Literature DB >> 26639763

Glutathione-triggered activation of the model of pro-oligonucleotide with benzyl protecting groups at the internucleotide linkage.

Hisao Saneyoshi1, Kazuhiko Kondo2, Naoki Sagawa2, Akira Ono3.   

Abstract

We have examined substituted benzyl protecting groups for the phosphodiester in oligodeoxyribonucleotides. Stability of the protecting groups in buffer and rates of deprotection by glutathione (GSH) were strongly influenced by benzyl ring substituents.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Glutathione; Nucleic acid-based therapeutics; Prodrug; Protecting group

Mesh:

Substances:

Year:  2015        PMID: 26639763     DOI: 10.1016/j.bmcl.2015.11.064

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

Review 1.  Stimuli-responsive oligonucleotides in prodrug-based approaches for gene silencing.

Authors:  Françoise Debart; Christelle Dupouy; Jean-Jacques Vasseur
Journal:  Beilstein J Org Chem       Date:  2018-02-19       Impact factor: 2.883

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.