Metabolic β-Hydroxylation and N-Oxidation of N′-Nitrosonornicotine

Stephen S. Hecht, Chi hong B. Chen, Dietrich Hoffmann

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29 Scopus citations

Abstract

3ʹ-Hydroxy-N′-nitrosonornicotine (2), 4-hydroxy-N′-nitrosonornicotine (3), and N′-nitrosonornicotine 1-N-oxide (4) were synthesized and identified as metabolites in the F-344 rat of the tobacco-specific carcinogen N′-nitrosonornicotine (1). For the synthesis of 2, myosmine (5) was converted to 3ʹ-bromomyosmine (6). Displacement by acetate and hydrolysis gave 3ʹ-hydroxymyosmine (7), which was reduced and nitrosated to give 2. 4ʹ-Hydroxymyosmine (13), the precursor to 3, was prepared by ammonolysis of l, 2-epoxy-4-(N-morpholino)-4-(3-pyridyl)-4-cyanobutane (10). N′-Nitrosonornicotine 1-N-oxide (4) was prepared by m-chloroperbenzoic acid oxidation of 1. When 1 was incubated with liver microsomes from Aroclor-pretreated F-344 rats, trace amounts of 2 and 3 were produced and 4 was a major metabolite. The urine from rats treated with N′-nitrosonornicotine-2ʹ- 14C contained only trace amounts of 2 and 3, whereas 4 accounted for 6.7-9.4% of the dose.

Original languageEnglish (US)
Pages (from-to)1175-1178
Number of pages4
JournalJournal of medicinal chemistry
Volume23
Issue number11
DOIs
StatePublished - Nov 1 1980

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