Monosacáridos

2-Acetamido-2,6-dideoxy-D-galactose (2ADG) is a structural analogue of the natural monosaccharide 2,6-dideoxy-D-galactose. It has been shown to have an antimicrobial effect against aerobacter aerogenes in vitro. 2ADG is metabolized by glycosidases and methyl glycosides to form 1,4-anhydro-2,3,4,6 tetraacetamido-2,4,6 dideoxy D galactose. This compound inhibits the growth of bacterial strains that are resistant to polymyxin b., such as Pseudomonas aeruginosa. The inhibition of these bacteria is due to the inhibition of the synthesis of their outer membrane lipopolysaccharides by 2ADG. The antibacterial activity is also attributed to its ability to inhibit the metabolism of glycan molecules in some bacteria

Substrate for glucuronosyltransferases

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.

2-Deoxy-1,3,4,6-tetra-O-pivaloyl-D-glucopyranose is a glycosylation sugar that belongs to the category of complex carbohydrates. It is a methylated sugar that can be fluorinated or modified with other saccharides. This product can be custom synthesized and has high purity.

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

Synthetic carbohydrate building block

1,2,3,4,6-Penta-O-benzyl-b-D-thiogalactopyranoside is a custom synthesis that is a complex carbohydrate. It has a CAS number of 210358-01-3 and a molecular weight of 603. It is modified with saccharide, methylation, glycosylation, and carbonyl groups. This product is available in high purity and without fluorination or synthetic modification.

4-Deoxy-4-fluoro-D-glucopyranose is a fluorinated sugar that is found in the roots of Glycyrrhiza uralensis. It can inhibit glycosylation by blocking the stepwise addition of glucose to the growing oligosaccharide chain. 4-Deoxy-4-fluoro-D-glucopyranose also has biological activities, such as antiinflammatory and antitumor properties. This compound is an analog of D-arabinose and D-xylulose, which are found in many plants. 4DFG can be used to synthesize glycosides with various substituents on the hydroxyl group.

2,3,4,5-Tetra-O-acetyl-D-ribononitrile is a custom synthesis chemical. It is an Oligosaccharide, Polysaccharide, Modification and has the CAS No. 25546-50-3. It can be used as a Fluorination reagent in Synthetic Chemistry and Click modification. The purity of this chemical is high and it has a Custom synthesis. 2,3,4,5-Tetra-O-acetyl-D-ribononitrile is synthesized by Methylation and Glycosylation of sugar molecule with acetyl group. This chemical can be used to modify saccharide and carbohydrate molecules.

The 4-methoxyphenyl 2,3,6-tri-O-benzoyl-b-D-galactopyranoside (4MP) is a coagulation factor that inhibits the activity of coagulation factors Xa and IIa. The compound has been shown to be reactive with the detection methods used for other coagulation factors. The sensitivity of 4MP to detection was assessed using a battery of detection methods. 4MP was found to be more reactive than other compounds studied with regard to the use of an immunoassay for detection. This compound has hepatotoxic effects and can cause cell death in vitro. Cell culture studies show that 4MP causes membrane permeabilization and cellular uptake by bacteria.

Inhibitor of alpha-glucosidase II

Sucrose-6-acetic ester is a product of the reaction between sucrose and acetic anhydride. It is a white crystalline compound that reacts with chlorinating agents to form sulfoxide compounds. Sucrose-6-acetic ester can be converted to acetylsalicylic acid, which is used to synthesize aspirin. The reaction selectivity of this process relies on the enzyme catalysis of acetylation and triphosgene as well as an acidic or basic catalyst. Acetylation is carried out in organic solvents and requires a crystallization process for purification. This product also has fatty acid properties, which are insoluble in water and other polar solvents.