Bioorganic and Medicinal Chemistry p. 5941 - 5952 (2016)
Update date:2022-08-11
Topics:
Lougiakis, Nikolaos
Gavriil, Efthymios-Spyridon
Kairis, Markelos
Sioupouli, Georgia
Lambrinidis, George
Benaki, Dimitra
Krypotou, Emilia
Mikros, Emmanuel
Marakos, Panagiotis
Pouli, Nicole
Diallinas, George
In the course of our study on fungal purine transporters, a number of new 3-deazapurine analogues have been rationally designed, based on the interaction of purine substrates with the Aspergillus nidulans FcyB carrier, and synthesized following an effective synthetic procedure. Certain derivatives have been found to specifically inhibit FcyB-mediated [3H]-adenine uptake. Molecular simulations have been performed, suggesting that all active compounds interact with FcyB through the formation of hydrogen bonds with Asn163, while the insertion of hydrophobic fragments at position 9 and N6 of 3-deazaadenine enhanced the inhibition.
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