Rosemeyer H, Seela F
J Med Chem. 1979 Dec;22(12):1545-7. doi: 10.1021/jm00198a023.
Condensation of 6-azauridine with ethyl levulinate, followed by saponification or phosphorylation, leads to 2',3'-O-[1-(2-carboxyethyl)ethylidene]-6-azauridine and its 5'-monophosphate. The latter was coupled to 6-aminohexylagarose via its carboxylic group. Using the same synthetic route, agarose-linked uridine 5'-monophosphate has been prepared. Both polymers show specific binding toward orotidine-5'-monophosphate decarboxylase. The immobilized inhibitor (6-azauridine 5'-monophosphat) binds the enzyme more strongly than the immobilized uridine 5'-monophosphate. Both resins have been used to separate orotidine-5'-monophosphate decarboxylase from orotidine-5'-monophosphate pyrophosphorylase.
6-氮杂尿苷与乙酰丙酸乙酯缩合,随后进行皂化或磷酸化反应,生成2',3'-O-[1-(2-羧乙基)亚乙基]-6-氮杂尿苷及其5'-单磷酸酯。后者通过其羧基与6-氨基己基琼脂糖偶联。采用相同的合成路线,制备了琼脂糖连接的尿苷5'-单磷酸酯。两种聚合物均对乳清苷-5'-单磷酸脱羧酶表现出特异性结合。固定化抑制剂(6-氮杂尿苷5'-单磷酸酯)比固定化尿苷5'-单磷酸酯更强烈地结合该酶。两种树脂均已用于从乳清苷-5'-单磷酸焦磷酸化酶中分离乳清苷-5'-单磷酸脱羧酶。