Paper
Synthesis of p-nitrophenyl 2-acetamido-2-deoxy-3-O--?-galactopyranosyl-?-galactopyranosides
Published May 1, 1976 · K. Matta
Carbohydrate Research
Q2 SJR score
16
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
P-nitrophenyl 2-acetamido-2-deoxy-3-O-?-galactopyranosyl-?-galactopyranosides can be synthesized by a similar reaction-sequence, yielding crystalline products.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
Synthesis of p-nitrophenyl 2-acetamido-2-deoxy-O-β-Dgalactopyranosyl-β-D-glucopyranosides☆
P-nitrophenyl 2-acetamido-2-deoxy-3-O--D-galactopyranosyl--D-glucopyranoside and p-nitrophenyl 2-acetamido-2-deoxy-6-O--D-galact
1975·24citations·K. Matta et al.·Carbohydrate Research
Carbohydrate Research
Structure of the carbohydrate of antifreeze glycoproteins from an antarctic fish
The structure of the glycoproteins from Trematomus borchgrevinki fish shows that they are composed of repeating units of a diglycosyltripeptide, Ala-Ala-Thr-Odisaccharide, with a /I-galactosyl residue bound to
1975·69citations·W. Shier et al.·FEBS Letters
FEBS Letters
Structure of the O-glycosidically linked carbohydrate units of fetuin.
Fetuin contains three O-glycosidically linked carbohydrate units attached to serine and threonine residues, with two serine and one threonine residue involved in carbohydrate attachment.
1974·507citations·R. Spiro et al.·The Journal of biological chemistry
The Journal of biological chemistry
A rapid procedure for derivatizing agarose with a variety of carbohydrates: Its use for affinity chromatography of lectins
This study presents a rapid method for derivatizing agarose with various sugars, enabling the purification of lectins by affinity chromatography, potentially benefiting studies of carbohydrates-specific proteins.
1974·49citations·R. Bloch et al.·FEBS Letters
FEBS Letters
Sialyltransferase acceptor activity of "antifreeze" glycoproteins from an antarctic fish.
"Antifreeze" glycoproteins from the Antarctic fish T. borchgrevinki effectively accept N-acetylneuraminic acid, suggesting they evolved during adaptation to a freezing environment by losing the ability to transfer sialic acid to the glycoprotein structure.
1974·15citations·W. Shier et al.·Biochemical and biophysical research communications
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Citations
Conformational analysis of the carbohydrate portion of T and TN haptens by NMR spectroscopy and molecular modeling
The carbohydrate portion of T and TN haptens adopts a quasi-parallel orientation, with hydroxyl groups relatively mobile and the crotyl chain showing significant segmental mobility in all three solvents.
1994·5citations·S. Hanessian et al.·Tetrahedron
Tetrahedron
ProcessingO-glycan core 1, Galβ1-3GalNAcα-R. Specificities of core 2, UDP-GlcNAc: Galβ1-3GalNAc-R(GlcNAc to GalNAc) β6-N-acetylglucosaminyltransferase and CMP-sialic acid:Galβ1-3GalNAc-R α3-sialyltransferase
Core 2 6-GlcNAc-T and 3-SA-T enzymes in leukemia cells show tissue-specific kinetic differences, suggesting potential targets for developing inhibitors of O-glycan biosynthesis.
1993·21citations·W. Kuhns et al.·Glycoconjugate Journal
Glycoconjugate Journal
Direct access to neoglycoproteins and glycopolymers from single precursors. Synthesis of T-antigen and N-acetyl-lactosamine-β-D-(1→6)-α-D-GalNAc conjugates
This study demonstrates a method for synthesizing neoglycoprotein and glycopolymer conjugates from single precursors, useful for immunochemical research.
1992·5citations·R. Roy et al.·Bioorganic & Medicinal Chemistry Letters
Bioorganic & Medicinal Chemistry Letters
Combined Chemical and Enzymatic Synthesis of a Disialylated Tetrasaccharide Analogous to M and N Bloodgroup Determinants of Glycophorin a
Disialylated tetrasaccharide 8 can be synthesized using a combination of chemical and enzyme methods, providing a potential tool for studying bloodgroup determinants in glycophorin a.
1988·18citations·H. T. de Heij et al.·Journal of Carbohydrate Chemistry
Journal of Carbohydrate Chemistry
Synthesis of methyl 2-acetamido-2-deoxy-3-O-(β-d-galactopyranosyl)-α-d-galactopyranoside from a corresponding thioglycoside derivative
This study demonstrates the successful synthesis of methyl 2-acetamido-2-deoxy-3-O-(-d-galactopyranosyl)--d-galactopyranoside from a corresponding thioglycoside derivative using halide i
1987·2citations·M. Haraldsson et al.·Glycoconjugate Journal
Glycoconjugate Journal
Substrate specificity and other properties of the beta-D-galactosidase from Aspergillus niger.
The beta-D-galactosidase from Aspergillus niger efficiently hydrolyzes -Gal-(13)-Gal, -Gal-(13)-Gal-1OC 6H4 NO 2 -p, and -G
1983·24citations·D. Sykes et al.·Carbohydrate research
Carbohydrate research
Synthesis of 3-O-(2-acetamido-2-deoxy-3-O-β-d-galactopyranosyl-β-d-galactopyranosyl)-1,2-di-O-tetradecyl-sn-glycerol☆
This study presents a stereo- and regio-selective synthesis of 3-O-(2-acetamido-2-deoxy-3-O--d-galactopyranosyl--d-galactopyranosyl)-1,2-di-O
1982·20citations·T. Ogawa et al.·Carbohydrate Research
Carbohydrate Research