[11C] Methyl-losartan as a potential ligand for PET imaging angiotensin II AT1 receptors

被引:11
|
作者
Hadizad, Tayebeh [1 ]
Collins, Jeffrey [1 ]
Antoun, Rawad E. [1 ,2 ]
Beanlands, Rob S. [1 ,2 ]
DaSilva, Jean N. [1 ,2 ]
机构
[1] Univ Ottawa, Inst Heart, Cardiac PET Ctr, Ottawa, ON, Canada
[2] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
来源
JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS | 2011年 / 54卷 / 12期
基金
加拿大健康研究院;
关键词
tetrazol-protected losartan; C-11] methylation; HCl hydrolysis; cardiovascular disorder; ANTAGONIST; NONPEPTIDE; HYPERTENSION; SYSTEM;
D O I
10.1002/jlcr.1917
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The renin-angiotensin system regulates blood pressure via activation of the angiotensin II type 1 receptor (AT(1)R). The AT(1)R is involved in the pathology of cardiac and renal diseases such as heart failure and diabetic nephropathy. The aim of this study was to synthesize and characterize the O-[C-11] methylated derivative of the clinically used AT(1) receptor blocker losartan as a novel AT(1)R PET imaging radioligand. [C-11] Methyl-losartan was reliably synthesized (n >= 40) via methylation of tetrazole-protected losartan followed by deprotection using HCl in an overall yield of 30%-60% (decay-corrected from [C-11] Mel). Radiochemical purity was > 99% and specific activity 700-3600mCi/mu mol.
引用
收藏
页码:754 / 757
页数:4
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