Monosaccharides

<p>Emodin 1-glucoside is a natural anthraquinone glycoside that is produced by plants and has been shown to have cytotoxic effects against human cells. Emodin 1-glucoside inhibits the function of enzymes, such as glycosidases, phosphatases, and proteases. This compound is activated by calcium ions and has been shown to disrupt mitochondrial membrane potential. Emodin 1-glucoside also inhibits sugar residues and has shown significant cytotoxicity against cultured human cells at higher concentrations. It may be used as a medicine for the treatment of inflammation or cancer.</p>

<p>Phenyl-beta-D-thioglucopyranoside is a heterocycloalkyl compound that contains a phenyl group and a beta-D-thioglucopyranoside. It is used as an intermediate in the production of pharmaceuticals, yellow dye, and cancer drugs. Phenyl-beta-D-thioglucopyranoside binds to the cell membrane of cancer cells and induces apoptosis by inhibiting the synthesis of proteins. This compound also has alkenyl and haloalkyl groups, which may be important for its biological activity. Phenyl-beta-D-thioglucopyranoside can be crystallized in two different forms: one with a crystalline form, which is yellow; the other with a crystalline form, which is colorless.</p>

<p>Used for preparation of biologically active compounds</p>

<p>Allyl 2-acetamido-2-deoxy-a-D-glucopyranoside is a synthetic oligosaccharide that has the ability to bind to the O antigen of bacterial cells. It is used in vaccines as an adjuvant and has been shown to increase antibody production and provide protection against Shigella, a bacterial infection. This compound also shows chemoenzymatic activity, which allows for regiospecifically catalytic conversion of glycosides. Allyl 2-acetamido-2-deoxy-a-D-glucopyranoside binds to specific microbial enzymes that contain an acceptor site, with its catalytic function being activated by these enzymes.</p>

<p>Methyl 2,3,4-tri-O-benzyl-α-D-glucuronide benzyl ester is a Carbohydrate. It is soluble in water and insoluble in alcohol. The molecular weight of Methyl 2,3,4-tri-O-benzyl-α-D-glucuronide benzyl ester is 584.1 g/mol. The CAS Registry Number for Methyl 2,3,4-tri-O-benzyl-α-D-glucuronide benzyl ester is 14279733.</p>

<p>4-Methoxyphenyl 3-O-benzyl-a-D-mannopyranoside is a synthetic carbohydrate that has been modified with a click reaction. It is an Oligosaccharide, which is a type of Carbohydrate, and has a saccharide sequence. This product is used in the synthesis of complex carbohydrates. The product has high purity and custom synthesis capabilities.</p>

<p>Peonidin-3-O-arabinoside chloride is a flavonol glycoside that is found in the plant peony and inhibits lipid absorption. It has inhibitory properties on fat absorption in vitro. Peonidin-3-O-arabinoside chloride also inhibits the activity of enzymes that break down dietary fats, such as pancreatic lipase, thereby preventing fat absorption. This compound has been shown to lower serum cholesterol levels and reduce blood pressure in vivo human trials. Peonidin-3-O-arabinoside chloride is extracted from the bark of the tree species Paeonia suffruticosa and is used as an ingredient in some weight loss supplements.</p>

<p>Phenyl-beta-D-thioglucuronic acid is a drug that is used to treat inflammatory diseases and autoimmune diseases. It is a basic structure that has been shown to have anti-estrogenic effects in vitro, although the mechanism of action is not well understood. Phenyl-beta-D-thioglucuronic acid can be crosslinked with proteins to form a matrix for wound healing. This drug has also been shown to be a potent inhibitor of proteases, and may inhibit other enzymes such as matrix metalloproteinases and serine proteases.</p>

<p>3-Hydroxydesloratadine b-D-glucuronide sodium salt is a carbohydrate that is used as an intermediate in the synthesis of saccharides. It can be modified to make it more soluble in water by adding fluorine atoms, which increases its solubility and bioavailability. 3-Hydroxydesloratadine b-D-glucuronide sodium salt is synthesized using a custom synthesis method with high purity and high yield. It has glycosylation, methylation, and click modification done on it during the synthesis process.</p>

<p>L-Daunosamine hydrochloride is a fluorinated sugar that is synthesized in the laboratory. It has been used for the modification of polysaccharides and other saccharides. L-Daunosamine hydrochloride is a monosaccharide that can be found in several complex carbohydrates. The CAS number for this chemical is 19196-51-1. This chemical has a high purity level, which makes it valuable for use as a synthetic material.</p>

<p>2,3,5-Tri-O-benzyl-b-D-ribofuranose is a synthetic monosaccharide that is used in the synthesis of complex carbohydrates such as glycosylation and polysaccharides. One use for this chemical is to modify the sugar moiety with methyl groups, yielding 2,3,5-tri-O-methyl b-D-ribofuranose. This modification helps prevent the sugar from being metabolized by enzymes in the body. The chemical can also be fluorinated to yield 2,3,5-trifluoro b-D-ribofuranose.</p>

<p>A beta glycoside with an alkyne handle suitable to click chemistry</p>

<p>Inositol is a member of the B-vitamin family and is classified as a sugar alcohol. It has a structural similarity to glucose and can be synthesized by plants, bacteria, and mammals. Inositol is found in high concentrations in the brain and liver. Inositol has been shown to inhibit guanine nucleotide-binding proteins (G proteins) and ryanodine receptor channels in HL-60 cells. It also inhibits cancer cell proliferation and suppresses ovarian activity. Inositol appears to work by binding to the inositol-1,4,5-trisphosphate receptor on the surface of cells, thereby inhibiting intracellular calcium release from its storage site within the endoplasmic reticulum. The effects of inositol are mediated by dinucleotide phosphate or p-nitrophenyl phosphate.</p>

<p>4-Methylphenyl 2,3,4-tri-O-benzyl-b-L-thiofucopyranoside is a custom synthesis of an oligosaccharide. It is a complex carbohydrate with CAS No. that belongs to the class of saccharide and sugar. Polysaccharides are made up of several monosaccharides linked together by glycosidic bonds, which are formed by the action of enzymes called glycosyltransferases or glycosidases. Glycosylation is the process in which a sugar molecule (usually glucose) is added to another molecule by means of a glycosidic bond. Carbohydrates are one type of macromolecule and they are important sources of energy in living things. They also play important roles in cell walls and as structural components in plants and animals. The chemical modification carried out on this compound is methylation, which refers to the addition of one or more methyl</p>

<p>Substrate for xylosyltransferases</p>

<p>L-Fucose-1-phosphate disodium salt is a high purity, synthetic, fluorinated carbohydrate that is used to modify saccharides. This modification can be accomplished by methylation or glycosylation. L-Fucose-1-phosphate disodium salt has been shown to be useful for glycosylation reactions with click chemistry. It has been shown to have a wide range of applications including modification of oligosaccharides and polysaccharides in the field of biotechnology.</p>

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

<p>2-Acetamido-2,4-dideoxy-4-fluoro-D-glucopyranose (2ADFG) is a glycosaminoglycan that inhibits the biosynthesis of glycosaminoglycans by binding to the enzyme UDP-N-acetylglucosamine 2-epimerase. It is used in cellular control experiments to determine if cells are hepatocytes or not. This compound binds to glycosaminoglycans and prevents them from being synthesized, which leads to cell death. The binding of 2ADFG also results in a decrease in cellular protein synthesis and an increase in cellular lysosomal activity.</p>

<p>Building block for polymers synthesis, ionic liquids and chiral auxiliaries</p>

<p>1,6-Anhydro-2,3,4-tri-O-benzyl-b-D-glucopyranose is a polymer that can be synthesized by copolymerizing the monomer with other reagents. The acetal linkage between the two glucose units allows for a cyclic structure, and this compound is soluble in water and methanol. 1,6-Anhydro-2,3,4-tri-O-benzyl-b-D-glucopyranose has been used to synthesize a variety of polymers such as polyacetals and polyesters.</p>

<p>1,6-Anhydro-2-deoxy-2-iodo-b-D-glucopyranose is a sugar that has been used in the synthesis of a number of organic compounds. It is an intermolecular hydrogen bond donor, and it forms hydrogen bonds with other molecules. The molecular structure of 1,6-Anhydro-2-deoxy-2-iodo-b-D-glucopyranose consists of a six carbon chain with three hydroxyl groups and two ether groups.</p>

<p>3-Deoxy-3-fluoro-D-galactose (3DFGal) is a potential drug that has been shown to shift the metabolic pathway of gram-positive pathogens from glycolysis to gluconeogenesis. This compound may be used as a tool for studying the enzymatic reaction catalyzed by galactokinase, which is involved in the conversion of 3DFGal to D-galactose. 3DFGal is a stereospecific carbohydrate and can be used as a substrate for biochemical studies. The bacterial surface profile of 3DFGal has been investigated and it has been found that 3DFGal is not significantly toxic to Gram-negative bacteria. The kinetics of 3DFGal hydrolysis have been studied and it was found that the hydrolysis rate was increased when the solution was acidified with hydrofluoric acid.</p>

<p>4-Methoxyphenyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-b-D-glucopyranoside is a complex carbohydrate that has been modified with methylation and glycosylation. It has been synthesized using the following reactants: 4-(methoxy)phenol, benzaldehyde, and 2,3,4,6,-tetraacetylpiperidine. This product has a CAS number of 129575–88–8 and is available for custom synthesis in quantities from 1 gram to 50 kilograms. This product is used as a custom synthesis for oligosaccharides or polysaccharides.</p>

<p>Methyl a-D-xylopyranoside is an iron chelator that can be used as a mycobacterial drug candidate. It binds to both ferric and ferrous iron, and has been shown to inhibit the uptake of ferric iron by Mycobacterium tuberculosis. It also inhibits the synthesis of siderophores, which are molecules produced by bacteria in order to acquire iron from their environment. Methyl a-D-xylopyranoside does not bind to the alpha-d-glucopyranoside moiety typically found in iron complexes. This is due to its hydroxamate group, which causes it to have an increased affinity for Fe3+. This compound is active against gram negative bacteria such as E. coli and Salmonella enterica serovar Typhimurium, but not against gram positive organisms such as Staphylococcus aureus or Streptococcus pneumoniae.</p>

<p>3,5-Di-O-benzoyl-2-deoxy-2,2-difluoro-D-ribonic acid-1,4-lactone (3DBR) is a nucleoside that has been shown to have antiaging properties. It has been found to be an effective scavenger of peroxyl radicals and reactive oxygen species (ROS). 3DBR also inhibits the formation of aluminum oxide and styrene by catalyzing the salt formation reaction. This compound also has anti-tumour activity and can be used as a chemotherapeutic agent for the treatment of cancer. It is heat resistant and can be combined with gemcitabine hydrochloride in chemotherapy.</p>

<p>2,3,4,6-Tetra-O-acetyl-a-D-glucopyranosyl chloride (TAOC) is a nuclear magnetic resonance (NMR) probe that has been used to study the structure of nuclei. It is synthesised by reacting acetyl chloride with sucrose in a reaction catalyzed by sodium hydroxide. The compound can be detected in quadrupole and resonance spectroscopy due to its high sensitivity to nuclear magnetic resonance. This NMR probe is typically used to study the structures of nuclei or for the analysis of polysaccharides.</p>

<p>1,2,3,4-Tetra-O-benzyl-a-D-mannopyranoside is an active drug that belongs to the group of thyromimetics. It is a prodrug that is hydrolyzed in vivo to 1,2,3,4-tetra-O-acetyl-a-D-mannopyranose. This drug has been shown to be effective in treating nervous system diseases such as sclerosis and endogenous disease. The acetylation of the benzyl group on this molecule prevents it from being metabolized by enzymes that are found in the liver. The unmodified form of this drug is rapidly absorbed into the blood and reaches high concentrations quickly.</p>

<p>2,3,5-Tri-O-benzyl-L-arabinofuranose is a benzyl ester of an anomeric mixture that can be prepared by hydrogenolysis of 2,3,5-tri-O-benzyl L-arabinofuranose. It is an experimental compound that may be used for the synthesis of optical anomers or as a starting material for the preparation of other compounds. The reactivity of the carbonyl group in this compound is determined by the steric hindrance from the benzyl esters. This compound also has chloride and trifluoromethanesulfonic acid esters.</p>

<p>β,β-Trehalose is a carbohydrate that is synthesized by the expression of a trehalose synthase enzyme from the yeast Saccharomyces cerevisiae. β,β-Trehalose is an acidic sugar with two glucose subunits. It has been shown to have an enzymatic mechanism similar to that of glucose. β,β-Trehalose has been found to increase the solubility and stability of proteins in acidic phs (pHs) by binding to hydroxyl groups on protein surfaces. β,β-Trehalose also binds to alcohols such as ethanol and methanol, which may be due to its ability to form hydrogen bonds between oxygen atoms. This sugar also forms hexamers in solution, which may contribute to its effectiveness as a stabilizer for proteins and other molecules. The optimum ph for β,β-trehalose synthesis is around 5.5-6.0 and it can be used at higher ph</p>

<p>1,2,3,4,6-Penta-O-acetyl-D-mannopyranose is an organic chemical compound that belongs to the group of sugars. It is a synthetic compound that can be used as an analytical reagent in hepg2 cells and chloride. 1,2,3,4,6-Penta-O-acetyl-D-mannopyranose has been shown to have a protective effect against adenosine receptors and phosphotungstic acid in brain cells. This sugar also has a strong affinity for lectins and can be used to study the binding of sugars to proteins by titration calorimetry.</p>

<p>4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside is an extracellular calcium modulator that can be used to treat viral infections. It binds to the viral envelope and alters the virus's ability to fuse with cells. 4MPTAA also has antiviral activity against herpes simplex virus type 1 (HSV1) and influenza A virus (IAV). The compound also has anticancer activity by blocking the growth of cancer cells. 4MPTAA can be used for the treatment of microprocessor viruses such as tenella and myxoma. This drug also has a structural analysis profile that can be accessed using a variety of methodologies, including thermodynamic profiling and coagulation profiling.</p>

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

<p>2-Chloroethyl-b-D-fructopyranoside is a stable reagent that is used to prepare 2,4-dichloroacetophenone (2,4-DAAP), which can be used as a crosslinking agent. This reagent is reactive and should be handled with care. It forms a hemoglobin adduct by reacting with the amino groups of hemoglobin. The reaction can be catalyzed by dialdehydes. Affinities for tissue proteins are created through stepwise reactions involving ring-opening reactions or methemoglobin formation. 2-Chloroethyl-b-D-fructopyranoside can be used to synthesize a polymerized affinity column by using the ring opening reaction in an affinity chromatography process.</p>

<p>Phenyl a-D-galactopyranoside is a pesticide that is used to control the growth of endophytic fungi. It has been shown to have an antibacterial effect against Gram-positive bacteria and can be used as a fungicide. Phenyl a-D-galactopyranoside can be synthesized from the corresponding synthons, which are 3-hydroxybenzoic acid and 4-methylphenol. This compound contains a carbonyl group and hydroxyl group that are reactive with enzymes such as esterases, glucuronidases, and glutathione reductase, which hydrolyzes it into its inactive form.</p>

<p>fucosylation inhibitor</p>

<p>sugar nucleotide</p>

<p>Butyl a-D-glucopyranoside is an antimicrobial agent that inhibits the growth of photosynthetic organisms. It has been shown to have high cytotoxicity against Gram-positive bacteria, including Enterobacter and Bacillus. Butyl a-D-glucopyranoside also exhibits strong antimicrobial activity against Gram-negative bacteria such as Escherichia coli, Salmonella enterica, Klebsiella pneumoniae, and Pseudomonas aeruginosa. This compound also has potent activity against fungi and yeast. The mechanism of action is not known but may involve the inhibition of tyrosol synthesis or the disruption of microbial membranes.</p>

<p>Building block for the synthesis of 2'-​C-​methyl substituted nucleosides</p>

<p>Custom synthesis of D-glucuronic acid, sodium salt monohydrate.</p>

<p>Magnesium L-lactate is a form of magnesium that is found in the human body, and it is often used to treat women with depressive disorders. This drug works by reducing the synthesis of cholesterol and increasing the level of serotonin in the brain. Magnesium L-lactate is not readily absorbed by the body, so it has low bioavailability. It also has an adverse effect on heart rate and cardiac rhythm, so people who have these conditions should avoid using this drug. The particle size of this drug is high, which can lead to low bioavailability.</p>

<p>2,7-Anhydro-D-sedoheptulose-2,3,4,5,6,7-13C6 is a custom synthesis of a complex carbohydrate. It is an oligosaccharide that is modified with methylation and glycosylation. This compound has been synthesized by Click modification and fluorination. 2,7-Anhydro-D-sedoheptulose-2,3,4,5,6,7-13C6 is water soluble and has a high purity. It is used as a research tool in the field of saccharides and carbohydrates.</p>

<p>Acetamido-2-deoxy-b-D-glucopyranosyl L-asparagine is used in studies of Aspartylglycosaminuria (AGU) which is a rare, inherited lysosomal storage disease caused by a deficiency in the enzyme aspartylglucosaminidase.</p>

<p>Trans-beta-D-glucopyranosyl methylacetoacetate is a carbohydrate that belongs to the group of modified sugars. It is a synthetic compound and can be custom synthesized for your specific needs. This product has a high purity and can be used in research or as a starting material for the synthesis of other compounds. Trans-beta-D-glucopyranosyl methylacetoacetate is an oligosaccharide that can be fluorinated, methylated, glycosylated, or click modified. This product is also available in various grades, such as standard and high purity.</p>

<p>The compound 1,7,7a-Triepialexine is an alkaloid that is found in plants of the genus Trientalis. It has been shown to have anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis. The compound also has a stereoselective synthesis and a stereoselective syntheses.</p>

<p>Leucine-​derived gamma-hydroxynitrile glucoside</p>

<p>N-Acetyl-L-talosaminuronic acid is a natural product that has been shown to have anti-inflammatory activity in experimental models of inflammatory bowel disease. N-Acetyl-L-talosaminuronic acid inhibits the production of proinflammatory cytokines, such as tumor necrosis factor alpha (TNFα), by binding to TNFα receptors on the surface of cells. This can be attributed to its ability to inhibit ATP levels and reduce oxidative stress, which are both factors that contribute to inflammation. N-Acetyl-L-talosaminuronic acid also has been shown to inhibit inflammatory responses in human monocytes and neutrophils. It binds specifically to her2+ breast cancer cells and inhibits their growth in culture. Furthermore, it has been shown to have cytotoxic effects on bladder cancer cells and can be used for the treatment of bladder cancer.</p>

<p>D-Glucose-13C6 is a complex carbohydrate, which is composed of a glucose molecule with one carbon atom labeled as C6. It is used to study the structure of carbohydrates and their interactions with proteins. D-Glucose-13C6 also has applications in the study of diseases such as Alzheimer's disease, Parkinson's disease, diabetes mellitus type 2, and cancer. In addition, this molecule can be used to measure plasma glucose concentrations in humans or animals. D-Glucose-13C6 is not active against bacteria such as Pseudomonas aeruginosa or Escherichia coli. The synthesis of D-glucose-13C6 requires anhydrous dextrose and unlabeled glucose.</p>

<p>Iminosugar 1 is a fluorinated saccharide that belongs to the group of carbohydrates. It is synthesized by the modification of glucose with a fluorine atom. This modification prevents crystallization and increases solubility in water. Iminosugar 1 has been modified by methylation and glycosylation to increase its stability. This product is available as a custom synthesis, and has high purity.</p>

<p>Methyl 3-O-benzyl-D-glucopyranoside is a custom synthesis. It is a complex carbohydrate that is an oligosaccharide, polysaccharide, and modified saccharide. Methyl 3-O-benzyl-D-glucopyranoside can be synthesized from glucose with the use of methylation, glycosylation, or carbonylation reactions. The product has been fluorinated to yield a high purity product. This product can be used for click modifications or sugar chemistry experiments.</p>

<p>Methyl β-D-maltopyranoside is a disaccharide that is an aglycon of maltosides. It has been shown to bind to the active site of alpha-d-glucopyranosidases, which are enzymes that hydrolyze alpha-d-glucopyranosides. Methyl β-D-maltopyranoside has also been shown to interact with dihedral angles and hydroxyl groups in the enzyme binding region, which may be due to conformational changes in the enzyme's active site. The kinetic constants for methyl β-D-maltopyranoside have been calculated by using an algorithm.</p>