Monosaccharides

<p>2,3,4,6-Tetra-O-benzoyl-1-deoxy-D-arabino-hex-1-enopyranose is a glycosyl compound that has been synthesized by the elimination of trifluoride and alcohols. It is used as a starting material for the synthesis of other compounds. This compound can react with halides to form etherate or ester derivatives. 2,3,4,6-Tetra-O-benzoyl-1-deoxy-D-arabino hexane can also be reacted with boron trifluoride or boron trifluoride etherate to form eliminations.</p>

<p>2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl azide is a chemical compound that has been synthesized and studied by X-ray crystallography. It is an azide derivative of β-D-glucopyranosyl acetate. The structure of this compound was solved using x-ray crystallographic techniques.</p>

<p>2,3,4,6-Tetra-O-benzyl-a-D-glucopyranosyl fluoride is a modification of a carbohydrate. It is a complex carbohydrate that has the CAS No. 89025-46-7 and is custom synthesized. The product contains an oligosaccharide and high purity that are synthetic and monosaccharides that are methylated, glycosylated, and polysaccharides that are sugars with fluorination. The product also contains saccharides with glycosylation and polysaccharide sugar units.</p>

<p>Hexadecyl-D-xylopyranoside is a synthetic sugar that has been fluorinated and methylated. It is a complex carbohydrate that belongs to the group of modified sugars. This product has many applications in the synthesis of oligosaccharides and saccharides, as well as in glycosylation reactions. Hexadecyl-D-xylopyranoside can be used in custom syntheses, and has been shown to have high purity with a CAS No. 115211-19-3.</p>

<p>4-Methoxyphenyl 3-O-allyl-4,6-O-benzylidene-b-D-galactopyranoside is a galactoside that is commonly found in plants. The biosynthesis of this molecule has been studied in the bacteria N. meningitidis and it has been shown that it can be synthesized from fatty acids. 4-Methoxyphenyl 3-O-allyl-4,6-O-benzylidene b -D -galactopyranoside can be used as a HIV drug, as it inhibits the growth of HIV cells by inhibiting protein synthesis and RNA transcription. This molecule is also able to inhibit cancer cell proliferation in vitro.</p>

<p>Phenyl 4,6-O-benzylidene-b-D-glucopyranoside is a white crystalline powder that belongs to the group of glycoconjugates. It has been made by the modification of glycosides and saccharides. This product can be used as a fluorination agent in organic synthesis, or as a click modification in carbohydrate chemistry. Phenyl 4,6-O-benzylidene-b-D-glucopyranoside can also be used for glycosylation reactions and methylation reactions.</p>

<p>2-Acetamido-2-deoxy-4,6-O-isopropylidene-D-glucopyranose is a modification of 2,3,4,5,6 tetraacetamido 1,2,3,4,5 pentaoxo 1,2 deoxy D glucose. It is an oligosaccharide that has been synthesized for the first time in 1977. The monosaccharide can be methylated and glycosylated to form polysaccharides such as mannans and galactans. The chemical structure of this product can be modified with fluorination or saccharide substitution.</p>

<p>Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an enzyme that catalyzes the conversion of glyceraldehyde-3-phosphate to 1,3 bisphosphoglycerate. GAPDH is involved in glycolysis and the pentose phosphate pathway. It has been shown to be an important player in mediating cellular responses to hypoxia, inflammation, and oxidative stress. The glyceraldehyde-3-phosphate dehydrogenase gene has been found to be mutated in a number of cancers including breast cancer and colon cancer. This gene also has a role in inflammatory lesion development as well as energy metabolism. GAPDH also participates in the biochemical reactions that lead to neuronal death during neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease.</p>

<p>2,3,5-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-D-arabinofuranose is an organic compound that belongs to the group of furan derivatives. The configuration of this molecule was determined to be (2S,3S) by the use of stereoselective synthesis. It can be synthesized from a benzaldehyde and a ribofuranosyl chloride with a yield of about 95%. This compound has been shown to react with azides in a catalytic transfer reaction yielding yields of up to 100%.</p>

<p>Colchicoside is a natural compound that belongs to the chemical family of phenylpropanoids. It is used in the treatment of gout and pseudogout, and has been shown to be effective against demecolcine-induced hemolytic activity. Colchicoside has also shown to be an analog for other compounds with toxicological studies, such as hydrochloric acid and potassium dichromate. The toxicity studies performed on colchicoside have shown that it can cause damage to cells in culture by inhibiting DNA repair mechanisms.</p>

<p>Glycogen phosphorylase inhibitor</p>

<p>2,3,4,6-Tetra-O-benzoyl-D-galactopyranose is a glycoside. It is synthesized by the glycosylation of galactose with benzoic acid chloride in the presence of sodium carbonate. This compound is a natural product that can be found in plants and animals. 2,3,4,6-Tetra-O-benzoyl-D-galactopyranose has been shown to inhibit topoisomerase I and II activity in mammalian cells and induce the uptake of galactose into human adenocarcinoma cells. The yields of this compound are low and it has not been studied extensively due to its limited availability.</p>

<p>3-Deoxygalactosone is a reactive compound that is formed by the reaction of glyoxal and galactose. The glyoxal molecule reacts with the hydroxyl group on the galactose to form a new aldehyde, which can then react with another molecule of glyoxal or galactose to form 3-deoxygalactosone. 3-Deoxygalactosone has been shown to have health effects in clinical studies. It also has been shown to decrease the dry weight of rats fed a high-fat diet. This compound also is an intermediate in the formation of 5-hydroxymethylfurfural, which is produced during the Maillard reaction between sugars and amino acids. 3-Deoxygalactosone binds to proteins, forming hydrogen bonds with amino acid side chains and affecting their biological function.</p>

<p>Antioxidant; antibacterial; suppresses LPS-induced inflammatory response</p>

<p>4, 6-O-Ethylidene-D-glucopyranose is a glucose analogue that inhibits sugar transport. It has been shown to inhibit glucose transport by binding to the hydroxyl group on the red cell membrane. This binding prevents the sugar from entering the cell and as a result, glucose accumulates in the blood. 4, 6-O-Ethylidene-D-glucopyranose also binds to tryptophan fluorescence and inhibits cytochalasin B binding to tryptophans that are located on the plasma membrane of eukaryotic cells.</p>

<p>1,3,4,6-Tetra-O-benzyl-b-D-galactopyranoside is a custom synthesis that has been modified with methylation and fluorination. It is an oligosaccharide composed of saccharides linked by glycosidic bonds. Carbohydrates are polymers of monosaccharides, which can be classified as either simple sugars or complex carbohydrates. This product is a high purity, synthetic sugar that is suitable for use in the synthesis of complex carbohydrate polymers.</p>

<p>Ginsenoside F1 is a natural compound found in ginseng. It is believed to have anti-cancer properties. Ginsenoside F1 has been shown to inhibit the proliferation of HL-60 cells and have an apoptotic effect by regulating mitochondrial membrane potential and activating the apoptotic pathway. The mechanism of action for the anti-cancer activity of Ginsenoside F1 may be due to its ability to inhibit angiogenesis, which is needed for cancer cell proliferation. Ginsenoside F1 also inhibits the growth of skin cancer cells in mice by regulating microvessel density. This compound has been found in foods such as soybeans, rice, peanuts, and kiwifruit.</p>

<p>Tert-butyl 2-deoxy-L-ribopyranoside is a synthetic monosaccharide that can be used in the synthesis of polysaccharides and oligosaccharides. It is also used for fluorination reactions, such as click modification. This compound can be custom synthesized to order, and it is available in high purity. Tert-butyl 2-deoxy-L-ribopyranoside can be modified with a variety of different functional groups, including methylation. It has an CAS number of 1032153-57-3.</p>

<p>N-Acetyl-2-O-methyl-b-D-neuraminic acid (AOMBNA) is a modification of sialic acid. It is an N-acetylated, O-methylated analogue of b-D-neuraminic acid. AOMBNA is synthesized by the chemical modification of D,L -erythro -2,3,4,6 tetra hydro sialic acid with methyl bromo acetate in the presence of sodium methoxide. The product can be purified by crystallization from dichloromethane and methanol mixture. AOMBNA has been used in complex carbohydrate synthesis and glycosylation reactions.</p>

<p>D-Glucono-1,5-lactone is a chemical compound that is a member of the class of compounds known as diketones. It can be used in chemical biology and polymer chemistry to probe hydrogen bonding interactions, polymer compositions, and redox potentials. D-Glucono-1,5-lactone has been shown to inhibit the growth of cells in culture by inhibiting DNA synthesis. This inhibition is due to its ability to bind with high affinity to nucleic acids and prevent the formation of the enzyme complexes required for transcription and replication. The effects are reversible.</p>