Product Name | Resveratrol |
Description |
Antioxidant |
Purity | >98% |
CAS No. | 501-36-0 |
Molecular Formula | C14H12O3 |
Molecular Weight | 228.25 |
Field of Use | Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only. |
Storage Temperature | -20ºC |
Shipping Temperature | Shipped Ambient |
Product Type | Antioxidant |
Solubility | Soluble to 100 mM in DMSO and to 100 mM in ethanol |
Source | Synthetic |
Appearance | Off-White Solid |
SMILES | C1=CC(=CC=C1/C=C/C2=CC(=CC(=C2)O)O)O |
InChI | InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+ |
InChIKey | LUKBXSAWLPMMSZ-OWOJBTEDSA-N |
Safety Phrases |
Classification: Caution: Substance not yet fully tested. Safety Phrases: S22 - Do not breathe dust S24/25 - Avoid contact with skin and eyes S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection Hazard Phrases: H302-H315-H317-H318-H335 Precautionary Phrases: P261-P280-P305 + P351 + P338 |
Cite This Product | Resveratrol (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-264) |
Alternative Names | 5-[(E)-2-(4-Hydroxyphenyl)vinyl]-1,3-benzenediol |
Research Areas | Cancer, Oxidative Stress |
PubChem ID | 445154 |
Scientific Background | Resveratrol is a stilbenoid and a phytoalexin produced naturally by several plants. Its effects are numerous and include anti-cancer (1), anti-inflammatory (2), anti-fungal and has other beneficial cardiovascular effects. It has been proposed that Mn SOD is increased by the pathwayRESV-SIRT1/Nad+- FOXO3a- MnSOD (3). In terms of its anti-cancer properties, resveratrol modulates the transcription factor NF-KB and inhibition of the cytochrome P450 enzyme (1, 4). |
References |
1. Leiro J., et al. (2005) Int Immunopharm. 5(2): 393-406. 2. Gentilli M., et al. (2001) Life Sciences. 68(11): 1317-1321. 3. Robb E.L., et al. (2008) Biochem Biophys Res Commun. 367(2): 406-412. 4. Chun Y.J., Kim M.Y., Guengerich F.P. (1999) Biochem Biophys Res Commun. 262(1): 20-24. |
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