Weight | 361.825 g/mol |
---|---|
Formula | C19H20ClNO4 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 7 |
bezafibrate (41859-67-0)
Cedur · BM15.075 · Regadrin B
Score:
#937 in Biochemistry
,
#2472 in Biology
,
#3085 in Chemistry
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- Angiographic assessment of effects of bezafibrate on progression of coronary artery disease in young male postinfarction patients. (The Lancet, 1996)
- Bezafibrate for the secondary prevention of myocardial infarction in patients with metabolic syndrome. (JAMA Internal Medicine, 2005)
- Abnormalities in very low, low and high density lipoproteins in hypertriglyceridemia. Reversal toward normal with bezafibrate treatment. (Journal of Clinical Investigation, 1984)
- Cardiovascular Outcomes in Type 2 Diabetes: A double-blind placebo-controlled study of bezafibrate: the St. Mary's, Ealing, Northwick Park Diabetes Cardiovascular Disease Prevention (SENDCAP) Study (Diabetes Care, 1998)
- Plasma concentrations of active lovastatin acid are markedly increased by gemfibrozil but not by bezafibrate. (Clinical Pharmacology & Therapeutics, 2001)
- Effects of bezafibrate, PPAR pan-agonist, and GW501516, PPAR agonist, on development of steatohepatitis in mice fed a methionine- and choline-deficient diet (European Journal of Pharmacology, 2006)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Cedur
- BM15.075
- Regadrin B
- Bfizal
- Beza Lande
- Befibrat
- Bezacur
- Beza Puren
- BezaLande
- BM 15.075
- Eulitop
- Solibay
- Lipox
- Bezabeta
- Difaterol
- Bezafibrat PB
- Azufibrat
- Bezamerck
- BezaPuren
- Sklerofibrat
- Bezafisal
- Reducterol
- durabezur
- Beza-Puren
- Bezalip
- BM-15.075
- Beza-Lande
-
SMILESCC(C)(C(=O)O)OC1=CC=C(C=C1)CCNC(=O)C2=CC=C(C=C2)Cl
-
InChIKeyIIBYAHWJQTYFKB-UHFFFAOYSA-N
- Pubchem - bezafibrate
- Wikipedia - bezafibrate
Bezafibrate (marketed as Bezalip and various other brand names) is a fibrate drug used as a lipid-lowering agent to treat hyperlipidaemia. It helps to lower LDL cholesterol and triglyceride in the blood, and increase HDL.
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Synthesis
4-CHLOROBENZOYL CHLORIDE
+
Propanoic acid, 2-[4-(2-aminoethyl)phenoxy]-2-methyl-
(Schotten-Baumann amide from acid)
4-CHLOROBENZAMIDE
+
Reactant
(Alkylation of primary amines)
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