Synthesis, Characterization and Evaluation of 5α, 6β-Dihalo Androsterone Derivatives as 5α-Reductase Inhibitors

    May 2022 in “ Current Enzyme Inhibition ”
    Akanksha Sharma, Priyanka S. Rana, Poonam Arora … Neelima Dhingra
    Studysummary This study found that the synthesized compound 7b exhibited higher 5α-reductase inhibitory activity, increased solubility, and dissolution compared to finasteride, suggesting its potential as a lead compound for benign prostatic hyperplasia treatment.
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    Research cited in this study 9

    1. Synthesis and Biological Evaluation of 3-Tetrazolo Steroidal Analogs: Novel Class of 5α-Reductase Inhibitors Bioorganic & Medicinal Chemistry · 2015
    2. Steroid 5α-Reductase as a Novel Therapeutic Target for Schizophrenia and Other Neuropsychiatric Disorders Current Pharmaceutical Design · 2011
    3. Synthesis, Antiproliferative, Acute Toxicity and Assessment of Antiandrogenic Activities of Some Newly Synthesized Steroidal Lactams European Journal of Medicinal Chemistry · 2010
    4. Saturable Binding of Finasteride to Steroid 5α-Reductase as Determinant of Nonlinear Pharmacokinetics Drug Metabolism and Pharmacokinetics · 2010
    5. Selective Non-Steroidal Inhibitors of 5α-Reductase Type 1 Journal of steroid biochemistry and molecular biology/˜The œJournal of steroid biochemistry and molecular biology · 2004
    6. A Stability-Indicating HPLC Method to Determine Finasteride in a Tablet Formulation Journal of Liquid Chromatography & Related Technologies · 2002
    7. New Progesterone Esters as 5α-Reductase Inhibitors Chemical & Pharmaceutical Bulletin · 2001
    8. Androgenic and Anti-Androgenic Effects of Progesterone Derivatives with Different Halogens as Substituents at the C-6 Position Steroids · 1999
    9. The Enzyme and Inhibitors of 4-Ene-3-Oxosteroid 5α-Oxidoreductase Steroids · 1995

    Related research 1

    1. The Clinical Development of a 5α-Reductase Inhibitor, Finasteride The Journal of Steroid Biochemistry and Molecular Biology · 1990