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[18] [19] Clinic data also note it does not disrupt hormonal pathways targeted by finasteride, making it attractive for users sensitive to hormone-based treatments
Dwivedi S, Rendn-Huerta EP, Ortiz-Navarrete V, Montao LF
Hepatic cytochrome P450 3A4, 3A5, and fetal-predominant 3A7 catalyze regio- and stereoselective hydroxylation, leading to urinary excretion of conjugated metabolites
doi: 10.1155/2021/9924314
