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A major biliary metabolite of the hepatocarcinogen, N,N-dimethyl-4-aminoazobenzene (DAB), in the rat was identified as N-(glutathion-S-methylene)-4-aminoazobenzene (GS-CH2-AB). This conjugate was(More)
The synthetic model ultimate carcinogen N-benzoyloxy-N-methyl-4-aminoazobenzene reacted in vitro with either calf thymus or rat liver DNA to yield approximately 1 bound residue per 1,000 nucleotides.(More)
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