Literature DB >> 2842187

A route to 2',5'-oligoadenylates with increased stability towards phosphodiesterases.

A V Itkes1, O N Kartasheva, S N Mikhailov, G P Moiseyev, W Pfleiderer, R Charubala, G I Yakovlev.   

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.

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Year:  1988        PMID: 2842187     DOI: 10.1016/0014-5793(88)80048-6

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

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Authors:  Kong-Jiang Wang; James P Ferris
Journal:  Orig Life Evol Biosph       Date:  2005-06       Impact factor: 1.950

2.  Locked and unlocked nucleosides in functional nucleic acids.

Authors:  Holger Doessing; Birte Vester
Journal:  Molecules       Date:  2011-05-27       Impact factor: 4.411

3.  G-rich VEGF aptamer with locked and unlocked nucleic acid modifications exhibits a unique G-quadruplex fold.

Authors:  Maja Marušič; Rakesh N Veedu; Jesper Wengel; Janez Plavec
Journal:  Nucleic Acids Res       Date:  2013-08-08       Impact factor: 16.971

  3 in total

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