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The aim of this examine should be to characterize the metabolites of EAM-2201 in human hepatocytes obtained in vitro and those in liver and urine specimens acquired in vivo through the autopsy of the EAM-2201 abuser.
Our in vitro results suggest that EAM-2201 ought to be examined with regards to likely in vivo pharmacokinetic drug–drug interactions a result of time-dependent inhibition of CYP2C8, CYP2C9, CYP2C19 and CYP3A4 functions and competitive inhibition of UGT1A3 activity.
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Then, the inhibitor focus that supports 50 percent the maximal level of inhibition (Ki) and maximal rate of enzyme inhibition (kinact) values were calculated making use of the next equation with Enzyme Kinetics application:
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