QSAR study on species differences in microsomal N-oxygenation of N,N-dimethylalkylamines

Author:

Devínsky Ferdinand1,Gorrod John W1

Affiliation:

1. Chelsea Department of Pharmacy, King’s College London (KQC), University of London, Manresa Road, London SW3 6LX, UK

Abstract

Abstract The metabolic N-oxygenation of nine long chain N,N-dimethylalkylamines and tri-n-butylamine has been studied using hepatic microsomal homogenates from mice, dogs and guinea-pigs. The relative oxidizability of amines (ROA) was correlated with structure, lipophilicity and nucleophilicity parameters of substrates and corresponding amine oxides formed in this biological reaction. The highest conversion of amines to N-oxides was found with male guinea-pig, followed by dog (male, female) and the lowest amount of amine oxides has been produced with male mice microsomal homogenates. The analyses were carried out by GLC and the results quantified using QSAR methodology. ROA is parabolically dependent upon structure and physicochemical properties of the substrates and products which was proved by the high statistical significance of the regression equations. The biological N-oxygenation of these amines is controlled by lipophilicity, stereochemistry and electronic effects.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference19 articles.

1. Minimal Statistical Data for Structure-Function Correlations;Craig;J. Med. Chem.,1971

2. Microsomal N-oxidation of Long Chain N, N-dimethyl alkylamines: Quantitative Structure-Activity Relationships;Devínsky;Eur. J. Drug. Metab. Pharmacokin.,1987

3. Amine Oxides. I. Synthesis, 1H-n.m.r., and infrared spectra of 4-Alkylmorpholine-N-oxides;Devínsky;Chem. Zvesti,1978

4. Amine Oxides. VII. Synthesis, IR Spectra, and antimicrobial activity of 1,4-dialkyl piperazine dioxides;Devínsky;Collect. Czech. Chem. Commun.,1982

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