Novel quinoxaline derivatives for in vivo imaging of β-amyloid plaques in the brain

被引:29
作者
Cui, Mengchao [1 ,2 ]
Ono, Masahiro [1 ]
Kimura, Hiroyuki [1 ]
Liu, Boli [2 ]
Saji, Hideo [1 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
[2] Beijing Normal Univ, Key Lab Radiopharmaceut, Minist Educ, Coll Chem, Beijing 100875, Peoples R China
基金
日本学术振兴会;
关键词
Alzheimer's disease; beta-Amyloid; Imaging agent; Binding assay; Autoradiography; ALZHEIMERS-DISEASE; RADIOLIGAND; BIODISTRIBUTION; HYPOTHESIS; DOSIMETRY;
D O I
10.1016/j.bmcl.2011.05.079
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In a search for new probes to detect beta-amyloid plaques in the brain of patients with Alzheimer's disease (AD), we have synthesized and evaluated a series of quinoxaline derivatives containing a '6+6-6' ring system. These quinoxaline derivatives showed excellent affinity for A beta(1) (42) aggregates with K(i) values ranging from 2.6 to 10.7 nM. Autoradiography with sections of brain tissue from an animal model of AD mice (APP/PS1) and AD patients revealed that [(125)I]5 labeled beta-amyloid plaques specifically. In biodistribution experiments using normal mice, [(125)I]5 displayed high uptake (6.03% ID/g at 2 min) into and a moderately fast washout from the brain. Although additional refinements are needed to decrease the lipophilicity and improve the washout rate, the quinoxaline scaffold may be useful as a backbone structure to develop novel beta-amyloid imaging agents. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4193 / 4196
页数:4
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