Synthesis of aminomethyl and amino analogs of 5-benzylacyclouridine and 5-benzyloxybenzylacyclouridine
作者:Shih Hsi Chu、Zhi Hao Chen、Zun Yao Weng、Elizabeth C. Rowe、Edward Chu、Ming-Yu Wang Chu
DOI:10.1002/jhet.5570240418
日期:1987.7
Amino analogs of BAU (5-benzylacyclouridine) and BBAU (5-benzyloxybenzylacyclouridine) and their 2′-hydroxymethyl derivatives were synthesized for evaluation as inhibitors of uridine phosphorylase and hence potential cancer chemotherapeutic agents. Both aminomethyl analogs were found to be potent inhibitors of this enzyme and good potentiators of the anti-tumor action of FUdR.
合成了BAU(5-苄基环上尿苷)和BBAU(5-苄氧基苄基环上尿苷)的氨基类似物及其2'-羟甲基衍生物,作为尿苷磷酸化酶抑制剂和潜在的癌症化学治疗剂的评估对象。发现两种氨基甲基类似物都是该酶的有效抑制剂,也是FUdR的抗肿瘤作用的良好增强剂。