Dimepregnen

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Dimepregnen is a synthetic, steroidal progestogen with antigonadotropic effects, which was developed by Schering AG in the 1960s but was never marketed. It is a derivative of progesterone and is related to other 19-norprogesterone derivatives such as gestronol, gestonorone, gestonorone caproate, and nomegestrol acetate.

Chemistry[edit | edit source]

Dimepregnen is a synthetic steroid and a derivative of progesterone. It is more specifically a derivative of 17α-hydroxyprogesterone and is a member of the 19-norprogesterone and 17α-hydroxyprogesterone groups of progestogens. Dimepregnen is closely related to gestronol (17α-hydroxy-19-norprogesterone), gestonorone (17α-hydroxy-19-norprogesterone 3-cyclopentyl enol ether), gestonorone caproate (17α-hydroxy-19-norprogesterone 3-cyclopentyl enol ether caproate), and nomegestrol acetate (17α-hydroxy-6-methyl-19-norprogesterone acetate).

Pharmacology[edit | edit source]

As a progestogen, dimepregnen has antigonadotropic effects. It works by binding to and activating the progesterone receptor, which inhibits the release of gonadotropin-releasing hormone from the hypothalamus. This in turn suppresses the release of follicle-stimulating hormone and luteinizing hormone from the anterior pituitary, thereby inhibiting ovulation and preventing pregnancy.

History[edit | edit source]

Dimepregnen was developed by the pharmaceutical company Schering AG in the 1960s. Despite its development, it was never marketed for medical use.

See also[edit | edit source]

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Contributors: Prab R. Tumpati, MD