首页 | 本学科首页   官方微博 | 高级检索  
检索        


5-substituted derivatives of 6-halogeno-3-((2-(S)-azetidinyl)methoxy)pyridine and 6-halogeno-3-((2-(S)-pyrrolidinyl)methoxy)pyridine with low picomolar affinity for alpha4beta2 nicotinic acetylcholine receptor and wide range of lipophilicity: potential probes for imaging with positron emission tomography
Authors:Zhang Yi  Pavlova Olga A  Chefer Svetlana I  Hall Andrew W  Kurian Varughese  Brown LaVerne L  Kimes Alane S  Mukhin Alexey G  Horti Andrew G
Institution:Neuroimaging Research Branch, Intramural Research Program, National Institute on Drug Abuse, NIH, DHHS, 5500 Nathan Shock Drive, Baltimore, Maryland 21224, USA.
Abstract:Potential positron emission tomography (PET) ligands with low picomolar affinity at the nicotinic acetylcholine receptor (nAChR) and with lipophilicity (log D) ranging from -1.6 to +1.5 have been synthesized. Most members of the series, which are derivatives of 5-substituted-6-halogeno-A-85380, exhibited a higher binding affinity at alpha4beta2-nAChRs than epibatidine. An analysis, by molecular modeling, revealed an important role of the orientation of the additional heterocyclic ring on the binding affinity of the ligands with nAChRs. The existing nicotinic pharmacophore models do not accommodate this finding. Two compounds of the series, 6-(18)F]fluoro-5-(pyridin-3-yl)-A-85380 ((18)F]31) and 6-chloro-3-((2-(S)-azetidinyl)methoxy)-5-(2-(18)F]fluoropyridin-5-yl)pyridine) ((18)F]35), were radiolabeled with (18)F. Comparison of PET data for (18)F]31 and 2-(18)F]FA shows the influence of lipophilicity on the binding potential. Our recent PET studies with (18)F]35 demonstrated that its binding potential values in Rhesus monkey brain were ca. 2.5 times those of 2-(18)F]FA. Therefore, (18)F]35 and several other members of the series, when radiolabeled, will be suitable for quantitative imaging of extrathalamic nAChRs.
Keywords:
本文献已被 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号