Syringetin

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Syringetin
Chemical structure of syringetin
Names
IUPAC name
3,5,7-trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4H-chromen-4-one
Other names
3',5'-O-Dimethylmyricetin
3',5'-Dimethoxy-3,5,7,4'-tetrahydroxyflavone
3,5,7,4'-tetrahydroxy-3',5'dimethoxyflavone
Identifiers
4423-37-4 YesY
ChEBI CHEBI:18215 N
ChEMBL ChEMBL489142 N
ChemSpider 4445230 N
Jmol 3D model Interactive image
PubChem 5281953
  • InChI=1S/C17H14O8/c1-23-11-3-7(4-12(24-2)14(11)20)17-16(22)15(21)13-9(19)5-8(18)6-10(13)25-17/h3-6,18-20,22H,1-2H3 N
    Key: UZMAPBJVXOGOFT-UHFFFAOYSA-N N
  • InChI=1/C17H14O8/c1-23-11-3-7(4-12(24-2)14(11)20)17-16(22)15(21)13-9(19)5-8(18)6-10(13)25-17/h3-6,18-20,22H,1-2H3
    Key: UZMAPBJVXOGOFT-UHFFFAOYAJ
  • COc1cc(cc(OC)c1O)C=3Oc2cc(O)cc(O)c2C(=O)C=3O
Properties
C17H14O8
Molar mass 346.28 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Syringetin is an O-methylated flavonol, a type of flavonoid. It is found in red grape (absent in white grape),[1] in Lysimachia congestiflora[2] and in Vaccinium uliginosum (bog billberries).[3] It is one of the phenolic compounds present in wine.[4]

It induces human osteoblast differentiation through bone morphogenetic protein-2/extracellular signal-regulated kinase 1/2 pathway.[5]

Metabolism

Syringetin is formed from laricitrin by the action of the enzyme laricitrin 5'-O-methyltransferase[1][6] (myricetin O-methyltransferase).[7]

Glycosides

References

  1. 1.0 1.1 1.2 Metabolite Profiling of Grape: Flavonols and Anthocyanins. Fulvio Mattivi, Raffaele Guzzon, Urska Vrhovsek, Marco Stefanini and Riccardo Velasco, J. Agric. Food Chem., 2006, 54 (20), pp 7692–7702
  2. Flavonol glycosides from Lysimachia congestiflora. Jian Guo, , Dong-Lei Yu, Lizhen Xu, Min Zhu and Shi-Lin Yang, Phytochemistry, Volume 48, Issue 8, August 1998, Pages 1445-1447
  3. Anthocyanin and Flavonol Variation in Bog Bilberries (Vaccinium uliginosum L.) in Finland. Anja K. Lätti, Laura Jaakola, Kaisu R. Riihinen and Pirjo S. Kainulainen, J. Agric. Food Chem., 2010, 58 (1), pp 427–433
  4. Syringetin, a flavonoid derivative in grape and wine, induces human osteoblast differentiation through bone morphogenetic protein-2/extracellular signal-regulated kinase 1/2 pathway. Ya-Ling Hsu, Hsin-Lin Liang, Chih-Hsing Hung and Po-Lin Kuo, Molecular Nutrition & Food Research, Volume 53 Issue 11, Pages 1452-1461
  5. Syringetin, a flavonoid derivative in grape and wine, induces human osteoblast differentiation through bone morphogenetic protein-2/extracellular signal-regulated kinase 1/2 pathway. Hsu Ya-Ling, Liang Hsin-Lin, Hung Chih-Hsing and Kuo Po-Lin, Molecular nutrition & food research, 2009, vol. 53, no11, pp. 1452-1461
  6. laricitrin 5'-O-methyltransferase on amigo.geneontology.org
  7. Syringetin biosynthetis pathway on metacyc.org
  8. Syringetin-3-O-galactoside on www.massbank.jp
  9. 9.0 9.1 Syringetin-3-O-glucoside on www.massbank.jp
  10. Characterisation of Phenolic Constituents from Juvenile and Mature Needles of Norway Spruce by Means of High Performance Liquid Chromatography-Mass Spectrometry. Rune Slimestad and Kurt Hostettmann, Phytochemical Analysis, Volume 7 Issue 1, pp 42-48
  11. New flavonol glycosides from the needles of Larix sibirica. N. A. Tyukavkina, S. A. Medvedeva and S. Z. Ivanova, Chemistry of Natural Compounds, Volume 10, Number 2 / march 1974
  12. Syringetin 3-O-(6″-acetyl)-β-glucopyranoside and other flavonols from needles of norway spruce, Picea abies. Rune Slimestad, Øyvind M. Andersen, George W. Francis, Andrew Marston and Kurt Hostettmann, Phytochemistry, Volume 40, Issue 5, November 1995, Pages 1537-1542