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Finasteride may treat baldness but less effective for those with 5α-reductase deficiency.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

Nitrendipine and nifedipine effectively block muscle contractions, while papaverine relaxes them and minoxidil needs high amounts to work.

Plant steroid hormones show growth, health, and medicinal benefits in various organisms, including potential for treating diseases.

Fluconazole is an effective antifungal medication with potential side effects and lacks official analytical methods for its determination.

New research on prostamide F2α has led to treatments for glaucoma and eyelash growth and may have more medical uses.

Flutamide effectively treats female pattern hair loss with low doses showing good liver tolerance.

Topical finasteride and flutamide reduce gland size and enzyme activity, with flutamide being more potent, potentially treating acne, seborrhea, hirsutism, and androgenic alopecia.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

Skin and hair can regenerate after injury due to changes in gene activity, with potential links to how cancer spreads. Future research should focus on how new hair follicles form and the processes that trigger their creation.

Finasteride may affect fetal brain development and increase arousal, but more research is needed for safety confirmation.

Some hormone-related drugs may protect brain cells in Parkinson's disease differently in men and women.

Minoxidil can cause allergic reactions, but testing helps identify the cause.

A natural steroid in the body may protect against eye damage in glaucoma.

Optimized film improves finasteride skin absorption and treatment efficiency.

Parkinson's disease is linked to skin disorders and skin cells help in studying the disease.

Dutasteride protects dopamine neurons in Parkinson's mice, but Finasteride doesn't.

Nanoparticles effectively deliver water-insoluble drugs to hair follicles, stimulating hair growth without irritating the skin.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Male rats have androgen receptors in their liver, which are different from proteins that bind estrogen.

Newer low-dose oral contraceptives with less androgenic effects improve patient compliance.

α-Tocopheryl acetate is well absorbed through healthy skin.

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

New chemicals were made that can block an enzyme linked to hair loss, prostate growth, and acne.

Minoxidil needs specific structure to block lysyl hydroxylase; exploring alternatives may keep benefits without this effect.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

Flutamide, dutasteride, and finasteride dissolve differently in supercritical carbon dioxide, with dutasteride dissolving the least.

Different halogens on progesterone derivatives can either block or mimic male hormone effects, depending on their type and amount.

Human hair has more unsaturated fats inside than on the surface, and certain lipids may help bind the outer and inner layers together.

Finasteride breakdown products found in bile and urine, helps understand drug safety and effectiveness.