Monosaccharides

<p>Mitiglinide-acyl-b-D-glucuronide is a custom synthesis of an oligosaccharide and polysaccharide that has been fluorinated, modified and then acylated. This reagent is available in high purity and with a modification of methylation. It is a complex carbohydrate with high purity that is obtained by modifying the sugar monomer. Mitiglinide-acyl-b-D-glucuronide is a synthetic monosaccharide that has been modified with polysaccharides and saccharides to produce a product with high purity.</p>

<p>1,2,3,4-Tetra-O-pivaloyl-6-O-(tert-butyldiphenylsilyl)-b-D-galactopyranose is a high purity custom synthesis of a sugar. It is a fluorinated tetra saccharide with an unusual 1,2,3,4 linkage that has been modified with methyl groups at the 2 and 6 positions. The modification of this compound with silylation has made it resistant to enzymatic degradation. This compound has shown anti-inflammatory activities in animal models and can be used as an adjuvant therapy for inflammatory bowel disease.</p>

<p>1,2,3,4-Tetra-O-benzoyl-6-O-trityl-b-D-glucopyranose is a custom synthesis that can be used for methylation and Click modification. This compound is an oligosaccharide consisting of sugar molecules linked by glycosidic bonds. It is a polysaccharide with a saccharide repeating unit composed of monosaccharides. The carbohydrate chain contains 1,2,3,4 tetra O benzoyl groups and 6 O trityl groups. This product has a high purity and can be used in the synthesis of other compounds.<br>1,2,3,4 Tetra O benzoyl 6 O trityl b D glucopyranose (1) was synthesized from 4-(2'-hydroxyethyl)benzaldehyde (2), 4-(2'-hydroxyethyl)benzoic acid (3),</p>

2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-thioglucopyranose is a synthetic monosaccharide that belongs to the group of complex carbohydrates. It has CAS No. 10043-46-6 and is used in glycosylation reactions. The fluorination of the sugar can be done by using a Click modification or methylation reaction. This product has been custom synthesized and can be ordered with high purity.

<p>Glucose 6-phosphatase substrate</p>

<p>1-Octylamino-1-deoxy-D-glucitol is a natural product that is extracted from the bark of the tree Streptomyces griseorubens. It has been shown to have a diastereomeric ratio of 97:3 and an optical purity of 98%. The thermodynamic properties of this compound are determined by the reaction time, which can vary from 1 to 24 hours. The enantiomers are separated by chromatography or crystallization, and the solubility data is determined at 25°C.</p>

<p>Low-calorie sweetener; additive in detergents, cosmetics, and pharmaceuticals</p>

<p>Intermediate for the anomeric modification of Fuc, including fucosylation</p>

<p>Starting material for chiral-pool based synthesis of modified nucleosides</p>

<p>1,3,4,6-Tetra-O-acetyl-a-D-glucopyranose is a synthon that is used as a synthetic intermediate for the synthesis of other compounds. It is also a reactive compound that can be used to synthesize carboxylic acids and hydroxy ketones by reaction with water or alcohols. 1,3,4,6-Tetra-O-acetyl-a-D-glucopyranose can also be converted into esters by reaction with alcohols.</p>

<p>4-Acetamidophenyl b-D-glucuronide sodium salt is a pharmaceutical drug that is a metabolite of acetaminophen. It can be detected in the urine by biochips, which are microarrays that contain immobilized binding sites for specific analytes. The analysis of 4-acetamidophenyl b-D-glucuronide sodium salt in urine is used to screen for the use of acetaminophen and to identify cytochrome P450 2C19 (CYP2C19) activity. This drug can also be detected by spectrometric methods using biochemical assays on plates or hepatocytes and mass spectrometric detection methods using liquid chromatography/mass spectrometry (LC/MS). Acetaminophen has been shown to have toxic effects on the liver, kidneys, and lungs in humans, as well as on diode photoluminescence.</p>

<p>Apigenin is a flavone, which is a type of phenolic compound. It is one of the most widely distributed plant flavonoids found in nature. Apigenin has been shown to inhibit glucose uptake and intestinal transport in mice. Apigenin also has been shown to have anti-inflammatory properties, as well as the ability to suppress the growth of cancer cells in vitro. The expression of apigenin was observed after incubation with caco-2 cells and was upregulated when maltose was added to the media. Apigenin can be used as an additive for food products that are high in sugar content, such as cakes and cookies.</p>

<p>Propyl b-D-glucuronide is a synthetic compound that belongs to the family of carbohydrates. It has a fluorinated hydroxyl group at the C3 position and an esterified carboxylic acid at the C1 position. This compound can be used as a building block for oligosaccharides and polysaccharides, which are complex carbohydrates. Propyl b-D-glucuronide is soluble in water and has a molecular weight of 176.</p>

<p>Resource for the synthesis of Clofarabine and other bioactive arabinosides</p>

<p>L-Rhamnose diethyl mercaptal is an antiperspirant and deodorant that is used in combination with other ingredients to reduce or eliminate body odor. It is a supplement, often found in combinations with other compounds such as neodymium and radium. This compound works by preventing the formation of sweat from the apocrine glands, which reduces underarm wetness and body odor. L-Rhamnose diethyl mercaptal also has antimicrobial properties that help prevent bacterial growth on the skin surface.</p>

<p>Methyl 4,6-O-benzylidene-a-D-mannopyranoside is a hexadecanoic acid that is mediated by the target cell. It has been shown to inhibit the growth of bacteria and cancer cells in vitro. Methyl 4,6-O-benzylidene-a-D-mannopyranoside also possesses an antibacterial activity with a low mammalian toxicity. This compound is hydrolyzed by esterases or glucuronidases, oxidized by cytochrome P450 enzymes, reduced by glutathione reductase, or conjugated with glucuronic acid. The residue of this compound has been shown to be carcinogenic in vivo and in vitro. Anticancer activity of this compound may be due to its ability to disrupt DNA synthesis and induce apoptosis of cancer cells.</p>

<p>Methyl 3-amino-3-deoxy-a-D-mannopyranoside HCl is a potent antioxidant that has been shown to protect cells from lipid peroxidation and protein oxidation. It also inhibits the formation of toxic reactive oxygen species, such as hydroxyl radicals. This compound has been shown to have protection against oxidative stress in cell culture studies. Methyl 3-amino-3-deoxy-a-D-mannopyranoside HCl is an inhibitor of the enzyme catalase, which may be responsible for its antioxidant activity. This compound also inhibits population growth in an aerobic environment, as well as catalase and dismutase activity in a population of bacteria. Methyl 3-amino-3-deoxy-a-D-mannopyranoside HCl is resistant to solanum tuberosum and solanum tuberosum extract and is oxidized by peroxidases found in plants.</p>

<p>Phenyl 3,6,2',3',4',6'-hexa-O-acetyl-2-deoxy-2-trichloroacetamido-b-D-thiolactoside is a custom synthesis. It is an oligosaccharide and polysaccharide with a high purity and modification. This compound has a CAS No., and is an Oligosaccharide and Polysaccharide. Phenyl 3,6,2',3',4',6'-hexa-O-acetyl-2-deoxy-2-trichloroacetamido-b-D-thiolactoside is a sugar which is synthesized by Monosaccharides.</p>

<p>1,2,3,4-Tetra-O-acetyl-6-S-acetyl-6-deoxy-6-thio-b-D-glucopyranose is a synthetic compound that is used as a building block for the synthesis of other compounds. It is an acetylated oligosaccharide that can be modified with fluorine atoms to form 1,2,3,4-tetra-[F]fluoro-[F]deoxy-[F]thio-[F]hexose. This product has high purity and can be used in glycosylation reactions.</p>

<p>This is a custom synthesis of a carbohydrate. It is a methylated, glycosylated, fluorinated, complex carbohydrate that can be synthesized to any desired degree of substitution. This product has been designed for use as a fluorescent tag or label in biochemistry and cell biology research. It is modified at the anomeric position with an acetyl group and an azide group. The acetyl group confers solubility in water, while the azide group confers fluorescence. The modifications also allow for click chemistry reactions, which are used in protein labeling and activation studies.</p>