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Structure of 55486-09-4
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5-Methyl-2′-O-methyl-uridine features a methyl group at the 5-position and a 2′-O-methyl modification, enhancing nuclease resistance and metabolic stability. This dual substitution improves cellular uptake and structural rigidity, making it ideal for antisense oligonucleotide design and RNA therapeutics development.
5-Methyl-2′-O-methyl-uridine serves as a valuable nucleoside building block for the synthesis of modified oligonucleotides, offering enhanced nuclease resistance and improved binding affinity. Its 5-methyl substitution increases hydrophobicity and stabilizes base pairing, while the 2′-O-methyl modification enhances metabolic stability and facilitates efficient coupling in solid-phase synthesis. The compound exhibits excellent bench stability and is compatible with standard phosphoramidite protocols, enabling reliable incorporation into antisense agents and RNA therapeutics.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: