Monosaccharides

<p>Zearalenone 14-glucuronide is a custom synthesis. It is a complex carbohydrate, which is an oligosaccharide that has been modified by methylation and glycosylation. Zearalenone 14-glucuronide is a polysaccharide with a saccharide backbone and various modifications at the ends of the sugar chains. This product has been fluorinated to provide high purity.</p>

<p>5-(Galactosylhydroxy)-L-lysine is a metabolite that is found in human urine and serum. It is a basic compound with a hydroxyl group, which can be used as a biomarker for metabolic disorders and pharmacological treatments. 5-(Galactosylhydroxy)-L-lysine has been shown to have the potential to be used as a treatment for protein synthesis disorders. The mechanism of this reaction is still unknown, but it has been found that the optimum pH for this reaction is between 7 and 8.</p>

<p>Methyl 2-deoxy-2-fluoro-b-D-glucopyranoside is a synthetic glycosylation product that is prepared by monosaccharide and polysaccharide modification. This fluorinated sugar has high purity and is easy to handle. It can be used in the synthesis of oligosaccharides, sugar chains, and other complex carbohydrate molecules. The CAS number for Methyl 2-deoxy-2-fluoro-b-D-glucopyranoside is 39110–58–2.</p>

<p>Methyl 3,5-di-O-(2,4-dichlorobenzyl)-2-keto-a-D-ribofuranoside is a synthetic carbohydrate that can be used as a building block in the synthesis of complex carbohydrates. This product is custom synthesized and has high purity. It is also glycosylated and methylated.</p>

<p>Suberoylanilide hydroxamic acid b-D-glucuronide (SAHA) is a histone deacetylase inhibitor that is used in the treatment of colorectal adenocarcinoma. It is orally administered and can cross the blood-brain barrier to inhibit HDACs in human liver cells. SAHA has been shown to be effective against a number of cancer cell lines, including colon, prostate, breast, lung, and leukemia cell lines. SAHA has also been shown to have clinical benefits in various cancers and has been found to be safe at doses up to 1g/day when given for 24 months. The most common side effects are thrombocytopenia and anorexia.</p>

<p>cis-Zeatin-o-glucoside is a naturally occurring cytokinin glycoside, which is a derivative of cis-zeatin conjugated with a glucose molecule. It is synthesized in various plant tissues and acts as an important signaling compound within the plant's hormonal network. The mode of action involves the regulation of cell division and differentiation, primarily through modulating the expression of specific genes and interacting with cytokinin receptors. This glycosylation potentially alters the transport, stability, and activity of the cytokinin, influencing its overall biological effect.</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>(-)-2,3-O-Isopropylidene-D-threitol is a chiral compound with two stereoisomers. It is a crystalline solid that melts at 71°C and has a population of 50%. (-)-2,3-O-Isopropylidene-D-threitol is an important intermediate for the synthesis of polyethers with chiral centers. The catalytic asymmetric synthesis of (-)-2,3-O-isopropylidene-D-threitol is achieved by alkylation of (+)-2,3-(dimethoxyphosphinyl)propane with isopropanol. This reaction can be used to produce polyethers with chiral centers in high yields and enantioselectivity.</p>

<p>Methyl a-L-arabinofuranoside is a microbial feed additive that is used to improve the quality of ruminal cellulose. This product has been shown to inhibit the activity of esterases and polysaccharides, which would otherwise break down cellulose so it can be digested by bacteria in the rumen. This supplement also inhibits microbial growth and has been shown to be an effective treatment for infectious diseases. Methyl a-L-arabinofuranoside is detectable in urine, feces, and milk one day after administration. It is broken down by uronic acid esterases into arabinose and methyl alcohol.</p>

<p>2,3,5-Tri-O-benzyl-D-arabinofuranose is a phosphorane that has been synthesised by the reaction of 2,3,5-trihydroxypentanoic acid and benzaldehyde. The synthesis of this compound involves the use of a stereoselective process to produce the desired product. This compound is able to inhibit both bacterial and fungal growth in vitro. Inhibition of bacterial growth is due to its ability to disrupt the synthesis of proteins and nucleic acids while the inhibition of fungal growth is due to its ability to interfere with chitin production.</p>

<p>Methyl 6-O-p-toluenesulfonyl-a-D-glucopyranoside is a custom synthesis. It is an oligosaccharide and polysaccharide that can be modified with methylation and glycosylation. The carbohydrate has a CAS number of 6619-09-6, and the purity is high. This product has been fluorinated for synthetic purposes.</p>

<p>A sugar phosphate</p>

<p>1,2:4,5-Di-O-isopropylidene-b-D-erythro-2,3-hexodiulo-2,6-pyranose is an acidic compound that is a constituent of the ginseng plant. It has been shown to have biochemical properties as well as bioactivities. It can be synthesized in vivo from the amino acid L-lysine by the enzyme diammonium glyoxalate reductase. The compound has two chiral centers and four stereogenic centers. It is a trisubstituted diastereomer with oxygenated ring opening and chemical structures consisting of a pyranose ring and an ethylene glycol moiety.</p>

<p>GDP-6-deoxy-a-D-talose is a synthetic oligosaccharide that can be modified to include fluorine, methylation, or other modifications. It has been synthesized for use in the modification of saccharides and complex carbohydrates. GDP-6-deoxy-a-D-talose is soluble in water and has a molecular weight of 519.</p>

<p>6-O-Hydroxyethyl-D-glucose (6OHEDG) is a homologue of glucose that has been synthesized by reacting paraformaldehyde with ethylene in the presence of a glucofuranose. It is used as a solute for uptake studies, hydrolyzates for ion-exchanges, and glucoses for preparative chromatographic techniques. 6OHEDG is also used as an analog to glucose in polyethylene glycols and anhydroglucoses.</p>

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

<p>2-Deoxy-2-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-L-glucose is a fluorophore that is used in biological imaging. It has been shown to have tumor vasculature targeting properties and can be used to diagnose cancer. The optimal reaction for 2DG is aerobic glycolysis, which occurs when the glucose concentration is high enough. This compound can be used as a carbon source for mammalian cells and has been shown to inhibit the growth of cells from tumors.</p>

<p>2-Acetamido-2-deoxy-b-D-glucopyranosylnitromethane is a natural product that can be found in the extract of gladiolus. It has been shown to have antimalarial activity against Plasmodium falciparum and other species. 2-Acetamido-2-deoxy-b-D-glucopyranosylnitromethane inhibits the growth of bacteria by binding to the 50S ribosomal subunit, preventing transcription and replication. The high frequency of human activity has been shown using a patch clamp technique on human erythrocytes. This active form is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.</p>

<p>D-Glycero-D-talo-heptose is a fluorescent probe used in fluorescence spectroscopy. It has been shown to bind to mannose and lyxose, which are carbohydrates with a structural similarity to D-glycero-D-manno-heptose. D-Glycero-D-talo-heptose undergoes dose dependent emission of light when excited at 488 nm. In addition, this compound can be used as a marker for liquid chromatography. The fluorescence of D -glycero -D -talo -heptose is quenched by the presence of ribose.</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>