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4,4'-亚甲基双(2-氯苯胺)可能的替代物的遗传毒性及其对大鼠肝脏药物代谢酶的影响。

Genotoxicity and effects on rat liver drug-metabolizing enzymes by possible substitutes for 4,4'-methylene bis(2-chloroaniline).

作者信息

Wu K, Bonin A M, Leslie C L, Baker R S, Stacey N H

机构信息

National Institute of Occupational Health and Safety, University of Sydney, NSW, Australia.

出版信息

Carcinogenesis. 1989 Nov;10(11):2119-22. doi: 10.1093/carcin/10.11.2119.

Abstract

The mutagenic properties of Ethacure 300, Cyanacure and Polacure 740M, all possible substitutes for the industrial carcinogen, 4,4'-methylene bis(2-chloroaniline), have been determined in Salmonella typhimurium strains TA100, TA98, TA1535 and TA1537. These data have been compared with the effects of these chemicals on ethoxyresorufin O-deethylase (EROD) activity and aldrin epoxidase (AE) activity in rat liver. Ethacure 300 was clearly positive in both TA100 and TA98 bacterial strains, while Cyanacure was positive only in TA100. Polacure 740M was negative in all strains. Ethacure 300 caused a 28-fold induction of EROD while Cyanacure caused a doubling. Polacure 740M was without effect. Neither Ethacure 300 nor Cyanacure affected AE, while Polacure 740M caused an increase at only the lower dose tested. Thus there was excellent correlation between mutagenicity and EROD induction. A similar correlation was noted for six other structurally related compounds giving support to the contention that the ability of a chemical to induce EROD bears some relationship to its carcinogenic potential.

摘要

已在鼠伤寒沙门氏菌TA100、TA98、TA1535和TA1537菌株中测定了乙硫脲300、氰脲酸和聚硫脲740M的诱变性,它们都是工业致癌物4,4'-亚甲基双(2-氯苯胺)的所有可能替代品。已将这些数据与这些化学物质对大鼠肝脏中乙氧基异吩恶唑酮O-脱乙基酶(EROD)活性和艾氏剂环氧化酶(AE)活性的影响进行了比较。乙硫脲300在TA100和TA98两种细菌菌株中均呈明显阳性,而氰脲酸仅在TA

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