Mesyl phosphoramidate oligonucleotides as potential splice-switching agents: impact of backbone structure on activity and intracellular localization
A series of 2′-deoxy and novel 2′-O-methyl and 2′-O-(2-methoxyethyl) (2′-MOE) oligonucleotides with internucleotide methanesulfonyl (mesyl, μ) or 1-butanesulfonyl (busyl, β) phosphoramidate groups has been synthesized for evaluation as potential splice-switching oligonucleotides. Evaluation of their...
Main Authors: | Hammond, SM, Sergeeva, OV, Melnikov, PA, Goli, L, Stoodley, J, Zatsepin, TS, Stetsenko, DA, Wood, MJA |
---|---|
Format: | Journal article |
Language: | English |
Published: |
Mary Ann Liebert
2021
|
Similar Items
-
Mesyl phosphoramidate backbone modified antisense oligonucleotides targeting miR-21 with enhanced in vivo therapeutic potency
by: Patutina, OA, et al.
Published: (2020) -
Structure-activity relationship study of mesyl and busyl phosphoramidate antisense oligonucleotides for unaided and PSMA-mediated uptake into prostate cancer cells
by: O. Sergeeva, et al.
Published: (2024-03-01) -
Novel Lipid-Oligonucleotide Conjugates Containing Long-Chain Sulfonyl Phosphoramidate Groups: Synthesis and Biological Properties
by: Alina Derzhalova, et al.
Published: (2021-01-01) -
Phosphoramidate Azole Oligonucleotides for Single Nucleotide Polymorphism Detection by PCR
by: Alexey S. Chubarov, et al.
Published: (2024-01-01) -
Solid-Phase Synthesis of Phosphorothioate/Phosphonothioate and Phosphoramidate/Phosphonamidate Oligonucleotides
by: Ondřej Kostov, et al.
Published: (2019-05-01)