Mexiletine
| Systematic (IUPAC) name | |
|---|---|
| (RS)-1-(2,6-dimethylphenoxy)propan-2-amine OR 2-(2-aminopropoxy)-1,3-dimethylbenzene |
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| Clinical data | |
| AHFS/Drugs.com | monograph |
| MedlinePlus | a607064 |
| Pregnancy cat. | B1 (AU) C (US) |
| Legal status | POM (UK) |
| Routes | Oral, IV |
| Pharmacokinetic data | |
| Bioavailability | 90% |
| Protein binding | 50-60% |
| Metabolism | Hepatic (CYP2D6 and 1A2- mediated) |
| Half-life | 10-12 hours |
| Excretion | Renal (10%) |
| Identifiers | |
| CAS number | 31828-71-4 |
| ATC code | C01BB02 |
| PubChem | CID 4178 |
| IUPHAR ligand | 2629 |
| DrugBank | DB00379 |
| ChemSpider | 4034 |
| UNII | 1U511HHV4Z |
| KEGG | D08215 |
| ChEBI | CHEBI:6916 |
| ChEMBL | CHEMBL558 |
| Chemical data | |
| Formula | C11H17NO |
| Mol. mass | 179.259 g/mol |
| SMILES | eMolecules & PubChem |
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Mexiletine (INN, sold under the trade name Mexitil) belongs to the Class IB anti-arrhythmic group of medicines. It is used to treat arrhythmias within the heart, or seriously irregular heartbeats. It slows conduction in the heart and makes the heart tissue less sensitive. Dizziness, heartburn, nausea, nervousness, trembling, unsteadiness are common side effects. It is available in injection and capsule form.
Class IB antiarrhythmics decrease action potential duration by shortening the repolarization phase. This is achieved by blocking sodium channels.1
Mexiletine may also be of use in patients experiencing refractory pain2 and is also effective for treating muscle stiffness resulting from myotonia congenita (Thomsen disease) or myotonic dystrophy (Steinert's disease).
References
- ^ Mexiletine, RxList.com
- ^ Sweetman S (ed.) (2002). Martindale: The complete drug reference (33rd ed.). London: Pharmaceutical Press. ISBN 0-85369-499-0.
Further reading
- Peck T; Hill S, Williams M (eds.) (2004). Pharmacology for Anaesthesia and Intensive Care (2nd ed.). Cambridge University Press. ISBN 0-521-68794-2.
External links
- MedlinePlus Drug Information: Mexiletine
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