Monosaccaridi

N-Methyldeoxynojirimycin is a monoclonal antibody that is a competitive inhibitor of the melanoma antigen gp75. It is also an inhibitor of oligosaccharide synthesis and has been shown to have anti-inflammatory properties. N-Methyldeoxynojirimycin binds to the golgi alpha-mannosidases, preventing them from processing high-mannose type oligosaccharides. This leads to decreased chemoattractant protein production by neutrophils, which are important in the inflammatory process. N-Methyldeoxynojirimycin has also been shown to inhibit myocardial infarct size and glomerular filtration rate in rats, as well as increase biochemical markers for inflammation, such as α subunit of α1 acid glycoprotein and basic fibroblast growth factor.

<p>2-Deoxy-1,3,4,6-tetra-O-pivaloyl-D-glucopyranose is a glycosylation sugar that belongs to the category of complex carbohydrates. It is a methylated sugar that can be fluorinated or modified with other saccharides. This product can be custom synthesized and has high purity.</p>

<p>2-Acetamido-2,6-dideoxy-D-galactose (2ADG) is a structural analogue of the natural monosaccharide 2,6-dideoxy-D-galactose. It has been shown to have an antimicrobial effect against aerobacter aerogenes in vitro. 2ADG is metabolized by glycosidases and methyl glycosides to form 1,4-anhydro-2,3,4,6 tetraacetamido-2,4,6 dideoxy D galactose. This compound inhibits the growth of bacterial strains that are resistant to polymyxin b., such as Pseudomonas aeruginosa. The inhibition of these bacteria is due to the inhibition of the synthesis of their outer membrane lipopolysaccharides by 2ADG. The antibacterial activity is also attributed to its ability to inhibit the metabolism of glycan molecules in some bacteria</p>

<p>2,3,4,6-Tetra-O-acetyl linamarin is a carbohydrate that belongs to the group of oligosaccharides. It is a complex carbohydrate that has been modified by fluorination and methylation. This product is custom synthesized and can be produced with high purity. The 2,3,4,6-Tetra-O-acetyl linamarin has been glycosylated and click modified.</p>

Abundant and critical component of natural glycans and glycoproteins

1,2,4,6-Tetra-O-acetyl-3-deoxy-D-galactose (1,2,4,6TDA) is a custom synthesis that is a complex carbohydrate. It has been modified with methylation and glycosylation. 1,2,4,6TDA is an oligosaccharide with a molecular weight of 498.06 Da and a CAS number of 90193-74-8. This product is high purity and can be fluorinated. This product can also be synthesized using the click modification reaction.

<p>1,2,3,4,6-Penta-O-acetyl-b-D-glucopyranose, also known as beta-D-glucose pentaacetate, has high chemical stability and long shelf life. This protected form of glucose is a key building block of any chemical synthesis of glucose-containing oligosaccharides or glycoconjugates. In the presence of Lewis acids it can be used as a glycosyl donor to make simple glycosides. In order to perform more complex glycosylations, it can be converted into more reactive donors, such as glycosyl halides or thioglycosides. Beta-D-glucose pentaacetate is also used as a food additive and flavouring agent.</p>

<p>2-Azido-2-deoxy-L-glucopyranose is a Custom synthesis, modification and fluorination of methylated glucopyranosides. This compound has been shown to be effective in the synthesis of mono-, oligo-, and polysaccharides. 2-Azido-2-deoxy-L-glucopyranose is used for the preparation of glycosylation reagents. It can also be used to modify saccharide chains with azide or alkyne functionalities. 2-Azido-2-deoxy-L-glucopyranose is an important building block for the synthesis of complex carbohydrates, such as polysaccharides, glycosylation reagents, and click chemistry compounds.</p>

Homomorph used to study the biological role of 6 hydroxyl group of glucose

Diethoxy phosphonyl 4,7,8,9-tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is a glycosylation agent that is used in the synthesis of complex carbohydrates. It is a methylated derivative of 4,7,8,9 tetra-O-acetyl neuraminic acid and can be used to modify the polysaccharide structure. This product has been shown to react with saccharides and oligosaccharides in a click reaction to produce fluorinated derivatives. Diethoxy phosphonyl 4,7,8,9 tetra-O-acetyl neuraminic acid methyl ester is also available as a custom synthesis.

Intermediate for the anomeric modification of GlcU, including glucuronylation

Resource for synthesis of non-natural ManNAc analogs and mannosaminyl donors

Methyl a-L-fucopyranoside is a natural product that has been shown to have many biological effects, including antioxidant and anti-inflammatory properties. It has been shown to inhibit the growth of bacteria by binding to the ribosome, preventing protein synthesis and cell division. The compound has also been shown to have anti-inflammatory effects in mice with inflammatory bowel disease. Methyl a-L-fucopyranoside inhibits the production of pro-inflammatory cytokines, such as interferon alfa-2b (IFNα2β), which is induced by IFNγ. This inhibition of IFNα2β activity may be due to methyl a-L-fucopyranoside's ability to bind to cytosolic calcium and inhibit its transport into the nucleus. Methyl a-L-fucopyranoside also blocks the production of antimicrobial peptides, such as defensins or cathelicidins.

The 2-azidoethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a custom synthesis in a high purity that can be methylated and modified for glycosylation. It is an azide sugar with the CAS number 142072-11-5. The product can be used for saccharide and polysaccharides modifications or click chemistry. This product is also available for custom synthesis.

<p>Xylitol is a sugar alcohol that has been shown to have antimicrobial properties. It is also used as a sweetener in chewing gum and toothpaste. Xylitol inhibits the growth of bacteria by binding to the enzyme adenosine triphosphate (ATP) synthase, which is required for energy metabolism. The binding of xylitol to ATP synthase prevents the formation of ATP and blocks bacterial growth, leading to cell death. Xylitol can be produced from xylose, a sugar found in plants and animals, through biochemical reactions that are catalyzed by enzymes such as xylitol dehydrogenase and xylulokinase. This process is anaerobic and does not require oxygen or organic nutrients. Xylitol has been shown to have physiological effects on wild-type strain bacteria such as Aerobacter aerogenes.</p>

<p>2,4-Di-O-methyl-D-glucose is a partially O-methylated glucose sugar.</p>

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

<p>Keratin-reducing component in cosmetic applications; used in Glc conjugation</p>

<p>Please enquire for more information about Benzyl-alpha-S-GalNAc including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

2,3,4-Tri-O-benzyl-D-glucuronide benzyl ester is a synthetic glycosylation product. It has been custom synthesized and modified with fluorination and methylation. This compound is an oligosaccharide that can be used as a pharmaceutical intermediate or in the synthesis of complex carbohydrates. 2,3,4-Tri-O-benzyl-D-glucuronide benzyl ester has been shown to have high purity and can be used for research purposes.

<p>Ferric carboxymaltose is a form of iron that is administered intravenously and is used to treat iron deficiency. Ferric carboxymaltose has been shown to be effective in treating iron deficiency anemia as well as other conditions, such as inflammation of the bowel or hematologic response. Ferric carboxymaltose binds to free iron in the blood and prevents it from oxidizing. Ferric carboxymaltose also exhibits an anti-inflammatory effect by inhibiting the production of pro-inflammatory cytokines and chemokines. The polymerase chain reaction (PCR) technique has been used to measure ferritin levels in the blood, which are then used to determine whether treatment with ferric carboxymaltose is necessary.</p>

Methyl 3,5-di-O-benzyl-b-D-ribofuranoside is a synthetic glycoconjugate. The methyl group at the 3 position of the ribose is substituted with a fluorine atom. This modification results in increased resistance to nucleases and enhanced cell penetration. Methyl 3,5-di-O-benzyl-b-D-ribofuranoside can be used for the synthesis of complex carbohydrates that are not accessible by other methods.

Hexadecyl-D-xylopyranoside is a synthetic sugar that has been fluorinated and methylated. It is a complex carbohydrate that belongs to the group of modified sugars. This product has many applications in the synthesis of oligosaccharides and saccharides, as well as in glycosylation reactions. Hexadecyl-D-xylopyranoside can be used in custom syntheses, and has been shown to have high purity with a CAS No. 115211-19-3.

<p>Phenyl 3-deoxy-3-fluoro-a-D-glucopyranoside is a modified oligosaccharide, which is synthesized by the glycosylation of 3,6-diaminohexanoic acid with phenyl boronic acid. This compound is also known as an anti-tuberculosis drug. It has been shown to inhibit bacterial growth by binding to DNA dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity has been shown using a patch clamp technique on human erythrocytes. Phenyl 3-deoxy-3-fluoro-a-D-glucopyranoside also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX1 secretion system protein) and inhibits cell growth in culture.</p>

4-Methoxyphenyl 3-O-allyl-2-azido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside (MPA) is a glycosylated antigen that has been shown to be specific for mycobacterium avium. It is a cytosolic calcium ionophore and can induce platelet membrane activation and coagulation. MPA has also been found to be chemoprotective in animal models of cancer. MPA can be used as an indicator of the body mass index (BMI).

The chemical profile of the methyl ester (Z)-3-hexen-1-yl b-D-glucopyranoside has been determined using high performance liquid chromatography. The compound is an anti-fungal agent and its main pharmacological effects are related to radical scavenging activity. It shows possible neuropharmacological activity, but further studies are required to confirm this. The chemical profile of Z)-3-hexen-1-yl b-D-glucopyranoside was found to be different from that of other compounds in the genus. This compound belongs to a group of compounds called aldehydes, which is characterized by methoxy and dimethoxy substitutions on the benzene ring. The compound is used in traditional Chinese medicine for the treatment of scopolin or codonopsis radix, which are two types of chinese medicinal herbs.

2-Azidoethyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside is a custom synthesis. It is a complex carbohydrate that has been modified with glycosylation and methylation. This saccharide is a glycoside of the simple sugar mannose and the amino acid 2-azidoethanol. The compound has been fluorinated to yield a stable molecule. This product is of high purity and can be used in the synthesis of other compounds.

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-a-D-mannopyranose (1,3,4,6-TA) is a stable analog of the glycosidic sugar 2,6-dideoxymannose. This compound has been shown to be a potent inhibitor of the synthesis of Neisseria meningitidis capsular polysaccharides and an effective vaccine adjuvant against Mycobacterium tuberculosis. 1,3,4,6-TA is also a competitive inhibitor for the enzyme mycothiol and other thioglycosidic enzymes that are involved in the biosynthesis of mycolic acids. 1,3,4,6-TA was synthesized from 2-(N'-bromoacetamido)-2'-deoxymannose by reaction with sodium azide in acetone. The structure is bicyclic with two

<p>Isosorbide dinitrate is a drug that belongs to the class of nitrates. It is used in the treatment of angina pectoris, as well as congestive heart failure and chronic heart failure. Isosorbide dinitrate has been shown to cause caspase-independent cell death in human leukemia cells and breast cancer cells. This may be due to its ability to inhibit mitochondrial membrane potential and interfere with intracellular calcium mobilization. The optimum concentration for isosorbide dinitrate is 10 µM, which inhibits the growth of bacteria, including Mycobacterium tuberculosis and Salmonella enterica serovar Typhimurium. The drug also inhibits the production of proinflammatory cytokines such as IL-1β, IL-6, and TNF-α by inhibiting c-jun phosphorylation. Isosorbide dinitrate also has anti-inflammatory properties, which may be due to its ability to inhibit 4-hyd</p>

D-Mannurono-6,3-lactone is a carbohydrate that can be found in plants. The compound is a monosaccharide and an isomer of D-mannose. It consists of 6 carbon atoms, 3 oxygen atoms, and 1 nitrogen atom. D-Mannurono-6,3-lactone has been shown to have kinetic properties that are different from other carbohydrates. The chromatographic method used to isolate the compound was based on its acidic properties. This acid hydrolysis allowed for the separation of the molecule into two components: one with a pK value of 4.5 and another with a pK value of 2.5. These components were then separated using a fluorimetric method due to their differing fluorescence intensities at 490 nm and 530 nm wavelengths. D-Mannurono-6,3-lactone has been shown to interact with fulvellum (an antibiotic). This interaction

<p>3-Deoxy-D-galactopyranose is a galectin that has been synthetically produced. It has shown to be an antagonist of galactoside, which may be useful in the treatment of type 2 diabetes. The synthetic method for this molecule is still being developed.</p>

Fluorescent substrate used to monitor glucose uptake

Donor for Koenigs-Knorr type galactosylation and other anomeric substitutions

<p>Glycogen phosphorylase inhibitor</p>

1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro-a-D-ribofuranose is a synthetic saccharide that can be used as a fluorinated carbohydrate. This compound has been shown to have high purity and can be custom synthesized with various functional groups. 1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro--aD ribofuranose is a methylated sugar that can be modified to include glycosylation or modification of the sugar with click chemistry. It has CAS number 704916121.

Inositol-1-phosphate is a precursor of inositol and is involved in the regulation of cell signalling. It has been shown to inhibit neuronal death by decreasing intracellular calcium levels. Inositol-1-phosphate also inhibits epidermal growth factor induced cytosolic calcium increase in hybridoma cells. Inositol-1-phosphate has been shown to be neuroprotective, which may be due to its ability to stimulate p2y receptors and inhibit neurokinin-1 receptor activities.

2-Hydroxydesipramine glucuronide is a metabolite of desipramine, which is a tricyclic antidepressant that inhibits the uptake of noradrenaline and 5-hydroxytryptamine. 2-Hydroxydesipramine glucuronide is formed by conjugation with glucuronic acid. It has been found in human urine and has been proposed as a biomarker for the clinical monitoring of patients taking desipramine. The pharmacological effects of 2-hydroxydesipramine glucuronide are similar to those of desipramine, but it is less potent and selective than its parent compound. This metabolite also has biliary excretion properties, which may be due to its small molecular size.

1,2,3,4,6-Penta-O-acetyl-β-D-mannopyranose is a custom synthesis of an oligosaccharide that is used in the modification of saccharides and complex carbohydrates. It has been used in the synthesis of glycosylations and methylations. This product is a fluorinated monosaccharide with high purity.

<p>Methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-a-D-glucopyranoside is a synthetic monosaccharide with a high purity. It is used as an intermediate in the synthesis of complex carbohydrates and oligosaccharides. Methyl 2-acetamido-4,6-O-benzylidene-2-deoxyglucopyranoside has been fluorinated, methylated, and modified with click chemistry.</p>

2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone is an organic compound that belongs to the class of lactones. It is a chiral molecule with two asymmetric carbons and four stereogenic atoms. This compound can be used for the synthesis of optically active compounds. It is also a precursor for the synthesis of morpholines and phosphonates. 2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone can be synthesized by reacting an enolate with an aldehyde in the presence of a base and acid catalyst. The acid catalyst causes elimination of water from the enolate to produce the desired product.

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>L-Gulonic acid-1,4-lactone is an ascorbic acid derivative that inhibits the production of matrix metalloproteinases (MMPs) and other enzymes. L-Gulonic acid-1,4-lactone has been shown to inhibit the activity of MMPs in hl-60 cells, which may be due to its ability to chelate metal ions, such as zinc and copper. This molecule also has a stabilizing effect on collagen type I because it prevents cross linking between lysine amino acids. The discovery process for this molecule was found by screening clones from a cDNA library with biochemical properties similar to those of ascorbic acid. This molecule has been shown to inhibit the activation of protein kinase C (PKC) and phosphorylation of extracellular signal regulated kinase (ERK). L-Gulonic acid-1,4-lactone is metabolized through plant metabolism</p>

1,3,4,6-Tetra-O-acetyl-2-[[2-(acetylthio)acetyl]amino]-2-deoxy-D-galactopyranose is a modified GalNAc analogue

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-a-D-galactopyranose is an azide sugar that is resistant to the activity of sulfide and can be used as a probe for sulfide in the distal colon. It has been shown that this sugar binds to recombinant human erythrocyte enzymes and inhibits their activities. The hydrolysis of this sugar by pancreatic enzymes has been shown to be dependent on the conformational state of the enzyme. This sugar also inhibits salivary amylase and intestinal sucrase activities.

<p>4-Deoxy-4-fluoro-D-glucopyranose is a fluorinated sugar that is found in the roots of Glycyrrhiza uralensis. It can inhibit glycosylation by blocking the stepwise addition of glucose to the growing oligosaccharide chain. 4-Deoxy-4-fluoro-D-glucopyranose also has biological activities, such as antiinflammatory and antitumor properties. This compound is an analog of D-arabinose and D-xylulose, which are found in many plants. 4DFG can be used to synthesize glycosides with various substituents on the hydroxyl group.</p>

Medicagenic acid 3,28-di-O-glucoside is a synthetic compound that is the product of a custom synthesis. It is a sugar with 1,2-linked glucose units. Medicagenic acid 3,28-di-O-glucoside is an intermediate in the synthesis of glycoconjugates. Medicagenic acid 3,28-di-O-glucoside can be modified to produce saccharides with various properties and functions. This compound has been modified by fluorination, methylation and click chemistry to produce medicagenic acid 3,28-di-O-[(2-(4′-[N′-(3′,5′'-dimethoxytrityl)-3H]thiophenyl)carbonyl]-6′-(4′-[N′-(3',5'-dimethoxytrityl)-3H]thiophenyl)methyl] glucopyranoside.

Building block for galectin-3 inhibitors based on 3’-modified LacNAc

<p>2,3,4,5-Tetra-O-acetyl-D-ribononitrile is a custom synthesis chemical. It is an Oligosaccharide, Polysaccharide, Modification and has the CAS No. 25546-50-3. It can be used as a Fluorination reagent in Synthetic Chemistry and Click modification. The purity of this chemical is high and it has a Custom synthesis. 2,3,4,5-Tetra-O-acetyl-D-ribononitrile is synthesized by Methylation and Glycosylation of sugar molecule with acetyl group. This chemical can be used to modify saccharide and carbohydrate molecules.</p>

2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl azide is a custom synthesis that is a complex carbohydrate. It is a glycosylation product of 2,3,4,6-tetraacetyl α--D--glucose and 2,3,6 -tri--O--acetyl--2--deoxy--β--D--glucopyranose. This compound has been modified by Click chemistry with 4-(dimethylamino)pyridine (DMAP). The modification has produced an acetamido group at the C2 position of the glucopyranoside moiety. The compound is available in high purity for research purposes.

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.