Herein, we report the synthesis of four new phenyl alkyl ether derivatives (7, 9–11) of the pyrazolo[1,5- a]pyrimidine acetamide class, all of which showed high binding affinity and selectivity for the TSPO and, in the case of the propyl, propargyl, and butyl ether derivatives, the ability to increase pregnenolone biosynthesis by 80–175% over baseline in rat C6 glioma cells. While these compounds fit our in silico generated pharmacophore for TSPO binding the current model does not account for the observed functional activity.
Pyrazolo[1,5-a]pyrimidine acetamides: 4-phenyl alkyl ether derivatives as potent ligands for the 18 KDa translocator protein (TSPO) / A. Reynolds; R. Hanani; D. Hibbs; A. Damont; E. Da Pozzo; S. Selleri; F. Dollé; C. Martini; M Kassiou. - In: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS. - ISSN 0960-894X. - STAMPA. - 20:(2010), pp. 5799-5802. [10.1016/j.bmcl.2010.07.135]
Pyrazolo[1,5-a]pyrimidine acetamides: 4-phenyl alkyl ether derivatives as potent ligands for the 18 KDa translocator protein (TSPO)
SELLERI, SILVIA;
2010
Abstract
Herein, we report the synthesis of four new phenyl alkyl ether derivatives (7, 9–11) of the pyrazolo[1,5- a]pyrimidine acetamide class, all of which showed high binding affinity and selectivity for the TSPO and, in the case of the propyl, propargyl, and butyl ether derivatives, the ability to increase pregnenolone biosynthesis by 80–175% over baseline in rat C6 glioma cells. While these compounds fit our in silico generated pharmacophore for TSPO binding the current model does not account for the observed functional activity.File | Dimensione | Formato | |
---|---|---|---|
id 396745.pdf
Accesso chiuso
Tipologia:
Versione finale referata (Postprint, Accepted manuscript)
Licenza:
Tutti i diritti riservati
Dimensione
373.38 kB
Formato
Adobe PDF
|
373.38 kB | Adobe PDF | Richiedi una copia |
I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.