Monossacáridos

<p>Muscarine chloride is a potent acetylcholine receptor agonist that causes activation of the postsynaptic membrane by increasing the K+ concentration and hyperpolarizing the membrane. Muscarine chloride increases spontaneous activity in muscle and ganglion cells, which may be due to its ability to activate cholinergic receptors. Muscarine chloride has been shown to cause paralysis of skeletal muscle when injected into frog sciatic nerve, which is caused by its ability to block nerve impulses. Muscarine chloride is effective at doses as low as 0.1 ug/kg and can be used for research purposes when activating acetylcholine receptors.br&gt; br&gt;</p>

Galactostatin is a protein synthesis inhibitor that binds to the l-tartaric acid site of the bacterial 30S ribosomal subunit. It inhibits the binding of aminoacyl-tRNA to the ribosome, preventing translation and inhibiting cell growth. Galactostatin has been shown to be effective against HIV infection in mammalian cells. This drug also has a chaperone effect that protects cells from heat or cold stress.

3-Deoxy-2-keto-D-xylonate lithium salt is a synthetic compound that is used in the synthesis of protamine. It is produced by the reduction of an aldehyde with borohydride. 3-Deoxy-2-keto-D-xylonate lithium salt has been shown to be active against E. cloacae, which can cause diarrhea and other gastrointestinal disorders. 3-Deoxy-2-keto-D-xylonate lithium salt inhibits the growth of E. cloacae by inhibiting glycolaldehyde reductase and aldolases, which are enzymes that are essential for glycolysis and citrate metabolism, respectively. The cleavage products formed by this reaction inhibit bacterial growth by interfering with cell wall biosynthesis, preventing protein synthesis, or blocking ATP production (oxidative phosphorylation).

<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.</p>

<p>D-Fructose-1,6-diphosphate dicalcium salt is essential for glycolysis to occur efficiently. It links to adenine nucleotides which regulate 6-phosphofructokinases (Pfks) that catalyze one of the rate limiting steps of glycolysis. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.</p>

<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.</p>

<p>1-Azido-1-deoxy-2-C-hydroxymethyl-2,3-O-isopropylidene -D-glucitol is a synthetic monosaccharide that can be used for glycosylation, methylation, and click modification. It is a complex carbohydrate with an Oligosaccharide structure. 1-Azido -1-deoxy -2 -C -hydroxymethyl -2,3 -O -isopropylidene D glucitol has been fluorinated. This compound is a sugar that has been modified with a Click modification. It is a sugar that has been synthesized and custom synthesized by high purity.</p>

<p>1,4-Anhydro-2,O:5,6-di-O-isopropylidene-2-C-(hydroxymethyl)-D-galactitol is a custom synthesis. It is commonly used in the modification of saccharides and oligosaccharides to produce fluorinated derivatives with various functional groups. The preparation of this compound has been described by Click chemistry.</p>

<p>1-Chloro-2-deoxy-3,5-di-O-toluoyl-a-D-ribofuranose (also known as Hoffer’s chlorosugar) is a synthetic building block used in nucleic acid research to afford an array of both alpha and beta linked 2’-deoxyribose derivatives. Naturally occurring nucleosides are typically beta linked and the efficient synthesis of alpha linked analogues, which are often more stable, offers access to interesting variations in 3D structure and biochemical reactivity.</p>

<p>3-Deoxy-D-glucose (3DG) is a molecule that belongs to the class of carbohydrates. It is an analog of D-glucose, which is the key substrate for the production of energy in mammalian cells. 3DG has been shown to inhibit the uptake of glucose by trypanosomes and also inhibits glycolysis in mammalian cells. The inhibition of glycolysis may be due to its ability to prevent the phosphorylation of glucose by hexokinase, thus blocking the conversion of glucose into glucose 6-phosphate. 3DG is biosynthesized from d-xylose, which is a five carbon sugar that can be oxidized to form CO2 and H2O.</p>

<p>1,2,3,4-Tetra-O-acetyl-D-[6-13C]glucuronide methyl ester is a custom synthesis that can be used for the methylation of saccharides and polysaccharides. It is also used to modify glycosides and oligosaccharides. This compound has a CAS number and can be modified with click chemistry. It is a high purity product that can be synthesized with fluorination or complex carbohydrates.</p>

<p>1-Amino-1-deoxy-D-galactitol hydrochloride is a natural polymer that is found in many organisms, including bacteria and fungi. It can be obtained by enzymatic conversion of galactose, which is an epimer of glucose. 1-Amino-1-deoxy-D-galactitol hydrochloride has been shown to have viscosity properties that are similar to those of natural polymers. This compound also has the ability to form hydrogen bonds with other molecules. 1-Amino-1-deoxy-D-galactitol hydrochloride is produced by chemoenzymatic reactions and can be used as a substitute for natural polymers in certain applications (e.g., food industry).</p>

<p>2,3-O-Isopropylidene-1-C-methyl-D-erythrose is a modified oligosaccharide that is synthesized from D-erythrose. It can be used in the synthesis of complex carbohydrates with various biological activities. It is a sugar that can be methylated, glycosylated, or fluorinated and has been shown to have anti-inflammatory properties.</p>

<p>Inhibitor of alpha-glucosidase II</p>

<p>2,3:4,5:6,7-Tri-O-isopropylidene-D-glycero-D-ido-heptonic acid methyl ester is an oligosaccharide that is a synthetic glycosylation product. It is a complex carbohydrate that has a high purity and CAS No. This compound can be custom synthesized to your specifications and modified in the lab with fluorination or methylation.</p>

<p>Please enquire for more information about GDP-L-fucose disodium including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3:4,5-Di-O-isopropylidene-1,6-di-O-benzyl-D-myo-inositol is a complex carbohydrate and a sugar. It is an oligosaccharide with two monosaccharides and a glycosidic linkage. It has been modified by methylation, fluorination and Click chemistry. This compound has been custom synthesized for high purity.</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>3,4,6-Tri-O-acetyl-D-glucal, also called 1,5-anhydro-2-deoxy-D-arabino-hex-1-enitol triacetate, is the acetate protected cyclic enol-ether (glycal) of D-glucose. 3,4,6-Tri-O-acetyl-D-glucal is a building block useful in the synthesis of a range of carbohydrates with the glucal double bond allowing other functional groups to be introduced. As an alkene, a glycal can undergo electrophilic addition across the double bond to introduce halogens and epoxides or be used to generate deoxy monosaccharides. 3,4,6-Tri-O-acetyl-D-glucal can undergo a Ferrier rearrangement with an alcohol and Lewis acid to give a 2,3-unsaturated product.</p>

<p>5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone is a synthetic monosaccharide with the molecular formula C8H14O5. It has a CAS number of 94697-68-4 and is available for custom synthesis. The chemical structure of 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone consists of a methyl group attached to the hydroxyl at position 1 and a fluoro group attached to the hydroxyl at position 4. 5,6--O--Isopropylidene--L--gulonic acid--1,4--lactone is not naturally occurring and is made by modification of glycosides. This compound can be used in click chemistry or complex carbohydrate reactions.</p>

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

<p>1-Octen-3-ol glucoside is a synthetic, fluorinated sugar that is modified with glycosylation, methylation, and click chemistry. It contains a high degree of purity and is custom synthesized to order. This product can be used as a substitute for other sugars in the production of oligosaccharides, saccharides, and polysaccharides.<br>1-Octen-3-ol glucoside has been shown to have various modifications including glycosylation, methylation, and click chemistry. It is often used when there are restrictions on the types of sugars that can be used in the synthesis of complex carbohydrates.</p>

<p>Building block for oligosaccharide synthesis</p>

<p>1-Hydroxymethyl-8-benzyloxy-3-methoxy-2,6-dioxabicyclo[3,2,1]octane is a sugar that can be modified with various functional groups. This compound is synthesized by modification of the 1S,3S,4R,8S configuration of 8-Benzyloxy-1-(hydroxymethyl)-3-methoxy-2,6 dioxabicyclo[3,2,1]octane. The synthesis can be performed in two steps: first the hydroxymethyl group is replaced by benzyloxymethyl using 1-(benzyloxy)propanol and then the methoxy group is replaced by a methoxy group with sodium methoxide.</p>

<p>3-Deoxy-D-gluconic acid is a chemical compound that has the chemical structure of C6H12O6. It is a white crystalline solid that can be found in nature as a reaction product of glucose and oxygen. 3-Deoxy-D-gluconic acid can also be synthesized by reacting D-glucose with nitrous acid or sulfur dioxide. 3-Deoxy-D-gluconic acid is an organic acid and has been shown to inhibit the growth of filamentous fungi by acting on their glycosidic bonds. This chemical compound has not been shown to have any adverse health effects in humans, although it may cause irritation if it comes into contact with skin or eyes.</p>

<p>UDP-a-D-galactose disodium salt (UDP-Gal) is a sugar-nucleotide substrate of galactosyltransferases. It’s used as the donor of galactose in the biosyntheses of glycoproteins and glycolipids. Its low cellular content is also hypothetically linked to the defective galactosylation in galactosemia.</p>

<p>3-Deoxy-L-threo-2-hexulosaric acid is a sugar that is modified by the addition of a fluorine atom to one of its hydroxyl groups. 3-Deoxy-L-threo-2-hexulosaric acid is used in the synthesis of complex carbohydrates and oligosaccharides. It is also used in the modification of saccharides, sugars, and polysaccharides. 3-Deoxy-L-threo-2-hexulosaric acid can be custom synthesized according to your specifications. It can be synthesized with high purity at our labs.</p>

<p>Please enquire for more information about D-Fructose 1-phosphate disodium including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl α-D- glucopyranoside is a methylated sugar used as an inhibitor of lectin-conjugate binding. Methyl α-D- glucopyranoside is commonly used in protein purification for eluting glycoproteins and other glycoconjugates from affinity chromatography columns of agarose lectin. Methyl α-D- glucopyranoside is also known as Methyl alpha-D-glucoside or alpha-Methyl-glucoside.</p>

<p>Building block for polymers synthesis, ionic liquids and chiral auxiliaries</p>

<p>3,4-O-Isopropylidene-D-arabinose is a synthetic compound that has been used as an active analogue for the study of nucleophile reactions. 3,4-O-Isopropylidene-D-arabinose undergoes nucleophilic addition with potassium azide to form a thiazolidine intermediate. The stereospecificity of this reaction was shown by the chemists and biochemists who synthesized it. It has also been shown to react with an anion in a similar manner. This chemical is used in the synthesis of d-arabinose, which can be used for the production of other compounds.</p>

<p>Please enquire for more information about 2-Deoxy-2-fluoro-D-galactose including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>D-Glucuronolactone is supposed to be involved in detoxification processes.</p>

<p>a-Acetobromo-D-xylose is an oligosaccharide sugar used in glycosylation and polysaccharide modifications. It is synthesized by the fluorination of xylose with acetic acid, bromine, and a base. The product is purified by vacuum distillation and recrystallization. In addition to its use as a carbohydrate, this product can be modified using methylation or click chemistry to create derivatives.</p>

<p>L-Xylose is a monosaccharide that is found in many plants. It is used as a sweetener, and also has been shown to be beneficial in the treatment of diabetic neuropathy. L-Xylose can be metabolized by the enzyme xylitol dehydrogenase to produce energy for the cell. The enzyme catalyzes the conversion of xylitol to D-xylulose and then D-xylulose 1-phosphate, which can be converted into ATP for use by cells. L-Xylose is not metabolized by bacterial enzymes and does not affect blood sugar levels. L-Xylose has been shown to have an effect on taste perception, with a sweet taste at concentrations of 10 milligrams per liter (mg/L). This sweet taste is due to its hydroxymethyl group on the C2 position, which reacts with sodium ions in the mouth. The optimum pH for L-xylose</p>

<p>Di-O-isopropylidene psicose is a synthetic sugar that is a modification of the natural compound, psicose. It can be used for the synthesis of oligosaccharides, polysaccharides and other complex carbohydrates. Di-O-isopropylidene psicose can be methylated and glycosylated to form other sugar derivatives or fluorinated to form fluoroquinolones. This sugar has been shown to have high purity and stability under a wide range of conditions.</p>

<p>L-Fucose is a monosaccharide that is an important component of glycoproteins and glycolipids. L-Fucose is also found in the cell wall of bacteria. The most abundant sources of L-fucose are from the hydrolysis of lactose or sucrose by bacteria, or as a result of intestinal microbial fermentation. L-Fucose has been shown to be involved in the regulation of many metabolic processes, including the glomerular filtration rate and sephadex g-100 binding capacity in the kidney. It has also been shown to improve growth in infant rats with protein malnutrition. The enzyme that catalyzes the conversion of D-arabinose to L-fucose is known as fucokinase.</p>

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

<p>3-Azido-3-deoxy-5,6-O-isopropylidene-D-allonic acid g-lactone is a modification of the sugar allose. It is an oligosaccharide that contains a complex carbohydrate. It can be custom synthesized and has high purity, making it suitable for use in pharmaceuticals. 3-Azido-3-deoxy-5,6-O-isopropylidene-D allonic acid g lactone is a methylated sugar, which means that it has had one of its hydroxyl groups replaced with a methyl group. It is also glycosylated, meaning that it has been modified by the addition of carbohydrates to its structure. The carbons in 3ADODAGL are found in the form of ring structures, which are known as saccharides.</p>

<p>Isopropyl-β-D-thioglucuronic acid is a β-D-glucuronidase inducer. It enhances the sensitivity of β-glucuronidase assays in E. coli.</p>

<p>2,4,6-Tri-O-benzyl-3-O-benzyl-D-mannopyranose is a modification of the monosaccharide D-mannopyranose. It is a carbohydrate that can be custom synthesized and has high purity with a CAS number. The 2,4,6-tri-O-benzoyl group can be used for glycosylation reactions to produce polysaccharides. This modification also has the ability to be fluorinated or methylated by using the corresponding reagents.<br>2,4,6-Tri-O-benzoyl-3-O-benzyl mannopyranose is an oligosaccharide that can serve as a building block for more complicated carbohydrates like polysaccharides. It has not been shown to have any toxicity in animals and is used as a food additive in some countries.</p>

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

<p>L-Guluronic acid sodium is a monosaccharide that plays a crucial role in cardiac health. It is involved in the uptake and utilization of polyene carbohydrates, carotenoids, and fatty acids by human myocardial cells. L-Guluronic acid sodium has been shown to enhance the bioavailability of these essential nutrients, promoting optimal heart function. Additionally, this compound acts as a reactive analog, mimicking the effects of certain molecules involved in mammalian cell signaling pathways. This unique property makes L-Guluronic acid sodium a potential therapeutic agent for various cardiovascular conditions and may have implications in other areas such as stent technology and cancer research.</p>

<p>GDP-D-mannose is a natural mannosyl donor and substrate for mannosyltransferases that catalyses mannosylation, for instance during the synthesis of the trimannoside core of complex, high-mannose or hybrid N-glycans. GDP-D-mannose is widely used in (chemo)enzymatic synthesis of oligosaccharides and its biosynthesis occurs from glucose-6-phosphate over several steps. GDP-D-mannose consists of a D-mannose unit, α-glycosydically linked to the nucleotide guanosine diphosphate (GDP). Examples of this important reaction would be the transfer of mannosyl moieties onto the dolichol-P-P-GlcNAc2 precursor of N-glycans in the endoplasmatic reticulum, with release of GDP, or the mannosylation reactions during GPI-anchor (bio)synthesis. GDP-D-mannose has also been used for the in vitro synthesis of b-mannan oligosaccharides.</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. It has 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>2-Keto-L-galactonic acid is a chemical compound that belongs to the group of fatty acids. It is produced by the degradation of polyunsaturated fatty acids and has been shown to be a potential control agent for hepatic steatosis. 2-Keto-L-galactonic acid also inhibits the synthesis of dinucleotide phosphate in rat liver cells, leading to an accumulation of intracellular potassium ion. This compound inhibits the uptake of glucose by activating ATPase, which leads to an increase in intracellular pH. The uptake of 2-keto-L-galactonic acid into cells has been shown using cell culture experiments with wild type and mutant strains.</p>

<p>Glycol ethers are compounds that are used as solvents and plasticizers. They have been shown to inhibit the activity of enzymes, such as glucose-6-phosphate dehydrogenase, which is involved in the conversion of glucose to phosphate. Glycol ethers also promote sugar transport by inhibiting the sodium-dependent glucose transporter (SGLT). This transport mechanism is important for maintaining normal blood sugar levels and preventing diabetic neuropathy. Glycol ethers are also anti-diabetic agents that can increase insulin sensitivity by stimulating insulin release from pancreatic beta cells and improving the response of peripheral tissues to insulin stimulation.</p>

<p>Please enquire for more information about 2-Keto-L-gluconic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-O-Methyl-β-D-glucuronic acid is a β-glucuronidase inducer.</p>

<p>D-Allose pentaacetate is a modified oligosaccharide that can be used as a synthetic intermediate in the production of complex carbohydrates. It has been shown to have high purity and is easily synthesized in a laboratory setting. D-Allose pentaacetate is a monosaccharide with five acetate groups that can be methylated or glycosylated, which makes it an ideal candidate for modification. D-Allose pentaacetate has CAS No. 144071-49-8 and can be found on PubChem CID: 1215965.</p>

<p>Used in synthetic organic chemistry and natural product synthesis. Induces apoptosis by inhibiting the synthesis and increasing the efflux of glutathione. It is used for synthesis of optically active dipyrrolyl alkanols from pyrroles on the surface of montmorillonite KSF clay.</p>

<p>6-Deoxy-6-fluoro-D-glucose is a molecule that belongs to the group of glucose analogs. It has been shown that 6-deoxy-6-fluoro-D-glucose, or dF6G, induces apoptosis in MCF7 cells through inhibition of glut1, the rate limiting enzyme for glycolysis. The structural analysis of the compound showed that it contains a fluorine atom at C2 and an oxygen atom at C3. The kinetic studies revealed that dF6G reacts with H2O in a 1:1 stoichiometric ratio to form hydrogen fluoride and 6-deoxyhexoate. 6dF6G has been shown to have pharmacokinetic properties similar to glucose and it can be used as an alternative source of energy by many organisms including aerobacter aerogenes.</p>

<p>1-Deoxy-L-allitol is a naturally occurring compound found in human urine. It has been shown to have a role in the regulation of glucose metabolism, as it is catalysed by liver enzymes and can affect the synthesis of glycogen. 1-Deoxy-L-allitol also has been found to be an activator of t-cells, which are immune cells that help regulate the body's response to infection.</p>

<p>1,2:5,6-Di-O-isopropylidene-a-L-glucofuranose is a monosaccharide that is a component of the fatty acid biosynthesis pathway. It has been shown to be important in clinical relevance, because it can inhibit viral replication by binding to the virus as a nucleophile and attacking the glycosidic bond. This monosaccharide also inhibits the growth of liver cells by binding to a receptor on the cell surface. 1,2:5,6-Di-O-isopropylidene-a-L-glucofuranose binds specifically to nucleophilic sites on proteins and has been shown to have antiinflammatory properties through its inhibition of prostaglandin synthesis.</p>

<p>L-Glucurono-3,6-lactone is an acetonide that is a derivative of L-glucose. L-Glucurono-3,6-lactone can be used as a precursor for the synthesis of polyhydroxybutyrate (PHB).</p>

<p>Ribulose 5-phosphate sodium is a chemical that can be used to inhibit the enzyme ribulose phosphate reductase. Ribulose 5-phosphate sodium has been shown to inhibit glycolaldehyde production in the chloroplasts of plants, effectively reducing the amount of carbon dioxide produced. This chemical has also been shown to have an inhibitory effect on other enzymes involved in carbon fixation and assimilation. The effectiveness of this chemical is dependent on the specific plant species and environmental conditions.</p>

<p>Reference compound for metabolites of the pentosephosphate pathway</p>

<p>3-Phenyl-2-propenylbeta-D-glucopyranoside is a flavonoid that has been shown to have inhibitory properties. It has been used as an analytical method for the diagnosis of bronchial reactivity. The high resistance of 3-phenyl-2-propenylbeta-D-glucopyranoside to oxidation and reduction make it an interesting candidate for antiinflammatory agents. When testing the effects of this compound on human bronchial tissue, it was found that 3-phenyl-2-propenylbeta-D-glucopyranoside inhibited allergic symptoms by inhibiting the release of inflammatory mediators such as histamine and leukotrienes, which are released in response to allergens and other irritants in the airways. The use of this compound may be useful in the treatment of asthma patients who suffer from allergic reactions to dust, pollen, or animal dander.</p>

<p>Propranolol-2-O-b-D-glucuronide is a metabolite of propranolol hydrochloride. It has been shown to have low bioavailability in humans and rats. Propranolol-2-O-b-D-glucuronide is eliminated via the kidney, with an elimination rate that is faster than the parent drug propranolol hydrochloride. The glucuronide conjugate of propranolol, which is found in urine samples, has been shown to be a potential biomarker for glomerular filtration rate and renal function.</p>

<p>2-O-Benzoyl-4,6-O-benzylidene-a-D-glucopyranoside is a synthetic carbohydrate with a structure that is similar to that of glucose. It has been shown to have anti-inflammatory properties in animal models and can be used for the treatment of inflammatory bowel disease and Crohn's disease. This compound has also been shown to inhibit the growth of bacteria such as Streptococcus pyogenes, Staphylococcus aureus, and Escherichia coli. 2-O-Benzoyl-4,6-O-benzylidene--aD glucopyranoside is soluble in water and has high purity with an average of 98%.</p>

<p>D-ribulose-5-phosphate sodium is a nucleotide sugar that is one of the ribonucleotides, which are fundamental components of RNA. D-ribulose 5-phosphate sodium has been shown to be an intermediate in the metabolism of ribulose and catalyzes the oxidation of d-arabinose. This enzyme also catalyses the synthesis of fatty acids and participates in reactions involving glycerolipids and phospholipids. The reaction mechanism involves a double displacement with simultaneous attack by a water molecule on C2' and C3'. When deuterium is present, it affects the rate of these reactions in a way that depends on the orientation of the substrate to the enzyme.</p>

<p>D-Xylulose 5-phosphate sodium salt is a synthetic monosaccharide that can be used in the synthesis of oligosaccharides, polysaccharides, and complex carbohydrates. It is also used in glycosylation reactions. D-Xylulose 5-phosphate sodium salt has been fluorinated to provide better stability and solubility. The compound has a molecular weight of 206.06 g/mol and a CAS number of 105931-44-0. This product is available for custom synthesis upon request.</p>

<p>3,4-O-Carbonyl-D-galactal is a custom synthesis that can be used to modify oligosaccharides, carbohydrates or complex carbohydrates. It has a high purity and is non-toxic in humans. 3,4-O-Carbonyl-D-galactal has been fluorinated and saccharide modified. This product has CAS No. 149847-26-7 and can be synthesized with methylation and glycosylation.</p>

<p>10-Beta-D-glucopyranosyl-1,8-dihydroxy-3-(hydroxymethyl)-anthrone heptaacetate is a synthetic saccharide that can be used as a fluorescent probe. It is synthesized by reacting methyl anthrone with 10-beta-D-glucopyranosyl chloride and sodium hydroxide under basic conditions. The fluorination of the compound leads to its fluorescent properties. This product has been custom synthesized for use in click chemistry reactions.</p>

<p>2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-a-D-galactopyranose is a fluorinated complex carbohydrate that has been modified by methylation and acetylation. This product is a custom synthesis that has not been previously described in the scientific literature. It is synthesized from 2, 3, 4, 6 tetraacetyl alpha D galactopyranoside and 2 deoxy alpha D galactopyranose. The chemical properties of this compound are similar to those of other complex carbohydrates such as glycogen and heparin.</p>

<p>Methyl D-arabinofuranoside is an antimycobacterial agent that inhibits the synthesis of mycolic acids, which are important components of the cell wall of Mycobacterium tuberculosis. Methyl D-arabinofuranoside has been shown to be active against drug-resistant strains and has been well tolerated by animals. This compound can be synthesized from 2,4-dichlorophenylacetic acid and arabinose in two steps. The first step involves a three-component condensation reaction with sodium hydroxide, hydrochloric acid, and 2,4-dichlorophenylacetic acid. The second step is a nucleophilic attack on the pyran ring of methyl D-arabinofuranoside with hypophosphorous acid. Methyl D-arabinofuranoside can also be prepared by reacting sodium nitrosobenzene with sodium benzene sulfinate in alcoholic solution</p>

<p>Thioglucosides are a type of sugar that is modified with a thiol group at the C-3 position. A thioglucose can be synthesized by methylation, click modification, and fluorination. Thioglucoses have been used in the past for the production of oligosaccharides and polysaccharides, as well as in complex carbohydrate research. They are also used in the production of high purity monosaccharide sugars. This product is available for custom synthesis to meet your needs.</p>

<p>3'-a-Sialyl-N-acetyllactosamine sodium salt is a high purity, custom synthesis sugar. It has been modified with fluorination, glycosylation, and methylation to provide the desired properties. This product is also available in other forms such as monosaccharide and saccharide. 3'-a-Sialyl-N-acetyllactosamine sodium salt can be used in various applications including Click modification, fluoroamination, glycosylation, carbonylation and methylation. CAS No. 350697-53-9</p>

<p>Ramipril-D5 acyl-b-D-glucuronide is a custom synthesis of the complex carbohydrate, oligosaccharide. It has been modified with saccharide, methylation, glycosylation, and click modification. Ramipril-D5 acyl-b-D-glucuronide is a high purity product that has been fluorinated and synthesized.</p>

<p>9,10-Dimethoxy-pterocarpane-3-O-b-D-glucoside is a custom synthesis that is a polysaccharide with a complex carbohydrate structure. The chemical name for this compound is 9,10-dimethoxy-pterocarpane-3-O-[4′″-(1″″′′)-b′″'-D-glucopyranosyl]-3′′′,4′″’,6′"’] bibenzyl. This compound has been modified by methylation and glycosylation. It can be used in the treatment of cancer and diabetes due to its high purity and fluorination. 9,10-Dimethoxy pterocarpane 3β O glucoside is a sugar or saccharide that can be found in plants such as the roots of tobacco plants. The modification of this sugar by methylation and glycosylation makes it more</p>

<p>4,7,8,9-Tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is a modified form of sialic acid. This compound is a glycosylation product that has been modified with methyl groups and fluorine atoms. The fluorination of the molecule increases its stability and prevents it from being hydrolyzed by enzymes such as β-galactosidase. 4,7,8,9-Tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is often used in the synthesis of polysaccharides and oligosaccharides for medical purposes. This compound can be custom synthesized for research purposes or to meet special requirements.</p>

<p>The chemical name of this compound is 2-(Acetylamino)-1-O-benzyl-2-deoxy-3,4-O-isopropylidene-6-O-(2,3,4,6-tetra-O-acetylbDgalactopyranosyl)-Dgalactopyranoside. It is a synthetic compound and its molecular formula is C17H22N2O8. The molecular weight of this compound is 412.46 g/mol. CAS No. 352273-66-6</p>

<p>4-Deoxy-D-glucose is a sugar that is synthesized by the condensation of two molecules of erythrose. It has been shown to be an efficient donor substrate for nucleophilic attack, which can lead to the synthesis of glycosides and other natural products. 4-Deoxy-D-glucose is also a competitive inhibitor of uridine diphosphate (UDP) glucose, which is an enzyme involved in the biosynthesis of UDP sugars and glycoproteins. The concentration of 4-deoxy-D-glucose affects its catalytic mechanism, as it acts as a competitive inhibitor at high concentrations. Molecular modeling has revealed that this molecule adopts a chair conformation with significant solvent exposure.</p>

<p>2-Amino-2-deoxy-D-xylose is a metal chelator that can be used in the treatment of infections caused by bacteria. It has been shown to have synergistic effects with metaperiodate, a compound that inhibits bacterial growth by blocking the synthesis of folic acid. 2-Amino-2-deoxy-D-xylose also chelates and removes heavy metals such as mercury and lead from the bloodstream and other tissues. In addition, this drug is an efficient method for producing amino function pyrimidine nucleosides, which are precursors to DNA and RNA synthesis. The metal chelate ring is formed through dehydration of a furanose molecule with a chloride ion. This leads to an advanced carbohydrate product that contains chlorine.</p>

<p>Please enquire for more information about N’-Nitrosonornicotine N-β-D-glucuronide (mixture of diastereomers) hydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2,4,6-Tetra-O-acetyl-3-O-carbamoyl-D-mannopyranose is a synthetic sugar that belongs to the class of glycosides. It can be used in the synthesis of oligosaccharides and polysaccharides. This product is custom synthesized on request and can be modified with fluorination, methylation or click modification. It is available in high purity and has a CAS number of 99748-11-5.</p>

<p>Methyl 3,4-O-isopropylidene-L-threonate is a chromatographic chiral compound that is synthesized by the reaction of malonate and aspartyl amide. This product can be used to determine the stereochemistry of other chiral compounds. It is an endocannabinoid that has been found to have anti-inflammatory activities in animals. Methyl 3,4-O-isopropylidene-L-threonate has also been shown to have antiobesity effects in mice fed a high fat diet and may be used as a synthetic carbohydrate replacement for diabetics.</p>

<p>Methyl 2,3,5-tri-O-acetyl-D-arabinofuranoside is a monosaccharide that is used in the synthesis of carbohydrates. It has been shown to inhibit the growth of Rhizopus stolonifer and other fungi. Methyl 2,3,5-tri-O-acetyl-D-arabinofuranoside has also been used for the quantitative analysis of deacetylated sugars. A chromatographic method was developed using an ion exchange resin and methyl glycosides as standards. The sugar was quantified by electron ionization mass spectrometry (EI) after conversion to its trimethylsilyl ether derivatives with triethylamine in methylene chloride. The spectrum obtained from EI analysis showed the presence of anomeric proton peaks at m/z 184 and 186, indicating that this sugar contains two anomeric hydroxyl groups on the same carbon atom.</p>

<p>Methyl 2,3,4-tri-O-benzyl-b-L-thiofucopyranoside is a glycosyl acceptor that can be used in the synthesis of oligosaccharides. It is also an intermediate for the production of antifungal drugs such as fluconazole.</p>

<p>Decyl D-glucopyranoside is a sodium salt of decyl D-glucopyranoside that is used as a detergent additive in cleaning compositions. Decyl D-glucopyranoside has shown antimicrobial activity against both Gram-positive and Gram-negative bacteria, including methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. Decyl D-glucopyranoside has also been shown to have chemical stability at high temperatures, making it useful in the manufacture of lacrimal gland preparations and cationic surfactants.</p>

<p>1-Deoxy-1-nitro-L-glucitol is a potent apoptosis-inducing compound that has shown promising results in cancer research. It is an analog of vanillin and nintedanib, two well-known cancer cell inhibitors. 1-Deoxy-1-nitro-L-glucitol has been shown to inhibit the activity of several kinases, including those involved in tumor growth and progression. In addition, it has been found to be effective against various types of cancer cells, including Chinese hamster ovary cells and human bladder cancer cells. This compound also exhibits synergistic effects with other anti-cancer drugs such as glimepiride and apomorphine. The presence of 1-Deoxy-1-nitro-L-glucitol in urine may serve as a potential biomarker for the diagnosis and monitoring of certain cancers.</p>

<p>Ribitol is a sugar alcohol that is found in all living organisms. It is also used as a source of carbon and energy in the form of D-ribitol-5-phosphate, which can be synthesized from ribose 5-phosphate by means of an enzymatic reaction. Ribitol 5 phosphate is used for the synthesis of monoclonal antibodies, which are useful for studying enzyme activities, immunoassays, and cell surface receptors. This compound has been shown to have regulatory effects on the expression of genes encoding fatty acid biosynthesis enzymes. Ribitol 5 phosphate has been detected using magnetic resonance spectroscopy techniques in glycan structures and galacturonic acid residues.</p>

<p>Salacinol is a naturally occurring sulfonium ion, which is a bioactive compound found primarily in the roots and stems of the plant Salacia reticulata. This plant is native to regions of South Asia, particularly India and Sri Lanka, and is traditionally used in Ayurvedic medicine. Salacinol's mode of action involves the inhibition of alpha-glucosidase, an enzyme responsible for breaking down carbohydrates into glucose. By inhibiting this enzyme, salacinol reduces the postprandial rise in blood glucose levels, thus demonstrating antidiabetic potential.</p>