Parameters Piceatannol Resveratrol
Nomenclature 3,3′,4′,5-trans-trihydroxystilbene 3,4′,5-trans-trihydroxystilbene
Spectrophotometric analysis in ethanol Absorbs maximally at 322 nm Absorbs maximally at 308 nm.
Content in grapes About 4-times lower than  resveratrol about 4-times higher than  piceatannol
Inhibitory activity Does not inhibit CYP2E1 (Cytochrome P450 2E1) Inhibits CYP2E1 (Cytochrome P450 2E1)
Scavenging activity Show stronger activity to scavenge free radicals. Higher rate constant of reaction with linoleate (LOO•)
Concentration of  piceatannol required  to scavenge O2•- is 1200 times lower than that of Resveratrol
Lower rate constant of reaction with linoleate (LOO•)
Substrate of enzyme catechol-O-methyltransferase (COMT) Substrate of  enzyme catechol-O-methyltransferase (COMT) due to presence of  extra 3’-OH group Not a substrate of enzyme catechol-O-methyltransferase (COMT)
Inhibition of  MRP1-mediated transport of 2′,7′-bis-(carboxypropyl)-5(6)-carboxyfluorescein (BCPCF) from
human erythrocytes
Show moderate activity Ineffective
Hormetic effect Piceatannol-induced hormetic response has been reported Not reported till now
TPA-induced NFkB DNA binding Inhibits NFkB DNAbinding to a greater extent inhibits NFkB DNAbinding to a lesser extent
Table 3: Table showing distinction between piceatannol and resveratrol [6,15,18,25].