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Catalog Number:
42256
Gal[2346Ac]β(1-3)GlcNPhth[46Bzd]-β-MP
Purity:
≥ 97% (HPLC)
Synonym(s):
4-Methoxyphenyl3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside
Documents
$334.10 /1G
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Product Information

Gal[2346Ac]β(1-3)GlcNPhth[46Bzd]-β-MP is a specialized glycan derivative engineered for advanced carbohydrate research. This compound features functionalized acetyl and benzyl groups, providing enhanced stability and specificity for chemical synthesis and structural analysis. Its unique β(1-3) glycosidic linkage supports studies of glycan assembly and interactions within biological systems.

Widely used in glycomics, this derivative is ideal for applications such as glycan synthesis, glycan-based drug discovery, and the development of diagnostic tools. It also aids in exploring glycan-protein interactions and the role of glycosylation in cell signaling and immune responses. Gal[2346Ac]β(1-3)GlcNPhth[46Bzd]-β-MP offers reliable performance, making it a preferred choice for researchers in both academia and industry.

Synonyms
4-Methoxyphenyl3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside
Purity
≥ 97% (HPLC)
Molecular Formula
C42H43NO17
Molecular Weight
833.8
Appearance
White to off-white powder
Optical Rotation
a20D = 9 - 13 ° (C=1 in CHCl3)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-Methoxyphenyl3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside
Purity
≥ 97% (HPLC)
Molecular Formula
C42H43NO17
Molecular Weight
833.8
Appearance
White to off-white powder
Optical Rotation
a20D = 9 - 13 ° (C=1 in CHCl3)
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications
Gal[2346Ac]β(1-3)GlcNPhth[46Bzd]-β-MP is widely utilized in research focused on:
  • Glycosylation studies: Serves as a model compound for analyzing β(1→3) glycosidic linkages, aiding in understanding glycan biosynthesis and function.
  • Enzymatic synthesis research: Assists in exploring efficient and regioselective methods for producing β(1→3) galactosides, contributing to advancements in green chemistry. :contentReference[oaicite:0]{index=0}
  • Glycoconjugate development: Utilized in the synthesis of complex glycoconjugates, facilitating studies on cell-cell communication and molecular recognition.
  • Lectin interaction assays: Aids in investigating the binding specificity of lectins to β(1→3) linked glycans, important for understanding immune responses.
  • Pharmaceutical research: Supports the design of glycan-based therapeutics, enhancing drug targeting and efficacy.

Citations