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. Author manuscript; available in PMC: 2011 Jan 5.
Published in final edited form as: Nutr Cancer. 2006;54(1):47–57. doi: 10.1207/s15327914nc5401_6

Figure 1.

Figure 1

Hydroxylation pathway of N-nitrosomethylbenzylamine (NMBA) metabolism at the methylene carbon in the rat esophagus. NMBA metabolism involving α-hydroxylation at the methylene carbon atom at the N-nitroso group results in the formation of benzaldehyde and reactive methyl diazonium ions. The reactive intermediate forms both N7 and the highly mutagenic O6 adduct on guanine.