Ipsapirone

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Ipsapirone


Ipsapirone is an anxiolytic and serotonin agonist of the azapirone chemical class. It was first developed in the 1980s by Bristol-Myers Squibb, a multinational pharmaceutical company. Ipsapirone is primarily used in the treatment of anxiety disorders, although it has also been investigated for use in the treatment of other conditions such as depression and schizophrenia.

Chemistry[edit | edit source]

Ipsapirone belongs to the azapirone class of compounds, which are characterized by their pyrimidinylpiperazine component. The chemical structure of ipsapirone is similar to that of other azapirones such as buspirone and gepirone, which also have anxiolytic and serotonin agonist properties.

Pharmacology[edit | edit source]

Ipsapirone acts as a selective 5-HT1A receptor agonist, meaning it binds to and activates this specific subtype of serotonin receptor. The 5-HT1A receptor is involved in various neurological processes, including anxiety, depression, sleep, and cognition. By activating this receptor, ipsapirone can exert anxiolytic and antidepressant effects.

Clinical Use[edit | edit source]

Ipsapirone has been used in the treatment of generalized anxiety disorder (GAD). It has been shown to reduce symptoms of anxiety, such as restlessness, tension, and worry. In addition to its use in GAD, ipsapirone has been investigated for potential use in the treatment of depression and schizophrenia, although more research is needed in these areas.

Side Effects[edit | edit source]

Like all medications, ipsapirone can cause side effects. Common side effects include dizziness, headache, and nausea. Less common side effects can include changes in mood or behavior, such as agitation, confusion, or hallucinations. If these or any other side effects occur, they should be reported to a healthcare provider immediately.

See Also[edit | edit source]


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Contributors: Prab R. Tumpati, MD