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

Researchers made new compounds that could potentially be developed into anticancer drugs.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Phenylpropanoid sucrose esters show potential as anticancer agents.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

The research found a link between certain molecular features and the biological activity of BC3, which can help identify or create new active compounds.

A new compound was made that might help treat diseases related to male hormones.

Certain compounds reduced hamster flank organ size by inhibiting 5α-reductase, like finasteride, without affecting androgen receptors.

P2X₃-IR fibers are widespread in rat skin and likely help detect pain.

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

The neighborhood face index (NFI) accurately predicts properties of complex molecules.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

The study created a model to help design new inhibitors for steroidal 5α-reductase enzymes.

Three specific 4-azasteroid-2-oximes showed strong enzyme inhibition, but less than finasteride.

New pregnane derivatives were more effective than finasteride at inhibiting a key enzyme for male pattern baldness.

PADI4 enzyme slows down cell growth in developing hair follicles.

The research helps understand how finasteride works and aids drug development.

A new method efficiently modifies alkenes to create useful medicinal compounds.

Samcyprone ointment is effective for treating common warts if a sensitization reaction occurs first.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

The tested hair dye ingredients do not form harmful oxidized metabolites in the liver.

The more lipophilic the progesterone derivative, the better it binds to androgen receptors and has antiandrogenic effects.

PM-9, like finasteride, may help treat certain diseases by blocking a key enzyme.

Some newly made compounds can block an enzyme linked to hair loss and prostate growth, with one in particular being very selective.

Researchers created 10 new compounds similar to cercidin, which could lead to new antibiotics.

The piRNA pathway genes are crucial in early development and may influence sex differentiation through hormone regulation.

Scientists created iodinated arylhydantoins and arylthiohydantoins that could potentially be used for imaging prostate cancer. Some versions with specific side-chains showed high potential for this use.