Flunitrazepam
This potent benzodiazepine has strong sedative, hypnotic, and muscle-relaxant properties and has been used medically for severe insomnia and as a pre-anesthetic agent. Due to its potential for misuse and association with drug-facilitated assault, it is tightly controlled or banned in many countries.
الوزن الجزيئي
313,2800 g/mol
LogP
2,10
TPSA
78,50 Ų
قاعدة ليبينسكي للخمسة
ناجح
آلية العمل
Enhances the effect of gamma-aminobutyric acid (GABA) at GABA-A receptors by binding to an allosteric site and increasing the frequency of chloride ion channel opening. This produces anxiolytic, sedative, hypnotic, and anticonvulsant effects.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Enhances the effect of gamma-aminobutyric acid (GABA) at GABA-A receptors by binding to an allosteric site and increasing the frequency of chloride ion channel opening. This produces anxiolytic, sedative, hypnotic, …
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
CN1C(=O)CN=C(c2ccccc2F)c2cc([N+](=O)[O-])ccc21
InChI
InChI=1S/C16H12FN3O3/c1-19-14-7-6-10(20(22)23)8-12(14)16(18-9-15(19)21)11-4-2-3-5-13(11)17/h2-8H,9H2,1H3
Molecular Formula
C16H12FN3O3
HBD / HBA
- / 5
الروابط القابلة للدوران
1
الذرات الثقيلة
23
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
الأسئلة الشائعة
This potent benzodiazepine has strong sedative, hypnotic, and muscle-relaxant properties and has been used medically for severe insomnia and as a pre-anesthetic agent. Due to its potential for misuse and association with drug-facilitated assault, it is tightly controlled or banned in many countries.
Enhances the effect of gamma-aminobutyric acid (GABA) at GABA-A receptors by binding to an allosteric site and increasing the frequency of chloride ion channel opening. This produces anxiolytic, sedative, hypnotic, and anticonvulsant effects.
Yes, Flunitrazepam is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL13280. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 3380. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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