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The new compound is a promising, less toxic alternative to finasteride for treating prostate issues.

Scientists in India found a safer and efficient way to make a type of medicine called hydantoins from carbamates, which also worked well in making the seizure medicine, Ethotoin.

Metabolite 7 is a strong inhibitor for Alzheimer's disease management.

Finasteride reduces certain behaviors caused by D1-like receptor agonists but not by D2-like receptor agonists in mice.

A new method efficiently creates biaryl N-oxides with potential for cancer treatment and drug development.

Alstonia boonei phytochemicals show promise as alternative treatments for BPH with fewer side effects than current drugs.

11β-Hydroxylase inhibitors help prevent seizures in mice by boosting natural neurosteroid production.

Five preservatives may disrupt hormone function and need more health and environmental risk assessment.

Duloxetine, escitalopram, and finasteride may be effective against bacteria and fungi.

The salts have diverse molecular packing with significant hydrogen interactions.

Compounds 15, 20, and 25 are strong inhibitors of human steroid 5α-reductase type 2.

The optimized Cinchonine gel effectively fights acne bacteria and is safe for twice-daily use.

The nature of the side chain in RU 58841 derivatives greatly affects its AR affinity, with the N-(iodopropenyl) derivative 13 showing the highest AR binding affinity, suggesting its potential for developing high-affinity radioiodinated AR radioligands.

Cepharanthine shows promise as a COVID-19 treatment.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

The MXD/24HA salt is more effective for hair growth than raw MXD.

Method can accurately measure five BPH drugs at once.

New steroidal compounds moderately block an enzyme related to testosterone conversion, less effectively than finasteride.

New steroidal compounds could be effective for treating conditions related to 5α-reductase enzyme activity.

Monocyclic aromatic compounds are important for developing various drugs and treatments.

New compounds similar to cromakalim were less effective at inhibiting insulin release but improved in solubility and one acted as a calcium entry blocker, not a potassium channel opener.

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

Treated hair can fight dandruff and odor even after several washes.

Ozenoxacin reduces sebum production, helping manage acne.

Lowering the dose of ziprasidone can cause sudden restlessness and urge to move in patients.

Notopterygii rhizoma et radix (Qiang Huo) can effectively treat psoriasis by reducing skin symptoms and inflammation.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.

The compound 4c effectively inhibits the enzyme linked to hair loss.