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Topical 17 alpha-propylmesterolone increases hair cell growth in androgenetic alopecia.

Dihydrotestosterone gel improved well-being and sexual function in older men without negatively affecting prostate health.

Finasteride, a drug used for anti-hyperplasia, can be effectively delivered in the form of matrix tablets.

Combining tadalafil and finasteride improves their solubility and effectiveness.

Blocking the enzyme 11β-HSD1 might help treat obesity and metabolic issues.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

Finasteride affects urinary steroid profiles and can potentially hide steroid abuse in sports drug testing.

Dihydrotestosterone (DHT) is crucial for conditions like male-pattern baldness and acne, and measuring a byproduct, androstanediol glucuronide, is a better way to assess DHT's effects than DHT blood levels.

Modifying steroidal inhibitors shows promise for developing new cancer treatments.

Nandrolone phenylpropionate injections thickened the skin and enlarged oil glands in female hairless hamsters.

5α-reductases increase epitestosterone's effect on androgen receptors.

The dutasteride nanoemulsion could improve hair loss treatment by enhancing drug penetration and retention in hair follicles.

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

Dihydrotestosterone (DHT) and its active metabolites play a key role in various diseases, and the development of 5α-reductase inhibitors can help treat these conditions.

Synthetic 19-norprogestins promote bone cell growth and function through their non-phenolic metabolites.

A new method was developed to measure and assess the activity and inhibition of the enzyme steroid 5α-reductase.

Using β-cyclodextrin derivatives improves the solubility and bioavailability of steroidal drugs.

Diane and Androcur 10 improved acne and seborrhea in most women, and hirsutism and alopecia in about half.

Some cannabinoid derivatives may be more effective than current drugs at targeting proteins relevant to prostate cancer treatment.

Epristeride's metabolism involves key metabolites and proteins, affecting its use in doping tests.

A new method was created to test the effectiveness of Dihydrotestosterone (DHT) inhibitors, like finasteride and dutasteride, in human and fish cells. The results showed fish cells are more sensitive to these treatments, and dutasteride works better than finasteride in all tested cells.

The method effectively identifies banned substances in hair loss and skin disease cosmetics.

A new compound, 3a, effectively fights prostate cancer better than finasteride.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

Finasteride's molecular properties and active sites were identified using computational methods.

The new progesterone derivatives effectively inhibit 5α-reductase and bind to the androgen receptor.