Flumedroxone acetate

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Flumedroxone Acetate is a synthetic, steroidal progestin that was never marketed. It is a derivative of progesterone and was synthesized in the late 1960s.

Chemistry[edit | edit source]

Flumedroxone acetate, also known as 6α-fluoro-17α-hydroxyprogesterone acetate, is a synthetic pregnane steroid and a derivative of progesterone. It is specifically a derivative of 17α-hydroxyprogesterone with a fluorine atom at the C6α position and an acetate group at the C17α position.

Pharmacology[edit | edit source]

As a progestin, flumedroxone acetate has progestogenic activity. It binds to and activates the progesterone receptor, thereby exerting its effects. Progestogens like flumedroxone acetate are responsible for changes in the endometrium that prepare it for implantation of a fertilized egg and maintenance of pregnancy.

History[edit | edit source]

Flumedroxone acetate was synthesized in the late 1960s as part of a series of modifications to progesterone aimed at improving its pharmacological properties. Despite its synthesis and initial study, it was never marketed.

See also[edit | edit source]

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