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CAS 115142-60-4

:

O-6-Deoxy-alpha-L-galactopyranosyl-(1-6)-O-[O-beta-D-galactopyranosyl-(1-3)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-[O-beta-D-galactopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-2)]-O-alpha-D-mannopyranosyl-(1-3)-O-[O-beta-D-galactopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-2)-alpha-D-mannopyranosyl-(1-6)]-O-beta-D-mannopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)]-2-(acetylamino)-2-deoxy-D-glucose

Description:
The chemical substance known as O-6-Deoxy-alpha-L-galactopyranosyl-(1-6)-O-[O-beta-D-galactopyranosyl-(1-3)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-[O-beta-D-galactopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-2)]-O-alpha-D-mannopyranosyl-(1-3)-O-[O-beta-D-galactopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-2)-alpha-D-mannopyranosyl-(1-6)]-O-beta-D-mannopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)]-2-(acetylamino)-2-deoxy-D-glucose, with CAS number 115142-60-4, is a complex glycosylated compound characterized by multiple sugar units linked through various glycosidic bonds. This structure features a combination of deoxy sugars, acetylamino groups, and multiple galactopyranosyl and glucopyranosyl residues, indicating its potential biological significance, particularly in cellular recognition processes. The presence of acetylamino groups suggests that it may play a role in modulating interactions with proteins or other biomolecules. Its intricate structure may also imply specific solubility and stability characteristics, which could influence its reactivity and potential applications in biochemistry or pharmaceuticals. Overall, this compound exemplifies the complexity of carbohydrate chemistry and its implications in biological systems.
Formula:C82H137N5O60
Synonyms:
  • D-Glucose, O-6-deoxy-α-L-galactopyranosyl-(1→6)-O-[O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-[O-β-D-galactopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)]-O-α-D-mannopyranosyl-(1→3)-O-[O-β-D-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-...
  • O-6-Deoxy-alpha-L-galactopyranosyl-(1-6)-O-[O-beta-D-galactopyranosyl-(1-3)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-[O-beta-D-galactopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-2)]-O-alpha-D-mannopyranosyl-(1-3)-O-[O-beta-D-galactopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-2)-alpha-D-mannopyranosyl-(1-6)]-O-beta-D-mannopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)]-2-(acetylamino)-2-deoxy-D-glucose
  • NA3F N-Glycan
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  • NA3F N-Glycan
    Biosynth
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    NA3F N-Glycan

    CAS:
    <p>NA3F is a N-glycan that is found on various glycoproteins and glycolipids. It consists of sialic acid, galactose, and fucose sugars in the ratio 3:2:1. NA3F N-glycans are synthesized by the removal of the terminal sialic acid residue from an Asn-linked oligosaccharide precursor. These types of glycans are found on high mannose (HMan) and hybrid (HHyb) glycans. The synthesis of NA3F N-glycan requires the activity of two enzymes: peptidase and sialyltransferase. The enzyme peptidase cleaves an α(1,4)-linked oligosaccharide at the nonreducing end to form a free α(1,6) linked oligosaccharide with a terminal α(1,2) linked mannose residue. This process releases the terminal</p>
    Formula:C82H137N5O60
    Purity:Min. 95%
    Molecular weight:2,152.96 g/mol

    Ref: 3D-ON28969

    10mg
    8,976.00€