Vernakalant

drug
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Also known as Vernakalant (Hydrochloride)

Summary

Vernakalant (CHEMBL2111112) is an approved small molecule (ATC C01BG11); indicated across 3 conditions including atrial fibrillation and atrial flutter.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: C01BG11
  • Indications: 3 conditions
  • Clinical trials: 8
  • Chemistry: 349.5 Da · C20H31NO4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2111112
NameVernakalant
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID9930049
ATCC01BG11
Molecular formulaC20H31NO4
Molecular weight349.5
InChIKeyVBHQKCBVWWUUKN-KZNAEPCWSA-N

SMILES: COC1=C(C=C(C=C1)CCO[C@@H]2CCCC[C@H]2N3CC[C@H](C3)O)OC

IUPAC name: (3R)-1-[(1R,2R)-2-[2-(3,4-dimethoxyphenyl)ethoxy]cyclohexyl]pyrrolidin-3-ol

Also known as: Vernakalant, VERNAKALANT, vernakalant, Vernakalant (Hydrochloride)

Parent form; salt/anhydrous children: CHEMBL2107383

Patent coverage: 96 distinct patent families (262 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Sodium-dependent serotonin transporter.

Bioactivity

ChEMBL activities: 1 potent at pChembl ≥ 5 of 1 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
SLC6A45.98AC501040nMCHEMBL_ACT_25151846

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

3 indications (1 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
atrial fibrillation3MONDO:0004981EFO:0000275
atrial flutter2MONDO:0005310EFO:0003911

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 8.

Phase distribution

PhaseTrials
PHASE44
PHASE33
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01627106PHASE4WITHDRAWNA Study Comparing Vernakalant Therapy to Amiodarone Therapy in Acute Management of Recent Onset Atrial Fibrillation (AF) (MK-6621-055)
NCT01646281PHASE4UNKNOWNVernakalant Versus Flecainide: Atrial Contractility
NCT03005366PHASE4COMPLETEDPredictive Factors to Effectively Terminate Paroxysmal Atrial Fibrillation by Blocking Atrial Selective Ionic Currents
NCT04485195PHASE4COMPLETEDRAFF4 Trial: Vernakalant vs. Procainamide for Acute Atrial Fibrillation in the Emergency Department
NCT04748991PHASE3NOT_YET_RECRUITINGVernakalant Versus Amiodarone for Post-operative Atrial Fibrillation in Cardiac Surgery Patients
NCT00668759PHASE3COMPLETEDA Phase III Superiority Study of Vernakalant vs Amiodarone in Subjects With Recent Onset Atrial Fibrillation
NCT00989001PHASE3TERMINATEDA Phase 3b Study of Vernakalant Injection in Patients With Recent Onset Symptomatic Atrial Fibrillation (AF)(MK-6621-045)
NCT01370629Not specifiedCOMPLETEDStudy of Normal Conditions of Use, Dosing, and Safety of Intravenous (IV) Administration of Vernakalant (MK-6621-049)

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).