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Xenobiotica
the fate of foreign compounds in biological systems
Volume 10, 1980 - Issue 3
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Research Article

The metabolic fate of a herbicidal methylmercapto-s-triazine (cyanatryn) in the rat

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Pages 169-185 | Received 19 Jul 1979, Published online: 22 Sep 2008
 

Abstract

1. A major route of metabolism of the methylmercaptotriazine herbicide cyanatryn involves S-oxygenation.

2. The S-oxide reacts spontaneously with glutathione affording a conjugate, which is eliminated in the bile, and a mercapturic acid which is eliminated in the urine.

3. A small proportion of the administered dose was covalently bound to a component of the blood, probably haemoglobin. This was shown to be dependent on the formation of the S-oxide and on the species of animal studied.

4. No reactivity of the S-oxide towards DNA in vivo, or in vitro could be demonstrated.

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