N-azidoacetylgalactosamine-tetraacylated (Ac4GaINAz)

N-azidoacetylgalactosamine-tetraacylated (Ac4GaINAz)
  • CAS No.:653600-56-7

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  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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N-azidoacetylgalactosamine-tetraacylated (Ac4GaINAz) Basic information
Product Name:N-azidoacetylgalactosamine-tetraacylated (Ac4GaINAz)
Synonyms:N-azidoacetylgalactosamine-tetraacylated (Ac4GaINAz);N-Azidoacetylgalactosamine-tetraacylated;Ac4GalNAz;N-Azidoacetylgalactosamine, Acylated;2-[(2-Azidoacetyl) amino] -2-deoxy-1,3,4,6- tetra-O-acetyl-D-galac- topyranose;1,3,4,6-Tetra-O-acetyl-N-azidoacetylgalactosamine;1,3,4,6-Tetra-O-acetyl-2-[(azidoacetyl)amino]-2-deoxy-β-D-galactopyranos;N-N-azidoacetylgalactosamine-tetraacylated (Ac4GalNAz)
CAS:653600-56-7
MF:C16H22N4O10
MW:430.37
EINECS:
Product Categories:
Mol File:653600-56-7.mol
N-azidoacetylgalactosamine-tetraacylated (Ac4GaINAz) Chemical Properties
storage temp. -20°C
form powder or crystals
Safety Information
MSDS Information
N-azidoacetylgalactosamine-tetraacylated (Ac4GaINAz) Usage And Synthesis
DescriptionThe unnatural azido-containing monosaccharide building block. The azide moiety can be used for modification though chemoselective ligation chemistries including CuAAC, Cu-free click reaction or Staudinger ligation. The acetyl groups increase solubility in many solvents and make handling of this reagent easier.
UsesN-Azidoacetylgalactosamine-tetraacylated (Ac4GalNAz) provides the first part of a simple and robust two-step technique that helps identify and characterize cell surface sialic acid-containing glycoproteins. The azide-modified protein can be detected by reaction with alkynes. For example alkynes labeled with a fluorescent probe or a biotin can be used. The acetyl groups increase cell permeability and allow the unnatural sugars to easily pass through the cell membrane. Carboxyesterases remove the acetyl groups once the monosaccharide is in the cell.
ApplicationN-Azidoacetylgalactosamine-tetraacylated (Ac4GalNAz) provides the first part of a simple and robust two-step technique that helps identify and characterize cell surface sialic acid-containing glycoproteins. The azide-modified protein can be detected by reaction with alkynes. For example alkynes labeled with a fluorescent probe or a biotin can be used. The acetyl groups increase cell permeability and allow the unnatural sugars to easily pass through the cell membrane. Carboxyesterases remove the acetyl groups once the monosaccharide is in the cell.
N-azidoacetylgalactosamine-tetraacylated (Ac4GaINAz) Preparation Products And Raw materials

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