(Q28319083)

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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

scientific article (publication date: April 1979)

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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 (English)

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B. Ketterer

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A111801

26 November 2022

F. Kadlubar

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A111801

26 November 2022

T. Flammang

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A111801

26 November 2022

T. Carne

4

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A111801

26 November 2022

G. Enderby

5

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A111801

26 November 2022

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April 1979

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https://api.elsevier.com/content/article/PII:0009279779900656?httpAccept=text/xml

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10.1016/0009-2797(79)90065-6

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26 November 2022

https://api.elsevier.com/content/article/PII:0009279779900656?httpAccept=text/plain

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10.1016/0009-2797(79)90065-6

https://api.crossref.org/works/10.1016/0009-2797(79)90065-6

26 November 2022

Chemico-biological Interactions

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25

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1

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7-21

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Microsomal N-oxidation of the hepatocarcinogen N-methyl-4-aminoazobenzene and the reactivity of N-hydroxy-N-methyl-4-aminoazobenzene

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Hepatic metabolism of N-hydroxy-N-methyl-4-aminoazobenzene and other N-hydroxy arylamines to reactive sulfuric acid esters

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3-methylmercapto-N-methyl-4-aminoazobenzene: an alkaline-degradation product of a labile protein-bound dye in the livers of rats fed N,N-dimethyl-4-aminoazobenzene

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Studies on structures of polar dyes derived from the liver proteins of rats fed N-methyl-4-aminoazobenzene. II. Identity of synthetic 3-(homocystein-S-yl)-N-methyl-4-aminoazobenzene with the major polar dye P2b

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Studies on structures of polar dyes derived from the liver proteins of rats fed N-methyl-4-aminoazobenzene. 3. Tyrosine and homocysteine sulfoxide polar dyes

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Structures of hepatic nucleic acid-bound dyes in rats given the carcinogen N-methyl-4-aminoazobenzene

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The isolation of carcinogen-binding protein from livers of rats given 4-dimethylaminoazobenzene

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Purification and properties of the principal liver protein conjugate of a hepatic carcinogen

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The principal liver carcinogen-protein conjugate after a single dose of hepatic azocarcinogen

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A low-molecular-weight protein from rat liver that resembles ligandin in its binding properties

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The formation of mercapturic acids. 1. Formation of mercapturic acid and the levels of glutathione in tissues

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The Conjugation of Aminoazo Dye Metabolites with a Tripeptide and Specific Soluble Proteins of the Liver Soluble Cytoplasm of the Rat

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AZO DYES AND RAT LIVER GLUTATHIONE

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Glutathione and Gamma Glutamyl Transpeptidase in Rat Liver During Chemical Carcinogenesis23

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Biochemistry of Glutathione

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Enhancement of azo dye carcinogenesis by dietary sodium sulphate

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Glutathione S-transferases in the metabolism of foreign compounds

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