» Articles » PMID: 7389036

Binding of Nitroreduction Products of Misonidazole to Nucleic Acids and Protein

Overview
Specialties Oncology
Pharmacology
Date 1980 Jan 1
PMID 7389036
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

[14C]Misonidazole was reduced with zinc dust in aqueous solution in the presence of ammonium chloride. When the reduction mixture was allowed to react with calf thymus DNA and the reaction mixture was dialyzed, radioactivity was detected in the DNA fraction. Bovine albumin, after reaction with the reduction mixture and subsequent Bio-Gel P-2 column chromatography, was also found to be radioactive. The hydroxylamine derivative of misonidazole was detected in the reduction mixture. It is postulated that binding of nitroreduction products of misonidazole to cellular macromolecules is a probable mechanism for the cytotoxicity of misonidazole.

Citing Articles

Sulphydryls, ascorbate and oxygen as modifiers of the toxicity and metabolism of misonidazole in vitro.

Taylor Y, Rauth A Br J Cancer. 1980; 41(6):892-900.

PMID: 7426314 PMC: 2010364. DOI: 10.1038/bjc.1980.166.


In vitro metabolism of misonidazole.

Josephy P, Palcic B, SKARSGARD L Br J Cancer. 1981; 43(4):443-50.

PMID: 7236487 PMC: 2010618. DOI: 10.1038/bjc.1981.65.