Monosaccharides

<p>N-Amyl b-D-glucopyranoside is a monosaccharide with a glucose residue at the 1 position and an amyl group at the 2 position. It is a synthetic sugar that can be used as a starting material in glycosylation reactions to modify oligosaccharides, saccharides, and complex carbohydrates. N-Amyl b-D-glucopyranoside can also be fluorinated, methylated, or modified by click chemistry to produce novel compounds. N-Amyl b-D-glucopyranoside is typically obtained by the glycosylation of amylamine with dibenzoyl glucose in the presence of an acid catalyst. This reaction produces a mixture of mono-, di-, tri-, tetra-, penta-, hexa-, hepta-, octa-, nona-, deca-, undeca-, dodeca-, and tetradecasaccharides, which</p>

<p>Gypsogenin-3-O-glucuronide is a saponin found in the roots of Gypsophila paniculata, a plant native to China. It has been shown to have anti-inflammatory and anti-tumor activities. Gypsogenin-3-O-glucuronide has been shown to inhibit tumor growth in mice by inhibiting protein synthesis. The pentasaccharides that make up gypsogenin are present in different proportions, which leads to differences in the biological activity of this compound. This is one of the reasons why saponins have not yet been fully explored for potential use in medicine.</p>

<p>Glycolytic inhibitor; pro-apoptotic; anti-cancer agent</p>

<p>Synthetic building block</p>

<p>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).</p>

<p>Ethyl 2,3-di-O-benzyl-4,6-O-benzylidene-a-D-thiomannopyranoside is a custom synthesis of an oligosaccharide with a complex carbohydrate structure. It can be modified to suit customer specifications. This product has been fluorinated and is available in high purity. Ethyl 2,3-di-O-benzyl-4,6-O-benzylidene-a-D-thiomannopyranoside is a sugar that can be used for the synthesis of polysaccharides and saccharides. It has been synthesized by methylation and Click modification.</p>

<p>1,2,3,5,6-Penta-O-acetyl-D-galactofuranose is a condensation product of a 4-methylumbelliferone with the anomeric form of D-galactose. It is a white crystalline solid that can be obtained in yields up to 200 g per multigram of reactants. This compound has been shown to react with chloride ion and zinc chloride at elevated temperatures to yield the corresponding chloride or zinc salt. The crystal structure of this compound has been studied by x-ray diffraction and found to have an anomeric configuration and a space group P2(1)22(1). Carbohydrates are polyhydroxyaldehydes or polyhydroxyketones containing at least one hemiacetal or hemiketal group in their structure. The general formula for carbohydrates is (Cx(H2O)y)z where x is usually 2 or 3, y is</p>

<p>Fluorinated glucose analog</p>

<p>α-D-Mannose-1-phosphate sodium is a synthetically made mannose phosphate. This compound is used in the synthesis of oligosaccharides and glycoproteins.</p>

<p>Constituent of RNA; important resource for RNA- and DNA-related syntheses</p>

<p>2-Deoxy-2-fluoro-L-fucose (2FF) is a fluorinated analogue of fucose that can be converted to GDP (Guanosine Diphosphate)-2FF in vitro, a competitive inhibitor of alpha-1,3-fucosyltransferase V. It can also be metabolised inside the cell to a substrate-based inhibitor of fucosyltransferases. 2FF reduces fucosylation of IgG in antibodies, which increases therapeutic efficacies of antibodies that cause antibody-dependent cellular cytotoxicity.</p>

<p>2,3,4,6-Tetra-O-pivaloyl-β-D-glucopyranoside is a carbohydrate modified with fluorination and methylation. It is also a synthetic oligosaccharide that has been glycosylated. This product can be custom synthesized to meet your needs. We offer high purity and custom synthesis for this product.</p>

<p>3,5-((R)-Benzylidene)-6-deoxy-L-glucono-1,4-lactone is a synthesized sugar that can be modified to include fluorination, glycosylation, methylation and other modifications. It is an oligosaccharide with a saccharide backbone made up of glucose units. The monosaccharides are galactose and glucuronic acid. 3,5-(R) Benzylidene)-6-deoxy-L-glucono-1,4-lactone is used in the synthesis of complex carbohydrates for research purposes.</p>

<p>Ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-b-D-thioglucopyranoside is a modified sugar that is used as an intermediate in the synthesis of saccharides and oligosaccharides. It is synthesized by a modification of the Knorr reaction. This product has been shown to be high purity and can be custom synthesized with a variety of functional groups, such as fluorination. Ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-b-D-thioglucopyranoside is also available in CAS No. 11764719.</p>

<p>3-O-Benzyl-D-glucopyranose is a molecule that has been optimized for its autodock score. It binds to the active site of peptidases, which are enzymes that break down proteins in the body. 3-O-Benzyl-D-glucopyranose is a nauclea that can be used as a pharmacokinetic (PK) or pharmacodynamic (PD) inhibitor. Nauclea have shown effectiveness against diabetes by preventing the breakdown of glucose, which is an important energy source for cells. 3-O-Benzyl-D-glucopyranose has also been found to be an effective inhibitor of DPPIV, which is an enzyme involved in breaking down insulin and other hormones in blood circulation. In vitro studies have shown that it may also have antiaging properties due to its ability to inhibit production of inflammatory cytokines such as IL1β, IL6, and TNFα.</p>

<p>Mannose (Man) is the C2 epimer of glucose with one hydroxyl group axial which by Hudsons rules makes it slightly less stable than glucose (Hudson, 1948). However, mannose is very common in plants and animals, and occurs in many polysaccharides, such as, galactomannans (e.g. Guar, Locust Bean Gum), mananns (e.g. Ivory Nut Mannan), Spruce Galactoglucomannan, Gum Ghatti (Whistler, 1993) and baker’s yeast (Saccharomyces cerevisiae) (Manners, 1973). Mannose is one of the key mammalian monosaccharides (Glucose, Galactose, Mannose, Fucose, N-Acetyl Glucosamine, N-Acetyl galactosamine and Sialic acid) and occurs in N-linked glycans where it is a core oligosaccharide (Gabius, 2009).</p>

<p>Phenyl b-L-thiofucopyranoside is a custom-synthesized, fluorinated, modified sugar that is used in the synthesis of oligosaccharides and polysaccharides. This compound is an excellent choice for methylation reactions due to its high reactivity and stability under harsh conditions. Phenyl b-L-thiofucopyranoside can be used as a precursor for the synthesis of saccharide derivatives, such as monosaccharides and complex carbohydrates. It has been shown to be stable to heat and pH extremes, making it ideal for use in organic syntheses.</p>

<p>Isopropyl-a-D-thiomannopyranoside is a custom synthesis that is a methylated oligosaccharide. It has been modified by click chemistry to introduce an acetate group at the C4 position of the mannose residue. This product may be used in the preparation of polysaccharides, saccharides and carbohydrates. Isopropyl-a-D-thiomannopyranoside is a white solid that is soluble in methanol and ethanol but insoluble in water. It has been shown to have high purity and high chemical stability.</p>

<p>Please enquire for more information about 2-(2-Aminoethoxy)ethyl 6-deoxy-α-L-mannopyranoside including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3,5-Tri-O-p-chlorobenzoyl-b-D-ribofuranosyl chloride is a glycosylation inhibitor that inhibits the synthesis of complex carbohydrates. It is used in the preparation of oligosaccharides and sugar derivatives. 2,3,5-Tri-O-p-chlorobenzoyl-b-D-ribofuranosyl chloride is synthesized by reacting an activated glycosylin with chloroformic acid in the presence of sodium hydroxide. This reaction can also be carried out with a variety of sugars including dextrose, fructose and glucose. Methylation at the 2 position of the benzoyl group can be accomplished by refluxing 2,3,5 -tri -O -p -chlorobenzoyl b -D -ribofuranosyl chloride with methyl iodide in dry acetone for 4 hrs. The methylated product can be purified</p>