Monosacáridos

Dodecyldeoxynojirimycin is a polyketide natural product that has been shown to be a potent inhibitor of the synthesis of mannose-containing glycoproteins, including glucans and chitooligosaccharides. It binds to the active site of glucan synthetase and prevents the formation of glucose residues, which blocks glucan biosynthesis. Dodecyldeoxynojirimycin has also been shown to have anti-inflammatory properties.

2,3,4,6-Tetra-O-acetyl-a-D-glucopyranosyl chloride (TAOC) is a nuclear magnetic resonance (NMR) probe that has been used to study the structure of nuclei. It is synthesised by reacting acetyl chloride with sucrose in a reaction catalyzed by sodium hydroxide. The compound can be detected in quadrupole and resonance spectroscopy due to its high sensitivity to nuclear magnetic resonance. This NMR probe is typically used to study the structures of nuclei or for the analysis of polysaccharides.

2’-(N-Hexadecanoylamino)-4’-nitrophenyl-b-D-galactopyranoside is a synthetic substrate that is used to diagnose and monitor brain diseases. It can be used in the diagnosis of Alzheimer's disease by measuring the amount of amniotic fluid that leaks into the brain. The rate of hydrolysis of this substrate has been shown to be higher in patients with Alzheimer's disease than in healthy controls. This synthetic substrate is also useful for monitoring the activity of taurocholate galactohydrolase, which is an enzyme that breaks down bile salts and plays a role in cholesterol metabolism. The rate of hydrolysis has been found to be increased in patients with Parkinson's disease, but not in those with Alzheimer's disease or healthy controls. 2’-(N-Hexadecanoylamino)-4’-nitrophenyl-b-D-galactop

Trans,trans-3,4-Dihydroxy-D-proline is a custom synthesis that has been fluorinated and methylated. It is a polysaccharide with a sugar backbone of an oligosaccharide or saccharide. The carbons in the backbone are connected by glycosylation to form a complex carbohydrate. This product has CAS No.

fucosylation inhibitor

2-Iodoethyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside is a high purity custom synthesis that can be modified with Click chemistry. It can be synthesized by modification of methylated glycosides and saccharides. This product has been shown to have a wide range of applications in the areas of fluorination, glycosylation, and methylation. The sugar moiety is an oligosaccharide made up of one or more monosaccharides (simple sugars) joined together by glycosidic bonds. This product is often found in complex carbohydrates such as glycogen and starch.

Allyl alpha-D-glucopyranoside is an optical isomer of D-glucose that is used in the synthesis of a number of synthetic trisaccharides, including maltotriose. Allyl alpha-D-glucopyranoside is also a potent antibacterial agent and has been shown to be active against Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. Allyl alpha-D-glucopyranoside has hydrophilic and hydrophobic properties, which makes it soluble in both water and organic solvents. This compound can also form stable complexes with metal cations such as sodium and potassium, making it useful for tissue culture experiments.

Component of plant, especially grape, glucuronoxylans

2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-N'-(2-aminophenyl)thiourea is a fluorinated glycoside that is synthesized by the coupling of an acetyl group with an aminophenylthiourea. The synthesis of this compound can be customized for specific carbohydrate requirements. This product has been shown to be effective in the modification of complex carbohydrates such as polysaccharides and glycans. It is also useful for applications involving glycosylation and methylation reactions.

Methyl β-L-arabinopyranoside is a stereochemically pure monosaccharide that has been used to calibrate and quantify the conformational, stereochemical, and spectrometric methods. Methyl β-L-arabinopyranoside has a conformation that is restricted by the presence of an α-hydroxyl group at C2. The chloride ion can be used to monitor this conformation. The diameter of methyl β-L-arabinopyranoside can be measured with a micropipette and monitored using an aerosol detector. Methyl β-L-arabinopyranoside can also be quantified by mass spectrometry or spectrophotometry. The conformational, stereochemical, and spectrometric methods have been calibrated using methyl β-L-arabinopyranoside as a standard to determine their accuracy in measuring the size of other molecules.

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The interaction of 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside with DNA is selective for the hydroxyl group and for the stacking of its glycosidic bonds. The data obtained from the spectra show that this compound interacts with the sugar moiety of nucleosides to yield a product with a lower melting point. The binding constants are high and the yields are low.