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Our in vitro success propose that EAM-2201 should be examined regarding potential in vivo pharmacokinetic drug–drug interactions due to time-dependent inhibition of CYP2C8, CYP2C9, CYP2C19 and CYP3A4 activities and aggressive inhibition of UGT1A3 exercise.
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 more info vivo through the autopsy of the EAM-2201 abuser.
Our in vitro outcomes recommend that EAM-2201 needs to be examined regarding likely in vivo pharmacokinetic drug–drug interactions due to time-dependent inhibition of CYP2C8, CYP2C9, CYP2C19 and CYP3A4 functions and competitive inhibition of UGT1A3 activity.
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