Dofetilide
Antiarrhythmic — CARDIOVASCULAR SYSTEM
Also known as: tikosyn, UK 68798, UK-68,798
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Dofetilide is an ofp drug in the Antiarrhythmic class catalogued in DrugCentral. It was first approved by the FDA in 1999. DrugCentral lists 3 molecular targets, including KCNH2, KCNH1 and KCNK2. Recorded indications include Atrial fibrillation, Cardioversion of Atrial Fibrillation and Cardioversion of Atrial Flutter.
- Approval status: ofp (first approved 1999 by the FDA).
- Drug class: Antiarrhythmic.
- Molecular targets: KCNH2, KCNH1 and KCNK2 (3 listed in DrugCentral).
- Indications: Atrial fibrillation, Cardioversion of Atrial Fibrillation and Cardioversion of Atrial Flutter.
- ATC code: C01BD04 (Antiarrhythmics, class III).
- Molecular formula: C19H27N3O5S2; molecular weight 441.56 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (3)
- Atrial fibrillation
- Cardioversion of Atrial Fibrillation
- Cardioversion of Atrial Flutter
Contraindications (12)
- Acute nephropathy
- Anorexia nervosa
- Congenital long QT syndrome
- Disease of liver
- Hyperhidrosis
- Hypokalemia
- Hypomagnesemia
- Kidney disease
- Prolonged QT interval
- Severe diarrhea
- Torsades de pointes
- Vomiting
Mechanism & targets
| Established pharmacologic class | Antiarrhythmic |
|---|
Molecular targets (3)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Potassium voltage-gated channel subfamily H member 2 | KCNH2 | blocker | Ki 8.19 |
| Potassium voltage-gated channel subfamily H member 1 | KCNH1 | blocker | IC50 7.50 |
| Potassium channel subfamily K member 2 | KCNK2 | unknown | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1999-10-01 | FDA | — | PFIZER |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
C01BD04 | CARDIOVASCULAR SYSTEM › CARDIAC THERAPY › ANTIARRHYTHMICS, CLASS I AND III › Antiarrhythmics, class III |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Electrocardiogram QT prolonged | 962.9 |
| Torsade de pointes | 504.7 |
| Ventricular tachycardia | 313.3 |
| Atrial fibrillation | 271.9 |
| Death | 244.8 |
| Arrhythmia | 155.4 |
| Palpitations | 116.7 |
| Ventricular fibrillation | 112.1 |
| Cardiac arrest | 88.2 |
| Therapy cessation | 86.6 |
| Atrial flutter | 83.3 |
| Cardioversion | 80.7 |
Chemical structure
| Molecular formula | C19H27N3O5S2 |
|---|---|
| Molecular weight | 441.56 g/mol |
| CAS number | 115256-11-6 |
| InChIKey | IXTMWRCNAAVVAI-UHFFFAOYSA-N |
| PubChem CID | 71329 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Dofetilide used for?
DrugCentral lists the following indications for Dofetilide: Atrial fibrillation, Cardioversion of Atrial Fibrillation and Cardioversion of Atrial Flutter.
How does Dofetilide work?
Its molecular targets in DrugCentral include KCNH2 (blocker), KCNH1 (blocker) and KCNK2.
When was Dofetilide first approved?
Dofetilide was first approved by the FDA in 1999.
What drug class does Dofetilide belong to?
Dofetilide is in the Antiarrhythmic class.
What is the chemical formula of Dofetilide?
Dofetilide has the molecular formula C19H27N3O5S2 and a molecular weight of 441.56 g/mol.
Browse: all drugs starting with D · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 942 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL473 — compound record and bioactivity
- PubChem CID 71329 — chemical identifiers
- DrugBank DB00204 — drug record
- FDA UNII R4Z9X1N2ND — substance identity
- DailyMed: FDA labels for Dofetilide — current prescribing information (label search)
- UniProt Q12809 (KCNH2) — target protein
- UniProt O95259 (KCNH1) — target protein
- UniProt O95069 (KCNK2) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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