1993176-75-2

N3-Gly-Gly-Gly-OH Chemical Structure
1993176-75-2

Chemical Structure

N3-Gly-Gly-Gly-OH

  • CAS 番号: 1993176-75-2
  • Formula:C6H9N5O4
  • Molecular Weight:215.17

IUPAC Name: (2-azidoacetyl)glycylglycine

InChIKey: JAMMEZNHAILDJV-UHFFFAOYSA-N

SMILES: [N-]=[N+]=NCC(NCC(NCC(O)=O)=O)=O

Biological Activity: N3-Gly-Gly-Gly-OH is a oligo-Gly click chemistry reagent containing an azide group. Oligo-Gly also has been used as linker to combine different subunits of dimeric or oligomeric proteins or to create artificial multi-domain proteins. By modification into Gly-Gly-Gly-Ser motifs high solubility can be achieved[1][2][3]. N3-Gly-Gly-Gly-OH 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.

製品番号 製品名 純度 製品説明 Pricing
HY-151746
N3-Gly-Gly-Gly-OH 97.49% N3-Gly-Gly-Gly-OH is a oligo-Gly click chemistry reagent containing an azide group. Oligo-Gly also has been used as linker to combine different subunits of dimeric or oligomeric proteins or to create artificial multi-domain proteins. By modification into Gly-Gly-Gly-Ser motifs high solubility can be achieved. N3-Gly-Gly-Gly-OH 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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