Monosaccaridi

<p>6-O-Trityl-D-mannopyranose is a modified sugar that has been synthesized for use as a glycosylation agent. It is an O-glycoside of mannose and is usually used in the synthesis of complex carbohydrates. 6-O-Trityl-D-mannopyranose can be fluorinated, methylated, or click modified to produce desired derivatives. This product can also be used to modify saccharides or oligosaccharides.</p>

<p>D-Glucose is a sugar that is used in the production of polysaccharides and glycosylations. It can be modified with fluorination, saccharide methylation, or glycosylation. D-Glucose can be synthesized by the custom synthesis of an oligosaccharide. This product has high purity, and is both monosaccharide and complex carbohydrate.</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>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>

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>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>

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.

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

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.

2,3,4,6-Tetra-O-pivaloyl-b-D-galactopyranosyl isothiocyanate is a custom synthesis that has complex carbohydrate as its main component. It is a modified saccharide with chemical modifications such as methylation, glycosylation, and fluorination. It also contains one or more sugars. The CAS number for this product is 147948-52-5. This product has high purity and can be synthesized according to customer specifications.

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.

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>Substrate for N-acetylglucosaminyltransferases</p>

Building block for synthesis of oligosaccharides

<p>D-Glucuronic acid methyl ester is an acidic, carbohydrate-binding molecule. It has been shown to bind to sugar residues in proteins and form covalent linkages with ester linkages. D-Glucuronic acid methyl ester has also been shown to be effective for the treatment of pentosan polysulfate sodium (PPS) induced inflammation in animal models. D-Glucuronic acid methyl ester binds to the monoclonal antibodies that are used for structural analysis of glycosidic bonds and oligosaccharides. The hydroxyl group on the molecule can form hydrogen bonds with other molecules, which may explain its usefulness as a magnetic resonance spectroscopy probe.</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>

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>2,3,4,6-Tetra-O-acetyl-D-mannopyranosyl fluoride is a methylated, fluorinated oligosaccharide. It is a custom synthesis and can be used as a monosaccharide to modify polysaccharides or saccharides. The modification of the sugar with 2,3,4,6-Tetra-O-acetyl-D-mannopyranosyl fluoride increases the water solubility of the complex carbohydrate and its ability to be synthesized into other compounds. This product is high purity and has been modified with fluorine for better stability.</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>

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>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>

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.

Inhibits the Maillard reaction between glucose and glycine

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>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>Short-term marker of glycemic control</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>3,4,6-Tri-O-benzyl-D-galactal is a hydrogen bond donor and has been shown to have physiological activities. It was found to increase the number of lymphocytes in unimmunized mice. It also inhibits the growth of psoralea virus. The glycosidic bond between 3,4,6-tri-O-benzyl-D-galactal and glucose produces a product with an acetylated hydroxyl group and an aldehyde group. This type of bond is stereoselective and benzofuran derivatives are formed from the reaction. 3,4,6-Tri-O-benzyl-D-galactal has been shown to have anticancer activity against cancer cells in laboratory experiments.</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>

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

<p>6-Chloro-6-deoxy-D-glucose is a sugar that is used as a carbon source in the process of spermatozoa production. It has been shown to increase the fertility of animals by increasing the uptake of phosphorus pentachloride and ganglion cells in the testes. This drug also has contraceptive and antifertility effects, which may be due to its ability to inhibit the uptake of adenine nucleotide in cells. 6-Chloro-6-deoxy-D-glucose may have a role in ATP levels, with intracellular levels being higher than those in control analysis.</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>

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.

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.

1,6-Anhydro-2-azido-2-deoxy-b-D-glucopyranose is a sugar. It belongs to the group of carbohydrates and has a molecular weight of 198.15 g/mol. The CAS number for this compound is 67546-20-7. 1,6-Anhydro-2-azido-2,3,4,5,6,7,8,9,10,-hexahydroxybenzoate (1) is an intermediate in the synthesis of 1,6 anhydro 2 azido 2 deoxy b D glucopyranose (2). In this reaction 2 are reacted with sodium azide and potassium hydroxide in ethanol to give 2 as a white crystalline solid with mp 169°C. This product can be used as a monosaccharide or modified monosaccharide for glycosylation or methylation reactions.

<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>Substrate for glucuronosyltransferases</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>Scyllo-inosamine is a redox potential that belongs to the class of antimicrobial agents. It is derived from the amino acid inosine, which is found in RNA and DNA. Scyllo-inosamine has been shown to inhibit bacterial growth by inhibiting protein synthesis. It also acts as an aminotransferase inhibitor, which may be used for the treatment of certain human pathogens. Scyllo-inosamine has been shown to have beneficial effects on the regulation of benzyl groups and hydroxyl group reactions. It has also been shown to inhibit polymerase chain reaction activity and titration calorimetry activity.</p>

<p>3,5,6-Tri-O-benzyl-1,2-O-isopropylidene-a-D-glucofuranose is a synthetic monosaccharide that has been fluorinated at the C3 position. It is an oligosaccharide with a complex carbohydrate structure. This glycosylation product can be custom synthesized and has been modified by methylation. 3,5,6-Tri-O-benzyl-1,2-O-isopropylidene Glucuronic acid can be used in the synthesis of polysaccharides or as a sugar for click chemistry. The chemical formula is C13H28O4F3 and its molecular weight is 322.32 g/mol.</p>

Intermediate for β-glucosides; potential PET surface modification reagent

<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>

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.

Methyl α-L-daunosamide hydrochloride is a drug that inhibits the production of DNA. It is used to treat infectious diseases such as malaria, in which it can inhibit the growth of the parasite by preventing DNA replication and transcription. The methyl α-L-daunosamide hydrochloride molecule is a polymerase chain inhibitor that binds to the enzyme adriamycin synthetase, which catalyzes the conversion of daunosamine into adriamycin. This binding prevents the formation of stable complexes with the target enzymes and blocks their activity, leading to inhibition of DNA synthesis and transcription. Methyl α-L-daunosamide hydrochloride has been shown to inhibit glycan biosynthesis in rat liver microsomes and does not have significant interactions with other drugs or with glycan in human serum.

<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>

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>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>

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>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>

N1-a-L-Arabinopyranosylamino-guanidine HCl is a carbohydrate that belongs to the class of oligosaccharides. It is a synthetic compound, which is custom synthesized for use in research. This product has been shown to be high purity and is methylated, glycosylated, and click modified. The CAS number 109853-78-3 refers to the chemical name of this product. The molecular weight of N1-a-L-Arabinopyranosylamino-guanidine HCl is 597.14 g/mol with an empirical formula C8H23N2O6.

2,4,7,8-Tetra-O-acetyl-9-azido-9-deoxy-N-acetylneuraminic acid methyl ester is a high purity synthetic compound that has been modified for use in Click chemistry. It is a monosaccharide with an acetyl group on the 2' position and an azido group on the 9' position of the sugar. This compound is used in fluoroination reactions to modify sugars and oligosaccharides. It can also be used in glycosylation reactions to attach monosaccharides and saccharides to proteins or other molecules.

<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>

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>Precursor for the preparation of abasic nucleoside analogues</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>

Homomorph used to study the biological role of 6 hydroxyl group of glucose

Ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-b-D-thiogalactopyranoside is a high purity custom synthesis sugar. This product contains the Click modification, fluorination and glycosylation modifications. It can be used in the synthesis of oligosaccharides, monosaccharides and saccharides. Ethyl 2,3-di-O-benzoyl-4,6-O-benzylidenebDthiogalactopyranoside is used to synthesize complex carbohydrates.

<p>Diethoxy phosphonyl 4,7,8,9-tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is a glycosylation agent that is used in the synthesis of complex carbohydrates. It is a methylated derivative of 4,7,8,9 tetra-O-acetyl neuraminic acid and can be used to modify the polysaccharide structure. This product has been shown to react with saccharides and oligosaccharides in a click reaction to produce fluorinated derivatives. Diethoxy phosphonyl 4,7,8,9 tetra-O-acetyl neuraminic acid methyl ester is also available as a custom synthesis.</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>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>

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>

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

Intermediate for the anomeric modification of GlcU, including glucuronylation

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

2,3,5-Tri-O-benzyl-D-lyxofuranose is a custom organic synthesis. The product is an Oligosaccharide and Polysaccharide that belongs to the carbohydrate family. It can be used for methylation reactions and click chemistry modifications with other molecules. This product has been found to have high purity, and it can be used in various applications such as Fluorination, complex carbohydrate, and Modification. 2,3,5-Tri-O-benzyl-D-lyxofuranose is a monosaccharide sugar that has a molecular weight of 327.24 g/mol and a melting point of 155°C.

Phenyl-beta-D-glucuronic acid monohydrate is a genotoxic agent that is metabolized to S-phenylmercapturic acid. This metabolite can be detected in urine as an indicator of exposure to the compound. Phenyl-beta-D-glucuronic acid monohydrate has been shown to have toxic effects on humans, such as decreasing the glomerular filtration rate and increasing reactive oxygen species levels. It also decreases antioxidant vitamin levels and causes blood disorders, including hemolytic anemia. Phenyl-beta-D-glucuronic acid monohydrate may also be used for the treatment of autoimmune diseases by inhibiting certain enzymes involved in inflammation and immune response.

3-Deoxygalactosone is a reactive compound that is formed by the reaction of glyoxal and galactose. The glyoxal molecule reacts with the hydroxyl group on the galactose to form a new aldehyde, which can then react with another molecule of glyoxal or galactose to form 3-deoxygalactosone. 3-Deoxygalactosone has been shown to have health effects in clinical studies. It also has been shown to decrease the dry weight of rats fed a high-fat diet. This compound also is an intermediate in the formation of 5-hydroxymethylfurfural, which is produced during the Maillard reaction between sugars and amino acids. 3-Deoxygalactosone binds to proteins, forming hydrogen bonds with amino acid side chains and affecting their biological function.

<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>Colchicoside is a natural compound that belongs to the chemical family of phenylpropanoids. It is used in the treatment of gout and pseudogout, and has been shown to be effective against demecolcine-induced hemolytic activity. Colchicoside has also shown to be an analog for other compounds with toxicological studies, such as hydrochloric acid and potassium dichromate. The toxicity studies performed on colchicoside have shown that it can cause damage to cells in culture by inhibiting DNA repair mechanisms.</p>

<p>Isopropylbeta-D-glucopyranoside is a chemical compound that has been studied for its antibacterial activity. It has been shown to inhibit the growth of bacteria by reacting with fatty acids in the cell membrane, which leads to the disruption of the cell membrane and death. Isopropylbeta-D-glucopyranoside is a member of the sugar alcohols class, and it can be synthesized from glucose, fatty acid, and hydrochloric acid using an acid catalyst. The reaction system is typically carried out in microcapsules.</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>Phenyl 3-deoxy-3-fluoro-a-D-glucopyranoside is a modified oligosaccharide, which is synthesized by the glycosylation of 3,6-diaminohexanoic acid with phenyl boronic acid. This compound is also known as an anti-tuberculosis drug. It has been shown to inhibit bacterial growth by binding to DNA dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity has been shown using a patch clamp technique on human erythrocytes. Phenyl 3-deoxy-3-fluoro-a-D-glucopyranoside also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX1 secretion system protein) and inhibits cell growth in culture.</p>

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-a-D-mannopyranose (1,3,4,6-TA) is a stable analog of the glycosidic sugar 2,6-dideoxymannose. This compound has been shown to be a potent inhibitor of the synthesis of Neisseria meningitidis capsular polysaccharides and an effective vaccine adjuvant against Mycobacterium tuberculosis. 1,3,4,6-TA is also a competitive inhibitor for the enzyme mycothiol and other thioglycosidic enzymes that are involved in the biosynthesis of mycolic acids. 1,3,4,6-TA was synthesized from 2-(N'-bromoacetamido)-2'-deoxymannose by reaction with sodium azide in acetone. The structure is bicyclic with two

4-Methoxyphenyl 3-O-allyl-2-azido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside (MPA) is a glycosylated antigen that has been shown to be specific for mycobacterium avium. It is a cytosolic calcium ionophore and can induce platelet membrane activation and coagulation. MPA has also been found to be chemoprotective in animal models of cancer. MPA can be used as an indicator of the body mass index (BMI).