Article · Wikipedia archive · Last revised Jun 21, 2026

Astringin

Astringin is a stilbenoid, the 3-β-D-glucoside of piceatannol. It can be found in the bark of Picea sitchensis and Picea abies.

Last revised
Jun 21, 2026
Read time
≈ 1 min
Length
294 w
Citations
6
Source
Astringin
Chemical structure of astringin
Chemical structure of astringin source ↗
Names
IUPAC name
3-[(E)-2-(2,3-Dihydroxyphenyl)ethen-1-yl]-5-hydroxyphenyl β-D-glucopyranoside
Systematic IUPAC name
(2S,3R,4S,5S,6R)-2-{3-[(E)-2-(3,4-Dihydroxyphenyl)ethen-1-yl]-5-hydroxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
UNII
  • InChI=1S/C20H22O9/c21-9-16-17(25)18(26)19(27)20(29-16)28-13-6-11(5-12(22)8-13)2-1-10-3-4-14(23)15(24)7-10/h1-8,16-27H,9H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1 checkY
    Key: PERPNFLGJXUDDW-CUYWLFDKSA-N checkY
  • InChI=1/C20H22O9/c21-9-16-17(25)18(26)19(27)20(29-16)28-13-6-11(5-12(22)8-13)2-1-10-3-4-14(23)15(24)7-10/h1-8,16-27H,9H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1
    Key: PERPNFLGJXUDDW-CUYWLFDKBH
  • O(c2cc(O)cc(\C=C\c1ccc(O)c(O)c1)c2)[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)CO
Properties
C20H22O9
Molar mass 406.387 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Astringin is a stilbenoid, the 3-β-D-glucoside of piceatannol.1 It can be found in the bark of Picea sitchensis23 and Picea abies (Norway spruce).4

It is also present in Vitis vinifera cells cultures5 and in wine.6

See also

See also

References

References

  1. CID 5281712 from PubChem
  2. Aritomi, Masakazu; Donnelly, Dervilla M.X. (1976). "Stilbene glucosides in the bark of Picea sitchensis". Phytochemistry. 15 (12): 2006–2008. Bibcode:1976PChem..15.2006A. doi:10.1016/S0031-9422(00)88881-0.
  3. Toscano Underwood, Claudia D.; Pearce, Raymond B. (1991). "Astringin and isorhapontin distribution in Sitka spruce trees". Phytochemistry. 30 (7): 2183–2189. Bibcode:1991PChem..30.2183T. doi:10.1016/0031-9422(91)83610-W.
  4. Lindberg, M.; Lundgren, L.; Gref, R.; Johansson, M. (1992). "Stilbenes and resin acids in relation to the penetration of Heterobasidion annosum through the bark of Picea abies". European Journal of Forest Pathology. 22 (2): 95–106. doi:10.1111/j.1439-0329.1992.tb01436.x.
  5. Mérillon, J. M.; Fauconneau, B.; Teguo, P. W.; Barrier, L.; Vercauteren, J.; Huguet, F. (1997). "Antioxidant activity of the stilbene astringin, newly extracted from Vitis vinifera cell cultures". Clinical Chemistry. 43 (6 Pt 1): 1092–1093. doi:10.1093/clinchem/43.6.1092. PMID 9191572.
  6. Vitrac, Xavier; Bornet, Aurélie; Vanderlinde, Regina; Valls, Josep; Richard, Tristan; Delaunay, Jean-Claude; Mérillon, Jean-Michel; Teissédre, Pierre-Louis (2005). "Determination of Stilbenes (δ-viniferin, trans-astringin, trans-piceid, cis- and trans-resveratrol, ε-viniferin) in Brazilian Wines". Journal of Agricultural and Food Chemistry. 53 (14): 5664–9. doi:10.1021/jf050122g. PMID 15998130.