Literature DB >> 826256

Allylisopropylacetamide preferentially interacts with the phenobarbital-inducible form of rat hepatic microsomal P-450.

M B Baird, L S Birnbaum, H B Samis, H R Massie, J A Zimmerman.   

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Year:  1976        PMID： 826256     DOI： 10.1016/0006-2952(76)90042-3

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN： 0006-2952            Impact factor:   5.858


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  3 in total

Review 1.  Multiple forms of inducible drug-metabolizing enzymes: a reasonable mechanism by which any organism can cope with adversity.

Authors:  D W Nebert
Journal:  Mol Cell Biochem       Date:  1979-09-28       Impact factor: 3.396

2.  N-alkylation of the haem moiety of cytochrome P-450 caused by substituted dihydropyridines. Preferential attack of different pyrrole nitrogen atoms after induction of various cytochrome P-450 isoenzymes.

Authors:  F De Matteis; A H Gibbs; C Hollands
Journal:  Biochem J       Date:  1983-05-01       Impact factor: 3.857

3.  Formation of cytochrome P-450 containing haem or cobalt-protoporphyrin in liver homogenates of rats treated with phenobarbital and allylisopropylacetamide.

Authors:  H L Bonkovsky; J F Sinclair; J F Healey; P R Sinclair; E L Smith
Journal:  Biochem J       Date:  1984-09-01       Impact factor: 3.857
  3 in total

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