d-galactose-d-1

D-Galactose-d-1 is the deuterated form of D-Galactose. D-Galactose is a naturally occurring hexose and serves as the C-4 epimer of glucose.

D-Melibiose (Galalpha1-6Glcbeta) is a reducing disaccharide formed by an alpha-1, 6 linkage between galactose and glucose (D-Gal-α(1→6)-D-Glc).

Propargyl-PEG4-tetra-Ac-beta-D-galactose is a PEGylated proteolysis-targeting chimera (PROTAC) linker used for PROTAC synthesis [1].

6-O-2-Propyn-1-yl-D-galactose functions as an irreversible glycolinker, facilitating the attachment of cytotoxic drugs for applications in antibody-drug conjugation (ADC).

Galactose 1-dehydrogenase, pseudomonas fluorescens, a dehydrogenase found in Pseudomonas fluorescens, facilitates the oxidation of L-arabinose and D-galactose, utilizing NADP+/NAD+ as a cofactor. This enzyme is employed in diagnostic assays to quantify total galactose levels and serves as a biocatalyst in the production of galacturonic acid salts.

Anticanceragent 232 (compound 12f) is a sugar hybrid designed from 1-azide glycosides derived from d-glucose, d-galactose, and d-mannose. The IC50 values for this compound are 1.05 μM against MCF-7 cells and 18.03 μM for MDA-MB231 cells.

AMOR is unique to plant cell walls and enhances plant fertilization efficiency and capacity

6-O-beta-D-Galactopyranosyl-D-galactose, a disaccharide, is a constituent of the polysaccharide backbone characterized by beta-(1→6) glycoside linkages, with a side chain attached to the primary chain through a beta-(1→3) bond.

Galactose 1-phosphate Potassium salt (α-D-Galactose-1-phosphate Dipotassium Pentahydrate) is an intermediate in the galactose metabolism and nucleotide sugars metabolism pathways.

Galactokinase (BiGalK), a phosphotransferase, catalyzes the ATP-dependent phosphorylation of α-D-galactose to galactose 1-phosphate [1].

Lactodifucotetraose (Difucosyllactose), a tetrasaccharide extracted from human milk, consists of one D-glucose, one D-galactose, and two L-fucose molecules [1].

α-Lactose (hydrate) (α-D-Lactose (hydrate)), the primary carbohydrate in mammalian milk, consists of two sugar units: glucose and galactose, and exists as two anomers, α and β. It serves various roles in the food and pharmaceutical industries, including as a free-flowing or agglomerating agent, and a diluent for pigments, flavors, or enzymes [1] [2] [3].

β-D-Galactose pentaacetate, a negative regulator of insulin, possesses plasma membrane penetrating ability and can be hydrolyzed by intracellular esterases. It inhibits leucine-induced insulin release in Wistar rat islets, potentially preventing excessive insulin release in pathological conditions [1].

1-Amino-1-deoxy-β-D-galactose (β-D-Galactosylamine) is a galactose analog utilized as a competitive inhibitor. It facilitates the separation, purification, identification, differentiation, and characterization of β-D-galactosidases and galactose oxidases.

UDP-a-D-Galactose disodium salt is a donor substrate for galactosyltransferases employed in the biosynthesis of galactose-containing oligosaccharides[1].

D-Melibiose (Standard) is the standard substance of D-Melibiose, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. D-Melibiose (Galalpha1-6Glcbeta) is a reducing disaccharide formed by an alpha-1, 6 linkage between galactose and glucose (D-Gal-α(1→6)-D-Glc).

Isocampneoside I, an acylated phenethyl oligosaccharide isolated from Cistanche deserticola (Orobanchaceae), inhibits D-galactose-induced cytotoxicity and protects primary hepatocytes in mice [1].

1-Thio-β-D-galactose, Sodium Salt is a biochemical reagent used in glycoscience research. Glycoscience examines the structure, synthesis, biology, and evolution of sugars, encompassing carbohydrate chemistry, enzymology of glycans, protein-glycan interactions, and the role of glycans in biological systems. It is closely linked to fundamental research, biomedicine, and biotechnology.