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Synthesis of a new class of uridine phosphorylase inhibitors
Authors:Diane L. Levesque  Eng-Chi Wang  Dau-Chang Wei  Cherng-Chyi Tzeng  Raymond P. Panzica  Fardos N. M. Naguib  Mahmoud H. El Kouni
Abstract:A new series of potent uridine phosphorylase inhibitors have been prepared from barbituric acid. Among them, 1-[(2-hydroxyethoxy)methyl]-5-)(m--benzyloxy)benzylbarbituric acid ( 37 , BBBA) is the most promising having a Ki value of 1.1 ± 0.2 nM with uridine phosphorylase from human liver. The new inhibitors are easily synthesized and are better inhibitors of human uridine phosphorylase than their uracil counterparts.
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