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pubmed-article:15469019pubmed:abstractTextThe linoleyl alcohol oxidation catalyzed by potato tuber 5-lipoxygenase was found to be efficiently inhibited by stable nitroxyl radicals: 1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl 1-bicyclo[2,2,2]octane-1-carboxylate, 1-adamantylacetate, dodecanoate, and octadecanoate. The dependence of apparent IC50 values on the rotational correlation times of times of 4-hydroxy-1-oxyl-2,2,6,6-tetramethylpiperidine and its derivatives in model micellar systems was analyzed. The inhibition mechanism was proposed; it involves the interaction of hydrophobic nitroxyl radical with the intermediate radical enzyme-substrate complex.lld:pubmed
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pubmed-article:15469019pubmed:authorpubmed-author:Mel'nikA KAKlld:pubmed
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pubmed-article:15469019pubmed:pagination436-40lld:pubmed
pubmed-article:15469019pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:15469019pubmed:articleTitle[Hydrophobic nitroxyl radicals inhibit linoleyl alcohol oxidation by 5-lipoxygenase].lld:pubmed
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pubmed-article:15469019pubmed:publicationTypeEnglish Abstractlld:pubmed