Prunus avium - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Prunus avium - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Prunus avium - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Prunus avium - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID64403fbcb6b5e002326029
Scientific name Prunus avium
Authority (L.) L.
First published in Flora Svecica 165. 1755

Description Top

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Synonyms Top

Scientific name Authority First published in
Prunus cerasus var. bigarella L. Sp. Pl. : 475 (1753)
Prunus cerasus var. duracina L. Sp. Pl. : 475 (1753)
Prunus cerasus var. juliana L. Sp. Pl. : 474 (1753)
Cerasus pallida M.Roem. Fam. Nat. Syn. Monogr. 3: 69 (1847)
Druparia avium [Clairv.] Man. Herbor. Suisse : 159 (1811)
Prunus nigricans Ehrh. Beitr. Naturk. 7: 126 (1792)
Prunus varia Ehrh. Beitr. Naturk. 7: 127 (1792)
Prunus duracina Sweet Hort. Brit. : 134 (1826)
Cerasus anglica Poit. & Turpin Traité Arbr. Fruit. 2: n.º 27 (1811)
Cerasus avicularis Dulac Fl. Hautes-Pyrénées : 301 (1867)
Cerasus nigra Mill. Gard. Dict. ed. 8 : Cerasus n.º 2 (1768)
Cerasus nigricans Borkh. Arch. Bot. (Leipzig) 1(2): 38 (1797)
Cerasus varia Borkh. Arch. Bot. (Leipzig) 1(2): 38 (1797)
Cerasus dulcis G.Gaertn., B.Mey. & Scherb. Oekon. Fl. Wetterau 2: 181 (1800)
Prunus cerasus var. avium L. Sp. Pl. : 474 (1753)
Prunus avium subsp. juliana (L.) Schübl. & G.Martens Fl. Würtemberg : 311 (1834)
Prunus cerasus var. dulcis L. Sp. Pl. : 474 (1753)
Cerasus avium var. duracina (L.) Lej. & Courtois Comp. Fl. Belg. 2: 129 (1831)

Common names Top

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Language Common/alternative name
English gean, wild cherry
English sweet cherry
English wild cherry
English gean
English bird cherry

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Area

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Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Eastern Asia
      • Korea
    • Middle Asia
      • Kazakhstan
      • Tadzhikistan
      • Turkmenistan
    • Western Asia
      • Afghanistan
      • Cyprus
      • Iran
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Pakistan
      • West Himalaya
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Victoria
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • West Virginia
    • Northwestern U.S.A.
      • Idaho
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southeastern U.S.A.
      • Delaware
      • District Of Columbia
      • Kentucky
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Utah
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001005630
UNII 9PLM3OM8VL
Canadensys 8859
USDA Plants PRAV
Tropicos 27801088
INPN 116043
Flora of Italy 2229
KEW urn:lsid:ipni.org:names:30093848-2
The Plant List rjp-383
Missouri Botanical Garden 286442
Open Tree Of Life 162547
Observations.org 7261
NCBI Taxonomy 42229
NBN Atlas NBNSYS0000003417
Nature Serve 2.137270
IUCN Red List 172064
IPNI 30093848-2
iNaturalist 61964
IFPNI 68DC1FFF-EC28-40CE-850A-3FB35A1388D6
GBIF 3020791
Freebase /m/06lqtp
EPPO PRNAV
EOL 231737
Elurikkus 9659
Calflora (Californian flora) 9204
US Library of Congress sh85131169
USDA GRIN 29844
Wikipedia Prunus_avium

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
GCF_002207925.1 PAV_r1.0 Scaffold Kazusa DNA Research Institute 2017-06-12 327.0x 259.74 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
A dataset of 40’000 trees with section-wise measured stem diameter and branch volume from across Switzerland Didion M, Herold A, Thürig E, Topuz S, Vulovic Z, Abegg M, Nitzsche J, Stillhard J, Glatthorn J Sci Data 09-May-2024
PMCID:PMC11082132
doi:10.1038/s41597-024-03336-7
PMID:38724536
Comparative analysis of POD genes and their expression under multiple hormones in Pyrus bretschenedri Li G, Manzoor MA, Wang G, Huang S, Ding X, Abdullah M, Zhang M, Song C BMC Genom Data 06-May-2024
PMCID:PMC11075270
doi:10.1186/s12863-024-01229-7
PMID:38711007
A modified CTAB method for the extraction of high-quality RNA from mono-and dicotyledonous plants rich in secondary metabolites Kiss T, Karácsony Z, Gomba-Tóth A, Szabadi KL, Spitzmüller Z, Hegyi-Kaló J, Cels T, Otto M, Golen R, Hegyi ÁI, Geml J, Váczy KZ Plant Methods 04-May-2024
PMCID:PMC11069240
doi:10.1186/s13007-024-01198-z
PMID:38704591
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
Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview Szmechtyk T, Małecka M Materials (Basel) 30-Apr-2024
PMCID:PMC11084627
doi:10.3390/ma17092123
PMID:38730929
A comprehensive review on pharmacognosy, phytochemistry and pharmacological activities of 8 potent Prunus species of southeast Asia Shikha A, Adarsh K, Ankit KS, Harshwardhan S, Suresh T, Pradeep K J Tradit Chin Med 30-Apr-2024
PMCID:PMC11077151
doi:10.19852/j.cnki.jtcm.2024.03.002
PMID:38767647
A View on the Chemical and Biological Attributes of Five Edible Fruits after Finishing Their Shelf Life: Studies on Caco-2 Cells Pirvu LC, Rusu N, Bazdoaca C, Androne E, Neagu G, Albulescu A Int J Mol Sci 29-Apr-2024
PMCID:PMC11084482
doi:10.3390/ijms25094848
PMID:38732066
Genetic and molecular regulation of chilling requirements in pear: breeding for climate change resilience Gabay G, Flaishman MA Front Plant Sci 26-Apr-2024
PMCID:PMC11082341
doi:10.3389/fpls.2024.1347527
PMID:38736438
Antibiotic Resistance in Plant Pathogenic Bacteria: Recent Data and Environmental Impact of Unchecked Use and the Potential of Biocontrol Agents as an Eco-Friendly Alternative Islam T, Haque MA, Barai HR, Istiaq A, Kim JJ Plants (Basel) 18-Apr-2024
PMCID:PMC11054394
doi:10.3390/plants13081135
PMID:38674544
GATA transcription factor in common bean: A comprehensive genome-wide functional characterization, identification, and abiotic stress response evaluation Abdulla MF, Mostafa K, Aydin A, Kavas M, Aksoy E Plant Mol Biol 17-Apr-2024
PMCID:PMC11024004
doi:10.1007/s11103-024-01443-y
PMID:38630371
Evolutionary Conservation in Protein–Protein Interactions and Structures of the Elongator Sub-Complex ELP456 from Arabidopsis and Yeast Jun SE, Cho KH, Schaffrath R, Kim GT Int J Mol Sci 15-Apr-2024
PMCID:PMC11050213
doi:10.3390/ijms25084370
PMID:38673955
Isothermal Nucleic Acid Amplification-Based Lateral Flow Testing for the Detection of Plant Viruses Song X, Cao Y, Yan F Int J Mol Sci 11-Apr-2024
PMCID:PMC11050433
doi:10.3390/ijms25084237
PMID:38673821
A Comprehensive Analysis of the Peanut SQUAMOSA Promoter Binding Protein-like Gene Family and How AhSPL5 Enhances Salt Tolerance in Transgenic Arabidopsis Sun X, Zhang L, Xu W, Zheng J, Yan M, Zhao M, Wang X, Yin Y Plants (Basel) 09-Apr-2024
PMCID:PMC11055087
doi:10.3390/plants13081057
PMID:38674467
Genetic dissection of the tissue‐specific roles of type III effectors and phytotoxins in the pathogenicity of Pseudomonas syringae pv. syringae to cherry Vadillo‐Dieguez A, Zeng Z, Mansfield JW, Grinberg NF, Lynn SC, Gregg A, Connell J, Harrison RJ, Jackson RW, Hulin MT Mol Plant Pathol 08-Apr-2024
PMCID:PMC11002349
doi:10.1111/mpp.13451
PMID:38590135
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

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,3S,4R,4aS,8aR)-3,4a,8,8-tetramethyl-4-[(2E)-3-methylpenta-2,4-dienyl]-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol 162949319 Click to see CC(=CCC1C2(CCCC(C2CC(C1(C)O)O)(C)C)C)C=C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
4,5,12-Trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-13-ene-9-carboxylic acid 131752584 Click to see CC12C(C=CC3(C1C(C45C3CC(C(C4)(C(=C)C5)O)O)C(=O)O)OC2=O)O 362.40 unknown https://doi.org/10.1016/0031-9422(93)85204-5
5-Hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-12-ene-9-carboxylic acid 12310158 Click to see CC12C=CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 330.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
5,13-Dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid 4658943 Click to see CC12CC(CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellic acid 6466 Click to see CC12C(C=CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin 1 3509874 Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A1 5280379 Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A29 14605548 Click to see CC12CC(CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A5 5281988 Click to see CC12C=CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 330.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A8 5280607 Click to see CC12C3C(C45CC(=C)C(C4)(CCC5C3(CC(C1O)O)OC2=O)O)C(=O)O 364.40 unknown https://doi.org/10.1016/S0031-9422(99)00597-X
Gibberellin A87 101663385 Click to see CC12C(C=CC3(C1C(C45C3CC(C(C4)(C(=C)C5)O)O)C(=O)O)OC2=O)O 362.40 unknown https://doi.org/10.1016/0031-9422(93)85204-5
Gibberellins 522636 Click to see CC12C(C=CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
8-Formyl-12-hydroxy-4-methyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid 4632015 Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
Gibberellin A19 5460209 Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)86860-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273102/
Urs-12-ene-3,28-diol, (3beta)- 3266408 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273102/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273102/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Oxalic Acid 971 Click to see C(=O)(C(=O)O)O 90.03 unknown https://doi.org/10.1111/J.1469-8137.1988.TB04193.X
Succinic Acid 1110 Click to see C(CC(=O)O)C(=O)O 118.09 unknown https://doi.org/10.1515/BCHM2.1922.122.1-3.46
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
D-Lactic acid 61503 Click to see CC(C(=O)O)O 90.08 unknown https://doi.org/10.1515/BCHM2.1922.122.1-3.46
Lactic Acid 612 Click to see CC(C(=O)O)O 90.08 unknown https://doi.org/10.1515/BCHM2.1922.122.1-3.46
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid 222656 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown https://doi.org/10.1515/BCHM2.1922.122.1-3.46
Malic Acid 525 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown https://doi.org/10.1515/BCHM2.1922.122.1-3.46
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3S,4R,5S)-1,3,4-Trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-cyclohexane-1-carboxylic acid 14158101 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1021/JF030595S
3-p-Coumaroylquinic acid 9945785 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1021/JF00050A015
https://doi.org/10.1016/S0023-6438(03)00143-9
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1021/JF00050A015
https://doi.org/10.1021/JF030595S
https://doi.org/10.1016/0021-9673(96)00169-0
https://doi.org/10.1016/S0031-9422(00)97746-X
https://doi.org/10.1016/S0023-6438(03)00143-9
Isochlorogenic acid 5315832 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1021/JF030595S
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1021/JF00050A015
https://doi.org/10.1016/S0023-6438(03)00143-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
4,5-Dihydroxy-3-methoxy-6-(2,4,5-trihydroxyoxan-3-yl)oxyoxane-2-carboxylic acid 14078718 Click to see COC1C(C(C(OC1C(=O)O)OC2C(C(COC2O)O)O)O)O 340.28 unknown https://doi.org/10.1139/V61-340
Qchfhxzdzvjvjc-ifwyrxgasa- 21635776 Click to see COC1C(C(C(OC1C(=O)O)OC2C(C(COC2O)O)O)O)O 340.28 unknown https://doi.org/10.1139/V61-340
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3R,4S,5R,6R)-6-[(3R,4S,5R,6R)-6-hydroxy-4,5-dimethoxyoxan-3-yl]oxy-4,5-dimethoxyoxan-3-ol 163028371 Click to see COC1C(COC(C1OC)OC2COC(C(C2OC)OC)O)O 338.35 unknown https://doi.org/10.1139/V61-340
6-(6-Hydroxy-4,5-dimethoxyoxan-3-yl)oxy-4,5-dimethoxyoxan-3-ol 163028370 Click to see COC1C(COC(C1OC)OC2COC(C(C2OC)OC)O)O 338.35 unknown https://doi.org/10.1139/V61-340
alpha-Maltose 439341 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see C(C(C(C(C(=O)CO)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
D-Fructose 2723872 Click to see C1C(C(C(C(O1)(CO)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
6-Deoxy-Hexose 840 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
alpha-D-GALACTOSE 439357 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
alpha-D-Mannose 185698 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
alpha-L-Rhamnose 439710 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
Alpha-d-xylopyranose 6027 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
beta-L-Arabinopyranose 439764 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
Pentose 229 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Sorbitol 5780 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
5,9,10-Trihydroxy-7-(3-hydroxy-3-methylbutyl)-8-(3-methylbut-2-enyl)furo[2,3-c]xanthen-6-one 162937039 Click to see CC(=CCC1=C(C2=C(C(=C1O)O)OC3=C(C2=O)C(=CC4=C3C=CO4)O)CCC(C)(C)O)C 438.50 unknown https://doi.org/10.1016/0031-9422(83)83029-5
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
(1S,3R,4R,5S,8S)-3,4,8-trihydroxy-2,6-dioxabicyclo[3.2.1]octan-7-one 101719890 Click to see C1(C2C(C(OC1C(=O)O2)O)O)O 176.12 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
D-Mannuronicacidlactone 14178454 Click to see C1(C2C(C(OC1C(=O)O2)O)O)O 176.12 unknown https://doi.org/10.1016/S0031-9422(00)85322-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
2-hydroxy-2-methyl-N-[(2S)-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-2-yl]propanamide 162854059 Click to see CC(C)(C(=O)NC1CCCN1C(=O)C=CC2=CC=CC=C2)O 302.37 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/0021-9673(96)00169-0
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/0031-9422(83)83029-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+/-)-Epicatechin 255538 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/JF030595S
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/10.1016/J.PHYTOCHEM.2009.08.018
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/10.1016/S0031-9422(00)97746-X
https://doi.org/10.1021/JF030595S
https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Epicatechin 72276 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/JF030595S
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/JA01559A059
(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/10.1016/J.PHYTOCHEM.2009.08.018
https://doi.org/10.1021/JA01559A059
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/10.1016/J.PHYTOCHEM.2009.08.018
https://doi.org/10.1021/JA01559A059
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/JA01559A059
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
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/10.1016/0304-4238(78)90069-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1556/AALIM.31.2002.1.7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3S,4R,5R,6S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 9955335 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1021/JF030595S
(2S,4R,5S)-2-[[(3R,6R)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 163185847 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown https://doi.org/10.1021/JF030595S
Cyanidin 3-O-galactoside 441699 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
cyanidin 3-O-sophoroside 11169452 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 611.50 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Keracyanin cation 441674 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown https://doi.org/10.1016/S0308-8146(01)00231-X
https://doi.org/10.1078/0944-7113-00053
https://doi.org/10.1021/JF00050A015
https://doi.org/10.1016/S0023-6438(03)00143-9
https://doi.org/10.1021/JF030595S
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1021/JF00050A015
https://doi.org/10.1021/JF030595S
https://doi.org/10.1016/S0308-8146(01)00231-X
https://doi.org/10.1016/S0023-6438(03)00143-9
Pelargonidin 3-O-rutinoside 443917 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC=C(C=C5)O)O)O)O)O)O)O)O)O 579.50 unknown https://doi.org/10.1016/S0308-8146(01)00231-X
https://doi.org/10.1021/JF00050A015
https://doi.org/10.1016/J.FOODCHEM.2007.08.004
https://doi.org/10.1016/S0023-6438(03)00143-9
Peonidin 3-rutinoside 90470732 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O)O 609.60 unknown https://doi.org/10.1021/JF00050A015
https://doi.org/10.1016/S0308-8146(01)00231-X
https://doi.org/10.1016/S0023-6438(03)00143-9
Peonidin-3-glucoside 443654 Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O 463.40 unknown https://doi.org/10.1016/S0308-8146(01)00231-X
https://doi.org/10.1021/JF00050A015
https://doi.org/10.1016/S0023-6438(03)00143-9
Petunidin 3-galactoside 14311149 Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 479.40 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
1-[2-Hydroxy-4-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 72732169 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/10.1016/0031-9422(91)84200-C
3,5,7-trihydroxy-2-[4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 154496826 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)83951-5
Genkwanin 5-glucoside 11293760 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC=C(C=C4)O 446.40 unknown https://doi.org/10.1016/0031-9422(91)84200-C
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 54579866 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/JF030595S
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
5,7-dihydroxy-2-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]-3-[(2R,3R,4R,5S,6S)-3,4,5-trihydroxy-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxychromen-4-one 162979621 Click to see CC1C(C(C(C(O1)OC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C=C(C=C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 920.80 unknown https://doi.org/10.1016/S0031-9422(00)83951-5
5,7-Dihydroxy-2-[2-hydroxy-4-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]-3-[3,4,5-trihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxychromen-4-one 162979620 Click to see CC1C(C(C(C(O1)OC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C=C(C=C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 920.80 unknown https://doi.org/10.1016/S0031-9422(00)83951-5
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
Malvidin 3-O-arabinoside 25079994 Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(CO4)O)O)O)O)O 463.40 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(00)97746-X
https://doi.org/10.1016/0304-4238(78)90069-9
https://doi.org/10.1021/JF030595S
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4',5-Dihydroxy-7-glucosyloxyflavanone 124300887 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/10.1016/S0031-9422(00)97746-X
https://doi.org/10.1111/J.1399-3054.1985.TB02366.X
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/JA01559A059
5-Hydroxy-2-[4-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[3,4,5-trihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxychromen-4-one 163045404 Click to see CC1C(C(C(C(O1)OC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=C(C=C(C=C6)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O)O 920.80 unknown https://doi.org/10.1016/S0031-9422(00)83951-5
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/10.1111/J.1399-3054.1985.TB02366.X
https://doi.org/10.1021/JA01559A059
https://doi.org/10.1016/S0031-9422(00)97746-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Dihydrowogonin 11491431 Click to see COC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
S-Dihydrowogonin 10265977 Click to see COC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.08.018
> 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/JA01559A059
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-Hydroxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14311197 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/10.1016/S0031-9422(00)97795-1
4H-1-Benzopyran-4-one, 5-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-7-methoxy- 184974 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/10.1016/S0031-9422(00)97795-1
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/JA01559A059
Genistoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/JA01559A059
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/10.1016/S0031-9422(00)97795-1
> 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/JA01559A059

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