Desmethylflunitrazepam

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Desmethylflunitrazepam[edit | edit source]

Chemical structure of Desmethylflunitrazepam

Desmethylflunitrazepam is a benzodiazepine derivative and an active metabolite of flunitrazepam, commonly known by the brand name Rohypnol. It is known for its sedative, anxiolytic, muscle relaxant, and anticonvulsant properties. Desmethylflunitrazepam is primarily used in the context of its parent compound, flunitrazepam, which is a potent hypnotic agent.

Pharmacology[edit | edit source]

Desmethylflunitrazepam acts on the central nervous system by enhancing the effect of the neurotransmitter gamma-aminobutyric acid (GABA) at the GABA_A receptor. This action results in increased neuronal inhibition, leading to the sedative and anxiolytic effects characteristic of benzodiazepines.

Metabolism[edit | edit source]

Desmethylflunitrazepam is formed in the body as a result of the metabolism of flunitrazepam. The primary metabolic pathway involves the N-demethylation of flunitrazepam, which is catalyzed by the cytochrome P450 enzyme system in the liver. This metabolite retains pharmacological activity and contributes to the overall effects of flunitrazepam.

Clinical Use[edit | edit source]

While desmethylflunitrazepam itself is not marketed as a separate pharmaceutical product, its presence is significant in the context of flunitrazepam use. Flunitrazepam is prescribed for the short-term treatment of severe insomnia and is sometimes used as a premedication in surgical procedures due to its strong sedative effects.

Legal Status[edit | edit source]

Due to its association with flunitrazepam, desmethylflunitrazepam is subject to similar legal restrictions. Flunitrazepam is classified as a Schedule IV controlled substance under the Controlled Substances Act in the United States and is similarly regulated in many other countries due to concerns about its potential for abuse and its use in drug-facilitated crimes.

Related Pages[edit | edit source]


Benzodiazipines[edit source]

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