Dimestrol: Difference between revisions

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[[Category:Synthetic estrogens]]
[[Category:Synthetic estrogens]]
[[Category:Hormone replacement therapy]]
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File:Dimestrol.svg|Dimestrol
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Revision as of 01:01, 20 February 2025

Overview of the synthetic estrogen Dimestrol


Dimestrol
INN
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PubChem
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Dimestrol is a synthetic estrogen that was historically used in hormone replacement therapy and for other medical purposes. It is a derivative of diethylstilbestrol (DES), a nonsteroidal estrogen.

Chemical Structure

Dimestrol is a stilbestrol derivative, characterized by its two phenolic rings connected by a carbon-carbon double bond. The chemical structure of Dimestrol is similar to that of diethylstilbestrol, with modifications that affect its pharmacological properties.

Pharmacology

Dimestrol acts as an agonist of the estrogen receptor, mimicking the effects of natural estrogens in the body. It binds to estrogen receptors in various tissues, leading to the activation of estrogen-responsive genes. This action is responsible for its effects on the reproductive system, bone density, and other estrogen-sensitive tissues.

Medical Uses

Historically, Dimestrol was used in the treatment of menopausal symptoms, such as hot flashes and vaginal atrophy. It was also used in certain cases of hypogonadism and delayed puberty in females. However, due to concerns about the safety of synthetic estrogens, its use has declined.

Safety and Side Effects

Like other synthetic estrogens, Dimestrol has been associated with an increased risk of thromboembolic events, breast cancer, and other estrogen-related side effects. The use of Dimestrol and similar compounds has been largely replaced by safer alternatives in modern medical practice.

History

Dimestrol was developed in the mid-20th century as part of a broader effort to create effective synthetic estrogens. It was one of several compounds used in hormone replacement therapy before the risks associated with synthetic estrogens became widely recognized.

Related Compounds

Dimestrol is chemically related to other synthetic estrogens, such as diethylstilbestrol and hexestrol. These compounds share a similar mechanism of action but differ in their pharmacokinetic properties and safety profiles.

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