Flunitrazolam

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Flunitrazolam is a benzodiazepine derivative that is structurally related to flunitrazepam and triazolam. It is known for its potent sedative, hypnotic, and anxiolytic properties. Flunitrazolam is not approved for medical use in many countries and is often encountered in the context of recreational drug use.

Chemical Structure and Properties[edit | edit source]

Flunitrazolam belongs to the benzodiazepine class of drugs, which are characterized by their core chemical structure: a benzene ring fused to a diazepine ring. The chemical formula of flunitrazolam is C17H12FN5O2, and its molecular weight is 337.31 g/mol. The compound features a fluorine atom at the 2' position of the benzene ring and a triazole ring fused to the diazepine ring.

Pharmacology[edit | edit source]

Flunitrazolam 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 its sedative and anxiolytic effects. The drug has a high affinity for the GABA_A receptor, which contributes to its potency.

Effects and Uses[edit | edit source]

The primary effects of flunitrazolam include:

Due to its high potency, flunitrazolam is often used in very small doses. It is not commonly prescribed in clinical settings due to the risk of dependence, tolerance, and abuse.

Legal Status[edit | edit source]

Flunitrazolam is classified as a controlled substance in many countries. Its legal status varies, but it is generally subject to strict regulations due to its potential for abuse and lack of approved medical use.

Side Effects[edit | edit source]

Common side effects of flunitrazolam include:

In cases of overdose, flunitrazolam can cause severe respiratory depression, coma, and even death.

History[edit | edit source]

Flunitrazolam was first synthesized in the late 20th century as part of research into new benzodiazepine derivatives. Despite its potent effects, it has not been widely adopted for medical use.

See Also[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD