Pyranose

α-D-Glucopyranose, 2,3,4,6-tetraacetate is a biochemical assay reagent.

1,2,3,4-Tetra-O-acetyl-β-D-glucopyranose, 96% (1,2,3,4-Tetra-O-acetyl-beta-D-glucopyranose, 96%) can be used in glycobiology research to study glycosylation mechanisms, glycosidic bond formation, and stereochemistry.

2,3,4,6-Tetra-O-acetyl-D-glucopyranose, 96% can be used in simulated glycosylation experiments.

6-Deoxy-D-glucose is an inhibitor of glucose oxidation. 6-Deoxy-D-glucose is a structural homomorph of D-glucose, and can be used for study of D-glucose transport.

2-Keto-D-Glucose (D-Glucosone) is a key intermediate in a secondary metabolic pathway leading to the antibiotic Cortalcerone. 2-Keto-D-Glucose is also an intermediate in the conversion of D-glucose into D-fructose. 2-Keto-D-Glucose is found in various natural sources, including fungi, algae, and shellfish.

\alpha-D-glucose is a monosaccharide that has a more significant insulin stimulating effect than beta-D-glucose.

6-Azido-6-deoxy-D-galactose, 95% can be used as a substrate in enzymology to study the activity and specificity of galactosyltransferases and other glycosylation enzymes.

α-D-Galactose pentaacetate (Pentaacetyl-α-D-galactopyranose) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

D-Galactose-6-O-sulfate sodium salt (D-Galactose-6-O-sulphate sodium salt) is a sulfated derivative of D-Galactose (HY-N0210). D-Galactose-6-O-sulfate sodium salt does not block the binding of ganglioside antibody DG2 to solid-phase sulfatides.

6-Azido-6-deoxy-D-glucose, 95% is used for visualizing protein-specific glycosylation in living cells.

D-Glucose 6-phosphate potassium is a biologically active compound that has the activity of being a substrate for glucose-6-phosphate isomerase. D-Glucose 6-phosphate potassium can participate in the sugar metabolism process and promote the production and utilization of energy in cells.

Chloro 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranose 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.

2-Azido-2-deoxy-D-galactose, 98% can be applied in glycobiology, can be glycosylated by glycopeptides, and can be used for the synthesis of glycoconjugates.

α-D-Galactose is a isomer of D-galactose (HY-N0210). α-D-Galactose is a polysaccharide and can be used as a carbon source.

4,6-O-ethylidene-α-D-glucose (Ethylidene-glucose), a glucose derivative, is a competitive exofacial binding-site inhibitor on glucose transporter 1 (GLUT1) with a K_i of 12 mM for wild-type 2-deoxy-D-glucose transport.

Hexyl-β-D-glucopyranoside, 98% is typically used as a mild nonionic detergent.

Tetra-O-benzyl-δ-D-Gluconolactone (2,3,4,6-Tetra-O-benzyl-D-glucono-1,5-lactone) is a 1,5-sugar lactone and protected D-glucono-1,5-lactone, which serves as a synthetic intermediate in the field of carbohydrate chemistry. Tetra-O-benzyl-δ-D-Gluconolactone acts as a model substrate for zinc-mediated Barbier allylation, crotylation and propargylation reactions.

4-Aminophenyl-α-D-mannopyranoside, 98% is a mannopyranoside. 4-Aminophenyl-α-D-mannopyranoside, 98%, after conjugation to the surface of liposomes, can enhance delivery to the mouse brain via GLUT1- and GLUT3-mediated transport. 4-Aminophenyl-α-D-mannopyranoside, 98% can be detected as a characteristic glycoside in the metabolomics of fermented foods and is considered a potential health-related metabolic marker. 4-Aminophenyl-α-D-mannopyranoside, 98% can be used in studies of glycosylation processes and enzyme-substrate interactions.

Ethyl D-glucopyranoside can be used in glycobiology research.

Thioglucose is a thiosugar with antioxidant properties. Thioglucose acts as an H₂S/polysulfide donor to elevate intracellular sulfane sulfur levels and promote hydropersulfide formation. Thioglucose reduces the endocytosis of gold nanoparticles by phagocytes, enhances cytotoxicity and improves biocompatibility by increasing their adsorption on the surface of cancer cells. Thioglucose can be engineered into a stimulus-responsive prodrug or functional reagent for the development of targeted nanocarriers, and is used in studies related to human breast adenocarcinoma and cervical cancer.