
doi:10.1021/acsomega.1c04053
PMID:35071863
Selection of a core collection of Prunus sibirica L. germplasm by a stepwise clustering method using simple sequence repeat markers Sun Y, Dong S, Liu Q, Chen J, Pan J, Zhang J PLoS One 19-Nov-2021
PMCID:PMC8604298
doi:10.1371/journal.pone.0260097
PMID:34797843
Xuanfei Baidu Decoction protects against macrophages induced inflammation and pulmonary fibrosis via inhibiting IL-6/STAT3 signaling pathway Wang Y, Sang X, Shao R, Qin H, Chen X, Xue Z, Li L, Wang Y, Zhu Y, Chang Y, Gao X, Zhang B, Zhang H, Yang J J Ethnopharmacol 01-Oct-2021
PMCID:PMC9715986
doi:10.1016/j.jep.2021.114701
PMID:34606948

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
(R)-mandelonitrile 9548674 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
(S)-Mandelonitrile 439767 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
Benzaldehyde, oxime, (Z)- 5324470 Click to see C1=CC=C(C=C1)C=NO 121.14 unknown via CMAUP database
Mandelonitrile 10758 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown via CMAUP database
> Homogeneous non-metal compounds / Other non-metal organides / Other non-metal nitrides
Cyanide ion 5975 Click to see [C-]#N 26.02 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z)-9,10-dideuteriooctadec-9-enoic acid 13011408 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 284.50 unknown via CMAUP database
Elaidic Acid 637517 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
(2R,5R,9S,10R,11R,12S)-5,12-Dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid 193311 Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown via CMAUP database
CID 439329 439329 Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown via CMAUP database
CID 443464 443464 Click to see CC12C=CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 330.40 unknown via CMAUP database
GA29 5460028 Click to see CC12CC(CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown via CMAUP database
Gibberellin A1 5280379 Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown via CMAUP database
Gibberellin A29 14605548 Click to see CC12CC(CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown via CMAUP database
Gibberellin A5 5281988 Click to see CC12C=CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 330.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
6-Chromanol, 2,8-dimethyl-2-(4,8,12-trimethyltridecyl)- 586537 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown via CMAUP database
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
delta-Tocopherol 92094 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown via CMAUP database
DL-alpha-Tocopherol 2116 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
gamma-Tocopherol 92729 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 unknown via CMAUP database
Tocopherols 14986 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 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
Amygdalin 656516 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
Benzeneacetonitrile, (R)- 656495 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
Isoamygdalin 2180 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
Neoamygdalin 441462 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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(Z)-2-hexenal 6428782 Click to see CCCC=CC=O 98.14 unknown via CMAUP database
2-Hexenal 5281168 Click to see CCCC=CC=O 98.14 unknown via CMAUP database

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