Monosaccharides

<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>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>

<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>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-Deoxy-2,2-difluoro-D-erythro-pentonic acid gamma-lactone is a modification of the natural pentose sugar erythrose. It is a white crystalline powder that can be used for the synthesis of oligosaccharides, polysaccharides, and other complex carbohydrates. 2DFPGL can be found in various glycosylation and methylation reactions in the synthesis of saccharides. It has been shown to act as a competitive inhibitor of glucose uptake by cells.</p>

<p>A sugar phosphate</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>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>Succinyl activated n-acetylglucosamine.</p>

<p>2-Acetamido-6-azido-2,6-dideoxy-D-glucopyranose is a synthetic compound with an azide functional handle, so set up for click chemistry</p>

<p>2-Deoxy-L-xylose is a sugar that is produced by the reduction of 2-deoxy-d-galactose. It has been shown to be an acceptor in enzymatic reactions, such as those catalyzed by alcohol dehydrogenase and sulfoxide reductase. 2-Deoxy-L-xylose has been shown to have antibacterial properties against some strains of bacteria, including typhimurium. This sugar also exhibits antiplasmodial activity against Plasmodium falciparum and can be used for the synthesis of L-xylulose, which is an important intermediate for the biosynthesis of malic acid.</p>

<p>Fructose-3-phosphate sodium salt is a reactive sugar molecule that belongs to the group of monosaccharides. It can be used as a cross-linking agent in polymerization reactions, such as those used in sample preparation for animal experiments or for magnetic resonance spectroscopy. Fructose-3-phosphate sodium salt is also used as a reactant in nephrology dialysis and has been shown to have beneficial effects on diabetic patients. This compound has the ability to increase the concentration of galactitol, a nonmetabolized form of glucose that can only be obtained from the diet. Galactitol is produced by the liver when blood glucose levels are high and helps to lower blood glucose levels through its action on insulin secretion and peripheral tissue sensitivity. Fructose-3-phosphate sodium salt may also act as an anti-inflammatory agent by inhibiting prostaglandin synthesis, which may be due to its inhibition of prostaglandin synthesis</p>

<p>2-Acetamido-2-deoxy-D-gluconhydroximo-1,5-lactone is a farnesyltransferase inhibitor that belongs to the group of techniques. It is used in the diagnosis of relapsed and resistant multiple myeloma. This drug has been shown to be a potent inductor of apoptosis in vitro and in vivo through inhibition of protein synthesis. 2-Acetamido-2-deoxy-D-gluconhydroximo-1,5-lactone also inhibits the growth of tumor cells and can be used as a potential chemotherapeutic agent for pediatric patients with relapsed or resistant myeloma.</p>

<p>Isosaccharinic acid is a bacterial strain that produces isosaccharinic acid as its main fatty acid. The thermodynamic data for the reaction mechanism of the conversion of glucose to isosaccharinic acid has been determined. Isosaccharinic acid formation is catalyzed by an enzyme called glycosyl-glycerate dehydrogenase, which converts glycerate to 3-hydroxypropanoic acid and then to 3-oxopropanoate before it undergoes decarboxylation and reduction to form isosaccharinic acid. Radionuclides such as TcO4 are used in chemical ionization mass spectrometry for the detection of this compound in samples. Neutral pH, high activation energies, and low binding constants are all factors that affect the stability of this molecule.</p>

<p>CMP-N-acetylneuraminic acid 9-sp-biotin is a biotinylated sugar nucleotide</p>

<p>Daunorubicin-d3 is a fluorinated, monosaccharide, synthetic, oligosaccharide and complex carbohydrate. Custom synthesis of Daunorubicin-d3 is available with glycosylation, methylation and other modifications. Daunorubicin-d3 has CAS No. 1614-68-8 and purity &gt;99%.</p>

<p>5-Thio-N-acetylglucosamine is a microtubule inhibitor that binds to o-glcnac, a posttranslational modification of proteins that regulates the morphology and cycling of stem cells. 5-Thio-N-acetylglucosamine has been shown to inhibit the transcriptional activity of o-glcnacase, an enzyme that catalyzes the conversion of o-glcnac to glucosamine. This drug also inhibits the metabolic activity of neural progenitor cells, which may be due to its ability to regulate subpopulations with concomitant expression of markers such as Oct4 and Sox2.</p>

<p>2,4-Bis(acetylamino)-2,4,6-trideoxy-D-galactose (BTDG) is a nitro derivative of L-threonine that has been derivatized with an acetyl group and a molecule of 2,4,6-trideoxygalactose. BTDG has been shown to be safe in clinical trials for vaccine development against life-threatening diseases. It is the first glycopolymer approved by the FDA for clinical use in humans. This drug has been shown to increase the antibody response and improve protection against influenza virus infection. BTDG also inhibits bacterial replication by blocking protein synthesis in some bacteria and inhibiting glycolysis in others.</p>

<p>A seven carbon sugar</p>