{"title":"抗氧化剂修复色氨酸自由基","authors":"Slobodan V. Jovanovic, Michael G. Simic","doi":"10.1016/0748-5514(85)90016-9","DOIUrl":null,"url":null,"abstract":"<div><p>Oxidizing free radicals with redox potential greater than 1 V generate indole radicals, R-Ind<sup>⨥</sup> and R-Ind·, as in tryptophan. These resonance-stabilized free radicals can be repaired efficiently with electron donors (<em>k</em> = 5 × 10<sup>6</sup> − 1.3 × 10<sup>9</sup> dm<sup>3</sup> mol<sup>−</sup> s<sup>−</sup>) such as ascorbate, <em>N</em>,<em>N</em>,<em>N</em>′,<em>N</em>′-tetramethyl-<em>p</em>-phenylenediamine dihydrochloride (TMPD), and phenolic antioxidants. Sulfhydryl compounds, which are good H-atom donors, were found to be relatively unreactive (<em>k</em> < 10<sup>6</sup> dm<sup>3</sup> mol<sup>−1</sup>s<sup>−1</sup>). These indole radicals were also found to be unreactive with oxygen (<em>k</em> < 10<sup>6</sup> dm<sup>3</sup> mol<sup>−1</sup> s<sup>−1</sup>).</p></div>","PeriodicalId":77737,"journal":{"name":"Journal of free radicals in biology & medicine","volume":"1 2","pages":"Pages 125-129"},"PeriodicalIF":0.0000,"publicationDate":"1985-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0748-5514(85)90016-9","citationCount":"51","resultStr":"{\"title\":\"Repair of tryptophan radicals by antioxidants\",\"authors\":\"Slobodan V. Jovanovic, Michael G. Simic\",\"doi\":\"10.1016/0748-5514(85)90016-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Oxidizing free radicals with redox potential greater than 1 V generate indole radicals, R-Ind<sup>⨥</sup> and R-Ind·, as in tryptophan. These resonance-stabilized free radicals can be repaired efficiently with electron donors (<em>k</em> = 5 × 10<sup>6</sup> − 1.3 × 10<sup>9</sup> dm<sup>3</sup> mol<sup>−</sup> s<sup>−</sup>) such as ascorbate, <em>N</em>,<em>N</em>,<em>N</em>′,<em>N</em>′-tetramethyl-<em>p</em>-phenylenediamine dihydrochloride (TMPD), and phenolic antioxidants. Sulfhydryl compounds, which are good H-atom donors, were found to be relatively unreactive (<em>k</em> < 10<sup>6</sup> dm<sup>3</sup> mol<sup>−1</sup>s<sup>−1</sup>). These indole radicals were also found to be unreactive with oxygen (<em>k</em> < 10<sup>6</sup> dm<sup>3</sup> mol<sup>−1</sup> s<sup>−1</sup>).</p></div>\",\"PeriodicalId\":77737,\"journal\":{\"name\":\"Journal of free radicals in biology & medicine\",\"volume\":\"1 2\",\"pages\":\"Pages 125-129\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1985-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0748-5514(85)90016-9\",\"citationCount\":\"51\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of free radicals in biology & medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0748551485900169\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of free radicals in biology & medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0748551485900169","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Oxidizing free radicals with redox potential greater than 1 V generate indole radicals, R-Ind⨥ and R-Ind·, as in tryptophan. These resonance-stabilized free radicals can be repaired efficiently with electron donors (k = 5 × 106 − 1.3 × 109 dm3 mol− s−) such as ascorbate, N,N,N′,N′-tetramethyl-p-phenylenediamine dihydrochloride (TMPD), and phenolic antioxidants. Sulfhydryl compounds, which are good H-atom donors, were found to be relatively unreactive (k < 106 dm3 mol−1s−1). These indole radicals were also found to be unreactive with oxygen (k < 106 dm3 mol−1 s−1).