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5-alpha-reductase type II (SRD5A2) is a microsomal enzyme that catalyzes the conversion of testosterone to dihydrotestosterone (DHT), a more potent androgen. This reaction is essential for normal male sexual differentiation and development. Mutations in SRD5A2 can cause 5-alpha reductase deficiency, leading to underdeveloped or ambiguous external genitalia in genetic males. It is also implicated in prostate cancer and is the target of drugs like finasteride used to treat benign prostatic hyperplasia and androgenetic alopecia.
Inhibition of 5-alpha reductase type II, preventing the conversion of testosterone to dihydrotestosterone (DHT)
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