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Finasteride and minoxidil together promote hair growth better than either alone.

Finasteride doesn't affect hormone levels in normal men.

A new method was created to test the effectiveness of Dihydrotestosterone (DHT) inhibitors, like finasteride and dutasteride, in human and fish cells. The results showed fish cells are more sensitive to these treatments, and dutasteride works better than finasteride in all tested cells.

Finasteride affects male rat genitalia development, causing abnormalities during specific pregnancy days.

Finasteride doesn't affect antipyrine metabolism, so interactions with cytochrome P-450 enzyme drugs are unlikely.

Finasteride, a drug that changes testosterone to a different hormone, was studied and its effects over time were modeled successfully.

Finasteride effectively treats male pattern hair loss with a 1 mg daily dose.

Curcuma aeruginosa extract combined with minoxidil effectively treats male-pattern baldness.

Finasteride reduces dihydrotestosterone, increases testosterone, and may treat hirsutism in women.

Compound 4 is a promising treatment for hair loss with low toxicity.

Four-amino acid part makes enzyme sensitive to finasteride.

Finasteride reduces hairiness and androgen levels in women with unexplained excessive hair growth.

High doses of finasteride cause cell growth and tumors in mice.

Finasteride temporarily lowers male rat fertility without affecting libido.

New steroid compounds effectively inhibit 5α-reductase and may treat hair loss.

5α-reductase inhibitors like finasteride may not be effective or safe for transgender individuals, and more research is needed.

Finasteride may affect PNMT, causing side effects.

Finasteride causes abnormal growth in male mice cells at high doses.

Finasteride effectively treats BPH, but needs more trials to understand potential.

Long-term finasteride use doesn't change bone density or metabolism.

PNU157706 reduced rat sperm movement and fertility without affecting offspring health.

Finasteride effectively inhibits 5α reductase, while plant extracts like Permixon and Bazoton don't show significant results.

Finasteride exposure in pregnancy causes genital abnormalities in male rats.

Finasteride boosts morphine's pain relief, stops tolerance, and reduces withdrawal in rats.

Finasteride's molecular properties and active sites were identified using computational methods.

The PW91 method is best for calculating the basic physical and chemical properties of Finasteride, a drug used for prostate issues and hair loss.

Low dose finasteride decreases certain steroids, possibly increasing depression risk.

Finasteride effectively reduces hair growth in women with idiopathic hirsutism, but requires careful contraception during treatment.

The new compounds moderately block a specific enzyme and strongly counteract a male hormone, suggesting potential for treating certain male-related health conditions.

Finasteride and dutasteride are effective for long-term treatment of enlarged prostates but have sexual side effects and a risk of high-grade prostate cancer.