2305415-75-0

5’-Azido-5’-deoxy-2’-O,4’-C-methyleneuridine Chemical Structure
2305415-75-0

Chemical Structure

5’-Azido-5’-deoxy-2’-O,4’-C-methyleneuridine

  • CAS No.: 2305415-75-0
  • Formula:C10H11N5O5
  • Molecular Weight:281.22

IUPAC Name: 1-((1S,3R,4R,7S)-1-(azidomethyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)pyrimidine-2,4(1H,3H)-dione

InChIKey: PFXWOPNWYGPHBA-JIOCBJNQSA-N

SMILES: O[C@@H]1[C@@]2(CN=[N+]=[N-])O[C@@H](N3C(NC(C=C3)=O)=O)[C@@H]1OC2

Biological Activity: 5’-Azido-5’-deoxy-2’-O,4’-C-methyleneuridine 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[1]. 5’-Azido-5’-deoxy-2’-O,4’-C-methyleneuridine 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. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

Cat. No. Product Name Purity Description Pricing
HY-154042
5’-Azido-5’-deoxy-2’-O,4’-C-methyleneuridine 5’-Azido-5’-deoxy-2’-O,4’-C-methyleneuridine 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,4’-C-methyleneuridine 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. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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