Resveratrol

Mfr.No.	SIH-264
Alternative Names	5-[(E)-2-(4-Hydroxyphenyl)vinyl]-1,3-benzenediol
Appearance	Off-White Solid
Function	Antioxidant
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
Mode Of Action	Antioxidant
Molecular Formula	C14H12O3
Pubchem Cid	445154
Research Area	Cancer ; Oxidative Stress
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
Smiles	C1=CC(=CC=C1/C=C/C2=CC(=CC(=C2)O)O)O
Field Of Use	Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
Cas Number	501-36-0
Molecular Weight	228.25
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).
Solubility	Soluble to 100 mM in DMSO and to 100 mM in ethanol
Source	Synthetic
Adr Code	Non-hazardous
Country Of Origin	Canada
Tarriff Code	3822.00.1090

Reference	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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Combination SKU	Supplier No.	Size	Your price	Quantity
BHB11900086-1	SIH-264-100MG	100 mg	$52		Add to Cart
BHB11900086-2	SIH-264-500MG	500 mg	$215		Add to Cart