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A route to 2',5'-oligoadenylates with increased stability towards phosphodiesterases
A V Itkes1, Karpeisky MYa, O N Kartasheva
1Institute of Molecular Biology, USSR Academy of Sciences, Moscow.
FEBS Letters
|August 29, 1988
Abstract:
The rates of enzymatic hydrolysis of 2',5'-oligoadenylates and their synthetic analogs have been measured. These compounds were treated with either NIH 3T3 cell lysates, mouse liver homogenates or snake venom phosphodiesterase. All analogs with 3'-terminal acyclic nucleoside residues demonstrated greater stability compared with the natural compound adenylyl(2'-5')adenylyl(2'-5')adenosine.