Prazepam

CHEMBL969 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
324.8 g/mol
LogP
3.6
Phase
4

Prazepam is a long-acting benzodiazepine anxiolytic that potentiates the inhibitory neurotransmitter GABA at the GABA-A receptor by allosterically enhancing chloride ion conductance, producing anxiolytic, sedative, anticonvulsant, and muscle relaxant effects. It serves as a prodrug, being converted to the active metabolite desmethyldiazepam (nordazepam), and is used for the treatment of anxiety disorders.

分子量

324.8000 g/mol

LogP

3.60

TPSA

32.70 Ų

Lipinski 五规则

符合

作用机制

Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

机制

Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.

二维结构

SVG PNG

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SMILES

O=C1CN=C(c2ccccc2)c2cc(Cl)ccc2N1CC1CC1

InChI

InChI=1S/C19H17ClN2O/c20-15-8-9-17-16(10-15)19(14-4-2-1-3-5-14)21-11-18(23)22(17)12-13-6-7-13/h1-5,8-10,13H,6-7,11-12H2

Molecular Formula

C19H17ClN2O

HBD / HBA

- / 2

可旋转键数

3

重原子数

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.

常见问题

Prazepam is a long-acting benzodiazepine anxiolytic that potentiates the inhibitory neurotransmitter GABA at the GABA-A receptor by allosterically enhancing chloride ion conductance, producing anxiolytic, sedative, anticonvulsant, and muscle relaxant effects. It serves as a prodrug, being converted to the active metabolite desmethyldiazepam (nordazepam), and is used for the treatment of anxiety disorders.

Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.

Yes, Prazepam is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL969. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 4890. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

医疗免责声明

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.