Search

everythinglearnresearchcommunity

for

Search:↓

The medications 5α-reductase inhibitors and spironolactone are generally safe for breast cancer patients on endocrine therapies and do not significantly increase breast cancer risk.

FCE 28260 is a stronger and longer-lasting inhibitor of 5α-reductase than finasteride, which may make it a better treatment for certain medical conditions.

Researchers developed a new method to find substances in herbs that can block a specific enzyme linked to hair loss.

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

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

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

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

Reducing 5α-reductase activity helps endometrial cells differentiate, aiding pregnancy.

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

HST and HST/F promote hair growth and may help treat alopecia.

5α-reductase inhibitors may prevent prostate cancer but could also raise the risk of more severe cancers.

Finasteride safely lowers DHT levels without affecting testosterone.

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

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

Finasteride slowly binds to 5-alpha-reductase, affecting enzyme stability and inhibitor potency.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Finasteride may treat baldness but less effective for those with 5α-reductase deficiency.

Antidepressants, 5α-reductase inhibitors, and isotretinoin can cause long-lasting sexual dysfunction.

Four new compounds were more effective than finasteride in treating prostate issues and hair loss, with one being 100 times more active and safe for use.

An extract from Quercus acutissima bark was found to reduce sebum production and block an enzyme linked to acne.

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

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

New compounds may soon be tested to treat excessive hair growth in women.

Researchers found new potential but less potent rat enzyme inhibitors using a 3D model.

Some newly made compounds are promising for treating enlarged prostate, hair loss, viruses, and prostate cancer, and might be better than current drugs.

Progesterone byproduct 5αP stimulates mammary tumor growth, but finasteride can suppress it.

Women with PCOS have higher 5α-reductase activity, which may be linked to insulin resistance.

New compounds show promise for treating hair loss, enlarged prostate, and prostate cancer, with some being more effective and having different side effects than current treatments.

Special nanoparticles increased skin absorption of hair loss treatments with fewer side effects.