2021-08-30T12:45:07Z
2021-08-30T12:45:07Z
2013-07-15
2021-08-30T12:45:07Z
Oligoribonucleotide conjugates carrying apolar carbohydrates at the 5′-end and the corresponding siRNA duplexes have been prepared using phosphoramidite chemistry. All the carbohydrate-siRNA derivatives were compatible with RNA interference machinery if transfected with oligofectamine. In the absence of a transfection agent, some of them exerted certain reduction of gene expression. Double-tailed permethylated glucose conjugated to siRNA through a long spacer inhibited gene expression up to 26% compared to the scrambled duplex. Such modifications contribute positively to the stability of oligoribonucleotides against 5′-exonuclease degradation.
Article
Accepted version
English
RNA; Oligonucleòtids; Química orgànica; RNA; Oligonucleotides; Organic chemistry
Elsevier Ltd
Versió postprint del document publicat a: https://doi.org/10.1016/j.bmcl.2013.05.065
Bioorganic & Medicinal Chemistry Letters, 2013, vol. 23, num. 14, p. 4048-4051
https://doi.org/10.1016/j.bmcl.2013.05.065
(c) Elsevier Ltd, 2013