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JNJ-56142060 is the primary active metabolite of apalutamide, which is a small molecule androgen receptor antagonist developed for the treatment of prostate cancer. It is formed via metabolic conversion following oral administration of apalutamide. Like the parent compound, JNJ-56142060 acts as an androgen receptor antagonist and plays an important role in mediating the therapeutic effect of apalutamide. Both apalutamide and JNJ-56142060 induce CYP3A4 in human hepatocytes and have been studied for their pharmacokinetic and pharmacodynamic properties in castration-resistant prostate cancer.
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