Volinanserin
| Clinical data | |
|---|---|
| Other names | MDL-100,907; MDL-100907; MDL100907; M100907; M-100907; M-100,907 |
| Routes of administration | Oral |
| Drug class | Serotonin 5-HT2A receptor antagonist |
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| Pharmacokinetic data | |
| Onset of action | Tmax: 1–2.5 hours |
| Elimination half-life | 6.6 hours (range 4.5–9.8 hours) |
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| IUPHAR/BPS | |
| ChemSpider | |
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| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.123.797 |
| Chemical and physical data | |
| Formula | C22H28FNO3 |
| Molar mass | 373.468 g·mol−1 |
| 3D model (JSmol) | |
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Volinanserin (INN; developmental code MDL-100,907) is a highly selective 5-HT2A receptor antagonist that is frequently used in scientific research to investigate the function of the 5-HT2A receptor. It was also tested in clinical trials as a potential antipsychotic, antidepressant, and treatment for insomnia but was never marketed. The drug reached phase 3 trials for schizophrenia and insomnia prior to the discontinuation of its development in the late 2000s. It is taken orally.