Product Information
- DSLNH-IO-(N-Acetyl-a-neuraminosyl)-(2?3)-O-b-D-galactopyranosyl-(1?3)-O-2-acetamido-2-deoxy-b-D-glucopyranosyl-(1?3)-O-[O-(N-acetyl -a-neuraminosyl)-(2?6)-O-b-D-galactopyranosyl-(1?4)-2-acetamido)-2-deoxy-b-D-glucopyranosyl-(1?6)]-O-b-D-galactopyrano
- 5-(acetylamino)-2-[(6-{[5-(acetylamino)-6-[(4-{[3-(acetylamino)-4-{[4-{[5-(acetylamino)-2-carboxy-6-hydroxy-4-(1,2,3-trihydroxypropyl)tetrahydro-2H-pyran-2-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-5-hydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-6-[1-(1,2-dihydroxyethyl)-2,3-dihydroxy-4-oxobutoxy]-3,5-dihydroxytetrahydro-2H-pyran-2-yl)methoxy]-4-hydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl]oxy}-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)methoxy]-4-hydroxy-6-(1,2,3-trihydroxypropyl)tetrahydro-2H-pyran-2-carboxylic acid (non-preferred name)
- 5-Acetamido-2-[2-[3-Acetamido-2-[2-[[3-Acetamido-5-[6-[[5-Acetamido-2-Carboxy-4-Hydroxy-6-(1,2,3-Trihydroxypropyl)Oxan-2-Yl]Oxymethyl]-3,4,5-Trihydroxyoxan-2-Yl]Oxy-4-Hydroxy-6-(Hydroxymethyl)Oxan-2-Yl]Oxymethyl]-3,5-Dihydroxy-6-(1,2,4,5-Tetrahydroxy-6-Oxohexan-3-Yl)Oxyoxan-4-Yl]Oxy-5-Hydroxy-6-(Hydroxymethyl)Oxan-4-Yl]Oxy-3,5-Dihydroxy-6-(Hydroxymethyl)Oxan-4-Yl]Oxy-6-Hydroxy-4-(1,2,3-Trihydroxypropyl)Oxane-2-Carboxylic Acid
- <span class="text-smallcaps">D</smallcap>-Glucose, O-(N-acetyl-α-neuraminosyl)-(2→3)-O-β-<smallcap>D</smallcap>-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→3)-O-[O-(N-acetyl-α-neuraminosyl)-(2→6)-O-β-<smallcap>D</smallcap>-galactopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→6)]-O-β-<smallcap>D</span>-galactopyranosyl-(1→4)-
- Dslnh-I
- O-(N-Acetyl-α-neuraminosyl)-(2→3)-O-β-<span class="text-smallcaps">D</smallcap>-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→3)-O-[O-(N-acetyl-α-neuraminosyl)-(2→6)-O-β-<smallcap>D</smallcap>-galactopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→6)]-O-β-<smallcap>D</smallcap>-galactopyranosyl-(1→4)-<smallcap>D</span>-glucose
Disialyllacto-N-hexaose I is a complex carbohydrate that belongs to a class of saccharides called polysaccharides. Disialyllacto-N-hexaose I is synthesized through the methylation and glycosylation of sucrose. It has been modified by Click chemistry with a maleimide group to create an amide bond between the terminal alpha position on the glucose residue and the terminal alpha position on the N-acetylglucosamine residue. This modification can be used for Polysaccharide analysis, such as MALDI TOF MS. Disialyllacto-N-hexaose I has a CAS number of 137636-98-7 and has been shown to have high purity without any impurities or contaminants.
Chemical properties
Technical inquiry about: 3D-OD64737 Disialyllacto-N-hexaose I
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