Megestrol caproate: Difference between revisions
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{{Short description|A synthetic progestin used in hormone therapy}} | |||
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'''Megestrol caproate''' is a [[synthetic progestin]] used in [[hormone therapy]]. It is a derivative of [[megestrol]], a [[progesterone]] analog, and is primarily utilized for its [[progestogenic]] effects. | |||
Megestrol caproate is | |||
== | ==Pharmacology== | ||
===Mechanism of Action=== | |||
Megestrol caproate functions by binding to the [[progesterone receptor]], mimicking the effects of natural progesterone. This interaction leads to changes in the [[endometrium]] and influences the [[hypothalamic-pituitary-gonadal axis]], ultimately affecting [[ovulation]] and [[menstrual cycle]] regulation. | |||
===Pharmacokinetics=== | |||
The pharmacokinetic profile of megestrol caproate involves its absorption, distribution, metabolism, and excretion. It is administered via [[intramuscular injection]], allowing for a slow release and prolonged action. The drug is metabolized in the [[liver]] and excreted primarily through the [[urinary system]]. | |||
== | ==Clinical Uses== | ||
Megestrol caproate is | Megestrol caproate is used in various clinical settings, including: | ||
* [[Hormone replacement therapy]] | |||
* [[Contraception]] | |||
* Treatment of [[endometriosis]] | |||
* Management of [[menstrual disorders]] | |||
==Side Effects== | |||
Common side effects of megestrol caproate include: | |||
* [[Weight gain]] | |||
* [[Fluid retention]] | |||
* [[Mood changes]] | |||
* [[Nausea]] | |||
== | ==Synthesis== | ||
The synthesis of megestrol caproate involves the chemical modification of megestrol, incorporating a caproate ester group to enhance its pharmacological properties. This modification increases the drug's [[lipophilicity]], allowing for a longer duration of action. | |||
== | ==Related Compounds== | ||
Megestrol caproate is | Megestrol caproate is related to other progestins such as [[medroxyprogesterone acetate]] and [[norethindrone]]. These compounds share similar mechanisms of action but differ in their chemical structure and clinical applications. | ||
== | ==Related pages== | ||
* [[ | * [[Progestin]] | ||
* [[ | * [[Hormone therapy]] | ||
* [[ | * [[Progesterone]] | ||
* [[Endometriosis]] | |||
[[Category:Progestogens]] | [[Category:Progestogens]] | ||
[[Category: | [[Category:Synthetic hormones]] | ||
[[Category: | [[Category:Contraception]] | ||
Latest revision as of 11:12, 15 February 2025
A synthetic progestin used in hormone therapy
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Megestrol caproate is a synthetic progestin used in hormone therapy. It is a derivative of megestrol, a progesterone analog, and is primarily utilized for its progestogenic effects.
Pharmacology[edit]
Mechanism of Action[edit]
Megestrol caproate functions by binding to the progesterone receptor, mimicking the effects of natural progesterone. This interaction leads to changes in the endometrium and influences the hypothalamic-pituitary-gonadal axis, ultimately affecting ovulation and menstrual cycle regulation.
Pharmacokinetics[edit]
The pharmacokinetic profile of megestrol caproate involves its absorption, distribution, metabolism, and excretion. It is administered via intramuscular injection, allowing for a slow release and prolonged action. The drug is metabolized in the liver and excreted primarily through the urinary system.
Clinical Uses[edit]
Megestrol caproate is used in various clinical settings, including:
- Hormone replacement therapy
- Contraception
- Treatment of endometriosis
- Management of menstrual disorders
Side Effects[edit]
Common side effects of megestrol caproate include:
Synthesis[edit]
The synthesis of megestrol caproate involves the chemical modification of megestrol, incorporating a caproate ester group to enhance its pharmacological properties. This modification increases the drug's lipophilicity, allowing for a longer duration of action.
Related Compounds[edit]
Megestrol caproate is related to other progestins such as medroxyprogesterone acetate and norethindrone. These compounds share similar mechanisms of action but differ in their chemical structure and clinical applications.