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Research 30 of 351
- Design, synthesis and biological evaluation of novel 3-oxo-4-oxa-5α-androst-17β-amide derivatives as dual 5α-reductase inhibitors and androgen receptor antagonists
- A Convenient Synthesis of (16S,20S)-3β-Hydroxy-5α-pregnane-20,16-carbolactam and Its N-alkyl Derivatives
- 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
- Synthesis and in Vitro Evaluation of 4-Substituted N-(1,1-Dimethylethyl)-3-oxo-4-androstene-17.beta.-carboxamides as 5.alpha.-Reductase Inhibitors and Antiandrogens
- 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
- A review on computer‐aided chemogenomics and drug repositioning for rationalCOVID‐19 drug discovery
- Chemical profiles and pharmacological attributes of Apis cerana indica beehives using combined experimental and computer-aided studies
- Homeodynamic Rejuvenation: an adaptive framework for resetting skin aging
- Enzymes
- Synthesis and structural characterization of a new dinuclear platinum(III) complex, [Pt<sub>2</sub>Cl<sub>4</sub>(NH<sub>3</sub>)<sub>2</sub>{μ-HN=C(O)Bu<sup>t</sup>}<sub>2</sub>]
- Hair Depigmentation Is a Biological Readout for Pharmacological Inhibition of KIT in Mice and Humans
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Local and Systemic Reduction by Topical Finasteride or Flutamide of Hamster Flank Organ Size and Enzyme Activity
- Bioequivalence Study of Finasteride
- Topical niacinamide does not stimulate hair growth based on the existing body of evidence
- Novel Lead Generation through Hypothetical Pharmacophore Three-Dimensional Database Searching: Discovery of Isoflavonoids as Nonsteroidal Inhibitors of Rat 5α-Reductase
- Repositioning Old Drugs for New Battles: The Expanding Role of Drug Repurposing in Cancer, Inflammation, and Metabolic Disease.
- Pharmacological evidences for the extracts and secondary metabolites from plants of the genus Hibiscus
- 2-Substituted 4-(Thio)chromenone 6-<i>O</i>-Sulfamates: Potent Inhibitors of Human Steroid Sulfatase
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Sulfatase inhibitors: a patent review
- Novel inhibitors of 5α-reductase
- Effect of C-ring modifications in benzo[c]quinolizin-3-ones, new selective inhibitors of human 5α-reductase 1
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- DETERMINATION OF FINASTERIDE AND RELATED COMPOUNDS BY REVERSED-PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY. I. CHOOSING THE MOBILE PHASE COMPOSITION
- Chapter 23. Therapeutic Control of Androgen Action
- Pharmacological Options for Treatment of Hyperandrogenic Disorders
- Dermatological medications and local therapeutics
- Steroid Hormones
- Development and evaluation of crystalline inclusion complex of finasteride using electrospraying as a novel approach