Metabolism of 2-(2-thienyl)allylamine hydrochloride in the rat: identification of a novel metabolite.

Abstract

A novel metabolite, 2-(2-thienyl)propionic acid, is formed in vivo from 2-(2-thienyl)allylamine hydrochloride. Mass spectral analysis suggested 2-(2-thienyl)propionic acid formation involves loss of the amine moiety followed by reduction of the olefinic group.

Cite this paper

@article{Gordon1987MetabolismO2, title={Metabolism of 2-(2-thienyl)allylamine hydrochloride in the rat: identification of a novel metabolite.}, author={William Perry Gordon and Joseph R. McCarthy and So Young Chang}, journal={Biochemical and biophysical research communications}, year={1987}, volume={145 1}, pages={575-80} }