Trimetazidine
| Clinical data | |
|---|---|
| Trade names | Angintriz | 
| AHFS/Drugs.com | International Drug Names | 
| Routes of administration | Oral | 
| ATC code | |
| Legal status | |
| Legal status | 
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| Pharmacokinetic data | |
| Bioavailability | completely absorbed at around 5 hours, steady state is reached by 60th hour | 
| Protein binding | low (16%) | 
| Metabolism | minimal | 
| Elimination half-life | 7 to 12 hours | 
| Excretion | mainly renal (unchanged), exposure is increased in renal impairment – on average by four-fold in subjects with severe renal impairment (CrCl <30 ml/min) | 
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| CAS Number | |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.023.355 | 
| Chemical and physical data | |
| Formula | C14H22N2O3 | 
| Molar mass | 266.341 g·mol−1 | 
| 3D model (JSmol) | |
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| (what is this?) (verify) | |
Trimetazidine (IUPAC: 1-(2,3,4-trimethoxybenzyl)piperazine) is a drug sold under many brand names for angina pectoris (chest pain associated with impaired blood flow to the heart). Trimetazidine is described as the first cytoprotective anti-ischemic agent developed and marketed by Laboratoires Servier (France). It is an anti-ischemic (antianginal) metabolic agent of the fatty acid oxidation inhibitor class, meaning that it improves the heart muscle's ability to use glucose as a fuel by inhibiting its use of fatty acid metabolism. It has become controversial for its use as a performance-enhancing drug, with several scandals involving its use erupting at successive Olympic games.