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Both injectable contraceptives lower testosterone and SHBG levels, with NET-EN having a greater effect than DMPA-IM.

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

Norplant implants lower some androgen levels but don't significantly change sexual function.

Norgestimate is the most effective birth control progestin for reducing an enzyme linked to acne and excessive hair growth in women.

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.

Neogynon effectively prevents pregnancy but may cause side effects like headaches and menstrual changes.

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

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

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

Strontium ranelate is no longer available for treatment.

Trienones are more effective at inhibiting the enzyme linked to hair loss than dienones.

Stiripentol shows promise as a potential treatment for androgen-related diseases but needs more testing.

Ovulation inhibitors effectively treat menstrual issues and improve fertility but can have side effects.

New nonsteroidal molecules can potentially increase dihydrotestosterone in neurons by blocking certain enzymes, without affecting prostate and seminal vesicle weight.

New steroidal compounds could be effective for treating conditions related to 5α-reductase enzyme activity.

New sulfur-containing steroid analogs show promise for more targeted medical treatments.

Combining a GnRH agonist with a low-dose oral contraceptive is more effective and safer for treating hirsutism than using either alone.

Bolandiol, a synthetic steroid, builds muscle and bone without greatly affecting sex glands, and works differently from other hormones.

Hormonal contraceptives may reduce social behavior and sexual motivation by lowering allopregnanolone levels.

New steroids were effective in blocking male hormone receptors in hamster prostates.

Two non-steroidal antiandrogens, RU 58841 and RU 56187, form a common metabolite at different rates, which may influence their effects; RU 56187 could be used for prostate cancer treatment and RU 58841 for acne treatment.

New progesterone-based compounds can block male hormones.

Scientists made the first metal-based compounds from a nonsteroidal antiandrogen drug, which showed potential in fighting both hormone-dependent and independent prostate cancer cells.

High doses of norethindrone acetate in rats caused various organ changes but didn't significantly increase tumor rates.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

Certain hydroxycinnamate derivatives may effectively inhibit enzymes linked to hair loss with low toxicity.

A new method effectively predicts estrogen-related health effects for early screening.

Certain progesterone derivatives can inhibit enzymes and reduce androgenic activity, potentially affecting prostate growth.

Norethindrone and levonorgestrel can enhance or inhibit root growth in Arabidopsis thaliana depending on the concentration.