42 citations
,
February 1998 in “The Journal of Steroid Biochemistry and Molecular Biology”
This study found that PNU 157706 is a highly potent inhibitor of human 5α-reductase enzymes, showing a stronger and longer-lasting antiprostatic effect in rats compared to finasteride.
12 citations
,
April 1995 in “Journal of Medicinal Chemistry”
In this study, 4-substituted N-(1,1-dimethylethyl)-3-oxo-4-androstene-17.beta.-carboxamides were synthesized and evaluated in vitro as potential 5 alpha-reductaseinhibitors and antiandrogens.
11 citations
,
January 2000 in “The Journal of Steroid Biochemistry and Molecular Biology”
This study found that LY320236 is a competitive inhibitor of type I and a non-competitive inhibitor of typeII steroid 5alpha-reductase, indicating its potential as a dualinhibitor with differing modes of activity.
1 citations
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January 2015 in “Hair therapy & transplantation”
This study found that dutasteride increased hair growth metrics significantly more than finasteride in Korean men with AGA, but a meta-analysis suggests no overall significant efficacy difference between the two drugs.
Finasteride may pose a risk during pregnancy, so using a condom is recommended if a partner is pregnant. It is advised to stop finasteride before trying to conceive due to potential effects on fetal development.
The conversation discusses the effectiveness of hair loss treatments, specifically finasteride and dutasteride. The conclusion is that dutasteride significantly reduces DHT levels and may be more effective than finasteride for long-term hair retention, with some users reporting personal experiences and side effects.