{"title":"Validity of a linear Hammett plot for the stability of some carcinogenic 1-aryl-3,3-dimethyltriazenes in an aqueous system.","authors":"G F Kolar, R Preussmann","doi":"10.1515/znb-1971-0919","DOIUrl":null,"url":null,"abstract":"The stability of fourteen carcinogenic 1-aryl-3,3-dimethyltriazenes to hydrolysis in 0.15 ᴍ phosphate buffer, pH 7.0, at 37° was determined spectroscopically. The data gave an unexpectedly wide span of half-lives resulting in a linear Hammett plot with a reaction constant, ρ= -4.7. These results are in complete agreement with the currently accepted mechanisms of carcinogenic activity associated with this class of compounds. The rapid liberation of a diazonium cation from the labile triazenes (t½, less than 2 × 102 min) seems to be responsible for the induction of local tumours; however, an enzymic activation is necessary for the systemic carcinogenic activity of the compounds stable to hydrolysis (t½, more than 2 × 102 min). Convincing experimental evidence is thus provided for two different mechanisms of activity which are operative within a single class of chemical carcinogens.","PeriodicalId":23706,"journal":{"name":"Zeitschrift fur Naturforschung. Teil B, Chemie, Biochemie, Biophysik, Biologie und verwandte Gebiete","volume":"26 9","pages":"950-3"},"PeriodicalIF":0.0000,"publicationDate":"1971-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1515/znb-1971-0919","citationCount":"30","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift fur Naturforschung. Teil B, Chemie, Biochemie, Biophysik, Biologie und verwandte Gebiete","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/znb-1971-0919","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 30
Abstract
The stability of fourteen carcinogenic 1-aryl-3,3-dimethyltriazenes to hydrolysis in 0.15 ᴍ phosphate buffer, pH 7.0, at 37° was determined spectroscopically. The data gave an unexpectedly wide span of half-lives resulting in a linear Hammett plot with a reaction constant, ρ= -4.7. These results are in complete agreement with the currently accepted mechanisms of carcinogenic activity associated with this class of compounds. The rapid liberation of a diazonium cation from the labile triazenes (t½, less than 2 × 102 min) seems to be responsible for the induction of local tumours; however, an enzymic activation is necessary for the systemic carcinogenic activity of the compounds stable to hydrolysis (t½, more than 2 × 102 min). Convincing experimental evidence is thus provided for two different mechanisms of activity which are operative within a single class of chemical carcinogens.