Resveratroloside

For research use only. Not for therapeutic Use.

  • CAT Number: R041529
  • CAS Number: 38963-95-0
  • Molecular Formula: C20H22O8
  • Molecular Weight: 390.388
  • Purity: ≥95%
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<p>
<span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">Resveratroloside (CAS&nbsp;38963-95-0)&nbsp;is a compound that shows cancer-chemopreventive and antioxidative activity through study. It is due to being a derivative of Resveratrol which is a minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1, and it also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression.</span></span></p>


Catalog Number R041529
CAS Number 38963-95-0
Synonyms

4-[(1E)-2-(3,5-Dihydroxyphenyl)ethenyl]phenyl β-D-Glucopyranoside;?(E)-4-[2-(3,5-Dihydroxyphenyl)ethenyl]phenyl β-D-Glucopyranoside; 3,4’,5-Trihydroxystilbene 4’-mono-β-D-glycopyranoside; Resveratrol 4’-O-β-D-glucopyranoside;

Molecular Formula C20H22O8
Purity ≥95%
Target Glucosidase
Storage Store at -20C
IUPAC Name (2S,3R,4S,5S,6R)-2-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
InChI InChI=1S/C20H22O8/c21-10-16-17(24)18(25)19(26)20(28-16)27-15-5-3-11(4-6-15)1-2-12-7-13(22)9-14(23)8-12/h1-9,16-26H,10H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1
InChIKey RUOKEYJFAJITAG-CUYWLFDKSA-N
SMILES C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O
Reference

<p>
<span style="color:#000000;"><span style="font-size:12px;"><span style="font-family:arial,helvetica,sans-serif;">1.Powell, Richard G., et al. &quot;Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the Poaceae.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Phytochemistry</i>&nbsp;35.2 (1994): 335-338.<br />
2.Jeandet, P., et al. &quot;Production of the phytoalexin resveratrol by grapes as a response to Botrytis attack under natural conditions.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Journal of Phytopathology</i>&nbsp;143.3 (1995): 135-139.<br />
3.Mattivi, Fulvio, Fabiano Reniero, and Siegfried Korhammer. &quot;Isolation, characterization, and evolution in red wine vinification of resveratrol monomers.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Journal of Agricultural and Food Chemistry</i>&nbsp;43.7 (1995): 1820-1823.<br />
4.Kim, Hyo Jin, et al. &quot;Antioxidative activity of resveratrol and its derivatives isolated from seeds of Paeonia lactiflora.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Bioscience, biotechnology, and biochemistry</i>&nbsp;66.9 (2002): 1990-1993.</span></span></span></p>

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