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Bisphenol-A (BPA) increases connections between brain cells and boosts their activity, but it blocks the effects of a male hormone on brain cell plasticity.

The study found ways to create important compounds for male health from olive waste.

Researchers developed new compounds that target the androgen receptor effectively with fewer side effects.

A man had bad reactions to a hair loss treatment called DNCB.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

Combining finasteride with dimethyl-β-cyclodextrin improves its absorption and bioavailability.

Finasteride is made through a series of chemical reactions starting from a specific intermediate compound.

Biodegradable polymers can improve cannabinoid delivery but need more clinical trials.

TCDD reduces EGF receptors in the liver, affecting growth and development.

Mercuric triflate is an effective catalyst for various organic reactions, working well at room temperature with high yields.

Long-term exposure to benzene increases skin diseases, blood disorders, and liver problems.

Calancardin B may help reduce inflammation in immune cells.

4-(4-Phenoxybenzoyl)benzoic acid derivatives can both increase and decrease certain types of reactive oxygen species, and may be relevant to hair loss.

Certain changes to the B-ring of androgen receptor ligands can increase their effectiveness for potential treatments of muscle and bone conditions.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

Androgen receptor inactivation delays skin cancer onset and reduces incidence in mice, with gender differences in susceptibility.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

The nanocomposite effectively targets lung cancer cells without harming normal cells.

PM-9 and finasteride effectively inhibit the enzyme that converts testosterone to DHT.

Flutamide, dutasteride, and finasteride dissolve differently in supercritical carbon dioxide, with dutasteride dissolving the least.

Impure benzeneseleninic anhydride samples cause lower finasteride intermediate yields.

Scientists made the first metal-based compounds from a nonsteroidal antiandrogen drug, which showed potential in fighting both hormone-dependent and independent prostate cancer cells.

Fetal environments contain various chemicals that may disrupt hormones.

The process efficiently converts α-pinene oxide to campholenic aldehyde using a special catalyst, achieving high yields quickly.

The research found that compound 6, a newly created steroid, is more effective at inhibiting 5α-reductase (an enzyme) than current treatments, suggesting it could be a better option for treating urinary tract symptoms in men.

Low-dose bisphenol A increases prostate size in rats by affecting certain enzymes.

Finasteride modifies 5-alpha-reductases through a two-step process, affecting inhibitor potency and possibly causing side effects.