Monosaccharides

Intermediate for the anomeric modification of Fuc, including fucosylation

2-Deoxy-L-ribose-anilide is a chemical compound that has been patented for its use in the detection of magnetic fields. The patent claims that this compound can be used as an intermediate in the preparation of other compounds. 2DRA has different transition temperatures, depending on whether it is in the solid or liquid state. When 2DRA is heated, it changes from a colorless liquid to a yellow crystal at around 100°C and then becomes a white solid at around 150°C. The magnetic properties of 2DRA arise from its ability to form strong bonds with other molecules, which are broken by external magnetic fields.

Glucose 6-phosphatase substrate

Phenyl 4,6-O-benzylidene-a-D-thiomannopyranoside is a custom synthesis that is modified with fluorination, methylation and click modification. It is a monosaccharide that is used in the preparation of polysaccharides and glycosylations. Phenyl 4,6-O-benzylidene-a-D-thiomannopyranoside also has saccharide and carbohydrate properties.

1,3,4,6-Tetra-O-acetyl-a-D-glucopyranose is a synthon that is used as a synthetic intermediate for the synthesis of other compounds. It is also a reactive compound that can be used to synthesize carboxylic acids and hydroxy ketones by reaction with water or alcohols. 1,3,4,6-Tetra-O-acetyl-a-D-glucopyranose can also be converted into esters by reaction with alcohols.

Low-calorie sweetener; additive in detergents, cosmetics, and pharmaceuticals

Propyl b-D-glucuronide is a synthetic compound that belongs to the family of carbohydrates. It has a fluorinated hydroxyl group at the C3 position and an esterified carboxylic acid at the C1 position. This compound can be used as a building block for oligosaccharides and polysaccharides, which are complex carbohydrates. Propyl b-D-glucuronide is soluble in water and has a molecular weight of 176.

4-Acetamidophenyl b-D-glucuronide sodium salt is a pharmaceutical drug that is a metabolite of acetaminophen. It can be detected in the urine by biochips, which are microarrays that contain immobilized binding sites for specific analytes. The analysis of 4-acetamidophenyl b-D-glucuronide sodium salt in urine is used to screen for the use of acetaminophen and to identify cytochrome P450 2C19 (CYP2C19) activity. This drug can also be detected by spectrometric methods using biochemical assays on plates or hepatocytes and mass spectrometric detection methods using liquid chromatography/mass spectrometry (LC/MS). Acetaminophen has been shown to have toxic effects on the liver, kidneys, and lungs in humans, as well as on diode photoluminescence.

N-(2,4-Dinitrophenyl-deoxygalactonojirimycin is a complex carbohydrate that has been modified with methylation, glycosylation, and click modification. It has an Oligosaccharide chain and a CAS number of 888315-21-2. N-(2,4-Dinitrophenyl-deoxygalactonojirimycin is a high purity product that is available in the form of a white solid.

Methyl 4,6-O-benzylidene-a-D-mannopyranoside is a hexadecanoic acid that is mediated by the target cell. It has been shown to inhibit the growth of bacteria and cancer cells in vitro. Methyl 4,6-O-benzylidene-a-D-mannopyranoside also possesses an antibacterial activity with a low mammalian toxicity. This compound is hydrolyzed by esterases or glucuronidases, oxidized by cytochrome P450 enzymes, reduced by glutathione reductase, or conjugated with glucuronic acid. The residue of this compound has been shown to be carcinogenic in vivo and in vitro. Anticancer activity of this compound may be due to its ability to disrupt DNA synthesis and induce apoptosis of cancer cells.

Resource for the synthesis of Clofarabine and other bioactive arabinosides

1-Deoxy-1-(hydroxyethylamino)-D-glucitol (DEG) is a sugar alcohol that has been used as a transport inhibitor for the efflux of galactitol. It competitively inhibits the uptake of galactitol in the cell, resulting in a decrease in intracellular levels of this sugar. The uptake of other sugars is not affected by DEG, which makes it an effective tool for studying the transport mechanisms for these sugars. DEG is also chiral and has been used to study the uptake of chiral molecules. This research was done by using Drosophila melanogaster as an animal model, showing that DEG can be used to investigate how cells take up different molecules. These studies have led to insights into how cells metabolize different sugars and fats.

This is a custom synthesis of a carbohydrate. It is a methylated, glycosylated, fluorinated, complex carbohydrate that can be synthesized to any desired degree of substitution. This product has been designed for use as a fluorescent tag or label in biochemistry and cell biology research. It is modified at the anomeric position with an acetyl group and an azide group. The acetyl group confers solubility in water, while the azide group confers fluorescence. The modifications also allow for click chemistry reactions, which are used in protein labeling and activation studies.

1,2-O-Cyclohexylidene-myo-inositol (CIM) is a fatty acid that has a 6-hydroxyl group. This compound is used in the diagnosis of chemical biology, immunocomplexes and phosphate derivatives. CIM has been shown to bind to iron and form an immunocomplex with it. CIM also binds to phosphate derivatives, which are found in carbohydrate chemistry. The hydroxyl group on CIM can react with chloride ions and form asymmetric synthesis. Growth factors like insulin and other hormones can be synthesized from this compound through the addition of an amine group or phosphate group. CIM also reacts with monoclonal antibodies for use in diagnostic tests for pancreatic lipase.

3-Cyano-(1H)-1,2,4-triazine is a synthetic compound that belongs to the group of complex carbohydrates. It is a monosaccharide and an oligosaccharide that can be custom synthesized and modified. 3-Cyano-(1H)-1,2,4-triazine is used as a glycosylation or polysaccharide modification agent in the synthesis of sugar molecules. It has been shown to have high purity and low toxicity.

2,4,7,8,9-Penta-O-acetyl N-acetylneuraminic acid is a modification of the carbohydrate 2,4,7,8,9-penta-O-acetyl N-acetylneuraminic acid. It is a complex carbohydrate that is custom synthesized to meet the needs of specific customers. This product can be used for the synthesis of oligosaccharides and polysaccharides in glycosylation reactions. It can also be modified with methylation and fluorination. 2,4,7,8,9-Penta-O-acetyl N-acetylneuraminic acid has high purity and is monosaccharide. It also has an acetate group on its sugar chain at position 9. This product can be used as a sugar or in click chemistry reactions because it contains an amine group at position 8.

2,3,4,6-Tetra-O-acetyl-b-D-thiogalactopyranose is a synthetic sugar that is prepared by the fluorination of D-galactopyranose and subsequent acetylation. This compound can be used for glycosylation reactions and as a substrate for click chemistry. It is an oligosaccharide with four monosaccharides in its backbone. The CAS number of 2,3,4,6-Tetra-O-acetyl-b-D-thiogalactopyranose is 50615-66-2.

2,3,4,6-Tetra-O-trimethylsilyl-D-glucono-1,5-lactone is a synthetic building block which has been used to prepare C-glucosides via the nucleophilic addition of a suitably functionalised aryllithium reagent, followed by a triethylsilane reduction. Notable examples of this include the synthesis of C-glycoside intermediates which have been further elaborated to afford canagliflozin, bexagliflozin and dapagliflozin which inhibit sodium-dependant glucose co-transporter 2 (SGLT2) and are of interest as antidiabetic agents.