Zipeprol
Zipeprol is a centrally acting antitussive agent that suppresses cough through mechanisms involving both central opioid receptor activity and local anesthetic properties, rather than acting primarily on the cough center as codeine does. It has been used in some countries for symptomatic relief of non-productive cough associated with respiratory tract infections. Its potential for abuse and dependence due to opioid-related psychotropic effects led to restrictions or withdrawal in many markets.
Molecular Weight
384.5000 g/mol
LogP
2.20
TPSA
45.20 Ų
Lipinski RO5
Pass
Mechanism of Action
Blocks voltage-gated sodium channels in nerve cell membranes, preventing the generation and conduction of nerve impulses. This produces reversible loss of sensation in the area of application.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Blocks voltage-gated sodium channels in nerve cell membranes, preventing the generation and conduction of nerve impulses. This produces reversible loss of sensation in the area of application.
2D Structure
Cite this structure
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SMILES
COC(CN1CCN(CC(O)C(OC)c2ccccc2)CC1)c1ccccc1
InChI
InChI=1S/C23H32N2O3/c1-27-22(19-9-5-3-6-10-19)18-25-15-13-24(14-16-25)17-21(26)23(28-2)20-11-7-4-8-12-20/h3-12,21-23,26H,13-18H2,1-2H3
Molecular Formula
C23H32N2O3
HBD / HBA
1 / 5
Rotatable Bonds
9
Heavy Atoms
28
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.
Frequently Asked Questions
Zipeprol is a centrally acting antitussive agent that suppresses cough through mechanisms involving both central opioid receptor activity and local anesthetic properties, rather than acting primarily on the cough center as codeine does. It has been used in some countries for symptomatic relief of non-productive cough associated with respiratory tract infections. Its potential for abuse and dependence due to opioid-related psychotropic effects led to restrictions or withdrawal in many markets.
Blocks voltage-gated sodium channels in nerve cell membranes, preventing the generation and conduction of nerve impulses. This produces reversible loss of sensation in the area of application.
Yes, Zipeprol 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). CHEMBL2105497. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 36910. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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