Design and synthesis of 6-fluoropurine acyclonucleosides: potential prodrugs of acyclovir and ganciclovir

Dae Kee Kim, Hee Kap Kim, Young Bok Chae

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)1309-1312
Number of pages4
JournalBioorganic and Medicinal Chemistry Letters
Volume4
Issue number11
DOIs
StatePublished - 9 Jun 1994

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