Guanidine−Acylguanidine Bioisosteric Approach in the Design of Radioligands: Synthesis of a Tritium-Labeled<i>N</i><sup>G</sup>-Propionylargininamide ([<sup>3</sup>H]-UR-MK114) as a Highly Potent and Selective Neuropeptide Y Y<sub>1</sub>Receptor Antagonist
Max Keller(University of Regensburg), Armin Buschauer(University of Regensburg), Christoph Hutzler(University of Regensburg), Annette G. Beck‐Sickinger(Leipzig University of Applied Sciences), Nathalie Pop(University of Regensburg), Günther Bernhardt(University of Regensburg)
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