Ethynerone: Difference between revisions

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== Ethynerone ==
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Latest revision as of 01:04, 20 February 2025

File:Progestin-induced tumors in beagle dogs.png

Ethynerone is a synthetic progestogen that was developed in the mid-20th century. It is a derivative of testosterone and is structurally related to other synthetic progestogens such as norethisterone and ethisterone. Ethynerone was primarily investigated for its potential use in hormonal contraception and hormone replacement therapy.

Chemical Structure[edit]

Ethynerone belongs to the class of 19-nortestosterone derivatives. Its chemical structure is characterized by the presence of an ethynyl group at the 17α position of the steroid nucleus, which is a common feature among many synthetic progestogens. This modification enhances the oral bioavailability and progestogenic activity of the compound.

Mechanism of Action[edit]

As a progestogen, ethynerone exerts its effects by binding to the progesterone receptors in target tissues. This binding mimics the action of natural progesterone, leading to changes in the endometrium that are necessary for the maintenance of pregnancy and the regulation of the menstrual cycle. Ethynerone also has some degree of androgenic activity due to its structural similarity to testosterone.

Clinical Uses[edit]

Ethynerone was investigated for several clinical applications, including:

However, ethynerone was not widely adopted in clinical practice, and its use has been largely supplanted by other synthetic progestogens with more favorable profiles.

Side Effects[edit]

The side effects of ethynerone are similar to those of other synthetic progestogens and may include:

History and Development[edit]

Ethynerone was developed during the 1950s and 1960s, a period of significant advancements in the field of synthetic progestogens. The development of ethynerone and related compounds was driven by the need for effective and reliable hormonal contraceptives and hormone replacement therapies.

See Also[edit]

References[edit]

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External Links[edit]


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