Comutagenesis--V: rapid conversion of 2-hydroxyl-amino-3-methylpyridineto 2-amino-3-methylpyridine by a hepatic S9 preparation.
J W Gorrod, T G Altuntas
Index: Eur. J. Drug Metab. Pharmacokinet. 22(4) , 341-4, (1997)
Full Text: HTML
Abstract
The in vitro metabolism of 2-hydroxylamino-3-methylpyridine has been investigated using arochlor 1254 pretreated rat S9 mixtures. 2-Hydroxylamino-3-methylpyridine is rapidly converted to the parent amine 2-amino-3-methylpyridine. No further oxidation products of 2-hydroxylamino-3-methylpyridine (i.e. nitroso or nitro) were detected under the HPLC conditions used. This observation may explain our previous findings on the in vitro metabolism of 2-amino-3-methylpyridine where no hydroxylamino metabolite was detected.
Related Compounds
Related Articles:
2011-02-01
[J. Enzyme Inhib. Med. Chem. 26(1) , 104-14, (2011)]
1997-11-01
[Xenobiotica 27(11) , 1103-11, (1997)]
1997-01-01
[Anticancer Res. 17(5A) , 3485-91, (1997)]
1997-01-01
[Anticancer Res. 17(6D) , 4479-82, (1997)]