Monosaccharides

2,3,4,6-Tetra-O-benzyl-1,5-di-O-mesyl-D-glucitol is a substituted sugar alcohol that can exist as either an intramolecular or an intermolecular isomer. The intramolecular isomer has a carboxylate group in the 6 position and the intermolecular isomer has a propionate group in the 6 position. 2,3,4,6-Tetra-O-benzyl-1,5-di-O-mesyl-D-glucitol has conformational properties that depend on which substituent occupies the 4 position. Benzene rings are more flexible than benzyloxy groups. The geometry of 2,3,4,6 - Tetra - O - benzyl - 1 , 5 - di - O - mesyl - D - glucitol changes from chair to boat with substitution at position

Fluconazole D-glucuronide is a synthetic, fluorinated sugar that has been modified with a glycosylation. It is synthesized by reacting fluconazole with the sugar glucuronic acid in the presence of an enzyme called glycosyltransferase. Fluconazole D-glucuronide is a custom synthesis, and it can be used as a pharmaceutical intermediate to produce other compounds. Fluconazole D-glucuronide is also used as an analytical standard for quantifying fluconazole in biological samples.

Iminosugar 1 is a fluorinated saccharide that belongs to the group of carbohydrates. It is synthesized by the modification of glucose with a fluorine atom. This modification prevents crystallization and increases solubility in water. Iminosugar 1 has been modified by methylation and glycosylation to increase its stability. This product is available as a custom synthesis, and has high purity.

2,5-Anhydro-D-mannofuranose oxime is a glycosylation inhibitor that prevents the formation of glycosidic bonds. It is used in the synthesis of complex carbohydrates, such as polysaccharides and oligosaccharides. This compound can be fluorinated or methylated to produce 2,5-anhydro-D-mannofuranose oxime derivatives that are useful for click chemistry. 2,5-Anhydro-D-mannofuranose oxime has been shown to inhibit the enzymatic conversion of mannitol to mannose and fructose by blocking the enzyme alpha mannosidase. The high purity of this compound makes it suitable for use in a variety of reactions, including glycobiology studies and carbohydrate modifications.

Main metabolite of antiretroviral drug Abacavir with potent activity against human immunodeficiency virus type 1 (HIV-1). Abacavir is eliminated by hepatic metabolism to two major metabolites: 5’-glucuronide formed by uridine diphosphate glucuronyl transferase and 5’-carboxylate formed by cytosolic alcohol dehydrogenase.

6-Amino-6-deoxy-L-sorbose is a sugar that is metabolized by the body to produce energy. This compound has been shown to be an effective antidiabetic, as it may inhibit glucose production in the liver and enhance insulin sensitivity. 6-Amino-6-deoxy-L-sorbose is a nutrient that can be found in food sources such as bananas, potatoes, and soybeans. It can also be synthesized from various plant sources. The biosynthesis of this compound is dependent on a number of enzymes, including L-arabinose 1 phosphate dehydrogenase.

Glucose covalently bound to BSA through a 3 atom spacer.

(S)-3-((2R,3S,5S)-5-Allyl-3-(benzyloxy)-4-oxotetrahydrofuran-2-yl)propane-1,2-diyl dibenzoate is a small molecule that inhibits the activity of the epidermal growth factor receptor (EGFR). The EGFR is a transmembrane protein that binds to and signals through growth factor proteins. Inhibition of EGFR signaling prevents activation of downstream proteins such as extracellular signal regulated kinase 1/2 and phosphatidylinositol 3 kinase. This stabilized form has been shown to inhibit the growth of tumor cells in vitro and in vivo.