| Weight | 228.247 g/mol |
|---|---|
| Formula | C14H12O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Resveratrol (501-36-0)
Score:
#12 in Biochemistry
,
#81 in Biology
,
#84 in Chemistry
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- Cancer chemopreventive activity of resveratrol, a natural product derived from grapes. (Science, 1997)
- Resveratrol improves health and survival of mice on a high-calorie diet. (Nature, 2006)
- Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alpha. (Cell, 2006)
- Therapeutic potential of resveratrol: the in vivo evidence (Nature Reviews Drug Discovery, 2006)
- Biological effects of resveratrol. (Life Sciences, 2000)
- Role of Resveratrol in Prevention and Therapy of Cancer: Preclinical and Clinical Studies (Anticancer Research, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O
-
InChIKeyLUKBXSAWLPMMSZ-UHFFFAOYSA-N
- Pubchem - Resveratrol
- Wikipedia - resveratrol
Resveratrol (3,5,4-trihydroxy-trans-stilbene) is a stilbenoid, a type of natural phenol, and a phytoalexin produced by several plants in response to injury or, when the plant is under attack by pathogens such as bacteria or fungi. Sources of resveratrol in food include the skin of grapes, blueberries, raspberries, mulberries. Although it is used as a dietary supplement, there is no good evidence that consuming resveratrol affects life expectancy or human health.
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
Reactant
+
4-CHLOROPHENOL
(Heck terminal vinyl)
Reactant
+
4-CHLOROPHENOL
(Stille)
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Resveratrol
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