Monosaccharides

<p>Short-term marker of glycemic control</p>

<p>D-Glucosamine 6-phosphate is a non-essential amino acid that belongs to the group of nucleotide sugar phosphates. It is a metabolite of the sugar D-glucose and it plays an important role in the energy metabolism of bacteria, plants, and animals. It has been shown to have anti-cancer effects on prostate cancer cells. D-Glucosamine 6-phosphate inhibits methyltransferase activity by binding to the enzyme's active site. This inhibition prevents DNA synthesis, leading to cell death. The structural analysis has been done using NMR spectroscopy on d-arabinose as a model substrate.</p>

<p>3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranosyl fluoride is a synthetic glycoside that has been synthesized by the click modification of a fluorinated saccharide. The compound has an acetyl group at C3 and C6 positions with an OCH3 group at the C4 position. This compound has been used in glycosylation reactions to modify the carbohydrate moiety of peptides and proteins. It has also been used in research on complex carbohydrate chemistry.</p>

<p>2-Amino-b-L-arabinofurano[1,2:4,5]oxazoline is a custom synthesis. It is a white to off-white powder with a molecular weight of 264.50 and a melting point of about 160°C. The purity of this compound is &gt;98% by HPLC analysis. This product has been modified with glycosylation, methylation, click modification, fluorination, saccharide modification, sugar modification, and oligosaccharide modification.</p>

<p>Phenyl β-D-thiogalactopyranoside is a selective inhibitor of galectin-3, which mediates the growth and metastasis of cancer cells. Phenyl β-D-thiogalactopyranoside has been shown to inhibit the binding of galectin-3 to its receptor on cancer cells, thereby blocking the activation of signaling pathways that promote cell proliferation and survival. The crystalline form can be used as a reagent for the determination of glucose in aqueous solutions.</p>

<p>2,3-O-Isopropylidene-D-glyceraldehyde is an acetal protected glyceraldehyde building block for use in organic chemistry. The aldehyde group of 2,3-O-Isopropylidene-D-glyceraldehyde is left unprotected which allows for a range of reactions to be performed. These include aldol condensations, olefinations, Grignard reactions and imine formation, including reductive amination.</p>

<p>2-Deoxy-L-ribose-anilide is a chemical compound that has been patented for its use in the detection of magnetic fields. The patent claims that this compound can be used as an intermediate in the preparation of other compounds. 2DRA has different transition temperatures, depending on whether it is in the solid or liquid state. When 2DRA is heated, it changes from a colorless liquid to a yellow crystal at around 100°C and then becomes a white solid at around 150°C. The magnetic properties of 2DRA arise from its ability to form strong bonds with other molecules, which are broken by external magnetic fields.</p>

<p>5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone is a synthetic monosaccharide with the molecular formula C8H14O5. It has a CAS number of 94697-68-4 and is available for custom synthesis. The chemical structure of 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone consists of a methyl group attached to the hydroxyl at position 1 and a fluoro group attached to the hydroxyl at position 4. 5,6--O--Isopropylidene--L--gulonic acid--1,4--lactone is not naturally occurring and is made by modification of glycosides. This compound can be used in click chemistry or complex carbohydrate reactions.</p>

<p>3,4-Di-O-methyl-D-glucose is a partially protected glucose .It is found in the exudates of certain plants.</p>

<p>3-O-Allyl-1,2-O-isopropylidene-α-D-galactofuranose is a synthetic glycoside that can be custom synthesized. It is a fluorinated monosaccharide that reacts with an allyl group to form an allyl glycoside. This modification increases the solubility of the molecule and can make it soluble in organic solvents. 3-O-Allyl-1,2-O-isopropylidene α D galactofuranose is used to modify saccharides or complex carbohydrates for use in research.</p>

<p>The galactosyl diglyceride (GalDG) is a lipid molecule that is found naturally in plants. The chemical formula for GalDG is C22H44O8 and it has a molecular weight of 464.36 g/mol. This lipid molecule is composed of two fatty acid chains, one glycerol molecule and one galactose molecule. It can be synthesized with the help of a transition metal catalyst and an oxidizing agent such as hydrogen peroxide or sodium hypochlorite. When heated to a temperature of about 200-250 degrees Celsius, the transformation process takes place which results in the conversion of the lamellar phase to the crystalline phase. The diffraction method was used to determine its crystal structure and it was found that this lipid molecule has a lamellar phase at room temperature but transforms into a crystalline phase when heated to 250 degrees Celsius. The diffraction pattern obtained from x-ray diffraction analysis indicated that this</p>

<p>11-Dehydroxygrevilloside B is a natural glycoside compound, which is primarily isolated from the plant genus Grevillea. This genus is known for its rich diversity of secondary metabolites with various biological activities. The mode of action of 11-Dehydroxygrevilloside B involves interactions with specific molecular targets, potentially influencing biochemical pathways associated with inflammation, oxidative stress, or other cellular processes. Its exact mechanism is still under research, aiming to unravel its potential therapeutic or protective effects. Applications of 11-Dehydroxygrevilloside B are mainly within the realm of biochemical and pharmacological research, where it serves as a subject for in vitro or in vivo experiments to explore its efficacy and safety profile. Its study contributes to understanding how plant-derived compounds can be harnessed for medicinal purposes and augments the exploration of novel drug candidates from natural sources.</p>

<p>Methyl b-D-mannopyranoside isopropylate is a high purity synthetic oligosaccharide. It has been custom synthesized and fluorinated with methyl groups on the sugar ring. It can be used for glycosylation, modification, and synthesis of saccharides. This product can also be used as a complex carbohydrate in the food industry.</p>

<p>Glucosylceramide (Glc-Cer) is the common precursor in the biosynthesis of most glycosphingolipids, with exception of some Gal-Cer derivatives, such as, GM4. Glucosylceramide consists of a glucosyl moiety which is β-O-glycosydically linked to ceramide, which itself, consists of the long-chain aminoalcohol sphingosine and a fatty acid. Glucosylceramide (also called glucocerebroside) is synthesised enzymatically, by the glucosylceramide synthase-catalysed with the addition of a glucose residue to ceramide. Glucosylceramide is involved in the regulation of various cellular events and also serves as a main constituent in liposome formulations.</p>

<p>1-O-Methyl-β-D-glucopyranoside is a β-glucosidase inducer.</p>

<p>L-Talose is a type of sugar that is found in plants and animals. It is a stereoselective, synthetic carbohydrate with the chemical formula C12H24O11. L-Talose has an anhydrous dextrose equivalent (DE) of 180. L-Talose is synthesized from D-glucal and D-talonol by a recombinant protein. The immobilization process has been shown to be successful for the production of L-talose as it prevents the loss of product due to adsorption on the surface of the reactor. Molecular modeling was used to determine that L-talose binds to carbonyl groups more strongly than other types of molecules. Anhydrous dextrose was shown to be an effective acceptor for L-talose because it reacts with hydroxyl groups at room temperature and pressure conditions. The nmr spectra show that the hydroxyl group interacts with hydrogen bonding and coordinate covalent bonding</p>

<p>L-Altrose is a carbohydrate that is used as a nutrient and sweetener. It is a dextrose monomer with an L-arabinose side chain. L-Altrose has been shown to be a stereoselective carbon source that can be used in the synthesis of various biologically active compounds, such as antibiotics. L-Altrose has also been shown to stimulate growth of yeast cells in the absence of oxygen by providing an extracellular carbon source. This compound can be hydrolyzed by ring-opening or benzoylation reactions to yield dextrose.</p>

<p>Ethyl b-D-galactopyranoside is a galactosylated glycoside that can be synthesized by the transfer of an acetyl group from ethyl alcohol to a sugar. It has antibacterial activity and is used in solvents as a stabilizer. The chemical structure of this compound consists of two benzene rings with an -OH group on one end, which are linked together by a covalent bond. The spacing between these two benzene rings is important for the stability of this compound, and it will break down when there is not enough space for the electron clouds to interact with each other. Ethyl b-D-galactopyranoside has been shown to be effective against tuberculosis bacteria, Mycobacterium tuberculosis, and Mycobacterium avium complex.</p>

<p>Phenyl b-D-thioglucuronide is a synthetic molecule that has been used in studies of the carotid, abdominal and symmetric techniques. It can be used to study water absorption and squamous cell growth. Phenyl b-D-thioglucuronide has been used as a crosslinking agent for optical imaging techniques, such as fluorescence microscopy and confocal microscopy. The basic protein form of phenyl b-D-thioglucuronide is found in the human brain and spinal cord. There have been reports that phenyl b-D-thioglucuronide causes death and teratomas in mice when injected into the sigmoid colon or teratoma. Phenyl b-D-thioglucuronide also causes neuroinflammation, which may be due to its ability to induce matrix metalloproteinase production.</p>

<p>L-glucose is a monosaccharide that is an important source of energy for the human body. The glucose molecule consists of 6 carbon atoms, 12 hydrogen atoms and 6 oxygen atoms. Glucose enters cells with the help of insulin and ATP-sensitive potassium channels. It has been shown that L-glucose can inhibit viral replication in vitro, such as HIV and herpes simplex virus type 1 (HSV-1). L-Glucose may be used to treat squamous carcinoma by reducing the redox potential in cancer cells. L-Glucose inhibits the growth of c. glabrata by inhibiting transcription activators and enzymes involved in glycolysis. L-Glucose also has hypoglycemic effects on humans by reducing cortisol concentrations in human serum.</p>