Lewin G, Rolland Y, Privat S, Breugnot C, Lenaers A, Vilaine J P, Baltaze J P, Poisson J
Laboratoire de Pharmacognosie, Faculté de Pharmacie, Caen, France.
J Nat Prod. 1995 Dec;58(12):1840-7. doi: 10.1021/np50126a006.
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.