This article may be too technical for most readers to understand.(February 2022) |
Clinical data | |
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AHFS/Drugs.com | International Drug Names |
Routes of administration | Oral |
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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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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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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).[1] 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.