DESIGN AND SYNTHESIS OF 6-FLUOROPURINE ACYCLONUCLEOSIDES - POTENTIAL PRODRUGS OF ACYCLOVIR AND GANCICLOVIR

被引:15
作者
KIM, DK
KIM, HK
CHAE, YB
机构
关键词
D O I
10.1016/S0960-894X(01)80350-4
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
6-Fluoropurine acyclonucleosides 6 and 7 have been prepared as potential prodrugs of acyclovir and ganciclovir. It has been found that compounds 6 and 7 are 11.6 and 7.6 times more efficiently metabolized to acyclovir and ganciclovir by adenosine deaminase than the corresponding 6-aminopurine acyclonucleosides 4 and 12, respectively.
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页码:1309 / 1312
页数:4
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