Bepridil Hydrochloride

CHEMBL1200382 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
403.0 g/mol
LogP
Phase
4

The hydrochloride salt of bepridil, a calcium channel blocker historically used for angina and heart rhythm disorders. It was withdrawn from widespread clinical use due to its risk of causing life-threatening ventricular arrhythmias, particularly in patients with underlying heart conditions. It remains a reference compound in cardiac research.

Peso molecular

403,0000 g/mol

TPSA

15,70 Ų

Áreas terapéuticas

Mecanismo de acción

Blocks L-type voltage-gated calcium channels in vascular smooth muscle and cardiac myocytes, reducing calcium influx during depolarization. This produces vasodilation, decreased myocardial contractility, and reduced heart rate.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Blocks L-type voltage-gated calcium channels in vascular smooth muscle and cardiac myocytes, reducing calcium influx during depolarization. This produces vasodilation, decreased myocardial contractility, and reduced heart rate.

Estructura 2D

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SMILES

CC(C)COCC(CN(Cc1ccccc1)c1ccccc1)N1CCCC1.Cl.O

InChI

InChI=1S/C24H34N2O.ClH.H2O/c1-21(2)19-27-20-24(25-15-9-10-16-25)18-26(23-13-7-4-8-14-23)17-22-11-5-3-6-12-22;;/h3-8,11-14,21,24H,9-10,15-20H2,1-2H3;1H;1H2

Molecular Formula

C24H35ClN2O

HBD / HBA

1 / 3

Enlaces Rotables

10

Átomos Pesados

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.

Preguntas frecuentes

The hydrochloride salt of bepridil, a calcium channel blocker historically used for angina and heart rhythm disorders. It was withdrawn from widespread clinical use due to its risk of causing life-threatening ventricular arrhythmias, particularly in patients with underlying heart conditions. It remains a reference compound in cardiac research.

Blocks L-type voltage-gated calcium channels in vascular smooth muscle and cardiac myocytes, reducing calcium influx during depolarization. This produces vasodilation, decreased myocardial contractility, and reduced heart rate.

Yes, Bepridil Hydrochloride 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). CHEMBL1200382. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 50088. Chemical information database.

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

Aviso médico

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.