Monossacáridos

UDP-D-galactosamine disodium salt is a type of sugar that is a substrate for UDP-glucuronosyltransferase (UGT), which catalyzes the transfer of galactose from UDP-D-galactose to other molecules. The product of this reaction is UDP-D-galacturonic acid. It is produced in the liver, where it participates in the synthesis of glycoproteins, glycolipids, and glycosaminoglycans. In addition, it can be found in the distal tubule of the kidney and in leukemia cells. The histological analysis of rat liver tissue showed that UDP-D-galactosamine disodium salt is present in hepatocytes. This sugar also helps with protein synthesis and activates uridine, which can be used as a carbon source. Histological analysis also revealed that UDP-D-galactosamine disodium salt plays an important role in glucose metabolism, as well as

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.

4,7,8,9-Tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is a modified form of sialic acid. This compound is a glycosylation product that has been modified with methyl groups and fluorine atoms. The fluorination of the molecule increases its stability and prevents it from being hydrolyzed by enzymes such as β-galactosidase. 4,7,8,9-Tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is often used in the synthesis of polysaccharides and oligosaccharides for medical purposes. This compound can be custom synthesized for research purposes or to meet special requirements.

Cyanidin-3-O-sophoroside chloride (CAS: 6279-21-6) is a naturally occurring phenolic compound that has been isolated from the roots of Sophora flavescens. This compound is a glycosylated form of protocatechuic acid, which is an organic compound with antioxidant properties. The surface methodology on tissue structure showed that this compound can react with nucleophilic radicals and scavenge free radicals in the presence of chloride ions, which is important for its dietary and medicinal value. COS has also been shown to have anti-inflammatory activities in a model system by inhibiting the production of prostaglandins. COS can be extracted from plants by acidic hydrolysis or preparative high performance liquid chromatography.

1-O-Acetyl-2,3,5-tri-O-benzyl-L-ribofuranose is a modified form of ribofuranose. It is a polymer that contains three or more monosaccharides linked together by glycosidic bonds. It has been modified with methyl groups and fluorine atoms to enhance its properties. This compound can be used in the synthesis of oligosaccharides, which are complex carbohydrates that are not found in nature and have potential applications as drugs.

ADP-4-deoxy-D-glucose is a carbohydrate derivative that has been modified with fluorination. ADP-4 is a methylated, custom synthesized oligosaccharide that contains saccharide and polysaccharide chains. It is not commercially available and must be custom synthesized. The modification of the sugar to ADP-4 involves the addition of one or more atoms of fluorine and may be accomplished by click chemistry. This product has high purity and can be used as a research reagent in the synthesis of complex carbohydrates.

Ethyl a-D-thioglucopyranoside is an organic compound that is used as a precursor in the synthesis of complex sugars. Ethyl a-D-thioglucopyranoside is an oligosaccharide that contains a methylated and glycosylated sugar. The glycosidic bond in this product can be modified by fluorination to give ethyl 2,3,4,5-tetrafluorothioglucopyranoside.

Astragaloside II is a natural compound that has been shown to have anti-inflammatory effects in vitro and in vivo. Astragaloside II inhibits the production of inflammatory mediators by inhibiting phosphodiesterase and cyclooxygenase pathways. It also has a matrix effect on the cells, which may be due to its ability to activate protein kinase C. This compound also has an analytical method, which consists of HPLC with UV detection at 210 nm.

L-altronojirimycin is a diterpene glycoside that belongs to the group of natural products that have inhibitory properties against lipid peroxidation. It has been shown to decrease the concentration of 1,2-dipalmitoylglycerophosphocholine (DPPC) in primary cells and reduce the rate of lipid peroxidation in a concentration-dependent manner. L-altronojirimycin inhibits the activity of enzymes such as acetylcholinesterase and phospholipase A2, which are involved in inflammation. This drug has also been shown to have cardioprotective effects and inhibit mutations in cardiac muscle cells. L-altronojirimycin has been tested for its long-term efficacy and shown to be effective against both bowel disease and cardiac effects.

2-Amino-2-deoxy-D-idose is a sugar that is found in the cell walls of bacteria. It has been shown to be an inhibitor of the enzymes that catalyze the acetylation and methylenecyclopropanes reactions, which are necessary for bacterial growth. 2-Amino-2-deoxy-D-idose binds to copper ions, preventing them from binding with the enzymes. This drug also chelates metals such as zinc, iron, and manganese to prevent their use by bacteria.

a-L-Fucose-1-phosphate is a Glycosylation, complex carbohydrate, Methylation, Click modification, Polysaccharide, Fluorination, saccharide, Modification, sugar, Oligosaccharide and Synthetic product. a-L-Fucose-1-phosphate is available for custom synthesis and can be ordered with high purity.

Pentaric acid is a crystalline, monocarboxylic acid with a hydroxyl group. It is used as an inhibitor of corrosion in metal and as a disinfectant. Pentaric acid can be found in urine samples and has been shown to be an effective inhibitor of the enzymatic reaction that produces azobenzene, which is associated with the development of bladder cancer. This compound also inhibits the growth of bacteria. Pentaric acid is used as an additive in some detergents and soaps because it can inhibit the growth of bacteria on surfaces.
Pentaric acid was first synthesized by German chemist Otto Wohlert in 1834. Hydrogen ions are released when pentaric acid dissolves in water, lowering the pH level and causing corrosion to metal surfaces. The corrosion inhibition properties of pentaric acid have been known since its discovery, but its anti-bacterial properties were not discovered until recently when researchers found that pentar