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Glutathione adducts of N-methyl-4-aminoazobenzene formed in vivo and by reaction of N-benzoyloxy-N-methyl-4-aminoazobenzene with glutathione

✍ Scribed by Brian Ketterer; Fred Kadlubar; Thomas Flammang; Tom Carne; Graham Enderby

Book ID: 113136029
Publisher: Elsevier Science
Year: 1979
Tongue: English
Weight: 1002 KB
Volume: 25
Category: Article
ISSN: 0009-2797
DOI: 10.1016/0009-2797(79)90065-6

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The new compound N-methyl-4-nitrosoacetanilide w a ~. coupled with ~niIine-~H(ring-G) in ethanol-acetic acid and the resulting azoamide was hydrolyzed in alkali to give a high yield o j N-methyl-4-aminoazobenzene labelled in the prime ring. ## INTRODUCTION. N-Methyl-4-aminoazobenzene, a hepatocar