The synthesis and pharmacological properties of a novel type of vasorelaxan
t hybrid compounds are described. The investigated compounds are based on f
luorinated 4-aryl-1,4-dihydropyridines (1,4-DHP), which are known calcium c
hannel blockers, and/or from fluorinated analogues of pinacidil, an opener
of ATP-sensitive potassium channels. Benzimidazole analogues of hypotensive
preparation losartan with fluorine-containing substituents in positions 2
and 5, as well as at heterocyclic nitrogen atom of benzimidazole ring are d
iscussed. (C) 2001 Elsevier Science B.V. All rights reserved.