2016
DOI: 10.1016/j.bmcl.2016.10.033
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Inhibition of plasma lipid oxidation induced by peroxyl radicals, peroxynitrite, hypochlorite, 15-lipoxygenase, and singlet oxygen by clinical drugs

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Cited by 6 publications
(2 citation statements)
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“…Edaravone can scavenge 1 O 2 that is generated by activated human neutrophils [ 66 ] and by photoactivated Rose Bengal [ 67 ]. The plasma lipid peroxidation caused by 1 O 2 , however, cannot be suppressed by edaravone and other clinical drugs with antioxidant ability, which include roglitazone, probucol, carvedilol, pentoxifylline and ebselen, although they exhibit suppressive effects on lipid peroxidation caused by free radicals, peroxynitrite, hypochlorite, and lipoxygenase reactions [ 68 ]. Because blood plasma contains high concentrations of proteins and many other compounds that could potentially interfere with the scavenging reaction by these chemicals, such biological compounds may have influenced the results.…”
Section: Fundamental Knowledge Of the Biochemical Properties Of ...mentioning
confidence: 99%
“…Edaravone can scavenge 1 O 2 that is generated by activated human neutrophils [ 66 ] and by photoactivated Rose Bengal [ 67 ]. The plasma lipid peroxidation caused by 1 O 2 , however, cannot be suppressed by edaravone and other clinical drugs with antioxidant ability, which include roglitazone, probucol, carvedilol, pentoxifylline and ebselen, although they exhibit suppressive effects on lipid peroxidation caused by free radicals, peroxynitrite, hypochlorite, and lipoxygenase reactions [ 68 ]. Because blood plasma contains high concentrations of proteins and many other compounds that could potentially interfere with the scavenging reaction by these chemicals, such biological compounds may have influenced the results.…”
Section: Fundamental Knowledge Of the Biochemical Properties Of ...mentioning
confidence: 99%
“…Hydroperoxides can generate alkoxy radical RO upon the breaking of their oxygen–oxygen bonds or other compounds such as aldehydes, acids and hydrocarbons upon the breaking of their carbon–carbon bonds. In addition, RO can also be decomposed into ketones, alcohols and aldehydes, such as the secondary oxidation products malondialdehyde (MDA), α, β-unsaturated aldehyde and hexanal [ 15 , 16 , 17 ].…”
Section: Introductionmentioning
confidence: 99%