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dc.contributor.authorPirouzpanah, S
dc.contributor.authorHanaee, J
dc.contributor.authorRazavieh, SV
dc.contributor.authorRashidi, MR
dc.date.accessioned2018-08-26T08:16:52Z
dc.date.available2018-08-26T08:16:52Z
dc.date.issued2009
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51137
dc.description.abstractFlavonoids are an important group of natural compounds that can interfere with the activity of some enzymes. In this study, effects of various flavonoids on aldehyde oxidase (AO) activity were evaluated in vitro. AO was partially purified from guinea pig liver. The effects of 12 flavonoids from three subclasses of flavon-3-ol, flavan-3-ol and flavanone on the oxidation of vanillin and phenanthridine as substrates of AO and xanthine as a substrate of xanthine oxidase (XO) were investigated spectrophotometrically. Among the 12 flavonoids, myricetin and quercetin were the most potent inhibitors of both AO and XO. In general, the oxidation of vanillin was more inhibited by flavonoids than that of phenanthridine. Almost all of the flavonoids inhibited AO activity more potently than XO, which was more evident with non-planner flavanols. A planner structure seems to be essential for a potent inhibitory effect and any substitution by sugar moieties reduces the inhibitory effects. This study could provide a new insight into AO natural inhibitors with potential to lead to some food-drug interactions.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY
dc.subjectFlavonoids
dc.subjectaldehyde oxidase
dc.subjectxanthine oxidase
dc.subjectinhibition
dc.titleInhibitory effects of flavonoids on aldehyde oxidase activity
dc.typeArticle
dc.citation.volume24
dc.citation.issue1
dc.citation.spage14
dc.citation.epage21
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1080/14756360701841301


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