- Concerning Model Metabolites of the Carcinogen 4-Nitroquinoline 1-Oxide. Reactivity of 1-Acetoxy-4-(hydroxyimino)-1,4-dihydroquinoline
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1-Acetoxy-4-(hydroxyimino)-1,4-dihydroquinoline is obtained by hydrolysis of 1-acetoxy-4-(acetoxyimino)-1,4-dihydroquinoline under strongly acidic conditions.At pH 1 the monoacetate is protonated and on hydrolysis affords only 1-hydroxy-4-(hydroxyimino)-1,4-dihydroquinoline.Above pH 1 on hydrolysis the monoacetate affords a complex product mixture including 4-(hydroxyamino)quinoline and 4-nitrosoquinoline.Comparison of the above behavior of 1-acetoxy-4-(hydroxyamino)-1,4-dihydroquinoline with that of 1-hydroxy-4-(acetoxyimino)-1,4-dihydroquinoline at a neutral pH suggests that the former type of ester is less likely to be important in those steps initiating oncogenesis.In contrast the latter type of monoester or diesters corresponding to 1-acetoxy-4-(acetoxyimino)-1,4-dihydroquinoline by their ability to generate nitrenium ion intermediates and undergo attack by nucleophiles at the 3-position are likely intermediates in the process of oncogenesis.Further aspects of their likely biological role are discussed.
- Demeunynck, Martine,Tohme, Najat,Lhomme, Marie-France,Mellor, John M.,Lhomme, Jean
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p. 405 - 410
(2007/10/02)
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- 1-ACETOXY-4-HYDROXYMINO-1,4-DIHYDROQUINOLINE, A REACTIVE INTERMEDIATE DERIVED FROM THE POTENT CARCINOGEN 4-NITROQUINOLINE N-OXIDE
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The title compound, a new monoester of the carcinogenic metabolite 4-hydroxyaminoquinoline 1-oxide, has been prepared as its crystalline hydrochloride and its decomposition in acidic and basic media examined.
- Demeunynck, Martine,Lhomme, Marie France,Lhomme, Jean
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p. 3189 - 3192
(2007/10/02)
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