FIELD: biotechnology.
SUBSTANCE: invention relates to biologically stable oligonucleotide derivatives with modified phosphate groups which can be used in pharmaceutical industry. Disclosed is a novel modified oligonucleotide with length of 5–21 nucleotides for binding with RNA and activation of RNase H, containing at least one group, corresponding to formula (III)
(III),
where B is a natural nitrogen base, R is a hydrogen atom, a nucleotide or oligonucleotide residue, R1 is a hydrogen atom, a nucleotide or oligonucleotide residue, R2 is independently selected from a group comprising C1-6alkyl, p-methylphenyl, o-nitrophenyl, effective for in vitro binding with RNA and activation of RNase H, to produce a therapeutic agent, aimed at selective suppression of expression of undesired genes by binding with RNA and its hydrolytic cleavage through activation of RNase H cell enzyme.
EFFECT: disclosed are modified oligonucleotides which activate RNase H.
7 cl, 35 ex, 36 dwg
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Authors
Dates
2021-01-14—Published
2017-02-21—Filed