A new series of amino-3,5-dicyanopyridines (3–28) as analogues of the adenosine hA2Breceptor agonist BAY60-6583 (compound 1) was synthesized. All the compounds that interact with the hA2Badenosine receptor display EC50values in the range 9–350 nM behaving as partial agonists, with the only exception being the 2-[4-(4-acetamidophenyl)-6-amino-3,5-dicyanopyridin-2-yl]thioacetamide (8) which shows a full agonist profile. Moreover, the 2-[(1H-imidazol-2-yl)methylthio)]-6-amino-4-(4-cyclopropylmethoxy-phenyl)pyridine-3,5-dicarbonitrile (15) turns out to be 3-fold more active than 1 although less selective. This result can be considered a real breakthrough due to the currently limited number of non-adenosine hA2BAR agonists reported in literature. To simulate the binding mode of nucleoside and non-nucleoside agonists at the hA2BAR, molecular docking studies were performed at homology models of this AR subtype developed by using two crystal structures of agonist-bound A2AAR as templates. These investigations allowed us to represent a hypothetical binding mode of hA2Breceptor agonists belonging to the amino-3,5-dicyanopyridine series and to rationalize the observed SAR.
The aminopyridine-3,5-dicarbonitrile core for the design of new non-nucleoside-like agonists of the human adenosine A2B receptor
Varani, Katia;Vincenzi, Fabrizio;
2018
Abstract
A new series of amino-3,5-dicyanopyridines (3–28) as analogues of the adenosine hA2Breceptor agonist BAY60-6583 (compound 1) was synthesized. All the compounds that interact with the hA2Badenosine receptor display EC50values in the range 9–350 nM behaving as partial agonists, with the only exception being the 2-[4-(4-acetamidophenyl)-6-amino-3,5-dicyanopyridin-2-yl]thioacetamide (8) which shows a full agonist profile. Moreover, the 2-[(1H-imidazol-2-yl)methylthio)]-6-amino-4-(4-cyclopropylmethoxy-phenyl)pyridine-3,5-dicarbonitrile (15) turns out to be 3-fold more active than 1 although less selective. This result can be considered a real breakthrough due to the currently limited number of non-adenosine hA2BAR agonists reported in literature. To simulate the binding mode of nucleoside and non-nucleoside agonists at the hA2BAR, molecular docking studies were performed at homology models of this AR subtype developed by using two crystal structures of agonist-bound A2AAR as templates. These investigations allowed us to represent a hypothetical binding mode of hA2Breceptor agonists belonging to the amino-3,5-dicyanopyridine series and to rationalize the observed SAR.File | Dimensione | Formato | |
---|---|---|---|
Betti Eur J Med Chem 2018.pdf
solo gestori archivio
Descrizione: Full text editoriale
Tipologia:
Full text (versione editoriale)
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
1.82 MB
Formato
Adobe PDF
|
1.82 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
EJMECH-D-17-02921R1.pdf
accesso aperto
Descrizione: Pre print
Tipologia:
Pre-print
Licenza:
PUBBLICO - Pubblico con Copyright
Dimensione
569.89 kB
Formato
Adobe PDF
|
569.89 kB | Adobe PDF | Visualizza/Apri |
I documenti in SFERA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.