alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc

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6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc href="ProdSupplierGNCB3349720_EN.htm">alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc Suppliers list
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alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc Basic information
Product Name:alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc
Synonyms:N-acetylneuraminyl-L-lacto-N-neo-*hexaose from hu;N-ACETYLNEURAMINYL-L-LACTO-N-NEO-HEXAOSE FROM HUMA;n-acetylneuraminyllacto-n-neohexaose;α-neunac-(2→6)-β-gal-(1→4)-β-glcnac-(1→3)(β-gal-[1→4]-β-glcnac[1→6])-β-gal-(1→4)-glc;N-Acetylneuraminyl-L-lacto-N-neo-hexaose, Sialyllacto-N-neo-hexaose, α-NeuNAc-(2-6)-β-Gal-(1-4)-β-GlcNAc-(1-3)(β-Gal-[1-4]-β-GlcNAc[1-6])-β-Gal-(1-4)-Glc;SIALYLLACTO-N-NEO-HEXAOSE;N-ACETYLNEURAMINYL-L-LACTO-N-NEO-HEXAOSE;D-Glucose, O-(N-acetyl-α-neuraminosyl)-(2→6)-O-β-D-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-[O-β-D-galactopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)]-O-β-D-galactopyranosyl-(1→4)-
CAS:118023-83-9
MF:C51H85N3O39
MW:1364.22
EINECS:
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Mol File:118023-83-9.mol
alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc Structure
alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc Chemical Properties
Boiling point 1708.8±65.0 °C(Predicted)
density 1.75±0.1 g/cm3(Predicted)
storage temp. −20°C
pka2.01±0.70(Predicted)
Safety Information
WGK Germany 3
MSDS Information
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SigmaAldrich English
alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc Usage And Synthesis
UsesSialyllacto-N-neohexaose II is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].
DefinitionChEBI: N-Acetylneuraminyllacto-N-neohexaose is a member of neuraminic acids.
References[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922
alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc Preparation Products And Raw materials
Tag:alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc(118023-83-9) Related Product Information
4-O-(6-O-[2-Acetamido-2-deoxy-beta-D-gluco-pyranosyl]-beta-D-galacto-pyranosyl)-D-gluco-pyranose alpha-Neu5Ac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3]-beta-Gal-[1->4]-Glc sodium salt alpha-Neunac-[2->6]-beta-Gal-[1->4]-beta-GlcNAc-[1->3][beta-Gal-(1->4)-beta-GlcNAc(1->6)]-beta-Gal-[1->4]-Glc 6-O-[2-Acetamido-2-deoxy-4-O-(beta-D-galactopyranosyl)-beta-D-glucopyranosyl]-D-galactopyranose Amyl 2-acetamido-2-deoxy-beta-D-glucopyranoside Lacto-N-neotetraose (tetrahydro-2H-pyran-2-ylmethoxy)acetic acid 6-SIALYL-N-ACETYLLACTOSAMINE* HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE