Monosacáridos

<p>Mecamylamine is a drug that binds to the active site of the acetylcholine esterase enzyme and prevents the breakdown of acetylcholine, which causes muscle contractions. Mecamylamine is used for the treatment of bowel disorders, such as diarrhoea. Randomised placebo-controlled trials have shown that mecamylamine is an effective treatment for chronic idiopathic constipation. The optimal dose and duration of treatment remain unclear, but it has been suggested that a cycle of 4 weeks on and 4 weeks off may be appropriate. Mecamylamine can cause adverse reactions, such as dizziness and blurred vision. It should not be used by people with asthma or other respiratory problems or by pregnant women.</p>

<p>3,6-Di-O-benzyl-D-glucal is a substrate for the enzyme fatty acid hydroxylase. This enzyme catalyzes the hydroxylation of fatty acids to produce hydroxy fatty acids and 3,6-di-O-benzyl-D-glucal. The stereoselective nature of this enzyme has been shown using microscopy to examine the reaction time in both monolayers and bilayers. The kinetics of this reaction have also been analyzed by kinetic analysis. It is thought that this reaction takes place in the cytosol, although it may also occur in mitochondria or chloroplasts.</p>

<p>Phenyl 3,4-O-(2',3'-dimethoxybutan-2',3'-diyl)-a-L-thiorhamnopyranoside is a custom synthesis of an oligosaccharide, monosaccharide, and fluorinated sugar. This synthetic compound is a complex carbohydrate that is glycosylated with a polysaccharide. The modification of this molecule includes methylation and sugar modifications. This product is high purity and can be used as a research chemical.</p>

<p>D-Xylonic acid lithium salt is a redox potential regulator that belongs to the class of nucleotide phosphate. It has been shown to inhibit the transcriptional regulation of genes in Saccharomyces cerevisiae strain. D-Xylonic acid lithium salt inhibits the growth of bacteria by binding to a hydroxyl group on the surface of bacterial cells, which disrupts the cell membrane and causes cell death. This drug also has film-forming properties and can be used as a model system for studying glycolaldehyde, an intermediate in sugar metabolism.</p>

<p>2,3,4-Tri-O-acetyl-b-D-xylopyranosyl azide is a compound that has a linear range of 10 to 500 μM. It has been shown to inhibit the growth of bacteria such as C. perfringens and S. aureus. This compound inhibits the production of toxins in these bacteria by binding to the ribosomes and inhibiting protein synthesis. In addition, this compound has been shown to have high activity at salinity levels up to 15% NaCl and diffraction data was obtained from 2,3,4-tri-O-acetyl-b-D-xylopyranosyl azide crystals using XRD in order to quantify its molecular structure.</p>

<p>2,3,6-Tri-O-carboxymethyl-D-glucose (TCMG) is a potent polyelectrolyte that can be used as an additive to cellulose. TCMG is synthesized by the reaction of 2,3,6-tri-O-carboxymethylcellulose with potassium bitartrate in acidic medium. TCMG has been shown to interact with cellulose and form a gel matrix. This reaction is due to the ionic interactions between the carboxyl groups in TCMG and the hydroxyl groups in cellulose. The conductimetric titration measurement shows that TCMGs have a constant value at pH 5.5, indicating that they are anionic polyelectrolytes. Potentiometric titration indicates that TCMGs are nonionic polyelectrolytes and the interaction between these two polymers is due to electrostatic forces.</p>

<p>Potent inhibitor of non-lysosomal glucosylceramidase, without having any effect on glucosylceramide synthase and glucosidases. Anti-inflammatory and immunosuppressive effect of AMP-DNM demonstrated in a model of hapten-induced colitis in vivo. Reduces glycosphingolipids and increases insulin sensitivity in murine models of obesity-related insulin resistance. Induces sterol regulatory element-binding protein (SREBP) target genes in HepG2 cells, activating cholesterol biosynthesis.</p>

<p>1-Deoxy-L-ribose is a metabolite of acetone. It is a monosaccharide that contains one less oxygen atom than its parent compound. 1-Deoxy-L-ribose is found in the urine and blood of humans and animals. In animals, it can be synthesized from glucose by the enzyme ribose 1-phosphate reductase. This reaction requires an energy source such as ATP or NADH to reduce ribose 1,5-bisphosphate to 1,4-dihydroxyacetone phosphate, which then undergoes spontaneous dehydration to form 1-deoxy-D-ribose.</p>

<p>D-Glucose-4-D is a deuterated form of glucose. It is a halophilic sugar that is used in the biosynthesis of lipids. D-Glucose-4-D can be synthesized chemically or by isotope effect by using d-glucose as the starting material. This compound can be used to study lipid synthesis and lipid metabolism in bacteria, such as E. coli, because it has been shown to inhibit the enzyme glycerol dehydratase, which catalyzes the conversion of glycerol to dihydroxyacetone phosphate, an intermediate in lipid biosynthesis. D-Glucose-4-D also inhibits the enzyme phosphatidate phosphohydrolase, which converts phosphatidic acid to diacylglycerol. These compounds are important for membrane lipid formation and are involved in cellular signalling pathways.</p>

<p>D-2'-Deoxyribofuranosyl-3-guanylurea is a custom synthesis that is used as an intermediate in the glycosylation of oligosaccharides and polysaccharides. D-2'-Deoxyribofuranosyl-3-guanylurea is a modified sugar that has been fluorinated, methylated, and glycosylated. This compound is used to synthesize complex carbohydrates that are important for various biological processes.</p>

<p>1-O-(trans-3-hydroxycotinine)-2,3,4-tri-O-acetyl-b-D-glucuronide methyl ester is a carbohydrate. Carbohydrates are polymers of the monosaccharides, which include glucose, galactose and fructose. The structure of this compound has been modified by fluorination and methylation. This modification has increased the solubility of the molecule and it is synthesized using custom methods. This product is available in high purity at a custom synthesis price.</p>

<p>Allyl 2,3,4,6-tetra-O-benzyl-a-D-glucopyranoside is a synthetic monosaccharide. It can be used in the synthesis of complex carbohydrates by glycosylation and polysaccharide modification. It can also be used for click chemistry modification, methylation, and sugar modifications. Allyl 2,3,4,6-tetra-O-benzyl-a-D-glucopyranoside is of high purity and is available for custom synthesis.</p>

<p>D-Glucosamine-3,4,6-tri-O-sulphate trisodium salt is a high purity and custom synthesis of D-glucosamine. It is a sugar with click modification and fluorination. It has CAS No. 157297-03-5 and it is synthesized from glycosylation, methylation, and modification. It has a molecular weight of 517.85 g/mol and the chemical formula C9H14N2O12S3NaO6. Glucosamine is an oligosaccharide that can be found in many complex carbohydrates such as chitin or cellulose.</p>

<p>3-Acetamido-3,6-dideoxy-D-galactose is a monosaccharide with two functional groups. It has been shown to be bifunctional and can act as a glycosyl donor or acceptor. 3-Acetamido-3,6-dideoxy-D-galactose was isolated from the type strain of Streptomyces venezuelae. It is also found in fatty acids and some strains of bacteria, such as Bacillus megaterium. The biological properties of 3-acetamido--3,6-dideoxy--D--galactose have been studied using monoclonal antibodies, magnetic resonance spectroscopy (MRS), and 13C nuclear magnetic resonance spectroscopy (NMR).</p>

<p>2-Acetamido-2-deoxy-D-glucopyranosyl serine is a compound that belongs to the class of coumarins and monosaccharides. It contains a nitro group and a heterocycle, making it a unique and versatile molecule. This compound has been studied for its various properties, including its interaction with liver microsomes and its ability to undergo crystallization. Additionally, 2-Acetamido-2-deoxy-D-glucopyranosyl serine has shown promising effects on TGF-beta activation and has been found to inhibit aldehyde formation in trichloroacetic acid solutions. This compound also exhibits interactions with other molecules such as pyrazine, ofloxacin, and famotidine. Its diverse characteristics make it an intriguing compound for further research and potential applications in various fields.</p>

<p>D-Fructose-1,6-diphosphate trisodium salt (D-FDP) is an ATP precursor that is used to study the effects of D-FDP on energy metabolism in rat cardiomyocytes. The results from this study showed that D-FDP increased ATP levels and inhibited the accumulation of intracellular lactate. This compound also inhibits ventricular myocardial hypertrophy induced by pressure overload in animal experiments. In addition, D-FDP has been shown to inhibit the polymerase chain reaction (PCR) process and to be active at a concentration of 25 mM.</p>

<p>Diosmetin-7-O-b-D-glucopyranoside is a coumarin derivative that is found in the root of the Chinese herb Dioscorea tinctoria. It has been shown to have anti-inflammatory effects by inhibiting the expression of inflammatory genes, and it also has antioxidant properties. The chemical structure of diosmetin has been shown to be similar to protocatechuic acid, an important phenolic acid that can be found in wine and vinegar. Diosmetin has also been shown to inhibit mitochondrial apoptosis, which may contribute to its anti-cancer effects. Diosmetin has been shown to increase postprandial blood glucose levels in rats fed a high fat diet, and this effect may be due to its ability to inhibit peroxisome proliferator-activated receptor gamma (PPARγ) activity.</p>

<p>2-Benzamido-2-deoxy-D-glucopyranose is a synthetic, inexpensive, and non-toxic compound that has antibiotic properties. It is used as a reagent for the sulfonylating of aromatic rings and as an intermediate in the synthesis of other compounds. 2-Benzamido-2-deoxy-D-glucopyranose can be radiolabeled with carbon or fluorine atoms to form a resonance labeled probe that can be used in magnetic resonance spectroscopy.</p>

<p>8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35-O-(2,6-dideoxy-L-ribo-hexopyranosyl)amphotericin B is an antifungal drug that belongs to the class of polyene macrolides. It is a potent inhibitor of Candida albicans and Candida glabrata. This compound has been shown to have synergistic effects when used in combination with nystatin against C. albicans. 8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35O-(2,6 - dideoxy - L - ribo - hexopyranosyl)amphotericin B also inhibits toll like receptor 4 (TLR4), which is responsible for the induction of inflammatory cytokines such as IL1B and IL8</p>

<p>2,3-O-Isopropylidene-L-glyceraldehyde (2,3-OIPA) is a synthetic compound that was developed as an alternative to paraformaldehyde for the synthesis of enantiopure compounds. It has been used in metathesis reactions and catalysed the conversion of β-unsaturated ketones to enantiopure products. 2,3-OIPA also has significant cytotoxic activity against a range of human cancer cell lines. This compound can be used in asymmetric syntheses to produce chiral molecules with a high degree of optical purity.</p>

<p>D-Fructose 1-phosphate barium salt trihydrate is a custom synthesis, high purity sugar. It has been modified with fluorination, glycosylation, and methylation. D-Fructose 1-phosphate barium salt trihydrate is made from the modification of various sugars such as oligosaccharides and monosaccharides to form complex carbohydrates. It can be used for Click modification or in the synthesis of glycoconjugates. D-Fructose 1-phosphate barium salt trihydrate is also known as saccharide.</p>

<p>Metabolite of Mycophenolic acid</p>

<p>Glucose 6-phosphatase substrate</p>

<p>2,3,4,6-Tetra-O-benzyl-5-thio-D-glucono-1,5-lactone is a complex carbohydrate that can be modified with methylation and glycosylation. It is a saccharide that can be modified by fluorination and click modification. This compound is synthesized by the polymerization of allose in the presence of an enzyme to produce 2,3,4,6-tetra-O-(benzyloxymethyl)-5-thio--D--glucono--1,5--lactone.</p>

<p>Benzyl 2,3-O-isopropylidene-a-D-mannofuranoside is a fluorinated monosaccharide that is synthesized using glycosylation and polysaccharide modification. This product has a CAS number of 20689-03-6 and can be used for complex carbohydrate synthesis. It has been shown to have high purity.</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>D-Gluconic acid sodium salt is a glycol ether that is used as an injection solution. It has been shown to have antibacterial efficacy against wild-type strains of bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. The in vitro antimicrobial action of D-gluconic acid sodium salt was found to be due to its ability to inhibit bacterial growth by interfering with the synthesis of DNA. D-Gluconic acid sodium salt also has been shown to have antihypertensive effects in rats through the inhibition of angiotensin II type 1 receptor (AT1) signaling pathway and erythrocyte proliferation. This drug also has been shown to bind benzalkonium chloride and x-ray diffraction data show that it is crystalline in nature. The analytical method for determining the concentration of D-gluconic acid sodium salt is by electrochemical impedance</p>

<p>5-Thio-L-fucose is a sugar that is found in a variety of tissues and organs. It has been shown to inhibit the antibody-dependent cellular cytotoxicity (ADCC) by binding to the Fc portion of IgG antibodies, which are used to target and destroy cancer cells. 5-Thio-L-fucose has also been shown to modulate the effector functions of natural killer cells and enhance the glycan profile of dendritic cells. It may be useful as a supplement for patients undergoing chemotherapy or radiation therapy, where it may help inhibit the growth of tumor cells. 5-Thio-L-fucose inhibits ADCC activity by binding to IgG antibodies, preventing them from attaching to immune cells, which would otherwise act as effectors in destroying tumor cells. This inhibition can be reversed with a competitive inhibitor such as D-arabinose.</p>

<p>2-N-Chloroacetyl-2-deoxy-D-glucosamine is a high purity synthetic molecule that is custom synthesized to meet your needs. This product is a sugar with the following Click modification, fluorination, glycosylation, and methylation. 2-N-Chloroacetyl-2-deoxy-D-glucosamine has CAS No. 1334320-67-0. The molecular weight of this compound is 514.25 g/mol. This product can be used in the synthesis of oligosaccharides and monosaccharides as well as saccharides, which are complex carbohydrates.</p>

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

<p>2-Deoxy-2-fluoro-D-fucose is a custom synthesis, which is a complex carbohydrate. It has CAS No. and polysaccharide modification and can be methylated, glycosylated, or fluorinated. The molecular weight of this product is high purity and it can be used as a sugar or carbohydrate. Click modification is possible with 2-deoxy-2 fluoro-D-fucose.</p>

<p>β-Estradiol 3-(β-D-glucuronide) 17-sulfate dipotassium is a synthetic, nonsteroidal estrogen with a high affinity for the human estrogen receptor. It is used in the treatment of various types of breast cancer and as hormone replacement therapy. β-Estradiol 3-(β-D-glucuronide) 17-sulfate dipotassium is a part of the drug class selective estrogen receptor modulators (SERMs). The compound has been shown to have antiestrogenic activity through its ability to compete with estradiol for binding to the estrogen receptor. This compound also has some antiandrogenic effects and can inhibit sex hormone binding globulin (SHBG), leading to increased levels of free testosterone in blood plasma.</p>

<p>D-Arabinose-5-phosphate is an intermediate in the pentose phosphate pathway. It is synthesized from D-xylulose-5-phosphate by xylitol dehydrogenase. D-Arabinose-5-phosphate inhibits the enzyme xylitol dehydrogenase, which converts xylulose to d-xylulose, and thus prevents the formation of 5-hydroxyisoxazole phosphate, a precursor to the synthesis of NADPH. In this way, it blocks the synthesis of NADPH, which is essential for aerobic metabolism. This inhibition leads to a decrease in ATP production and consequently cell death.</p>

<p>5-azido-5-deoxy-D-arabinose is a compound derived from Aquilaria sinensis that has various biological activities. It has been shown to modulate transmembrane conductance by interacting with fatty acid-binding proteins and divalent metal ions. Additionally, it can regulate the activity of potassium channels, which play a crucial role in cellular function. 5-azido-5-deoxy-D-arabinose is known for its reactive properties and can form covalent adducts with nucleophilic residues in proteins, affecting their structure and function. This compound has also been studied for its potential therapeutic applications, such as enhancing the delivery of iron sucrose through electrode-based systems or improving the bioavailability of drugs like ketorolac or creatine. Furthermore, 5-azido-5-deoxy-D-arabinose exhibits interesting carbohydrate chemistry, making it a valuable tool for carbohydrate synthesis and modification. Its diverse characteristics and unique properties make it an intriguing compound for further</p>

<p>Beta-rutinose is a potent kinase inhibitor that has shown anti-tumor activity in Chinese hamster ovary (CHO) cells. It inhibits the activity of cyclin-dependent kinases, which are essential for cell division and proliferation. Beta-rutinose has been shown to induce apoptosis in human cancer cells, making it a promising candidate for anticancer therapy. This compound is an analog of rutin, a flavonoid found in many plants, and has been shown to have potent anticancer effects in vitro and in vivo. Beta-rutinose inhibits the growth of cancer cells by blocking the activity of specific kinases involved in tumor progression, making it an attractive target for developing new cancer therapies. Additionally, this compound has been found to be effective at reducing protein levels associated with cancer cell growth and proliferation.</p>

<p>D-Galacturono-6,3-lactone is a fatty acid that is part of the glucuronolactone family and has been shown to have anti-obesity effects in vitro. D-Galacturono-6,3-lactone has been synthesized from sodium citrate and hydrochloric acid in the presence of magnesium salt, and the product was purified by crystallization. It has also been shown to inhibit aminotransferase activity and increase locomotor activity. D-Galacturono-6,3-lactone has a ph optimum of 4.5, which can be determined by an analytical method involving the measurement of hydrogen ion concentration.</p>

<p>N-Acetylmuramic acid 6-phosphate is a molecule that belongs to the class of compounds known as nucleotide phosphates. It is an intermediate in the biosynthesis of peptidoglycan, which is a major component of bacterial cell walls. N-Acetylmuramic acid 6-phosphate is synthesized from ATP and N-acetylmuramic acid by hydrolysis. The reaction mechanism for this transformation involves an imine intermediate, which can be formed through the action of two molecules of ATP and one molecule of N-acetylmuramic acid. This reaction is catalyzed by an enzyme called heterocyst. The enzyme kinetics for this transformation are influenced by many factors, including temperature, pH, and substrate concentration.</p>

<p>1,2,3,4-Tetra-O-acetyl-D-glucuronide methyl ester is a lactone that can be used as a precursor for the synthesis of various types of compounds. The chemical structure was determined by high-resolution x-ray diffraction to be a planar molecule with two conformations: one where the four acetyl groups are on different sides and another where they are all on the same side. The latter conformation is more stable due to the dihedral angle between the hydroxyl group and carbonyl group. This compound is an intermediate in synthesizing 2-(4'-hydroxybenzoyl)-1,2,3,4-tetra-O-acetyl-.alpha.-D-.beta.-D glucopyranoside methyl ester by reacting with 3-(3'-azido)benzaldehyde. The single crystal x-ray diffraction study revealed that this compound has a conformation</p>

<p>Methyl 4-C-[[(methylsulfonyl)oxy]methyl]-3-O-benzyl-1,2-di-O-acetyl 5-methanesulfonate D-erythro-pentofuranose is a methylated saccharide used in the synthesis of LNA amidites</p>

<p>D-Glucose-6-phosphate barium salt is a custom synthesis that is prepared by modification of D-glucose with phosphoric acid, fluorination, methylation, and monosaccharide. This compound is a synthetic carbohydrate that belongs to the category of oligosaccharides and polysaccharides. It has a molecular weight of 583.12 g/mol and an empirical formula of C7H8O10P2Ba. The CAS number for this compound is 150400-00-3.</p>

<p>2,5-Anhydro-1,3-O-isopropylidene-6-O-trityl-D-glucitol is a complex carbohydrate that is synthesized by the modification of glucose. This product has been modified with methylation and glycosylation.<br>2,5-Anhydro-1,3-O-isopropylidene-6-O-trityl--D--glucitol is a white powder that is soluble in water and ethanol. <br>It can be used for fluoroquinolone resistance studies, which are important for developing new antibiotics to combat bacterial infections.</p>

<p>3,6’-Disinapoyl sucrose is a saponin that has been shown to be neuroprotective and antidepressant. It is also able to increase the absorption of drugs in the gastrointestinal tract. 3,6’-Disinapoyl sucrose was found to have neurotrophic effects on neurons and inhibit glutamate-induced excitotoxicity. 3,6’-Disinapoyl sucrose has been shown to inhibit the mineralocorticoid receptor in vitro and may be useful as an antihypertensive agent. 3,6’-Disinapoyl sucrose can be used for clinical use in the treatment of depression and other neurological disorders such as Alzheimer's disease.</p>

<p>Bacillithiol (BSH) is a low molecular weight thiol molecule produced in Bacilli, which is also found in Firmicutes bacteria. It plays an important role in maintaining the balance of reactive oxygen species within cells and detoxifying certain harmful compounds. It is the α-anomeric glycoside of L-cysteinyl-D-glucosamine with L-malic acid and it seems to have antioxidant properties. Bacillithiol plays an important role in bacterial redox homeostasis and plays an important role in the detoxification of electrophiles as it is a cofactor for FosB (thiol transferase). <br>This is the salt form (trifluoroacetic acid salt, TFA) of Bacillithiol.</p>

<p>1,2,3,4,6-Penta-O-acetyl-D-galactopyranose is an analog of the natural pentoses that binds to the mitochondrial membrane and inhibits the production of pro-inflammatory cytokines. This drug has been shown to inhibit the binding of lysophosphatidic acid (LPA) to its receptor by substituting for LPA in this binding site. 1,2,3,4,6-Penta-O-acetyl-D-galactopyranose also inhibits the expression of proinflammatory cytokines such as interleukin 6 (IL6) and IL1β in a dose dependent manner. This drug is also capable of inhibiting phosphotungstic acid from binding to a monolayer surface and can be used as a glycopolymer for cell culture. It has been shown that 1,2,3,4,6-Penta-O-acetyl</p>

<p>Pseudaminic acid is a sugar molecule that is found in the cell walls of bacteria, where it provides structural support. It is synthesized enzymatically by transferring the terminal hydroxyl group from glucose-1-phosphate to glycerol-3-phosphate. Pseudaminic acid can be chemoenzymatically synthesized in a scalable manner and has been shown to inhibit the growth of infectious bacteria in biological studies. Structural studies have revealed that pseudaminic acid contains an hydroxyl group and two glycosidic bonds, which are formed between the carbon atom at position C2 and C6 of glucose. This molecule also has an ester linkage between C1 and C2 of mannose. Pseudaminic acid is biosynthesized through a series of reactions that involve phosphorylation, dephosphorylation, and oxidation. This molecule also participates in protein glycosylation as well as water molecules that hydrogen bond</p>

<p>1,2,3,4-Tetra-O-benzyl-6-O-trityl-a-D-mannopyranose is a methylated form of mannopyranose. It can be custom synthesized and modified with various functional groups to produce a wide range of saccharide derivatives and oligosaccharides. The 1,2,3,4-tetra-O-benzyl group is commonly used for glycosylation reactions because it can be easily removed by acid hydrolysis. The methylation of the sugar molecule also increases its stability and prevents further reactions from occurring. This product is available in high purity and has been fluorinated on one or more hydroxyl groups to make it resistant to hydrolysis.</p>

<p>Methyl 2-deoxy-5-O-toluoyl-L-ribofuranoside is a high purity, custom synthesis, methylated, Glycosylation and Oligosaccharide. It has CAS No. 676598-19-9 and is Glycosylated and Methylated. This complex carbohydrate is a synthetic, monosaccharide or saccharide that can be modified with fluorination, Click modification or glycosylation.</p>

<p>Ferulic acid acyl-b-D-glucoside is a flavonoid compound that has been shown to have antioxidant properties. It is found in plants and can be synthesized by the enzyme phenylalanine ammonia-lyase. Ferulic acid acyl-b-D-glucoside is insoluble in water, but soluble in organic solvents such as ethanol and acetone. The chemical composition of ferulic acid acyl-b-D-glucoside is not well understood, but it has been shown to contain chalcone, chlorogenic acids, aldehydes, celosianin, and betanidin.</p>

<p>Lectins are carbohydrate-binding proteins that can be classified into different types based on their specificities for glycan structures. One of the most common types is the N-acetyl-D-glucosamine (NAG) lectin, which binds to oligomers of NAG and related sugars. Lectins are used to activate cells and induce cell death. The dodecyl NAG lectin has been shown to bind to glucocerebrosides in a reductively irreversible manner and has been used as a model for such interactions. This lectin is also inexpensively produced from a synthetic benzylidene acetal, which can be made from commercially available materials. It has been shown that this lectin binds to polyacrylamide gels in an SDS-polyacrylamide gel electrophoresis, with a pH optimum at 7.0 and an amino acid composition that includes glutamic acid, glutamine, asparagine, ser</p>

<p>2-Acetamido-1,3,6-tri-O-acetyl-2,4-dideoxy-4-fluoro-D-glucopyranose is a high purity synthetic glycosylate with a custom synthesis. It is an oligosaccharide that has been modified for fluorination and methylation. This product is used as an intermediate in the production of complex carbohydrates.</p>