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- Synthesis and 5α-Reductase Inhibitory Activity of C21 Steroids Having 1,4-diene or 4,6-diene 20-ones and 4-Azasteroid 20-Oximes
- Novel inhibitors of 5α-reductase
- An overview on 5α-reductase inhibitors
- Effect of C-ring modifications in benzo[c]quinolizin-3-ones, new selective inhibitors of human 5α-reductase 1
- Steroid 5α-reductase inhibition by polymethoxyflavones
- Exploring the Inhibitory Potential of Phytosterols β-Sitosterol, Stigmasterol, and Campesterol on 5-Alpha Reductase Activity in the Human Prostate: An In Vitro and In Silico Approach
- Caffeic acid N-[3,5-bis(trifluoromethyl)phenyl] amide as a non-steroidal inhibitor for steroid 5α-reductase type 1 using a human keratinocyte cell-based assay and molecular dynamics
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- 13C-NMR study of 4-azasteroids in solution and solid state
- Synthesis of a 4-azasteroid hormones compound
- Azasteroids as inhibitors of testosterone 5α-reductase in mammalian skin
- Synthesis and in vitro study of 17β-[N-ureylene-N,N′-disubstituted]-4-methyl-4-aza-5α-androstan-3-ones as selective inhibitors of type I 5α-reductase
- Dutasteride in Androgenetic Alopecia: An Update
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Alopecia - the search for novel agents continues
- A concise review- Development of an analytical method and validation of dutasteride
- 5α-Reductase Inhibitors, Chemical and Clinical Models
- 12 Treatment of hirsutism with 5α-reductase inhibitors
- Steroid 5α-Reductase Inhibitors
- 5α‐Reductase inhibitors and prostatic disease
- A Connection between the Mitochondrial Permeability Transition Pore, Autophagy, and Cerebral Amyloidogenesis
- Pharmacodynamic modeling of finasteride, a 5 alpha-reductase inhibitor.
- New Synthesis of Finasteride
- Species Differences in Prostatic Steroid 5<i>α</i>-Reductases of Rat, Dog, and Human
- FORMULATION AND EVALUATION OF FINASTERIDE SUSTAINED-RELEASE MATRIX TABLETS USING DIFFERENT RATE CONTROLLING POLYMERS
- FINASTERIDE AS A TREATMENT FOR MALE ANDROGENETIC ALOPECIA
- Generation of comparative pharmacophoric model for steroidal 5α-reductase I and II inhibitors: A 3D-QSAR study on 6-azasteroids
- Experimental Assessment of 3-<i>meta</i>-Pyridine-1,2,4-Oxadiazole Deoxycholic Acid Derivative as a Prototype of 5-α-Reductase Inhibitors <i>in silico</i> and <i>in vivo</i> Models
- Crystal Structure of 3-Oxo-4-Aza-5-Alpha-Androstone-17 β-Tert-Butyl Carboxamide with an O···H–(C, N) Acceptor Four-Center Hydrogen Bond