摘要

The substitution of a hydroxyl group by a fluorine atom in a potential drug is an efficient reaction that can, in principle, improve its pharmacological properties. Herein, the synthesis of the novel compound 5%26apos;-fluoro-5%26apos;-deoxyacadesine (5%26apos;-F-AICAR), a strict analogue of AICAR that cannot be 5%26apos;-phosphorylated to ZMP by cellular kinases, is reported.

  • 出版日期2012-11