metabolites
Formation of these metabolites was inhibited significantly (>50%) by       13-cis retinoic acid, a CYP2C8 inhibitor, but not by furafylline, quinidine or       ketoconazole.
Formation of these  @SUBJECT$  was  @PREDICAT$  significantly (>50%) by        @OBJECT$ , a CYP2C8 inhibitor, but not by furafylline, quinidine or       ketoconazole.