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细胞色素P-450将四氯化碳代谢为光气的还原-氧化机制。

Reductive-oxygenation mechanism of metabolism of carbon tetrachloride to phosgene by cytochrome P-450.

作者信息

Pohl L R, Schulick R D, Highet R J, George J W

出版信息

Mol Pharmacol. 1984 Mar;25(2):318-21.

PMID:6700577
Abstract

The mechanism of metabolism of carbon tetrachloride (CCl4) to phosgene (COCl2) in rat liver microsomes was investigated. When the oxygen dependency of the reaction was studied, it was found that the rate of the reaction increased as the oxygen concentration in the reaction atmosphere was decreased from 100% to 5%. Decreasing the oxygen concentration below 5% caused a decrease in the rate of the reaction. The reaction was not inhibited by superoxide dismutase or catalase nor was it supported by cumene hydroperoxide. A reconstituted form of cytochrome P-450 from phenobarbital-pretreated rats metabolized CCl4 to COCl2. These results are consistent with a mechanism we call reductive oxygenation. The first step of the reaction is the cytochrome P-450-dependent reductive dechlorination of CCl4 to trichloromethyl radical (CCl3.). This intermediate is trapped by oxygen to form trichloromethylperoxyl radical (CCl3OO.), which decomposes to COCl2 and possibly an electrophilic form of chlorine.

摘要

研究了大鼠肝微粒体中四氯化碳(CCl4)代谢为光气(COCl2)的机制。当研究该反应对氧气的依赖性时,发现随着反应气氛中氧气浓度从100%降至5%,反应速率增加。将氧气浓度降至5%以下会导致反应速率下降。该反应不受超氧化物歧化酶或过氧化氢酶的抑制,也不受异丙苯过氧化氢的促进。来自苯巴比妥预处理大鼠的重组细胞色素P-450将CCl4代谢为COCl2。这些结果与我们称为还原氧化的机制一致。反应的第一步是细胞色素P-450依赖的将CCl4还原脱氯为三氯甲基自由基(CCl3·)。该中间体被氧气捕获形成三氯甲基过氧自由基(CCl3OO·),其分解为COCl2并可能生成亲电形式的氯。

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