79541-46-1

4-Azidophlorizin Chemical Structure
79541-46-1

Chemical Structure

4-Azidophlorizin

  • CAS No.: 79541-46-1
  • Formula:C21H23N3O9
  • Molecular Weight:461.42

IUPAC Name: 3-(4-azidophenyl)-1-(2,4-dihydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)phenyl)propan-1-one

InChIKey: AXCDEMZKQHNYNE-QNDFHXLGSA-N

SMILES: [N-]=[N+]=NC(C=C1)=CC=C1CCC(C2=C(C=C(C=C2O)O)O[C@@H]3O[C@@H]([C@H]([C@@H]([C@H]3O)O)O)CO)=O

Biological Activity: 4-Azidophlorizin is a high affinity probe and photoaffinity label for the glucose transporter in brush border membranes[1]. 4-Azidophlorizin 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-147115
4-Azidophlorizin 4-Azidophlorizin is a high affinity probe and photoaffinity label for the glucose transporter in brush border membranes. 4-Azidophlorizin 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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