- Bezafibrate
drugbox
IUPAC_name = 2- [4- [2- [(4-chlorobenzoyl)amino]
ethyl] phenoxy] -2-methyl-propanoic acid
width = 145px
CAS_number = 41859-67-0
ATC_prefix = C10
ATC_suffix = AB02
ATC_supplemental=
PubChem = 39042
DrugBank =
chemical_formula =
C=19 | H=20 | N=1 | I= | Br= | Cl=1 | F= | O=4 | P= | S= | Se= | Na=
molecular_weight = 361.819
bioavailability =
protein_bound =
metabolism =
elimination_half-life =
excretion =
pregnancy_category =
legal_status = RX/POM
dependency_liability = N/A
routes_of_administration = oralBezafibrate (Bezalip and various other brand names) is a
fibrate drug used for the treatment ofhyperlipidaemia . It helps to lower LDL cholesterol andtriglyceride in theblood , and increase HDL.History
Bezafibrate was first introduced by
Boehringer Mannheim in 1977.Mode of action
Like the other fibrates, bezafibrate is an agonist of PPARα; some studies suggest it may have some activity on PPARγ and PPARδ as well.
Uses
Bezafibrate improves markers of
combined hyperlipidemia , effectively reducing LDL and triglycerides and improving HDL levels. [Secondary prevention by raising HDL cholesterol and reducing triglycerides in patients with coronary artery disease: the Bezafibrate Infarction Prevention (BIP) study. "Circulation" 2000;102:21-7. PMID 10880410.] The main effect on cardiovascular morbidity is in patients with themetabolic syndrome , the features of which are attenuated by bezafibrate. [Tenenbaum A, Motro M, Fisman EZ, Tanne D, Boyko V, Behar S. Bezafibrate for the secondary prevention of myocardial infarction in patients with metabolic syndrome. "Arch Intern Med" 2005;165:1154-60. PMID 15911729.] Studies show that in patients with impaired glucose tolerance, bezafibrate may delay progress to diabetes [Tenenbaum A, Motro M, Fisman EZ, Schwammenthal E, Adler Y, Goldenberg I, Leor J, Boyko V, Mandelzweig L, Behar S. Peroxisome proliferator-activated receptor ligand bezafibrate for prevention of type 2 diabetes mellitus in patients with coronary artery disease. "Circulation" 2004;109:2197-202. PMID 15123532] , and in those withinsulin resistance it slowed progress in the HOMA severity marker. [Tenenbaum A, Fisman EZ, Boyko V, Benderly M, Tanne D, Haim M, Matas Z, Motro M, Behar S. Attenuation of progression of insulin resistance in patients with coronary artery disease by bezafibrate. "Arch Intern Med" 2006;166:737-41. PMID 16606809.]ide-effects
The main toxicity is hepatic (abnormal liver enzymes), and
myopathy and rarelyrhabdomyolysis have been reported.Other uses
The Australian biotech company
Giaconda combines bezafibrate withchenodeoxycholic acid in an anti-hepatitis C drug combination called Hepaconda.References
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