{"title":"一些致癌的1-芳基-3,3-二甲基三氮在水体系中稳定性的线性哈米特图的有效性。","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":"{\"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}","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}
Validity of a linear Hammett plot for the stability of some carcinogenic 1-aryl-3,3-dimethyltriazenes in an aqueous system.
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.