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CAS 187733-72-8

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Uridine, 5′-deoxy-5′-iodo-5-methyl-2′-O-methyl-

Description:
Uridine, 5′-deoxy-5′-iodo-5-methyl-2′-O-methyl- is a modified nucleoside that features several unique structural characteristics. It is a derivative of uridine, which is a nucleoside composed of a ribose sugar and the nitrogenous base uracil. In this specific compound, the ribose sugar has been modified at the 5′ position, where a deoxy group and an iodine atom are present, along with a methyl group. Additionally, the 2′ position of the ribose sugar is substituted with a methoxy group, enhancing its stability and potentially influencing its biological activity. Such modifications can affect the nucleoside's interaction with nucleic acids and enzymes, making it of interest in biochemical research and therapeutic applications. The presence of iodine may also impart unique properties, such as increased lipophilicity or altered binding affinities. Overall, this compound exemplifies the diverse modifications that can be made to nucleosides to explore their functional roles in biological systems.
Formula:C11H15IN2O5
InChI:InChI=1S/C11H15IN2O5/c1-5-4-14(11(17)13-9(5)16)10-8(18-2)7(15)6(3-12)19-10/h4,6-8,10,15H,3H2,1-2H3,(H,13,16,17)/t6-,7-,8-,10-/m1/s1
InChI key:InChIKey=HTLVQJXEEODLKI-FDDDBJFASA-N
SMILES:O(C)[C@H]1[C@@H](O[C@H](CI)[C@H]1O)N2C(=O)NC(=O)C(C)=C2
Synonyms:
  • Uridine, 5′-deoxy-5′-iodo-5-methyl-2′-O-methyl-
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Found 2 products.
  • 5'-Deoxy-5'-iodo-2'-O-methyl-5-methyluridine
    Targetmol
    + Info

    5'-Deoxy-5'-iodo-2'-O-methyl-5-methyluridine

    CAS:
    <p>Nucleoside Derivatives - 5’-Modified nucleosides, Halo-nucleosides, 2’-Modified nucleosides</p>
    Formula:C11H15IN2O5
    Color and Shape:Solid
    Molecular weight:382.15

    Ref: TM-TNU1153

  • 5’-Deoxy-5’-iodo-2’-O-methyl-5-methyluridine
    Biosynth
    + Info

    5’-Deoxy-5’-iodo-2’-O-methyl-5-methyluridine

    CAS:
    <p>5’-Deoxy-5’-iodo-2’-O-methyl-5-methyluridine is a monophosphate nucleoside. It is an antiviral and anticancer agent that inhibits viral replication by inhibiting the synthesis of viral DNA. It also has been shown to have antitumor activity, but it can only be used in cancer treatments when combined with other drugs such as 5FU. The chemical formula for 5’-Deoxy-5’-iodo-2’O methyl -5 methyl uridine is C10H14N4O8P.</p>
    Purity:Min. 95%

    Ref: 3D-ND163035

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