Jacobi S, Hoffmann H
Institut für Pharmazeutische Chemie, Johann Wolfgang Goethe-Universität, Frankfurt am Main.
Arch Pharm (Weinheim). 1990 Oct;323(10):825-7. doi: 10.1002/ardp.19903231002.
The 1H-benzotriazole-carboxylic acid esters under investigation were almost - with the exception of the tert.-butylester - completely hydrolyzed by rat liver microsomes. Some substrates were metabolically oxidized to a very small extent (less than 1%) yielding small amounts of possibly toxic metabolites after inhibition of the esterases with paraoxone.