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|Title:||alpha1-Adrenoceptor Antagonists. Rational Design, Synthesis and Biological Evaluation of New Trazodone-like Compounds||Authors:||L., Betti
|Issue Date:||2002||Project:||None||Journal:||BIOORGANIC & MEDICINAL CHEMISTRY LETTERS||Abstract:||
A rational design approach has been applied to synthesize a novel class of compounds with affinity for α1 adrenergic receptors (AR). Molecular structures are characterized by a benzimidazolylpyridazinone or an imidazolylpyridazinone moiety, an original fragment in the field of the arylpiperazine compounds with α1-AR blocking properties. A 1.1 nM affinity toward α1-AR was found for compound 3, the most active of this series.
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