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A new, efficient method has been developed to detect darolutamide and thalidomide, drugs used for certain hair loss and prostate cancer treatments, in pharmaceuticals and body fluids.

Testosterone, progesterone, and levonorgestrel change enzyme levels related to fat production in hamster skin, which could affect skin oil and acne.

Scientists made new substances that can block an enzyme linked to prostate issues and hair loss, with potential for creating a new treatment.

Cabergoline is more effective and has fewer side effects than bromocriptine for treating women with hyperprolactinemic amenorrhea.

Three cost-effective methods accurately measure finasteride in pharmaceuticals, better than current techniques.

New compounds were made that effectively block a specific enzyme related to androgen conditions.

Higher 3α,5α-THP levels in the brain may reduce depression in pregnant rats.

Researchers found new potential treatments for conditions related to the androgen receptor, like male hormonal contraception, by testing thousands of compounds.

A simple and eco-friendly method was developed to make finasteride Form-I using water.

The method effectively detects residual solvents in finasteride raw materials.

Researchers found potential urine markers for polycystic ovary syndrome, including testosterone-glucuronide and 11α-hydroxyprogesterone, which may help diagnose the condition.

Blocking progesterone metabolism can cause depression-like behavior in mice.

Progesterone affects GABA_A receptor function by altering δ subunit levels.

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

A reliable method was created to measure dutasteride and related molecules in capsules.

Steroid hormones change the size, charge, and stability of DPPC liposomes.

Coal tar shampoo increases enzyme activity in hair follicles, enhancing carcinogen binding to DNA.

D-004 may be a natural alternative to finasteride for treating enlarged prostate and male baldness.

A new, less toxic and more efficient method to create the anti-baldness compound RU58841 was developed in 2014.

MENT could be a better option than testosterone for male hormone therapy and birth control because it works well at lower doses and has fewer side effects on the prostate.

Progesterone significantly reduces neuroblastoma tumor growth without harming healthy cells.

A 17-year-old female with adrenogenital syndrome produces very high levels of androgens, which prevent complete feminization despite high estrogen doses.

Cyproterone acetate is effective for treating hirsutism and acne in women by blocking androgens in the skin and also works as a contraceptive.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

3-tetrazolo steroidal analogs can strongly inhibit the enzyme linked to hair loss.

Two accurate methods were developed to measure finasteride in tablets.

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

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

LC-MS/MS is essential for accurately detecting pregnanes in pregnant mares.

Fetal environments contain various chemicals that may disrupt hormones.