Monosaccharides

<p>Ziyuglycoside II is a steroidal alkaloid that has been shown to have anti-angiogenic properties. It is a natural compound extracted from the Chinese herb ziyuglycoside. This compound has been shown to inhibit the activation of toll-like receptor 4, which plays an important role in inflammation and immunity. Ziyuglycoside II also inhibits the production of reactive oxygen species and autophagy, leading to cell death by apoptosis. This compound has been shown to be effective against bowel disease and epithelial mesenchymal transition (EMT). Ziyuglycoside II has also been shown to have matrix effects on the cells Hl-60, which are related to tumor metastasis.</p>

<p>1,2:3,5-Di-O-Isopropylidene-a-L-xylofuranose is a fluorinated sugar that is used as a building block in the synthesis of complex carbohydrates and oligosaccharides. It has a CAS number of 131156-47-3. 1,2:3,5-Di-O-Isopropylidene-a-L-xylofuranose is an active component in the modification of saccharide and polysaccharide structures by click chemistry. It can be modified with various functional groups such as methylation or monosaccharide to produce specific compounds. This product is available for custom synthesis.</p>

<p>N1-b-D-arabinopyranosylamino-guanidine HCl is a modified carbohydrate. It is a synthetic monosaccharide that is custom synthesized by methylation and glycosylation. This product has high purity and can be used for modification of saccharides or oligosaccharides to create new carbohydrates with desired properties.</p>

<p>Benzyl 4,6-O-benzylidine-b-D-galactopyranoside is a benzoylated sugar. It is prepared by reacting benzoyl chloride with benzene and then with the sugar in an equimolar ratio. The reaction proceeds via a nucleophilic substitution at the 2' position of the sugar followed by an elimination of water. Benzyl 4,6-O-benzylidine-b-D-galactopyranoside reacts with dibutyltin to form a benzoylated tin compound that can be used as a catalyst for organic synthesis.</p>

<p>Methyl 2,3,4-tri-O-acetyl-b-D-glucopyranuronosyl azide is a fluorinated carbohydrate. It is a monosaccharide and an oligosaccharide that is synthesized from a synthetic glycosylation reaction. This product can be used in the production of polysaccharides or as a click modification to modify the sugar moiety of other molecules. Methyl 2,3,4-tri-O-acetyl-b-D-glucopyranuronosyl azide has CAS No. 67776-38-9 and is available in high purity.</p>

<p>1,2,3,5,6-Penta-O-benzoyl-D-galactofuranose is a sugar that is custom synthesized and can be modified with fluorination. This product has a CAS number of 138811-45-7 and is high purity. It can be used in glycosylation, oligosaccharide synthesis, methylation, monosaccharide synthesis and polysaccharide synthesis. It is an important building block for the modification of complex carbohydrates.</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>2,3-O-Isopropylidene-1-O-methyl-D-ribosic acid is a synthetic glycosylate that can be used to modify saccharides and oligosaccharides. It is a methylated form of ribose and has been shown to inhibit the glycosylation reactions of glycogen. 2,3-O-Isopropylidene-1-O-methyl-D-ribosic acid is also known to react with fluorine in order to produce a variety of fluorinated carbohydrates. This product has high purity and can be used for custom synthesis of carbohydrates. The CAS number for this product is 54622-95-6.</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>2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl isothiocyanate (TGIT) is a compound that mimics the melanoma antigen. It has been used to identify human pathogens in biological samples and has shown to have an antibody response. TGIT has also been used as a fluorescent probe for nucleic acids in analytical methods and polymerase chain reaction. This chemical can be used as a fluorescence detector in titration calorimetry. TGIT is not acutely toxic, but can cause cell lysis when combined with trifluoroacetic acid.</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>Enhances dissolution of soil minerals; intermediate in L-ascorbic acid syntheses</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>Methyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranoside is an antiperspirant that prevents the formation of sweat. It is a mixture of two active ingredients: methyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranoside and zinc oxide. The former inhibits the formation of sweat by binding to the protein in eccrine glands and preventing it from absorbing chloride ions. Zinc oxide reduces body odor by binding to sulfur compounds that are secreted by bacteria on skin surfaces. Methyl 2,3,5-triO-benzoyl arabinofuranoside and zinc oxide are used as a combination for their complementary effects.</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>1,3,5-Tri-O-benzoyl-2-O-(1H-imidazole-1-sulfonate)-a-D-ribofuranose (TBIR) is a fatty acid that is synthesized by the condensation of 1,3,5-triacetylbenzene with 2,4,6,-trichlorobenzoyl chloride in the presence of triethylamine and sodium methoxide. TBIR has been shown to be suitable for fabricating polyesters and polyamides. TBIR also has the ability to modify membranes. This modification occurs when TBIR reacts with phospholipids in the membrane bilayer by inserting itself into the membrane bilayer. The mesoporous nature of TBIR allows for diffusional transport through its pores as well as an increased surface area for reactions. It also has a large diameter and branched chains that make it suitable for</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>2-Acétamido-3,4,6-tri-O-acetyl-2-deoxy-D-glucopyranose is a cytotoxic glycoside that can be used as an intermediate in the synthesis of saponins. It has been shown to yield high yields of trifluoromethanesulfonate (TFM) when reacted with glycosyl acceptors such as albizia bark extract. The TFM may then be used for the synthesis of nitromethane and alcohols. This compound also reacts with oleanolic acid to form an anomeric mixture that can be used to yield 2,3,4,6 tetraacetylated 2 deoxyglucose.</p>

<p>1,2:5,6-Di-O-isopropylidene-a-D-ribo-hexofuranose-3-ulose monohydrate is a fluorinated carbohydrate that has been synthesized in our lab. It is a complex carbohydrate and can be used as a building block for glycosylation. The synthesis of this compound is done through the use of click chemistry to modify the sugar. We have high purity levels for this compound and can provide custom synthesis services for your needs.</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>E-Retinyl b-glucuronide is a metabolite of vitamin A that is formed in the liver by glucuronidation of retinol. It has been shown to have immunomodulatory effects and can be used to activate various immune cells, such as T lymphocytes, monocytes, and natural killer cells. E-Retinyl b-glucuronide binds to cell surface antigens and induces the expression of surface markers on mononuclear cells. In vitro studies have shown that this metabolite has growth-promoting activity for certain types of cancerous cells including colon carcinoma, breast carcinoma, and thyroid carcinoma. E-Retinyl b-glucuronide is also known to inhibit the binding of 13-cis retinoic acid to its receptor, thereby preventing the activation of genes in target tissues.</p>

<p>Glucose 6-phosphatase substrate</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>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>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>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>L-Erythrose is a monosaccharide that contains an hydroxyl group on the second carbon atom. It can be synthesized by a synthetic scheme involving glycolaldehyde and hydroxylamine. L-Erythrose has been shown to inhibit the enzyme phosphoglycerate kinase, which converts 2-phosphoglycerate into phosphoenolpyruvate. L-Erythrose has also been shown to inhibit dehydroascorbic acid reductase, which converts dehydroascorbic acid into ascorbic acid, and galactitol reductase, which converts galactitol into D-tagatose. The mutant strain of Escherichia coli K12 that was engineered to produce L-erythrose showed a decreased susceptibility to phage infection and an increased resistance to oxidative stress. In addition, the polyol pathway in E. coli was induced by L-erythrose treatment.</p>

<p>Resource for the industrial synthesis of ascorbic acid alias Vitamin C</p>

<p>Methyl α-L-rhamnopyranoside is a conjugate molecule made via a Fisher glycosylation with MeOH. It has been shown to have pesticidal activities and can be used in the production of pesticides or glycoconjugates. Methyl α-L-rhamnopyranoside is of interest as a vaccine adjuvant, due to its ability to activate the immune system. This compound also has anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</p>

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

<p>a-D-Mannopyranosyl L-threonine is a carbohydrate with the molecular formula C6H14O5. It is a white crystalline powder that has a sweet taste. This product can be used as an ingredient in food and beverage products, such as confectionery products, soft drinks, dairy products, baked goods, and chewing gum. It may also be used in pharmaceuticals, such as chewable tablets or capsules for oral use.</p>

<p>1,2,3,4-Tetra-O-acetyl-6-O-trityl-b-D-mannopyranose is a synthetic sugar that can be used as a building block for the synthesis of oligosaccharides. It is also used to alter the properties of sugars and polysaccharides by modifying their glycosidic linkages. The product is insoluble in water and organic solvents. It is stable under acidic conditions and can be hydrolyzed with acids or alkalis. It is also soluble in methanol and methylene chloride. The CAS number for this product is 92621-31-3.End&gt;</p>

<p>Methyl a-D-fucopyranoside is a monoclonal antibody that binds to the O-antigen of the polysaccharide chain. It is a synthetic trisaccharide consisting of an o-antigen, an α-linked D-fucose residue, and an α-linked galactose residue. This antibody interacts with the serologic subtypes of Group A Streptococcus, but not with other serogroups. Methyl a-D-fucopyranoside utilizes conformational epitopes and disaccharides which are not accessible to other antibodies in order to bind to the o-antigen. The o-antigen is composed of two serologically distinct regions: one region for binding by anti-A antibodies, and another for binding by anti-B antibodies.</p>

<p>Please enquire for more information about 2-[(1E)-2-[6-(β-D-Galactopyranosyloxy)-2,3-dihydro-1H-xanthen-4-yl]ethenyl]-3,3-dimethyl-1-propyl-3H-indolium iodide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3,4,6-Tetra-O-benzoyl-α-D-glucopyranosyl bromide is a derivative of vitamin A. It has been used as a carbonate for the synthesis of retinol, tetrabenzoate and other related compounds. The compound is soluble in water and has shown growth promoting activity in studies with Salmonella typhimurium. 2,3,4,6-Tetra-O-benzoyl-α-D-glucopyranosyl bromide is metabolized to retinol by hydrolysis or oxidation. It can also be converted into tetrabenzoate by oxidation followed by reduction of the 4′ position hydroxyl group.</p>

<p>Phenyl 2,3,4,6-tetra-O-acetyl-a-D-thiomannopyranoside is an analog of a sugar molecule. This compound can be synthesized by the metathesis reaction between phenyl 2,3,4,6-tetra-O-acetyl-α-(2′→3′)-D-thiomannopyranoside and bis(trimethylsilyl) sulfate in the presence of polyphosphoric acid and potassium sulfate. The yield of this synthesis is high and can be increased with the addition of potassium sulfonate as a cofactor.</p>

<p>L-Idonic acid sodium is a plant hormone that regulates carbohydrate metabolism. It has been shown to regulate the synthesis of galacturonic acid and malic acid, which are important for the production of glucose. L-Idonic acid sodium also regulates the synthesis of fatty acids, which are important for cell membrane formation. L-Idonic acid sodium is an intermediate in the biosynthesis of l-tartaric acid, which is an enzyme substrate. The gene product that encodes this molecule has been characterized as a protein with a molecular weight of approximately 9,000 daltons and a hydroxyl group on C-3.</p>

<p>Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside is a high purity natural carbohydrate. It is an oligosaccharide that can be custom synthesized to meet your requirements. Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido b D glucopyranoside has many modifications including click and fluorination. Its CAS number is 76101 13 8. This product can be used for modification, glycosylation and fluorination in the synthesis of complex carbohydrates.<br>!-- <br>--&gt;<br>!-- <br>--&gt;</p>

<p>1,5-Anhydro-2,3,4-tri-O-benzoyl-D-threo-pent-1-enitol is a high purity compound that is synthesized from D-threo pent 1 enitol. It is a sugar that belongs to the category of complex carbohydrates. This product can be custom synthesized and modified according to customer requirements.</p>

<p>2,3,4,6-Tetra-O-acetyl-a-D-glucopyranosyl trichloroacetimidate (2TG) is a mannose targeting agent that can be used to target specific cells in the body. This compound has been shown to inhibit the growth of cancer cells and induce photodynamic therapy. 2TG is a conjugate that consists of a 6-phosphate group attached to an acetylated mannose molecule. The 6-phosphate group is an important feature for tumor targeting, as it allows for the attachment of other molecules such as monoclonal antibodies and drugs. 2TG functions by binding with high affinity to glycoproteins on the surface of cancer cells and animal tissues. These glycoproteins are found in large quantities on the surface of cancer cells and animal tissue, which makes them good targets for anti-cancer drug development.</p>

<p>Tetracycline 10-O-b-D-galactopyranoside is a tetracycline antibiotic that has been modified with a fluorinating agent to increase its water solubility. Tetracycline 10-O-b-D-galactopyranoside is the most active of the tetracyclines for the treatment of infections caused by mycoplasmas, rickettsias, and chlamydiae. It inhibits protein synthesis in these bacteria by binding to ribosomes. This drug also has an inhibitory effect on the growth of Mycobacterium tuberculosis and Mycobacterium avium complex.</p>

<p>6-O-Malonylglycitin is a glycosylated flavonoid that belongs to the group of isoflavones. It is found in a variety of plants, including soybeans and fava beans. 6-O-Malonylglycitin has been shown to be an effective inhibitor of β-glucosidase activity at temperatures below 37°C, which overlaps with the range of temperatures where it inhibits glycitein production. This inhibition may be due to its pleiotropic effects on various treatments, such as its ability to inhibit cancer cell growth by inhibiting protein synthesis and inducing apoptosis. 6-O-Malonylglycitin also has synergistic effects when used concomitantly with chromatographic markers, such as high performance liquid chromatography (HPLC), which can be used to analyze the levels of endogenous compounds in human blood samples.</p>

<p>1-O-Galloyl-b-D-glucose is a molecule that is found in plants and has been used as an inhibitor of p-hydroxybenzoic acid (PHBA) enzyme activities. 1OGG inhibits the growth of viruses by inhibiting the enzymatic activity of their RNA polymerases. It also inhibits mitochondrial membrane potential, which is vital for cellular respiration. 1OGG has shown to be active against urinary infections and opportunistic fungal infections such as Candida glabrata. In vitro assays have shown that it may have anti-inflammatory properties.</p>

<p>Kifunensine is a potent and specific inhibitor of plant and animal α-mannosidase I with IC50 in nanomolar range. It inhibits the enzyme isoforms in Golgi apparatus (GMI) and endoplasmatic reticulum (ERMI). The compound prevents mannose trimming on glycoproteins and shifts the glycoform content from complex to oligomannose type. It's used for the production of recombinant therapeutic glycoproteins with mannose rich N-linked glycans.</p>

<p>Methyl 2,3,4,6-tetra-O-benzyl-D-galactopyranoside is a trisaccharide that binds to the fluorescent chromophore. It has been shown to have strong binding activity and can be used for the labeling of carbohydrates. Methyl 2,3,4,6-tetra-O-benzyl-D-galactopyranoside is also used in assays to detect toxins or as a fluorescent label for polymers. This compound can be synthesized by reacting methyl 4,6-dibenzyloxybenzoate with glucose in methanol.</p>

<p>1,2-Di-O-acetyl-3-azido-3-deoxy-5-O-toluoyl-D-ribofuranose is a synthetic sugar that can be modified to produce oligosaccharides or polysaccharides. It has a CAS number of 120143-22-8 and is composed of a sugar molecule with an acetyl group on the 2' position and toluene sulfonyl group on the 3' position. This modification can be used for glycosylation or methylation reactions. 1,2-Di-O-acetyl -3,4,6,-triaminopyrimidine is also known as fluorinated ribofuranose.</p>

<p>Raspberry ketone glucoside is a hydrogenated, isopropyl palmitate fatty acid. It is a dietary supplement that has been shown to inhibit the activity of matrix metalloproteinases, which are enzymes that break down collagen in the skin and lead to wrinkles. Raspberry ketone glucoside also inhibits tyrosinase, an enzyme involved in the production of melanin. As a result, raspberry ketone glucoside has been shown to reduce pigmentation and inhibit UV-induced skin damage. Raspberry ketone glucoside may have an inhibitory effect on fatty acids by inhibiting the synthesis of fatty acids and reducing the number of fat cells in adipose tissue. This compound is also used as a crystallization aid for cellulose and as an organic solvent for food composition.</p>

<p>Please enquire for more information about 6-O-Desmethyl donepezil glucuronide sodium (Mixture of Diastereomers) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,5-Anhydro-2,3,4-tri-O-benzoyl-6-deoxy-D-arabino-hex-1-enitol is a high purity sugar with a click modification. It is a synthetic monosaccharide that is an important building block for complex carbohydrates. This compound can be modified through methylation, glycosylation, and custom synthesis to produce desired compounds. The 1,5 Anhydro 2,3,4 tri O benzoyl 6 deoxy D arabino hex 1 enitol has shown activity against the fluoroquinolone resistant bacteria Staphylococcus aureus and Mycobacterium tuberculosis. It has also been shown to inhibit the growth of cancer cells in vitro and in vivo.</p>

<p>Methyl b-D-thiogalactopyranoside (MTGP) is a cell lysis agent that can be used for diagnostic purposes to measure enzyme activities in cells. It is also used to determine the kinetic of an enzyme reaction, as well as its acid formation. MTGP has been shown to inhibit sugar transport and metabolism by binding to the sugar molecule and preventing it from passing through cellular membranes. This inhibition prevents the accumulation of proton gradients across the membrane, which disrupts ATP production and leads to cell death. MTGP is also an inhibitor of glucose-6-phosphate dehydrogenase (G6PDH), which converts glucose into sorbitol. Sorbitol accumulates intracellularly and leads to cell death by osmotic lysis.</p>

<p>Raloxifene 6-D-glucuronide is a synthetic compound that consists of the sugar raloxifene and the sugar glucuronic acid. It is a complex carbohydrate with a molecular weight of 569. Raloxifene 6-D-glucuronide is soluble in water and insoluble in most organic solvents. The compound has been modified by fluorination, which increases its stability in water, and by click modification. This compound has been shown to inhibit the activity of bacterial enzymes that are responsible for the synthesis of saccharides, such as oligosaccharides and polysaccharides.</p>

<p>D-Lyxonic acid potassium salt is a pentitol that is a stereospecific, aldonic, and nature D-glycosylamine. It can be synthesized by reacting phenylhydrazine with glycolic acid chloride in the presence of catalytic amounts of sodium hydroxide. The yield is about 98%. This compound has been shown to have anti-inflammatory properties when it reacts with hydrogen chloride to form D-lyxonic acid chloride. It also has been shown to inhibit the growth of bacteria and fungi by binding to the cell wall and inhibiting protein synthesis.</p>

<p>D-Galacturonic acid (GalA) is a hexuronic acid with the CH2OH at C5 of galactose replaced by a carboxyl group (Collins, 2006). D-galacturonic acid is abundant in pectic polysaccharides which are characterized by a high α-1,4 linked galacturonic acid content and include pectic acid (polygalacturonic acid), rhamnogalacturonan I (Oomen, 2002), rhamnogalacturonan (RG) II (Vidal, 2000), xylogalacturonan, and homogalacturonan. These polymers play roles in strengthening cell walls, cell adhesion and are established as part of signaling cascades that detect cell wall degradation upon pathogen attack.</p>

<p>a-D-Glucopyranosyl fluoride is an irreversible inhibitor of the enzyme glycosidase. This product has been used to study the kinetic and mechanism of human serum alpha-glucosidase, which is a key enzyme in the digestion of carbohydrates. Kinetic studies have shown that 4-hydroxycinnamic acid and glucose are competitive inhibitors of the enzyme. The reaction mechanism for this product involves hydrogen fluoride cleavage of the glycosidic bond. The optimum pH for this product is 7.</p>

<p>Glucose (Glu) is the most common carbohydrate on the planet, found in all living organisms and is the major source of metabolic energy for plants and animals. Glucose is a building block in numerous oligosaccharides and polysaccharides. It is present in blood and milk, in gangliosides and in N- and O-linked glycans (Collins, 2006). Glucose is wrongly called a simple sugar because in solution it exists in five forms: two six membered rings (α/β), two five membered rings (α/β) and a straight chain form, a system known as mutarotation (Robyt, 2012). The proportions of different glucose forms are dictated by temperature and pH. D-Glucose is optically active (dextrorotary) and L-Glucose is its enantiomer (Levorotary). Its hydroxyl groups are all equatorial, providing maximum stability, according to Hudsons rules (Hudson, 1948).</p>

<p>2,3,5-Tri-O-benzyl-L-xylofuranose is a sugar molecule that has been modified to inhibit glycosidases. 2,3,5-Tri-O-benzyl-L-xylofuranose is an iminosugar that inhibits the enzyme β-glucosidase and α-galactosidase. The compound is not metabolized and it binds to the enzyme's active site. 2,3,5-Tri-O-benzyl L xylofuranose has been shown to be effective at inhibiting all of the glycosidases tested in this study with inhibition potencies ranging from 0.1 mM to 10 mM. This compound also inhibits epoxides and cyclic enzymes such as azido reductase and dihydropyrimidine dehydrogenase.</p>

<p>N-acetylneuraminic acid derivative and a useful tool for the study of sialic acid binding to its ligands. It was previously used for such purpose in studies on the influenza binding to hemagglutinin. This compound was also used for investigation of Clostridium botulinum toxin binding to various sugars.</p>

<p>1,3,4,6-Tetra-O-acetyl-2-deoxy-2-fluoro-D-galactopyranose is a fluorinated sugar that is used in the synthesis of glycosides. It is a synthetic compound that is prepared by reacting 1,3,4,6-tetraacetyl galactose with potassium bifluoride and diethyl oxalate in presence of anhydrous sodium sulfate. The product obtained has the following structural formula: The chemical name for this compound is 1,3,4,6-Tetraacetyl -2-[(1R)-1-(ethoxycarbonyl)propyl]-2-(fluorooxymethyl) -D-galactopyranose. The CAS number for this compound is 83697–45–4.</p>

<p>Phenyl b-L-thiofucopyranoside is a custom-synthesized, fluorinated, modified sugar that is used in the synthesis of oligosaccharides and polysaccharides. This compound is an excellent choice for methylation reactions due to its high reactivity and stability under harsh conditions. Phenyl b-L-thiofucopyranoside can be used as a precursor for the synthesis of saccharide derivatives, such as monosaccharides and complex carbohydrates. It has been shown to be stable to heat and pH extremes, making it ideal for use in organic syntheses.</p>

<p>3-Deoxy-3-fluoro-D-allose is a chemical compound with the molecular formula CHNO. It has been shown to have potential as a contrast agent for magnetic resonance imaging (MRI) and positron emission tomography (PET). The conformation of 3-Deoxy-3-fluoro-D-allose is similar to that of glucose, but it does not inhibit the uptake of glucose by erythrocytes or the transport of glucose across cell membranes. 3DFA has been shown to be taken up by cells in the brain, kidney, and liver. The uptake and distribution of 3DFA in these tissues was dependent on serum protein concentrations.</p>

<p>1,4-Anhydro-D-erythritol is a sugar alcohol that can be found in various plants and fruits. It is a reaction product of D-erythrose and glycerol, with an average formation rate of 10%. The hydroxyl group on the 1,4-anhydro-D-erythritol molecule reacts with methyl glycosides to produce an ester. Trifluoromethanesulfonic acid is used as a catalyst in this process, which activates the hydroxyl group on the molecule. The reaction mechanism for this process involves three steps: elimination of water, dehydration of the hydroxyl group, and addition of methyl glycoside. This process results in a new molecule called 1,4-anhydro-D-erythritol methyl ester (AEME). AEME has been shown to have conformational properties that are different from those of its parent compound. The conformational</p>

<p>D-Xylose-5-phosphate disodium salt is a Custom synthesis that has been fluorinated, methylated, and modified with a click reaction. D-Xylose-5-phosphate disodium salt is also an oligosaccharide and polysaccharide. The CAS No. for this compound is 1083083-57-1.</p>

<p>D-Salicin is a naturally occurring compound, classified as a biologically active glycoside. It is acquired from the bark of willow trees, primarily species within the genus Salix. The primary mode of action of D-Salicin involves its metabolic conversion into salicylic acid within the human body. This conversion occurs in the gastrointestinal tract and bloodstream, ultimately displaying effects similar to non-steroidal anti-inflammatory drugs (NSAIDs).</p>

<p>4-Methoxyphenyl 2-deoxy-3-benzyl-4,6-O-(4-methoxybenzylidene)-2-phthalimido-b-D-glucopyranoside is a custom synthesis that has been modified with fluorination and carbamoylation. This product is an oligosaccharide that belongs to the group of polysaccharides. It is a complex carbohydrate that has been synthesized from monosaccharides and sugar. 4MPBGP is soluble in water and has high purity levels.<br>*The following content was automatically generated by eCommerce software:</p>

<p>Resource for the 6-O-modification of Glc e.g. in glucuronic acid synthesis</p>

<p>Salicylic acid-acyl-b-D-glucuronide is an anti-inflammatory compound that is found in the urine of diabetic patients. It has been shown to inhibit the production of a number of proinflammatory compounds, including prostaglandin E2 (PGE2), in human serum. Salicylic acid-acyl-b-D-glucuronide is formed by the reaction of salicylic acid with acetylsalicylic acid. The rate of formation is dependent on the concentration of salicylic acid and pH. The reactive product can form covalent adducts with tyrosinase and other proteins, leading to inhibition of tyrosinase activity and melanin synthesis.</p>

<p>Voglibose is a competitive inhibitor of α-glucosidase used for the control of blood sugar levels in patients with type 2 diabetes mellitus. The compound binds reversibly to intestinal carbohydrate-active digestive enzymes with α-glucosidase activity, inhibits breakdown of complex sugars and consequently delays the absorption of glucose into blood.</p>

<p>L-Xylonic acid-1,4-lactone is an enzyme that functions as a glycolytic enzyme. It catalyzes the conversion of D-xylose to L-xylonic acid and L-xylonic acid-1,4-lactone. This enzyme is expressed in leukemia HL60 cells and is activated by acidic conditions. L-Xylonic acid-1,4-lactone has been shown to be catabolized by the enzyme xylanase. The kinetic properties of this reaction have been studied using mass spectrometric techniques and biochemical methods. The rate of the reaction was found to be dependent on the presence of divalent cations (Mg2+ or Ca2+) or monovalent ions (Na+ or K+). L-Xylonic acid 1,4 lactone also catabolizes glucose with a similar rate constant.</p>

<p>3,4-Di-O-acetyl-L-arabinal is a synthetic compound that belongs to the class of monofluorides. It has been synthesized from l-arabinose by a stereoselective process, with triflic acid as the catalyst and propargylation as the key step. The synthetic pathway starts from an acid hydrolysis of L-arabinose to yield 3,4-di-O-acetyl-L-arabinonic acid. This acid is then converted to 3,4 diacetyl L arabinonic acid with acetic anhydride and acetic acid in the presence of triethylamine. The final product is then obtained by reacting this intermediate with 1 equivalent of sodium fluoride in tetrahydrofuran (THF) using catalytic reduction with sodium borohydride at 0 °C. The major advantage of this synthetic process is that it provides two stereoisomers: (</p>

<p>2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl azide is a catalyst that has been used in the production of carbonate catalysts. It can also be used to reoxidize metallic catalysts.</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>Simvastatin acyl-b-D-glucuronide is a synthetic compound that is not naturally occurring. It has a molecular weight of 571.67 and the CAS number 463962-56-3. The chemical formula for this compound is C30H44O8 and its structural formula is shown below. The purity of this product is &gt;99% and it has been modified with fluorination to improve solubility in water.</p>

<p>Phenylethyl-beta-D-glucopyranoside is a phenolic compound that is found in plants such as Echinacea. Phenylethyl-beta-D-glucopyranoside has been shown to inhibit tumor cell proliferation by increasing the levels of enzyme catalysis and enzyme activity, and decreasing the levels of protocatechuic acid. This compound also inhibits fatty acid synthesis, which may be due to its ability to inhibit the production of 4-hydroxycinnamic acid via inhibition of the enzyme acyl coenzyme A:cholesterol acyltransferase. The cyanobacterial strain Synechococcus elongatus PCC 7942 was found to produce phenylethyl glucoside, an iridoid glucoside with high cytotoxic activity against human tumor cells.</p>

<p>D-Threonic acid-1,4,-lactone is a methylated saccharide that is prepared by the oxidation of D-threo-aldose. It can be used as a building block in the synthesis of glycosylates, oligosaccharides, and polysaccharides. The compound has been shown to inhibit the growth of Mycobacterium tuberculosis and Mycobacterium avium complex. D-Threonic acid-1,4,-lactone can also be fluorinated for use as an imaging agent for positron emission tomography (PET).</p>

<p>Telmisartan acyl-b-D-glucuronide is a drug metabolite that is formed by the conjugation of telmisartan with glucuronic acid. Telmisartan acyl-b-D-glucuronide is activated in vivo and reversibly inhibits the enzyme creatine kinase, which is involved in the metabolism of creatine to creatinine. The effective dose for this compound has been shown to be 10 mg/kg (orally) in humans. Telmisartan acyl-b-D-glucuronide has been shown to be an at1 receptor antagonist and may have some antihypertensive effects via modulation of ion channels. This drug also appears to have some proliferative effects on cells that are inhibited by radiation.</p>

<p>Methyl β-L-arabinopyranoside is a stereochemically pure monosaccharide that has been used to calibrate and quantify the conformational, stereochemical, and spectrometric methods. Methyl β-L-arabinopyranoside has a conformation that is restricted by the presence of an α-hydroxyl group at C2. The chloride ion can be used to monitor this conformation. The diameter of methyl β-L-arabinopyranoside can be measured with a micropipette and monitored using an aerosol detector. Methyl β-L-arabinopyranoside can also be quantified by mass spectrometry or spectrophotometry. The conformational, stereochemical, and spectrometric methods have been calibrated using methyl β-L-arabinopyranoside as a standard to determine their accuracy in measuring the size of other molecules.</p>

<p>Methyl 2-deoxy-3,5-di-O-toluoyl-L-ribofuranoside is a custom synthesis that is a complex carbohydrate that is used in the modification of saccharides. It has been shown to be able to methylate and glycosylate carbohydrates and can be fluorinated for use in click chemistry experiments. Methyl 2-deoxy-3,5-di-O-toluoyl-L-ribofuranoside is highly pure and can be synthesized with high yield.</p>