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Vitisin A (stilbenoid)

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Revision as of 19:22, 19 May 2011 by Nono64 (talk | contribs) (opposite effect to hopeaphenol)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff) For other uses, see Vitisin A (disambiguation).
Vitisin A
Chemical structure of vitisin A
Identifiers
CAS Number
3D model (JSmol)
PubChem CID
CompTox Dashboard (EPA)
SMILES
  • C1=CC(=CC=C1C2C(C3=CC(=CC4=C3C(C(O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C26)O)O)O)C7=C(C=CC(=C7)C=CC8=CC(=CC9=C8C(C(O9)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O)O
Properties
Chemical formula C56H42O12
Molar mass 906.92 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

Vitisin A is a resveratrol tetramer found in Vitis.

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

References

  1. 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
  2. Vitisin A inhibits adipocyte differentiation through cell cycle arrest in 3T3-L1 cells. Soon-hee Kim, Hee-Sook Park, Myoung-su Lee, Yong-Jin Cho, Young-Sup Kim, Jin-Taek Hwang, Mi Jeong Sung, Myung Sunny Kim and Dae Young Kwon, Biochemical and Biophysical Research Communications, Volume 372, Issue 1, 18 July 2008, Pages 108-113 doi:10.1016/j.bbrc.2008.04.188, PMID 18482581
  3. Vitisin A suppresses LPS-induced NO production by inhibiting ERK, p38, and NF-KB activation in RAW 264.7 cells. Mi Jeong Sung, Davaatseren Munkhtugs, Kim Won, Sung Kwang Park, Kim Soon-Hee, Haeng Jeon Hur, Myung Sunny Kim, Kim Young-Sup and Dae Young Kwon, International immunopharmacology, 2009, vol. 9, no3, pp. 319-323, INIST 21253190

External links

Type of stilbenoids (molecules with a C6-C2-C6 backbone)
Types


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