Bivalent Ligands for the Serotonin 5-HT3 Receptor

被引:12
|
作者
Cappelli, Andrea [1 ,2 ]
Manini, Monica [1 ,2 ]
Paolino, Marco [1 ,2 ]
Gallelli, Andrea [1 ,2 ]
Anzini, Maurizio [1 ,2 ]
Mennuni, Laura [3 ]
Del Cadia, Marta [4 ]
De Rienzo, Francesca [4 ,5 ]
Menziani, M. Cristina [4 ]
Vomero, Salvatore [1 ,2 ]
机构
[1] Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy
[2] Univ Siena, European Res Ctr Drug Discovery & Dev, I-53100 Siena, Italy
[3] Rottapharm Madaus, I-20052 Monza, Italy
[4] Univ Modena & Reggio Emilia, Dipartimento Chim, I-41100 Modena, Italy
[5] CNR, Ist Nanosci, Ctr S3, I-41125 Modena, Italy
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2011年 / 2卷 / 08期
关键词
Serotonin receptors; 5-HT3; bivalent ligands; multivalency; molecular modeling; BINDING; RECOGNITION; DOMAIN; SITES;
D O I
10.1021/ml2000388
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The serotonin 5-HT3 receptor is a ligand-gated ion channel, which by virtue of its pentameric architecture, can be considered to be an intriguing example of intrinsically multivalent biological receptors. This paper describes a general design approach to the study of multivalency in this multimeric ion channel. Bivalent ligands for 5-HT3 receptor have been designed by linking an arylpiperazine moiety to probes showing. different functional features. Both homobivalent and heterobivalent ligands have shown 5-HT3 receptor affinity in the nanomolar range, providing evidence for the viability of our design approach. Moreover, the high affinity shown by homobivalent ligands suggests that bivalency is a promising approach in 5-HT3 receptor modulation and provides the rational basis for applying the concepts of multivalency to the study of 5-HT3 receptor function.
引用
收藏
页码:571 / 576
页数:6
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