Literature DB >> 725322

Decreased toxicity of the N-methyl analogs of acetaminophen and phenacetin.

S D Nelson, A J Forte, R J McMurtry.   

Abstract

The N-methyl analogs of p-hydroxyacetanilide (acetaminophen) and p-ethoxyacetanilide (phenacetin) were prepared and tested for toxicity. N-Methylacetaminophen was found to cause no hepatic necrosis in mice, rats, or hamsters in doses that caused massive hepatic necrosis in the same animals when acetaminophen was administered. Neither acetaminophen nor its N-methylated analog caused methemoglobinemia at these dose levels. Fischer rats that were administered large doses of acetaminophen (900 mg/kg s.c.) sustained necrosis in the proximal renal tubules, whereas N-methylacetaminophen caused no renal injury at higher dose levels (1800 mg/kg s.c.). N-Methylphenacetin caused no observable hepatic necrosis in 3-methylcholanthrene (3-MC) pretreated hamsters at dose levels higher than those in which phenacetin caused hepatic necrosis. Also, in contrast to phenacetin, N-methylphenacetin did not cause extensive methemoglobinemia in mice, rats, or hamsters.

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Year:  1978        PMID: 725322

Source DB:  PubMed          Journal:  Res Commun Chem Pathol Pharmacol        ISSN: 0034-5164


  1 in total

1.  Human keratin 8 variants promote mouse acetaminophen hepatotoxicity coupled with c-jun amino-terminal kinase activation and protein adduct formation.

Authors:  Nurdan Guldiken; Qin Zhou; Ozlem Kucukoglu; Melanie Rehm; Kateryna Levada; Annika Gross; Raymond Kwan; Laura P James; Christian Trautwein; M Bishr Omary; Pavel Strnad
Journal:  Hepatology       Date:  2015-07-03       Impact factor: 17.425

  1 in total

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