Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sergio Menegon"'
Publikováno v:
Intercâmbio. 49:113-137
A investigação da declamação suscita interesse por sua carga expressiva. O propósito deste trabalho é investigar, por meio de um experimento fonético, os efeitos impressivos causados nos ouvintes por declamações do Soneto da Fidelidade. Na a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ef2fc578716311a5f7e909b0a9900ec
https://doi.org/10.23925/2237.759x.2021v49.56747
https://doi.org/10.23925/2237.759x.2021v49.56747
Autor:
Lorenza Pirona, Roberto Dilernia, Valerio Tazzari, Carlo De Toma, Anna Elisa Valsecchi, Sergio Menegon, Silvia Caligari, Matteo Marco Longhi, Fabio Frigerio, Giulio Vistoli, Giulio Rastelli, Davide Graziani, Elisa Callegari, Luca Pinzi, Carlo Riva
Publikováno v:
Journal of medicinal chemistry. 62(3)
Negative allosteric modulators (NAMs) of the metabotropic glutamate receptor 5 (mGlu5) hold great promise for the treatment of a variety of central nervous system disorders. We have recently reported that prop-2-ynylidenecycloalkylamine derivatives a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f8cc91852a3dd23ac7c42dd4f1845fe
https://pubmed.ncbi.nlm.nih.gov/30624919
https://pubmed.ncbi.nlm.nih.gov/30624919
Autor:
Massimo Nabissi, Sergio Menegon, Consuelo Amantini, Alessandro Piergentili, Yogita Farande, Valerio Farfariello, Alessandro Bonifazi, Maria Pigini, Giorgio Santoni, Mario Giannella, Wilma Quaglia, Fabio Del Bello, Amedeo Leonardi, Elena Poggesi
Publikováno v:
Journal of Medicinal Chemistry. 56:584-588
5-HT1A receptor and α1-adrenoreceptor (α1-AR) binding sites recognized by the 1,4-dioxanes 2–4 display reversed stereochemical requirements. (S)-2 proved to be a potent 5-HT1A receptor agonist high...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ec745c4c6644878c0af88ec2d8e0cac
https://doi.org/10.1021/jm301525w
https://doi.org/10.1021/jm301525w
Autor:
Antonio Cilia, Ilaria Bettinelli, Andrew Anighoro, Lorenza Pirona, Fabio Mangiarotti, Sergio Menegon, Carlo Riva, Elena Poggesi, Carlo De Toma, Giulio Rastelli, Matteo Marco Longhi, Davide Graziani
Publikováno v:
Bioorganicmedicinal chemistry. 23(13)
Metabotropic glutamate receptor 5 (mGlu 5 ) is a biological target implicated in major neurological and psychiatric disorders. In the present study, we have investigated structural determinants of the interaction of negative allosteric modulators (NA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::779b08083fdb1199db060eaffe4c0263
https://pubmed.ncbi.nlm.nih.gov/26014480
https://pubmed.ncbi.nlm.nih.gov/26014480
Autor:
Alessandro, Bonifazi, Alessandro, Piergentili, Fabio, Del Bello, Yogita, Farande, Mario, Giannella, Maria, Pigini, Consuelo, Amantini, Massimo, Nabissi, Valerio, Farfariello, Giorgio, Santoni, Elena, Poggesi, Amedeo, Leonardi, Sergio, Menegon, Wilma, Quaglia
Publikováno v:
Journal of medicinal chemistry. 56(2)
5-HT(1A) receptor and α(1)-adrenoreceptor (α(1)-AR) binding sites recognized by the 1,4-dioxanes 2-4 display reversed stereochemical requirements. (S)-2 proved to be a potent 5-HT(1A) receptor agonist highly selective over α(1)-AR subtypes. Chiral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5ff28c2267ff79bc8543511e32cb0b6b
https://pubmed.ncbi.nlm.nih.gov/23252794
https://pubmed.ncbi.nlm.nih.gov/23252794
Autor:
Sergio Menegon, Gabriele Amari, Bruno P. Imbimbo, Elisabetta Armani, Giulio Dondio, Luigi Radice, Elena La Porta, Maurizio Delcanale, Marco Bergamaschi, Alessandra Giardini, Paola Petrillo, Luca F. Raveglia, Francesca Scarpitta, Maurizio Civelli, Claudia Fossati, Giuseppe Giardina, Roberta Scudellaro, Andrea Rizzi, Enza Santoro, Gino Villetti, Stefano Radaelli, Riccardo Patacchini, Matilde Guala, Alberto Cerri, Franco Bassani, Ilaria Peretto
Publikováno v:
Journal of medicinal chemistry. 50(7)
Synthesis and biological activity of a novel class of quaternary ammonium salt muscarinic M3 receptor antagonists, showing high selectivity versus the M2 receptor, are described. Selected compounds exhibited potent anticholinergic properties, in isol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91046415b7dfab24bbe538b4df6de1dc
https://pubmed.ncbi.nlm.nih.gov/17352463
https://pubmed.ncbi.nlm.nih.gov/17352463
Autor:
Ilaria Peretto, Claudia Fossati, Giuseppe A. M. Giardina, Alessandra Giardini, Matilde Guala, Elena La Porta, Paola Petrillo, Stefano Radaelli, Luigi Radice, Luca F. Raveglia, Enza Santoro, Roberta Scudellaro, Francesca Scarpitta, Alberto Cerri, Sergio Menegon, Giulio M. Dondio, Andrea Rizzi, Elisabetta Armani, Gabriele Amari, Maurizio Civelli
Publikováno v:
Journal of Medicinal Chemistry; Apr2007, Vol. 50 Issue 7, p1693-1697, 5p