228088-38-8Relevant articles and documents
Synthesis and biological activity of some new flavonyl-2,4-thiazolidinediones
Bozdag-Duendar, Oya,Verspohl, Eugen J.,Das-Evcimen, Net,Kaup, Rebecca M.,Bauer, Katrin,Sarikaya, Mutlu,Evranos, Beguem,Ertan, Rahmiye
, p. 6747 - 6751 (2008/12/23)
A new series of flavonyl-2,4-thiazolidinediones (Va-c, VIa-c) was prepared by Knoevenagel reaction. The synthesized compounds were tested for their ability to inhibit rat kidney aldose reductase (AR) and for their insulinotropic activities in INS-1 cells.
Synthesis of some 4-[3' or 4'-(4 H-4-oxo-1-benzopyran-2-yl)phenyl]-1,4- dihydropyridine derivatives as potential calcium channel antagonists
Tuncbilek,Ertan
, p. 255 - 259 (2007/10/03)
In this study, the synthesis of new flavonoid derivatives, which possess a 1,4-dihydropyridine (1,4-DHP) moiety on the phenyl ring of flavone were realized. 3' or 4'-Formyl-flavones were synthesized, then the aldehyde groups of these compounds were converted to the 1,4-DHP moiety by the Hantzsch method. A series of 23 new derivatives having different substituents at C-3 and C-5 of the 1,4-DHP ring were prepared. Two compounds (8a, 8b) were tested for their calcium channel blocker activity and 8b exhibited the best result.