The kinetics and spectra of the reactions of clozapine with compounds I and
II of myeloperoxidase were investigated using both single- and sequential-
mixing stopped-flow techniques, steady-state kinetics, and spectrophotometr
ic measurements. The results show conclusively that both compounds I and II
are reduced in one-electron reactions with clozapine, At pH 7.0 the rate c
onstant for compound I reacting with clozapine is (1.5 +/- 0.1) x 10(6) M-1
s(-1) and for compound II (4.8 +/- 0.1) x 10(4) M-1 s(-1). The physiologic
al pH of 7.4 was found to be optimal for the oxidation of clozapine by comp
ound I. The rate constant for compound I reacting with ascorbate is (1.1 +/
- 0.1) x 10(6) M-1 s(-1) and for compound II (1.1 +/- 0.2) x 10(4) M-1 s(-1
), both obtained at pH 7.0, Experiments with both clozapine and ascorbate p
resent showed that ascorbate acts both as a competitive inhibitor and free
radical scavenger. (C) 1999 Academic Press.