Discovery of a Novel Hybrid from Finasteride and Epristeride as 5α-Reductase Inhibitor

    Zhiyi Yao, Ping Zhu, Minmin Zhang … Chenzhong Liao
    Studysummary This study found that a new hybrid compound designed from finasteride and epristeride was a potent inhibitor of 5α-reductase with a mechanism similar to finasteride.
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    Research cited in this study 3

    1. Inhibition of Human Steroid 5β-Reductase (AKR1D1) by Finasteride and Structure of the Enzyme-Inhibitor Complex Journal of Biological Chemistry · 2009
    2. Finasteride and the Hair Cycle Journal of The American Academy of Dermatology · 2000
    3. Structure of Human Type II 5 Alpha-Reductase Gene Endocrinology · 1992

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    4. Mechanism-Based Inhibition of Human Steroid 5α-Reductase by Finasteride: Enzyme-Catalyzed Formation of NADP-Dihydrofinasteride, a Potent Bisubstrate Analog Inhibitor Journal of the American Chemical Society · 1996