Methyl 2-O-Allyl-3-O-(2’,3’,4’,6’-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside产品图

Methyl 2-O-Allyl-3-O-(2’,3’,4’

,6’-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside
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  • 欧美
  • M285000
  • 2025年07月16日
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    • 文献和实验
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    • 保存条件:

      咨询甄准

    • 保质期:

      咨询甄准

    • 英文名:

      Methyl 2-O-Allyl-3-O-(2’,3’,4’,6’-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside

    • 库存:

      1

    • 供应商:

      上海甄准

    • CAS号:

      81555-75-1

    • 规格:

      50mg

    C24H36O15

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    图标文献和实验
    相关实验
    • Synthesis of 2-O-Alkyloligoribonucleotides

      2′-O -Alkyloligoribonucleotides possess properties that render them ideally suited for studying RNA processing and for the affinity chromatography of RNA-protein complexes. Particularly useful compounds are those in which alkyl is methyl (1 –

    • Optimizing Splice-Switching Oligomer Sequences Using 2-O-Methyl Phosphorothioate Chemistry

      and then a set of oligomers complementary to the acceptor and donor splice sites, as well as intra-exonic regions predicted to contain exon splice enhancers, are designed and synthesized as 2′-O-methyl-modified bases on a phosphorothioate backbone (2OMeAOs

    • Chemical Synthesis of 2-O-Alkylated siRNAs

      available 2�-O-methyl ribosides, 2′-alkyl groups bearing positive charges are especially promising candidates. We have shown that in a proper formulation they are superior to unmodified siRNAs. This may be due to enhanced stability and most probably

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