2,3,5,4'-Tetrahydroxystilbene 2-O-β-D-glucoside

• CAT Number: I004980
• CAS Number: 82373-94-2
• Molecular Formula: C20H22O9
• Molecular Weight: 406.38
• Purity: ≥95%
• Solubility: DMSO
• Storage: Store at -20°C
• IUPAC Name: (2S,3R,4S,5S,6R)-2-[2,4-dihydroxy-6-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
• InChI: InChI=1S/C20H22O9/c21-9-15-16(25)17(26)18(27)20(28-15)29-19-11(7-13(23)8-14(19)24)4-1-10-2-5-12(22)6-3-10/h1-8,15-18,20-27H,9H2/b4-1+/t15-,16-,17+,18-,20+/m1/s1
• InChIKey: JAYVHSBYKLLDJC-DSNJPTTOSA-N
• SMILES: C1=CC(=CC=C1/C=C/C2=C(C(=CC(=C2)O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O

2,3,5,4′-Tetrahydroxystilbene 2-O-β-D-glucoside（Cat No.:I004980）is a natural flavonoid glycoside, a derivative of stilbene, commonly found in various plants, including grapes and Japanese knotweed. It is a potent antioxidant with potential anti-inflammatory, anti-cancer, and neuroprotective properties. The compound is known for its ability to scavenge free radicals and modulate oxidative stress, which may contribute to its therapeutic potential in cardiovascular diseases, neurodegenerative conditions, and cancer prevention. Studies suggest it could also support skin health and delay aging processes. Further research is needed to fully explore its pharmacological properties and clinical applications.

Reference

[1]. Kimura Y et al. Effects of stilbenes on arachidonate metabolism in leukocytes. Biochim Biophys Acta. 1985 Apr 25;834(2):275-8.