| Weight | 244.246 g/mol |
|---|---|
| Formula | C14H12O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
piceatannol (10083-24-6, 4339-71-3)
Score:
#1295 in Biochemistry
,
#3175 in Biology
,
#3972 in Chemistry
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- Resveratrol, Pterostilbene, and Piceatannol in Vaccinium Berries (Journal of Agricultural and Food Chemistry, 2004)
- Inhibition of mast cell Fc epsilon R1-mediated signaling and effector function by the Syk-selective inhibitor, piceatannol (Journal of Biological Chemistry, 1994)
- The cancer preventative agent resveratrol is converted to the anticancer agent piceatannol by the cytochrome P450 enzyme CYP1B1 (British Journal of Cancer, 2002)
- Piceatannol Inhibits TNF-Induced NF-B Activation and NF-B-Mediated Gene Expression Through Suppression of IB Kinase and p65 Phosphorylation (Journal of Immunology, 2002)
- Piceatannol (3,4,3,5-tetrahydroxy-trans-stilbene) is a naturally occurring protein-tyrosine kinase inhibitor (Biochemical and Biophysical Research Communications, 1989)
- Biological activity of piceatannol: Leaving the shadow of resveratrol (Mutation Research-reviews in Mutation Research, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O
-
InChIKeyCDRPUGZCRXZLFL-UHFFFAOYSA-N
- Pubchem - piceatannol
- Wikipedia - piceatannol
Piceatannol is a stilbenoid, a type of phenolic compound.
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Most-cited Publications
Areas of Application
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
Reactant
+
5-Chlororesorcinol
(Stille)
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piceatannol
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