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Ishige sinicola extract helps bone-building cells grow and mature, which could aid in treating osteoporosis.

Menthol-based microemulsions improve skin delivery of finasteride and silodosin.

The conclusion is that a new test was created to find substances that affect specific ion channels, and it works well for drug discovery.

Matrix effects in LC-MS can be managed but not completely avoided.

New sulfur-containing steroid analogs show promise for more targeted medical treatments.

Compounds from Ziziphus spina-christi roots show strong antibacterial and antioxidant potential.

A new method improves betulin delivery in experiments, showing promise against certain tumors.

New itaconate prodrugs improve its absorption and effectiveness for treating inflammation.

A new, efficient method creates sulfinimidate esters from sulfenamides and alcohols without metals.

New steroid derivatives show promise as anticancer agents, even against resistant cells.

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

PSI-MS quickly and accurately measures finasteride in tablets, helping with quality control.

A new method creates valuable compounds for drug discovery by breaking traditional chemical rules.

The hydrogel effectively treats oral mucositis by reducing oxidative damage and bacterial infection.

Compound 15a was effective in inhibiting 5α-reductase.

Thiadiazole chitosan conjugates improve hair manageability, moisture, and protection in conditioners.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

A new antiandrogen compound was made and its detailed three-dimensional shape was described.

Ishige sinicola extract may help prevent muscle atrophy through its antioxidant and anti-inflammatory effects.

New isatin-gallate hybrids show promise as antioxidants, cancer treatments, and coronavirus inhibitors.

New gel formulas without ethanol and propylene glycol, containing a minoxidil-methyl-β-cyclodextrin complex, have been created for treating hair loss.

Benzo[c]quinolizin-3-ones are effective nonsteroidal inhibitors of human steroid 5α-reductase 1.

The MPA-ISO cocrystal improved solubility and dissolution rate, while the others did not.

A new method creates unique chemical structures that could improve drug discovery.

Mimicking the steroid A-ring may help create effective enzyme inhibitors for prostate disease treatment.

Compound 1 showed promising anticancer activity.

Toluene diisocyanate exposure can cause immune sensitization by interacting with proteins in hair follicles and sebaceous glands.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.