Taleranol
Taleranol is a synthetic estrogen that was developed in the 1960s. It is a member of the steroidal estrogen class of drugs, which also includes substances such as estradiol, estriol, and ethinylestradiol. Taleranol is not currently used in medical practice, but it has been studied for potential uses in the treatment of menopausal symptoms and osteoporosis.
History[edit | edit source]
Taleranol was first synthesized in the 1960s by the pharmaceutical company Eli Lilly. It was one of many synthetic estrogens developed during this time period, as researchers sought to create drugs that could mimic the effects of natural estrogens without causing unwanted side effects.
Pharmacology[edit | edit source]
Like other steroidal estrogens, taleranol works by binding to estrogen receptors in the body. These receptors are found in many different tissues, including the breast, uterus, brain, and bone. When taleranol binds to these receptors, it triggers a series of biochemical reactions that can lead to various physiological effects.
Potential Uses[edit | edit source]
Although taleranol is not currently used in medical practice, it has been studied for potential uses in the treatment of menopausal symptoms and osteoporosis. Some research suggests that it may be effective in reducing hot flashes, night sweats, and other symptoms associated with menopause. Other studies have suggested that it may help to prevent bone loss in postmenopausal women, potentially reducing the risk of osteoporosis.
Safety and Side Effects[edit | edit source]
Like other synthetic estrogens, taleranol has been associated with a number of potential side effects. These can include nausea, vomiting, breast tenderness, and menstrual irregularities. In addition, long-term use of synthetic estrogens has been linked to an increased risk of certain types of cancer, including breast cancer and endometrial cancer.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD