European Journal of Drug Metabolism and Pharmacokinetics 1997-01-01

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

  • 3-Methylpyridin-2-...

Related Articles:

Synthesis and characterisation of two novel proton transfer compounds and their inhibition studies on carbonic anhydrase isoenzymes.

2011-02-01

[J. Enzyme Inhib. Med. Chem. 26(1) , 104-14, (2011)]

Comutagenesis-III. In vitro metabolism of 2-amino-3-methylpyridine: the effect of various potential inhibitors, activators and inducers.

1997-11-01

[Xenobiotica 27(11) , 1103-11, (1997)]

Comutagenesis-I: the in vitro metabolism of 2-amino-3-methylpyridine.

1997-01-01

[Anticancer Res. 17(5A) , 3485-91, (1997)]

Comutagenesis-IV in vitro metabolism of the comutagen 2-amino-3-methylpyridine: species differences and metabolic interaction with norharman.

1997-01-01

[Anticancer Res. 17(6D) , 4479-82, (1997)]

More Articles...