Search

everythinglearnresearchcommunity

for

Search:↓

Compounds 15, 20, and 25 are strong inhibitors of human steroid 5α-reductase type 2.

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

Smaller substituents at C-17 enhance the inhibitory activity of progesterone derivatives on 5alpha-reductase.

Pesticides can cause reproductive and adrenal health issues.

5 alpha reductase inhibitors can cause sexual, cognitive, and muscle side effects, and may slightly increase aggressive cancer risk.

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

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

New niosomal formulation effectively delivers aminexil through rat skin.

Selective androgen receptor modulators (SARMs) are a promising type of drug for various health conditions due to their targeted actions.

AH-001 could be a safer and more effective treatment for hair loss.

Targeting amphiregulin may improve treatment for fibrosis and cancer.

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

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

New pyrazole-based inhibitors show promise for treating metabolic diseases and other conditions.

Houttuynia cordata compounds may help with anti-aging and hair loss.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Weak endocrine disruptors in mixtures can have significant effects and should be considered in risk assessments.

Certain drugs can cause early hair growth in mice by affecting the nerves.

Cyproterone acetate effectively treats hirsutism and related conditions.

Disruption of glycinergic circuits increases pain sensitivity, suggesting new pain treatment options.

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

Researchers developed new compounds that target the androgen receptor effectively with fewer side effects.

Chlormadinone acetate is a strong, well-tolerated hormone used in birth control and hormone therapy with benefits for menstrual pain and skin conditions.

Certain compounds, especially those with a propionic substituent, could potentially be new treatments for hair loss and similar disorders.

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

Basic drugs like amphetamine are absorbed more in darker hair than lighter hair.

Neurosteroids help control dopamine responses in the brain.

Dihydroartemisinin helps reduce prostate enlargement in rats by stopping the growth of prostate cells.