Monosaccharides

<p>2,3,4,6-Tetra-O-acetyl-β-D-mannopyranosyl azide is a crystallographic technique that can be used to determine the structure of molecules. This technique involves the use of x-ray diffraction analysis to produce images of crystal structures. The technique is useful for determining the three dimensional structure of molecules that are too small to be seen with other techniques such as electron microscopy.</p>

<p>D-Ribopyranosyl amine is a heterocyclic compound that can be synthesized from ethyl formate and thiourea. The synthesis of this compound has been studied using techniques such as hydrogen bonding, high yield, and optical rotation. D-Ribopyranosyl amine is an aminoimidazole derivative with a decarboxylation reaction to produce uridine. This process can be carried out in acetone or dimethylformamide solvent, which produces the α-form of the molecule. The 1H NMR spectra of D-ribopyranosyl amine have peaks at 3.8 ppm, 2.5 ppm, and 2.0 ppm, while the 13C NMR spectrum peaks are found at 79.2 ppm and 131.9 ppm</p>

<p>3,4,6-Tri-O-acetyl-2-O-trifluoromethanesulfonyl-b-D-mannopyranosyl azide is a chemically synthesized compound that can be used for methylation reactions. It is an Oligosaccharide with a molecular weight of 597.5 and contains the following structural features: A saccharide composed of three monosaccharides (D-glucose, D-mannose, and D-galactose), which is bonded by alpha 1,6 linkages. The chemical formula is C12H14F3N3O8. The CAS number is 1159265-99-2.</p>

<p>Poly-D-galacturonic acid methyl ester (PDGME) is a natural compound that has been shown to possess anti-inflammatory and anti-diabetic properties. PDGME has been shown to increase the expression of pro-apoptotic proteins in mouse macrophages, as well as inhibit the activity of toll-like receptor 4, which may be due to its ability to induce caspase-independent cell death. PDGME also inhibits the growth of Clostridium difficile and other bacteria by inhibiting their enzyme activities. PDGME is water soluble and can be used as a reagent for biochemical studies.</p>

<p>Intermediate for β-glucosides; potential PET surface modification reagent</p>

<p>2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-glucohydroximo-1,5-lactone is a methylated sugar. It is a white to off white powder with a molecular weight of 518. The chemical formula for 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy--D--glucohydroximo--1,5--lactone is C16H26N2O8 and the structural formula is as follows:br&gt;</p>

<p>Chitobiose 2HCl is a synthetic sugar that has been modified using Click chemistry. It is a fluorescent sugar that can be used as an indicator for protein-sugar interactions. Chitobiose 2HCl is soluble in water and has a molecular weight of 258.078 g/mol.</p>

<p>D-Mannonic acid-1,4-lactone is a recombinant carbohydrate that is synthesized from l-ribose and l-arabinose. It has lysozyme inhibitory activity. D-Mannonic acid-1,4-lactone can be used to study the synthesis of lactones by escherichia coli and their inhibitory effects on lysozyme. The compound consists of two stereoisomers: dl-mannonic acid and ldl-mannonic acid. It can be detected by liquid chromatography (LC) and electrophoresis.</p>

<p>Isopropyl 2-acetamido-2-deoxy-α-D-glucopyranoside is a modification of an oligosaccharide. It has been synthesized and characterized by NMR spectroscopy. This carbohydrate is custom synthesized as a complex carbohydrate. It is also a synthetic carbohydrate. Isopropyl 2-acetamido-2-deoxy-α-D-glucopyranoside is used as a monosaccharide, in glycosylation, methylation, polysaccharides, and other sugar chemistry reactions. Isopropyl 2-acetamido-2-deoxy-α-D-glucopyranoside can be used for fluorination or saccharides.</p>

<p>4-Methoxyphenyl a-D-mannopyranoside is a fluorinated monosaccharide. It is synthesized by the reaction of 4-methoxyphenol with an aldose in the presence of sodium hydroxide and sulfuric acid. The product is purified by chromatography with silica gel and eluted with methanol. This compound is also used to produce polysaccharides, glycosyls, oligosaccharides, or complex carbohydrates through glycosylation or polysaccaride synthesis. 4-Methoxyphenyl a-D-mannopyranoside can be modified to produce methylated, acetalized, or deoxygenated derivatives for use in click chemistry reactions.</p>

<p>3-O-Methanesulfonyl-D-glucopyranose is a high purity, custom synthesis sugar that can be modified with fluorination, glycosylation, methylation and modification. It is also synthesized from glycoaldehyde and methanesulfonic acid in the presence of sodium hydroxide and sodium acetate. 3-O-Methanesulfonyl-D-glucopyranose can be used to synthesize saccharides and oligosaccharides. This compound is soluble in water and has a boiling point of 218°C at 760 mmHg. It is slightly soluble in methanol, ethanol and acetone. 3-O-Methanesulfonyl-D-glucopyranose has a CAS number of 40631-95-6.</p>

<p>2,3,4,6-Tetra-O-benzyl-D-glucopyranose is a selectively protected intermediate, where the anomeric 1-O-hydroxyl group is free. This hemiacetal has been used successfully as an intermediate for glucosylation couplings, where it was converted into 2,3,4,6-tetra-O-benzyl-D-glucopyranose trichloroacetimidate using trichloroacetonitrile in the presence of a base such as potassium carbonate and DBU. Importantly, this imidate donor with no neighbouring participating groups is commonly used for the selective formation of α-glucosides. 2,3,4,6-tetra-O-benzyl-D-glucopyranose can also be oxidized to the lactone, or reduced to give the open chain form. Additionally, 2,3,4,6-tetra-O-benzyl-D-glucopyranose can be used for the preparation of glucono-1,5-lactone hydrazine, which was used, in-turn, to form a glucosylidene-spirocyclopropane.</p>

<p>2,3,5-Tri-O-benzyl-b-D-xylofuranose is a synthetic carbohydrate with a complex structure. It is an oligosaccharide that has been modified by methylation and glycosylation. It has a molecular weight of 582.16 g/mol and the CAS number is 1174234-12-8.</p>

<p>UDP-2-deoxy-2-fluoro-D-galactose is a methylated and fluorinated saccharide that is used in click chemistry. It is a synthetic compound that can be custom synthesized to create polysaccharides or oligosaccharides. This product has high purity and can be modified with glycosylation, methylation, and other modifications.</p>

<p>Methyl 6-amino-6-deoxy-a-D-glucopyranoside is a saccharide with a molecular weight of 362.4 g/mol. This carbohydrate is fluorinated and modified with an amine group on the C1 position, which makes it a complex carbohydrate. It can be custom synthesized to order and has high purity. CAS No. 5155-47-5</p>

<p>2,3,4-Tri-O-benzyl-D-glucopyranose is a thioglucoside that can be synthesized from D-glucose and benzyl bromide. This compound is a protonated nucleophile with a hydroxyl group that can interact with the sulfur of a thiol or disulfide group. The interaction between 2,3,4-tri-O-benzyl-D-glucopyranose and S. aureus has been shown to be dependent on the concentration of 2,3,4 tri O benzyl glucopyranose. The reaction between this compound and oligosaccharides led to the formation of dioxane ring structures that were hydrophobic.</p>

<p>Substrate for N-acetylglucosaminyltransferases</p>

<p>Building block for synthesis of oligosaccharides</p>

<p>Alpha-Chloralose (max. 20% beta-anomer) is a chemical compound primarily used as a sedative and for rodent control. It is synthesized through a chemical reaction involving glucose and chloral, creating a substance with unique physiological properties. Its mode of action primarily involves depressing the central nervous system, leading to reduced responsiveness and hypothermia in targeted organisms. Alpha-Chloralose induces symptoms that facilitate its application as a tranquilizer, particularly in small mammals and birds during scientific research. Additionally, due to its efficacy in lowering metabolic rates, it is utilized as a rodenticide. Within this context, it serves to humanely control rodent populations by inducing hypothermic conditions, leading to a humane death. Its dual functionality—both as a sedative and a rodenticide—makes it a versatile tool in scientific research and pest management. The specification of a maximum 20% beta-anomer content ensures a standardized formulation, enhancing its reliability and consistency for experimental and practical applications.</p>

<p>2-Deoxy-2-fluoro-D-mannose is known for its antiviral properties as a sugar analog and glycosylation inhibitor. It works by inhibiting the glycosylation of viral envelope proteins, which can prevent viral replication and reduce viral infectivity. Studies have shown that 2-deoxy-2-fluoro-D-mannose can inhibit the replication of various viruses, including influenza A virus, human immunodeficiency virus (HIV), and hepatitis C virus (HCV). Inhibition of viral glycosylation by 2-Deoxy-2-fluoro-D-mannose can also enhance the effectiveness of some antiviral drugs, making them more potent.</p>

<p>DNA-binding agent</p>

<p>Phenyl 3,4-O-isopropylidene-b-D-thiogalactopyranoside is a custom synthesis of the complex carbohydrate Oligosaccharide, Polysaccharide. It belongs to Modification, saccharide, Methylation, Glycosylation, Carbohydrate. Phenyl 3,4-O-isopropylidene-b-D-thiogalactopyranoside can be used for Click modification, sugar and High purity. This compound is Fluorinated and Synthetic.</p>

<p>Methyl-2,3,4-tri-O-benzoyl-6-deoxy-alpha-D-glucopyranoside is a modification of the sugar molecule. It is a monosaccharide that has been modified with methylation and fluorination. This product can be used in the synthesis of saccharides, polysaccharides, oligosaccharides and complex carbohydrates. Methyl 2,3,4-tri-O-benzoyl 6 deoxy alpha D -glucopyranoside is one of many compounds that can be used to synthesize glycosylations.</p>

<p>1,3,6-Tri-O-galloylglucose is an extract of the fruit of Terminalia catappa and Terminalia citrina. It has been shown to have antimicrobial activity against a variety of bacteria and fungi. The antimicrobial activity may be due to its ability to chelate metal ions or inhibit their activities. Punicalagin also has tannin content, which may contribute to its antimicrobial properties.</p>

<p>D-Lyxono-1,4-lactone is an inhibitor of the enzyme fucosidase. It competitively inhibits the enzyme, but does not inhibit other hydroxamic acids such as enantiomers of D-lyxono-1,4-lactone. D-Lyxono-1,4-lactone has been used to treat HIV and AIDS because it prevents viral replication by blocking the synthesis of glycoproteins in the virus's envelope. It also has inhibitory effects on tumor cells that are not dependent on fucosidase activity. Magnetic resonance spectroscopy (NMR) studies have shown that d-lyxono-1,4-lactone binds to human liver cells and blocks the binding site for cytotoxic molecules in these cells. The molecular modelling study has demonstrated that d-lyxono 1,4 lactone binds to a specific site on human HLA class II molecule and reduces its</p>

<p>Tetra-O-acetyl-6-O-trityl-a-D-mannopyranose is a synthetic glycoside that is used as an intermediate in the synthesis of oligosaccharides. It has been modified with a fluorine atom at C1 to form 1,2,3,4-tetra-O-acetyl 6-(trifluoromethyl)-a-D mannopyranoside. This modification can be done through a click reaction. Tetra-O acetyl 6-(trifluoromethyl)-a D mannopyranoside is soluble in water and has a melting point of about 210°C.</p>

<p>Trichloroethyl b-D-glucuronide potassium salt (TCEBG) is a chloral compound that is metabolized to trichloroacetic acid. It has been shown to be carcinogenic in rats, but not in mice. Trichloroethyl b-D-glucuronide potassium salt has been used as an experimental agent for the synthesis of monoclonal antibodies. TCEBG binds to rat liver microsomes and CD1 mouse liver microsomes, which may be due to its high lipophilicity. TCEBG also disrupts cell membranes and induces cell death by inhibiting protein synthesis at the ribosome level.</p>

<p>2,3,4,6-Tetra-O-benzyl-a-D-glucopyranosyl chloride is a cholic acid derivative that is used as a bile acid. It has been shown to be effective in the treatment of gallstones and other conditions involving hypercholesterolemia and cholesterol gallstones. 2,3,4,6-Tetra-O-benzyl-a-D-glucopyranosyl chloride is synthesized by coupling acetyl chloride with 2,3,4,6 tetra O benzyl a D glucopyranoside. The acetate group is then removed to form the desired product.</p>

<p>CMP-Neu5Ac sodium salt (CMP-sialic acid) is a compound of the monosaccharide N-acetylneuraminic acid (Neu5Ac) O-linked with the nucleotide cytidine-5’-monophosphate (CMP). CMP-sialic acid is a substrate for sialyltransferases, which attach sialic acid to a growing oligosaccharide chain. This sugar nucleotide is produced in cytoplasm and then transported into Golgi lumen by a nucleotide-sugar transporter, where it is used in sialylation reactions on glycoproteins and glycolipids.</p>

<p>Inhibits the Maillard reaction between glucose and glycine</p>

<p>D-Mannojirimycin hydrogensulfite, an iminosugar analogue of Mannose, is a potent inhibitor of alpha-mannosidase.</p>

<p>Short-term marker of glycemic control</p>

<p>D-Xylonic acid calcium salt hydrate is a product that is made from the hydrolysis of cellulose. It is a byproduct of the production of d-xylose and can be used as a nutritional supplement or an additive in animal feed. D-Xylonic acid calcium salt hydrate has been shown to have an uptake rate in aerobic conditions that is ten times higher than glucose, which makes it more economical for use in the production of d-xylose. D-Xylonic acid calcium salt hydrate can be catalyzed to produce yields for d-glucose and d-xylose, which are both important monosaccharides. The catalytic process also produces d-gluconic acid and aerobic oxidation produces d-xylose, making it possible to recycle these products.</p>

<p>2,3,4-Tri-O-acetyl-D-arabinopyranosyl bromide - Stabilised with 2% CaCO3 is an organic compound that belongs to the group of glycosylations. It is a sugar derivative of arabinose and has been fluorinated with trifluoromethanesulfonic acid. This product is custom synthesized and can be used for Glycosylation reactions as well as methylations and click modifications. It is also a complex carbohydrate and can be used in the production of polysaccharides. The CAS number for this compound is 113889-50-2 and it has a monosaccharide content of 100%. This product is available for purchase at high purity.</p>

<p>Inhibitor of viral, bacterial and animal sialidase</p>

<p>2,3,5-Tri-O-benzyl-D-arabino-1,4-lactone is a carbonyl compound that has been used to synthesize carbonyl compounds. It has been shown to catalyze the formation of benzaldehyde from acetoacetic ester in the presence of hydrochloric acid. The melting point of 2,3,5-tri-O-benzyl-D-arabino-1,4--lactone is reported to be between 138° and 141°C.</p>

<p>3-Deoxypentulose is a kinetic, reactive and chromatographic compound that belongs to the family of glycolysis. It is present in small amounts in the blood and is derived from pentose sugars. The reaction mechanism of 3-deoxypentulose can be divided into two steps: glyoxal formation and hydroxide solution modification. In the first step, 3-deoxypentulose reacts with glucose to form glyoxal. In the second step, 3-deoxypentulose reacts with hydroxide solution to form galactose, which can further react with other compounds or be modified by enzymatic reactions. This compound has been used as a tagatose substitute in food products and as an oligosaccharide modifier. Recently, it has been shown that 3-deoxypentulose may be used as a chemical probe for studying glycolic acid synthesis in bacteria.</p>

<p>2-Methoxycarbonylphenyl b-D-glucopyranoside is a modification that can be used to synthesize complex carbohydrates. It is an oligosaccharide, which consists of a series of monosaccharides linked together by glycosidic bonds. The synthesis of this compound requires the use of methylation and fluorination reactions. This product has high purity and can be used for a variety of purposes, including as a sugar or as a polysaccharide.</p>

<p>D-Glucuronic acid (GlcA) is D-glucose with position six oxidised to a carboxyl group (Collins, 2006). It is a common component of a number of gums and mucilages structurally related to pectins, where it is can be present as a terminal non reducing end residue (Renard, 1999). Glucuronic acid is also found in bacterial polysaccharides, such as, xanthan gum produced by Xanthomonas campestris (Faria, 2011), and in glycosaminoglycans, such as, heparan sulfate (Casale, 2020).</p>

<p>L-Talitol is a naturally occurring sugar alcohol that is found in the human body and in many vegetables, fruits, and grains. It has been shown to be a potent inhibitor of the bacterium Klebsiella aerogenes. L-talitol has been used as a model system to study the effect of matrix on the growth of cells. It has also been shown to have chronic pulmonary effects and to be effective for treating selenium deficiency. L-talitol can inhibit b-raf by binding to the hydroxyl group on its kinase domain and inhibiting downstream signaling pathways. This inhibition leads to reduced levels of transcriptional regulation in cells, which may be due to decreased protein synthesis or increased degradation of mRNA. L-Talitol also inhibits d-talitol dehydrogenase, which results in an increase in d-talitol concentrations in cells.</p>

<p>3,5,6-Trichloro-2-pyridinol b-D-glucuronide is a synthetic glycosylate that has been modified by fluorination and methylation. It is used as an intermediate in the manufacture of a variety of saccharides and oligosaccharides. The sugar has been synthesized to have a high purity. 3,5,6-Trichloro-2-pyridinol b-D-glucuronide is a complex carbohydrate that can be modified using click chemistry. Click chemistry is a modification technique that uses copper (II) ions as catalysts for the formation of carbon–carbon bonds. This process can be used to modify saccharides and oligosaccharides with functional groups such as amines, thiols, alcohols, carboxylic acids, or nitriles.</p>

<p>L-Allono-1,4-lactone is a molecule with a stereocenter. It has been shown to be a target molecule for glycosidase inhibitors. The inhibition of the enzyme by L-allono-1,4-lactone may be due to its ability to form a hydrogen bond with the oxygen atom in the active site of the enzyme and its hydroxyl group that can form an additional hydrogen bond with water molecules. This inhibition prevents the transfer of glucose from one substrate to another, which leads to inefficient glycosidase activity. The synthesis of L-allono-1,4-lactone has been studied using piperidine as a starting material.</p>

<p>Indomethacin acyl-b-D-glucuronide is a prodrug of indomethacin. It is absorbed through the stomach and small intestine and metabolized in the liver. The pharmacokinetic parameters are not as well understood as with other drugs, but it has been shown that indomethacin acyl-b-D-glucuronide has a higher systemic exposure than indomethacin. This may be due to an increase in absorption or faster elimination. Indomethacin acyl-b-D-glucuronide is used for the treatment of pain and inflammation associated with rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, gouty arthritis, and bursitis.</p>

<p>Methyl 3,5-di-O-benzyl-b-D-ribofuranoside is a synthetic glycoconjugate. The methyl group at the 3 position of the ribose is substituted with a fluorine atom. This modification results in increased resistance to nucleases and enhanced cell penetration. Methyl 3,5-di-O-benzyl-b-D-ribofuranoside can be used for the synthesis of complex carbohydrates that are not accessible by other methods.</p>

<p>Substrate for glucuronosyltransferases</p>

<p>2,3,4-Tri-O-acetyl-1,6-anhydro-b-D-galactopyranose is a sugar that has been modified with fluorination. This modification is done in an effort to increase the solubility of this product. It is also used as the backbone for other sugars in order to create complex carbohydrates or polysaccharides. In addition, 2,3,4-Tri-O-acetyl-1,6-anhydro-b-D-galactopyranose can be methylated and glycosylated in order to modify its properties. This product is available for custom synthesis and has a purity level of 99%.</p>

<p>1,3,4,6-Tetra-O-benzoyl-a-D-fructofuranose is a fluorinated monosaccharide. It is an artificial sugar that has been modified with a benzoyl group at the 1 position and a tetra-O-benzoyl group at the 3 position. This compound has been synthesized using a custom synthesis. The compound is soluble in water and ethanol and can be used as a glycosylation or polysaccharide modification reagent. Click chemistry reactions have been performed on this compound to introduce methyl groups to the 4 and 6 positions of the sugar ring. The purity of this product is &gt;99%.</p>

<p>3,4,6-Tri-O-benzyl-D-glucal is a benzyl protected, 2,3 unsaturated glucal used as a chiral intermediate. The C2-C3 double bond of the pyranose ring can be modified via a variety of reactions including: hydrogenation, oxidation, hydroxylation, and aminohydroxylation, to generate structural complexity. 3,4,6-Tri-O-benzyl-D-glucal also minimizes tedious protecting-group strategies required for fully oxygenated sugars. The products of 2,3 unsaturated glycosides as chiral intermediates have played a role in the synthesis of many biologically active compounds, such as, nucleosides and modified sugar derivatives.</p>

<p>This is a Custom Synthesis of a 1,2,4,6-Tetra-O-acetyl-3-O-benzyl-D-glucopyranose. The desired product is an Oligosaccharide with a complex carbohydrate structure. It has been Fluorinated and Methylated in order to create the desired product. Modification and Click Modification have also been performed on this molecule.</p>

<p>2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-Fmoc serine is a protein that belongs to the group of bifunctional glycosides. It is used in recombinant virus production as a component of the viral coat protein (VP). 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-Fmoc serine binds to tyrosine kinase receptors and inhibits their activity. This inhibition prevents cell adhesion and migration and can cause tumor regression in some cancers. 2,3,4,6-Tetra-O-acetyl-b-D--glucopyranosyl--Fmoc serine also has antiviral activity due to its ability to inhibit the replication of viruses containing RNA genomes.</p>

<p>2,3,4,6-Tetra-O-benzoyl-b-D-glucopyranosyl cyanide is a quaternary ammonium salt that is found in the cenozoic sequence of samples. It has been suggested that this compound may be a new source of radiocarbon.</p>

<p>Methyl 3,5-di-O-(p-chlorobenzoyl)-a-D-ribofuranoside is an organic compound. It is a synthetic product that is used in the synthesis of saccharides and polysaccharides. This chemical can be modified with Click chemistry to create a glycosylate or fluorinated complex carbohydrate. The compound has CAS number 62700-92-3 and can be custom synthesized to meet customer specifications.</p>

<p>Please enquire for more information about Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Acetamido-1,3,4,6-tetra-O-benzyl-2-deoxy-b-D-thioglucopyranose is a modification of the natural molecule glucose. It is an Oligosaccharide with a complex carbohydrate structure. The molecule has been custom synthesized and is synthesized to be of high purity. It has CAS No.: 52268-42-9. 2-Acetamido-1,3,4,6-tetra-O-benzyl-2-deoxyglucopyranose is a Monosaccharide that can be methylated and glycosylated to form Polysaccharides. This molecule can be used as a sugar in food products or as a Fluorination agent for other molecules.</p>

<p>Genistin is an isoflavone found in soybeans and other plants. It has antioxidative properties, which may be due to its ability to scavenge free radicals. Genistin also has protein-binding activity, and it can inhibit the growth of certain insects by binding to their DNA. Genistin can also bind to a number of enzymes and affect their activities, including amylase, chymotrypsin, trypsin, and lipase. It is also involved in energy metabolism and protein synthesis. The physiological effects of genistin are not well understood but may be related to its ability to act as a phytoestrogen or mimic estrogen.</p>

<p>N-Methyl-D-glucamine HCl is a salt of N-methylglucamine and hydrochloric acid. It is used as a buffer to maintain the pH of solutions at a desired level. N-Methyl-D-glucamine HCl has an inhibition constant (Ki) of 0.5 mM for glutamate, which can be used to measure the concentration of glutamate in tissue samples or reaction mixtures. This compound also inhibits locomotor activity, and its effect on blood pressure may be due to its ability to inhibit amines. The Ki for chloride is approximately 2 mM, and it can be used to measure the concentration of chloride in solution.</p>

<p>N-Methyldeoxynojirimycin is a monoclonal antibody that is a competitive inhibitor of the melanoma antigen gp75. It is also an inhibitor of oligosaccharide synthesis and has been shown to have anti-inflammatory properties. N-Methyldeoxynojirimycin binds to the golgi alpha-mannosidases, preventing them from processing high-mannose type oligosaccharides. This leads to decreased chemoattractant protein production by neutrophils, which are important in the inflammatory process. N-Methyldeoxynojirimycin has also been shown to inhibit myocardial infarct size and glomerular filtration rate in rats, as well as increase biochemical markers for inflammation, such as α subunit of α1 acid glycoprotein and basic fibroblast growth factor.</p>

<p>2-Deoxy-1,3,4,6-tetra-O-pivaloyl-D-glucopyranose is a glycosylation sugar that belongs to the category of complex carbohydrates. It is a methylated sugar that can be fluorinated or modified with other saccharides. This product can be custom synthesized and has high purity.</p>

<p>2-Acetamido-2,6-dideoxy-D-galactose (2ADG) is a structural analogue of the natural monosaccharide 2,6-dideoxy-D-galactose. It has been shown to have an antimicrobial effect against aerobacter aerogenes in vitro. 2ADG is metabolized by glycosidases and methyl glycosides to form 1,4-anhydro-2,3,4,6 tetraacetamido-2,4,6 dideoxy D galactose. This compound inhibits the growth of bacterial strains that are resistant to polymyxin b., such as Pseudomonas aeruginosa. The inhibition of these bacteria is due to the inhibition of the synthesis of their outer membrane lipopolysaccharides by 2ADG. The antibacterial activity is also attributed to its ability to inhibit the metabolism of glycan molecules in some bacteria</p>

<p>Intermediate for the anomeric modification of GlcU, including glucuronylation</p>

<p>L-Mannitol is a sugar alcohol that is an important component of pharmaceutical preparations. It is used as a preservative, diluent, and sweetener in many pharmaceutical products. L-Mannitol has been shown to have anti-inflammatory properties and may help prevent allergic reactions by inhibiting the production of prostaglandin D2. L-Mannitol also inhibits the activity of xylitol dehydrogenase, which prevents the conversion of xylitol to DHA, an intermediate metabolite that can cause tissue damage in animals and humans. L-Mannitol has been shown to have a laxative effect when taken orally or injected as an intravenous solution. This property may be due to its ability to stimulate chloride secretion from intestinal cells and increase water reabsorption from the colon. L-Mannitol is also used as a chromatographic matrix for saponins and conjugates with other amino acids.</p>

<p>1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-L-mannopyranose is a carbohydrate that is synthesized by the modification of the glycosylation process. It is a methylated and fluorinated oligosaccharide with a high purity. This product is available for custom synthesis in order to meet specific customer requirements.</p>

<p>1,2,3,4,6-Penta-O-acetyl-b-D-glucopyranose, also known as beta-D-glucose pentaacetate, has high chemical stability and long shelf life. This protected form of glucose is a key building block of any chemical synthesis of glucose-containing oligosaccharides or glycoconjugates. In the presence of Lewis acids it can be used as a glycosyl donor to make simple glycosides. In order to perform more complex glycosylations, it can be converted into more reactive donors, such as glycosyl halides or thioglycosides. Beta-D-glucose pentaacetate is also used as a food additive and flavouring agent.</p>

<p>2-Azido-2-deoxy-L-glucopyranose is a Custom synthesis, modification and fluorination of methylated glucopyranosides. This compound has been shown to be effective in the synthesis of mono-, oligo-, and polysaccharides. 2-Azido-2-deoxy-L-glucopyranose is used for the preparation of glycosylation reagents. It can also be used to modify saccharide chains with azide or alkyne functionalities. 2-Azido-2-deoxy-L-glucopyranose is an important building block for the synthesis of complex carbohydrates, such as polysaccharides, glycosylation reagents, and click chemistry compounds.</p>

<p>Homomorph used to study the biological role of 6 hydroxyl group of glucose</p>

<p>3-Amino-3-deoxy-1,2:5,6-di-O-isopropylidene-a-D-glucofuranose is a synthetic, custom carbohydrate with a saccharide backbone. The modification of this molecule includes methylation and fluorination. 3-Amino-3-deoxy-1,2:5,6-di-O-isopropylidene is a modification on the saccharide backbone. This molecule is also synthesized with click chemistry to produce an amine functionality at the reducing end of the sugar. This product has high purity and can be used in research or as an intermediate for other compounds.</p>

<p>2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone is an organic compound that belongs to the class of lactones. It is a chiral molecule with two asymmetric carbons and four stereogenic atoms. This compound can be used for the synthesis of optically active compounds. It is also a precursor for the synthesis of morpholines and phosphonates. 2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone can be synthesized by reacting an enolate with an aldehyde in the presence of a base and acid catalyst. The acid catalyst causes elimination of water from the enolate to produce the desired product.</p>

<p>Synthetic carbohydrate building block</p>

<p>3,4-Di-O-acetyl-D-fucal is a synthetic carbohydrate with two orientations. It is a synthon for the synthesis of carbohydrates and can be used as a ligand in biomolecular design. The synthetic carbohydrate has been shown to have chemotherapeutic effects, which may be due to its ability to inhibit glycan synthesis. This synthetic carbohydrate also has conformational parameters that are similar to those of natural fucose, which makes it an attractive candidate as a potential drug target.</p>

<p>Methyl a-L-fucopyranoside is a natural product that has been shown to have many biological effects, including antioxidant and anti-inflammatory properties. It has been shown to inhibit the growth of bacteria by binding to the ribosome, preventing protein synthesis and cell division. The compound has also been shown to have anti-inflammatory effects in mice with inflammatory bowel disease. Methyl a-L-fucopyranoside inhibits the production of pro-inflammatory cytokines, such as interferon alfa-2b (IFNα2β), which is induced by IFNγ. This inhibition of IFNα2β activity may be due to methyl a-L-fucopyranoside's ability to bind to cytosolic calcium and inhibit its transport into the nucleus. Methyl a-L-fucopyranoside also blocks the production of antimicrobial peptides, such as defensins or cathelicidins.</p>

<p>The 2-azidoethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a custom synthesis in a high purity that can be methylated and modified for glycosylation. It is an azide sugar with the CAS number 142072-11-5. The product can be used for saccharide and polysaccharides modifications or click chemistry. This product is also available for custom synthesis.</p>

<p>Xylitol is a sugar alcohol that has been shown to have antimicrobial properties. It is also used as a sweetener in chewing gum and toothpaste. Xylitol inhibits the growth of bacteria by binding to the enzyme adenosine triphosphate (ATP) synthase, which is required for energy metabolism. The binding of xylitol to ATP synthase prevents the formation of ATP and blocks bacterial growth, leading to cell death. Xylitol can be produced from xylose, a sugar found in plants and animals, through biochemical reactions that are catalyzed by enzymes such as xylitol dehydrogenase and xylulokinase. This process is anaerobic and does not require oxygen or organic nutrients. Xylitol has been shown to have physiological effects on wild-type strain bacteria such as Aerobacter aerogenes.</p>

<p>2,4-Di-O-methyl-D-glucose is a partially O-methylated glucose sugar.</p>

<p>Intermediate in the synthesis of tofogliflozin</p>

<p>1-Deoxy-L-mannitol is an effective oral hypoglycemic agent that has been used in the treatment of diabetes. It is a sugar alcohol with a chemical structure similar to glucose and erythritol. 1-Deoxy-L-mannitol is absorbed by the small intestine and enters the bloodstream after being hydrolyzed by pancreatic enzymes. It inhibits fatty acid synthesis, which leads to decreased levels of acetyl coenzyme A and increased levels of carnitine, leading to activation of fatty acid oxidation in liver cells. This drug also inhibits phosphatase activity, which leads to decreased production of glycerophosphate from triphosphate. This process results in an increase in intracellular pH and a decrease in plasma glucose concentration. The use of 1-deoxy-L-mannitol for the treatment of diabetes was first reported by George Cahill and his colleagues at Harvard University in 1967. It was shown that this drug could reduce blood sugar</p>

<p>Keratin-reducing component in cosmetic applications; used in Glc conjugation</p>

<p>Please enquire for more information about Benzyl-alpha-S-GalNAc including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3,4-Tri-O-benzyl-D-glucuronide benzyl ester is a synthetic glycosylation product. It has been custom synthesized and modified with fluorination and methylation. This compound is an oligosaccharide that can be used as a pharmaceutical intermediate or in the synthesis of complex carbohydrates. 2,3,4-Tri-O-benzyl-D-glucuronide benzyl ester has been shown to have high purity and can be used for research purposes.</p>

<p>Ferric carboxymaltose is a form of iron that is administered intravenously and is used to treat iron deficiency. Ferric carboxymaltose has been shown to be effective in treating iron deficiency anemia as well as other conditions, such as inflammation of the bowel or hematologic response. Ferric carboxymaltose binds to free iron in the blood and prevents it from oxidizing. Ferric carboxymaltose also exhibits an anti-inflammatory effect by inhibiting the production of pro-inflammatory cytokines and chemokines. The polymerase chain reaction (PCR) technique has been used to measure ferritin levels in the blood, which are then used to determine whether treatment with ferric carboxymaltose is necessary.</p>

<p>Delphinidin 3-galactoside chloride is a natural organic compound that belongs to the flavonol glycosides. It is a pigment that has been identified in flowers and fruits, such as the fruit tree. This compound exhibits antioxidant properties and can scavenge radicals, which may be due to its ability to inhibit dehydroascorbate reductase activity. Delphinidin 3-galactoside chloride also has an effect on high cholesterol levels, which may be due to its ability to inhibit HMG-CoA reductase activity. In addition, it has been shown that this compound can inhibit the growth of human pathogens such as P. aeruginosa and S. aureus.</p>