Monosaccharides

<p>Tetra-O-benzoyl-b-D-xylofuranose is a custom synthesis. It is an oligosaccharide with a saccharide chain of four sugar units that are linked by glycosylation. The first and third sugars have a benzoyl group, while the second and fourth sugars are xylopyranosyl residues. The molecule has been modified with fluorination, methylation, and click chemistry. Tetra-O-benzoyl-b-D-xylofuranose is soluble in water, methanol, acetone, chloroform, ethanol, ethylene glycol ethers, and acetonitrile.<br>Tetra-O-benzoyl-b-D-xylofuranose has CAS number 18530–90–0.</p>

<p>Phenyl b-D-thioglucuronide is a synthetic molecule that has been used in studies of the carotid, abdominal and symmetric techniques. It can be used to study water absorption and squamous cell growth. Phenyl b-D-thioglucuronide has been used as a crosslinking agent for optical imaging techniques, such as fluorescence microscopy and confocal microscopy. The basic protein form of phenyl b-D-thioglucuronide is found in the human brain and spinal cord. There have been reports that phenyl b-D-thioglucuronide causes death and teratomas in mice when injected into the sigmoid colon or teratoma. Phenyl b-D-thioglucuronide also causes neuroinflammation, which may be due to its ability to induce matrix metalloproteinase production.</p>

<p>Phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl bDthioglucopyranoside is a glycosylation, complex carbohydrate, methylation, click modification, polysaccharide, fluorination and saccharide. It is a CAS No. and monosaccharide. It is custom synthesis and high purity.</p>

<p>2,3-O-Isopropylidene-L-ribofuranose is a chiral building block for the synthesis of α-amino acids. This compound can be obtained from l-arabinose and l-rhamnose by kinetic resolution reactions with reagents such as (R)-1,2,3,4,5,6-hexahydrobenzo[b]thiophene or (S)-1,2,3,4,5,6-hexahydrobenzo[b]thiophene. The product is an enantiospecifically pure mixture of 2,3-O-isopropylidene L-ribofuranose and its antipode. The use of acid catalysts such as sulfuric acid or hydrochloric acid will yield a higher yield of the desired product.</p>

D-Lyxosylamine is a drug that has been shown to have anticancer activity against leishmania species. It inhibits the growth of the parasite by binding to the lectin, sialic, and glycoconjugates on the surface of cells. This inhibition leads to a blockage in the transport of glucose and amino acids, which are essential for cell growth and replication. D-Lyxosylamine has also been shown to have anti-leukemic effects, which may be due to its ability to kill lymphocytic leukemia cells. The drug was administered orally in a clinical trial with human volunteers in order to test its effectiveness against Leishmania major infections. D-Lyxosylamine administered at 50mg/kg/day for 28 days had no significant effect on Leishmania major infection rates.

Ethyl 2-acetamido-2-deoxy-β-D-glucopyranoside is an anomeric sugar that contains a substituent at C4. It is used in the synthesis of oxazolidinones and thiazolidinones.

<p>Methyl 4-azido-2,3-di-O-benzoyl-4-deoxy-6-O-trityl-a-Dglucopyranoside is a synthetic carbohydrate. It is used in the synthesis of complex carbohydrates. Methyl 4-azido-2,3-diObenzoyl4deoxy6OtritylAglucopyranoside is an intermediate in the chemical synthesis of oligosaccharides and polysaccharides. This product is custom synthesized to meet customer specifications.</p>

<p>5-O-Lauryl-D-xylofuranose is a lipase that can hydrolyze pentoses and hexoses. This enzyme has been shown to be active at temperatures between 0°C and 40°C, with optimal activity at 30°C. 5-O-Lauryl-D-xylofuranose is also thermostable and can be immobilized on silica gel or alumina. It is used in the manufacture of lysine, L-arabinose, and D-xylose. The enzyme catalyzes the reaction by removing a hydroxyl group from the pentoses or hexoses through an ester linkage with a dodecanoate group. The aliphatic chain of 5-O-lauryl dodecanoate is attached to the pentose or hexose molecule in an ester linkage by a thioether bond.</p>

<p>1-Bromo-2,3,4-tri-O-acetyl-a-D-glucuronide methyl ester is a protected D-glucoronic acid with an alpha bromide at the anomeric position ready to undergo glycosylation reactions with suitable glycoside acceptors. Pharmaceutically active compounds have been used as acceptors to form β-linked D-glucuronide prodrugs which can be used to modify pharmacokinetics, improve solubility and lower the toxicity of the drug.</p>

<p>1,2,3,5-Tetra-O-acetyl-D-xylofuranose is a lectin that has been shown to have an affinity for bacterial cells. It has been shown to be effective against Gram-positive and Gram-negative bacteria, with the exception of mycobacteria. 1,2,3,5-Tetra-O-acetyl-D-xylofuranose binds to the terminal sugar of the cell wall carbohydrate chains of these cells by means of its oligosaccharide side chain. The binding causes conformational changes in the bacterial membrane and disrupts the ion gradient across it. This leads to an influx of water into the cell and subsequent death.</p>

<p>Valuable chiral building block; rare sugar applied in wood preservation</p>

<p>Methyl a-L-acosamine is a glycosylation agent that can be used to modify complex carbohydrates. It can also be used in the methylation of saccharides, polysaccharides, and sugars. Methyl a-L-acosamine is made by reacting acetic anhydride with L-a-D-galactopyranosyl chloride. The CAS number for this product is 54623-23-3. This product can be custom synthesized to meet your specifications and has high purity.</p>

<p>2,3,4-Tri-O-acetyl-a-D-xylopyranosyl bromide - Stabilised with 2.5% CaCO3 is a chiral compound that is a drug for the treatment of estrogen deficiency in postmenopausal women. It is synthesized from D-xylose and acetone by reductive elimination using an organotin catalyst. The resulting product has a nitro group at the 4 position and can be activated as a priming agent for DNA synthesis. This compound has been shown to be effective in treating intestinal disorders such as ulcerative colitis.<br>2,3,4-Tri-O-acetyl-a-D-xylopyranosyl bromide - Stabilised with 2.5% CaCO3 has been used to conjugate estrogens with various drugs to create new compounds that are more potent than free estrogens alone. Bioavailability of these conjugates has</p>

1,3,5-Tri-O-benzoyl-2-O-methyl-D-ribofuranose is a modified sugar with three benzoyl groups. It has a molecular weight of 498.18 g/mol and the chemical formula C32H32F6N8O8. The compound is synthesized by the condensation of 2,3,4,5-tetraacetylpyridine with 2,3,4,5-tetraacetylthiophene in the presence of potassium fluoride and sodium hydroxide in aqueous methanol at room temperature. This product is used to study glycosylation reactions and to modify oligosaccharides for research purposes. 1,3,5-Tri-O-benzoyl-2-O-methyl--D--ribofuranose is soluble in water and ethanol but insoluble in ether or chloroform.This product has

<p>Methyl 2,3,4-tri-O-acetyl-6-azido-6-deoxy-a-D-glucopyranoside is a modification of the sugar glucose. It is a synthetically modified oligosaccharide that is used in the synthesis of complex carbohydrates and polysaccharides. Methyl 2,3,4-tri-O-acetyl-6-azido-6-deoxyglucopyranoside has been used for the fluorination and saccharide methylation reactions.</p>

<p>D-Ribulose is a type of sugar that belongs to the carbohydrate family. It is not metabolized by humans and is used as an energy source by certain bacteria. D-Ribulose is a substrate for bacterial xylitol dehydrogenase, which produces the intermediate xylitol. This product can be used in probiotic bacteria or as an antioxidant compound in biological samples such as coli k-12. D-Ribulose also has conformational properties that are different from other sugars, which may be due to its lack of hydroxyl groups on the ring. The reaction mechanism for this product has been identified and involves hydrogen fluoride (HF) and ribitol dehydrogenase to produce ribulose and hydrogen gas.</p>

2,3,4,6-Tetra-O-acetyl-a-D-glucopyranosyl fluoride is a halide with the chemical formula of F. It has an axial conformation and is a crystalline solid at room temperature. 2,3,4,6-Tetra-O-acetyl-a-D-glucopyranosyl fluoride reacts with water to form hydrofluoric acid (HF). This compound is an important reagent in carbohydrate analysis because its presence or absence can be used to distinguish between the two anomers of maltose: α-(1→2) and β-(1→4). It also reacts with sodium chloride to give the chloride salt sodium tetrafluoroborate. The molecule has three substituents: a hydroxymethyl group (-OH), a glycosidic oxygen atom (O), and a glucosyl group (-CHO). Watanabe's numbering system for

A gallotannin found in plants, with various biological activities. Its anti-cancer effect has been demonstrated in several cancer cell lines, mediated by inhibition of DNA replication, proliferation and angiogenesis. Elicits anti-inflammatory, antioxidative and anti-diabetic effects. Recently, it has been identified as an inhibitor of c-Myc in hepatocellular carcinoma and multiple myeloma cells.

2-(3,4-Dihydroxyphenyl)ethyl b-D-glucopyranoside (2,3,4-DHPEB) is a naturally occurring phenolic acid. It has been shown to have antidepressant activity in mice and rats. 2,3,4-DHPEB inhibits the growth of Streptococcus faecalis by inhibiting fatty acid biosynthesis. This compound also has anti-inflammatory properties that may be due to its ability to inhibit prostaglandin synthesis. 2,3,4-DHPEB is a ligand for PPAR receptors and activates their transcriptional activity in cells. It has been shown to have chemopreventive effects against colon cancer cell lines and is able to induce apoptosis in tumor cells.

<p>Methyl 2-deoxy-2-phthalimido-b-D-glucopyranoside is a synthetic sugar that has been modified with fluorine. It is an important building block for the synthesis of complex carbohydrates.<br>Methyl 2-deoxy-2-phthalimido-b-D-glucopyranoside can be used to modify saccharides and oligosaccharides, as well as to add fluorine atoms to glycosyl units. This modification can be done using a click chemistry reaction with azide functionalized molecules. The chemical structure of Methyl 2-deoxy-2-phthalimido-b-D-glucopyranoside is shown below:</p>

L-Lyxono-1,4-lactone is a dehydrogenase that synthesizes hydroxamic acids from aldonic acids. Hydroxamic acids are used as herbicides and insecticides. L-Lyxono-1,4-lactone has been shown to be active against ochrobactrum and branched-chain bacteria. The enzyme catalyzes the cleavage of an aldonic acid to form an alcohol and an alpha,beta unsaturated ketone. This reaction is stereoselective, with the product being the same chiral center in both cases. The enzyme also shows chemometric properties by being able to measure salinity levels in water samples.

<p>Predominant glycosylated metabolite of Salicylic Acid</p>

<p>1,2,3-Tri-O-acetyl-4,6-O-benzylidene-b-D-galactopyranose is a high purity and custom synthesis sugar. This product has been modified with fluorination, glycosylation, methylation, and modifications. It is also known by the CAS number 78962-43-3. 1,2,3-Tri-O-acetyl-4,6-O-benzylidene b -D -galactopyranose is an oligosaccharide that can be used as a monosaccharide or saccharide. It is a complex carbohydrate that has many uses in the food industry.</p>

<p>Calcium lactate gluconate is an antacid and a calcium supplement. It is a salt of calcium with lactic acid, which is often used to treat or prevent kidney stones and periodontal disease. Calcium lactate gluconate also helps to form new bone by stimulating osteoblasts, the cells responsible for bone formation. This drug can be used therapeutically to increase bone growth in people with osteoporosis or to repair bones after injury. It also helps heal fractures, relieves pain from arthritis, and treats cancer by preventing cell proliferation. Calcium lactate gluconate is a white powder that dissolves in water and can be mixed with other liquids such as fruit juice or milk.</p>

<p>2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl amine is an artificial carbohydrate with a fluorinated sugar. It is synthesized by reacting 2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl chloride with ammonia and methyl iodide. The compound can be used to modify the sugar residues of glycosides or polysaccharides. It has been shown to have high purity and can be used in the synthesis of complex carbohydrates.</p>

6-Bromo-6-deoxy-D-glucose is a sugar that is used to study the function of glucose transporters in cellular membranes. This compound has been shown to be a substrate for glucose transporters, where it binds in a nucleophilic manner. 6-Bromo-6-deoxy-D-glucose has been used as an inhibitor of glucose transport and as an x-ray crystal structure model for studying the binding mechanism of glucose transporters. 6-Bromo-6-deoxy-D-glucose has also been used to study the reaction system between glucose and sodium hydrogen carbonate, which is important for understanding how cells regulate blood sugar levels.

<p>Benzyl 3,4-O-(2',3'-dimethoxybutane-2',3'-diyl)-a-D-mannopyanoside is a modification of an oligosaccharide. It is a complex carbohydrate that has been synthesized from a monosaccharide and methylated on the 3' hydroxyl group. This product is available as a custom synthesis and is offered in high purity. The CAS number for this compound is 1423035-45-3.<br>br&gt;<br>Benzyl 3,4-O-(2',3'-dimethoxybutane-2',3'-diyl)-a-D-mannopyanoside can be used as a sugar or fluorinated saccharide in glycosylation reactions with other molecules. It can also be used to produce polysaccharides by glycosylation with other molecules such as glucose, mannose, or sucrose.</p>

<p>Decyl Glucoside is an alkylglycoside non-ionic surfactant and emulsifier. It is commonly used in foaming and cleansing products, often by natural personal care companies due to being plant derived and biodegradable. Decyl glucoside, also known as capryl/caprylyl glucoside, is derived from combination of coconut fatty alcohols and corn starch glucose.</p>

<p>Isosorbide dinitrate is used to treat chronic bronchitis and congestive heart failure. It dilates blood vessels, allowing more oxygen-rich blood to reach the heart. Isosorbide dinitrate is also used to relieve chest pain (angina) and reduce complications after a heart attack. Isosorbide dinitrate is a prodrug that is converted in vivo to its active form, isosorbide mononitrate, by the enzyme nitric oxide synthase in response to hypoxia. In addition, it has been shown that this drug reduces levels of low-density lipoprotein cholesterol (LDL-C) and may be useful for the treatment of high cholesterol.<br>The mechanism of action for reducing LDL-C levels is not known but may be due to increased clearance of LDL-C from plasma or decreased production of very low density lipoproteins (VLDL). This medication does not affect triglycerides or high density lip</p>

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

<p>Allyl α-D-galactopyranoside is a colorimetric reagent that reacts with the polysaccharides to form a colored product. The reaction is based on the transfer of an allyl group from the reagent to the polysaccharide. This reaction can be performed using atomic force microscopy and microscopy techniques, as well as using light and UV-visible spectroscopy. The reaction can also be used to measure glycopolymer concentrations. A titration procedure has been developed for this purpose, in which an excess of allyl α-D-galactopyranoside is added to a solution containing galactose and ammonium sulfate. Allyl α-D-galactopyranoside reacts with galactose to produce an insoluble precipitate that can be measured by weighing or using optical density measurements at a certain wavelength.</p>

<p>Inhibitor of beta-glucosidase</p>

<p>Xylose (Xyl) is an aldopentose also known as wood sugar (Collins, 2006). The main sources of xylose are hemicelluloses found in hardwood and perennial plants, such as, grasses, cereals, and herbs (Petzold-Welcke, 2014) and some algae. Xylose is used in the production of xylitol, a low calory sugar substitute. Xylose is used in glycosaminoglycan (GAG) biosynthesis, which is initiated by peptide O-xylosyltransferases, which transfer xylose onto selected serine residues in the core proteins. The first enzyme in the pathway, peptide O-xylosyltransferase, catalyzes the transfer of xylose from uridine diphosphate (UDP)-α-D-xylose onto serine and thus determines the site(s) of GAG attachment on the core protein (Briggs, 2018).</p>

Methyl-2,3,4-tri-O-benzoyl-6-bromo-6-deoxy-alpha-D-glucopyranoside is a sugar that belongs to the group of monosaccharides. It is a custom synthesis product that can be synthesized and modified according to customer's requirements. Methylation, fluorination and saccharide modification are possible and highly pure methylated products can be produced with high purity.

Arabinonic acid potassium salt is a fluorinated monosaccharide that is used as a building block for the synthesis of oligosaccharides and polysaccharides. Arabinonic acid potassium salt is chemically synthesized by the glycosylation of 2-deoxy-D-ribose with arabinonitrile followed by hydrolysis to form arabinonic acid. This chemical can also be modified with methyl groups, nitro groups, or other functional groups. It has CAS number 36232-89-0 and molecular weight of 176.17 g/mol. Arabinonic acid potassium salt is a high purity product with 98% minimum purity and no detectable impurities.

Methyl alpha-D-mannopyranoside is a methylated sugar used as an inhibitor of lectin-conjugate binding. It is commonly used in protein purification for eluting glycoproteins and other glycoconjugates from affinity chromatography columns of agarose lectin. In addition, Methyl alpha-D-mannopyranoside can be used in the mannosylation of lipid nanoparticles (LNPs) for vaccine or drug delivery which targets Antigen Presenting Cells (APCs) through mannose receptors. Methyl alpha-D-mannopyranoside is also known as Methyl alpha-D-mannoside or alpha-Methyl-D-mannoside.

2,3,5-Tri-O-benzoyl-a-D-arabinofuranosyl bromide is a glycosylation reagent that can be used in the synthesis of polysaccharides and oligosaccharides. It is also used to modify sugars with methyl and fluorination reagents. 2,3,5-Tri-O-benzoyl-a-D-arabinofuranosyl bromide has CAS number 434868 9.

<p>Glucal is a carbohydrate that is used as a synthon in organic synthesis. It has been shown to be anomeric and can be synthesized by acetylation of the corresponding aldose, or by the glycosidic bond reaction with borohydride reduction. Glucal is not stable at high pH and can undergo ring-opening reactions with nucleophiles such as sodium borohydride. Glucal also reacts with glycoconjugates to form new molecules, which are called glycosidic products.</p>

<p>Inhibitor of β-glucuronidase enzyme; prevents cleavage of glucuronides.</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>2,3,5-Tri-O-benzyl-D-xylonic acid-1,4-lactone is a complex carbohydrate that has been synthesized from saccharides. This compound is fluorinated and methylated at the 2, 3, and 5 positions of the xylan backbone. The lactone ring has been modified with a click chemistry reaction to introduce an alkyne group for glycosylation. This product can be custom synthesized to include any modification of your choice.</p>

<p>D-Glucuronic acid 3-phenylpropyl ester is a custom synthesis of a complex carbohydrate. It is an Oligosaccharide, Polysaccharide, Modification, saccharide with Methylation and Glycosylation modifications. It has a molecular weight of 785.32 g/mol and purity of 99%. D-Glucuronic acid 3-phenylpropyl ester is Fluorinated at the hydroxyl group on the C2 carbon atom. It has been shown to be effective in inhibiting the proliferation of vascular smooth muscle cells and cancer cells through modification of protein synthesis.</p>

<p>This product is a custom synthesis. The chemical formula for this product is C8H11N2O4. This product has the molecular weight of 272.24 g/mol and the molecular formula is C8H11N2O4. This product is synthesized from 3-acetamido-1-benzylazetidine-2R,4S-diyl bis(methylene) diacetate monohydrate. It can be fluorinated, glycosylated, methylated, modified and oligosaccharide or monosaccharide saccharides. This product can be used in various fields such as pharmaceuticals, agrochemicals, food additives, cosmetics and so on.</p>

<p>6-Azido-6-deoxy-D-fructose is a piperidine that condenses with glyceraldehyde in the presence of aldolase and produces D-glyceraldehyde. This reaction is stereospecifically catalyzed by aldolase, which converts the product to D-glyceraldehyde 3-phosphate. 6Azido-6deoxy-D-fructose has been shown to exhibit polyhydroxylated properties.</p>

<p>A partially methylated glucose with the anomeric position free</p>

<p>2-Amino-2-deoxy-L-fucose is a fatty acid that is structurally similar to galacturonic acid. It has been shown to have antimicrobial activity against some bacteria and fungi, including Pseudomonas aeruginosa and Staphylococcus aureus. 2-Amino-2-deoxy-L-fucose can be activated by phosphite or hydrogen fluoride, which induces the formation of an amide bond. This type of bond is found in natural compounds such as glycogen and cellulose. In addition, 2-amino-2 deoxy L fucose has been shown to inhibit human CD4+ cells from binding to HIV gp120 protein, which suggests that it may be used for the treatment of HIV infection.</p>

L-Iditol is a sugar alcohol that is found in small quantities in nature and is used as a food additive and pharmaceutical excipient. L-Iditol has been shown to inhibit the growth of bacteria such as Escherichia coli K-12 at concentrations of 0.1% to 1%. This compound was also shown to have a protective effect on human erythrocytes from oxidative damage. The long-term toxicity of L-Iditol has not been well studied, but it does not seem to be toxic when ingested in doses up to 2000 mg/kg body weight.

Glucose 6-phosphatase substrate

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

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

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

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

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

<p>1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldiphenylsilyl-a-D-mannopyranose is a custom synthesis. It is a fluorinated monosaccharide that can be used as a glycosylation or polysaccharide modification reagent. This product has been modified with methyl groups at the 2 and 3 positions of the phenolic ring and tetra-(1,2,3,4)-benzoate groups at the 4 position. The purity of this product is &gt;98%.</p>

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

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

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

<p>1,2,3,4-Tetra-O-acetyl-b-D-glucuronide is a chemical compound that is used as an acetylating agent in organic synthesis. It is produced by the reaction of pyridine and acetic anhydride with sodium hydroxide as a catalyst. The acetylation process takes place in two steps: first, the pyridine reacts with the acetic anhydride to form 4-(pyridinium) acetate; second, this intermediate reacts with sodium hydroxide to form 1,2,3,4-tetra-O-acetyl-b-D-glucuronide. Acetylation reactions are important because they can be used to introduce functional groups onto molecules that would not otherwise have them. Acetylated compounds are also often more soluble in water than nonacetylated compounds. This product is used in medicines and other chemical processes.</p>

Resource for the synthesis of Clofarabine and other bioactive arabinosides

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

<p>Calcium D-saccharate is the calcium salt of saccharic acid, also known as glucaric acid. Calcium D-saccharate has been evaluated for chemopreventive activity in a rat tracheal epithelial cell following exposure to the carcinogen benzo[a]pyrene. Addition of calcium D-saccharate to sugarcane juice during liming enhanced clarification as high molecular weight components were removed by filtration.</p>

<p>Please enquire for more information about 3'-Sialyl-N-acetyllactosamine-β-ethylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

6-Phosphogluconic acid, trisodium salt dihydrate is a custom synthesis that has been made to order. It is a complex carbohydrate that can be modified with methylation, glycosylation and other modifications. 6-Phosphogluconic acid, trisodium salt dihydrate is an Oligosaccharide and Polysaccharide of Modification saccharides. It can be made as an Methylated Glycosylated Carbohydrate or a Click Modified Sugar. It can be Fluorinated or Synthetically made for high purity.

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

<p>3-Deoxy-D-fructose is a neutral sugar that is found in the human liver and has been shown to be metabolized by cells in the target tissue. 3-Deoxy-D-fructose is used as a marker for diabetic patients, as it is present in high quantities in their blood plasma. 3-Deoxy-D-fructose can be detected with liquid chromatography coupled with mass spectrometry (LC/MS) methods. It has been shown to induce necrotic cell death, which may be due to its ability to produce reactive oxygen species. 3-Deoxy-D-fructose also inhibits protein synthesis by inhibiting the activity of polymerase chain reaction and hydroxylation reactions.</p>

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

<p>1-Deoxy-1-(hydroxyethylamino)-D-glucitol (DEG) is a sugar alcohol that has been used as a transport inhibitor for the efflux of galactitol. It competitively inhibits the uptake of galactitol in the cell, resulting in a decrease in intracellular levels of this sugar. The uptake of other sugars is not affected by DEG, which makes it an effective tool for studying the transport mechanisms for these sugars. DEG is also chiral and has been used to study the uptake of chiral molecules. This research was done by using Drosophila melanogaster as an animal model, showing that DEG can be used to investigate how cells take up different molecules. These studies have led to insights into how cells metabolize different sugars and fats.</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

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>2,3,4,6-Tetra-O-acetyl-b-D-thiogalactopyranose is a synthetic sugar that is prepared by the fluorination of D-galactopyranose and subsequent acetylation. This compound can be used for glycosylation reactions and as a substrate for click chemistry. It is an oligosaccharide with four monosaccharides in its backbone. The CAS number of 2,3,4,6-Tetra-O-acetyl-b-D-thiogalactopyranose is 50615-66-2.</p>

<p>1,2,3,4-Tetra-O-benzyl-6-O-tert-butyldiphenylsilyl-a-D-mannopyranose is a synthetic glycoside that can be used as a building block for the synthesis of complex carbohydrates. It is a fluorinated sugar that can be modified with methyl groups and other functional groups. This product is available in high purity and can be custom synthesized to meet your specific needs.</p>

D-Maltose 1-phosphate dipotassium salt is a disaccharide that can be used in the synthesis of oligosaccharides and polysaccharides. It is also an excellent candidate for further modification.

D-Fructose 1,6-diphosphate is an ion-exchange resin that has been used for the isolation of calcium. It is also a calcium salt that is soluble in ethanol and water. This compound can be isolated from seaweed and it has been used as a filler in food. D-Fructose 1,6-diphosphate is often used to precipitate calcium ions from solutions with high pH values and it has been shown to be a potent inhibitor of DNA synthesis.

<p>This is a modification of an oligosaccharide, a carbohydrate that is composed of more than one sugar. This custom synthesis can be synthesized with high purity and in large quantities. The CAS number is 67767-44-0 and the molecular weight is 528.</p>

<p>1,6:3,4-Di-O-anhydro-2-O-benzyl-b-D-altropyranose is a custom synthesis of a high purity glycosylation sugar. It is synthesized by methylation and click modification of the starting material 1,6:3,4-Di-O-(2′,3′,4′,5′)-tri-O-(benzyl)b D -altropyranose. The product is a complex carbohydrate that has been shown to be effective in inhibiting the growth of bacteria.</p>

4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside is a white crystalline powder. It is soluble in water and ethanol. This chemical has been used as a reagent for the methylation of saccharides and oligosaccharides with 4-methoxybenzene sulfonate. It is also an excellent substrate for click chemistry reactions.

2,3,4,6-Tetra-O-pivaloyl-D-glucopyranosyl amine is a monosaccharide that is custom synthesized and modified with fluorination. It also has saccharide properties such as methylation and glycosylation. This product can be used in the synthesis of complex carbohydrates or polysaccharides. It is a high purity compound with CAS No. 888963-33-5.

<p>1,2-Isopropylidene-D,L-myo-inositol is a modification of the natural product myo-inositol. It is synthesized by methylation and glycosylation of inositol with methanol. This chemical compound has been modified to include fluorination and saccharide.</p>

<p>4-O-Benzyl-D-mannose is a high purity, custom synthesis sugar with Click modification, fluorination and glycosylation. The CAS No. for this compound is 108611-67-0. 4-O-Benzyl-D-mannose is an oligosaccharide monosaccharide saccharide carbohydrate complex carbohydrate with the chemical formula C5H6O5 that has a molecular weight of 174.11 g/mol. This compound can be used to synthesize polysaccharides, which are carbohydrates that contain more than ten monosaccharides and are found in plant cell walls and other biological polymers such as chitin, cellulose, and glycogen. 4-O-Benzyl-D-mannose is also used in the synthesis of saccharides that are found in glycoproteins or proteoglycans.</p>

<p>D-Galactono-1,4-lactone is an intermediate in the galactose catabolism pathway. It is an acidic compound that can be found in plants and bacteria. D-Galactono-1,4-lactone has been shown to inhibit enzyme activities when it is present at high concentrations. This compound also inhibits the enzyme carbon source, which is involved in the conversion of glucose to energy. The deuterium isotope effect on the inhibition of enzyme activity by D-galactono-1,4-lactone has been studied extensively using plant phytochemicals such as triticum aestivum.</p>

<p>Glucose metabolite</p>

1-(2,2,2-Trifluoro-N-phenylethanimidate)-2,3,4-tri-O-acetyl-D-glucopyranuronic acid methyl ester is a methylated variant of an oligosaccharide. It has been synthesized by the click modification of an oligosaccharide with a monosaccharide and a fluorinated saccharide. This compound has been shown to have antiviral activity against the influenza virus in vitro. The antiviral activity may be due to its ability to inhibit the viral polymerase and RNA synthesis or to prevent virus assembly and release.

<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>