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Research 30 of 709
- Effect of Saw Palmetto Supplements on Androgen-Sensitive LNCaP Human Prostate Cancer Cell Number and Syrian Hamster Flank Organ Growth
- Relative binding affinity of novel steroids to androgen receptors in hamster prostate
- Comparison Between Two Different Hamster Models used for the Determination of Testosterone and Finasteride Activity
- Molecular Interactions of New Pregnenedione Derivatives
- Activity of steroid 4 and derivatives 4a–4f as inhibitors of the enzyme 5α-reductase 1
- Novel C-6 substituted and unsubstituted pregnane derivatives as 5α-reductase inhibitors and their effect on hamster flank organs diameter size
- Local and Systemic Reduction by Topical Finasteride or Flutamide of Hamster Flank Organ Size and Enzyme Activity
- New 5?-reductase inhibitors: In vitro and in vivo effects
- Synthesis and Pharmacological Evaluation of New Progesterone Esters as 5.ALPHA.-Reductase Inhibitors
- New ester derivatives of dehydroepiandrosterone as 5α-reductase inhibitors
- Ezetimibe Reduces Enlarged Prostate in an Animal Model of Benign Prostatic Hyperplasia
- In vitro and In vivo Effects of 17β-N-(4-phenylcarbamoyl) androst-4-en-3- one Derivatives as 5a-reductase Inhibitors on Androgen-dependent Glands
- Adrenal steroid precursors exert potent androgenic action in the hamster sebaceous glands of flank organs and ears.
- Steroid 5α-Reductase Inhibitors
- Anti-androgenic effect of sesquiterpenes isolated from the rhizomes of Curcuma aeruginosa Roxb.
- New Aromatic Esters of Progesterone as Antiandrogens
- New Progesterone Esters as 5.ALPHA.-Reductase Inhibitors.
- Pharmacological Profile of 9,11-Dehydrocortexolone 17α-Butyrate (CB-03-04), a New Androgen Antagonist with Antigonadotropic Activity
- Biological activity of novel progesterone derivatives having a bulky ester side chains at C-3
- Synthesis and biological evaluation of esters of 16-formyl-17-methoxy-dehydroepiandrosterone derivatives as inhibitors of 5α-reductase type 2
- In vivo and in vitro effect of novel 4,16-pregnadiene-6,20-dione derivatives, as 5α-reductase inhibitors
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Protective role of agomelatine via modulation of TLR4/NF-κB: NLRP3/IL-1β signaling pathways in testosterone-induced benign prostatic hyperplasia in rats
- Endocrine treatment of benign prostatichypertrophy: Current concepts
- Prostate-Sparing Effects in Primates of the Potent Androgen 7α-Methyl-19-Nortestosterone: A Potential Alternative to Testosterone for Androgen Replacement and Male Contraception1
- Rat steroid 5α-reductase kinetic characteristics: Extreme pH-dependency of the type II isozyme in prostate and epididymis homogenates
- The promoter of an androgen dependent gene in the hamster flank organ
- Hormonal control of 5.ALPHA.-reductase activity in hamster sebaceous glands.
- Molecular interactions of natural and synthetic steroids in female hamsters’ flank organs
- Evaluation of New Pregnane Derivatives as 5.ALPHA.-Reductase Inhibitor.