Dienestrol diacetate: Difference between revisions
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{{DISPLAYTITLE:Dienestrol diacetate}} | |||
== | == Overview == | ||
Dienestrol diacetate | [[File:Dienestrol_diacetate.svg|thumb|right|Chemical structure of dienestrol diacetate]] | ||
'''Dienestrol diacetate''' is a synthetic nonsteroidal estrogen of the [[stilbestrol]] group, which is related to [[diethylstilbestrol]]. It is an [[acetate ester]] of [[dienestrol]], and it has been used in [[hormone replacement therapy]] and for the treatment of [[menopausal symptoms]]. | |||
== | == Chemical Properties == | ||
Dienestrol diacetate | Dienestrol diacetate is characterized by its chemical structure, which includes two acetate groups attached to the dienestrol molecule. This modification enhances its [[lipophilicity]], allowing for better absorption and prolonged action in the body. | ||
== | == Mechanism of Action == | ||
As an estrogen, dienestrol diacetate binds to and activates the [[estrogen receptor]]s in various tissues. This activation leads to the transcription of estrogen-responsive genes, which are involved in the regulation of the [[reproductive system]], [[bone density]], and [[lipid metabolism]]. | |||
== | == Clinical Uses == | ||
Dienestrol diacetate has been used primarily in the management of menopausal symptoms such as [[hot flashes]], [[vaginal atrophy]], and [[osteoporosis]]. It has also been used in certain cases of [[hypogonadism]] and [[ovarian failure]]. | |||
== | == Side Effects == | ||
The use of dienestrol diacetate, like other estrogens, can be associated with side effects such as [[nausea]], [[breast tenderness]], and an increased risk of [[thromboembolic events]]. Long-term use may also be associated with an increased risk of [[endometrial cancer]] and [[breast cancer]]. | |||
== Pharmacokinetics == | |||
Dienestrol diacetate is administered orally and is metabolized in the liver. The acetate groups are hydrolyzed to release the active dienestrol, which then exerts its estrogenic effects. The drug is excreted primarily in the urine. | |||
== Related Compounds == | |||
* [[Diethylstilbestrol]] | |||
* [[Estradiol]] | |||
* [[Ethinylestradiol]] | |||
== Related Pages == | |||
* [[Estrogen]] | * [[Estrogen]] | ||
* [[Hormone replacement therapy]] | * [[Hormone replacement therapy]] | ||
* [[ | * [[Menopause]] | ||
[[Category:Estrogens]] | [[Category:Estrogens]] | ||
[[Category: | [[Category:Hormones]] | ||
[[Category:Pharmacology]] | |||
Latest revision as of 06:36, 16 February 2025
Overview[edit]

Dienestrol diacetate is a synthetic nonsteroidal estrogen of the stilbestrol group, which is related to diethylstilbestrol. It is an acetate ester of dienestrol, and it has been used in hormone replacement therapy and for the treatment of menopausal symptoms.
Chemical Properties[edit]
Dienestrol diacetate is characterized by its chemical structure, which includes two acetate groups attached to the dienestrol molecule. This modification enhances its lipophilicity, allowing for better absorption and prolonged action in the body.
Mechanism of Action[edit]
As an estrogen, dienestrol diacetate binds to and activates the estrogen receptors in various tissues. This activation leads to the transcription of estrogen-responsive genes, which are involved in the regulation of the reproductive system, bone density, and lipid metabolism.
Clinical Uses[edit]
Dienestrol diacetate has been used primarily in the management of menopausal symptoms such as hot flashes, vaginal atrophy, and osteoporosis. It has also been used in certain cases of hypogonadism and ovarian failure.
Side Effects[edit]
The use of dienestrol diacetate, like other estrogens, can be associated with side effects such as nausea, breast tenderness, and an increased risk of thromboembolic events. Long-term use may also be associated with an increased risk of endometrial cancer and breast cancer.
Pharmacokinetics[edit]
Dienestrol diacetate is administered orally and is metabolized in the liver. The acetate groups are hydrolyzed to release the active dienestrol, which then exerts its estrogenic effects. The drug is excreted primarily in the urine.