Analogs of JHU75528, a PET ligand for imaging of cerebral cannabinoid receptors (CBI): Development of ligands with optimized lipophilicity and binding affinity

被引:13
作者
Fan, Hong [1 ]
Kotsikorou, Evangelia [2 ]
Hoffman, Alexander F. [3 ]
Ravert, Hayden T. [1 ]
Holt, Daniel [1 ]
Hurst, Dow P. [2 ]
Lupica, Carl R. [3 ]
Reggio, Patricia H. [2 ]
Dannals, Robert F. [1 ]
Horti, Andrew G. [1 ]
机构
[1] Johns Hopkins Univ Hosp, Sch Med, Dept Radiol, Div Nucl Med,PET Ctr, Baltimore, MD 21287 USA
[2] Univ N Carolina, Dept Chem & Biochem, Ctr Drug Discovery, Greensboro, NC 27402 USA
[3] NIDA, Intramural Res Program, Cellular Neurobiol Branch, Electrophysiol Res Unit, Baltimore, MD 21224 USA
关键词
Cannabinoid receptor; Carbon-11; JHU75528; Rimonabant; Positron emission tomography; Molecular modeling; Receptor docking; PREFRONTAL CORTEX; NUCLEUS-ACCUMBENS; F-18; SR144385; BRAIN; RADIOLIGANDS; LOCALIZATION; ANTAGONISTS; AGONIST; PHARMACOLOGY; RADIOTRACER;
D O I
10.1016/j.ejmech.2008.03.040
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cyano analogs of Rimonabant with high binding affinity for the cerebral cannabinoid receptor (CB1) and with optimized lipophilicity have been synthesized as potential positron emission tomography (PET) ligands. The best ligands of the series are optimal targets for the future radiolabeling with PET isotopes and in vivo evaluation as radioligands with enhanced properties for PET imaging of CB1 receptors in human subjects. Extracellular electrophysiological recordings in rodent brain slices demonstrated that JHU75528, 4, the lead compound of the new series, has functional CB antagonist properties that are consistent with its structural relationship to Rimonabant. Molecular modeling analysis revealed an important role of the binding of the cyano group with the CB1 binding pocket. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:593 / 608
页数:16
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