Clinical data | |
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Other names | Desmethylenzalutamide; Norenzalutamide |
Drug class | Nonsteroidal antiandrogen |
Pharmacokinetic data | |
Protein binding | 95%[1] |
Elimination half-life | 7.8 days[2][1] |
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Chemical and physical data | |
Formula | C20H14F4N4O2S |
Molar mass | 450.41 g·mol−1 |
3D model (JSmol) | |
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N-Desmethylenzalutamide is a nonsteroidal antiandrogen (NSAA) and the major metabolite of enzalutamide, an NSAA which is used as a hormonal antineoplastic agent in the treatment of metastatic prostate cancer.[3][4][2] It has similar activity to that of enzalutamide and, with enzalutamide therapy, circulates at similar concentrations to those of enzalutamide at steady state.[3][4][2] N-Desmethylenzalutamide is formed from enzalutamide in the liver by the cytochrome P450 enzymes CYP2C8 and CYP3A4.[4] It has a longer terminal half-life than enzalutamide (7.8 days versus 5.8 days).[2]