Vernakalant Hydrochloride

CHEMBL2107383 Phase 4 Одобрено Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
385.9 g/mol
LogP
Phase
4

Vernakalant hydrochloride is the hydrochloride salt of vernakalant, an atrial-selective antiarrhythmic agent approved for rapid cardioversion of recent-onset atrial fibrillation. It blocks atrial-specific potassium channels (IKur, IKAch) and sodium channels with use-dependent kinetics, terminating AF while sparing ventricular myocardium. The intravenous hydrochloride salt formulation enables rapid administration in clinical settings for acute AF management.

Молекулярная масса

385,9000 g/mol

TPSA

51,20 Ų

Терапевтические области

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D Структура

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SMILES

COc1ccc(CCO[C@@H]2CCCC[C@H]2N2CC[C@@H](O)C2)cc1OC.Cl

InChI

InChI=1S/C20H31NO4.ClH/c1-23-19-8-7-15(13-20(19)24-2)10-12-25-18-6-4-3-5-17(18)21-11-9-16(22)14-21;/h7-8,13,16-18,22H,3-6,9-12,14H2,1-2H3;1H/t16-,17-,18-;/m1./s1

Molecular Formula

C20H32ClNO4

HBD / HBA

2 / 5

Вращаемые Связи

7

Тяжёлые Атомы

26

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.

Часто задаваемые вопросы

Vernakalant hydrochloride is the hydrochloride salt of vernakalant, an atrial-selective antiarrhythmic agent approved for rapid cardioversion of recent-onset atrial fibrillation. It blocks atrial-specific potassium channels (IKur, IKAch) and sodium channels with use-dependent kinetics, terminating AF while sparing ventricular myocardium. The intravenous hydrochloride salt formulation enables rapid administration in clinical settings for acute AF management.

Yes, Vernakalant 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). CHEMBL2107383. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 9930048. Chemical information database.

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

Медицинский отказ от ответственности

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.