Monosacáridos

<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-Gulose is a sugar that has been shown to have inhibitory properties on blood glucose levels. It also has insulin-like effects and can be used as an alternative to insulin injections in patients with Type 1 diabetes. D-Gulose is metabolized by the liver into 5-deoxy-D-gluconic acid and then into glucose, which can then be used for cellular energy production. The rate constant for this process was determined in experiments using rat liver slices. D-Gulose may also have potent angiogenic effects, as it increased the proliferation of pluripotent cells and caused significant increases in growth factor β1 expression. D-Gulose may also have potential anti-cancer effects, as it inhibited nitrate reductase activity in tumor cells and decreased xanthine oxidase activity.</p>

<p>D-Fructose-1,6-diphosphate is a chemical that is found in the cytosol of cells. It is an intermediate in the metabolism of fructose and also has an important role in the synthesis of fatty acids and phospholipids. D-Fructose-1,6-diphosphate is an effective inhibitor of sodium succinate dehydrogenase, which converts succinate to fumarate. D-Fructose-1,6-diphosphate has a neutral pH profile and is not affected by changes in pH levels. The optimum pH for this compound is between 6.5 and 7.5. D-Fructose-1,6-diphosphate binds to proteins with unsaturated alkyl chains such as creatine kinase and glutamate dehydrogenase. It has been shown to have hemolytic effects on erythrocytes (red blood cells) at high concentrations, which may be due to its ability to bind</p>

<p>Octyl-beta-D-glucopyranoside is an alkylglycoside non-ionic detergent and is one of the most commonly used in membrane protein isolation. As it is uncharged, it is unlikely to cause protein denaturation or refolding issues, allowing for the isolation of intact macromolecular complexes without affecting protein-protein interactions. Octyl-beta-D-glucopyranoside, also known as octylglucoside or OG, forms small, uniformed micelles and has an aggregation number of between 27-100. It is readily dialyzable from membrane protein preparations due to its high Critical Micelle Concentration (CMC) of 18-20mM. Octyl-beta-D-glucopyranoside has similar uses and properties to that of another frequently used surfactant, Octyl-beta-D-thioglucopyranoside.</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>4,6-O-(4-Methoxybenzylidene)-1,2,3-tri-O-pivaloyl-b-D-glucopyranose is a Glycosylation compound that has been modified with methyl groups on the 4 and 6 carbons of the sugar. It is a complex carbohydrate that has been fluorinated at the C5 position. This product is available for custom synthesis in quantities of 10g or more. The CAS number for this compound is 13357007.</p>

<p>Glycerone phosphate is a cytosolic calcium (Ca2+) substrate molecule that is used to measure the activity of phospholipase A2, an enzyme that catalyzes the hydrolysis of membrane lipids. Glycerone phosphate has been shown to inhibit neuronal death and may be useful in treating neurodegenerative diseases such as Alzheimer's disease. Glycerone phosphate has also been shown to bind to monoclonal antibodies, which are proteins that bind specifically to antigens on the surface of cancer cells, thereby preventing them from binding to their corresponding receptors on healthy cells. This may limit the spread of tumor growth and increase their sensitivity to platinum-based chemotherapy.</p>

<p>5-Keto-D-gluconic acid potassium salt is a custom synthesis of 5-keto-D-gluconic acid, which is a monosaccharide. It is modified with fluorination and methylation at the C5 position. The chemical formula for 5-keto-D-gluconic acid potassium salt is C6H7O6K2. This compound has been used in the synthesis of oligosaccharides, saccharides, and polysaccharides.</p>

<p>3,4,6-Tri-O-allyl-D-glucal is a custom synthesis of a complex carbohydrate. It is an Oligosaccharide and Polysaccharide that can be modified by methylation and glycosylation. The product is a Modification of saccharides that has been shown to have Methylation, Glycosylation, Carbohydrate and Click modification. 3,4,6-Tri-O-allyl-D-glucal has CAS No. 434327-45-4 and is available in High purity with Fluorination.</p>

<p>D-Galactose-6-O-sulphate sodium salt is used as a diagnostic agent to measure the level of galactose in blood and tissues. The enzyme that hydrolyzes D-galactose-6-O-sulphate, galactose oxidase, is present in leukocytes and chorionic villi. The enzymatic assay for this chemical is based on the reaction between D-galactose and sulfite to form D-galactosulfonic acid. This reaction is catalysed by a sulphatase enzyme. A fluorimetric method can be used to measure the formation of D-galactosulfonic acid.</p>

<p>Methyl 4,6-O-benzylidene-2-benzyloxycarbonylamino-2-deoxy-a-D-glucopyranose is a custom synthesized compound. It is a polysaccharide that is modified with fluorine and methyl groups. The chemical structure of this compound includes a glucose molecule with an amino group at the C1 position and an acetyl group at the C4 position. This modification increases the solubility and stability of this compound. Methyl 4,6-O-benzylidene-2-benzyloxycarbonylamino-2-deoxy--A D glucopyranose has been used in research as a model for glycosylation.</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>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>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>1-Deoxy-1-nitro-D-galactitol is a methoxide that exhibits mutagenic activity. It reacts with nitromethane to form an intermediate, which then reacts with sodium methoxide to produce the final product. This product can be used as a precursor for other compounds.</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>2,3:4,6-Di-O-isopropylidene-α-L-sorbofuranose is a furanose sugar that is structurally similar to sorbose. It is a five membered ring with two stereocenters. The conformation of this molecule encompasses the techniques of dialkyl and furanose synthesis. This compound can be used as a vitamin and can be degraded by ozonation in water. 2,3:4,6-Di-O-isopropylidene-α-L-sorbofuranose is biodegradable and has been shown to have antiinflammatory properties.</p>

<p>2-Acetamido-1,3,4,6-tetra-O-benzyl-2-deoxy-a-D-glucopyranoside is a modification of the natural carbohydrate. It is an oligosaccharide synthesized with custom synthesis. The synthetic process involves the methylation and glycosylation of the monosaccharides. Fluorination and saccharide linkages are also used in the production of this compound. 2-Acetamido-1,3,4,6-tetra-O-benzyl-2-deoxyglucopyranoside can be used as a building block for complex carbohydrates or as a research reagent for glycobiology.</p>

<p>N-acetyl D-glucosamine (GlcNAc) is an aldohexose (2-acetamido-2-deoxyglucose) in which the hydroxyl group at position 2 is replaced by NHAc (Collins, 2006). N-acetyl D-glucosamine forms the exoskeletons of molluscs and insects as the building block of the polysaccharide chitin (Rudrapatnam, 2003). N-acetyl D-glucosamine is a key component of N- and O-linked glycans, present in glycolipids and the glycosaminoglycan hyaluronic acid (Fallacara, 2018). A recent study has suggested that N-acetyl D-glucosamine may have therapeutic potential for COVID-19 as it affects the spike protein-ACE2 receptor interaction during the infection with SARS-CoV-2 virus (Baysal, 2021).</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>N-[2-(4'-Methoxyphenylacetonitrile)]-2,3,4,6-tetra-O-pivaloyl-D-glucopyranoside is a custom synthesis of a carbohydrate. It is a synthetic saccharide that is modified by fluorination and methylation. This compound has high purity and can be custom synthesized to order.</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>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>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>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>Ethyl 3,5,6-tri-O-benzyl-D-glucofuranoside is a modification of the natural carbohydrate D-glucose and has been synthesized by methylation. This product has a purity of 99% and is made up of three monosaccharides: D-glucose, D-mannose, and D-galactose. It also contains an oligosaccharide chain that consists of 6 sugar units. Ethyl 3,5,6-tri-O-benzyl-D-glucofuranoside is insoluble in water but soluble in acetone. The molecular weight of this product is 522.2 g/mol.</p>

<p>N-Amyl b-D-glucopyranoside is a monosaccharide with a glucose residue at the 1 position and an amyl group at the 2 position. It is a synthetic sugar that can be used as a starting material in glycosylation reactions to modify oligosaccharides, saccharides, and complex carbohydrates. N-Amyl b-D-glucopyranoside can also be fluorinated, methylated, or modified by click chemistry to produce novel compounds. N-Amyl b-D-glucopyranoside is typically obtained by the glycosylation of amylamine with dibenzoyl glucose in the presence of an acid catalyst. This reaction produces a mixture of mono-, di-, tri-, tetra-, penta-, hexa-, hepta-, octa-, nona-, deca-, undeca-, dodeca-, and tetradecasaccharides, which</p>

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

<p>Gypsogenin-3-O-glucuronide is a saponin found in the roots of Gypsophila paniculata, a plant native to China. It has been shown to have anti-inflammatory and anti-tumor activities. Gypsogenin-3-O-glucuronide has been shown to inhibit tumor growth in mice by inhibiting protein synthesis. The pentasaccharides that make up gypsogenin are present in different proportions, which leads to differences in the biological activity of this compound. This is one of the reasons why saponins have not yet been fully explored for potential use in medicine.</p>

<p>D-Glucitol monostearate is a synthetic oligosaccharide that has been modified with fluorination, methylation, and click chemistry. It is the product of a custom synthesis and can be used as a sugar substitute or as a food additive. D-Glucitol monostearate is an off-white powder that can be used in pharmaceuticals or as food additives. It has been shown to have antiviral activity against Hepatitis C virus (HCV) and HIV replication.</p>

<p>Glycolytic inhibitor; pro-apoptotic; anti-cancer agent</p>

<p>2-C-Methyl-L-ribono-1,4-lactone is a crystallized carbohydrate that contains the enantiomers L and D. It is a chiral molecule with two asymmetric carbon atoms. The L form has a higher yield than the D form and can be synthesized from l-arabinose, dimethylamine, and isomerisation. This compound is also present in ketoses such as d-xylose and 1-deoxy-d-ribulose. 2CMLR1L4L acts as an inhibitor of the enzyme d-galactose dehydrogenase, which catalyzes the conversion of d-galactose to d-glucose. Cyanide can bind to this compound to form cyanohydrin adducts, which are toxic to cells.</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>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>Synthetic building block</p>

<p>2-Amino-2-deoxy-glucitol is a kinetic inhibitor of the enzyme glycogen phosphorylase, which catalyzes the rate-limiting step in glycogenolysis. It binds to the enzyme and blocks access to the active site by an amide group, thus inhibiting the phosphorylation of glucose residues. This prevents the breakdown of glycogen and leads to increased levels of blood sugar. 2-Amino-2-deoxy-glucitol is used as a treatment for pertussis (whooping cough) and as an adjunct therapy during insulin shock therapy for diabetic ketoacidosis. The drug has also been shown to bind to histidine residues on the enzyme and inhibit its activity.</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>2-Acetamido-2-deoxy-D-lyxojirimycin is a carbohydrate that is modified by fluorination, methylation, glycosylation, and click modification. The compound is a synthetic monosaccharide that is used in the synthesis of complex carbohydrates. 2-Acetamido-2-deoxy-D-lyxojirimycin has CAS number 1207673-74-2 and can be custom synthesized to meet your requirements for purity and quality.</p>

<p>D-Lyxono-1,4-lactone is a 4-deoxy-l-fucose derivative that is a potent inhibitor of bacterial growth. It is a highly effective antibiotic with a broad spectrum of activity against Gram-positive and Gram-negative bacteria. D-Lyxono-1,4-lactone has been shown to be active against multivorans, including Escherichia coli and Salmonella enterica serovar Typhimurium. This compound was found to be more active than antibiotics such as penicillin and streptomycin. The structure of D-Lyxono-1,4-lactone includes two hydroxamic acid groups that are connected by an acetal linkage to form the benzylidene acetal moiety. The optical enantiomers of this molecule have been characterized using high resolution NMR spectroscopy and magnetic resonance spectroscopy techniques.BR&gt;<br>Dosis: 250</p>

<p>D-Glucono-1,5-lactone is a chemical compound that is a member of the class of compounds known as diketones. It can be used in chemical biology and polymer chemistry to probe hydrogen bonding interactions, polymer compositions, and redox potentials. D-Glucono-1,5-lactone has been shown to inhibit the growth of cells in culture by inhibiting DNA synthesis. This inhibition is due to its ability to bind with high affinity to nucleic acids and prevent the formation of the enzyme complexes required for transcription and replication. The effects are reversible.</p>

<p>2-C-Azidomethyl-5-O-benzyl-1-O-tert.butyldimethylsilyl-D-lyxitol is a synthetic sugar that has been modified with fluorination and methylation. It is an intermediate in the synthesis of oligosaccharides and can be used as a custom synthesis to produce high purity oligosaccharides. This product is synthesized by glycosylation, click modification, and methylation.</p>

<p>Methyl 7,8,9-Tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-S-phenyl-2-thio-D-glycero -b-(1→4)-D-(1→3)-galacto-(1→4)-2-[N-[(1R,2R)-2-(methoxyimino)ethoxy]acetamido]-nonulopyranosylonate is a synthetic carbohydrate. It has been modified with methylation at position 7 and 8 of the sugar and click modification. Methyl 7,8,9 -triacetyl 5 -N, 4 -O carbonyl 3 , 5 -dideoxy 2 -S phenyl 2 -thiophenediol glycero b D galacto 2 nonulopyranoside is a complex carbohydrate.</p>

<p>Ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a compound with a molecular mass of 536.35 Da. It is an inhibitor of the enzyme catalase and has been shown to bind to monoclonal antibodies that are specific for human vascular endothelial growth factor (VEGF). This inhibition prevents the binding of VEGF to its receptor, which blocks the activation of the VEGF pathway. Ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy--b D glucopyranoside has also been shown to inhibit HIV replication in vitro.</p>

<p>Tert-butyl 2-deoxy-L-ribopyranoside is a synthetic monosaccharide that can be used in the synthesis of polysaccharides and oligosaccharides. It is also used for fluorination reactions, such as click modification. This compound can be custom synthesized to order, and it is available in high purity. Tert-butyl 2-deoxy-L-ribopyranoside can be modified with a variety of different functional groups, including methylation. It has an CAS number of 1032153-57-3.</p>

<p>2,3,4,6-Tetra-O-pivaloyl-β-D-glucopyranoside is a carbohydrate modified with fluorination and methylation. It is also a synthetic oligosaccharide that has been glycosylated. This product can be custom synthesized to meet your needs. We offer high purity and custom synthesis for this product.</p>

<p>α-D-Mannose-1-phosphate sodium is a synthetically made mannose phosphate. This compound is used in the synthesis of oligosaccharides and glycoproteins.</p>

<p>2-Deoxy-2-fluoro-L-fucose (2FF) is a fluorinated analogue of fucose that can be converted to GDP (Guanosine Diphosphate)-2FF in vitro, a competitive inhibitor of alpha-1,3-fucosyltransferase V. It can also be metabolised inside the cell to a substrate-based inhibitor of fucosyltransferases. 2FF reduces fucosylation of IgG in antibodies, which increases therapeutic efficacies of antibodies that cause antibody-dependent cellular cytotoxicity.</p>

<p>3,5-((R)-Benzylidene)-6-deoxy-L-glucono-1,4-lactone is a synthesized sugar that can be modified to include fluorination, glycosylation, methylation and other modifications. It is an oligosaccharide with a saccharide backbone made up of glucose units. The monosaccharides are galactose and glucuronic acid. 3,5-(R) Benzylidene)-6-deoxy-L-glucono-1,4-lactone is used in the synthesis of complex carbohydrates for research purposes.</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>2,4-Dideoxy-2,4-difluoro-D-glucose is a fluorinated glucose analog that has been synthesized to be used as an imaging agent for positron emission tomography (PET) and single photon emission computed tomography (SPECT). It is labeled with fluorine-18 and can be metabolically incorporated into the cellular glycolytic pathway. 2,4-Dideoxy-2,4-difluoro-D-glucose emits positrons that are detected by PET or SPECT cameras. The incorporation of 2,4-dideoxy-2,4-difluoro--D--glucose into the glycolytic pathway allows it to be used as a marker for positron emission tomography.</p>