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Finasteride


Mechanism of action:

Finasteride is a 5α-reductase inhibitor. 5α-reductase is responsible for converting testosterone into dihydrotestosterone. After binding to this enzyme, finasteride significantly reduces the production of dihydrotestosterone, thereby lowering dihydrotestosterone-mediated growth signaling in prostate tissue.

Reference(s):

1. Smith AB et al. (2009). Finasteride in the treatment of patients with benign prostatic hyperplasia: a review. Ther Clin Risk Manag. 


2. Agamia NF et al. (2016). Benign prostatic hyperplasia, metabolic syndrome and androgenic alopecia: Is there a possible relationship? Arab J Urol. 


3. Vaughan ED et al. (2003). Long-term experience with 5-alpha-reductase inhibitors. Rev Urol.

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