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On the Diversity of Oxidative Bioactivation Reactions on Nitrogen- Containing Xenobiotics

[ Vol. 3 , Issue. 4 ]

Author(s):

Amit S. Kalgutkar, Deepak K. Dalvie, John P. O'Donnell, Timothy J. Taylor and Diana C. Sahakian   Pages 379 - 424 ( 46 )

Abstract:


The unexpected occurrence of idiosyncratic drug reactions during late clinical trials or after a drug has been released can lead to a severe restriction in its use or failure to release / withdrawal. This leads to considerable uncertainty in drug development and has led to attempts to try to predict a drugs potential to cause such reactions. The biotransformation of relatively inert drugs to highly reactive metabolites, commonly referred to as “bioactivation”, is now recognized to be an obligatory step in several kinds of drug-induced adverse reactions. Reactive metabolites can be formed by most, if not all, of the enzymes that are involved in drug metabolism. A major theme explored in this review includes the diversity of oxidative bioactivation reactions on nitrogencontaining xenobiotics including drugs. A variety of Phase I enzymes including P450, MAO, and peroxidases bioactivate nitrogen-containing xenobiotics via direct oxidations on the nitrogen atom leading to reactive intermediates or by oxidation at an alternate site in the molecule; for the metabolite to be reactive via the latter sequence nitrogen participation in required. Examples of direct oxidations on nitrogen include the N-oxidation of aromatic amines (e.g. procainamide), single electron N-oxidation of imides (e.g. phenytoin), or α-carbon oxidations of arylalkyl- or alkylamines (e.g. mianserin), to reactive nitroso, nitrogen free radical and iminium species, respectively. Examples of indirect bioactivation are highlighted with aromatic amines (e.g. diclofenac) that undergo p-hydroxylation resulting in the formation of paminophenols, two-electron oxidation of which results in the formation of reactive quinoneimines. Potential strategies that could be utilized in the screening of novel bioactivation pathways are also discussed.

Keywords:

n xenobiotic, oxidative bioactivation

Affiliation:

Pharmacokinetics, Dynamics, andMetabolism Department, PGRD, Groton, CT 06340. USA



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