| Weight | 228.247 g/mol |
|---|---|
| Formula | C14H12O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
cis-resveratrol (61434-67-1)
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#1656 in Physics
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#5083 in Chemistry
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- Direct HPLC Analysis of cis- and trans-Resveratrol and Piceid Isomers in Spanish Red Vitis vinifera Wines (Journal of Agricultural and Food Chemistry, 1995)
- Determination of Stilbenes (trans-Astringin, cis- and trans-Piceid, and cis- and trans-Resveratrol) in Portuguese Wines (Journal of Agricultural and Food Chemistry, 1999)
- Comparative studies of the antioxidant effects of cis- and trans-resveratrol. (Current Medicinal Chemistry, 2006)
- Effects of cis-resveratrol on inflammatory murine macrophages: antioxidant activity and down-regulation of inflammatory genes. (Journal of Leukocyte Biology, 2004)
- Inhibitory effects of cis- and trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity (Biochemical and Biophysical Research Communications, 2006)
- Antiplatelet activity of cis-resveratrol (Drugs Under Experimental and Clinical Research, 1996)
-
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 - cis-resveratrol
- Wikipedia - (Z)-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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