Monosaccharides

D-Altrose is an alpha-hydroxy acid that is synthesized from D-arabinose and trifluoroacetic acid. It has been shown to be a substrate for the synthesis of oligosaccharides, which are important in carbohydrate chemistry. This molecule can also be used as a reagent in the preparation of carbohydrates with a specific configuration at C2. One use of this product is in generating analytical methods that can distinguish between D-altrose and D-arabinose by monitoring the ratio of hydrogen fluoride to carbonyl group signals. D-Altrose may also be used in asymmetric synthesis, where it is a useful chiral building block for the construction of galacturonic acid derivatives.

D-Galactosamine (GalN) is an aldohexose (2-amino-2-deoxygalactose) in which the hydroxyl group at position 2 is replaced by an amino group (Collins, 2006). Galactosamine (as the N-acetyl derivative) forms a key part of both N- and O-linked glycoproteins, glycolipids and glycosaminoglycans. Treatment of experimental animals with D-galactosamine / lipopolysaccharide causes lethal liver injury characterized by apoptosis of the hepatocyte and it is used as a laboratory model to study the effect of therapeutic agents (Hirono, 2001).

Xylitol is a sugar alcohol that has been shown to have antimicrobial properties. It has been found to be effective in inhibiting the growth of bacteria, yeast, and fungi by disrupting their cell membranes. In addition, xylitol appears to have the ability to reduce plasma glucose levels in animals and humans. Xylitol has also been shown to inhibit the growth of bacteria in acidic environments by binding with proteins on the bacterial cell membrane. This binding prevents the transport of nutrients into the cell and results in cell death. Xylitol is not metabolized by human cells because it cannot be broken down into acetaldehyde or acetate. However, xylitol can be metabolized by certain types of liver cells.
Xylitol BP/EP is a drug that belongs to the class of antidiabetic agents used for lowering blood sugar levels in patients with diabetes mellitus type II (insulin-dependent diabetes). It is an exogenous insulin secretagogue that stimulates insulin secretion from pancreatic

Ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-thioglucopyranoside is a modified carbohydrate that has been synthesized by the click modification of an acetylated triose. This chemical was synthesized by reacting ethyl 2-(2'-deoxy-(1->4)-beta--D--glucopyranoside) with trimethylsilylacetamide and copper(I) chloride in dry tetrahydrofuran. This product has high purity and is used as a research tool for glycobiology.

Inhibitor of sialyltransferases

D-Galacturonic acid sodium salt is a salt form of D-galacturonic acid. It is an extract from seaweed and has been shown to have the ability to be absorbed in the intestines. This compound can be used as a diagnostic tool, such as for detecting strontium or radioactive isotopes in urine samples. The esters of this compound have been shown to have chelating activity and may be useful as reagents in analytical chemistry.

Inhibitor of O-GlcNAcase

3,4,6-Tri-O-acetyl-D-glucal, also called 1,5-anhydro-2-deoxy-D-arabino-hex-1-enitol triacetate, is the acetate protected cyclic enol-ether (glycal) of D-glucose. 3,4,6-Tri-O-acetyl-D-glucal is a building block useful in the synthesis of a range of carbohydrates with the glucal double bond allowing other functional groups to be introduced. As an alkene, a glycal can undergo electrophilic addition across the double bond to introduce halogens and epoxides or be used to generate deoxy monosaccharides. 3,4,6-Tri-O-acetyl-D-glucal can undergo a Ferrier rearrangement with an alcohol and Lewis acid to give a 2,3-unsaturated product.

2-Acetamido-1,6-anhydro-2-deoxy-b-D-glucopyranose is widely used in carbohydrate chemistry. It is used as reagent for the synthesis of oligosaccharides and also as a precursor in the synthesis of oligopeptides. 2-Acetamido-1,6-anhydro-2-deoxy-b-D-glucopyranose is an analog of levoglucosan, a compound that is often used to trace for biomass burning in enviromental chemistry studies.

Scyllo-inosamine is a redox potential that belongs to the class of antimicrobial agents. It is derived from the amino acid inosine, which is found in RNA and DNA. Scyllo-inosamine has been shown to inhibit bacterial growth by inhibiting protein synthesis. It also acts as an aminotransferase inhibitor, which may be used for the treatment of certain human pathogens. Scyllo-inosamine has been shown to have beneficial effects on the regulation of benzyl groups and hydroxyl group reactions. It has also been shown to inhibit polymerase chain reaction activity and titration calorimetry activity.

A beta glycoside with an alkyne handle suitable to click chemistry

Custom synthesis of D-glucuronic acid, sodium salt monohydrate.

Valuable chiral building block; rare sugar applied in wood preservation

2,3,4-Tri-O-acetyl-a-D-xylopyranosyl bromide - Stabilised with 2.5% CaCO3 is a chiral compound that is a drug for the treatment of estrogen deficiency in postmenopausal women. It is synthesized from D-xylose and acetone by reductive elimination using an organotin catalyst. The resulting product has a nitro group at the 4 position and can be activated as a priming agent for DNA synthesis. This compound has been shown to be effective in treating intestinal disorders such as ulcerative colitis.
2,3,4-Tri-O-acetyl-a-D-xylopyranosyl bromide - Stabilised with 2.5% CaCO3 has been used to conjugate estrogens with various drugs to create new compounds that are more potent than free estrogens alone. Bioavailability of these conjugates has

2-Deoxy-D-galactose is a metabolite of the carbohydrate galactose. It is found in the rat striatum and has been shown to inhibit glutamate dehydrogenase activity. 2-Deoxy-D-galactose also inhibits 2,3,4,5 tetrahydropyridine (MPTP) induced neurotoxicity in mice by increasing levels of uridine and nucleotides in the brain. This agent also has an effect on glomerular filtration rate and on protein synthesis. The glycoside derivatives of 2-deoxy-D-galactose are formed by joining a sugar molecule to hydroxyl group. These derivatives are then transported into cells via glucose transport proteins.

Decyl Glucoside is an alkylglycoside non-ionic surfactant and emulsifier. It is commonly used in foaming and cleansing products, often by natural personal care companies due to being plant derived and biodegradable. Decyl glucoside, also known as capryl/caprylyl glucoside, is derived from combination of coconut fatty alcohols and corn starch glucose.

b-D-Allopyranose is a monosaccharide that has been modified with fluorine. It is used as a substrate for the production of oligosaccharides and polysaccharides, which are important biomolecules in cell walls and membranes. b-D-Allopyranose can be customized to suit your needs with Click chemistry, Methylation, or other modifications. We offer high purity b-D-Allopyranose at competitive prices.

Benzyl 3,4-O-(2',3'-dimethoxybutane-2',3'-diyl)-a-D-mannopyanoside is a modification of an oligosaccharide. It is a complex carbohydrate that has been synthesized from a monosaccharide and methylated on the 3' hydroxyl group. This product is available as a custom synthesis and is offered in high purity. The CAS number for this compound is 1423035-45-3.
br>
Benzyl 3,4-O-(2',3'-dimethoxybutane-2',3'-diyl)-a-D-mannopyanoside can be used as a sugar or fluorinated saccharide in glycosylation reactions with other molecules. It can also be used to produce polysaccharides by glycosylation with other molecules such as glucose, mannose, or sucrose.