Monossacáridos

D-Glucose - monohydrate is a glucose molecule that is found in the blood stream. It is the preferred source of energy for the brain and has been shown to enhance brain function. Glucose is also used to maintain the water balance of cells and tissues, as well as to prevent or treat hypoglycemia. This molecule can be found in many foods, such as honey, corn syrup, molasses, fruits and fruit juices. D-Glucose - monohydrate has antibacterial efficacy against a number of bacteria including staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and Bacillus subtilis. It can also inhibit squamous cell carcinoma growth in vivo by preventing the proliferation of cancer cells. D-Glucose - monohydrate is structurally similar to adenosine diphosphate (ADP), which binds to dinucleotide phosphate (DP) enzymes that are involved in energy metabolism

1-Deoxy-1-vinylsulfonamido-b-D-glucuronide is a synthetic sugar. It is a member of the group of compounds called sulfonamides. This drug has high purity, and can be custom synthesized to meet specific requirements. 1-Deoxy-1-vinylsulfonamido-b-D-glucuronide is used in the synthesis of oligosaccharides, monosaccharides, and saccharides.

1-Deoxy-D-glucitol is a sugar alcohol that is a reduction product of glucose. It can be produced by the reduction of glucose 6-phosphate in muscle cells. The enzyme dehydrogenase catalyzes this reaction, which is influenced by the presence of gemini surfactants such as DMSO. 1-Deoxy-D-glucitol has been shown to have anti-fungal properties against Aspergillus parasiticus and other organisms. This activity may be due to its ability to inhibit phosphofructokinase, hexokinases, or other enzymes that are involved in the metabolism of glucose by these organisms.

1,3,4,6-Tetra-O-acetyl-2-deoxy-2-(tetrachlorophthalamido)-D-glucopyranose is a custom synthesis of methylated oligosaccharide. It is a complex carbohydrate that has been modified with fluorination and acetylation. This saccharide is a monosaccharide with a sugar group at the end of its carbon chain. It has high purity and is synthesized from natural sugars such as glucose or sucrose. The CAS number for this product is 174356-26-4.

4-O-Acetyl-3,6-di-O-tert-butyldimethylsilyl-D-galactal is a high purity, custom synthesis sugar. This compound has been modified with Click chemistry and fluorination. The modification has been shown to have glycosylation and methylation. This product is synthesized from a complex carbohydrate.

Versatile resource for organic synthesis, e.g. of the inhibitor swainsonine

D-Galactosamine-1-phosphate is a precursor of UDP-glucose and is used in the synthesis of fatty acids. D-Galactosamine-1-phosphate is synthesized by the enzyme UDP-glucose pyrophosphorylase, which catalyzes the reaction between UDP and D-galactose. It is expressed in strains that have been engineered to produce recombinant proteins. This product can be produced in vitro by a number of methods, including enzymatic or chemical synthesis. The enzyme activity of D-galactosamine 1 phosphate synthase is temperature dependent, with optimal activity at 40°C. This product has been shown to inhibit hepatitis virus production and lipid formation in vitro.

Benzyl N-acetyl-4,6-O-benzylidene-a-isomuramic acid is a high purity custom synthesis. It is a sugar that has been modified by click chemistry, fluorination, glycosylation, and methylation. The modification of this compound includes the addition of an acetamide group to the hydroxyl group on carbon 2 and a benzylidene acetal at carbon 4. This compound has been synthesized to be used as a monosaccharide or an oligosaccharide in complex carbohydrates.

2,3,4,6-Tetra-O-acetyl-b-D-galactopyranosyl-(N2-Fmoc)-L-serine is a chemical compound. The molecular formula of this compound is C20H32O5 and the molecular weight is 376.429 g/mol. The chemical structure of this compound contains a tetra acetyl bDgalactopyranosyl residue linked to an N2 substituted Lserine residue.

The 6-cyclohexylhexyl-4-O-(a-D-glucopyranosyl)-b-D-glucopyranoside is a monoclonal antibody that targets acetylcholine. It binds to nicotinic acetylcholine receptors in the nervous system, preventing the binding of acetylcholine and thereby inhibiting the transmission of nerve impulses. The antibody has been shown to inhibit multidrug resistance in cell culture. This may be due to its ability to bind hydroxyl groups on molecules that are known inhibitors of multidrug resistance. This drug also has an amphipathic nature, which allows it to penetrate lipid bilayers and membranes.

4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside is a membrane stabilizer that prevents the mesenchymal transition of cells. This compound inhibits the growth of human tumor cells in vitro and has been shown to be an anti-tumor agent. 4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside binds to DNA and RNA and blocks translation or transcription. It also prevents the formation of ternary complex by interfering with the binding between aminoacyl tRNA synthetases and their cognate tRNAs. The compound is activated by intestinal enzymes and is metabolized in human liver microsomes to a more reactive form that can bind to cellular macromolecules such as proteins.

Inhibitor and pharmacological chaperone of lysosomal β-glucosidase (glucosylceramidase). The compound binds to the unstable glucosidase active site during the folding and post-translational processing in Golgi apparatus and endoplasmatic reticulum. It is effective in stabilising the enzyme and preventing accumulation of glucosylceramides in models for Gaucher disease, especially in the ones carrying N370S mutation. In addition, it has antiviral activity against Hepatitis C virus, which is mediated by misfolding of viral glycoproteins in the presence of the inhibitor.

Methyl 2-deoxy-3,5-di-O-toluoyl-D-ribofuranoside is a carbohydrate compound that is a modification of the saccharide and oligosaccharide. It is fluorinated at the 3' position. The monosaccharide is synthesized from D-ribose and methylated at the 2' and 5' positions. Methyl 2-deoxy-3,5-di-O-toluoyl-D-ribofuranoside is a synthetic sugar that has been modified with glycosylation and Click chemistry.