Synthesis of 2',5'-oligoadenylate analogs possessing a linker moiety in the place of the second adenosine and their ability to activate human RNase L.

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Abstract

This paper describes the synthesis of 2',5'-oligoadenylate analogs possessing a linker moiety in the place of the second adenosine and their ability to activate human RNase L. Thus, 2-5A analogs (2a-c & 3a-c) possessing -O(CH(2)CH(2))nO- moieties (n = 1 approximately 3) or aromatic ring moieties were prepared. The EC(50) value of the 2-5A analog (2a) incorporating ethylene glycol showed 700 nM in RNase L activation activity.

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Nakamura, T., Ito, Y., Mochizuki, M., Ueno, Y., & Kitade, Y. (2007). Synthesis of 2’,5’-oligoadenylate analogs possessing a linker moiety in the place of the second adenosine and their ability to activate human RNase L. Nucleic Acids Symposium Series (2004), (51), 449–450. https://doi.org/10.1093/nass/nrm225

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