Synthesis and biological evaluation of 2-aminothiazoles and their amide derivatives on human adenosine receptors.: Lack of effect of 2-aminothiazoles as allosteric enhancers

被引:34
|
作者
Göblyös, A [1 ]
Santiago, SN [1 ]
Pietra, D [1 ]
Mulder-Krieger, T [1 ]
Künzel, JVD [1 ]
Brussee, J [1 ]
Ijzerman, AP [1 ]
机构
[1] Leiden Amsterdam Ctr Drug Res, Div Med Chem, NL-2300 RA Leiden, Netherlands
关键词
2-aminothiazoles; adenosine receptors; allosteric modulation; antagonism;
D O I
10.1016/j.bmc.2005.01.006
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
A number of 2-aminothiazoles (2a-e) and their amide derivatives (4-10) were prepared. The 2-aminothiazoles themselves were tested as allosteric enhancers of agonist binding to human adenosine A, receptors. In a variety of experimental set-ups the compounds did not show any such effect, in contrast to earlier findings by another research group. Subsequently the 2-aminothiazoles were used as intermediates in the synthesis of a number of amide derivatives of either aromatic (4-6) or aliphatic nature (7-10). Some of the compounds emerged as moderately active antagonists on human adenosine A(1) and/or A(2A) receptors with lower or negligible potency at adenosine A(3) receptors. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2079 / 2087
页数:9
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