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Structure of 207131-16-6
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2'-O,4'-C-Methyleneguanosine features a rigid bicyclic sugar moiety that locks the ribose in the North conformation, enhancing nuclease resistance and stabilizing RNA duplexes. This structural constraint improves binding affinity in antisense applications and supports efficient incorporation into oligonucleotides for therapeutic development.
2'-O,4'-C-Methyleneguanosine serves as a key nucleoside building block for the synthesis of antiviral agents and oligonucleotide therapeutics. Its constrained ribose ring enhances nuclease resistance while maintaining favorable hybridization properties. The methylene bridge between the 2' and 4' positions stabilizes the C3'-endo sugar conformation, facilitating incorporation into RNA analogs. This compound enables efficient phosphoramidate coupling and exhibits robust bench stability under standard synthetic conditions.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: