U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of ETOFIBRATE

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

HIDE SMILES / InChI
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.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q07869
Gene ID: 5465.0
Gene Symbol: PPARA
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
LIPO-MERZ RETARD

Approved Use

Lipo-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.
Primary
LIPO-MERZ RETARD

Approved Use

Lipo-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

PubMed

TitleDatePubMed
Human health risk assessment of pharmaceuticals in water: issues and challenges ahead.
2010-11
Methods of chromatographic determination of medicines decreasing the level of cholesterol.
2010-09-30
[Efficacy and safety of etofibrate in patients with non-proliferative diabetic retinopathy].
2009-07
Etofibrate enhances 123I-LDL-binding in human liver.
2009-02-07
Determination of etofibrate, fenofibrate, and atorvastatin in pharmaceutical preparations and plasma using differential pulse polarographic and square wave voltammetric techniques.
2008-11-05
Substituted tertiary phosphine Ru(II) organometallics: catalytic utility on the hydrolysis of etofibrate in pharmaceuticals.
2008-10
Peroxisome proliferator activated receptors and lipoprotein metabolism.
2008
High performance liquid chromatographic determination of etofibrate and its hydrolysis products.
2007-01-04
Fenofibrate: a novel formulation (Triglide) in the treatment of lipid disorders: a review.
2006
Influence of etofibrate on LDL-subtype distribution in patients with diabetic dyslipoproteinemia.
2003-09
Mass spectrometric monitoring of the degradation and elimination efficiency for hardly eliminable and hardly biodegradable polar compounds by membrane bioreactors.
2002
Effects of etofibrate upon the metabolism of chylomicron-like emulsions in patients with coronary artery disease.
2001-02-01
Etofibrate but not controlled-release niacin decreases LDL cholesterol and lipoprotein (a) in type IIb dyslipidemic subjects.
2001-02
Treatment of dyslipoproteinemia in the metabolic syndrome.
2001
Studies with etofibrate in the rat. Part I: Effects on glycerol, free fatty acid and triacylglycerol metabolism.
1988-11-04
Mitochondrial myopathy--a result of clofibrate/etofibrate treatment? Case report.
1985
Patents

Patents

Sample Use Guides

The recommended dose is 1 sustained-release capsule (500 mg) once daily. In special cases, up to 2 sustained-release capsules can be prescribed.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
ETOFIBRATE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
ETOFIBRATE [MI]
Preferred Name English
ETOFIBRATE [MART.]
Common Name English
Etofibrate [WHO-DD]
Common Name English
2-HYDROXYETHYL NICOTINATE 2-(P-CHLOROPHENOXY)-2-METHYLPROPIONATE (ESTER)
Common Name English
etofibrate [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QC10AB09
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
WHO-ATC C10AB09
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
NCI_THESAURUS C98150
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
Code System Code Type Description
INN
3616
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID80185521
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
SMS_ID
100000082103
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
DRUG BANK
DB08983
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
ECHA (EC/EINECS)
250-743-1
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
CAS
31637-97-5
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
PUBCHEM
65777
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
EVMPD
SUB07321MIG
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
WIKIPEDIA
ETOFIBRATE
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
MESH
C009746
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
ChEMBL
CHEMBL358150
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
NCI_THESAURUS
C65588
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
RXCUI
24609
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY RxNorm
FDA UNII
23TF67G79M
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
DRUG CENTRAL
1106
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY
MERCK INDEX
m5193
Created by admin on Mon Mar 31 18:21:41 GMT 2025 , Edited by admin on Mon Mar 31 18:21:41 GMT 2025
PRIMARY Merck Index