Monosaccaridi

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

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.

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>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>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>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>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>

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-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>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>

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>

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

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>1-D-4-O-Methyl-myo-inositol is a compound that belongs to the group of biological compounds. It has been shown to have hypoglycemic effects in a model system and to inhibit 3t3-l1 preadipocyte differentiation. This compound also inhibits the activity of enzymes involved in metabolic pathways, and has an effect on lipid metabolism in kidney beans. 1-D-4-O-Methyl-myo-inositol has been shown to have antiobesity properties as well as antihyperglycemic activities.</p>

<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>

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.

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.

<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>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>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>

<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.

Donor for Koenigs-Knorr type galactosylation and other anomeric substitutions

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.

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>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>

Inhibits the Maillard reaction between glucose and glycine

<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>N-Acetyl-L-xylosamine is a custom synthesis of a glycosylation product that contains an acetyl group and a xylosamine. It is used as a building block for the synthesis of complex carbohydrates. N-Acetyl-L-xylosamine can be modified with fluorination, saccharide, modification, sugar, or oligosaccharide to create custom products.</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>

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

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.

1,2:3,5-Di-O-isopropylidene-a-D-xylofuranose is a synthetic glycoside that is used in the synthesis of complex carbohydrates. It has been used for the modification of polysaccharides and oligosaccharides. This compound has also been modified with fluorine to form 1,2:3,5-Di-O-isopropylidene-a-D-(1'-fluoro)-xylofuranose. The chemical name of this product is CAS No. 20881-04-3.