Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H18ClNO5 |
| Molecular Weight | 363.792 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(OC1=CC=C(Cl)C=C1)C(=O)OCCOC(=O)C2=CN=CC=C2
InChI
InChIKey=XXRVYAFBUDSLJX-UHFFFAOYSA-N
InChI=1S/C18H18ClNO5/c1-18(2,25-15-7-5-14(19)6-8-15)17(22)24-11-10-23-16(21)13-4-3-9-20-12-13/h3-9,12H,10-11H2,1-2H3
Etofibrate is an ethylene glycol diester of clofibrate and nicotinic acid. The drug was used under the names Tricerol and Lipo-Merz, among the others, for the treatment of severe hypertriglyceridemia and mixed hyperlipidemia. The mechanism of etofibrate action implies activation of PPAR-alpha receptors.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: Q07869 Gene ID: 5465.0 Gene Symbol: PPARA Target Organism: Homo sapiens (Human) Sources: http://www.google.com/patents/WO2003088962A1 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | LIPO-MERZ RETARD Approved UseLipo-Merz retard is indicated as an adjuvant treatment for a diet or other non-drug therapies (eg exercise, weight loss) for the following diseases: (1) severe hypertriglyceridemia; (2) mixed hyperlipidemia. |
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| Primary | LIPO-MERZ RETARD Approved UseLipo-Merz retard is indicated as an adjuvant treatment for a diet or other non-drug therapies (eg exercise, weight loss) for the following diseases: (1) severe hypertriglyceridemia; (2) mixed hyperlipidemia. |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Human health risk assessment of pharmaceuticals in water: issues and challenges ahead. | 2010-11 |
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| Methods of chromatographic determination of medicines decreasing the level of cholesterol. | 2010-09-30 |
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| [Efficacy and safety of etofibrate in patients with non-proliferative diabetic retinopathy]. | 2009-07 |
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| Etofibrate enhances 123I-LDL-binding in human liver. | 2009-02-07 |
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| Determination of etofibrate, fenofibrate, and atorvastatin in pharmaceutical preparations and plasma using differential pulse polarographic and square wave voltammetric techniques. | 2008-11-05 |
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| Substituted tertiary phosphine Ru(II) organometallics: catalytic utility on the hydrolysis of etofibrate in pharmaceuticals. | 2008-10 |
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| Peroxisome proliferator activated receptors and lipoprotein metabolism. | 2008 |
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| High performance liquid chromatographic determination of etofibrate and its hydrolysis products. | 2007-01-04 |
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| Fenofibrate: a novel formulation (Triglide) in the treatment of lipid disorders: a review. | 2006 |
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| Influence of etofibrate on LDL-subtype distribution in patients with diabetic dyslipoproteinemia. | 2003-09 |
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| Mass spectrometric monitoring of the degradation and elimination efficiency for hardly eliminable and hardly biodegradable polar compounds by membrane bioreactors. | 2002 |
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| Effects of etofibrate upon the metabolism of chylomicron-like emulsions in patients with coronary artery disease. | 2001-02-01 |
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| Etofibrate but not controlled-release niacin decreases LDL cholesterol and lipoprotein (a) in type IIb dyslipidemic subjects. | 2001-02 |
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| Treatment of dyslipoproteinemia in the metabolic syndrome. | 2001 |
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| Studies with etofibrate in the rat. Part I: Effects on glycerol, free fatty acid and triacylglycerol metabolism. | 1988-11-04 |
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| Mitochondrial myopathy--a result of clofibrate/etofibrate treatment? Case report. | 1985 |
Patents
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Preferred Name | English | ||
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NCI_THESAURUS |
C98150
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ETOFIBRATE
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ACTIVE MOIETY