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Bivalent Ligands for the Serotonin 5-HT3 Receptor.
Cappelli, Andrea; Manini, Monica; Paolino, Marco; Gallelli, Andrea; Anzini, Maurizio; Mennuni, Laura; Del Cadia, Marta; De Rienzo, Francesca; Menziani, M Cristina; Vomero, Salvatore.
Afiliação
  • Cappelli A; Dipartimento Farmaco Chimico Tecnologico and European Research Centre for Drug Discovery and Development, Università di Siena , Via A. Moro, 53100 Siena, Italy.
  • Manini M; Dipartimento Farmaco Chimico Tecnologico and European Research Centre for Drug Discovery and Development, Università di Siena , Via A. Moro, 53100 Siena, Italy.
  • Paolino M; Dipartimento Farmaco Chimico Tecnologico and European Research Centre for Drug Discovery and Development, Università di Siena , Via A. Moro, 53100 Siena, Italy.
  • Gallelli A; Dipartimento Farmaco Chimico Tecnologico and European Research Centre for Drug Discovery and Development, Università di Siena , Via A. Moro, 53100 Siena, Italy.
  • Anzini M; Dipartimento Farmaco Chimico Tecnologico and European Research Centre for Drug Discovery and Development, Università di Siena , Via A. Moro, 53100 Siena, Italy.
  • Mennuni L; Rottapharm Madaus , Via Valosa di Sopra 9, 20052 Monza, Italy.
  • Del Cadia M; Dipartimento di Chimica, Università di Modena e Reggio Emilia , Via Campi 183, 41100 Modena, Italy.
  • De Rienzo F; Dipartimento di Chimica, Università di Modena e Reggio Emilia , Via Campi 183, 41100 Modena, Italy ; Centro S3, CNR-Istituto di Nanoscienze , Via Campi 213A, 41125 Modena, Italy.
  • Menziani MC; Dipartimento di Chimica, Università di Modena e Reggio Emilia , Via Campi 183, 41100 Modena, Italy.
  • Vomero S; Dipartimento Farmaco Chimico Tecnologico and European Research Centre for Drug Discovery and Development, Università di Siena , Via A. Moro, 53100 Siena, Italy.
ACS Med Chem Lett ; 2(8): 571-6, 2011 Aug 11.
Article em En | MEDLINE | ID: mdl-24900351
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Med Chem Lett Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Med Chem Lett Ano de publicação: 2011 Tipo de documento: Article