An investigation of possible transfer of S-methyl groups to the amino nitrogen of aminoazo dyes.
作者信息
Blunck J M, Hughes P E
出版信息
Oncology. 1968;22(2):118-28. doi: 10.1159/000224443.
PMID:4972153
Abstract
摘要
相似文献
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An investigation of possible transfer of S-methyl groups to the amino nitrogen of aminoazo dyes.关于S-甲基基团可能转移至氨基偶氮染料氨基氮的研究。
Oncology. 1968;22(2):118-28. doi: 10.1159/000224443.
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Early stage in the metabolism of aminoazo dyes in the liver of rats.大鼠肝脏中氨基偶氮染料代谢的早期阶段。
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The fate of N-alkyl groups in the course of binding of metabolites of several N-alkyl amino azo dyes to rat-liver proteins.几种N-烷基氨基偶氮染料代谢产物与大鼠肝脏蛋白质结合过程中N-烷基基团的命运。
Chem Biol Interact. 1970 Jun;2(1):41-5. doi: 10.1016/0009-2797(70)90036-0.
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[Binding to DNA and to hepatic proteins of 2 azo compounds with different carcinogenic properties].
C R Acad Hebd Seances Acad Sci D. 1973 Jan 8;276(2):235-8.
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Chemical structure of polar dyes isolated from the livers of rats administered carcinogenic aminoazo dyes.从给予致癌氨基偶氮染料的大鼠肝脏中分离出的极性染料的化学结构。
Biochem Biophys Res Commun. 1966 Sep 8;24(5):811-6. doi: 10.1016/0006-291x(66)90399-8.
6
Significance of bound dye and glutathione for aminoazo dye hepatocarcinogenesis.结合染料和谷胱甘肽在氨基偶氮染料诱导肝癌发生中的意义。
Chem Biol Interact. 1971 Apr;3(2):109-16. doi: 10.1016/0009-2797(71)90090-1.
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[Findings on the bond between cancerogenic azo compounds and proteins of the liver during hepatic cancerogenesis].[肝癌发生过程中致癌偶氮化合物与肝脏蛋白质之间的结合情况研究]
Boll Soc Ital Biol Sper. 1969 Jan 15;45(1):21-4.
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Identification of the amino acid residues that bind azo-dye in the soluble azo-dye carcinogen-binding proteins of rat liver.大鼠肝脏可溶性偶氮染料致癌物结合蛋白中与偶氮染料结合的氨基酸残基的鉴定。
Biochem J. 1968 Sep;109(3):37P. doi: 10.1042/bj1090037pa.
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Two biological reactive intermediates in aminoazo-dye carcinogenesis and their glutathione adducts.氨基偶氮染料致癌作用中的两种生物活性中间体及其谷胱甘肽加合物。
Adv Exp Med Biol. 1981;136 Pt B:1297-306.
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Involvement of tyrosine in the binding of carcinogenic aminoazo dyes to rat-liver proteins in vivo.酪氨酸在致癌性氨基偶氮染料与大鼠肝脏蛋白质的体内结合中的作用。
Chem Biol Interact. 1969 Oct;1(1):73-6. doi: 10.1016/0009-2797(69)90019-2.
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