Pipamperone
| Clinical data | |
|---|---|
| Trade names | Dipiperon | 
| Other names | Carpiperone, floropipamide, fluoropipamide, floropipamide hydrochloride (JAN), McN-JR 3345; R-3345 | 
| AHFS/Drugs.com | International Drug Names | 
| Routes of administration | Oral | 
| ATC code | |
| Legal status | |
| Legal status | 
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| Pharmacokinetic data | |
| Elimination half-life | 17-22 hours | 
| Duration of action | 0.5-1 hour | 
| Identifiers | |
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| IUPHAR/BPS | |
| DrugBank | |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.119.828 | 
| Chemical and physical data | |
| Formula | C21H30FN3O2 | 
| Molar mass | 375.488 g·mol−1 | 
| 3D model (JSmol) | |
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| (what is this?) (verify) | |
Pipamperone (INN, USAN, BAN), sold under the brand name Dipiperon, is a typical antipsychotic of the butyrophenone family used in the treatment of schizophrenia and as a sleep aid for depression. It is or has been marketed under brand names including Dipiperon, Dipiperal, Piperonil, Piperonyl, and Propitan. Pipamperone was discovered at Janssen Pharmaceutica in 1961, and entered clinical trials in the United States in 1963.