Monosaccharides

<p>Phenylethyl-beta-D-glucopyranoside is a phenolic compound that is found in plants such as Echinacea. Phenylethyl-beta-D-glucopyranoside has been shown to inhibit tumor cell proliferation by increasing the levels of enzyme catalysis and enzyme activity, and decreasing the levels of protocatechuic acid. This compound also inhibits fatty acid synthesis, which may be due to its ability to inhibit the production of 4-hydroxycinnamic acid via inhibition of the enzyme acyl coenzyme A:cholesterol acyltransferase. The cyanobacterial strain Synechococcus elongatus PCC 7942 was found to produce phenylethyl glucoside, an iridoid glucoside with high cytotoxic activity against human tumor cells.</p>

<p>N-(4-Bromobenzyliden)imino-2,3,4,6-tetra-O-pivaloyl-D-glucopyranoside is a custom synthesis that is an oligosaccharide. This product is a complex carbohydrate that can be modified with methylation, glycosylation and click modification. The saccharide unit in this product is a sugar or carbohydrate. It has high purity with fluorination and synthetic modifications.</p>

<p>N-Acetyl-3-fluoro-neuraminic acid sodium (AFNA) is an inhibitor that binds to the terminal sialic acid residue of the glycoprotein neuraminidase in influenza viruses, preventing the virus from attaching to cells. AFNA is a fluorinated derivative of mannosamine and is synthesized by reacting an aldolase with sulfur trifluoride. AFNA has been shown to inhibit sialidases and utilising enzymes, which are necessary for viral replication. AFNA also inhibits bacterial sialidases, which are required for the synthesis of cell wall components.</p>

<p>2-Acetamido-4,6-O-benzylidene-2-deoxy-D-galactopyranose is a fluorescent dye that binds to the hydroxyl group of nucleic acids. It can be used for microscopy of cells and bacteria in culture. This dye is also used for the measurement of cavitation activity. The dye is added at a concentration of 0.1% to the cell culture media. After 24 hours, it can then be observed with a microscope under UV light. 2-Acetamido-4,6-O-benzylidene-2-deoxy-D-galactopyranose has been shown to have lysis effects on cells such as agarose gels and mammalian cells, leading to cell death by apoptosis or necrosis. It's also used as an indicator in gel electrophoresis experiments because it can bind to DNA and RNA molecules, which makes</p>

<p>Please enquire for more information about 2,3-O-Isopropylidene-1,4-di-O-tosyl-D-threitol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The b-D-glucopyranosyl amine is a glucose analogue that has been shown to have biochemical properties. It is the hydrochloride salt form of the molecule, which can be found in human liver cells. B-D-glucopyranosyl amine has been shown to inhibit the growth of bacteria and fungi. This compound also has anti-inflammatory activities, as it inhibits the release of reactive oxygen species from neutrophils. B-D-glucopyranosyl amine is an anti-infective agent that specifically targets bacterial cell wall synthesis and inhibits their growth by binding to the enzyme β1-glycosidase. This compound is also able to bind to lipid membranes and induce membrane leakage, leading to cell death.</p>

<p>D-Threonic acid-1,4,-lactone is a methylated saccharide that is prepared by the oxidation of D-threo-aldose. It can be used as a building block in the synthesis of glycosylates, oligosaccharides, and polysaccharides. The compound has been shown to inhibit the growth of Mycobacterium tuberculosis and Mycobacterium avium complex. D-Threonic acid-1,4,-lactone can also be fluorinated for use as an imaging agent for positron emission tomography (PET).</p>

<p>2,3-O-Isopropylidene-D-erythronolactone is a chromophore that has been synthesised. It is a chiral heterocycle with an anion linker and a boron trifluoride etherate group. The carbon chain of 2,3-O-isopropylidene-D-erythronolactone has been found to be essential for its antibacterial activity against tuberculosis. This compound binds to the adenosine receptor in the bacterial cell membrane and inhibits bacterial growth.</p>

<p>2-Methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-a-D-glucopyrano)-[2,1-d]-2-oxazoline (TAO) is a molecule that is produced during the glycosylation of proteins. TAO has been shown to enhance chemotherapy by targeting and inhibiting the growth of cancer cells. TAO binds to the epidermal growth factor receptor (EGFR), which is a protein that regulates cell proliferation. TAO inhibits cancer cell growth by blocking the activation of EGFR and its downstream signaling pathways. This inhibition leads to tumor regression in xenografts in mice. TAO also blocks o-glycosylation, which is a process that enhances cancer therapy resistance.</p>

<p>L-Arabinose diethyldithioacetal is a potassium carbonate derivative of L-arabinose that reacts with sulfur to form 1,2-dithioketals. These dithioketals are used as glycosyl donors in the synthesis of L-fucitol and d-xylose. This reaction is catalyzed by acetobacter, which converts L-arabinose and carbon dioxide into acetaldehyde and acetic acid. The reaction mechanism for this transformation includes an epimerization of the hydroxyl group on the C5 position of L-arabinose to a hydroxyl group on C6, followed by glycosidation with sulfuric acid. The glycosidic bond formed between the hydroxyl group on C6 and the carbonyl group at C1 (in this case, from L-arabinose) is called an acetal linkage. In addition to being antithrombotic</p>

<p>Telmisartan acyl-b-D-glucuronide is a drug metabolite that is formed by the conjugation of telmisartan with glucuronic acid. Telmisartan acyl-b-D-glucuronide is activated in vivo and reversibly inhibits the enzyme creatine kinase, which is involved in the metabolism of creatine to creatinine. The effective dose for this compound has been shown to be 10 mg/kg (orally) in humans. Telmisartan acyl-b-D-glucuronide has been shown to be an at1 receptor antagonist and may have some antihypertensive effects via modulation of ion channels. This drug also appears to have some proliferative effects on cells that are inhibited by radiation.</p>

<p>Hesperetin 7-O-b-D-glucuronide is a metabolite of hesperetin, a flavonoid primarily sourced from citrus fruits. This compound is formed through the glucuronidation process, a metabolic pathway that modifies hesperetin to enhance its solubility and facilitate its excretion from the human body. Hesperetin 7-O-b-D-glucuronide exerts biological effects through various modes of action, including antioxidant and anti-inflammatory mechanisms. It is thought to scavenge free radicals and modulate inflammatory pathways by inhibiting specific enzymes and cytokines.In scientific research, Hesperetin 7-O-b-D-glucuronide is studied for its potential therapeutic applications, particularly its role in reducing oxidative stress and inflammation-related diseases. It has garnered attention in the context of cardiovascular health, neuroprotection, and metabolic disorders. The exploration of its bioavailability and specific interactions at the molecular level continues to provide insights into its promising applications in nutraceuticals and pharmaceuticals. Researchers investigate its efficacy and safety to better understand its potential role in disease prevention and therapy.</p>

<p>3-Azido-1-O-t-butyldimethylsilyl-2,3,6-trideoxy-b-L-arabinohexopyranose is a modified sugar. It is used as a building block in the synthesis of oligosaccharides and polysaccharides. This product is custom synthesized to customer's specifications and is available in high purity.</p>

<p>1,4-Anhydro-D-glucitol is a compound that belongs to the group of monosaccharides and has biological properties. It has also been used in the production of acetate extracts from fetal bovine erythrocytes. The ester linkages are formed between 1,4-anhydro-D-glucitol and sodium salt by reaction with acetic anhydride. The reaction mechanism has been studied in detail, and it was found that hydroxyl groups on the molecule react with sodium ions to form an ester linkage. This compound is toxicologically safe at high doses, but can become toxic at lower doses due to its acid formation potential.</p>

<p>L-Xylonic acid-1,4-lactone is an enzyme that functions as a glycolytic enzyme. It catalyzes the conversion of D-xylose to L-xylonic acid and L-xylonic acid-1,4-lactone. This enzyme is expressed in leukemia HL60 cells and is activated by acidic conditions. L-Xylonic acid-1,4-lactone has been shown to be catabolized by the enzyme xylanase. The kinetic properties of this reaction have been studied using mass spectrometric techniques and biochemical methods. The rate of the reaction was found to be dependent on the presence of divalent cations (Mg2+ or Ca2+) or monovalent ions (Na+ or K+). L-Xylonic acid 1,4 lactone also catabolizes glucose with a similar rate constant.</p>

<p>Phenyl 2,3,6-tri-O-acetyl-2-deoxy-2-trichloroacetamido-b-D-thioglucopyranoside is a monosaccharide with a molecular weight of 594.5. It is derived from the reaction of methyl acetate and benzene in the presence of sulfuric acid. Phenyl 2,3,6-tri-O-acetyl-2-deoxy-2-trichloroacetamido b D thioglucopyranoside is an intermediate in the synthesis of saccharides that are modified by click chemistry or modification. <br>This product has been shown to be synthesized with high purity and good yield. The product can be used for custom synthesis as well as glycosylation reactions. This product also has a CAS number and can be used for Click chemistry or modification reactions.</p>

<p>Methyl β-L-arabinopyranoside is a stereochemically pure monosaccharide that has been used to calibrate and quantify the conformational, stereochemical, and spectrometric methods. Methyl β-L-arabinopyranoside has a conformation that is restricted by the presence of an α-hydroxyl group at C2. The chloride ion can be used to monitor this conformation. The diameter of methyl β-L-arabinopyranoside can be measured with a micropipette and monitored using an aerosol detector. Methyl β-L-arabinopyranoside can also be quantified by mass spectrometry or spectrophotometry. The conformational, stereochemical, and spectrometric methods have been calibrated using methyl β-L-arabinopyranoside as a standard to determine their accuracy in measuring the size of other molecules.</p>

<p>2-Acetamido-1,3,4,6-tetra-O-benzyl-2-deoxy-a-D-glucopyranoside is a modification of the natural carbohydrate. It is an oligosaccharide synthesized with custom synthesis. The synthetic process involves the methylation and glycosylation of the monosaccharides. Fluorination and saccharide linkages are also used in the production of this compound. 2-Acetamido-1,3,4,6-tetra-O-benzyl-2-deoxyglucopyranoside can be used as a building block for complex carbohydrates or as a research reagent for glycobiology.</p>

<p>N-Acetyl-D-mannosaminuronic acid sodium (NAMSA) is a precursor to uridine and fatty acids. It is synthesized in vivo by the enzyme mannosaminase, which cleaves the glycosidic linkage of NAMSA to form uridine and mannose. NAMSA has been shown to be an essential gene product for S. aureus strains. The activity of NAMSA can be monitored using the assay of radioactive incorporation into sialic acid, which is coupled with gel chromatography. This compound has also been used as a monoclonal antibody to detect CD4+ cells in vitro, and was shown to inhibit the growth of infectious diseases such as Mycobacterium tuberculosis, Neisseria meningitidis, and Salmonella typhimurium.</p>

<p>Methyl 2,3-di-O-benzoyl-4,6-O-(4-methoxybenzylidene)-a-D-galactopyranoside is a fluorinated and methylated synthetic carbohydrate. It is an oligosaccharide that is synthesized from galactose and glucose by glycosylation and click modification. Methyl 2,3-di-O-benzoyl-4,6-O-(4-methoxybenzylidene)-a-D-galactopyranoside has CAS number: 6079410.</p>