Monosaccaridi

Intermediate for the anomeric modification of Fuc, including fucosylation

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Glucose 6-phosphatase substrate

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.

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.

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-O-Isopropylidene-D-glyceraldehyde is an acetal protected glyceraldehyde building block for use in organic chemistry. The aldehyde group of 2,3-O-Isopropylidene-D-glyceraldehyde is left unprotected which allows for a range of reactions to be performed. These include aldol condensations, olefinations, Grignard reactions and imine formation, including reductive amination.

Phenyl 3,6,2',3',4',6'-hexa-O-acetyl-2-deoxy-2-trichloroacetamido-b-D-thiolactoside is a custom synthesis. It is an oligosaccharide and polysaccharide with a high purity and modification. This compound has a CAS No., and is an Oligosaccharide and Polysaccharide. Phenyl 3,6,2',3',4',6'-hexa-O-acetyl-2-deoxy-2-trichloroacetamido-b-D-thiolactoside is a sugar which is synthesized by Monosaccharides.

4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside is a white crystalline powder. It is soluble in water and ethanol. This chemical has been used as a reagent for the methylation of saccharides and oligosaccharides with 4-methoxybenzene sulfonate. It is also an excellent substrate for click chemistry reactions.

D-Maltose 1-phosphate dipotassium salt is a disaccharide that can be used in the synthesis of oligosaccharides and polysaccharides. It is also an excellent candidate for further modification.

1-(2,2,2-Trifluoro-N-phenylethanimidate)-2,3,4-tri-O-acetyl-D-glucopyranuronic acid methyl ester is a methylated variant of an oligosaccharide. It has been synthesized by the click modification of an oligosaccharide with a monosaccharide and a fluorinated saccharide. This compound has been shown to have antiviral activity against the influenza virus in vitro. The antiviral activity may be due to its ability to inhibit the viral polymerase and RNA synthesis or to prevent virus assembly and release.

Glucose metabolite

L-Glucono-1,5-lactone is a crystalline compound that is used in structural biology and as a growth factor. It has been shown to inhibit the transfer of phosphate from ATP to protein substrates, binding to receptor sites and inhibiting the activity of enzymes such as protein kinase C. L-Glucono-1,5-lactone has also been shown to bind to an aluminum ion with a constant of 0.5 M. This binding inhibits the enzymatic activity of phosphatases that hydrolyze phosphate esters which are important for cellular metabolism.