Synthesis, biological evaluation and radiolabelling by 18F-fluoroarylation of a dopamine D3-selective ligand as prospective imaging probe for PET
作者:S.B. Höfling、S. Maschauer、H. Hübner、P. Gmeiner、H.-J. Wester、O. Prante、M.R. Heinrich
DOI:10.1016/j.bmcl.2010.09.142
日期:2010.12
Radical F-18-fluoroarylation with fluorine-18-labelled arenediazonium chlorides has been successfully applied to the radiochemical synthesis of the dopamine D-3-selective ligand SH 317 ([F-18]8). SH 317 has been evaluated as a new PET ligand candidate by in vivo experiments. (C) 2010 Elsevier Ltd. All rights reserved.