2-deoxy-d-glucose

2-Deoxy-D-glucose (2-DG) is an analog of glucose, an inhibitor of glycolysis. 2-Deoxy-D-glucose has antiviral activity, as well as inhibitory cell proliferation and apoptosis-inducing activity.

2-Deoxy-D-glucose 6-phosphate disodium is a glucose analog that inhibits glycolysis and inhibits the function of hexokinase and glucose-6-phosphate isomerase.

2-deoxy-D-Glucose-13C is intended for use as an internal standard for the quantification of 2-deoxy-D-glucose by GC- or LC-MS. 2-deoxy-D-Glucose (T6742) is a glucose antimetabolite and an inhibitor of glycolysis. It inhibits hexokinase, the enzyme that converts glucose to glucose-6-phosphate, as well as phosphoglucose isomerase, the enzyme that converts glucose-6-phosphate to fructose-6-phosphate.

2-Azido-2-deoxy-D-glucose (2-ADG) serves as a glycosylation inhibitor useful for investigating the mechanisms of glycosyltransferases.

2-Deoxy-D-glucose-D is the deuterated form of 2-Deoxy-D-glucose (T6742). This compound is a glucose analogue that acts as a glucose metabolism inhibitor by targeting hexokinase to hinder glycolysis.

2-Deoxy-D-glucose-13C6 is a 13C-labeled variant of 2-Deoxy-D-glucose. As a glucose analog, 2-Deoxy-D-glucose (T6742) functions as a glucose metabolism inhibitor by targeting hexokinase, thereby disrupting glycolysis.

2-Deoxy-D-Glucose-[13C6] (Standard) is a reference standard of 2-Deoxy-D-Glucose-[13C6] intended for quantitative analysis, quality control, and related biochemical research applications.

2-[(Azidoacetyl)amino]-2-deoxy-D-glucose, 98% has potential applications in glycobiology research.

2-Azido-2-deoxy-D-glucose tetraacetate has potential applications in glycobiology research.

2-Deoxy-D-glucose-tetraacetate is a biochemical reagent used in glycobiology research. Glycobiology examines the structure, synthesis, biology, and evolution of sugars. It encompasses carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan interactions, and the roles of glycans in biological systems. This field is closely linked to fundamental research, biomedicine, and biotechnology.

N-Acetyl-D-Glucosamine (NAG) is a monosaccharide derivative of glucose. It is released by the action of O-GlcNAcase, in mammalian systems from proteins that have been post-translationally modified with O-GlcNAc.

AD-2646 has antidepressant activity and inhibits 2-deoxy-D-glucose (2-DG)-induced gastric acid secretion.

AD-2646 FA has antidepressant activity and inhibits 2-deoxy-D-glucose (2-DG)-induced gastric acid secretion.

Glucosamine hydrochloride (Chitosamine hydrochloride) is commonly used as a treatment for osteoarthritis, although its acceptance as a medical therapy varies.

2-Deoxy-2-sulfoamino-D-glucose sodium (GlcN-2S) can potentially influence arthritis.

2-Deoxy-D-galactose is a glucose analog and glucose antagonist that inhibits the maintenance of hippocampal LTP and can suppress tumor growth by inhibiting the glycolytic process.

WP 1122 is an analog of 2-deoxy-D-glucose and acts as a potent cytotoxic agent. It functions as a glycolysis inhibitor and can be utilized in cancer research.

2-deoxy-2-fluoro-D-Glucose (2-FG) is a derivative of glucose with anticancer activity.1It inhibits the growth of 143B osteosarcoma cells grown under normoxic and hypoxic conditions when used at concentrations of 6 and 24 mM.

4,6-O-Ethylidene-α-D-glucose (Ethylidene-glucose), a derivative of glucose, serves as a competitive inhibitor for the exofacial binding site of glucose transporter 1 (GLUT1), exhibiting a Ki of 12 mM against wild-type 2-deoxy-D-glucose transport.

Homovanillic acid sulfate is used as a reagent to detect oxidative enzymes, and is associated with dopamine levels in the brain.In psychiatry and neuroscience, brain and cerebrospinal fluid levels of homovanillic acid are measured as a marker of metabolic

2-(Acetylamino)-2-deoxy-4-O-β-D-mannopyranosyl-D-glucose is a type of biochemical reagent used in glycobiology research. Glycobiology explores the structure, synthesis, biology, and evolution of sugars, involving carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. This field closely connects to fundamental research, biomedicine, and biotechnology.

1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucose is a biochemical reagent used in glycobiology research. Glycobiology explores the structure, synthesis, biology, and evolution of sugars. It encompasses carbohydrate chemistry, glycan synthesis and degradation enzymology, protein-glycan interactions, and the role of glycans in biological systems. This field is closely connected to fundamental research, biomedicine, and biotechnology.

2-(Acetylamino)-2-deoxy-4,6-O-(1-methylethylidene)-D-glucose is a biochemical reagent used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars, involving carbohydrate chemistry, glycoconjugate formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to fundamental research, biomedicine, and biotechnology.

2-(Acetylamino)-2-deoxy-4-O-(6-deoxy-α-L-galactopyranosyl)-D-glucose (Fuc-α-2-4-GlcNAc) is a biochemical reagent utilized in glycobiology research. This field focuses on the study of carbohydrate structure, synthesis, function, and evolution, encompassing carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan interactions, and the role of glycans in biological systems. Glycobiology is closely linked to fundamental research, biomedicine, and biotechnology.