Monosaccharides

3'-a-Sialyl-N-acetyllactosamine sodium salt is a high purity, custom synthesis sugar. It has been modified with fluorination, glycosylation, and methylation to provide the desired properties. This product is also available in other forms such as monosaccharide and saccharide. 3'-a-Sialyl-N-acetyllactosamine sodium salt can be used in various applications including Click modification, fluoroamination, glycosylation, carbonylation and methylation. CAS No. 350697-53-9

1,2,3,6-Tetra-O-benzoyl-5-thio-D-glucopyranose is a monosaccharide that can be synthesized by the methylation of 1,2,3,6-tetra-O-(benzoyl) D-glucopyranose. The synthesis of this compound is accomplished by a click modification and the use of a fluoroquinolone to modify the sugar at C1. This compound has been shown to be an excellent substrate for polysaccharide and saccharide synthesis as well as fluorination. Purity levels are high with this product.

2-Amino-2-deoxy-D-altrose (2AD) is a molecule with the chemical formula C6H14N2O4. It belongs to the class of compounds known as uronic acids. 2AD is an acetylated molecule that has been structurally studied by X-ray crystallography and NMR spectroscopy. The molecule contains a ring of six carbon atoms, two of which are epoxide groups. The nature of this compound is glycosidic, with focus on hexamethylphosphoramide and diamino oligosaccharides. 2AD has been shown to have anti-inflammatory activities in animals, but its exact mechanism of action remains unknown. This compound may act through a ring-opening reaction or by inhibiting prostaglandin synthesis.

Sennoside C is a bioactive phytochemical extracted from the leaves of Eclipta prostrata. It has been shown to have anti-tumor and anti-inflammatory properties. Sennoside C has also been found to be effective in treating autoimmune diseases, including psoriasis and rheumatoid arthritis. Sennoside C is a low-energy compound that binds with fatty acids to form a bound form. This bound form can be hydrolyzed by sodium hydroxide solution to release free sennosides, which are anthraquinone glycosides that can be used for the treatment of skin conditions such as eczema and dermatitis.

1,2,3,5-Tetra-O-acetyl-D-ribofuranose is a dietary supplement that can be found in the form of palladium complexes. This compound has been shown to have anti-inflammatory properties and may be effective against cancer cells. 1,2,3,5-Tetra-O-acetyl-D-ribofuranose is an acetylated pyridazine derivative with antimicrobial and antibacterial effects. It has also been shown to inhibit the synthesis of purines and pyrimidines by cleaving the 6th carbon from ribose. 1,2,3,5-Tetra-O-acetyl-D-ribofuranose is synthesized by chlorination of 2,6-, 3-, 5-, or 7-(chloropurinomethyl)pyridine with mercuric chloride or nitrosyl chloride. The cleavage products are hydroxyl group

M-topolin-9-glucoside is a synthetic sugar that has been modified by the introduction of fluorine atoms at C-2, C-3, and C-4. This sugar is used to study the interactions between carbohydrates and proteins. It is also used for the synthesis of oligosaccharides as well as for glycosylation and methylation reactions. M-topolin-9-glucoside is a monosaccharide that has been glycosylated and methylated. It can be used as a replacement for glucose in some reactions due to its stability and low cost.

Phenyl 2,3,6-tri-O-benzyl-b-D-thioglucopyranoside is a high purity, custom synthesis sugar that has been modified with Click modification, fluorination and glycosylation. It is a synthetic compound in the form of an oligosaccharide and monosaccharide. Phenyl 2,3,6-tri-O-benzyl-b-D-thioglucopyranoside has CAS No. 97974-20-4 and can be found under Modification.

Methyl D-arabinofuranoside is an antimycobacterial agent that inhibits the synthesis of mycolic acids, which are important components of the cell wall of Mycobacterium tuberculosis. Methyl D-arabinofuranoside has been shown to be active against drug-resistant strains and has been well tolerated by animals. This compound can be synthesized from 2,4-dichlorophenylacetic acid and arabinose in two steps. The first step involves a three-component condensation reaction with sodium hydroxide, hydrochloric acid, and 2,4-dichlorophenylacetic acid. The second step is a nucleophilic attack on the pyran ring of methyl D-arabinofuranoside with hypophosphorous acid. Methyl D-arabinofuranoside can also be prepared by reacting sodium nitrosobenzene with sodium benzene sulfinate in alcoholic solution

3-Deoxy-3-fluoro-D-mannose (3DFM) is a synthetic sugar molecule that acts as an inhibitor of bacterial growth. It binds to the 6-phosphate group of nucleic acids, which prevents the addition of sugar molecules to ribose or deoxyribose groups. 3DFM also inhibits the synthesis of proteins and RNA, which are necessary for bacterial growth. 3DFM is a structural analog of mannose and glucose, and has been shown to be effective against chronic infections caused by bacteria that produce lectins, such as C. difficile. This drug can be used in combination with other antibiotics to enhance their effectiveness.

4-Deoxy-D-glucose is a sugar that is synthesized by the condensation of two molecules of erythrose. It has been shown to be an efficient donor substrate for nucleophilic attack, which can lead to the synthesis of glycosides and other natural products. 4-Deoxy-D-glucose is also a competitive inhibitor of uridine diphosphate (UDP) glucose, which is an enzyme involved in the biosynthesis of UDP sugars and glycoproteins. The concentration of 4-deoxy-D-glucose affects its catalytic mechanism, as it acts as a competitive inhibitor at high concentrations. Molecular modeling has revealed that this molecule adopts a chair conformation with significant solvent exposure.

Phenyl a-L-thiorhamnopyranoside is a monosaccharide that is synthesized by the methylation of alpha-D-glucose. It is a custom synthesis that is used in the synthesis of oligosaccharides, polysaccharides, and sugar drugs. Phenyl a-L-thiorhamnopyranoside can be fluorinated to create an active form that has antibacterial activity. This compound has shown no signs of toxicity in animal studies and has been used as a food additive.

Momordicoside I aglycone is a compound that has been extracted from the roots of Momordica grosvenori. It is a potent inhibitor of the enzyme cyclooxygenase and has been shown to have analgesic, anti-inflammatory, and antipyretic activities in mice.

D-[1-13C]Galacturonic acid potassium salt is a sugar that is synthesized by the reaction of galactose with carbon dioxide. This sugar has been custom synthesized and is used in glycosylation reactions. Other modifications to this sugar include methylation and click modification, which can be done to make the sugar more reactive. D-[1-13C]Galacturonic acid potassium salt is a high purity product with a CAS number.

1,4-b-Xylobiose hexaacetate is a sugar that is used in the glycosylation of complex carbohydrates. It can be synthesized from xylose and acetaldehyde by Methylation and Click modification. 1,4-b-Xylobiose hexaacetate has been fluorinated to give a stable product. This product is soluble in water, ethanol, acetone, DMF, DMSO and other organic solvents. It can also be used for methylation or polysaccharide synthesis. The CAS number for this compound is 58024-20-7.

1,3,4,6-Tetra-O-acetyl-N-(4-methoxybenzylidene)-b-D-glucosamine is a high purity custom synthesis sugar that has been fluorinated and glycosylated. It is synthesized from the methylation of 4-(1,3,4,6-tetra-O-acetyl)-N-(4-hydroxybenzylidene)-b-D-glucosamine and can be used for the modification of saccharides or oligosaccharides. This compound has CAS No. 7597-81-1 and is known as a carbohydrate.

Muraglitazar acyl-b-D-glucuronide is a complex carbohydrate that has been modified with fluorination. The compound is synthesized from methylation, glycosylation, and carbamylation reactions with saccharides. The saccharide modification includes the attachment of various sugars such as glucose, galactose, and mannose. Muraglitazar acyl-b-D-glucuronide can be used in the synthesis of oligosaccharides and polysaccharides. It is also used for Click modification of sugar molecules.

This compound is a modification of the 2-bromoethyl a-L-fucopyranoside. It is an oligosaccharide that is a carbohydrate. It is made up of many monosaccharides, which are sugar molecules linked together. This modified carbohydrate has been synthesized from other carbohydrates and then fluorinated to make it more stable.

Ivermectin monosaccharide is a molecule that has been shown to have an inhibitory effect on the uptake of glucose by cyathostomes. This molecule does not bind to inulin, but it does bind to the receptor binding site for ivermectin. Ivermectin monosaccharide has been shown to have a high affinity for the receptor binding site and can be used as an alternative method for detecting low concentrations of ivermectin.

Sennoside D is a fatty acid that can be isolated from the sennosides found in the leaves of the plant Senna alata. It has been shown to have anti-tumor properties and may play a role in treating colon cancer, breast cancer, and skin cancer. Sennoside D has also been shown to be effective against autoimmune diseases such as arthritis, ulcerative colitis, and Crohn's disease. The low energy of this compound may be due to its formation rate. The hydroxide solution (NaOH) is used in the synthesis of this molecule because it binds with carbon dioxide molecules to form sodium bicarbonate and carbon dioxide gas which can then be captured by water. This process produces a high yield of sennoside D. In addition, the bound form of this molecule is soluble in organic solvents and insoluble in water, which makes it suitable for skin conditions as well as colon cancer treatments.

Pantothenic acid 2,4-di-O-b-D-galactopyranoside is a custom synthesis of Methylated Pantothenic Acid 2,4-Di-O-b-D-Galactopyranoside. The compound is an oligosaccharide composed of two glucose molecules and one galactose molecule. It contains a fluorine atom at the 4th position of the sugar chain. This modification was made to increase the solubility in water. Pantothenic acid 2,4-di-O-b-D-galactopyranoside can be used in industry as a food additive or pharmaceutical intermediate.

3-O-Triisopropylsilyl-D-galactal is a carbohydrate that belongs to the group of sugars. It is an oligosaccharide with a complex structure, which is synthesized from D-galactal by treatment with triisopropylsilyl chloride in pyridine. 3-O-Triisopropylsilyl-D-galactal is used as a reagent for the methylation and glycosylation of proteins and nucleic acids. This compound has been shown to inhibit the enzyme carboxypeptidase A, which may be due to its ability to act as an inhibitor of carbohydrate binding. 3-O-Triisopropylsilyl-D-galactal has also been shown to bind specifically to erythrocyte membranes, suggesting that it could be used as a potential diagnostic marker for glycogen storage diseases.

Benzyl 5-amino-5-deoxy-2,3-O-isopropylidene-6-O-trityl-a-L-gulofuranoside is a custom synthesis of an Oligosaccharide. It is a complex carbohydrate that has been modified by methylation and glycosylation. The saccharide in this compound is a sugar and it has been fluorinated. This product is of high purity and has been synthesized using click chemistry.

1,4:3,6-Dianhydro-2-O-methyl-D-glucitol is a modified sugar that belongs to the group of carbohydrates. It is synthesized by the modification of 1,4:3,6-dianhydro-2,5-diO-methyl D glucitol with methyl iodide and sodium methoxide. The compound is used in pharmaceuticals as an excipient and in cosmetics as a moisturizer. It has been shown to be effective against influenza A virus.

4-Aminobutyl b-D-galactopyranoside is a methylated saccharide that is also a glycosylation reaction product of 4-aminobutyl b-D-galactopyranoside. It has been modified with Click chemistry and fluorinated for use in carbohydrate research, including glycoprotein synthesis, carbohydrate modification, and oligosaccharide synthesis. 4-Aminobutyl b-D-galactopyranoside has been shown to be a potent inhibitor of the enzyme aminoglycoside adenyltransferase 1 (AGT1), which is involved in the synthesis of bacterial cell wall peptidoglycan. This compound has been used as a model for glycosylation reactions as it contains both an amino and sugar moiety.

Methyl 1-(5-fluoro-1H-2-oxopyrimidin-4-yl)-b-D-glucopyranuronate is an anticancer drug that inhibits β-glucuronidase. Methyl 1-(5-fluoro-1H-2-oxopyrimidin-4-yl)-b-D-glucopyranuronate is a colorless solid that has been recrystallized, purified, and analyzed for its chloride content. The function of this compound has been tested in vitro using tissue cultures and animal models. The reaction vessel used for the test was an acetonitrile solution with a pH between 7 and 8. The methylester form of methyl 1-(5-fluoro-1H--2--oxopyrimidin 4--yl)-b--D--glucopyranuronate reacts with sulphite to produce a green product with a colorimetric method

1,3,4,6-Tetra-O-acetyl-2-O-nonafluorobutane-sulfonyl-b-D-mannopyranose is a fluorinated saccharide that can be custom synthesized. It is a glycosylated carbohydrate with a 1,3,4,6 tetra acetyl substitution at the 2 position of the b D mannopyranose moiety. The chemical formula for this compound is C12H28O8FS2. It has been shown to have potential as an antihyperglycemic agent and has been found to be active in tumor models.

Tetra-O-acetyl-2-acetamido-2-deoxy-b-D-mannose is a modified sugar that is synthesized by the methylation of 2,4,6-trichloroacetimidate. This compound has been used in the synthesis of glycosylations and other modifications. Tetra-O-acetyl-2-acetamido-2-deoxy-b-D mannose can be custom synthesized to your specifications with high purity.

Methyl L-rhamnopyranoside is a sugar that is the product of the reaction between l-rhamnose and acetone. This compound has been used as a chiral building block for the synthesis of other sugars, such as D-arabinose and D-lyxose. The yield of this reaction depends on the concentration of potassium thioacetate and temperature. This compound can be obtained in two forms: (1) anomeric form, which is an intermediate in the synthesis of carbohydrates and (2) crystalline form, which is a white solid with melting point at 157.3°C. The anomeric form has a stereogenic center at carbon atom 3, whereas the crystalline form does not have any stereogenic centers. Methyl L-rhamnopyranoside also reacts with chlorination reagents to produce chlorinated derivatives, such as 2-chloro-3-(3′,4′-dimeth

1-Deoxy-L-ribose is a metabolite of acetone. It is a monosaccharide that contains one less oxygen atom than its parent compound. 1-Deoxy-L-ribose is found in the urine and blood of humans and animals. In animals, it can be synthesized from glucose by the enzyme ribose 1-phosphate reductase. This reaction requires an energy source such as ATP or NADH to reduce ribose 1,5-bisphosphate to 1,4-dihydroxyacetone phosphate, which then undergoes spontaneous dehydration to form 1-deoxy-D-ribose.

Thiamine galactoside is a custom synthesis of a monosaccharide. It is modified with fluorination, methylation and saccharide. The resulting product has a molecular weight of 578.08 g/mol and the chemical formula C24H34N6O18S2.

Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene-b-D-galactopyranoside is a custom synthesis that belongs to the class of complex carbohydrates. This compound is an oligosaccharide or a polysaccharide that has been modified by methylation and glycosylation. The modification of this saccharide with methyl groups allows for fluorination which is a click modification. Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene b -D galactopyranoside is synthesized via glycosylation followed by fluorination. This product can be used as a research chemical or in other applications.

Trimethylsilyl-2,3,4,6-tetra-O-benzyl-b-D-glucopyranoside is a modified carbohydrate that has been fluorinated and silylated. It is used as an intermediate in the synthesis of glycosylated compounds. Trimethylsilyl-2,3,4,6-tetra-O-benzyl-b-D-glucopyranoside can be custom synthesized to meet your needs. It is a white powder that is soluble in water and alcohols. The CAS number for this compound is 89825-08-1.

2-Amino-2,3,5-trideoxy-3-methyl-L-arabinonic acid-gamma-lactone hydrochloride is a lipid biosynthesis inhibitor that blocks the first step of this pathway by inhibiting the enzyme d-arabinose 4,5-diphosphate aldolase. This compound inhibits bacterial growth and leads to cell lysis. It has been shown to be active against cryptococcus neoformans and Candida neopformans. 2AADL has also been shown to inhibit the production of cell wall polysaccharides in C. neoformans and other fungi. 2AADL is thought to bind to the cell membrane through its alcohol group, which may lead to changes in the redox potential of the cells.

Ouabain is a potent inhibitor of the Na+/K+-ATPase pump in cardiac and skeletal muscles. It has been shown to inhibit signal pathways that are involved in the regulation of cellular membrane potentials, such as the michaelis–menten kinetics. Ouabain has also been found to be effective against syncytial virus infection. Ouabain inhibits viral replication by inhibiting cellular protein synthesis and reducing cell number due to its cytotoxic effects on myocardial cells. Ouabain has also been found to inhibit neuronal death induced by α1-adrenergic receptor agonists, such as p2y receptors.

Remdesivir impurity

3-Pyridinylmethylbeta-D-glucopyranoside is a sugar that can be custom synthesized. It is a white to off-white crystalline powder with an odorless taste and is soluble in water. 3-Pyridinylmethylbeta-D-glucopyranoside is used in the synthesis of glycosides, saccharides, oligosaccharides, and monosaccharides. This compound can also be modified with fluorination or methylation reactions. The use of this product has been shown to produce high purity compounds for use in pharmaceuticals, agrochemicals, and other chemical industries.

2-Acetamido -1,3,4,6-tetra-O-acetyl-2-deoxy-5-thio-a-D-glucopyranose is a custom synthesis. It is an oligosaccharide and polysaccharide. It is a carbohydrate that has been modified by fluorination and a click modification. The complex carbohydrate contains one monosaccharide sugar. 2AATG can be used in the synthesis of other carbohydrates.

3,2',3',4'-Tetra-O-acetyl-6,6'-di-O-tert-butyldimethylsilyl-lactal is a glycosylation agent that can be used in the synthesis of oligosaccharides and polysaccharides. It can be fluorinated to create a reactive site for methylation and click modification. 3,2',3',4'-Tetra-O-acetyl-6,6'-di-O-tert-butyldimethylsilyl-lactal is an acetylated lactal with a silyl ether protecting group. This product has been custom synthesized and is available in high purity.

L-Idaric acid is a novel anti-inflammatory agent that is a derivative of the endogenous compound d-glucuronic acid. It has been shown to have anti-inflammatory effects in animal studies as well as in human cell cultures and it has been shown to be safe for use in humans. L-Idaric acid inhibits the production of inflammatory mediators, such as prostaglandins, leukotrienes, and cytokines. L-Idaric acid also inhibits the activity of β-glucuronidase, which may be responsible for its ability to prevent the degradation of glucuronic acid derivatives.

2,4-O-Ethylidene-D-erythrose is a trimerization product of glyoxal and acetaldehyde. It is an aldehyde that can be used as a precursor to other compounds. The hydrated form of 2,4-O-ethylidene-D-erythrose has been rationalized by the mesoxalic acid and water molecules to form the trimer. This compound can be produced from the glycolaldehyde and sulfoxide in an oxidation reaction with hydrogen peroxide. The acetylation of 2,4-O-ethylidene-D-erythrose produces isoxazolidines which are stereoselective.

Methyl b-D-thioxylopyranoside is a synthetic sugar that is used in the synthesis of saccharides and oligosaccharides. It is also used to modify saccharides, such as glucosamine, by adding methyl groups to the sugar's hydroxyl group. Methyl b-D-thioxylopyranoside can be used for glycans with high purity and high yield. This product does not contain any other substances except for water and ethanol. The chemical formula for this product is C6H8O6.

5-Deoxy-L-lyxono-1,4-lactone is a crystalline solid that belongs to the class of hydroxamic acids. This compound has been shown to react with hydroxylamine in an aldonic reaction and to inhibit the enzyme xanthin oxidase. The monoclinic crystal structure of 5-Deoxy-L-lyxono-1,4-lactone was determined by XRD analysis. This compound is synthesized from glyoxylate and malonitrile in an efficient manner. It also inhibits glucose oxidation and can be used as an additive for food products.