Radiolabeled Small Molecule Protein Kinase Inhibitors for Imaging with PET or SPECT

被引:54
|
作者
Hicks, Justin W. [1 ]
VanBrocklin, Henry F. [2 ]
Wilson, Alan A. [3 ]
Houle, Sylvain [3 ]
Vasdev, Neil [1 ,3 ]
机构
[1] Univ Toronto, Dept Psychiat, Toronto, ON M5T 1R8, Canada
[2] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94107 USA
[3] Ctr Addict & Mental Hlth, PET Ctr, Toronto, ON M5T 1R8, Canada
来源
MOLECULES | 2010年 / 15卷 / 11期
关键词
molecular imaging; protein kinase; small molecules inhibitors; positron emission tomography; single photon emission computer tomography; GROWTH-FACTOR RECEPTOR; POSITRON-EMISSION-TOMOGRAPHY; TYROSINE KINASE; ANILINOQUINAZOLINE DERIVATIVES; BIOLOGICAL EVALUATION; EGFR INHIBITORS; CAPTIVE SOLVENT; VIVO EVALUATION; C-11; BIODISTRIBUTION;
D O I
10.3390/molecules15118260
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Imaging protein kinase expression with radiolabeled small molecule inhibitors has been actively pursued to monitor the clinical potential of targeted therapeutics and treatments as well as to determine kinase receptor density changes related to disease progression. The goal of the present review is to provide an overview of the breadth of radiolabeled small molecules that have been synthesized to target intracellular protein kinases, not only for imaging in oncology, but also for other areas of interest, particularly the central nervous system. Considerable radiotracer development has focused on imaging receptor tyrosine kinases of growth factors, protein kinases A, B and C, and glycogen synthase kinase-3 beta. Design considerations, structural attributes and relevant biological results are summarized.
引用
收藏
页码:8260 / 8278
页数:19
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