Monossacáridos

<p>Applications A carbohydrate metabolism regulator that has been shown to inhibit gluconeogenesis from lactate plus pyruvate and from substrates that enter the gluconeogenic pathway as triose phosphate.<br>References Joet, T., et al.: Biochem. J., 381, 905 (2004), Girardin, E., et al.: J. Biol. Chem., 280, 38059 (2005), Nghiem, N., et al.: App. Biochem. Biotechnol., 141, 335 (2007),<br></p>

<p>Applications Benzyl β-D-Glucopyranoside (cas# 4304-12-5) is a compound useful in organic synthesis.<br>References Yoshikawa, M., et al.: Chem. Pharm. Bull., 56, 1297 (2008), Takeda, Y., et al.: J. Nat. Med., 62, 476 (2008),<br></p>

<p>Applications Monosaccharide anhydrides, new markers of toasted oak wood used for ageing wines and distillates.<br>References Goldberg, D., et al.: J. Agric. Food Chem., 47, 3978 (1999), Fu, P., et al.: Environ. Sci. Technol., 43, 286 (2009),<br></p>

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

<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>3,4,6-Tri-O-allyl-D-glucal is a custom synthesis of a complex carbohydrate. It is an Oligosaccharide and Polysaccharide that can be modified by methylation and glycosylation. The product is a Modification of saccharides that has been shown to have Methylation, Glycosylation, Carbohydrate and Click modification. 3,4,6-Tri-O-allyl-D-glucal has CAS No. 434327-45-4 and is available in High purity with Fluorination.</p>

<p>L-Allose is a monosaccharide that has the chemical formula HOCH(OH)CH(OH)CHO. L-Allose is a stereoisomer of D-allose, which differs in the orientation of the hydroxyl group on its asymmetric carbon atom. L-Allose can be produced by condensation of glucose and galactose, or by hydrogenation of allulose. The enzyme immobilized on alumina catalyzes the synthesis in high yield. L-Allose has been used as a carbon source for molecular modeling studies and as an enzymatic reaction substrate in sugar alcohols production.</p>

<p>Glycerone phosphate is a cytosolic calcium (Ca2+) substrate molecule that is used to measure the activity of phospholipase A2, an enzyme that catalyzes the hydrolysis of membrane lipids. Glycerone phosphate has been shown to inhibit neuronal death and may be useful in treating neurodegenerative diseases such as Alzheimer's disease. Glycerone phosphate has also been shown to bind to monoclonal antibodies, which are proteins that bind specifically to antigens on the surface of cancer cells, thereby preventing them from binding to their corresponding receptors on healthy cells. This may limit the spread of tumor growth and increase their sensitivity to platinum-based chemotherapy.</p>

<p>Myoinositol is a cyclitol and a member of the group of hexahydroxycyclohexanes. It is found in many plants and animals, especially in brain tissue, and plays an important role as a component of cell membranes. Myoinositol has been shown to inhibit cellular glycosidases, which are enzymes that break down complex sugars. In addition, myoinositol has been shown to have anti-cancer properties. Myoinositol is used as an analytical reagent in phase chromatography to separate molecules based on their hydrophobicities. 1-D-3-Deoxy-myo-inositol also has corrosion inhibition properties and can be used as a pesticide or agrochemical.</p>

<p>D-myo-Inositol-2,4,5-triphosphate sodium salt is a phosphoinositide that is involved in the process of cell signaling. It mediates the release of intracellular calcium ions from the endoplasmic reticulum and is involved in a number of processes including protein synthesis and efflux. D-myo-Inositol-2,4,5-triphosphate sodium salt can be found in many cells and tissues, including the brain and gastrointestinal tract. The concentration of calcium ions affects the activity of this compound by enhancing or terminating its effects. In cells that are not stimulated by an agonist such as ionomycin, divalent cations can enhance the activity of this compound. When stimulated by an agonist like ionomycin, divalent cations will terminate its effects by binding to it more strongly than to guanosine residues. This dual effect on divalent cations enhances the specificity for D</p>

<p>1,2-O-Isopropylidene-b-L-arabinofuranose is a custom synthesis. It is modified by fluorination, methylation, and monosaccharide synthesis. This product can be used in the creation of oligosaccharides and saccharides. 1,2-O-Isopropylidene-b-L-arabinofuranose is a carbohydrate that has been glycosylated and polysaccharided with other sugars to form complex carbohydrates.</p>

<p>Building block for 3-O-modified glucosylamide-linked glyconconjugates</p>

<p>UDP-6-deoxy-6-fluoro-D-glucose is a chemical compound that is an intermediate in glucosyltransferase and 4 epimerase reactions. UDP-6-deoxy-6-fluoro-D-glucose is used in the enzymatic synthesis of oligosaccharides, which are important to the biology of E. coli. The structure of this compound has been determined by X ray crystallography, revealing that it is a beta anomer. UDP-6 deoxy 6 fluoro D glucose also shows promiscuity with other enzymes, such as kinases, and can be used as a substrate for profiling.</p>

<p>1,2:3,4-Diacetone-b-D-glucopyranoside is a glycosylation agent that is used in the synthesis of polysaccharides. It reacts with the hydroxyl groups of saccharide molecules to form glycosidic bonds. 1,2:3,4-Diacetone-b-D-glucopyranoside can be modified by methylation and fluorination reactions to produce different derivatives. This product is CAS No. 496879-67-5 and has a purity of &gt;98%.</p>

<p>Benzyl a-D-glucopyranoside is an organic compound with the chemical formula CHO. It is a benzoyl derivative of glucose, which has been shown to be useful in the synthesis of other glycosides. The reaction yield and condition are dependent on reaction temperature and yield rate. The chloride ion reacts with the benzoyl chloride to form an ester, which then hydrolyzes to produce the desired product and hydrogen chloride. The reaction can be carried out at room temperature or under reflux conditions.</p>

<p>2,3,4,6-Tetra-O-acetyl-D-mannopyranose is a glycosylated polysaccharide. It is a complex carbohydrate with a methylated D-mannopyranose backbone and an acetylated 2,3,4,6-tetraose sidechain. This product can be fluorinated or saccharified to make it more reactive for click chemistry. 2,3,4,6-Tetra-O-acetyl-D-mannopyranose has been custom synthesized in a high purity form that is suitable for use in various applications including polymeric materials and pharmaceuticals.</p>

<p>6-Deoxy-L-allitol is a white crystalline solid that melts at 122°C. It has an amorphous character and may be present as a mixture of rotations, form, and crystalline polymorphs. 6-Deoxy-L-allitol can be oxidized to its diol derivative by hydrogen peroxide or sodium periodate. This compound is soluble in water, methanol, and acetone. The molecular weight of this compound is 179.06 g/mol.</p>

<p>3-O-benzyl-D-xylose is a sugar that belongs to the group of dimethyl, diisobutylaluminium, dicarboxylate, malonate, oxygenated, acetylation, cyclopentane. It has been shown to be effective in cleavage and condensation reactions. 3-O-benzyl-D-xylose can be used in the synthesis of pyridinium chlorochromate and chlorochromate. This compound also reacts with pyridinium via hydride reduction and hydroxide cleavage.</p>

<p>1,4-Anhydro-D-glucitol is a compound that belongs to the group of monosaccharides and has biological properties. It has also been used in the production of acetate extracts from fetal bovine erythrocytes. The ester linkages are formed between 1,4-anhydro-D-glucitol and sodium salt by reaction with acetic anhydride. The reaction mechanism has been studied in detail, and it was found that hydroxyl groups on the molecule react with sodium ions to form an ester linkage. This compound is toxicologically safe at high doses, but can become toxic at lower doses due to its acid formation potential.</p>

<p>N-acetyl D-glucosamine (GlcNAc) is an aldohexose (2-acetamido-2-deoxyglucose) in which the hydroxyl group at position 2 is replaced by NHAc (Collins, 2006). N-acetyl D-glucosamine forms the exoskeletons of molluscs and insects as the building block of the polysaccharide chitin (Rudrapatnam, 2003). N-acetyl D-glucosamine is a key component of N- and O-linked glycans, present in glycolipids and the glycosaminoglycan hyaluronic acid (Fallacara, 2018). A recent study has suggested that N-acetyl D-glucosamine may have therapeutic potential for COVID-19 as it affects the spike protein-ACE2 receptor interaction during the infection with SARS-CoV-2 virus (Baysal, 2021).</p>