PMID: 2136916Jan 1, 1990Paper

Synthesis and characterization of iodobenzamide analogues: potential D-2 dopamine receptor imaging agents

Journal of Medicinal Chemistry
R A MurphyJ Billings

Abstract

(S)-N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-3-iodo-6- methoxybenzamide ([123I]IBZM) is a central nervous system (CNS) D-2 dopamine receptor imaging agent. In order to investigate the versatility of this parent structure in specific dopamine receptor localization and the potential for developing new dopamine receptor imaging agents, a series of new iodinated benzamides with fused ring systems, naphthalene (INAP) and benzofuran (IBF), was synthesized and radiolabeled, and the in vivo and in vitro biological properties were characterized. The best analogue of IBZM is IBF (21). The specific binding of [125I]IBF (21) with rat striatal tissue preparation was found to be saturable and displayed a Kd of 0.106 +/- 0.015 nM. Competition data of various receptor ligands for [125I]IBF (21) binding show the following rank order of potency: spiperone greater than IBF (21) greater than IBZM greater than (+)-butaclamol greater than (+/-)-ADTN,6,7 greater than ketanserin greater than SCH-23390 much greater than propranolol. The in vivo biodistribution results confirm that [125I]IBF (21) concentrated in the striatal area after iv injection into rats. The study demonstrates that [123I]IBF (21) is a potential agent for imaging CNS D-2 dopamin...Continue Reading

Citations

Jan 1, 1996·Nuclear Medicine and Biology·C H van DyckR B Innis
Mar 12, 2003·Bioorganic & Medicinal Chemistry·Younong YuEdmond J LaVoie
Jan 1, 1991·The Journal of Pharmacy and Pharmacology·V SoskićJ Petrović
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Nov 13, 2008·Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism·Kazuhiro ShibaHirofumi Mori
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