Oxyresveratrol

• CAT Number: I003025
• CAS Number: 29700-22-9
• Molecular Formula: C14H12O4
• Molecular Weight: 244.20
• Purity: ≥95%
• Synonyms: trans-2/’,3,4/’,5-Tetramethoxystilbene
• Solubility: DMSO: ≥ 34 mg/mL
• Storage: -20°C
• IUPAC Name: 4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol
• InChI: InChI=1S/C14H12O4/c15-11-4-3-10(14(18)8-11)2-1-9-5-12(16)7-13(17)6-9/h1-8,15-18H/b2-1+
• InChIKey: PDHAOJSHSJQANO-OWOJBTEDSA-N
• SMILES: C1=CC(=C(C=C1O)O)/C=C/C2=CC(=CC(=C2)O)O

Oxyresveratrol (Cat No.:I003025) is a naturally occurring polyphenolic compound found in various plant sources, including mulberries, grapes, and peanuts. It has gained attention for its potential health benefits and biological activities. Oxyresveratrol exhibits antioxidant, anti-inflammatory, and anticancer properties. It has been studied for its potential in inhibiting tumor growth, induce apoptosis (programmed cell death) in cancer cells, and suppress inflammatory processes. Additionally, oxyresveratrol has shown potential in protecting against oxidative stress and neurodegenerative diseases. Further research is underway to explore its therapeutic applications and understand its mechanisms of action.

Reference

[1]. Lorenz. et al. Oxyresveratrol and resveratrol are potent antioxidants and free radical scavengers: Effect on nitrosative and oxidative stress derived from microglial cells. Nitric Oxide 9(2) 64-76 (2003).
[2]. Kim, Y.M., Yun, J., Lee, C., et al. Oxyresveratrol and hydroxystilbene compounds. Inhbitory effect on tyrosinase and mechanism of action. J Biol Chem277(18) 16340-16344 (2002).
[3]. Shaida A Andrabi et al. Oxyresveratrol (trans-2,3′,4,5′-tetrahydroxystilbene) is neuroprotective and inhibits the apoptotic cell death in transient cerebral ischemia. Brain Res, 2004 Aug 13, 1017(1-2):98-107.