| scholarly article | Q13442814 |
| P50 | author | Roberta Bernini | Q83884121 |
| Carmela Spatafora | Q39647980 | ||
| P2093 | author name string | Maurizio Barontini | |
| P2860 | cites work | Inhibitory activity of stilbenes on Alzheimer's beta-amyloid fibrils in vitro. | Q51930765 |
| Antioxidant activity of resveratrol, piceatannol and 3,3',4,4',5,5'-hexahydroxy-trans-stilbene in three leukemia cell lines. | Q53343691 | ||
| Isolation, Identification, and Antioxidant Activity of Three Stilbene Glucosides Newly Extracted fromVitis viniferaCell Cultures | Q58985637 | ||
| Use of potato disc and brine shrimp bioassays to detect activity and isolate piceatannol as the antileukemic principle from the seeds of Euphorbia lagascae | Q71396639 | ||
| A stabilized formulation of IBX (SIBX) for safe oxidation reactions including a new oxidative demethylation of phenolic methyl aryl ethers | Q73732359 | ||
| Resveratrol inhibition of lipid peroxidation | Q73825377 | ||
| 2-Arylhydroxytyrosol derivatives via Suzuki-Miyaura cross-coupling | Q81610006 | ||
| Regioselective oxidation of phenols to o-quinones with o-iodoxybenzoic acid (IBX) | Q24670322 | ||
| Resveratrol, pterostilbene, and piceatannol in vaccinium berries | Q28272990 | ||
| Cancer chemopreventive activity of resveratrol, a natural product derived from grapes | Q28300555 | ||
| Therapeutic potential of resveratrol: the in vivo evidence | Q29547413 | ||
| Piceatannol, a hydroxylated analog of the chemopreventive agent resveratrol, is a potent inducer of apoptosis in the lymphoma cell line BJAB and in primary, leukemic lymphoblasts | Q33183062 | ||
| Biological effects of resveratrol | Q33841550 | ||
| A reappraisal of the potential chemopreventive and chemotherapeutic properties of resveratrol | Q34318127 | ||
| Wine, alcohol, platelets, and the French paradox for coronary heart disease | Q34538674 | ||
| Recent developments in the chemistry of polyvalent iodine compounds | Q34726970 | ||
| Molecular mechanism of the chemopreventive effect of resveratrol | Q35082245 | ||
| Phenolic acids enzymatic lipophilization. | Q36096296 | ||
| The cancer preventative agent resveratrol is converted to the anticancer agent piceatannol by the cytochrome P450 enzyme CYP1B1. | Q36644183 | ||
| Enzymatic hydroxylation of aromatic compounds | Q36707306 | ||
| A selective de-O-methylation of guaiacyl lignans to corresponding catechol derivatives by 2-iodoxybenzoic acid (IBX). The role of the catechol moiety on the toxicity of lignans. | Q39848208 | ||
| Structural characterization of the metabolites of hydroxytyrosol, the principal phenolic component in olive oil, in rats | Q43944710 | ||
| Resveratrol, a polyphenol found in grapes, suppresses oxidative damage and stimulates apoptosis during early colonic inflammation in rats | Q44795258 | ||
| The 3,4-dihydroxyl groups are important for trans-resveratrol analogs to exhibit enhanced antioxidant and apoptotic activities | Q44908805 | ||
| The grape and wine polyphenol piceatannol is a potent inducer of apoptosis in human SK-Mel-28 melanoma cells. | Q45017189 | ||
| Resveratrol analogues as selective cyclooxygenase-2 inhibitors: synthesis and structure-activity relationship | Q45090641 | ||
| Chemo-enzymatic synthesis and cell-growth inhibition activity of resveratrol analogues | Q45236576 | ||
| Antioxidant, prooxidant and cytotoxic activity of hydroxylated resveratrol analogues: structure-activity relationship. | Q45302719 | ||
| Plant catechols and their S-glutathionyl conjugates as antinitrosating agents: expedient synthesis and remarkable potency of 5-S-glutathionylpiceatannol. | Q45957355 | ||
| Convenient synthesis of hydroxytyrosol and its lipophilic derivatives from tyrosol or homovanillyl alcohol | Q46390028 | ||
| Production of stilbenoids from the callus of Arachis hypogaea: a novel source of the anticancer compound piceatannol | Q46482577 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 4669-4681 | |
| P577 | publication date | 2009-11-17 | |
| P1433 | published in | Molecules | Q151332 |
| P1476 | title | New lipophilic piceatannol derivatives exhibiting antioxidant activity prepared by aromatic hydroxylation with 2-iodoxybenzoic acid (IBX) | |
| P478 | volume | 14 |
| Q37832721 | 2-Iodoxybenzoic acid--a simple oxidant with a dazzling array of potential applications |
| Q92163186 | Antimicrobial activity of resveratrol-derived monomers and dimers against foodborne pathogens |
| Q93154617 | Inhibition of Pancreatic α-amylase by Resveratrol Derivatives: Biological Activity and Molecular Modelling Evidence for Cooperativity between Viniferin Enantiomers |
Search more.