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多种潜在的抑制剂、激活剂和诱导剂对3-取代吡啶体外N-氧化的影响。

The effect of various potential inhibitors, activators and inducers on the N-oxidation of 3-substituted pyridines in vitro.

作者信息

Gorrod J W, Damani L A

出版信息

Xenobiotica. 1979 Apr;9(4):219-26. doi: 10.3109/00498257909038724.

Abstract
  1. The N-oxidation of pyridine, 3-methylpyridine and 3-chloropyridine was inhibited by SKF525A and DPEA. The C-oxidation of 3-methylpyridine was also inhibited by these compounds. 2. The N-oxidation of these pyridines was also inhibited by various other nitrogenous substrates including n-octylamine. 3. Incubation in an atmosphere of carbon monoxide resulted in inhibition of both C- and N-oxidation of 3-methylpyridine. 4. Any treatment of microsomes which resulted in a reduction of cytochrome P-450 also produced a concomitant fall in N-oxidation of the pyridines. 5. Pretreatment of animals with phenobarbitone resulted in an increase in the N-oxidation of the pyridines. Pretreatment with 3-methylcholanthrene had no appreciable effect on the N-oxidation of the pyridines in vitro.
摘要
  1. 吡啶、3-甲基吡啶和3-氯吡啶的N-氧化受到SKF525A和DPEA的抑制。这些化合物也抑制3-甲基吡啶的C-氧化。2. 这些吡啶的N-氧化也受到包括正辛胺在内的各种其他含氮底物的抑制。3. 在一氧化碳气氛中孵育导致3-甲基吡啶的C-氧化和N-氧化均受到抑制。4. 任何导致细胞色素P-450减少的微粒体处理也会伴随吡啶N-氧化的下降。5. 用苯巴比妥预处理动物会导致吡啶N-氧化增加。用3-甲基胆蒽预处理对体外吡啶的N-氧化没有明显影响。

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