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A cyclic imine intermediate in the in vitro metabolic conversion of 1,6-diaminohexane to 6-aminohexanoic acid and caprolactam

 

作者: SubramanyamBabu,   CalleryPatrick S.,   GeelhaarLinda A.,   EgorinMerrill J.,  

 

期刊: Xenobiotica  (Taylor Available online 1989)
卷期: Volume 19, issue 1  

页码: 33-42

 

ISSN:0049-8254

 

年代: 1989

 

DOI:10.3109/00498258909034674

 

出版商: Taylor&Francis

 

数据来源: Taylor

 

摘要:

1. 3,4,5,6-Tetrahydro-2H-azepine is an intermediate in the enzyme-catalyzed conversion of 1,6-diaminohexane to 6-aminohexanoic acid and its corresponding lactam, caprolactam, by mammalian liver aldehyde oxidase.2. Identification of metabolites was based on analysis by gas chromatography-mass spectrometry and confirmed by comparison with the properties of authentic standards.3. The results indicate that the cell differentiating agent hexamethylene bisacetamide is converted into 1,6-diaminohexane, and its metabolism therefore involves diamine oxidase.4. The metabolic fate of 1,6-diaminohexane is similar to that of putrescine and cadaverine in that a cyclic imine is an intermediate in the formation of metabolites with ring (lactam) and chain (amino acid) structures.

 

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