Monossacáridos

<p>a-D-Galactosamine-1-phosphate is a synthetic, fluorinated glycosylation inhibitor. It inhibits the synthesis of complex carbohydrates and is used in biochemical research. This compound has been shown to inhibit the methylation of glycoproteins and polysaccharides. It also inhibits the phosphorylation of glycogen, which may be useful in cases of diabetes mellitus.</p>

<p>Phenyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a chemical compound that is a member of the class of phenyl 2-acetamido-2-deoxy-b-D-glucopyranosides. This compound has been shown to be anomeric, substituent and phenyl.</p>

<p>D-Xylulose is a sugar monomer found in the cell walls of bacteria. It is also present in human blood, where it is converted to xylitol. D-Xylulose has been shown to be an important component of bacterial cell wall synthesis and can be used as a probiotic for humans. The enzyme xylitol dehydrogenase catalyses the conversion of D-xylulose to xylitol. The reaction mechanism is thought to be similar to that of other enzymes in the glycolysis pathway, such as ribitol dehydrogenase, which converts ribitol to ribose 5-phosphate. This conversion can be achieved through two different methods: hydrogen fluoride or sodium hydroxide. D-Xylulose can also be used for analytical purposes, such as in the detection of trifluoroacetic acid (TFA) by gas chromatography and mass spectrometry.</p>

<p>Chloramphenicol glucuronide is an active metabolite of chloramphenicol. It can be detected in human serum and urine, as well as rat liver microsomes. Chloramphenicol glucuronide binds to the cytosolic protein, cytochrome b5 reductase, which inhibits protein synthesis and cell growth. This compound has been shown to be effective for treating infectious diseases such as typhoid fever, pelvic inflammatory disease, and pneumonia. The chloramphenicol glucuronide group also includes a number of other metabolites that are formed from chloramphenicol by conjugation with glucuronic acid.</p>

<p>D-Altrose is an alpha-hydroxy acid that is synthesized from D-arabinose and trifluoroacetic acid. It has been shown to be a substrate for the synthesis of oligosaccharides, which are important in carbohydrate chemistry. This molecule can also be used as a reagent in the preparation of carbohydrates with a specific configuration at C2. One use of this product is in generating analytical methods that can distinguish between D-altrose and D-arabinose by monitoring the ratio of hydrogen fluoride to carbonyl group signals. D-Altrose may also be used in asymmetric synthesis, where it is a useful chiral building block for the construction of galacturonic acid derivatives.</p>

<p>2,3,4,6-Tetra-O-pivaloyl-D-glucopyranosyl azide is an oligosaccharide that has been modified for use in the synthesis of complex carbohydrates. It is synthesized through a methylation reaction and then click chemistry. The resulting product is a high purity chemical that can be used to modify saccharides or sugars. 2,3,4,6-Tetra-O-pivaloyl-D-glucopyranosyl azide is a white crystalline solid with CAS No. 1251910-91-4.</p>

<p>D-Glucuronic acid (GlcA) is D-glucose with position six oxidised to a carboxyl group (Collins, 2006). It is a common component of a number of gums and mucilages structurally related to pectins, where it is can be present as a terminal non reducing end residue (Renard, 1999). Glucuronic acid is also found in bacterial polysaccharides, such as, xanthan gum produced by Xanthomonas campestris (Faria, 2011), and in glycosaminoglycans, such as, heparan sulfate (Casale, 2020).</p>

<p>3,4,6-Tri-O-benzyl-D-glucal is a benzyl protected, 2,3 unsaturated glucal used as a chiral intermediate. The C2-C3 double bond of the pyranose ring can be modified via a variety of reactions including: hydrogenation, oxidation, hydroxylation, and aminohydroxylation, to generate structural complexity. 3,4,6-Tri-O-benzyl-D-glucal also minimizes tedious protecting-group strategies required for fully oxygenated sugars. The products of 2,3 unsaturated glycosides as chiral intermediates have played a role in the synthesis of many biologically active compounds, such as, nucleosides and modified sugar derivatives.</p>

<p>Please enquire for more information about Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Butyldeoxymannojirimycin HCl is a custom synthesis, complex carbohydrate that is synthesized from Oligosaccharides and Polysaccharides. This product is modified with Methylation, Glycosylation, and Carbohydrate. It has the CAS No. 155501-85-2 and it is high purity and fluorinated. The product can be used in Synthetic applications such as Click modification, sugar, or Fluorination.</p>

<p>Ciclopirox-D11 D-glucuronide is a custom synthesis that has been modified by fluorination, methylation, and click modification. It is a monosaccharide that has been synthesized from glucose and contains a glycosylation site. This compound is also an oligosaccharide with saccharide subunits. It has been shown to be effective against fungi such as Trichophyton rubrum, Microsporum canis, and Epidermophyton floccosum. Ciclopirox-D11 D-glucuronide binds to the fungal cell wall by covalent bonding to the chitin in the fungal cell wall. This compound also inhibits the growth of bacteria such as Staphylococcus aureus and Clostridium perfringens by inhibiting protein synthesis due to its ability to bind to ribosomes.</p>

<p>Allo-3a-tetrahydro cortisol 3-O-b-D-glucuronide is a methylated glucuronide of allo-3a,4b,5,6,7,9b tetrahydrocortisol. It is a synthetic modification of the natural hormone cortisol and has been shown to stimulate glycogenolysis in rat liver cells. Allo-3a,4b,5,6,7,9b tetrahydrocortisol has been shown to have antiinflammatory effects on skin cells and has been used as an analgesic in veterinary medicine. The compound is also used for the preparation of polysaccharides and glycosylations.</p>

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

<p>Chiral building block for synthesis of carbohydrate and nucleoside derivatives</p>

<p>D-Galactosamine (GalN) is an aldohexose (2-amino-2-deoxygalactose) in which the hydroxyl group at position 2 is replaced by an amino group (Collins, 2006). Galactosamine (as the N-acetyl derivative) forms a key part of both N- and O-linked glycoproteins, glycolipids and glycosaminoglycans. Treatment of experimental animals with D-galactosamine / lipopolysaccharide causes lethal liver injury characterized by apoptosis of the hepatocyte and it is used as a laboratory model to study the effect of therapeutic agents (Hirono, 2001).</p>

<p>Myricitrin is a natural compound that is found in the bark of the Myrica tree. It has been shown to have antioxidant effects and pro-apoptotic activities. Myricitrin has been shown to induce apoptosis in HL-60 cells through activation of the caspase-3 pathway, which includes cleavage of poly (ADP-ribose) polymerase and activation of caspases. In addition, myricitrin induces apoptosis by binding to DNA and inhibiting transcription. The physiological effects of myricetin are similar to those of myricitrin due to their structural similarity. However, there is no data available on the anti-inflammatory properties or hypoglycemic effect of myricetin.</p>

<p>4-Pentenyl 4,6-O-benzylidene-2,3-phenylethylidene-a-D-mannopyranoside is a modification of the natural oligosaccharide, mannose. The complex carbohydrate is synthesized using a custom synthesis and has a high purity that meets the CAS No. requirements. This molecule has been fluorinated and saccharides have been methylated and glycosylated.</p>

<p>D-Xylonic acid-1,4-lactone is a substrate that participates in the synthesis of glyceric acid. It has been shown to be a synthetic substrate for benzyl groups and leukemia HL-60 cells. D-Xylonic acid-1,4-lactone can react with chloride ions to form D-xylose. The product of this reaction is an epimerization reaction that occurs when the hydroxyl group on the carbon atom adjacent to the carbonyl group (C1) reacts with a proton from water to form a double bond at C2. This conversion produces xylonic acid and lactone.</p>

<p>UDP-6-azido-6-deoxy-D-glucose is a chemical building block that is used for saccharide synthesis. The azide group can be reduced to give the amine which has been used to make a fluorescent tag for 5-(hydroxymethyl)cytosine in DNA. UDP-6-azido-6-deoxy-D-glucose has also been used to synthesise siderophore conjugates which can be used to deliver functional reagents across bacterial cell membranes.</p>

<p>D-Idose is a single-enantiomer sugar with a pyranose ring and an enantiomeric configuration. It is used in the treatment of bacterial infections and has been shown to be effective at inhibiting the growth of bacteria that are resistant to beta-lactam antibiotics, such as methicillin-resistant Staphylococcus aureus (MRSA). D-Idose is active against bacteria that do not produce beta-lactamase enzymes, such as Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>Tetra-O-acetyl-1-deoxy-D-arabinohexopyranose is a boron trifluoride etherate method for the synthesis of tetraacetylated 1-deoxyhexopyranoses. The yield of this reaction is dependent on the formamide concentration and the hydrogenation time. When formamide is used, the yields are greater than when it is not. This product can be used in a variety of reactions such as the synthesis of 2,3,4,6-tetraiodo-, 2,3,4,6-tetrahalogeno-, or 2,3,4,-trihalogeno hexoses by substitution with iodine or chlorine. Tetraacetylated 1-deoxyhexopyranoses can also be used to synthesize ethanethiols and other alcohols by elimination reactions.</p>

<p>Ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-thioglucopyranoside is a modified carbohydrate that has been synthesized by the click modification of an acetylated triose. This chemical was synthesized by reacting ethyl 2-(2'-deoxy-(1-&gt;4)-beta--D--glucopyranoside) with trimethylsilylacetamide and copper(I) chloride in dry tetrahydrofuran. This product has high purity and is used as a research tool for glycobiology.</p>

<p>Methyl 4,6-O-benzylidene-a-D-galactopyranoside is a high purity, custom synthesis, sugar modified product. It has a CAS No. 72904-85-9, and can be synthesized by the click modification of methyl 1,4-O-diacetyl D-mannopyranoside. The fluorination of the glucose moiety in this molecule is accomplished using NCS/BF3 complex in acetonitrile. Glycosylation is achieved using NEM/HBTU and DCC in DMF. The saccharide is then modified with methyl 4,6-O-benzylidene alditol acetate to yield Methyl 4,6-O-benzylidene a D galactopyranoside. This product can also be synthesized by the glycosylation of methyl 2,5 dihydroxyacetophenone with methyl</p>

<p>L-Arabonic acid-1,4-lactone (LL) is the product of the reaction between L-arabinose and trifluoroacetic acid. LL is an enantiomer of D-arabinose and has a pK a of 6.5, which makes it a weak base. This compound has been shown to be a hydroxyl group donor in human liver and is also used as a chaperone for protein folding.</p>

<p>Propyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a synthetic monosaccharide that has been fluorinated and methylated. It is a custom synthesis and can be modified to suit your needs. This compound has been glycosylated and click modified. The purity of this product is high and it's molecular weight is 798 Da.</p>

<p>3, 4- O- [(R) -Benzylidene] -2-O-trifluormethansulfonyl-D- ribonic acid d- lactone is a sugar derivative that is used as a reagent in organic synthesis. It has been used as a building block for the preparation of acetonitrile derivatives, which are useful for the synthesis of heterocycles. 3, 4- O- [(R) -Benzylidene] -2-O-trifluormethansulfonyl-D- ribonic acid d- lactone has also been shown to be an active site for catalyzing the reaction between nitroglycerin and trinitrate with dioxane as solvent. This compound can also be used to synthesize the antihypertensive drug hydroxypropanolamine by reacting with hydroxylamine and acetone in acidic conditions.</p>

<p>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.</p>

<p>Phenyl 2,3,4-tri-O-benzyl-b-L-thiofucopyranose is a synthetic monosaccharide that is modified with fluorine. It is also known as 3,4,6-tri-O-benzyl-2,3,4,6-tetra-O-(trifluoromethyl) fucopyranose. This compound is a complex carbohydrate that belongs to the group of glycoconjugates and polysaccharides. Phenyl 2,3,4-tri-O-benzyl-b-L-thiofucopyranose has been shown to be useful in glycosylation reactions as well as in click chemistry reactions. This compound can be used for the synthesis of oligosaccharides and polysaccharides with custom modifications. Phenyl 2,3,4 tri O benzyl b L thiof</p>

<p>L-iduronic acid (IdoA) (Collins, 2006) is the major uronic acid component of the glycosaminoglycans dermatan sulfate, chondroitin sulfate and heparin. Iduronic acid is also present in heparan sulfate, although in a minor amount relative to glucuronic acid. Glycosaminoglycans represent a physiologically important group of molecules involved in a variety of biological functions, such as, cell proliferation, cell-to-cell communication, wound healing, coagulation, morphogenesis, and pathogenesis. Glycosaminoglycans present an intriguing target for the design of new approaches for diagnostic and therapeutic agents against various infectious diseases (Kamhi, 2013).</p>

<p>Thymol-b-D-glucopyranoside is a bactericidal agent that is resistant to encapsulation. It has been shown to be effective against animals and typhimurium in an incubated population and endogenous deaminase inhibitor strategy. The porcine activated food chemistry and abattoir experiments show that thymol-b-D-glucopyranoside has the potential to reduce populations of bacteria in the gastrointestinal tract by inhibiting protein synthesis.</p>

<p>1,3:2,4-Bis(O-benzylidene)-D-sorbitol is a hydrogenated derivative of sorbitol. It is used in fatty acid devices and as a surfactant in hydrogenation reactions. 1,3:2,4-Bis(O-benzylidene)-D-sorbitol is an acidic compound that has a low molecular mass and is soluble in water. It reacts with magnesium oxide to form the corresponding magnesium salt. This derivative is also used in silicone residue removal and as an activated organic base.</p>

<p>Inhibitor of sialyltransferases</p>

<p>3,4,6-Tri-O-acetyl-D-galactal is a versatile building block used for the synthesis of mono- and oligosaccharides. The galactal double bond affords a ready means through which to introduce new functionality or introduce deoxy positions at the C1 and C2 positions to afford functionalised monosaccharides and also allows galactals to be used as glycosylation donors.</p>

<p>GDP-L-fucose is a natural fucosyl donor and substrate for fucosyltransferases (FUT) that catalyses the fucosylation of, for example, human milk oligosaccharides or glycoproteins. GDP-L-fucose is widely used in (chemo)enzymatic synthesis of glycans. Cymit Quimicaesis of GDP-L-fucose, a nucleotide sugar consisting of an L-fucose that is β-glycosidically linked to the nucleotide guanosine diphosphate (GDP), is achieved either through de novo synthesis via GDP-mannose or through a salvage pathway from free fucose. Fucosylation is catalysed by fucosyltransferases (~ 13 FUT genes have been identified in the human genome to date) to generate α-1,2, α-1,3, α-1-4 and α-1-6 linkages of fucose to other sugars, as well as direct linkages to peptides, with release of GDP (Lairson, 2008).</p>

<p>B-L-Fucopyranosylamine is a Custom synthesis, Modification, Fluorination, Methylation, Monosaccharide, Synthetic, Click modification, Oligosaccharide, saccharide, Glycosylation. It has CAS No. 103419-79-0 and Carbohydrate.</p>

<p>1,2,3,4-Tetra-O-acetyl-6-O-triphenylmethyl-b-D-glucopyranose (TATPG) is a carbohydrate that belongs to the family of saccharides. It is a synthetic sugar with a modified glycosidic linkage between the hexoses 1 and 2. The preparation of TATPG is through the modification of sugar with fluorination and glycosylation. TATPG has been used in Click chemistry to attach polymers and proteins to oligosaccharides or monosaccharides. This modification can be achieved through methylation or substitution reactions with other chemical groups such as acetate, phosphates, and thiols. This molecule has also been used in the synthesis of complex carbohydrates by modifying the glucose unit with glucose oxidase, which leads to the formation of D-arabinitol 1,5-.</p>

<p>2-Deoxy-D-galactose is a metabolite of the carbohydrate galactose. It is found in the rat striatum and has been shown to inhibit glutamate dehydrogenase activity. 2-Deoxy-D-galactose also inhibits 2,3,4,5 tetrahydropyridine (MPTP) induced neurotoxicity in mice by increasing levels of uridine and nucleotides in the brain. This agent also has an effect on glomerular filtration rate and on protein synthesis. The glycoside derivatives of 2-deoxy-D-galactose are formed by joining a sugar molecule to hydroxyl group. These derivatives are then transported into cells via glucose transport proteins.</p>

<p>Methyl 2,3,5-tri-O-benzoyl-b-D-arabinofuranoside is a custom synthesis of an Oligosaccharide with a molecular formula of C12H22O11. It has CAS No. 1093344-99-0 and Methylation, Glycosylation, Carbohydrate, Click modification, saccharide, sugar. This product is a high purity product that is Fluorination and Synthetic.</p>

<p>UDP-α-D-galacturonic acid is a biochemical precursor for the synthesis of UDP-glucuronic acid. It is an intermediate in the biosynthesis of glycosaminoglycans, proteoglycans and lipopolysaccharides. This compound has been shown to inhibit the growth of cancer cells by inducing apoptosis in vitro. The presence of this compound may be detected by its ability to act as a substrate for glucuronidation reactions.</p>

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

<p>n-Octyl-beta-D-thiogalactopyranoside is a modification of the sugar Galactose. It is a mono saccharide that can be found in the form of an oligosaccharide or polysaccharide. The modification of the sugar is done by methylation, glycosylation and fluorination. n-Octyl-beta-D-thiogalactopyranoside has CAS No. 42891-16-7 and can be found on PubChem CID: 5135624.</p>

<p>(3S, 4S, 5R) -3, 4- Dihydroxy- 5- (hydroxymethyl) -L- proline is a custom synthesis. It is a fluorinated, methylated, and modified monosaccharide with a polysaccharide sugar attached to a glycosylation site. The CAS number for this compound is not available.</p>

<p>b-D-Glucopyranosyl azide is a Glycosylation agent that is used in the synthesis of complex carbohydrates and oligosaccharides. It is also used for Click modification, fluorination, and polysaccharide modification. The compound is a white crystalline solid that is soluble in water at low concentrations. It has a molecular weight of 180.18 g/mol and melting point of 220°C.</p>

<p>Abundant and critical component of natural glycans and glycoproteins</p>

<p>b-D-Allopyranose is a monosaccharide that has been modified with fluorine. It is used as a substrate for the production of oligosaccharides and polysaccharides, which are important biomolecules in cell walls and membranes. b-D-Allopyranose can be customized to suit your needs with Click chemistry, Methylation, or other modifications. We offer high purity b-D-Allopyranose at competitive prices.</p>

<p>3-Deoxy-D-manno-2-octulosonic acid ammonium is a bioreactor that is used in the delipidation of fatty acids. It is one of the most effective natural compounds for removing lipids, and it has been shown to be effective in reducing the levels of galactose and cholesterol. 3-Deoxy-D-manno-2-octulosonic acid ammonium has also been shown to be an effective antigen that can be used as a marker for various microorganisms, such as typhimurium, enterobacter, and lettuce.</p>

<p>Propargyl a-D-galactopyranoside (PGAL) is a synthetic compound that belongs to the group of oligosaccharides. PGAL can be used in the synthesis of glycosylated saccharides, such as glycoproteins and glycolipids. The modification of PGAL with fluorine atoms is known to increase its stability. It has been shown that PGAL can be modified with methyl groups without affecting its chemical properties. Furthermore, PGAL can be modified with click chemistry reactions, which are chemoselective reactions that are catalyzed by copper(I) ions.</p>

<p>Used for the synthesis of 1β-O-acyl glucuronides</p>

<p>Sorbitan monostearate is a lipid-soluble compound that is used as a surfactant and emulsifier in food products. It has been found to be nontoxic when administered at concentrations up to 5000 mg/kg of body weight for 28 days. Sorbitan monostearate has been shown to be nontoxic in vitro, but the long-term toxicity of this compound has not been established. Sorbitan monostearate also exhibits hydrogen bonding interactions with calcium pantothenate, sodium salts, and coumarin derivatives. The model system used was an artificial membrane composed of chitosan quaternary ammonium and monolaurate. This study found that sorbitan monostearate is able to permeabilize the membrane at an optimum concentration.</p>

<p>2-C-Methyl-D-ribono-1,4-lactone is a ketose which is formed from the thermal rearrangement of d-xylose. It has been shown to be an acceptor for episulfide and an 1-deoxy-d-ribulose. 2-C-Methyl-D-ribono-1,4-lactone has been found to yield dimethylamine when heated with magnesium. This compound can be ion exchanged with calcium and magnesium. 2CMR was first synthesized by the reaction of L(+) lactic acid with dimethylamine in the presence of magnesium chloride. The product was purified by crystallization from water, yielding a white powder that melts at 230°C.</p>

<p>1,2,3,4,6-Penta-O-galloyl-a-D-glucopyranose is a natural compound that inhibits the Cox-2 enzyme and has anti-cancer properties. It induces cell death by increasing oxidative injury and suppressing autophagy. 1,2,3,4,6-Penta-O-galloyl-a-D-glucopyranose has been shown to reduce xenograft tumor growth in mice while causing no observable toxic effects on normal tissues. This compound also inhibits the proapoptotic protein Bax and promotes the expression of Bcl2 in 3T3L1 preadipocytes. The mechanism of action may be related to its ability to inhibit basic fibroblast proliferation and induce apoptosis in k562 cells.</p>

<p>2-Acetamido-2-deoxy-b-D-thioglucopyranose is a sugar with the chemical formula C6H14O7. It has been synthesized by Click chemistry to have an acetamido group on one of the carbon atoms and a 2,3,5-triiodo substituent on the other. The methylene protons at the 3 and 5 positions of the glycosidic linkage are fluorinated to give this modified sugar. It is also glycosylated with glucose to form a complex carbohydrate. 2-Acetamido-2-deoxy-b-D-thioglucopyranose has CAS number 781581-10-0 and a molecular weight of 318.19 g/mol.</p>

<p>1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-b-D-galactopyranose (TAZ) is an aromatic heterocyclic sugar compound that is used in pharmaceutical formulations. It has low toxicity and can be synthesized using a number of methods. TAZ has been shown to have antifungal effects against Candida albicans and antitumor effects against cancer cells. TAZ also inhibits the activity of teniposide, which is a drug used for the treatment of leukemia. TAZ may be effective against cancer cells by acting as an amido donor and changing the conformation of the cyclic peptide.</p>

<p>Scyllo-inositol is a sugar alcohol that is an effective inhibitor of inositol monophosphatase and phosphatidylinositol-4,5-bisphosphate 3-kinase. It has been shown to inhibit the activity of these enzymes in a model system, which may be due to its structural similarity to inositol. Scyllo-inositol has also been shown to have physiological effects on cell lysis and metabolic disorders. The inhibitory properties of scyllo-inositol have been evaluated using microdialysis probes and x-ray crystal structures.</p>

<p>Inhibits β-N-acetylglucosaminidase, also known as O-GlcNAcase (OGA), which cleaves the O-linked glycans from glycoproteins. Interferes with O-GlcNAc cycling and leads to the accumulation of O-GlcNAcylated proteins. Thiamet G elicits neuroprotective effects by modulating microglia/macrophages and inhibiting hyperphosphorylation of the microtubule-associated protein tau in models of stroke and Alzheimer’s disease. Thiamet G also has implications on diabetes and cardiovascular pathologies.</p>

<p>Donor for Koenigs-Knorr type mannosylation and other anomeric substitutions</p>

<p>a-D-Mannose-1-phosphate dipotassium salt (DMDK) is a synthetic oligosaccharide that was designed and synthesized for use as a potential drug in the treatment of cancer. DMDK has been shown to be an inhibitor of protein glycosylation, which may lead to the prevention of tumor formation. It also has anti-inflammatory properties and can inhibit the growth of bacteria by binding to bacterial 16S ribosomal RNA and inhibiting protein synthesis.</p>

<p>4-O-Methyl-D-glucose is an acidic sugar that is found in the cell walls of plants. It has been shown to have structural studies on plant cells, with ion-exchange and ester linkages. 4-O-Methyl-D-glucose is metabolized by microorganisms, including bacteria, fungi, and yeast. This sugar can be oxidized to form acid or oligosaccharides as well as oxidation products such as methylglyoxal. 4-O-Methyl-D-glucose is also used in the synthesis of mucopolysaccharides which make up the connective tissue of tumor cells. This sugar can be synthesized from D-mannose by a diazonium salt reaction followed by oxidation with sodium hypochlorite. The hydroxyl group on this sugar can be acetylated to form acetylated 4-O methyl glucose.</p>

<p>1,2,3,6-Tetra-O-benzyl-β-D-glucopyranoside is a synthetic compound that is produced by the modification of natural sugars. It was first synthesized by a team of chemists led by Professor Robert Burns Woodward. This molecule has been modified with methyl groups and fluorine atoms to improve its stability and to provide a more convenient method for its analysis. 1,2,3,6-Tetra-O-benzyl-β-D-glucopyranoside can be used in the synthesis of oligosaccharides and polysaccharides.</p>

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

<p>4-Aminophenyl a-D-mannopyranoside is a compound that has been shown to have anti-inflammatory properties. It is also used as a starting material in the synthesis of other drugs. Rats with chronic kidney disease were given 4-aminophenyl a-D-mannopyranoside daily for three weeks, and it was found that this compound prevented the development of kidney injury markers. This drug has also been shown to be effective against mouse strains with nervous system diseases. 4-Aminophenyl a-D-mannopyranoside binds to lysine residues on proteins and prevents the interactions between these residues and the amino acid glutathione, which is required for glut1 uptake in brain cells. This uptake is essential for cellular function, and therefore 4-aminophenyl a-D-mannopyranoside may be useful as chemotherapeutic treatment for brain cancer.</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>2-Acetamido-1,6-anhydro-2-deoxy-b-D-glucopyranose is widely used in carbohydrate chemistry. It is used as reagent for the synthesis of oligosaccharides and also as a precursor in the synthesis of oligopeptides. 2-Acetamido-1,6-anhydro-2-deoxy-b-D-glucopyranose is an analog of levoglucosan, a compound that is often used to trace for biomass burning in enviromental chemistry studies.</p>

<p>D-Glucal is a protonated d-glucal, which is a simple sugar. It reacts with the electron acceptor oxygen to form an oxidized product. This product can be reduced back to the original molecule by using a reducing agent, such as sodium borohydride or sodium dithionite. D-Glucal has been shown to inhibit the growth of tumor cells in mice that are resistant to other anticancer drugs. D-Glucal inhibits transcription and replication of DNA by binding to the DNA-dependent RNA polymerase and blocking its ability to transcribe messenger RNA (mRNA). The enzyme is also inhibited by glycosidic bond architectures that prevent it from binding to the DNA template strand. D-Glucal also has an effect on protein synthesis because it binds to proteins and prevents them from performing their normal functions.<br>D-Glucal has been used as a model system for studying cellular processes in mammalian cells, such as oxidation</p>

<p>4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-b-D-glucopyranosyl trichloroacetimidate is a methylated saccharide that can be obtained through the Click modification of an oligosaccharide. It is a custom synthesis that has been modified with fluorination. This product is available in high purity and has been glycosylated. It is also a synthetic carbohydrate with a complex structure.</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>A beta glycoside with an alkyne handle suitable to click chemistry</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>3,4-Di-O-acetyl-D-arabinal is a spiroketal monofluoride that is known to be an efficient method for the synthesis of β-unsaturated aldehydes. It can be prepared by the hydration of enantiopure allyl chloroformate followed by reductive elimination with triflic acid and acidic hydrolysis. 3,4-Di-O-acetyl-D-arabinal has been used in the synthesis of biologically active molecules such as polyketides, peptides and natural products.</p>

<p>1,2,3,4-Tetra-O-acetyl-α-L-fucopyranose is a chiral compound and it has been used as a biocatalyst in the industrial production of L-amino acids. The enantiomers are obtained by enzymatic hydrolysis of the racemic mixture with lipases. It has been shown that 1,2,3,4-Tetra-O-acetyl-α-L-fucopyranose is an enantioselective substrate for lipolytic enzymes. Lipolytic enzymes are also screened for lipase activity using this compound as a surrogate.</p>

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

<p>D-Mannose-6-phosphate disodium salt hydrate (DMDSP) is an endogenous pentose phosphate metabolite that is found in the human body. DMDSP is generated from the metabolism of mannose and glucose and functions as a regulator of metabolic intermediates. It has also been shown to inhibit bacterial growth and function as a competitive inhibitor of bacterial DNA gyrase, an enzyme that maintains the integrity of bacterial DNA. Genetic polymorphism in the DMDP gene may be associated with changes in response to DMDSP. The reductive amination reaction can be used to synthesize this compound from L-aspartic acid, malic enzyme, and nicotinamide adenine dinucleotide phosphate.</p>

<p>N-Acetyl D-mannosamine (ManNAc) is an aldohexose (2-acetamido-2-deoxymannose) in which the axial hydroxyl group at position 2 is replaced by a N-acetyl group (Collins, 2006). It has been reported that N-acetyl D-mannosamine supplementation, may provide novel means to break the link between obesity and hypertension (Peng, 2019). N-Acetyl-D-mannosamine and N-acetyl-D-glucosamine are the essential precursors of sialic acid, the specific monomer of polysialic acid, a bacterial pathogenic determinant, for example, Escherichia coli K1 uses both amino sugars as carbon sources. Glycoproteins normally have some level of glycan sialylation, but incomplete sialylation can reduce their therapeutic effect when produced recombinantly. To improve performance, cell lines and culture media can be adjusted. The GNE enzyme controls the efficiency of sialylation in human cell lines, making it crucial for producing effective recombinant glycoprotein drugs. Adding ManNAc and other supplements to culture media improves sialylation, which boosts drug yield, increases stability and half-life, and lowers immune reactions by reducing antibody formation.It has also been reported that ManNAc can be used as a treatment for hereditary inclusion body myopathy, an adult-onset, progressive neuromuscular disorder and also for renal disorders involving proteinuria and hematuria due to podocytopathy and/or segmental splitting of the glomerular basement membrane (Galeano, 2007).</p>

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

<p>6-O-Methyl-D-galactopyranose is a monosaccharide that is an important component of the glycosidic linkage in the plant galactomannans. 6-O-Methyl-D-galactopyranose has been shown to be a good substrate for immobilized lectin, which can be used in ionization techniques as well as to characterize glycoproteins and glycopeptides. 6-O-Methyl-D-galactopyranose has also been used in the identification of blood groups and amino acid analysis.</p>

<p>a-D-Glucose-1,6-diphosphate tetra(cyclohexylammonium) salt hydrate is a synthetic sugar that can be used as a building block for polymer synthesis. It is an oligosaccharide that is synthesized by the click reaction of methylated glucose and cyclohexane diamine. This compound has been shown to be effective in the synthesis of polysaccharides and glycoproteins.</p>

<p>Quinovosamine hydrochloride (QNH) is a fatty acid that belongs to the group of galacturonic acid. It has been shown to be biologically active in wild-type strains and in some bacterial strains, including Pseudomonas aeruginosa. QNH has also been used for preparation of monoclonal antibodies directed against receptor activity, which are activated by QNH.</p>

<p>D-Fructose 6-phosphate, disodium salt dihydrate (DFP) is a compound that is used as an extender in the preparation of semen extenders and as a plasma membrane stabilizer in cryopreserved spermatozoa. It has shown to preserve fertility in bubalus, which may be due to its ability to maintain mitochondrial transmembrane potential. DFP also has been shown to protect against acrosome reactions. This drug also has been found to increase sperm motility and maintain supravitality of spermatozoa.</p>