Abstract
The novel flavones 6-28, which display structural analogies with the two well-known lipid peroxidation inhibitors, probucol [1] and butylated hydroxytoluene [2], were synthesized and studied in vitro for their ability to inhibit the copper sulfate or endothelial cell-induced lipid peroxidation of human low-density lipoprotein (LDL). Most of the flavones were active in the range of 0.1-1 microM.
MeSH terms
-
Antioxidants / chemical synthesis*
-
Antioxidants / pharmacology*
-
Flavonoids / chemical synthesis*
-
Flavonoids / pharmacology
-
Humans
-
In Vitro Techniques
-
Lipid Peroxidation / drug effects*
-
Lipoproteins, LDL / chemistry*
-
Magnetic Resonance Spectroscopy
-
Oxidation-Reduction
-
Thiobarbituric Acid Reactive Substances / chemistry
Substances
-
Antioxidants
-
Flavonoids
-
Lipoproteins, LDL
-
Thiobarbituric Acid Reactive Substances