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Many men misuse oral contraceptive pills for things like hair growth and muscle gain.

Certain 4-azasteroids are effective at blocking the enzyme that processes testosterone in human skin and could help treat acne, excessive hair growth, and male pattern baldness.

The chemicals 17βC and its methyl ester can block the effects of testosterone on hamster skin but not the effects of DHT.

Higher androgen levels and site-specific AR expression cause sex-related skeletal differences, and certain steroids can boost AR expression and androgen effects in bone cells.

CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

Allopregnanolone may enhance alcohol's effects on dopamine neurons, influencing addiction risk.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

Anti-androgen drugs can treat conditions like prostate cancer and male pattern baldness by blocking effects of testosterone and DHT.

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

Steroids may not work well for alopecia areata because of high unoccupied receptors and low thioredoxin levels.

Certain pesticides and fungicides can interfere with male hormone functions, potentially causing reproductive issues in male rats.

Antiandrogens are effective for conditions like prostate cancer and skin issues, but more research is needed to confirm their benefits and minimize side effects.

Cyproterone acetate effectively treats hirsutism and related conditions.

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

Men with male-pattern baldness have higher levels of certain testosterone metabolites and may have more active androgen metabolism.

Some new progesterone derivatives are better at blocking testosterone conversion than a common drug.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

Compounds 4, 4b, and 4c effectively inhibit an enzyme linked to testosterone conversion without significant toxicity.

Analog 23 is a promising compound for prostate cancer treatment.

Cyproterone acetate is used to treat conditions like prostate cancer, early puberty, excessive sexual drive, and female androgenization by blocking male sex hormones.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

The method can measure multiple steroids in human hair to study long-term steroid metabolism, especially in newborns and children.

Steroidogenesis inhibitors change but don't stop androgen production in prostate cancer.

Antiandrogens can treat female hormonal conditions, but environmental ones may harm reproductive health.

Testosterone undecanoate increases lean mass and causes various physical changes in female-to-male transsexuals.

SARM-induced changes in the androgen receptor are specific to each ligand and affect stability and protein interactions.

New compounds were made that block an enzyme linked to breast cancer better than existing treatments.

5 Alpha-Reductase Inhibitors reduce the effects of testosterone by blocking its conversion into a stronger form.

Certain derivatives are more effective 5α-reductase type 2 inhibitors than finasteride.