Monosaccharides

2,3,4,6-Tetra-O-acetyl-D-mannopyranose is a stereoselective technique used for the production of trisaccharides. It is also an acetylated form of D-mannopyranose that is obtained by acetylation of D-mannopyranose with acetic anhydride in the presence of hydrochloric acid or pyridine. The compound can be obtained as either levorotatory or dextrorotatory isomers depending on whether the hydroxyl group or carbonyl group are in the axial position. 2,3,4,6-Tetra-O-acetyl-D-mannopyranose can be used as a substrate for enzyme preparations to produce aminoglycoside antibiotics such as hygromycin A. Acetylation increases the solubility and stability of this drug and reduces its toxicity to humans

1,2,3,4-Tetra-O-benzyl-6-O-trityl-a-D-mannopyranose is a methylated form of mannopyranose. It can be custom synthesized and modified with various functional groups to produce a wide range of saccharide derivatives and oligosaccharides. The 1,2,3,4-tetra-O-benzyl group is commonly used for glycosylation reactions because it can be easily removed by acid hydrolysis. The methylation of the sugar molecule also increases its stability and prevents further reactions from occurring. This product is available in high purity and has been fluorinated on one or more hydroxyl groups to make it resistant to hydrolysis.

<p>Methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-D-glycero-D-galacto-non-2-enonate is a synthetic oligosaccharide that is used in the synthesis of glycosides. The carbohydrate has been modified to include fluorination and glycosylation. This product can be custom synthesized to meet your specifications.</p>

<p>4-Nitrobenzyl b-D-thiogalactopyranoside is a synthetic glycosylation agent that can be used for the modification of saccharides and oligosaccharides. The product is available in different purity grades, custom synthesis, and custom modifications.</p>

Dipyridamole di-O-b-D-glucuronide is a fluorinated oligosaccharide that has been synthesized using the click chemistry reaction. It is a monosaccharide that has been glycosylated and modified with methyl groups to produce a high purity product. The carbohydrate consists of one or more sugar units linked by glycosidic bonds. Carbohydrates are classified by their number of sugar units and by the presence of other chemical groups such as phosphate, sulfate, or hydroxyl. This product is also used in the synthesis of complex carbohydrates and polysaccharides.

1,3,4,6-Tetra-O-acetyl-2-O-benzyl-a-D-mannopyranose (1) is a high purity monosaccharide that can be custom synthesized to meet the needs of your research. 1 is a synthetic compound that is fluorinated and glycosylated. It has been shown to be an efficient methylation and modification agent for saccharide synthesis. It also acts as a building block for oligosaccharides and complex carbohydrates.

<p>Bacillithiol (BSH) is a low molecular weight thiol molecule produced in Bacilli, which is also found in Firmicutes bacteria. It plays an important role in maintaining the balance of reactive oxygen species within cells and detoxifying certain harmful compounds. It is the α-anomeric glycoside of L-cysteinyl-D-glucosamine with L-malic acid and it seems to have antioxidant properties. Bacillithiol plays an important role in bacterial redox homeostasis and plays an important role in the detoxification of electrophiles as it is a cofactor for FosB (thiol transferase). <br>This is the salt form (trifluoroacetic acid salt, TFA) of Bacillithiol.</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>Pseudaminic acid is a sugar molecule that is found in the cell walls of bacteria, where it provides structural support. It is synthesized enzymatically by transferring the terminal hydroxyl group from glucose-1-phosphate to glycerol-3-phosphate. Pseudaminic acid can be chemoenzymatically synthesized in a scalable manner and has been shown to inhibit the growth of infectious bacteria in biological studies. Structural studies have revealed that pseudaminic acid contains an hydroxyl group and two glycosidic bonds, which are formed between the carbon atom at position C2 and C6 of glucose. This molecule also has an ester linkage between C1 and C2 of mannose. Pseudaminic acid is biosynthesized through a series of reactions that involve phosphorylation, dephosphorylation, and oxidation. This molecule also participates in protein glycosylation as well as water molecules that hydrogen bond</p>

<p>11a-Hydroxy progesterone b-D-glucuronide is a fluorinated steroid that is synthesized with high purity. It has been modified with methylation and glycosylation. 11a-Hydroxy progesterone b-D-glucuronide is a complex carbohydrate, which consists of saccharides in the form of oligosaccharides. The sugar in 11a-hydroxy progesterone b-D-glucuronide is a monosaccharide, which can be modified with fluorination or click chemistry to create a new compound. This product has CAS No. 77710-64-6 and can be custom synthesized to meet your specifications.</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>

Methyl 2-deoxy-L-ribofuranoside is an intermediate in the synthesis of l-arabinose. It can be obtained by the reaction of methyl 2,3-dideoxy-D-ribofuranoside with pivaloyl chloride. The antiviral activity of this compound has been shown by its ability to inhibit the replication of influenza A virus. Methyl 2-deoxy-L-ribofuranoside is a fluorinating agent that can be used for the synthesis of oligosaccharides and nucleosides. This intermediate also serves as a substrate for a number of organic reactions, including regioselective and stereoselective chlorination.

<p>2,4-Dinitrophenyl 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-b-D-galactoside is a glycosidase inhibitor that is used in the validation of β-glucosidases. It has been shown to inhibit the activity of a number of glycosidases, including α-, β-, and γ-. 2,4-Dinitrophenyl 3,4,6-tri-O-acetyl -2 -deoxy -2 -fluoro -b D galactoside inhibits the hydrolysis of oligosaccharides containing a terminal α-- or β--glucose moiety to produce smaller sugars. This compound can be used as an acceptor for spectrophotometric assays and as an analytical standard for measuring the degree of polymerization (DP) of oligosaccharides. The rate of its reaction with gly</p>

<p>A thio-sugar</p>

<p>5-Deoxy-D-ribose is a molecule that is an intermediate in the shikimate pathway, which produces the aromatic amino acids. 5-Deoxy-D-ribose can be synthesized from D-ribose and shikimic acid. The biosynthesis of 5-deoxy-D-ribose is catalyzed by the enzyme ribose 5'-phosphate kinase, which converts ribose 5'-phosphate to 5-deoxy--D--ribose phosphate. This reaction requires ATP as a source of energy, and it is inhibited by phosphoribosyl pyrophosphate (PRPP). The asymmetric synthesis of 5-deoxy--D--ribose has been achieved with a chiral Lewis acid catalyst. The molecular structure of 5-deoxy--D--ribose has been determined by NMR spectroscopy. Shikimate pathways are present in mammalian cells, but not in plants or bacteria.</p>

Intermediate in the synthesis of empagliflozin

<p>Cornuside is a natural compound that is found in the fruits of Cornus. It is a dihydrochalcone, which has been shown to have hypoglycemic effects and inhibit the activity of 5-hmf. Cornuside also inhibits the enzyme activities involved in energy metabolism, such as glucose-6-phosphate dehydrogenase and hexokinase. It has also been shown to have genotoxic properties and induce DNA damage. Cornuside may be useful for treating diabetes or cancer, but further research needs to be done before this can be confirmed.</p>

D-Arabinose-5-phosphate is an intermediate in the pentose phosphate pathway. It is synthesized from D-xylulose-5-phosphate by xylitol dehydrogenase. D-Arabinose-5-phosphate inhibits the enzyme xylitol dehydrogenase, which converts xylulose to d-xylulose, and thus prevents the formation of 5-hydroxyisoxazole phosphate, a precursor to the synthesis of NADPH. In this way, it blocks the synthesis of NADPH, which is essential for aerobic metabolism. This inhibition leads to a decrease in ATP production and consequently cell death.

Corchoionoside C is a natural compound classified as an iridoid glycoside. This compound is isolated from various plant species, particularly those within the Boraginaceae family. The mode of action of Corchoionoside C involves modulation of biological pathways, likely through its interaction with cellular enzymes and receptors, contributing to its potential therapeutic effects.

<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>