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Results for "

3’-Deoxy-3’-α-C-methyl-5-methyluridine

" in MedChemExpress (MCE) Product Catalog:

3

Inhibitors & Agonists

1

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-152393

    Nucleoside Antimetabolite/Analog Others
    3’-Deoxy-3’-α-C-methyl-5-methyluridine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .
    3’-<em>Deoxy</em>-3’-α-C-<em>methyl</em>-5-<em>methyluridine</em>
  • HY-154377

    Nucleoside Antimetabolite/Analog Cancer
    5’-Azido-5’-deoxy-2’-O-methyl-5-methyluridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc . 5'-Azido-5'-deoxy-2'-O-methyl-5-methyluridine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
    5'-Azido-5'-<em>deoxy</em>-2'-O-<em>methyl</em>-5-<em>methyluridine</em>
  • HY-154375

    Nucleoside Antimetabolite/Analog Cancer
    5’-Deoxy-5’-iodo-2’-O-methyl-5-methyluridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .
    5’-<em>Deoxy</em>-5’-iodo-2’-O-<em>methyl</em>-5-<em>methyluridine</em>

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