Monosacáridos

<p>4,6-O-Benzylidene-D-glucose is a potent inhibitor of the enzyme dibutyltin oxide, which is involved in the synthesis of energy. It has been shown to have clinical activity in rat cardiomyocytes and has been tested in clinical studies. 4,6-O-Benzylidene-D-glucose inhibits enzymes by forming hydrogen bonds with their substrates. This compound also interacts with hydrochloric acid to form a stable complex that prevents it from interacting with other molecules. 4,6-O-Benzylidene-D-glucose is rapidly broken down into glucose and benzaldehyde when it reacts with carbonyl groups or amines. The asymmetric synthesis of this compound can be achieved using an intramolecular hydrogen transfer reaction. <br>4,6-O-Benzylidene glucose is derived from D-mannose derivatives and contains a hydroxyl group on the central carbon</p>

<p>4-Methoxyphenyl 3-O-benzyl-a-D-mannopyranoside is a synthetic carbohydrate that has been modified with a click reaction. It is an Oligosaccharide, which is a type of Carbohydrate, and has a saccharide sequence. This product is used in the synthesis of complex carbohydrates. The product has high purity and custom synthesis capabilities.</p>

<p>1,2,3,4,6-Penta-O-pivaloyl-a-D-glucopyranoside is a synthetic carbohydrate that has been fluorinated and methylated. This product is a modification of the natural compound D-glucose. It is an oligosaccharide which contains six pivaloyl groups attached to the 1-, 2-, 3-, 4-, 6-, and 7-positions on the glucose molecule. This product can be used in the synthesis of polysaccharides and glycosylations.</p>

<p>2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl isothiocyanate (TGIT) is a compound that mimics the melanoma antigen. It has been used to identify human pathogens in biological samples and has shown to have an antibody response. TGIT has also been used as a fluorescent probe for nucleic acids in analytical methods and polymerase chain reaction. This chemical can be used as a fluorescence detector in titration calorimetry. TGIT is not acutely toxic, but can cause cell lysis when combined with trifluoroacetic acid.</p>

<p>3-Hydroxydesloratadine b-D-glucuronide sodium salt is a carbohydrate that is used as an intermediate in the synthesis of saccharides. It can be modified to make it more soluble in water by adding fluorine atoms, which increases its solubility and bioavailability. 3-Hydroxydesloratadine b-D-glucuronide sodium salt is synthesized using a custom synthesis method with high purity and high yield. It has glycosylation, methylation, and click modification done on it during the synthesis process.</p>

<p>L-Daunosamine hydrochloride is a fluorinated sugar that is synthesized in the laboratory. It has been used for the modification of polysaccharides and other saccharides. L-Daunosamine hydrochloride is a monosaccharide that can be found in several complex carbohydrates. The CAS number for this chemical is 19196-51-1. This chemical has a high purity level, which makes it valuable for use as a synthetic material.</p>

<p>Phenyl 3,4,6-tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-b-D-glucopyranoside is a glycosylation product of the naturally occurring phenyl 2,3,4,6-tetraacetate. It is a white to off white powder that is stable in air and water. Phenyl 3,4,6-triacetyl 1 -thio 2-(2,2,2 trichloroethoxyformamido) b D glucopyranoside is soluble in methanol and ethanol but insoluble in water. This compound has been used as a monosaccharide or polysaccharide modification for click chemistry and complex carbohydrate studies.</p>

<p>Methyl mandelate glucoside is a glycosylation product that is custom synthesized for its fluorination and methylation. The molecule has a complex structure, consisting of monosaccharides and polysaccharides. Methyl mandelate glucoside is a high-purity compound with a CAS number. This chemical is also modified by click chemistry to create an oligosaccharide.</p>

<p>Inositol is a member of the B-vitamin family and is classified as a sugar alcohol. It has a structural similarity to glucose and can be synthesized by plants, bacteria, and mammals. Inositol is found in high concentrations in the brain and liver. Inositol has been shown to inhibit guanine nucleotide-binding proteins (G proteins) and ryanodine receptor channels in HL-60 cells. It also inhibits cancer cell proliferation and suppresses ovarian activity. Inositol appears to work by binding to the inositol-1,4,5-trisphosphate receptor on the surface of cells, thereby inhibiting intracellular calcium release from its storage site within the endoplasmic reticulum. The effects of inositol are mediated by dinucleotide phosphate or p-nitrophenyl phosphate.</p>

<p>Arabinose is a pentose sugar that has been shown to have antimicrobial properties. It inhibits the growth of bacteria by binding to their ribosomes and interfering with protein synthesis. Arabinose has also been shown to inhibit the growth of bone cancer cells in mice, which may be due to its ability to stimulate the production of growth factor-β1. The biochemical properties of arabinose are similar to those of d-arabinose, an active analogue that is used as a water vapor pump inhibitor. X-ray crystal structures have been obtained for both compounds, and they show that they differ in the position of one hydrogen atom on the sugar ring.</p>

<p>3-Aminopropyl α-D-glucopyranoside is a monomer that can be used to produce polymers. It has been shown to be effective in methylation, saccharide and oligosaccharide modifications. 3-Aminopropyl α-D-glucopyranoside is an alpha glucosidase inhibitor. The compound also inhibits the action of other enzymes, such as glycosidases, which are responsible for breaking down glycogen and starch. 3-Aminopropyl α-D-glucopyranoside is a white powder with a melting point of about 150°C and boiling point of about 300°C.</p>

<p>L-Fucose-1-phosphate disodium salt is a high purity, synthetic, fluorinated carbohydrate that is used to modify saccharides. This modification can be accomplished by methylation or glycosylation. L-Fucose-1-phosphate disodium salt has been shown to be useful for glycosylation reactions with click chemistry. It has been shown to have a wide range of applications including modification of oligosaccharides and polysaccharides in the field of biotechnology.</p>

<p>Methyl 2-acetamido-2-deoxy-α-D-glucopyranoside is a fluorinated sugar that is used as a building block in the synthesis of complex carbohydrates. It can be custom synthesized to order with purity levels up to 99.8%. The modification process includes methylation, monosaccharide, and polysaccharide modifications. This product is not intended for use in humans or animals.</p>

<p>2-Acetamido-2,4-dideoxy-4-fluoro-D-glucopyranose (2ADFG) is a glycosaminoglycan that inhibits the biosynthesis of glycosaminoglycans by binding to the enzyme UDP-N-acetylglucosamine 2-epimerase. It is used in cellular control experiments to determine if cells are hepatocytes or not. This compound binds to glycosaminoglycans and prevents them from being synthesized, which leads to cell death. The binding of 2ADFG also results in a decrease in cellular protein synthesis and an increase in cellular lysosomal activity.</p>

<p>Superdisintegrant used in pharmaceutical formulations</p>

<p>1,6-Anhydro-2,3,4-tri-O-benzyl-b-D-glucopyranose is a polymer that can be synthesized by copolymerizing the monomer with other reagents. The acetal linkage between the two glucose units allows for a cyclic structure, and this compound is soluble in water and methanol. 1,6-Anhydro-2,3,4-tri-O-benzyl-b-D-glucopyranose has been used to synthesize a variety of polymers such as polyacetals and polyesters.</p>

<p>1,6-Anhydro-2-deoxy-2-iodo-b-D-glucopyranose is a sugar that has been used in the synthesis of a number of organic compounds. It is an intermolecular hydrogen bond donor, and it forms hydrogen bonds with other molecules. The molecular structure of 1,6-Anhydro-2-deoxy-2-iodo-b-D-glucopyranose consists of a six carbon chain with three hydroxyl groups and two ether groups.</p>

<p>3-Deoxy-3-fluoro-D-galactose (3DFGal) is a potential drug that has been shown to shift the metabolic pathway of gram-positive pathogens from glycolysis to gluconeogenesis. This compound may be used as a tool for studying the enzymatic reaction catalyzed by galactokinase, which is involved in the conversion of 3DFGal to D-galactose. 3DFGal is a stereospecific carbohydrate and can be used as a substrate for biochemical studies. The bacterial surface profile of 3DFGal has been investigated and it has been found that 3DFGal is not significantly toxic to Gram-negative bacteria. The kinetics of 3DFGal hydrolysis have been studied and it was found that the hydrolysis rate was increased when the solution was acidified with hydrofluoric acid.</p>

<p>6-O-Malonylglycitin is a glycosylated flavonoid that belongs to the group of isoflavones. It is found in a variety of plants, including soybeans and fava beans. 6-O-Malonylglycitin has been shown to be an effective inhibitor of β-glucosidase activity at temperatures below 37°C, which overlaps with the range of temperatures where it inhibits glycitein production. This inhibition may be due to its pleiotropic effects on various treatments, such as its ability to inhibit cancer cell growth by inhibiting protein synthesis and inducing apoptosis. 6-O-Malonylglycitin also has synergistic effects when used concomitantly with chromatographic markers, such as high performance liquid chromatography (HPLC), which can be used to analyze the levels of endogenous compounds in human blood samples.</p>

<p>D-Salicin is a naturally occurring compound, classified as a biologically active glycoside. It is acquired from the bark of willow trees, primarily species within the genus Salix. The primary mode of action of D-Salicin involves its metabolic conversion into salicylic acid within the human body. This conversion occurs in the gastrointestinal tract and bloodstream, ultimately displaying effects similar to non-steroidal anti-inflammatory drugs (NSAIDs).</p>