2006 (v1)
Publication
We report the design and synthesis of a new class of piperazine-pyridazinone analogs. The arylpiperazine moiety, the length of the spacer, and the terminal mol. fragment were varied to evaluate their influence in detg. the affinity of the new compds. toward the α1-adrenergic receptor (α1-AR), α2-adrenergic receptor (α2-AR), and the 5-HT1A...
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