New oligonucleotide analogues based on morpholine subunits joined by oxalyl diamide tether-Reference-Cited by-同舟云学术

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New oligonucleotide analogues based on morpholine subunits joined by oxalyl diamide tether

Published:2007-06 Issue:3 Volume:35 Page:258-275
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Abramova Tatiana V.,Kassakin Marat F.,Lomzov Alexander A.,Pyshnyi Dmitrii V.,Silnikov Vladimir N.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference37 articles.

1. Vinyl analogs of polynucleotides

2. Synthetic analogues of polynucleotides

3. Synthetic analogues of nucleic acids — a review

4. Antisence Research and Application,1993

5. Morpholino antisense oligomers: the case for an RNase H-independent structural type

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1. Design, Synthesis and Molecular Modeling Study of Conjugates of ADP and Morpholino Nucleosides as A Novel Class of Inhibitors of PARP-1, PARP-2 and PARP-3;International Journal of Molecular Sciences;2019-12-27

2. A new approach to precise thermodynamic characterization of hybridization properties of modified oligonucleotides: Comparative studies of deoxyribo- and glycine morpholine pentaadenines;Biophysical Chemistry;2018-03

3. Synthesis of a series of NAD+ analogues, potential inhibitors of PARP 1, using ADP conjugates functionalized at the terminal phosphate group;Russian Journal of Bioorganic Chemistry;2017-01

4. A versatile strategy for the design and synthesis of novel ADP conjugates and their evaluation as potential poly(ADP-ribose) polymerase 1 inhibitors;Molecular Diversity;2016-09-27

5. Effective Synthesis of Fluorescently Labeled Morpholino Nucleoside Triphosphate Derivatives;Nucleosides, Nucleotides and Nucleic Acids;2016-01-02

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