Monosaccharides

<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>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>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>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>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>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>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>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>(-)-2,3-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>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>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-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>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>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>CMP-N-acetylneuraminic acid 9-sp-biotin is a biotinylated sugar nucleotide</p>

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