致癌物N-羟基-N-2-芴基乙酰胺的O-葡糖醛酸在体外经酶促脱乙酰作用激活：芴基胺-tRNA加合物的形成。 - Suppr

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超能文献

Activation of the O-glucuronide of the carcinogen N-hydroxy-N-2-fluorenylacetamide by enzymatic deacetylation in vitro: formation of fluorenylamine-tRNA adducts.

作者信息

Cardona R A, King C M

出版信息

Biochem Pharmacol. 1976 May 1;25(9):1051-6. doi: 10.1016/0006-2952(76)90495-0.

DOI:10.1016/0006-2952(76)90495-0

PMID:5097

Abstract

摘要

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Activation of the O-glucuronide of the carcinogen N-hydroxy-N-2-fluorenylacetamide by enzymatic deacetylation in vitro: formation of fluorenylamine-tRNA adducts.致癌物N-羟基-N-2-芴基乙酰胺的O-葡糖醛酸在体外经酶促脱乙酰作用激活：芴基胺-tRNA加合物的形成。

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