Monosacáridos

2-Keto-L-gluonic acid hydrate, also called 2-oxo-gulonic acid hydrate, L-xylo-2-hexulosonic acid hydrate (2-KLG) and D-sorbosonic acid hydrate, is an important intermediate in the synthesis of L-ascorbic acid (vitamin C) and can be produced by modified E. herbicola.

2,3,4,6-Tetra-O-acetyl-D-glucopyranose is a carbohydrate that is used in the synthesis of besifloxacin. This compound has been studied as an analog for many other natural compounds and its derivatives have shown to be effective against bacteria such as Staphylococcus aureus and Clostridium perfringens. The acetyl groups on this molecule allow it to be easily converted into other compounds with desired properties. This compound has been found to be acidic and can be used as a medicinal preparation or analytical chemistry reagent. The hydroxyl group on the 2 carbon atom allows the molecule to form glycoside derivatives. The halides on this molecule are also important for making new molecules by replacing one of the hydrogen atoms with another halogen atom. The phenylpropanoid glycosides are found in plants and may contain an enantiomeric form of 2,3,4

Methyl 2,6-dideoxy-a-D-glucopyranoside is a custom synthesis of an oligosaccharide that is modified with fluorination. It is a saccharide, or carbohydrate, that has been methylated and glycosylated. The modification of this complex carbohydrate has been achieved through the use of the Click reaction. This product has been purified to high purity and is ready for use in research and development.

2,3,4-Tri-O-benzyl-L-rhamnopyranose is a chemical compound that belongs to the family of carbohydrates known as rhamnopyranoses. It is a derivative of L-rhamnose, which is a naturally occurring aldohexose sugar. The compound is often used as a glycosyl donor in the synthesis of oligosaccharides and glycoconjugates. The three benzyl groups in the molecule provide protection for the hydroxyl groups, allowing for selective deprotection and glycosylation. 2,3,4-Tri-O-benzyl-L-rhamnopyranose is also used as a precursor in the synthesis of various natural products.

L-Fucose-1-phosphate disodium salt is a high purity, synthetic, fluorinated carbohydrate that is used to modify saccharides. This modification can be accomplished by methylation or glycosylation. L-Fucose-1-phosphate disodium salt has been shown to be useful for glycosylation reactions with click chemistry. It has been shown to have a wide range of applications including modification of oligosaccharides and polysaccharides in the field of biotechnology.

D-Glucono-1,4-lactone is a sugar that is produced by the action of glucoamylase on starch or cellulose. It can be used as a source of food for yeast, in the production of polyesters and plastics, and as a precursor to vitamin C. The pH optimum for D-glucono-1,4-lactone production is between 3.5 and 4.5. X-ray crystal structures have shown that the enzyme binds to crystalline cellulose via hydrogen bonding interactions, which are formed by hydroxyl groups on the enzyme and carboxyl groups on crystalline cellulose. These interactions are important for the cleavage of glucose from crystalline cellulose by D-glucono-1,4-lactone. D-glucono-1,4-lactone has been shown to reduce blood glucose levels in rats with metabolic disorders when administered orally at doses

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.

Allyl 2-O-acetyl-3-O-benzyl-a-L-rhamnopyranoside is a synthetic monosaccharide that is used in the synthesis of complex carbohydrates. It has a CAS number of 940274-20-4 and may be modified with fluorine or methyl groups. Synthetic allyl 2-O-acetyl-3-O-benzyl-a -L -rhamnopyranoside is also known as "Methylated, Custom synthesis, Click modification, Oligosaccharide, Polysaccharide, saccharide, sugar."

Methyl 2,3,4-tri-O-methyl-α-D-glucopyranoside is a synthetic monosaccharide that has been fluorinated with bromine. The synthetic process for this compound is click chemistry, which involves the use of copper and a chiral ligand. Methyl 2,3,4-tri-O-methyl-α-D-glucopyranoside is an example of a carbohydrate modification. It is also an oligosaccharide that contains three monosaccharides.
Methyl 2,3,4-tri-O-methyl-α-D-glucopyranoside can be used in glycosylation or methylation reactions due to its high purity and custom synthesis. This compound can also be used as an Oligosaccharide due to its saccharide composition.

Glucose 6-phosphatase substrate

Ethyl 4,6-O-benzylidene-b-D-thiogalactopyranoside is a synthetically produced carbohydrate typically used as a building block in oligo-saccharide synthesis.

Inhibitor of lysosomal acid β-glucosidase (GlcCerase/glucocerebrosidase) with IC50 in nanomolar range for wildtype and mutant enzyme. It behaves as pharmacological chaperon by binding to instable GlcCerase active site at neutral pH values and facilitating the protein folding. In acidic lysosomes, isofagomine gets release from the enzyme active site. This results in increased levels of functional glucocerebrosidase and brings therapeutic benefits to patients with Gaucher disease.

7-Deoxy-D-glycero-L-ido-heptitol is a synthetic carbohydrate that is a methylated, saccharide and polysaccharide. It is a custom synthesis and can be modified with Click chemistry. This product has CAS number 90319-73-6 and can be modified with fluorination. 7DGHLH is a high purity product that has been synthesized from carbon dioxide and hydrogen gas. It is an oligosaccharide that has been glycosylated and is available in the form of a powder or liquid.

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.