Monosaccharides

Propylbeta-D-glucopyranoside is a sugar transport inhibitor that is used to inhibit bacterial growth. It has been shown to bind to the glucose transporter and quench tryptophan fluorescence in plant cells. This active form of Propylbeta-D-glucopyranoside also inhibits bacterial growth by binding to fatty acid esters and cytochalasin, modifiers of cell membrane permeability, which inhibit the synthesis of fatty acids. Microcapsules containing this drug have been shown to be effective against staphylococci and other bacteria. The activity of Propylbeta-D-glucopyranoside can be increased by hydrochloric acid or sodium hydroxide, which increase the solubility of its salts.

2-Deoxy-scyllo-inosose is a biochemical with an unknown function. It is not a substrate for any known enzyme, but has been shown to be a substrate for the synthesis of corynebacterium glutamicum. The reaction mechanism of 2-deoxy-scyllo-inosose is still unclear, but it has been proposed that this molecule undergoes dehydration and then undergoes an acid catalyzed aldol cyclization to form 3-aminohexanol. This reaction produces fluorescence resonance energy transfer in group p2 subtilisin.
2DOS is also an antimicrobial agent which exhibits activity against Gram positive bacteria such as Streptococcus pyogenes, Enterococcus faecalis, and Bacillus subtilis.

1-Deoxy-L-idonojirimycin hydrochloride is a chaperone that is structurally related to the natural substrate, L-idonojirimycin. It has been found to interact with recombinant human Hsp70 and Hsp90. 1-Deoxy-L-idonojirimycin hydrochloride enhances the kinetic and thermodynamic parameters of these chaperones in vitro. The structural analysis of this compound revealed that it binds to both Hsp70 and Hsp90, which may be due to its ability to mimic the natural substrate's binding site on these chaperones.

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.

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.

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.

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

L-Idaric acid 1,4-lactone is a synthetic glycosylidic sugar that can be modified with fluorine compounds to create a variety of derivatives. It is used as a monomer in the synthesis of oligosaccharides, polysaccharides, and complex carbohydrates. L-Idaric acid 1,4-lactone can also be synthesized from methyl erythritol tetraacetate and glycerol in the presence of acetic anhydride.

Hydroxyterbinafine b-D-glucuronide is a synthetic monosaccharide that has been modified by the addition of a fluorine atom. Hydroxyterbinafine b-D-glucuronide is an oligosaccharide or polysaccharide, which is composed of at least two saccharides. It is obtained from the hydrolysis of methylated hydroxyterbinafine. This compound has been shown to have antiviral, antifungal and anticancer activities.

2-Deoxy-2-fluoro-D-[1-13C]glucose is a pharmacopoeia that is used in the diagnosis of thyroid gland, myocardial ischemia and malignant tumors. It is also used for the study of glucose metabolism in the thyroid gland, cerebral cortex and myocardium. 2-Deoxy-2-fluoro-D-[1-13C]glucose binds to pyranose sugars and has been shown to be an effective agent in the treatment of malignant tumors. This drug has also been shown to inhibit glucose metabolism in the thyroid gland, cerebral cortex and myocardium.

6-Deoxy L-glucose is a sugar analogue that inhibits the transport of glucose in bacteria. It competes with glucose for binding to transporter proteins and prevents glucose from being transported into the cell. 6-Deoxy L-glucose has been shown to inhibit the growth of wild-type strains, such as E. coli K12, in a dose-dependent manner. The antibiotic also reduces ATP production by inhibiting enzymes critical for glycolysis and gluconeogenesis. 6-Deoxy L-glucose has an optimum pH of 7.5 and is activated by hydrochloric acid or hydroxyl groups at the gamma position.

Thioglucosides are a type of sugar that is modified with a thiol group at the C-3 position. A thioglucose can be synthesized by methylation, click modification, and fluorination. Thioglucoses have been used in the past for the production of oligosaccharides and polysaccharides, as well as in complex carbohydrate research. They are also used in the production of high purity monosaccharide sugars. This product is available for custom synthesis to meet your needs.

Solasodine 3-glucoside is a sugar that belongs to the group of oligosaccharides. It has been synthetically modified by fluorination, methylation, and click chemistry. Solasodine 3-glucoside is synthesized from sucrose in a glycosylation reaction with glucuronic acid and an aminoglycoside antibiotic. The sugar analogs are then converted to the desired saccharide structure by monosaccharide synthesis or polysaccharide synthesis. This product is custom synthesized to order for customers and can be modified to suit their needs with click chemistry and other modifications.

Laninamivir is an antiviral drug that inhibits the neuraminidase activity of influenza A and B viruses. It is a prodrug that is activated by esterases to form the active metabolite laninamivir carboxylate, which inhibits virus replication. Laninamivir has been shown to be effective against oseltamivir-resistant mutants and has been used in combination with oseltamivir as a treatment for pandemic influenza. Laninamivir has also been studied in pediatric patients with influenza-like symptoms, with significant reductions in symptom severity, duration of symptoms, and viral load.

D-Glucoheptose is a sugar that can be used as an alternative to sucrose in the food industry. It is obtained by hydrolysis of inulin, which is a complex carbohydrate that consists of chains of fructose molecules with terminal d-glucose residues. D-Glucoheptose has been shown to be metabolized by lysine residues, which are present in many proteins and enzymes that are involved in glucose metabolism. D-Glucoheptose also participates in reactions involving chondroitin sulfate and type strain interactions. It has been shown to have a hydroxyl group on the C2 position and methyl glycosides on the C3 position, as well as benzyl groups on the C6 position. The chemical composition of D-glucoheptose can be determined using chromatographic methods or analytical methods.

2-Methoxycarbonylphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside is a high purity and custom synthesis sugar that can be fluorinated and glycosylated. This molecule has been modified with methyl groups and is an oligosaccharide. It is a complex carbohydrate with saccharide units, which are monosaccharides or polysaccharides. CAS No. 7791-66-4

N6-Benzyladenine-3-glucoside is a carbohydrate that is modified with a click chemistry reaction. It is synthesized from D-mannose and 6-benzylaminopurine and has been glycosylated with 2,3,4,6-tetra-O-acetyl glucosamine. N6-Benzyladenine-3-glucoside is an important component of the bacterial cell wall. The compound consists of a single sugar chain and is fluorinated at the C2 position.