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Inamdar G.S.,Bv Patel Pharmaceutical Education And Research Development | Pandya A.N.,Bv Patel Pharmaceutical Education And Research Development | Thakar H.M.,Bv Patel Pharmaceutical Education And Research Development | Sudarsanam V.,Bv Patel Pharmaceutical Education And Research Development | And 5 more authors.
European Journal of Medicinal Chemistry | Year: 2013

A series of [5-substituted-4-phenyl-1,3-thiazol-2-yl] benzamide and furamide analogues were investigated in radioligand binding studies at adenosine receptor subtypes with an aim to obtain potent and selective adenosine receptor ligands. Benzamide and furamide linked to thiazole was found to be crucial for high adenosine receptor affinity. The most potent compound indentified in this study was 5d with low nanomolar affinity for all four adenosine receptor subtypes. Compounds 5a and 5g showed moderate selectivity for A2A adenosine receptors. Molecular docking versus all four human adenosine receptors combined with membrane molecular dynamics studies were performed to rationalise the peculiar selectivity profile of 5d antagonist. © 2013 Elsevier Masson SAS. All rights reserved.

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