Monosacáridos

<p>1,2,3,5-Tetra-O-benzoyl-a-D-xylofuranose is a glycosylated oligosaccharide with a tetra-O-benzoyl group at the nonreducing end. It can be synthesized by reacting benzaldehyde with 1,2,3,5-tetraacetyl xylose in the presence of sodium methoxide and acetic acid. The product can be fluorinated or methylated to produce other derivatives. This product is soluble in water and methanol and has a CAS number of 5432-87-1. It is available as a custom synthesis from catalog number SYN0000011.<br>!-- <br>--&gt;!-- <br>--&gt;!-- <br>--&gt;!-- <br>--&gt; !-- <br>--&gt;!-- <br>--&gt;!-- <br>--&gt;!-- <br>--&gt; !-- <br>--&gt;!-- <br>--&gt;!--</p>

<p>D-Glucosamine sulfate is a sugar that belongs to the group of polysaccharides. It is a natural compound that is found in the human body and is important for the synthesis of glycosaminoglycans, which are found in cartilage and synovial fluid. D-Glucosamine sulfate can also be used as a raw material for the production of methylated compounds or saccharides. This product can be custom synthesized in different forms (D-glucosamine sulfate sodium chloride, D-glucosamine sulfate potassium salt, D-glucosamine sulfate calcium salt) and with different purity levels depending on your requirements.</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>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>The 4-methoxyphenyl 2,3,6-tri-O-benzoyl-b-D-galactopyranoside (4MP) is a coagulation factor that inhibits the activity of coagulation factors Xa and IIa. The compound has been shown to be reactive with the detection methods used for other coagulation factors. The sensitivity of 4MP to detection was assessed using a battery of detection methods. 4MP was found to be more reactive than other compounds studied with regard to the use of an immunoassay for detection. This compound has hepatotoxic effects and can cause cell death in vitro. Cell culture studies show that 4MP causes membrane permeabilization and cellular uptake by bacteria.</p>

<p>1,2,3,4-Tetra-O-benzyl-β-D-glucopyranoside is a prodrug that becomes active after acetylation. It is an endogenous compound that has been shown to inhibit the synthesis of myelin and lipid peroxidation in rat brains. This drug has also been found to be effective in the treatment of amyotrophic lateral sclerosis (ALS). 1,2,3,4-Tetra-O-benzyl-β-D-glucopyranoside is unmodified and does not have any side effects on the nervous system. It can be used for the treatment of Parkinson's disease when combined with levodopa.</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>2-Methyl-(1,2-dideoxy-a-D-glucopyrano)-[2,1-d]-2-oxazoline is a high purity, custom synthesis carbohydrate. It has been fluorinated and methylated to increase its stability and resistance to proteases. This compound is used in the synthesis of oligosaccharides and polysaccharides. It can be glycosylated or click modified with thiol groups.</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>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>Custom synthesis of D-glucuronic acid, sodium salt monohydrate.</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>Lactitol is a polyol sugar alcohol that has been used in the treatment of chronic viral hepatitis. It is also used to treat constipation, irritable bowel syndrome, and other gastrointestinal disorders. Lactitol is metabolized by certain types of bacteria and can have a laxative effect. Lactitol is not absorbed in the human intestine and thus does not cause an increase in blood sugar levels. Lactitol has been shown to be effective against microbial translocation and bacterial overgrowth in the gut, which may be due to its ability to lower pge2 levels and inhibit histological changes.</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>

<p>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>