Monosacáridos

fucosylation inhibitor

1-Chloro-1-deoxyribitol is a methylating agent that can be used for the synthesis of complex carbohydrates, such as oligosaccharides and polysaccharides. It is also used in click chemistry to modify saccharides with fluoride or other reagents. 1-Chloro-1-deoxyribitol is highly pure and stable, and is available in monosaccharide form. This compound is a synthetic sugar that has been modified to contain chlorine atoms at both the hydroxyl groups.

Hesperetin 7,3'-O-b-D-glucuronide is a custom synthesis that can be synthesized with a variety of modifications including the addition of fluorine atoms. It is an oligosaccharide or polysaccharide consisting of saccharides. Hesperetin 7,3'-O-b-D-glucuronide is a white crystalline powder that has high purity and low impurities. It is an effective topical treatment for acne vulgaris and other skin conditions.

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

The compound 1,7,7a-Triepialexine is an alkaloid that is found in plants of the genus Trientalis. It has been shown to have anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis. The compound also has a stereoselective synthesis and a stereoselective syntheses.

2,3,4,6-Tetra-O-acetyl-β-D-thiogalactopyranose sodium salt is a high purity custom synthesis sugar with a click modification. The fluorination and glycosylation are carried out to give the desired product. It has CAS No. 73962-00-2 and is a synthetic carbohydrate that can be used in oligosaccharides, monosaccharides, saccharide and complex carbohydrates.

Resource for the industrial synthesis of ascorbic acid alias Vitamin C

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.

1,2:3,4-Di-O-isopropylidene-a-D-galactopyranose, also known as diacetone-D-galactose and galactose diacetonide, is a partially protected monosaccharide building block with isopropylidene groups on the 1,2 and 3,4 hydroxyls. The 6-hydroxyl is unprotected and able to undergo a variety of chemical transformations, such as glycosylation acting as a glycosyl acceptor to form 1,6-linked disaccharides.

L-Erythrulose is an organic compound that is a sugar alcohol. It can be synthesized from the aldol reaction of glycolaldehyde and dehydroascorbic acid, which are both found in natural sources. L-Erythrulose has shown to have intramolecular hydrogen transfer (H-transfer) reactions, where the hydroxyl group migrates from one C atom to another. This kinetic data was obtained using surface methodology on model systems containing l-erythrulose and bacteria with wild-type or mutant strains. The conformational properties of L-erythrulose were also investigated by comparing its chemical structures with those of other sugars.

2,3,4,6-Tetra-O-benzyl-D-glucopyranose is a selectively protected intermediate, where the anomeric 1-O-hydroxyl group is free. This hemiacetal has been used successfully as an intermediate for glucosylation couplings, where it was converted into 2,3,4,6-tetra-O-benzyl-D-glucopyranose trichloroacetimidate using trichloroacetonitrile in the presence of a base such as potassium carbonate and DBU. Importantly, this imidate donor with no neighbouring participating groups is commonly used for the selective formation of α-glucosides. 2,3,4,6-tetra-O-benzyl-D-glucopyranose can also be oxidized to the lactone, or reduced to give the open chain form. Additionally, 2,3,4,6-tetra-O-benzyl-D-glucopyranose can be used for the preparation of glucono-1,5-lactone hydrazine, which was used, in-turn, to form a glucosylidene-spirocyclopropane.