5-[3-(4-Arylpiperazin-1-yl) propyl]-1H-benzimidazoles and 5-[2-(4-arylpiperazin-1-yl) ethoxy]- 1H-benzimidazoles were synthesized and their affinity for the D1, D2 and 5-HT1A receptors examined. They expressed a rather high affinity for the D2 dopamine receptor. The main features of ligand–D2 receptor interactions revealed by docking analyses were: salt bridge between piperazine ring protonated N1 and Asp 86, hydrogen bonds of ligand ...