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- W2022222334 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." @default.
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- W2022222334 date "1993-10-01" @default.
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- W2022222334 title "Synthesis of a new class of uridine phosphorylase inhibitors" @default.
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- W2022222334 doi "https://doi.org/10.1002/jhet.5570300537" @default.
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