2183487-92-3

2’-Beta-C-Ethynyl inosine Chemical Structure
2183487-92-3

Chemical Structure

2’-Beta-C-Ethynyl inosine

  • CAS No.: 2183487-92-3
  • Formula:C12H12N4O5
  • Molecular Weight:292.25

IUPAC Name: 9-((2R,3R,4R,5R)-3-ethynyl-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1,9-dihydro-6H-purin-6-one

InChIKey: RSQIETLALZCXER-YUTYNTIBSA-N

SMILES: O[C@H]1[C@](O)(C#C)[C@H](N(C=N2)C3=C2C(NC=N3)=O)O[C@@H]1CO

Biological Activity: 2’-Beta-C-Ethynyl inosine 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]. 2’-Beta-C-Ethynyl inosine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

Cat. No. Product Name Purity Description Pricing
HY-152625
2’-Beta-C-Ethynyl inosine 2’-Beta-C-Ethynyl inosine 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. 2’-Beta-C-Ethynyl inosine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References