Veres Z, Szinai I, Szabolcs A, Ujszászy K, Dénes G
Central Research Institute for Chemistry, Hungarian Academy of Sciences, Budapest.
Drugs Exp Clin Res. 1987;13(10):615-21.
5-Ethyl-2,2'-anhydrouridine (ANEUR) proved to be a potent inhibitor of uridine phosphorylase isolated from sarcoma 180 cells with an apparent Ki (Ki(app) value of 99 nM. Coadministration of ANEUR with 5-fluorouridine (FUR) resulted in increased toxicity of FUR. The LD50 value of FUR alone was 9 mg/kg (when administered for 5 consecutive days) while the LD50 was 3 mg/kg when FUR was administered together with ANEUR in vivo. There was no significant difference in mean tumor weight on day 10 between control animals and animals treated with FUR (5 mg/kg/day for 3 days) or ANEUR (280 mg/kg/day for 3 days). When FUR was coadministered with ANEUR, mean tumor weight was 91% less than that of the untreated controls, showing that ANEUR, the potent URPase inhibitor, increases the antitumor effect of FUR.
5-乙基-2,2'-脱水尿苷(ANEUR)被证明是从肉瘤180细胞中分离出的尿苷磷酸化酶的有效抑制剂,其表观抑制常数(Ki(app)值)为99 nM。ANEUR与5-氟尿苷(FUR)共同给药会导致FUR的毒性增加。单独使用FUR时的半数致死剂量(LD50)为9 mg/kg(连续给药5天),而在体内将FUR与ANEUR一起给药时,LD50为3 mg/kg。在第10天,对照组动物与接受FUR(5 mg/kg/天,共3天)或ANEUR(280 mg/kg/天,共3天)治疗的动物之间的平均肿瘤重量没有显著差异。当FUR与ANEUR共同给药时,平均肿瘤重量比未治疗的对照组减少了91%,这表明强效的尿苷磷酸化酶抑制剂ANEUR增强了FUR的抗肿瘤作用。