摘要
可逆地结合放射性和正电子发射断层扫描(PET) 在体内脑蛋白质如酶、神经递质转运蛋白、受体和离子通道成像的发展,对生物医学神经精神疾病研究和药物发现和开发十分重要,但是基于目前的药物化学水平这是十分困难的。本文主要讨论了被科学家所考虑的脑靶蛋白PET显像放射性配体的发展。
关键词: PET,放射性配体,分子成像、正电子发射体、碳11、氟18、转运、血脑屏障
Current Medicinal Chemistry
Title:Considerations in the Development of Reversibly Binding PET Radioligands for Brain Imaging
Volume: 23 Issue: 18
Author(s): Victor W. Pike
Affiliation:
关键词: PET,放射性配体,分子成像、正电子发射体、碳11、氟18、转运、血脑屏障
摘要: The development of reversibly binding radioligands for imaging brain proteins in vivo, such as enzymes, neurotransmitter transporters, receptors and ion channels, with positron emission tomography (PET) is keenly sought for biomedical studies of neuropsychiatric disorders and for drug discovery and development, but is recognized as being highly challenging at the medicinal chemistry level. This article aims to compile and discuss the main considerations to be taken into account by chemists embarking on programs of radioligand development for PET imaging of brain protein targets.
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Cite this article as:
Victor W. Pike , Considerations in the Development of Reversibly Binding PET Radioligands for Brain Imaging, Current Medicinal Chemistry 2016; 23 (18) . https://dx.doi.org/10.2174/0929867323666160418114826
DOI https://dx.doi.org/10.2174/0929867323666160418114826 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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