Nilestriol

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Nilestriol[edit | edit source]

Chemical structure of Nilestriol

Nilestriol is a synthetic estrogen used in hormone replacement therapy and for the treatment of menopausal symptoms. It is a derivative of estriol, one of the three main estrogens produced by the human body. Nilestriol is known for its long-acting properties, making it a convenient option for patients requiring estrogen supplementation.

Chemical Properties[edit | edit source]

Nilestriol is a steroidal estrogen with a chemical structure similar to that of natural estrogens. Its molecular formula is C20H24O3. The presence of specific functional groups in its structure contributes to its estrogenic activity and its ability to bind to estrogen receptors in the body.

Mechanism of Action[edit | edit source]

Nilestriol functions by binding to estrogen receptors in various tissues, including the reproductive system, bone, and cardiovascular system. This binding activates the estrogen receptor, leading to the transcription of estrogen-responsive genes. The effects of Nilestriol are similar to those of natural estrogens, including the regulation of the menstrual cycle, maintenance of bone density, and modulation of lipid metabolism.

Clinical Uses[edit | edit source]

Nilestriol is primarily used in the management of menopausal symptoms such as hot flashes, vaginal atrophy, and osteoporosis. It is also used in hormone replacement therapy for women who have undergone oophorectomy or have hypoestrogenism.

Administration and Dosage[edit | edit source]

Nilestriol is typically administered orally. The dosage and frequency of administration depend on the specific condition being treated and the patient's response to therapy. Due to its long-acting nature, Nilestriol may be administered less frequently than other estrogens.

Side Effects[edit | edit source]

Common side effects of Nilestriol include nausea, breast tenderness, and headache. Long-term use of estrogens, including Nilestriol, may increase the risk of endometrial cancer, breast cancer, and thromboembolic events. Patients should be monitored regularly for these potential adverse effects.

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