|Elimination half-life||~42 hours|
|Chemical and physical data|
|Molar mass||319.185 g/mol g·mol−1|
|3D model (JSmol)|
|(what is this?)|
Diclazepam (Ro5-3448), also known as chlorodiazepam and 2′-chloro-diazepam, is a benzodiazepine and functional analog of diazepam. It was first synthesized by Leo Sternbach and his team at Hoffman-La Roche in 1960. It is not currently approved for use as a medication, but rather sold as an unscheduled substance. Efficacy and safety have not been tested in humans.
Metabolism of this compound has been assessed, revealing diclazepam has an approximate elimination half-life of 42 hours and undergoes N-demethylation to delorazepam, which can be detected in urine for 6 days following administration of the parent compound. Other metabolites detected were lorazepam and lormetazepam which were detectable in urine for 19 and 11 days, respectively, indicating hydroxylation by cytochrome P450 enzymes occurring concurrently with N-demethylation.
- Delorazepam (Nordiclazepam)
- Ro5-4864 (4′-Chlorodiazepam)
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- ‹See Tfd›US 3136815, ”Amino substituted benzophenone oximes and derivatives thereof”
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- “The Misuse of Drugs Act 1971 (Amendment) Order 2017”.