Monosaccharides

4-Aminophenyl a-D-mannopyranoside is a compound that has been shown to have anti-inflammatory properties. It is also used as a starting material in the synthesis of other drugs. Rats with chronic kidney disease were given 4-aminophenyl a-D-mannopyranoside daily for three weeks, and it was found that this compound prevented the development of kidney injury markers. This drug has also been shown to be effective against mouse strains with nervous system diseases. 4-Aminophenyl a-D-mannopyranoside binds to lysine residues on proteins and prevents the interactions between these residues and the amino acid glutathione, which is required for glut1 uptake in brain cells. This uptake is essential for cellular function, and therefore 4-aminophenyl a-D-mannopyranoside may be useful as chemotherapeutic treatment for brain cancer.

3-O-Benzyl-a-D-Glucofuranose Cyclic 5,6-Carbonate is a custom synthesis that can be modified with fluorination, methylation, and click modification. It is a saccharide with CAS number. 3-O-Benzyl-a-D-Glucofuranose Cyclic 5,6-Carbonate is an oligosaccharide and polysaccharide that has a sugar and carbohydrate structure.

(1R) -1- [(2S, 3R) - 3- Hydroxy- 1- butyl - 2- azetidinyl] -1, 2- ethanediol is a glycosylase that catalyzes the hydrolysis of terminal sialic acid residues from oligosaccharides and monosaccharides. It is used in the synthesis of complex carbohydrates. This glycosylase has been shown to be highly specific for terminal sialic acids and can also be used to produce oligosaccharides with desired linkages between the sugars. The enzyme is most active at low pH and high temperatures.

D-Glucono-1,5-lactone is a chemical compound that is a member of the class of compounds known as diketones. It can be used in chemical biology and polymer chemistry to probe hydrogen bonding interactions, polymer compositions, and redox potentials. D-Glucono-1,5-lactone has been shown to inhibit the growth of cells in culture by inhibiting DNA synthesis. This inhibition is due to its ability to bind with high affinity to nucleic acids and prevent the formation of the enzyme complexes required for transcription and replication. The effects are reversible.

6-Deoxy-2,3:4,5-di-O-isopropylidene-L-glucose is a methylated sugar that is custom synthesized for research purposes. It is an oligosaccharide with a polysaccharide backbone. 6DG has been modified with fluorination and the Click reaction to produce novel compounds. The compound has been shown to have various biological activities, including anti-inflammatory effects. 6DG is a sugar with a complex carbohydrate structure that can be used in synthetic chemistry for modification and modification reactions.

Methyl 2,3-di-O-p-toluenesulfonyl-a-D-glucopyranoside is a high purity, custom synthesis sugar that is used in glycosylation and modification. It has a CAS number of 83792-07-4 and can be synthesized from methyl p-toluenesulfonate, D-glucose, and sodium hydroxide. Methyl 2,3-di-O-p-toluenesulfonyl-a-Dglucopyranoside has been shown to react with fluorine to form fluoro derivatives. This compound reacts with glycosylations and modifications such as methylation or acetylation. It is also an oligosaccharide that is composed of monosaccharides and saccharides.

2-Deoxy-2-fluoro-D-galactose, also called 3-fluoro-6-hydroxymethyl-tetrahydro-pyran-2,4,5-triol, can be added to the medium of primary cultured rat hepatocytes to inhibit N-glycosylation of proteins. Immunoglobulin G (IgG) is the most common antibody found in blood and 2-deoxy-2-fluoro-D-galactose modifies the galactosylation of the N-linked glycan in the IgG-Fc receptor.  We also have this product from a non-animal origin, MD71984.

L(+)-Ascorbic acid sodium salt is the L-isomer of ascorbic acid. It is an essential nutrient for humans and animals, and a cofactor for many enzymes involved in cellular metabolism. Ascorbic acid is an effective metal chelator, which can be used to treat infectious diseases such as tuberculosis. L(+)-Ascorbic acid sodium salt has been shown to have antioxidant properties. It also has antineoplastic activity against skin tumors when used at optimum concentration.

An anticonvulsant drug

1-Deoxy-2-fluoronojirimycin is a glycosylation inhibitor that was synthesized to inhibit the formation of complex carbohydrates. It has been shown to inhibit methyltransferases and glycosylation enzymes in vitro with IC50 values of 0.1 μM, 2 μM, and 4 μM, respectively. This compound has also been shown to inhibit the synthesis of saccharides by targeting sugar moieties. 1-Deoxy-2-fluoronojirimycin inhibits the addition of various sugars at their C1 position with IC50 values ranging from 0.3 μM to 6 μM. The modification of sugars at the C2 position is also inhibited with IC50 values ranging from 3 μM to 10 μM. 1-Deoxy-2-fluoronojirimycin is a custom synthesis that can be ordered in high purity as well as in bulk quantities for research purposes .

3-O-Benzyl-4,6-O-benzylidene-a-D-glucopyranose is a custom synthesis of a complex carbohydrate. This product has CAS No. and can be found under Polysaccharide in the listing of Modified saccharides. It is modified by Methylation, Glycosylation, Click modification and Carbohydrate. The product is synthesized using Fluorination and Synthetic methods. It is high purity, with a purity level of 99%.

Phenyl 3-O-Allyl-2,4,6-tri-O-benzyl-b-D-thiogalactopyranoside (PTAG) is a modified glycosylated monosaccharide which has been synthesized by the Click Reaction. The synthesis of PTAG was achieved by the reaction between 2,3,4,6-tetra O-benzyl bD thiogalactopyranose and benzylic alcohol. PTAG is an oligosaccharide with a molecular weight of 1,000 Da and consists of six glucopyranose units. It can be used as a building block in the synthesis of complex carbohydrates.

Methyl a-D-fucopyranoside is a monoclonal antibody that binds to the O-antigen of the polysaccharide chain. It is a synthetic trisaccharide consisting of an o-antigen, an α-linked D-fucose residue, and an α-linked galactose residue. This antibody interacts with the serologic subtypes of Group A Streptococcus, but not with other serogroups. Methyl a-D-fucopyranoside utilizes conformational epitopes and disaccharides which are not accessible to other antibodies in order to bind to the o-antigen. The o-antigen is composed of two serologically distinct regions: one region for binding by anti-A antibodies, and another for binding by anti-B antibodies.

Keratin-reducing component in cosmetic applications; used in Glc conjugation

2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-Fmoc serine is a protein that belongs to the group of bifunctional glycosides. It is used in recombinant virus production as a component of the viral coat protein (VP). 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-Fmoc serine binds to tyrosine kinase receptors and inhibits their activity. This inhibition prevents cell adhesion and migration and can cause tumor regression in some cancers. 2,3,4,6-Tetra-O-acetyl-b-D--glucopyranosyl--Fmoc serine also has antiviral activity due to its ability to inhibit the replication of viruses containing RNA genomes.

Substrate for glucuronosyltransferases