Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9769296 | European Journal of Medicinal Chemistry | 2005 | 11 Pages |
Abstract
The synthesis of unsubstituted and halogen substituted 5-arylidene basic amide derivatives of imidazolidine-2,4-dione is described. Structural elucidation based on X-ray analysis was performed for four representative compounds. The effect of the studied compounds on the electrocardiogram was examined in vitro in the non-working heart perfusion test and that of an anti-arrhythmic activity in the rat coronary artery ligation-reperfusion model. The most active compound: (5Z)-(3-chloro)benzylidene-3-{2-[4-(hydroxyethyl)piperazin-1-yl]-2-oxoethyl}imidazolidine-2,4-dione has shown properties of the compounds belonging to class Ia, according to the Vaughan Williams classification. Chosen compounds evaluated in vivo were devoid of anticonvulsant and neurotoxical activity.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Elżbieta PÄkala, Katarzyna Stadnicka, Agnieszka Broda, MaÅgorzata Zygmunt, Barbara Filipek, Katarzyna KieÄ-Kononowicz,