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Hopeaphenol

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Hopeaphenol
Chemical structure of hopeaphenol
Identifiers
CAS Number
3D model (JSmol)
PubChem CID
CompTox Dashboard (EPA)
SMILES
  • OC(C=C1)=CC=C12OC3=CC(O)=CC4=C32()C(C=C(O)C=C5O)=C5(C6=CC=C(O)C=C6)4()7()(C8=CC=C(O)C=C8)C9=C(C=C(O)C=C9O)%10()C%11=C7C=C(O)C=C%11O%10C%12=CC=C(O)C=C%12
Properties
Chemical formula C56H42O12
Molar mass 906.940 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Hopeaphenol is a stilbenoid. It is a resveratrol tetramer isolated from wines.

It shows an opposite effect to vitisin A on apoptosis of myocytes isolated from adult rat heart.

See also

References

  1. Habiba Amira Guebailia, Kleopatra Chira, Tristan Richard, Teguiche Mabrouk, Aurélie Furiga, Xavier Vitrac, Jean-Pierre Monti, Jean-Claude Delaunay and Jean-Michel Mérillon (2006). "Hopeaphenol: The First Resveratrol Tetramer in Wines from North Africa". J. Agric. Food Chem. 54 (25): 9559–9564. doi:10.1021/jf062024g. PMID 17147446.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. Opposite Effects of Two Resveratrol (trans-3,5,4′-Trihydroxystilbene) Tetramers, Vitisin A and Hopeaphenol, on Apoptosis of Myocytes Isolated from Adult Rat Heart. Kazuhiko Seya, Kouta Kanemaru, Chiharu Sugimoto, Megumi Suzuki, Teruko Takeo, Shigeru Motomura, Haruo Kitahara, Masatake Niwa, Yoshiteru Oshima and Ken-Ichi Furukawa, JPET January 2009 vol. 328 no. 1 90-98, doi:10.1124/jpet.108.143172
Type of stilbenoids (molecules with a C6-C2-C6 backbone)
Types

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