Synthesis of 4′‐ C ‐(Aminoethyl)thymidine and 4′‐ C ‐[( N ‐Methyl)aminoethyl] Thymidine Nucleosides to Enhance DNA Stability-Reference-Cited by-同舟云学术

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Synthesis of 4′‐ C ‐(Aminoethyl)thymidine and 4′‐ C ‐[( N ‐Methyl)aminoethyl] Thymidine Nucleosides to Enhance DNA Stability

Published:2022-09 Issue:9 Volume:2 Page:
ISSN:2691-1299
Container-title:Current Protocols
language:en
Short-container-title:Current Protocols

Author:

Chandela Akash¹,Ueda Hiroki²,Ueno Yoshihito¹²

Affiliation:

1. Faculty of Applied Biological Sciences Gifu University Gifu Japan

2. Graduate School of Natural Science and Technology Gifu University Gifu Japan

Funder

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Medical Laboratory Technology,Health Informatics,General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cpz1.501

Reference16 articles.

1. ANTISENSE OLIGONUCLEOTIDES AS THERAPEUTIC AGENTS

2. Highly Nuclease-Resistant Phosphodiester-Type Oligodeoxynucleotides Containing 4‘α-C-Aminoalkylthymidines Form Thermally Stable Duplexes with DNA and RNA. A Candidate for Potent Antisense Molecules

3. Synthesis and properties of 4′-C-aminoalkyl-2′-fluoro-modified RNA oligomers

4. RNase H sequence preferences influence antisense oligonucleotide efficiency

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