Cyclobenzaprine Hydrochloride

CHEMBL1200636 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
311.8 g/mol
LogP
Phase
4

The hydrochloride salt form of cyclobenzaprine, a central muscle relaxant used for short-term relief of muscle spasms and pain. It reduces muscle hyperactivity through central nervous system depression without directly affecting muscles or the neuromuscular junction.

Molekularmasse

311,8000 g/mol

TPSA

3,20 Ų

Therapeutische Bereiche

Wirkmechanismus

Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.

2D-Struktur

SVG PNG

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SMILES

CN(C)CCC=C1c2ccccc2C=Cc2ccccc21.Cl

InChI

InChI=1S/C20H21N.ClH/c1-21(2)15-7-12-20-18-10-5-3-8-16(18)13-14-17-9-4-6-11-19(17)20;/h3-6,8-14H,7,15H2,1-2H3;1H

Molecular Formula

C20H22ClN

HBD / HBA

1 / 1

Rotierbare Bindungen

3

Schwere Atome

22

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.

Häufig gestellte Fragen

The hydrochloride salt form of cyclobenzaprine, a central muscle relaxant used for short-term relief of muscle spasms and pain. It reduces muscle hyperactivity through central nervous system depression without directly affecting muscles or the neuromuscular junction.

Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.

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

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200636. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 22576. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Medizinischer Haftungsausschluss

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.