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The acetylcholine receptor is an essential link between the brain and the muscles, so it is a sensitive location for attack. In this study, some reversible [diethylenetriaminepentaacetic acid–(amino acid)2] have been docked computationally to the active site of the acetylcholine receptor. The induced fit method was employed to perform the automolecular docking for these systems. The result of docking studies generated thermodynamic properties, such as free energy of bindings (Glide score) and their weak electrostatic interactions. On the basis of these results, scintigraphic imaging studies were performed in mice. Among the radiotracers evaluated in this study, compound derived from 5-hydroxytryptophan/tryptophan exhibited remarkable localization in the brain, whereas radiotracer derived from L-histidine shows moderate accumulation in the brain. Preliminary studies with these amino acid–based ligands are encouraging to carrying out further in vivo experiments for targeted imaging

molecular imaging

Design and Docking Studies of [Diethylenetriaminepentaacetic Acid–(Amino Acid)<sub>2</sub>] with Acetylcholine Receptor as a Molecular Imaging Agent for Single-Photon Emission Computed Tomographic Application

Design and Docking Studies of [Diethylenetriaminepentaacetic Acid–(Amino Acid)2] with Acetylcholine Receptor as a Molecular Imaging Agent for Single-Photon Emission Computed Tomographic Application

Design and Docking Studies of [Diethylenetriaminepentaacetic Acid–(Amino Acid)₂] with Acetylcholine Receptor as a Molecular Imaging Agent for Single-Photon Emission Computed Tomographic Application