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通过苯并[a]蒽和7,12-二甲基苯并[a]蒽的化学或酶促氧化形成二氢二醇。

The formation of dihydrodiols by the chemical or enzymic oxidation of benz[a] anthracene and 7,12-dimethylbenz[a] anthracene.

作者信息

Tierney B, Hewer A, MacNicoll A D, Giovanni Gervasi P, Rattle H, Walsh C, Grover P L, Sims P

出版信息

Chem Biol Interact. 1978 Nov;23(2):243-57. doi: 10.1016/0009-2797(78)90010-8.

Abstract

When benz[a] anthracene was oxidised in a reaction mixture containing ascorbic acid, ferrous sulphate and EDTA, the non-K-region dihydrodiols, trans-1,2-dihydro-1,2-dihydroxybenz[a] anthracene and trans-3,4-dihydro-3,4-dihydroxybenz[a] anthracene together with small amounts of the 8,9- and 10,11-dihydrodiols were formed. When oxidised in a similar system, 7,12-dimethylbenz[a] anthracene yielded the K-region dihydrodiol, trans-5,6-dihydro-5,6-dihydroxy-7,12-dimethylbenz[a] anthracene and the non-K-region dihydrodiols, trans-3,4-dihydro-3,4-dihydroxy-7,12-dimethylbenz[a] anthracene, trans-8,9-dihydro-8,9-dihydroxy-7,12-dimethylbenz[a] anthracene, trans-10,11-dihydro-10,11-dihydroxy-7,12-dimethylbenz[a] anthracene and a trace of the 1,2-dihydrodiol. The structures and sterochemistry of the dihydrodiols were established by comparisons of their UV spectra and chromatographic characteristics using HPLC with those of authentic compounds or, when no authentic compounds were available, by UV, NMR and mass spectral analysis. An examination by HPLC of the dihydrodiols formed in the metabolism, by rat-liver microsomal fractions, of benz[a] anthracene and 7,12-dimethylbenz[a] anthracene was carried out. The metabolic dihydriols were identified by comparisons of their chromatographic and UV or fluorescence spectral characteristics with compounds of known structures. The principle metabolic dihydriols formed from both benz[a] anthracene and 7,12-dimethylbenz[a] anthracene were the trans-5,6- and trans-8,9-dihydrodiols. The 1,2- and 10,11-dihydrodiols were identified as minor products of the metabolism of benz [a] anthracene and the tentative identification of the trans-3,4-dihydriol as a metabolite was made from fluorescence and chromatographic data. The minor metabolic dihydriols formed from 7,12-dimethylbenz[a] anthracene were the trans-3,4-dihydrodiol and the trans-10,11-dihydriol but the trans-1,2-dihydrodiol was not detected in the present study.

摘要

当苯并[a]蒽在含有抗坏血酸、硫酸亚铁和乙二胺四乙酸的反应混合物中被氧化时,会形成非K区域的二氢二醇,即反式-1,2-二氢-1,2-二羟基苯并[a]蒽和反式-3,4-二氢-3,4-二羟基苯并[a]蒽,以及少量的8,9-和10,11-二氢二醇。当7,12-二甲基苯并[a]蒽在类似体系中被氧化时,会产生K区域的二氢二醇,即反式-5,6-二氢-5,6-二羟基-7,12-二甲基苯并[a]蒽和非K区域的二氢二醇,即反式-3,4-二氢-3,4-二羟基-7,12-二甲基苯并[a]蒽、反式-8,9-二氢-8,9-二羟基-7,12-二甲基苯并[a]蒽、反式-10,11-二氢-10,11-二羟基-7,12-二甲基苯并[a]蒽以及微量的1,2-二氢二醇。通过将其紫外光谱和使用高效液相色谱的色谱特征与 authentic 化合物的特征进行比较,或者在没有 authentic 化合物时,通过紫外、核磁共振和质谱分析,确定了二氢二醇的结构和立体化学。利用高效液相色谱对大鼠肝微粒体部分代谢苯并[a]蒽和7,12-二甲基苯并[a]蒽形成的二氢二醇进行了检测。通过将其色谱和紫外或荧光光谱特征与已知结构的化合物进行比较,鉴定了代谢产生的二氢二醇。由苯并[a]蒽和7,12-二甲基苯并[a]蒽形成的主要代谢二氢二醇是反式-5,6-和反式-8,9-二氢二醇。1,2-和10,11-二氢二醇被鉴定为苯并[a]蒽代谢的次要产物,并且根据荧光和色谱数据初步鉴定反式-3,4-二氢二醇为一种代谢产物。由7,12-二甲基苯并[a]蒽形成的次要代谢二氢二醇是反式-3,4-二氢二醇和反式-10,11-二氢二醇,但在本研究中未检测到反式-1,2-二氢二醇。

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