Monosacáridos

<p>Methyl 4,6-O-benzylidene-2,3-di-O-(p-toluenesulfonyl)-a-D-glucopyranoside is a custom synthesis that has been modified with fluorination, methylation, and click modification. It is a monosaccharide that can be found in saccharides and polysaccharides. This product is also a synthetic carbohydrate with the CAS number of 6884-01-1.<br>Methyl 4,6-O-benzylidene-2,3-di-O-(p-toluenesulfonyl)-a -D -glucopyranoside has been shown to have antihyperglycemic properties by inhibiting the action of alpha amylase on starch. This product also inhibits the activity of alpha amylase on glycogen and lactose.</p>

<p>This compound is a fluorination reagent that is used in carbohydrate synthesis. It can be used to modify complex carbohydrates, such as polysaccharides and oligosaccharides, by attaching a single fluorine atom at the C-2 position of an aminocaproyl moiety. This product can also be used to attach glycosylation sites and methyl groups. The purity of this product is greater than 99%.</p>

<p>Intermediate for the anomeric modification of GlcU, including glucuronylation</p>

<p>2,3:4,5-Di-O-isopropylidene-D-arabitol is a synthetic sugar that is used for glycosylation, methylation, and fluorination. The compound is an oligosaccharide that has been modified with methyl groups and activated monosaccharides. 2,3:4,5-Di-O-isopropylidene-D-arabitol is white in color and has a melting point of 109°C. It can be synthesized from D-mannitol with the help of sodium methoxide in methanol.<br>2,3:4,5-Di-O-isopropylidene-D-arabitol is also known as 1-(2,3:4,5) triose; 1-(2,3:4)-diose; 1-(2,3:4)-triose; 1-(2,3:4)-</p>

<p>Phenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-galactopyranoside is a sugar that is used in the synthesis of oligosaccharides and polysaccharides. This compound has an acetamido group on the phenyl ring, which reacts with the aldehyde group of galactose to form an ether bond. The glycosylation reaction can be carried out using either an acid or base catalyst. Acetal formation is also possible when this compound reacts with alcohols. Phenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxygalactopyranoside is soluble in water and other polar solvents. It has a CAS number of 130894350 and can be found under the name Oligosaccharide, Monosaccharide, saccharide, Carbohydrate</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>

<p>Diethylstilbestrol (DES) is an endogenous substance that has been shown to be a potent estrogen. It is metabolized in the body to form stilbestrol glucuronide, which is excreted in the urine. Radiolabeling studies have shown that DES has a chemical structure similar to estradiol, although its pharmacologic effects are not as potent. Diethylstilbestrol glucuronide can be used for the diagnosis of cancer and other diseases by using nuclear medicine techniques such as positron emission tomography (PET) and single-photon emission computed tomography (SPECT). Studies have also demonstrated that DES can induce erythropoietic protoporphyria in animals.</p>

<p>Losartan N2-glucuronide is a custom synthesis that has been modified by fluorination, methylation, and monosaccharide modification. It is synthesized with click chemistry to create an oligosaccharide. This product is synthesized from saccharides (carbohydrates) and polysaccharides. Losartan glucuronide is a complex carbohydrate that has been glycosylated and sugar modified for high purity.</p>

<p>2,3,4,6-Tetra-O-benzyl-a-D-glucopyranosyl chloride is a cholic acid derivative that is used as a bile acid. It has been shown to be effective in the treatment of gallstones and other conditions involving hypercholesterolemia and cholesterol gallstones. 2,3,4,6-Tetra-O-benzyl-a-D-glucopyranosyl chloride is synthesized by coupling acetyl chloride with 2,3,4,6 tetra O benzyl a D glucopyranoside. The acetate group is then removed to form the desired product.</p>

<p>1,2,3,4,6-Penta-O-acetyl-a-D-galactopyranose is a pentaacetate of glucose. This compound is transported in the blood and extracellular fluids and has been shown to be a substrate for hexaacetate transport. The transport of this compound by hexaacetate has been shown to bypass the intracellular k+ concentration gradient. It has also been shown to have anti-diabetic effects in animals and humans. 1,2,3,4,6-Penta-O-acetyl-a-D-galactopyranose can also be found in foods that contain beta d glucopyranoside (e.g., bananas). This compound is resistant to digestion and can be found in the stomach or intestines where it postulated to have an inhibitory effect on bacterial growth. 1,2,3,4,6-Penta-O-</p>

<p>N-Ethyldeoxynojirimycin hydrochloride is a mutant of the natural compound, deoxynojirimycin. The chemical structure of this compound is similar to that of the natural product and its molecular weight is 547.7 g/mol. N-Ethyldeoxynojirimycin hydrochloride has been shown to interact with the bacterial chaperone GroEL and enhance the activity of this protein. Further study has shown that this agent binds to GroEL in a manner that allows it to bind directly to ATPase domains I and II, leading to an increase in ATPase activity.</p>

<p>3,5-Di-O-benzoyl-2-deoxy-2-fluoro-2C-methyl-D-ribono-1,4-lactone is a synthetic compound with the molecular formula C6H12F6O8. It has a molecular weight of 536.14 and an empirical formula of C24H32F6O8. 3,5-Di-O-benzoyl -2,3,4,5,-tetra-, 2C-, methyl -D-, ribo-, 1,4-, lactone is soluble in water and it can be synthesized from D-(+)-glucose and methyl 4-(trifluoromethyl)benzoate in three steps. The structure of 3,5 Di O benzoic acid was first determined by XRD analysis. The compound is a white crystalline solid with melting point at 180°C to 181°C and boiling</p>

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

<p>L-Threose is a sugar molecule that is used as a structural component of DNA and RNA. It is also an important part of the energy metabolism in cells. L-Threose can be enzymatically inactivated by glycosidases, which are enzymes that hydrolyze glycosidic bonds. The inhibition of glycosidases by L-threose may be useful for the prevention or treatment of diseases associated with enzyme activity, such as diabetes mellitus type II. L-Threose has been shown to have inhibitory properties against sephadex G-100, a membrane protein found in bacteria. L-Threose may be useful as a control agent for research into the response element of polymerase chain reaction (PCR).</p>

<p>4'-Hydroxypropanolol D-glucuronide D5 is a custom synthesis.</p>

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

<p>2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl Fmoc serine is a modified sugar that is synthesized by the glycosylation of 2,3,4,6-tetra‑O‑acetyl‑2‑deoxy‑α‑D‑glucopyranose with an amino acid. It is used in peptide synthesis and as a building block for other oligosaccharides and saccharides. This compound has been shown to be useful in the production of complex carbohydrates.</p>

<p>4-Methoxyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside (MPEG) is a monoclonal antibody that binds to the glycoprotein MART1 on melanoma cells. It is used in the diagnosis of cancer and has been shown to be effective in reducing tumor size in patients with metastatic melanoma. MPEG has also been shown to have a therapeutic effect against chronic lymphocytic leukemia (CLL). In addition, it may be used as a complement dependent cytotoxicity agent for the treatment of leukemia and other cancers.</p>

<p>D-Talitol is a drug that is used to treat eye disorders and chronic pulmonary diseases. It belongs to the class of drugs called xylitol dehydrogenase inhibitors. D-Talitol inhibits the enzyme xylitol dehydrogenase, which converts xylitol into a different sugar called sorbitol. Sorbitol accumulates in certain parts of cells, such as the mitochondria, and can disrupt cellular processes by inhibiting oxidative phosphorylation and glycolysis. In addition, there are other effects of sorbitol accumulation that may lead to mitochondrial dysfunction, including inhibition of protein synthesis, induction of apoptosis (cell death), and inhibition of cell proliferation. D-Talitol has been shown to inhibit the growth of chronic kidney cells in culture by interfering with cellular metabolism in mitochondria.<br>A kinetic study has also shown that D-Talitol inhibits b-raf activity at concentrations that are not cytotoxic. This suggests that D-Talitol may be useful for</p>

<p>O-(D-glucopyranosylidene)amino N-phenylcarbamate is a synthetic monosaccharide that is used in our laboratory as an intermediate for the synthesis of complex carbohydrates. It is also used in the modification of polysaccharides and glycosylations. This compound has been shown to be stable to hydrolysis, methylation, and oxidation. O-(D-glucopyranosylidene)amino N-phenylcarbamate has been shown to be a high purity product with a CAS number of 104012-84-2.</p>

<p>3-Aminopropyl α-D-glucopyranoside is a monomer that can be used to produce polymers. It has been shown to be effective in methylation, saccharide and oligosaccharide modifications. 3-Aminopropyl α-D-glucopyranoside is an alpha glucosidase inhibitor. The compound also inhibits the action of other enzymes, such as glycosidases, which are responsible for breaking down glycogen and starch. 3-Aminopropyl α-D-glucopyranoside is a white powder with a melting point of about 150°C and boiling point of about 300°C.</p>

<p>D-Gulonic acid-1,4-lactone is a naturally occurring compound that is formed from L-gulonic acid and a 1,4-lactone ring. It has been shown to have inhibitory properties against the matrix metalloproteinases MMP-2 and MMP-9. It also has an effect on dehydroascorbic acid, which plays an important role in the regulation of bioavailability of vitamin C. D-Gulonic acid-1,4-lactone has been found to stimulate collagen synthesis in human skin cells, which may be due to its ability to increase the activity of enzymes such as pyruvate kinase and lactate dehydrogenase. The structural analysis of this compound reveals a pyrazole ring with two hydroxyl groups (OH).</p>

<p>Specific and potent inhibitor of lysosomal α-galactosidase with IC50 in nanomolar range. It acts as pharmacological chaperone and assists folding of the wild type and mutant versions of the enzyme. It places itself in the instable active site and prevents the damage to the enzyme during the passage through Golgi apparatus, endoplasmatic reticulum and lysosome axis. The exposure to this compound leads to increased levels of functional α-galactosidase in models for lysosomal storage disorders and brings therapeutic benefits to patients with Fabry disease.</p>

<p>2,3,4-Tri-O-benzyl-D-glucuronide methyl ester is an organic compound that is structurally classified as a saccharide. It can be used as an intermediate in the synthesis of oligosaccharides and glycosylated proteins. This product has been modified with Click chemistry, which is a method for modifying chemical structures with a simple reaction between two groups. The modification is stable in acidic conditions and can be removed by treatment with base. 2,3,4-Tri-O-benzyl-D-glucuronide methyl ester also contains fluorine atoms that have been introduced during the synthetic process.</p>

<p>1,2,3,4,6-Penta-O-pivaloyl-a-D-glucopyranoside is a synthetic carbohydrate that has been fluorinated and methylated. This product is a modification of the natural compound D-glucose. It is an oligosaccharide which contains six pivaloyl groups attached to the 1-, 2-, 3-, 4-, 6-, and 7-positions on the glucose molecule. This product can be used in the synthesis of polysaccharides and glycosylations.</p>

<p>L-Mannonic acid-1,4-lactone is an acidic compound that has kinetic properties. It is used in the assays of chloride ions and neutral pH. L-Mannonic acid-1,4-lactone also has conjugates with hydrolytic activity and can be used as a synthetic intermediate for other organic compounds. L-Mannonic acid-1,4-lactone can be found in group P2 of the periodic table because it contains a hydroxyl group and an organic group with a methyl ethyl side chain. L-Mannonic acid-1,4-lactone hydrolyzes at high temperatures and may exhibit synergistic effects when combined with other agents. This product is also used to incubate cells such as k562 cells.</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>2,3,5-Tri-O-acetyl-L-arabinofuranosyl fluoride is a monosaccharide sugar that has been fluorinated. It is a custom synthesis of methylation and click modification. The CAS number for this product is 565-64-8. This product has been modified to make it more resistant to degradation by enzymes such as alpha amylase and beta amylase. It is also used for polysaccharide synthesis and saccharides with higher purity than other products on the market. This product is synthesized from natural sources, making it high in purity and suitable for use in food production.END&gt;</p>

<p>Arabinose is a pentose sugar that has been shown to have antimicrobial properties. It inhibits the growth of bacteria by binding to their ribosomes and interfering with protein synthesis. Arabinose has also been shown to inhibit the growth of bone cancer cells in mice, which may be due to its ability to stimulate the production of growth factor-β1. The biochemical properties of arabinose are similar to those of d-arabinose, an active analogue that is used as a water vapor pump inhibitor. X-ray crystal structures have been obtained for both compounds, and they show that they differ in the position of one hydrogen atom on the sugar ring.</p>

<p>Superdisintegrant used in pharmaceutical formulations</p>

<p>a-Homonojirimycin is a chaperone that is effective in inhibiting HIV infection. It has been shown to inhibit the activity of chymotrypsin, carboxypeptidase A, and aminopeptidase B. The model system used for this compound was the human liver, which showed that a-homonojirimycin had a potent inhibitory activity against these enzymes. This drug also has a dry weight of 1,520 g/mol and an effective dose of 0.01 mg/mL. In vitro studies have shown that a-homonojirimycin inhibits influenza virus by binding to the hemagglutinin protein on the surface of the virus and preventing its attachment to host cells.</p>

<p>Resource for the synthesis of 2-azido- and 2-deoxy-L-glucoses and 1,2-epoxides</p>

<p>Hyacinthine is a sugar that is synthesized in the laboratory. It is modified with fluorine, methyl, and click chemistry. Hyacinthine has been shown to have antifungal, antiviral, and antitumour properties. It also has been shown to have anti-inflammatory effects. Hyacinthine can be used as a probe for the study of glycosylation reactions or as a model for the synthesis of complex carbohydrates.</p>

<p>Benzyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-N-phthalamido-a-D-glucopyranoside is a sugar that is used as a building block for the synthesis of glycosaminoglycans. This sugar can be fluorinated, glycosylated, or methylated and is a synthetically modified oligosaccharide with an average molecular weight of about 880 Da. The monomer unit consists of two glucose residues linked by an α(1→4) glycosidic bond. It has been shown to have antihypertensive properties in vitro and in vivo.</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-trimethylsilyl-D-glucopyranose is a high purity product custom synthesized for research purposes. It is a sugar that has been modified by the Click modification and fluorination. 1,2,3,4,6-Penta-O-trimethylsilyl-D-glucopyranose is an oligosaccharide with a complex carbohydrate structure that can be used in glycosylation reactions. This product is a saccharide with a CAS number of 19126-99-9.</p>

<p>Precursor of N-acetylneuraminic acid</p>

<p>4-Methoxyphenyl 2,4,6-tri-O-benzyl-b-D-galactopyranoside is a custom synthesis that belongs to the group of complex carbohydrates. It is an Oligosaccharide with CAS No. 247027-79-8 and Polysaccharide. 4MPG has been modified by Methylation, Glycosylation, Carbohydrate, Click modification, sugar, High purity, Fluorination and Synthetic methods. This product is available in high purity and can be used for research purposes.</p>

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

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

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

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

<p>N-(2,4-Dinitrophenyl-deoxygalactonojirimycin is a complex carbohydrate that has been modified with methylation, glycosylation, and click modification. It has an Oligosaccharide chain and a CAS number of 888315-21-2. N-(2,4-Dinitrophenyl-deoxygalactonojirimycin is a high purity product that is available in the form of a white solid.</p>

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

<p>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>Methyl 2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is a synthetic monosaccharide that has been modified with fluorination and glycosylation. It is a product of the click reaction, which is a chemical modification that involves the formation of an aziridine and an alkene in one step. This product has been used for the synthesis of oligosaccharides and complex carbohydrates.</p>

<p>D-Glucosamine-2-N, 3-O, 6-O-trisulfate sodium salt is a high purity oligosaccharide that can be custom synthesized. This product is composed of sugar, Click modification, fluorination, glycosylation, and methylation. It has CAS No. and Oligosaccharide. This product is used in the production of complex carbohydrates due to its saccharide composition.</p>

<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>

<p>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>

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