Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14330
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dc.contributor.authorPhosrithong N.
dc.contributor.authorSamee W.
dc.contributor.authorNunthanavanit P.
dc.contributor.authorUngwitayatorn J.
dc.date.accessioned2021-04-05T03:34:13Z-
dc.date.available2021-04-05T03:34:13Z-
dc.date.issued2012
dc.identifier.issn17470277
dc.identifier.other2-s2.0-84860477134
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14330-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84860477134&doi=10.1111%2fj.1747-0285.2012.01368.x&partnerID=40&md5=ecb7ca1172e848acdb6ee9682a4ad3ce
dc.description.abstractForty-eight chromone derivatives were evaluated for their antioxidant activity using 2,2-diphenyl-1-picrylhydrazyl free radical scavenging assay, ferrous ions (Fe 2+) chelating activity test, total antioxidant activity test (Ferric thiocyanate and Thiobarbituric acid methods), and total reductive capability (potassium ferricyanide reduction). 7,8-Dihydroxy-2-(3′-trifluoromethylphenyl)-3-(3″-trifluoromethylbenzoyl) chromone 32 showed stronger radical scavenging and metal chelating activities than butylated hydroxytoluene, vitamin E, and trolox. Chromone derivatives that exhibited good radical scavenging and metal chelating also displayed strong total antioxidant and reductive power activities. The results obtained from this study indicated that the synthesized chromone derivatives have remarkable antioxidant activity. © 2012 John Wiley & Sons A/S.
dc.subjectchromone derivative
dc.subjectfisetin
dc.subjectluteolin
dc.subjectquercetin
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectdrug structure
dc.subjectin vitro study
dc.subjectpriority journal
dc.subjectChelating Agents
dc.subjectChromones
dc.subjectFerricyanides
dc.subjectFree Radical Scavengers
dc.subjectMetals
dc.subjectOxidation-Reduction
dc.titleIn Vitro Antioxidant Activity Study of Novel Chromone Derivatives
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationChemical Biology and Drug Design. Vol 79, No.6 (2012), p.981-989
dc.identifier.doi10.1111/j.1747-0285.2012.01368.x
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