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- 11α-Hydroxyprogesterone, a potent 11β-hydroxysteroid dehydrogenase inhibitor, is metabolised by steroid-5α-reductase and cytochrome P450 17α-hydroxylase/17,20-lyase to produce C11α-derivatives of 21-deoxycortisol and 11-hydroxyandrostenedione in vitro
- The Role of Cytochrome P-450 in Dermatology
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Finasteride, A Steroid 5α-Reductase Inhibitor, Does Not Affect the Oxidative Metabolism of Antipyrine
- The Challenging Consultation: Management of Melanoma
- Response to “Reply to effectiveness of dutasteride in a large series of patients with FFA in real clinical practice”
- Chapter 14 Principles of drug metabolism
- Interaction of antiretroviral medications with finasteride
- Anti-Acne Agents Attenuate FGFR2 Signal Transduction in Acne
- Metabolic pathways of eicosanoids—derivatives of arachidonic acid and their significance in skin
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