Rahnasto, M <br/><br/>
More potent inhibition of human CYP2A6 than mouse CYP2A5 enzyme activities by derivatives of phenylethylamine and benzaldehyde.  [electronic resource] 

 -  Xenobiotica; the fate of foreign compounds in biological systems  May 2003 
 - 529-39 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0049-8254 
<br/><br/><label>Standard No.: </label>10.1080/0049825031000085979  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Aryl Hydrocarbon Hydroxylases--antagonists & inhibitors<br/>Benzaldehydes--chemistry<br/>Binding, Competitive<br/>Cytochrome P-450 CYP2A6<br/>Cytochrome P450 Family 2<br/>Dose-Response Relationship, Drug<br/>Enzyme Inhibitors--pharmacology<br/>Humans<br/>Inhibitory Concentration 50<br/>Kinetics<br/>Mice<br/>Microsomes, Liver--enzymology<br/>Mixed Function Oxygenases--antagonists & inhibitors<br/>Phenethylamines--chemistry<br/>Regression Analysis<br/>Structure-Activity Relationship