In this paper, it is evidenced by the quantitative structu re-carcinogenic activity relation-ship (QSCAR) and the pattern recognition treatment of N-nitroso compounds (NNC) that thekey step of carcinogenesis induced b...In this paper, it is evidenced by the quantitative structu re-carcinogenic activity relation-ship (QSCAR) and the pattern recognition treatment of N-nitroso compounds (NNC) that thekey step of carcinogenesis induced by NNC is the cross-linking on the complementary basepair of DNA, through the bifunctional alkylation between α-carbon and another carbonwithin the same chain. The alkylation by the α-carbon atom is through the diazonium salt,but that by the atom other than the α-position is through the active ester formed from thehydroxylated metabolite of the chain. Therefore, the alkylation by the β-position of NNC,or by its γ-position under suitable conditions, of which the distances from the α-positionboth approach 2. 80-3. 00 A, would be the most favourable positions along with the α-posi-tion for the cross-linking to occur between the complementary base pairs of DNA, whichwill yield the carcinogenic activity of NNC. The above conception of bifunctional alkyla-tion can reduce the QSCAR of NNC展开更多
Di-region theory, the theory for the mechanism of carcinogenesis, has been extendedsuccessfully on the quantitative Structure-carcinogenic activity relationship (QSCAR) of 63aromatic amines. A quantitative equation fo...Di-region theory, the theory for the mechanism of carcinogenesis, has been extendedsuccessfully on the quantitative Structure-carcinogenic activity relationship (QSCAR) of 63aromatic amines. A quantitative equation for the QSCAR of aromatic amines has been estab-lished by the mechanism conception of the specialized di- functional alkylation between thenitrenium ion of the amino group and the epoxide of the aromatic ring. The agreementbetween calculation and experiment comes up to 98%. Thus, it can now express the puzzlingvariation of the carcinogenicity of aromatic amines, as a comprehensible structure-chemicalreactivity relationship.展开更多
By using the relationship equation of Partition coefficients with water solubilities for polycyclic aromatic hydrocarbons (PAHs), we have estimated the solubilities of PAHs. In addition the high-performance liquid chr...By using the relationship equation of Partition coefficients with water solubilities for polycyclic aromatic hydrocarbons (PAHs), we have estimated the solubilities of PAHs. In addition the high-performance liquid chromatograph (HPLC) method has been used for the indirect determination of solubilities of PAHs. t3ased on the di-region theory, We have studied the relationship of the solubilities of PAHs with carcinogenicity and introduced the solubility parameter into the di-region theory equation. The calculated carcinogenicity of PAHs from the obtained equation shows little difference from that calculated from Dai Qianhuan’s equation.展开更多
基金Project supported the National Natural Science Foundation of China.
文摘In this paper, it is evidenced by the quantitative structu re-carcinogenic activity relation-ship (QSCAR) and the pattern recognition treatment of N-nitroso compounds (NNC) that thekey step of carcinogenesis induced by NNC is the cross-linking on the complementary basepair of DNA, through the bifunctional alkylation between α-carbon and another carbonwithin the same chain. The alkylation by the α-carbon atom is through the diazonium salt,but that by the atom other than the α-position is through the active ester formed from thehydroxylated metabolite of the chain. Therefore, the alkylation by the β-position of NNC,or by its γ-position under suitable conditions, of which the distances from the α-positionboth approach 2. 80-3. 00 A, would be the most favourable positions along with the α-posi-tion for the cross-linking to occur between the complementary base pairs of DNA, whichwill yield the carcinogenic activity of NNC. The above conception of bifunctional alkyla-tion can reduce the QSCAR of NNC
基金Project supported by the National Natural Science Foundation of China.
文摘Di-region theory, the theory for the mechanism of carcinogenesis, has been extendedsuccessfully on the quantitative Structure-carcinogenic activity relationship (QSCAR) of 63aromatic amines. A quantitative equation for the QSCAR of aromatic amines has been estab-lished by the mechanism conception of the specialized di- functional alkylation between thenitrenium ion of the amino group and the epoxide of the aromatic ring. The agreementbetween calculation and experiment comes up to 98%. Thus, it can now express the puzzlingvariation of the carcinogenicity of aromatic amines, as a comprehensible structure-chemicalreactivity relationship.
文摘By using the relationship equation of Partition coefficients with water solubilities for polycyclic aromatic hydrocarbons (PAHs), we have estimated the solubilities of PAHs. In addition the high-performance liquid chromatograph (HPLC) method has been used for the indirect determination of solubilities of PAHs. t3ased on the di-region theory, We have studied the relationship of the solubilities of PAHs with carcinogenicity and introduced the solubility parameter into the di-region theory equation. The calculated carcinogenicity of PAHs from the obtained equation shows little difference from that calculated from Dai Qianhuan’s equation.
