Quazepam
| Clinical data | |
|---|---|
| Trade names | Doral |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a684001 |
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| Routes of administration | By mouth |
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| Pharmacokinetic data | |
| Bioavailability | 29–35% |
| Metabolism | Liver |
| Elimination half-life | 39 hours |
| Excretion | Kidney |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.048.329 |
| Chemical and physical data | |
| Formula | C17H11ClF4N2S |
| Molar mass | 386.79 g·mol−1 |
| 3D model (JSmol) | |
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| (what is this?) (verify) | |
Quazepam, sold under the brand name Doral among others, is a relatively long-acting benzodiazepine derivative drug developed by the Schering Corporation in the 1970s. Quazepam is used for the treatment of insomnia, including sleep induction and sleep maintenance. Quazepam induces impairment of motor function and has relatively (and uniquely) selective hypnotic and anticonvulsant properties with considerably less overdose potential than other benzodiazepines (due to its novel receptor-subtype selectivity). Quazepam is an effective hypnotic which induces and maintains sleep without disruption of the sleep architecture.
It was patented in 1970 and came into medical use in 1985.