Monosacáridos

<p>1,3,4,6-Tetra-O-acetyl-2-O-trifluoromethanesulfonyl-b-D-mannopyranose is a chemical compound that belongs to the group of fatty acids. It is a product of chemical reactions and has been shown to be able to react with positrons in an organic solution. This compound can also react with potassium ions in water vapor. The reaction solution is suitable for testing samples and cell culture.</p>

<p>2-Deoxy-D-ribose 5-phosphate sodium salt is a mutant of ribose 5-phosphate. It is an intermediate in the pentose phosphate pathway, which generates ribose 5-phosphate and NADPH. The 2nd step of this pathway is catalyzed by deacetylase, which converts acetaldehyde to acetyl CoA. 2-deoxy-D-ribose 5-phosphate sodium salt is also an oxidant that can react with hydrogen peroxide to form hydroxyl radicals. This intermediate has been shown to inhibit the growth of E. coli by causing mutations in the DNA and protein synthesis machinery, as well as by catalase activation.</p>

<p>2-Azido-2-deoxy-D-galactose is a disaccharide that is synthesized by the enzymatic addition of galactose to 2-azido-2-deoxyglucose. It has been shown to be antigenic in the test tube and is reactive with hydroxy groups. 2-Azido-2-deoxygalactose can be glycosylated by glycopeptides, which are glycoproteins containing one or more oligosaccharide chains covalently linked to a protein core. The hydrophilic nature of this sugar makes it an ideal candidate for conjugation with hydrophobic drugs such as antibiotics. This disaccharide was used in the synthesis of glycoconjugates, which are carbohydrate molecules attached to proteins or lipids, and can be found in bacteria such as Corynebacterium glutamicum. 2-Azido-2-deoxygalactose</p>

<p>2,5-Anhydro-D-glucitol is a sugar alcohol that is found naturally in the human body. It can be produced from D-glucose by the enzyme aldose reductase. This reaction involves an initial dehydration of D-glucose to form 2,5-anhydro-D-glucose, followed by a nucleophilic attack on the hydroxyl group of 2,5-anhydro-D-glucose by the phosphate group of ATP to form 2,5-anhydro-D-glucitol and ADP. The reaction mechanism for this process has been studied using kinetic and model studies. It has also been shown that metal ions are required for cationic polymerization reactions. A solid catalyst was used in this study because it could be easily removed after completion of the reaction. The 2,5-anhydro form of D-glucitol can undergo dehydration reactions to yield</p>

<p>This is a custom synthesis of (5R, 6R, 7R, 8S) -5, 7-dihydroxy-8- (hydroxymethyl) -1-azabicyclo[4.2.0]octan-2-one. This compound has been fluorinated and methylated and has a monosaccharide modification.</p>

<p>Phenyl 4,6-O-benzylidene-2-O-levulinoyl-3-O-(2-naphthylmethyl)-b-D-thioglucopyranoside is a fluorinated monosaccharide. It can be synthesized in a custom synthesis and is available with high purity. This product is an oligosaccharide, which has glycosylation and polysaccharide properties. Phenyl 4,6-O-benzylidene-2-O-levulinoyl-3-O-(2-naphthylmethyl)-b-D -thioglucopyranoside is also a complex carbohydrate that has been modified by methylation and acetalization.</p>

<p>D-Xylulose 5-phosphate sodium is a phosphorylated sugar derivative, which is a crucial intermediate in the pentose phosphate pathway, a metabolic pathway parallel to glycolysis. It is naturally sourced from biochemical processes within organisms where it plays a pivotal role in carbohydrate metabolism.The mode of action involves its function as a substrate in the non-oxidative phase of the pentose phosphate pathway, where it facilitates the interconversion of sugars necessary for nucleotide and amino acid biosynthesis. This intermediary step is vital for the production of ribose-5-phosphate and NADPH, which are essential for anabolic reactions and antioxidant defense mechanisms.D-Xylulose 5-phosphate sodium is predominantly used in biochemical research to study metabolic pathways. It helps researchers investigate cellular processes, understand disease mechanisms where metabolism is disrupted, and explore metabolic engineering applications. By examining its role and transformations, scientists gain insights into energy production, redox balance, and cellular growth, providing foundational knowledge crucial for the development of therapies targeting metabolic disorders and cancer.</p>

<p>D-Mannono-1,5-lactone is a custom synthesis. It is fluorinated to give 1,5-difluoro-D-mannono-1,4,6-lactone. The methylation of the C2 hydroxyl group and the C3 keto group gives 1,5-difluoro-D-mannono-1,4,6-(methylenedioxy)lactone. Click modification of this product with azide or acetylene gives 1,5-[(azido)-(acetylenyl)] D-mannono lactone or 1,5-[(acetylene)-(azido)] D manno lactone respectively. Monosaccharides can be synthesized from these products by glycosylation with a sugar donor. Polysaccharides can be synthesized from these products by glycosylation with a sugar donor and subsequent glycosidic linkage via an olig</p>

<p>D-Galactosamine is a glycosaminoglycan (GAG) that is found in the mammalian cell. N-Thioglycolyl-D-galactosamine is a synthetic analog of D-galactosamine that was developed to study the biosynthesis of GAGs and glycoconjugates in cells. This molecule can be activated by hematopoietic cells, which leads to an increase in o-glycosylation and galnac synthesis.</p>

<p>2-Azido-2-deoxy-D-glucose is the azido analogue of D-glucosamine and may be used as a metabolic chemical reporter by direct labelling of glycans. The azide group is used to link to a fluorescent marker, enabling secondary visualisation and identification of glycoproteins. The azide moiety of 2-azido-2-deoxy-D-glucose has been used to form triazoles via a 1,3-dipolar cycloaddition reaction in the synthesis of molecules with improved solubility used to inhibit p38a MAPK for anti-inflammation.</p>

<p>2,3-Di-O-benzyl-4-deoxy--L-fucose is a methylated derivative of the fucose monosaccharide. It is synthesized through a click reaction that involves the use of an azide group on the sugar and an alkyne group on a thiol reagent. The synthesis utilizes one step, yielding 2,3-Di-O-benzyl-4-deoxy--L-fucose in high purity with low residual starting material. The product has been modified for glycosylation and can be used in oligosaccharides or polysaccharides.</p>

<p>Diethylgalactarate is a polymer that is solid at room temperature. It has a yield value of 10%. Diethylgalactarate is soluble in organic solvents, but insoluble in water. This polymer has been shown to have good thermal stability and microstructure when used as a monomer with other polymers. Diethylgalactarate has also been shown to have high permeability, which makes it an ideal candidate for use in drug delivery systems.</p>

<p>This is a high purity, custom synthesis of (3S,5S) -1-Nonyl-3, 4, 5- piperidinetriol. The starting material is an oligosaccharide and the product has been synthesized by a click modification reaction. It is a complex carbohydrate that has been fluorinated at the 3 position of the sugar moiety. This compound has been glycosylated and methylated with a high degree of purity.</p>

<p>2-(Piperidine-2,6-dione-4-yl)-acetic acid is a modification of an oligosaccharide. It is a monosaccharide that has been methylated and glycosylated. 2-(Piperidine-2,6-dione-4-yl)-acetic acid can be used as a building block for the synthesis of complex carbohydrates. This compound has been synthesized by fluorination and saccharide.</p>

<p>UDP-N-Lev-galactosamine is a glycosylation agent that is used in the synthesis of complex carbohydrates, such as methylated and fluorinated saccharides. It can be used to modify saccharides, oligosaccharides, and sugars. This compound can also be used for the synthesis of monosaccharides. UDP-N-Lev-galactosamine is a custom synthesis that has been shown to have a high purity.</p>

<p>D-Talitol-1,6-diphosphate is a modified sugar. It is an oligosaccharide and polysaccharide composed of D-talitol and 1,6-diphosphate. This product can be used in the synthesis of complex carbohydrates or as a reagent for fluorination reactions. D-Talitol phosphates are also used to modify monosaccharides by methylation, click modification, or other modifications.</p>

<p>4,6-Dichloro-4,6-dideoxy-D-galactose (4,6DDG) is a chlorinated sugar that is used as a precursor for the synthesis of glycosides. It has been shown to react with cellulose to form 4,6-dichloro-4,6-dideoxycellulose. Chlorination of 4,6DDG at the hydroxyl group leads to the formation of 4,6-dichloro-4,6-dideoxyhydroxyl chloride (4,6DDH). The chlorination process can be done in two ways: nonreducing and reducing. The nonreducing chlorination process occurs by reacting 4,6DDG with chlorine and dimethylformamide. The reducing chlorination process occurs by reacting 4,6DDG with hydrogen chloride and sodium borohydride or lithium aluminum hydride. An excess of hydrogen chloride</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>a-D-Galacturonic acid 1-phosphate is a component of the polygalacturonate skeleton. It is an intermediate in the biosynthesis of d-galacturonic acid and galacturonic acid. This compound is also involved in cellular growth, as it is a precursor for uronic acids. The enzyme catalyzing the conversion of a-D-galacturonic acid 1-phosphate to uronic acid has been purified from Phaseolus vulgaris. It has been shown that this enzyme can be inhibited by phosphatase inhibitors such as pyridoxal phosphate, and that it can be activated by nucleotide analogs such as adenosine 5'-diphosphate (ADP) or cytidine 5'-triphosphate (CTP).</p>

<p>2-Deoxy-2-fluoro-D-ribofuranose is a dinucleoside that stabilizes the ribose moiety of uridine and guanosine, which are important for bacterial DNA replication. 2-Deoxy-2-fluoro-D-ribofuranose binds to the ribosomal enzyme Uridylate Kinase and inhibits its activity, thereby preventing the synthesis of nucleotide precursors. This product has been shown to be effective against bacteria such as Escherichia coli and Staphylococcus aureus. The hydration properties of 2-deoxy -2 fluorodeoxy D ribofuranose make it an ideal ligand for binding to enzymes in order to inhibit their function. The nature of this compound also makes it an ideal candidate for thermodynamic studies.</p>

<p>4-Deoxy-4-fluoro-D-mannose is a sugar that is an analog of 3-deoxy-3-fluoro-d-mannose. It is synthesized by the transfer of a 6-hydroxyl group from 6,6'-dideoxyadenosine to the C6 hydroxyl group of 3,6'-dihexadecylthio adenosine. 4,4'-Difluoro D-mannose is then obtained by hydrolysis and decarboxylation. This process can be catalyzed by enzyme catalysis with phosphofructokinase or hexokinase. 4,4'-Difluoro D mannose has been used in biochemical studies as an analog for 6,6'-dideoxydaunosine. It has also been used as a substrate for virus glycosylation and protein glycosylation in living cells. In addition, it has been shown to inhibit</p>

<p>N,O-Didesmethyl venlafaxine D-glucuronide is a custom synthesis, complex carbohydrate. It is an Oligosaccharide with CAS No. that is Polysaccharide and Modification. It has Methylation and Glycosylation. The saccharide in the molecule is a sugar or Carbohydrate and sugar. The high purity of the product makes it Fluorination and Synthetic.</p>

<p>Raloxifene-4'-D-glucuronide D4 lithium salt is a synthetic glycosylate drug, which belongs to the group of anti-estrogens. Raloxifene-4'-D-glucuronide D4 lithium salt is used for the treatment of postmenopausal osteoporosis and prevention of osteoporotic fractures in women with intact uterus. It has been shown to inhibit bone resorption, increase bone mineral density and reduce the incidence of vertebral fractures in postmenopausal women. Raloxifene-4'-D-glucuronide D4 lithium salt can be synthesized using a click chemistry reaction which involves the addition of an azide to an alkyne followed by copper catalysis and subsequent reduction with sodium borohydride. Synthesis of this compound can be achieved without any purification steps due to its high purity.</p>

<p>2,5-Anhydro-L-iditol is a kinetic product of transglycosylation. It has been shown to be stereoselective and can be used as an acid catalyst in the synthesis of furanic compounds. 2,5-Anhydro-L-iditol is also a nucleophilic reagent that can participate in reactions with hydrogen chloride and tetraose chloride. This compound is useful for the production of polyols and glycols via dehydration reactions. 2,5-Anhydro-L-iditol has been used in carbohydrate chemistry techniques.</p>

<p>1-Deoxy-1-nitro-L-mannitol is an irreversible inhibitor of the enzyme mannitol dehydrogenase. It also inhibits other enzymes, such as L-arabinose isomerase and L-azide amidohydrolase, which are involved in the biosynthesis of arabinose and azide. The synthesis of 1-deoxy-1 nitro mannitol can be achieved through a one step reaction with hydroxide and l-arabinose (or l-xylose) in the presence of carbonate or sulfate. This product can be used in syntheses of amphoteric compounds.</p>

<p>1,2,3,4-Tetra-O-acetyl-6-O-(tert-butyldiphenylsilyl)-a-D-mannopyranose is a custom synthesis that is a complex carbohydrate. It is an Oligosaccharide that is Polysaccharide and can be modified with Methylation and Glycosylation. It has a saccharide with a CAS No. 815589-29-8 and has been fluorinated. This product has high purity and can be synthesized to order.</p>

<p>5-Amino-3-β-D-ribofuranosylthiazolo[4,5-d]pyrimidin-2,7(3H,6H)-dione (ATZ) is a prodrug that is converted to the active drug ATZ. ATZ has been shown to be effective against hepatitis C virus in vitro assays and in vivo in animal models. It inhibits viral replication by inhibiting the protein synthesis of the virus and its ability to replicate. ATZ also has been shown to be effective against infectious diseases such as herpes simplex virus, inflammatory diseases such as rheumatoid arthritis, and cancer. The drug is an oral prodrug that must be activated by intestinal bacteria before it can be absorbed into the bloodstream. It is chemically stable and does not undergo significant metabolism after being absorbed into the body.</p>

<p>Isomaltol is a sugar alcohol that is used as a food additive. It is a white, crystalline powder that is soluble in water and has an intense sweet taste. Isomaltol is produced by hydrogenating the reducing ends of sucrose to form maltose, which then undergoes hydrolysis to form maltitol. Isomaltol can be used as a replacement for sugar in foods and drinks. Isomaltol has been shown to inhibit tyrosinase activity, which may be beneficial for skin care products. It also has antimicrobial properties due to its ability to react with aluminium ions.</p>

<p>Dodecyl maltoside (DDM) is a non-ionic detergent that consists of a hydrophilic maltose head and a hydrophobic long chain alkyl tail. It has a relatively low critical micelle concentration of 0.17 mM and is considered a gentle but powerful detergent. DDM is often the best tool for solubilising/crystallising membrane proteins. Membrane proteins usually have α-helical structures that are easily destroyed when the protein is released from its membrane environment. DDM can often preserve these structures during the solubilisation. In addition, membrane proteins can often be renatured when isolated with DDM.</p>

<p>2,4-Methanoglutamic acid is an amino acid that has been shown to have neuroprotective effects in animal models of excitotoxicity. It has been shown to reduce neuronal death at low concentrations and inhibit the uptake of glutamate into the brain cells. 2,4-Methanoglutamic acid binds to calcium ions and prevents the release of calcium from intracellular stores, thereby protecting against neuronal death. This compound has also been shown to be toxic in mammalian cell culture, but it is not yet known if this toxicity will occur in humans.</p>

<p>Emodin is a natural product that can be extracted from the rhizome of Curcuma aromatica, a chinese herb. It has been shown to have neuroprotective effects in animal studies and has been used as an adjuvant in the treatment of cervical cancer. Emodin also inhibits the replication of human immunodeficiency virus type 1 (HIV-1) and herpes simplex virus type 1 (HSV-1). Emodin is also active against microbial infection, including bacterial infections, such as those caused by Staphylococcus aureus, and viral infections, such as influenza A virus. The main mechanism of action of emodin is its inhibition of DNA synthesis by binding to viral dna or bacterial rna polymerase. Emodin has also been found to inhibit protein synthesis by binding to ribosomes. This drug binds to urea nitrogen molecules in bacteria and disrupts their growth by inhibiting protein synthesis.</p>

<p>Galactose from plant origin, animal free production</p>

<p>3,4-Di-O-acetyl-L-fucal is a phosphate derivative that is synthetically derived from ethyl diazoacetate. It has cytotoxic properties and is readily activated by phosphorylation to form the active form. 3,4-Di-O-acetyl-L-fucal has been shown to be effective against leukemia cells in vitro and may be useful as an adjuvant treatment for lymphocytic leukemia. 3,4-Di-O-acetyl-L-fucal also inhibits the growth of staphylococci in vitro, but it is not active against other bacteria such as Escherichia coli or Pseudomonas aeruginosa. The enantiomer of 3,4 Di O acetyl - L - fucal is inactive because it cannot be phosphorylated.</p>

<p>4-Deoxy-4-fluoro-D-glucosamine is a carbohydrate that is used as an inhibitor of the enzyme l1210. This enzyme is required for the biosynthesis of the glycoprotein on the surface of some types of leukemia cells. 4-Deoxy-4-fluoro-D-glucosamine has been shown to be effective in inhibiting leukemia cell growth, and in some cases it has been shown to induce tumor regression. It inhibits protein synthesis by binding to the enzymes responsible for this process.</p>

<p>4,6-O-Benzylidene-D-galactose is an anomer of D-galactose. It is a lectin that has been shown to inhibit the binding of amyloid beta to the cerebroside in the brain tissue. This activity may be due to its ability to form an amide bond with galactose, which is present in amyloid beta. 4,6-O-Benzylidene-D-galactose also has a coronary heart disease prevention effect and can help reduce cholesterol levels. Furthermore, it has been found to have anti-cancer properties and can help prevent the growth of cancerous cells by inhibiting protein synthesis. In addition, 4,6-O-Benzylidene-D-galactose can be used as a cationic surfactant or detergent composition for cleaning or treating surfaces.</p>

<p>Sedoheptulose-1-phosphate is a ribosomal metabolite that is produced by marine microorganisms. It is catabolized by sedoheptulose-7-phosphate kinase and converted to the pentose phosphate pathway. The metabolic profile of sedoheptulose-1-phosphate has been shown to be altered in response to environmental stress, such as changes in pH, oxygen levels, and temperature. Sedoheptulose-1-phosphate has also been shown to have structural properties similar to those of ATP and ADP, which may make it an important target for the development of antibiotics.</p>

<p>Epilactose is a monosaccharide with biological properties. It is the 2-epimer of lactulose, and can be synthesized from cellobiose by epimerase. Epilactose has been shown to have beneficial effects on bowel disease in mice, which may be related to its ability to stimulate intestinal motility and improve the intestinal microflora. Epilactose has also been shown to have anti-inflammatory activity in rats with colitis. Epilactose can be used as a structural probe for oligosaccharides, due to its ability to form hydrogen bonds with sugars. In addition, epilactose has been found in marine microalgae such as Chlorella pyrenoidosa, but not in higher plants or animals.</p>

<p>The aldopentose L-arabinose (Ara) is, after xylose, the second most abundant pentose in nature. It is found in plant cell walls as a component of polysaccharides, including: hemicelluloses, pectin, arabinogalactan-protein complexes and in exudate plant gums, such as: Gum Arabic (Fehér, 2018). L-arabinose is an important component of the mycobacterial cell wall and is involved in the synthesis of arabinogalactan and lipoarabinomannan, which suggests that it can modulate cell wall permeability and drug resistance. Mycobacterium smegmatis is a useful tool for research into Mycobacteria due to it being a "fast grower" and non-pathogenic (Zhou, 2019).</p>

<p>D-Arabitol (or D-Arabinitol) is the reduced alcohol form of Arabinose. Arabitol is a commonly used food supplement, it is comparably sweet to sucrose but the oral flora cannot metabolize Arabitol, and hence protects from caries. Arabitol plays also an important role in energy controlled diets since it is absorbed slowly by the human digestive tract and has a low caloric content. The differential metabolism of the Arabitol D- and L-forms suggested its use in microbiological diagnostics (Bernard, E.M. et al. 1981) and became a routine urine laboratory test: L-Arabitol is metabolized by a variety of different bacteria and fungi utilizing an arabitol dehydrogenase enzyme. Therefore, it serves as a biomarker for, e.g., invasive candidiasis, since an infection results in an elevated urine D-Arabitol/L-Arabitol (DA/LA) ratio. Cymit Quimica offers both isomers in research grade: D-Arabitol (A-8270) and L-Arabitol (A-8280).</p>

<p>Used to differentiate bacteria on the basis of carbohydrate fermentation abilities.</p>

<p>Donor for Koenigs-Knorr type galactosylation and other anomeric substitutions</p>

<p>High purity grade.  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.Due to its integral role in the formation of DNA, 2-Deoxy-D-ribose is critical in studies of genetic expression, DNA repair mechanisms, and the synthesis of nucleotides. Researchers utilize it extensively in molecular biology and biochemistry to understand cell replication and gene function, and it serves as a standard in research pertaining to oxidative stress, where its degradation may indicate the presence of reactive oxygen species. Additionally, it is involved in the development of various pharmacological agents, particularly those targeting cancer and viral infections, where the synthesis and function of DNA are pivotal aspects of pathogenesis and treatment response.</p>

<p>3,5-Dideoxy-N-(1-hexyl)-3,5-imino-D-xylopentitol is a synthetic monosaccharide that is used in the production of complex carbohydrates. It can be modified with fluorination and methylation to produce 3,5-dideoxy-N-(1-hexyl)-3,5-[(2-[(2,6-difluoro phenoxy)methyl]phenyl]imino)D-xylopentitol. The compound has been shown to have antiviral properties and has been used in the synthesis of glycosaminoglycans.</p>

<p>N-Acetyl-D-galactosamine-PAP-HSA is a complex carbohydrate that consists of a sugar, an acetyl group and a phosphate. This product is available in custom synthesis and modification. N-Acetyl-D-galactosamine-PAP-HSA can be used for the treatment of cancer, diabetes, liver disease, kidney disease and other diseases. It has been modified with fluorine groups to create new derivatives with improved properties.</p>

<p>3-C-Methyl-1-deoxy-psicose is a sugar that is used in the synthesis of complex carbohydrates. This synthetic sugar is synthesized by the click modification of 3,4-dihydroxybenzaldehyde with 1,2,3,4-tetraacetylated benzyl chloride. The compound has a molecular weight of 228.22 and an empirical formula of C6H8O6F2. It's CAS number is 52714-32-0 and it's Oligosaccharide number is 976.</p>

<p>L-Glucose is a monosaccharide that belongs to the group of carbohydrates. L-Glucose is an important energy source for living organisms and plays a role in many metabolic pathways, including glycolysis and gluconeogenesis, as well as cell signaling. It is also an essential component of DNA and RNA. L-Glucose has been shown to have effects on brain functions such as memory and learning ability, which may be due to its ability to signal neurons. L-Glucose can be used in model systems to study the effects of diabetes on cells and has been shown to have pluripotent effects on cells. In addition, this molecule has been shown to inhibit the growth of bacteria by binding to the enzyme polysaccharide kinase and reducing its activity. This inhibition leads to decreased synthesis of polysaccharides (e.g., glycogen) that are necessary for cell division.</p>

<p>Corn Cob Syrup is a custom synthesis of polysaccharides, which are complex carbohydrates. This syrup is made from corn cobs and has been modified with fluorine and methyl groups. The monosaccharides in this syrup have been modified with a click modification and the oligosaccharides have been modified with glycosylation. This product contains sugar that has been modified by glycosylation.</p>

<p>1,2-O-Isopropylidene-b-L-arabinofuranose is a custom synthesis. It is modified by fluorination, methylation, and monosaccharide synthesis. This product can be used in the creation of oligosaccharides and saccharides. 1,2-O-Isopropylidene-b-L-arabinofuranose is a carbohydrate that has been glycosylated and polysaccharided with other sugars to form complex carbohydrates.</p>

<p>Substrate for UDP-3-O-acyl-N-acetylglucosamine deacetylase (LpxC)</p>

<p>3-Epicasuarine is an Oligosaccharide, which is a carbohydrate with a low molecular weight. It has two monosaccharides, which are the structural units of carbohydrates. 3-Epicasuarine is a glycosylation product of sucrose and glycine and has been fluorinated at the 8-position. The chemical formula for 3-Epicasuarine is C6H14FO4S2. This compound can be custom synthesized to meet your specifications or it can be purchased from us at a reasonable price.<br>A variety of modifications are available including methylation, click chemistry, and modification with saccharride residues such as maltose or glucose.<br>3-Epicasuarine may be used in the synthesis of oligosaccharides or as an intermediate in the synthesis of complex carbohydrates. It has been shown to have high purity and can be synthesized at any desired purity level.</p>