Cyclofenil: Difference between revisions
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==Cyclofenil== | |||
[[File:Cyclofenil.svg|Cyclofenil chemical structure|thumb|right]] | |||
'''Cyclofenil''' is a nonsteroidal [[selective estrogen receptor modulator]] (SERM) that was primarily used in the treatment of [[infertility]] and [[menstrual disorders]]. It is known for its ability to modulate the [[estrogen receptor]]s in the body, exhibiting both estrogenic and antiestrogenic effects depending on the target tissue. | |||
Cyclofenil | |||
== | ===Chemical Properties=== | ||
Cyclofenil is a synthetic compound with the chemical formula C<sub>20</sub>H<sub>20</sub>O<sub>2</sub>. It is structurally related to other SERMs but is distinct in its specific configuration and functional groups, which contribute to its unique pharmacological profile. | |||
== | ===Mechanism of Action=== | ||
Cyclofenil acts by binding to estrogen receptors, where it can either mimic or block the effects of [[estrogen]] depending on the tissue type. In tissues such as the [[uterus]] and [[breast]], it can act as an antiestrogen, while in other tissues, it may exhibit estrogen-like activity. This dual action is characteristic of SERMs and is utilized therapeutically to achieve desired outcomes in different clinical scenarios. | |||
== | ===Clinical Uses=== | ||
Cyclofenil | Cyclofenil was primarily used to treat [[infertility]] in women by stimulating [[ovulation]]. It was also used to address certain [[menstrual disorders]] and to manage symptoms associated with [[menopause]]. However, its use has declined with the advent of newer and more effective treatments. | ||
== | ===Pharmacokinetics=== | ||
The pharmacokinetic profile of cyclofenil involves its absorption, distribution, metabolism, and excretion. After oral administration, cyclofenil is absorbed into the bloodstream and distributed throughout the body. It undergoes hepatic metabolism and is eventually excreted in the urine. | |||
== | ===Side Effects=== | ||
Like other SERMs, cyclofenil can cause a range of side effects. Common side effects include [[hot flashes]], [[nausea]], and [[headaches]]. In some cases, it may also lead to more serious effects such as [[thromboembolism]] or [[endometrial hyperplasia]]. | |||
===Discontinuation=== | |||
The use of cyclofenil has largely been discontinued in favor of newer medications that offer improved efficacy and safety profiles. However, it remains a compound of interest in the study of estrogen receptor modulation and its effects on various tissues. | |||
==Related Pages== | |||
* [[Selective estrogen receptor modulator]] | |||
* [[Infertility]] | |||
* [[Menstrual disorder]] | |||
* [[Estrogen receptor]] | |||
[[Category:Selective estrogen receptor modulators]] | |||
[[Category:Infertility treatments]] | |||
Latest revision as of 11:07, 23 March 2025
Cyclofenil[edit]

Cyclofenil is a nonsteroidal selective estrogen receptor modulator (SERM) that was primarily used in the treatment of infertility and menstrual disorders. It is known for its ability to modulate the estrogen receptors in the body, exhibiting both estrogenic and antiestrogenic effects depending on the target tissue.
Chemical Properties[edit]
Cyclofenil is a synthetic compound with the chemical formula C20H20O2. It is structurally related to other SERMs but is distinct in its specific configuration and functional groups, which contribute to its unique pharmacological profile.
Mechanism of Action[edit]
Cyclofenil acts by binding to estrogen receptors, where it can either mimic or block the effects of estrogen depending on the tissue type. In tissues such as the uterus and breast, it can act as an antiestrogen, while in other tissues, it may exhibit estrogen-like activity. This dual action is characteristic of SERMs and is utilized therapeutically to achieve desired outcomes in different clinical scenarios.
Clinical Uses[edit]
Cyclofenil was primarily used to treat infertility in women by stimulating ovulation. It was also used to address certain menstrual disorders and to manage symptoms associated with menopause. However, its use has declined with the advent of newer and more effective treatments.
Pharmacokinetics[edit]
The pharmacokinetic profile of cyclofenil involves its absorption, distribution, metabolism, and excretion. After oral administration, cyclofenil is absorbed into the bloodstream and distributed throughout the body. It undergoes hepatic metabolism and is eventually excreted in the urine.
Side Effects[edit]
Like other SERMs, cyclofenil can cause a range of side effects. Common side effects include hot flashes, nausea, and headaches. In some cases, it may also lead to more serious effects such as thromboembolism or endometrial hyperplasia.
Discontinuation[edit]
The use of cyclofenil has largely been discontinued in favor of newer medications that offer improved efficacy and safety profiles. However, it remains a compound of interest in the study of estrogen receptor modulation and its effects on various tissues.