Miller, N E <br/><br/>
Mechanism-based inactivation of the major beta-naphthoflavone-inducible isozyme of rat liver cytochrome P-450 by the chloramphenicol analog N-(2-p-nitrophenethyl)dichloroacetamide.  [electronic resource] 

 -  Drug metabolism and disposition: the biological fate of chemicals   
 - 846-51 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0090-9556 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acetamides--pharmacology<br/>Animals<br/>Benzoflavones--pharmacology<br/>Chloramphenicol--analogs & derivatives<br/>Cytochrome P-450 Enzyme Inhibitors<br/>Cytochrome P-450 Enzyme System--biosynthesis<br/>Enzyme Induction--drug effects<br/>Flavonoids--pharmacology<br/>In Vitro Techniques<br/>Isoenzymes--antagonists & inhibitors<br/>Male<br/>Microsomes, Liver--drug effects<br/>Mixed Function Oxygenases--metabolism<br/>NADPH-Ferrihemoprotein Reductase--metabolism<br/>Oxidation-Reduction<br/>Rats<br/>Rats, Inbred Strains<br/>beta-Naphthoflavone