Monossacáridos

<p>4-Chloro-4-deoxy-D-galactose is a high resistance carbon source that has been shown to be a more efficient method for the detection of organometallic molecules. 4-Chloro-4-deoxy-D-galactose can be synthesized from deionized water and an organometallic molecule. The compound was found to be effective in detecting liver cancer cells using a chemometric technique. This synthetic molecule also has a high detection limit and is an analytical method for detecting human liver metabolites.</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>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>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>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-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-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>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>The utilization of D-Erythrose 4-phosphate extends to various research applications, particularly in studying metabolic pathways and enzyme catalysis relevant to both prokaryotic and eukaryotic organisms.</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>1,2,3,4,6-Penta-O-acetyl-5-thio-D-glucose is a synthetic sugar that can be used as a building block in the synthesis of glycosides and oligosaccharides.</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>N-Acetylneuraminic acid 9-phosphate is a sugar phosphate</p>

<p>4,5,7-Tri-O-acetyl-2,6-anhydro-3-deoxy-D-lyxo-hept-2-enononitrile is a modified sugar molecule that has been synthesized and fluorinated. It has a high purity and can be custom synthesized to order. Click modification of this molecule is possible with the addition of a methyl group. This product is used in the synthesis of oligosaccharides and polysaccharides for glycosylation studies.</p>

<p>Ammonium 8-azido-3,8-dideoxy-D-manno-octulosonate is an oligosaccharide that is a modification of the natural polysaccharide mannoheptulose. It has been shown to be highly soluble in water and can be easily synthesized. Ammonium 8-azido-3,8-dideoxy-D-manno-octulosonate has been shown to inhibit the activity of glycosyltransferases and methyltransferases. This compound also has a high degree of purity, with minimal impurities or degradation products.</p>

<p>b-D-Galactose-sp-biotin is a glycosylation agent that can be used to modify proteins, polysaccharides, and other complex carbohydrates. It is synthesized by the modification of b-D-galactose with a spacer arm containing biotin. The compound can be modified with fluorine atoms or methyl groups. It can also be modified with click chemistry to produce a reactive site for further chemical modification. This compound has been shown to have high purity and stability, which makes it suitable for use in a variety of applications.</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>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>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>2,3,5-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>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>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>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>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>2-Thioethyl-b-D-glucopyranoside is a methylated saccharide with a molecular weight of 228.2 g/mol. It is soluble in water and aqueous solutions, and has an odorless taste. This compound is used as a synthetic intermediate for the preparation of other saccharides, such as starch, cellulose, and glycogen. 2-Thioethyl-b-D-glucopyranoside can be custom synthesized to meet your specifications.</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>α-D-Galactose-1-phosphate is a model organism for the study of galactose metabolism. It is an intermediate in the galactose pathway and provides a new approach to understanding the pathogenesis of metabolic disorders. α-D-Galactose-1-phosphate is involved in many enzymatic reactions, including the conversion of uridine diphosphoglucose (UDPG) to UDP glucose, which is a key step in glycolysis. The enzyme that catalyzes this reaction, UDP glucuronosyltransferase (UGT), has been shown to be defective in patients with galactosemia. α-D-Galactose 1 phosphate has also been used as a model for studying human gene expression, specifically protein genes. This molecule has been found to bind DNA polymerase II and inhibit transcriptional elongation at specific sites on DNA called RNA polymerase II pause sites.</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>Succinyl activated n-acetylglucosamine.</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>4,7-Anhydro-1,2,3-trideoxy-D-allo-oct-1-enitol is a modified sugar that has been synthesized for use in glycosylation reactions. It is a high purity product with no detectable impurities. Click modification of this product has been shown to be useful for glycosylation reactions. 4,7-Anhydro-1,2,3-trideoxy-D-allo-oct-1-enitol is also fluorinated and glycosylated. This product can be used in the synthesis of oligosaccharides and monosaccharides.</p>

<p>2,3,5-Tri-O-benzyl-1-a-D-arabinofuranosyl chloride is a patent antibiotic produced by Streptomyces antibioticus. It has potent anticancer activity and is being developed as an antitumor agent. 2,3,5-Tri-O-benzyl-1-a-D-arabinofuranosyl chloride inhibits cell proliferation by inhibiting DNA synthesis and protein synthesis. This compound also induces programmed cell death (apoptosis) in tumor cells. Vidarabine is a nucleoside analog that can be used to treat herpes virus infections of the eye or genital tract. Vidarabine is chemically synthesized from 2,3,5 tri O benzyl d arabinofuranosyl chloride and has been shown to have potential antitumor activity.</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>1,3-Di-O-acetyl-5-O-benzoyl-2-deoxy-D-xylofuranose is a complex carbohydrate that has been custom synthesized. It is a monosaccharide with a methyl group at the C1 position and an acetyl group at the C3 position. The chemical formula for 1,3 Di-O-acetyl 5 O benzoyl 2 deoxy D xylofuranose is C11H21NO6. The molecular weight of 1,3 Di O acetyl 5 O benzoyl 2 deoxy D xylofuranose is 277.27 g/mol. 1,3 Di O acetyl 5 O benzoyl 2 deoxy D xylofuranose may have glycosidic bonds and be used in the synthesis of other carbohydrates or as a reagent in organic chemistry reactions.</p>

<p>Methyl 1,2,3,4-tetra-O-acetyl-a-L-idopyranuronate is a carbohydrate standard that belongs to the group of L-iduronic acid derivatives. Methyl 1,2,3,4-tetra-O-acetyl-a-L-idopyranuronate is commonly used in the synthesis of glycosides and glycoconjugates. Its fluorescence properties make it useful for labeling and detection purposes in biochemical assays. This compound can also serve as a substrate for enzymes involved in carbohydrate metabolism. Overall, Methyl 1,2,3,4-tetra-O-acetyl-a-L-idopyranuronate is an essential tool for researchers in the field of glycobiology and biochemistry.</p>

<p>D-Idonic acid-1,4-lactone is a modification of a carbohydrate which can be custom synthesized. The product is an oligosaccharide that has a high purity and is synthetically produced. This product is composed of monosaccharides, methylation, glycosylation, polysaccharides and sugar. It also contains fluorination and saccharide.</p>

<p>Enantiomer of natural L-Rha 13C-labelled at carbons 1 and 2</p>

<p>Synthetically produced sugar nucleotide</p>

<p>2-Acetamido-2-deoxy-alpha- D-galactopyranosyl L-threonine is a synthetic sugar. It has a CAS number of 67315-18-8 and a molecular weight of 289.05 g/mol. This sugar is synthesized by the Click modification, fluorination, glycosylation, and methylation methods. The synthesis can be modified to produce 2-acetamido-2,3,4,5,-tetra deoxygalactose or 2 acetamido 4,6 deoxy galactose. This sugar also has saccharide properties as it is classified as an oligosaccharide or monosaccharide.</p>

<p>CMP-N-acetylneuraminic acid 9-sp-biotin is a biotinylated sugar nucleotide</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>D-Glucose ethylenedithioacetal is a biological agent. It is a white to off-white crystalline powder that has a molecular weight of 204.3. D-Glucose ethylenedithioacetal is soluble in water and ethanol, but not in ether or chloroform. It is stable in air, but will react with alkali to form the corresponding salt of D-glucose.</p>

<p>A seven carbon sugar</p>

<p>Galactostatin is a protein synthesis inhibitor that binds to the l-tartaric acid site of the bacterial 30S ribosomal subunit. It inhibits the binding of aminoacyl-tRNA to the ribosome, preventing translation and inhibiting cell growth. Galactostatin has been shown to be effective against HIV infection in mammalian cells. This drug also has a chaperone effect that protects cells from heat or cold stress.</p>

<p>3-Deoxy-2-keto-D-xylonate lithium salt is a synthetic compound that is used in the synthesis of protamine. It is produced by the reduction of an aldehyde with borohydride. 3-Deoxy-2-keto-D-xylonate lithium salt has been shown to be active against E. cloacae, which can cause diarrhea and other gastrointestinal disorders. 3-Deoxy-2-keto-D-xylonate lithium salt inhibits the growth of E. cloacae by inhibiting glycolaldehyde reductase and aldolases, which are enzymes that are essential for glycolysis and citrate metabolism, respectively. The cleavage products formed by this reaction inhibit bacterial growth by interfering with cell wall biosynthesis, preventing protein synthesis, or blocking ATP production (oxidative phosphorylation).</p>

<p>The enzyme aldolase, which is involved in the metabolism of carbohydrates, catalyzes the cleavage of 3-deoxy-2-keto-6-phospho-D-galactonate to form aldol and 6-phosphoglycerate. The reaction mechanism involves an initial dehydration step that converts the substrate to an enolate ion. This intermediate then reacts with water to produce aldol and 6-phosphoglycerate. The enzyme is active only at low pH levels due to its dependence on divalent cations. The enzyme is also inhibited by other substrates or products of the reaction, such as D-tagatose, D-sorbose, and maltophilia.</p>

<p>Dihydrozeatin-7-glucoside (DZG) is a plant hormone that belongs to the group of abscisic acid. It is biosynthesized from zeatin, an intermediate in the synthesis of the plant hormone gibberellin. DZG has been shown to regulate water loss in plants and plays a role in the regulation of photosynthesis and seed germination. The uptake of DZG by plant cells is complex and can be influenced by both physiological and environmental factors. It can be conjugated with small molecules such as typhasterol, which is found in tobacco leaves, or tabacum l., which is found in certain species of tobacco plants. Dihydrozeatin-7-glucoside also interacts with other hormones such as 24-epibrassinolide and regulates various biochemical processes such as protein synthesis and cell growth.</p>