Abstract
Antisense oligonucleotides with 2'-O-(2-[N,N-dimethyl)aminooxy]ethyl) or (2'-O-DMAOE) modification were synthesized and evaluated for nuclease resistance and pharmacology both in vitro and in vivo. This modification exhibits very high nuclease resistance and efficacy in various biological (ICAM-1, C-raf and PKC-alpha) targets.
MeSH terms
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Animals
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Cells, Cultured
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Endothelium, Vascular / drug effects
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Endothelium, Vascular / metabolism
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Female
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Humans
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Intercellular Adhesion Molecule-1 / biosynthesis
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Intercellular Adhesion Molecule-1 / genetics
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Mice
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Mice, Inbred BALB C
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Oligonucleotides, Antisense / chemical synthesis*
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Oligonucleotides, Antisense / genetics
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Oligonucleotides, Antisense / pharmacology*
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Organophosphorus Compounds / chemical synthesis
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RNA, Messenger / biosynthesis
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RNA, Messenger / genetics
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Ribonuclease H / genetics
Substances
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Oligonucleotides, Antisense
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Organophosphorus Compounds
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RNA, Messenger
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phosphoramidite
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Intercellular Adhesion Molecule-1
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Ribonuclease H