Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374308 | Bioorganic & Medicinal Chemistry Letters | 2010 | 5 Pages |
Abstract
Nâ²-Cyanoisonicotinamidine derivatives, linked to an arylpiperazine moiety, were prepared to identify highly selective and potent 5-HT1A ligands. Nâ²-Cyano-N-(3-(4-(pyridin-2-yl)piperazin-1-yl)propyl)isonicotinamidine (4o) with Ki = 0.038 nM, was the most active and selective derivative for the 5-HT1A receptor.
Keywords
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ferdinando Fiorino, Beatrice Severino, Francesca De Angelis, Elisa Perissutti, Elisa Magli, Francesco Frecentese, Antonella Esposito, Paola Massarelli, Cristina Nencini, Vincenzo Santagada, Giuseppe Caliendo,