Monosaccharides

<p>3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-b-D-mannopyranose is a synthetic monosaccharide that is used as a substrate for the production of various oligosaccharides and polysaccharides. This substance can be fluorinated to produce 3,4,6-tri-O-(3′,5′ -difluoro) acetyl-1,2:5′,6′ -di(O—ethoxyethylidene)-b-D mannopyranose. It has been shown that methylation of the C1 position in this compound results in a variety of different compounds with different properties. In addition to its use as a substrate in organic synthesis, 3,4,6 triacetyl 1,2:5', 6'-di(O—ethoxyethylidene)-b D mannopyranose is also</p>

<p>D-Gluconic acid sodium salt is a glycol ether that is used as an injection solution. It has been shown to have antibacterial efficacy against wild-type strains of bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. The in vitro antimicrobial action of D-gluconic acid sodium salt was found to be due to its ability to inhibit bacterial growth by interfering with the synthesis of DNA. D-Gluconic acid sodium salt also has been shown to have antihypertensive effects in rats through the inhibition of angiotensin II type 1 receptor (AT1) signaling pathway and erythrocyte proliferation. This drug also has been shown to bind benzalkonium chloride and x-ray diffraction data show that it is crystalline in nature. The analytical method for determining the concentration of D-gluconic acid sodium salt is by electrochemical impedance</p>

<p>N-5-Carboxypentyl-1-deoxygalactonojirimycin is an inhibitor of glycolipid hydrolase and a potential drug for the treatment of lysosomal storage disorders. N-5-Carboxypentyl-1-deoxygalactonojirimycin is derived from the natural product galactonojirimycin, which has been shown to inhibit glycolipid hydrolase in vitro. The compound was developed by modifying the peptide sequence to increase its affinity for the enzyme. N-5-Carboxypentyl-1-deoxygalactonojirimycin displays a higher affinity for glycolipid hydrolase than galactonojirimycin, and it also has a greater inhibitory effect on this enzyme.<br>N-5-Carboxypentyl-1-deoxygalactonojirimycin is</p>

<p>N-Acetyl-2,7-anhydro-a-neuraminic acid is a synthetic derivative of a naturally occurring sugar that is found in the human brain and other tissues. It has been proposed as a potential drug for the treatment of inflammatory bowel disease due to its ability to inhibit the growth of cells in the colon and prevent inflammation. N-Acetyl-2,7-anhydro-a-neuraminic acid has been shown to have antiinflammatory properties by inhibiting the synthesis of proinflammatory cytokines. This compound binds to an enzyme called galactosamine kinase, which is involved in making certain proteins that are necessary for inflammation. The chemical structure of N-Acetyl-2,7-anhydro-a-neuraminic acid was determined through structural analysis and carbon source titration calorimetry. Magnetic resonance spectroscopy showed that this compound reacts with water molecules and chemical ionization revealed that it</p>

<p>Lectins are carbohydrate-binding proteins that can be classified into different types based on their specificities for glycan structures. One of the most common types is the N-acetyl-D-glucosamine (NAG) lectin, which binds to oligomers of NAG and related sugars. Lectins are used to activate cells and induce cell death. The dodecyl NAG lectin has been shown to bind to glucocerebrosides in a reductively irreversible manner and has been used as a model for such interactions. This lectin is also inexpensively produced from a synthetic benzylidene acetal, which can be made from commercially available materials. It has been shown that this lectin binds to polyacrylamide gels in an SDS-polyacrylamide gel electrophoresis, with a pH optimum at 7.0 and an amino acid composition that includes glutamic acid, glutamine, asparagine, ser</p>

<p>Octanoyl b-D-glucosylamine is a synthetic compound that has been designed for use in the synthesis of complex carbohydrates. It is an octanoyl derivative of D-glucosamine, which is a sugar. This compound can be used for the modification of saccharides and polysaccharides, as well as sugars. It has been shown to be resistant to glycosylation and fluorination reactions.</p>

<p>N-Acetylmuramic acid 6-phosphate is a molecule that belongs to the class of compounds known as nucleotide phosphates. It is an intermediate in the biosynthesis of peptidoglycan, which is a major component of bacterial cell walls. N-Acetylmuramic acid 6-phosphate is synthesized from ATP and N-acetylmuramic acid by hydrolysis. The reaction mechanism for this transformation involves an imine intermediate, which can be formed through the action of two molecules of ATP and one molecule of N-acetylmuramic acid. This reaction is catalyzed by an enzyme called heterocyst. The enzyme kinetics for this transformation are influenced by many factors, including temperature, pH, and substrate concentration.</p>

<p>Please enquire for more information about N-(Formylamidino)-N-b-D-ribofuranosylurea including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methoxyphenyl b-D-galactopyranoside is a custom synthesis of a sugar with an active methyl group. It is synthesized by the Click modification of 4-hydroxyphenyl b-D-galactopyranoside and has been fluorinated. The glycosylation process has been carried out using glycone as a precursor to modify the monosaccharide and oligosaccharide. This product has a CAS number of 3150-20-7 and is considered a synthetic compound.</p>

<p>Methyl b-D-fructofuranoside is a chemical compound that is used in the production of esters and fatty acids. Methyl b-D-fructofuranoside is produced by a dehydration reaction between two molecules of acetone. The product of this reaction, methyl b-D-fructopyranoside, can be broken down into two molecules of acetone and one molecule each of methyl alcohol and carbon dioxide. This process is called alkylation. Furanocoumarin derivatives are often found in plants such as asperulosidic acid and quinquefasciatus. These compounds are found in many species of plant, but they are most concentrated in the roots of these plants because they are more metabolically active there than other parts of the plant. Environmental pollution can lead to high concentrations of furanocoumarins in plants, which can have toxic effects on organisms that come into contact with them.</p>

<p>N-Propionyl-D-glucosamine is a sugar used in the synthesis of peptidoglycan, a structural component of bacterial cell walls. N-Propionyl-D-glucosamine is synthesized from formaldehyde and propionic acid. It is used as an antibiotic to treat bacterial infections caused by Gram-positive bacteria such as streptococci and staphylococci. N-Propionyl-D-glucosamine has also been shown to have anti-fungal properties against Candida albicans and Saccharomyces cerevisiae. The biosynthesis of this compound takes place through phosphorylation of the amide group on the sugar residue, which is catalyzed by a number of enzymes including phosphotransacetylase, acetate kinase, and phosphoenolpyruvate synthase. This process requires ATP, phosphate ions, ammonium ion, and water molecules.</p>

<p>D-Fructose-1,6-diphosphate dibarium salt is a synthetic sugar that is used in the synthesis of oligosaccharides and polysaccharides. This compound can be custom synthesized to meet your specifications. D-Fructose-1,6-diphosphate dibarium salt has been shown to be soluble in water, ethanol, acetone, and chloroform. D-Fructose-1,6-diphosphate dibarium salt is a fluorinated carbohydrate with a purity of 99%. It can be modified with methylation or click modification for further applications.</p>

<p>D-Gluconic acid potassium salt is a glycol ether with biochemical properties that can be used to synthesize covalent linkages. It has been shown to have antimicrobial properties in wild-type strains of Escherichia coli and Salmonella typhimurium. D-Gluconic acid potassium salt has been shown to exhibit inhibitory effects on the synthesis of DNA, RNA, and protein, as well as enzyme activities. The matrix effect is an analytical method that measures the inhibition of bacterial growth in agar plates. Electrochemical impedance spectroscopy (EIS) is a technique that measures changes in electrical resistance when bacteria are placed on an electrode surface. This technique has been used to show that D-gluconic acid potassium salt exhibits inhibitory effects against group P2 enzymes, such as polymerase chain reaction (PCR), which is used for DNA replication and amplification.</p>

<p>8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35-O-(2,6-dideoxy-L-ribo-hexopyranosyl)amphotericin B is an antifungal drug that belongs to the class of polyene macrolides. It is a potent inhibitor of Candida albicans and Candida glabrata. This compound has been shown to have synergistic effects when used in combination with nystatin against C. albicans. 8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35O-(2,6 - dideoxy - L - ribo - hexopyranosyl)amphotericin B also inhibits toll like receptor 4 (TLR4), which is responsible for the induction of inflammatory cytokines such as IL1B and IL8</p>

<p>2,3,4,6-Tetra-O-benzyl-5-thio-D-glucono-1,5-lactone is a complex carbohydrate that can be modified with methylation and glycosylation. It is a saccharide that can be modified by fluorination and click modification. This compound is synthesized by the polymerization of allose in the presence of an enzyme to produce 2,3,4,6-tetra-O-(benzyloxymethyl)-5-thio--D--glucono--1,5--lactone.</p>

<p>Forodesine is a purine nucleoside that inhibits the nucleoside phosphorylase enzyme and prevents the synthesis of purines. It has minimal toxicity and is effective against intracellular targets such as mitochondria, which are important for apoptosis induction. Forodesine also inhibits the mcl-1 protein, which is an inhibitor of t-cell lymphomas. This drug has been shown to be effective in animal models of human lymphoma and leukemia.</p>

<p>a-D-Mannopyranosyl amine is a synthetic product that is used as a sugar donor in glycosylation reactions. It can be custom synthesized to suit the needs of the customer. The chemical structure contains a methyl group and an oxygen atom, which are both in their highest oxidation state. This product is not intended for use as a food additive or dietary supplement.</p>

<p>2-Deoxy-2-fluoro-D-fucose is a custom synthesis, which is a complex carbohydrate. It has CAS No. and polysaccharide modification and can be methylated, glycosylated, or fluorinated. The molecular weight of this product is high purity and it can be used as a sugar or carbohydrate. Click modification is possible with 2-deoxy-2 fluoro-D-fucose.</p>

<p>Please enquire for more information about D-Mannose tablets including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Thio-L-fucose is a sugar that is found in a variety of tissues and organs. It has been shown to inhibit the antibody-dependent cellular cytotoxicity (ADCC) by binding to the Fc portion of IgG antibodies, which are used to target and destroy cancer cells. 5-Thio-L-fucose has also been shown to modulate the effector functions of natural killer cells and enhance the glycan profile of dendritic cells. It may be useful as a supplement for patients undergoing chemotherapy or radiation therapy, where it may help inhibit the growth of tumor cells. 5-Thio-L-fucose inhibits ADCC activity by binding to IgG antibodies, preventing them from attaching to immune cells, which would otherwise act as effectors in destroying tumor cells. This inhibition can be reversed with a competitive inhibitor such as D-arabinose.</p>