In:
Chirality, Wiley, Vol. 18, No. 8 ( 2006-01), p. 592-598
Abstract:
RS‐8359, (±)‐4‐(4‐cyanoanilino)‐5,6‐dihydro‐7‐hydroxy‐7 H ‐cyclopenta[ d ]‐pyrimidine is a racemic compound with a selective and reversible monoamine oxidase A (MAO‐A) inhibition activity. The substrate and product enantioselectivity with respect to 2‐hydroxylation of RS‐8359 enantiomers was studied using mouse and rat liver microsomes. In mice, the ( S )‐enantiomer was transformed to the cis ‐diol metabolite, whereas the ( R )‐enantiomer to the trans ‐diol metabolite. The V max/ K m value for the formation of the cis ‐diol metabolite from the ( S )‐enantiomer was sevenfold greater than that for the formation of the trans ‐diol metabolite from the ( R )‐enantiomer. The greater V max/ K m value for the ( S )‐enantiomer was due to the tenfold smaller K m value compared to that for the ( R )‐enantiomer. The results were in fair agreement with the previously reported low plasma concentrations of the ( S )‐enantiomer and the high recovery of the cis ‐diol metabolite derived from the ( S )‐enantiomer in urine after oral administration of RS‐8359 to mice. Similarly to mice, in rats the ( R )‐enantiomer was transformed to the trans ‐diol metabolite, whereas the ( S )‐enantiomer yielded the cis ‐diol and trans ‐diol metabolites. The V max/ K m value for the ( R )‐enantiomer was larger than that for the ( S )‐enantiomer in rats, indicating that the low plasma concentration of the ( S )‐enantiomer in rats might be caused by a metabolic reaction other than P450‐dependent hydroxylation. CYP3A was shown to be responsible for the trans ‐diol formation from the ( R )‐enantiomer. Chirality, 2006. © 2006 Wiley‐Liss, Inc.
Type of Medium:
Online Resource
ISSN:
0899-0042
,
1520-636X
Language:
English
Publisher:
Wiley
Publication Date:
2006
detail.hit.zdb_id:
2001237-8
SSG:
12
SSG:
15,3
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