Quinidine
Antiarrhythmic — CARDIOVASCULAR SYSTEM
Also known as: beta-Quinidine, chinidin, conchinin, conchinine, conquinine, pitayine, quincardine, quindine, quinidine gluconate, quinidine HCl, quinidine hydrochloride, quinidine hydrochloride monohydrate
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Quinidine is an ofp drug in the Antiarrhythmic class catalogued in DrugCentral. It was first approved by the FDA in 1950. Its mechanism of action is classified as Cytochrome P450 2D6 Inhibitors. DrugCentral lists 23 molecular targets, including CHRM2, CYP2D6 and KCNH2. Recorded indications include Atrial fibrillation, Cardioversion of Atrial Fibrillation, Life-Threatening Ventricular Tachycardia and Malaria.
- Approval status: ofp (first approved 1950 by the FDA).
- Drug class: Antiarrhythmic; Cytochrome P450 2D6 Inhibitor.
- Mechanism of action: Cytochrome P450 2D6 Inhibitors.
- Molecular targets: CHRM2, CYP2D6, KCNH2 and BCHE (23 listed in DrugCentral).
- Indications: Atrial fibrillation, Cardioversion of Atrial Fibrillation, Life-Threatening Ventricular Tachycardia, Malaria and Pseudobulbar affect.
- ATC code: C01BA01 (Antiarrhythmics, class Ia).
- Molecular formula: C20H24N2O2; molecular weight 324.42 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (5)
- Atrial fibrillation
- Cardioversion of Atrial Fibrillation
- Life-Threatening Ventricular Tachycardia
- Malaria
- Pseudobulbar affect
Contraindications (25)
- Anemia due to enzyme deficiency
- Bradycardia
- Chronic heart failure
- Complete atrioventricular block
- Congenital long QT syndrome
- Digitalis Toxicity with AV Conduction Defects
- Disease of liver
- Esophageal dysmotility
- Hypokalemia
- Hypomagnesemia
- Kidney disease
- Left bundle branch block
- Left heart failure
- Left ventricular hypertrophy
- Low blood pressure
- Myasthenia gravis
- Non-specific intraventricular conduction delay
- Partial atrioventricular block
- Poisoning by digitalis glycoside
- Poisoning by quinidine
- Prolonged QT interval
- Psoriasis
- Pulmonary emphysema
- Thrombocytopenic disorder
- Torsades de pointes
Mechanism & targets
| Mechanism of action (MoA) | Cytochrome P450 2D6 Inhibitors |
|---|---|
| Established pharmacologic class | Antiarrhythmic; Cytochrome P450 2D6 Inhibitor |
Molecular targets (23)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Muscarinic acetylcholine receptor M2 | CHRM2 | unknown | Ki 8.12 |
| Cytochrome P450 2D6 | CYP2D6 | inhibitor | Ki 7.92 |
| Potassium voltage-gated channel subfamily H member 2 | KCNH2 | unknown | IC50 6.49 |
| Cholinesterase | BCHE | unknown | IC50 5.91 |
| Potassium voltage-gated channel subfamily H member 1 | KCNH1 | blocker | IC50 5.80 |
| Potassium voltage-gated channel subfamily D member 2 | Kcnd2 | unknown | IC50 5.66 |
| Multidrug resistance protein 1 | ABCB1 | unknown | Ki 5.59 |
| Sodium channel alpha subunits; brain (Types I, II, III) | SCN1A|SCN2A|SCN3A | blocker | IC50 5.49 |
| Potassium voltage-gated channel subfamily A member 5 | KCNA5 | blocker | Kd 5.20 |
| Sodium channel protein type 5 subunit alpha | SCN5A | blocker | IC50 5.16 |
| Cholinesterase | BCHE | unknown | IC50 5.13 |
| Sodium channel protein type 5 subunit alpha | Scn5a | blocker | IC50 5.00 |
| Multidrug and toxin extrusion protein 1 | SLC47A1 | unknown | IC50 4.95 |
| Potassium voltage-gated channel subfamily A member 7 | KCNA7 | blocker | Kd 4.80 |
| Potassium channel subfamily T member 1 | KCNT1 | unknown | IC50 4.80 |
| Equilibrative nucleoside transporter 4 | SLC29A4 | inhibitor | Ki 4.60 |
| Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 | HCN4 | unknown | IC50 4.11 |
| Solute carrier family 22 member 2 | SLC22A2 | unknown | IC50 4.06 |
| Potassium channel subfamily T member 1 | Kcnt1 | blocker | IC50 4.00 |
| Sodium channel subunit beta-4 | SCN4B | unknown | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1950-07-12 | FDA | — | LILLY |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
C01BA01 | CARDIOVASCULAR SYSTEM › CARDIAC THERAPY › ANTIARRHYTHMICS, CLASS I AND III › Antiarrhythmics, class Ia |
C01BA51 | CARDIOVASCULAR SYSTEM › CARDIAC THERAPY › ANTIARRHYTHMICS, CLASS I AND III › Antiarrhythmics, class Ia |
C01BA71 | CARDIOVASCULAR SYSTEM › CARDIAC THERAPY › ANTIARRHYTHMICS, CLASS I AND III › Antiarrhythmics, class Ia |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- FDA label: CYP2D6
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 | 96.9 |
| Gliosis | 94.2 |
| Polyserositis | 90.4 |
| Premature menopause | 87.3 |
| Ovarian failure | 85.1 |
| Pouchitis | 83.9 |
| Somatic symptom disorder | 75.7 |
| Antiphospholipid syndrome | 74.5 |
| Venous thrombosis limb | 65.3 |
| Drug ineffective | 63.6 |
| Multiple-drug resistance | 54.8 |
| Cardiac tamponade | 54.1 |
Chemical structure
| Molecular formula | C20H24N2O2 |
|---|---|
| Molecular weight | 324.42 g/mol |
| CAS number | — |
| InChIKey | LOUPRKONTZGTKE-LHHVKLHASA-N |
| PubChem CID | 441074 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Quinidine used for?
DrugCentral lists the following indications for Quinidine: Atrial fibrillation, Cardioversion of Atrial Fibrillation, Life-Threatening Ventricular Tachycardia, Malaria and Pseudobulbar affect.
How does Quinidine work?
Quinidine is classified as Cytochrome P450 2D6 Inhibitors; its molecular targets in DrugCentral include CHRM2, CYP2D6 (inhibitor), KCNH2 and BCHE.
When was Quinidine first approved?
Quinidine was first approved by the FDA in 1950.
What drug class does Quinidine belong to?
Quinidine is in the Antiarrhythmic class.
What is the chemical formula of Quinidine?
Quinidine has the molecular formula C20H24N2O2 and a molecular weight of 324.42 g/mol.
Browse: all drugs starting with Q · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 2346 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1200437 — compound record and bioactivity
- PubChem CID 441074 — chemical identifiers
- DrugBank DB00908 — drug record
- FDA UNII ITX08688JL — substance identity
- DailyMed: FDA labels for Quinidine — current prescribing information (label search)
- UniProt P08172 (CHRM2) — target protein
- UniProt P10635 (CYP2D6) — target protein
- UniProt Q12809 (KCNH2) — target protein
- UniProt P06276 (BCHE) — target protein
- UniProt O95259 (KCNH1) — target protein
- UniProt P08183 (ABCB1) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
- PharmGKB / CPIC — pharmacogenomic label annotations
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