Cyclobenzaprine Hydrochloride
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.
分子量
311.8000 g/mol
TPSA
3.20 Ų
治疗领域
作用机制
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)
Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.
二维结构
Cite this structure
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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
可旋转键数
3
重原子数
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.
常见问题
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.
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.
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