Monossacáridos

<p>1,4:3,6-Dianhydro-L-iditol is a synthetic compound that is used in pharmaceutical preparations and tissue culture. It has been shown to inhibit the growth of bacteria such as Staphylococcus aureus and Mycobacterium tuberculosis in vitro assays. The synthesis of 1,4:3,6-dianhydro-L-iditol involves intramolecular hydrogenation of fatty acids with alkanoic acids and the use of solid catalysts.</p>

<p>Please enquire for more information about N-(Formylamidino)-N-b-D-ribofuranosylurea including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5-Anhydro-1,3-O-isopropylidene-6-O-trityl-D-glucitol is a complex carbohydrate that is synthesized by the modification of glucose. This product has been modified with methylation and glycosylation.<br>2,5-Anhydro-1,3-O-isopropylidene-6-O-trityl--D--glucitol is a white powder that is soluble in water and ethanol. <br>It can be used for fluoroquinolone resistance studies, which are important for developing new antibiotics to combat bacterial infections.</p>

Onitin 2'-O-glucoside is a sugar that is custom synthesized and purified. It is a modification of oligosaccharides, complex carbohydrates, and polysaccharides. Onitin 2'-O-glucoside is an Oligosaccharide Carbohydrate which can be used in the synthesis of high purity monosaccharides and methylations. It also has the ability to form glycosylation with saccharides, such as glucose or fructose. This product can also be fluorinated to produce saccharides that are water soluble.

2,3-O-Isopropylidene-L-glyceraldehyde (2,3-OIPA) is a synthetic compound that was developed as an alternative to paraformaldehyde for the synthesis of enantiopure compounds. It has been used in metathesis reactions and catalysed the conversion of β-unsaturated ketones to enantiopure products. 2,3-OIPA also has significant cytotoxic activity against a range of human cancer cell lines. This compound can be used in asymmetric syntheses to produce chiral molecules with a high degree of optical purity.

<p>D-Sedoheptulose is a sugar that is a member of the pentoses. It has been shown to have a ph optimum of 4.5 and oxidizing potential of -0.18 V. It is also an important intermediate in carbohydrate metabolism and can be used as an energy source by cells. D-Sedoheptulose plays a role in transcriptional regulation and cellular physiology, as well as being involved in the production of acyl chains and disulfide bonds for proteins. D-Sedoheptulose has also been found to have synergic effects with other sugars such as glucose, sucrose, or fructose, which may be due to its ability to act as an inducer of reductive enzymes such as glucose-6-phosphate dehydrogenase (G6PD).</p>

<p>Please enquire for more information about D-Mannose tablets including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Deoxy-D-glucitol is a sugar alcohol that is a reduction product of glucose. It can be produced by the reduction of glucose 6-phosphate in muscle cells. The enzyme dehydrogenase catalyzes this reaction, which is influenced by the presence of gemini surfactants such as DMSO. 1-Deoxy-D-glucitol has been shown to have anti-fungal properties against Aspergillus parasiticus and other organisms. This activity may be due to its ability to inhibit phosphofructokinase, hexokinases, or other enzymes that are involved in the metabolism of glucose by these organisms.</p>

<p>a-D-Mannopyranosyl amine is a synthetic product that is used as a sugar donor in glycosylation reactions. It can be custom synthesized to suit the needs of the customer. The chemical structure contains a methyl group and an oxygen atom, which are both in their highest oxidation state. This product is not intended for use as a food additive or dietary supplement.</p>

<p>2-Deoxy-D-glucono-1,5-lactone is a crystalline compound that is isolated from the hydrolysis of D-gluconic acid. This compound has been found to be a diastereoisomeric product with a lactone ring and an epimerization process. It can also be synthesized by reacting epichlorohydrin with potassium hydroxide in the presence of a hydroxy group. 2DG is an elimination product of 2-deoxyglucose and has been shown to have antihyperglycemic effects due to its ability to inhibit glucose synthesis in the liver and muscle cells. This compound also inhibits protein synthesis in bacteria, which may lead to cell death.</p>

<p>Methyl b-D-fructofuranoside is a chemical compound that is used in the production of esters and fatty acids. Methyl b-D-fructofuranoside is produced by a dehydration reaction between two molecules of acetone. The product of this reaction, methyl b-D-fructopyranoside, can be broken down into two molecules of acetone and one molecule each of methyl alcohol and carbon dioxide. This process is called alkylation. Furanocoumarin derivatives are often found in plants such as asperulosidic acid and quinquefasciatus. These compounds are found in many species of plant, but they are most concentrated in the roots of these plants because they are more metabolically active there than other parts of the plant. Environmental pollution can lead to high concentrations of furanocoumarins in plants, which can have toxic effects on organisms that come into contact with them.</p>

<p>2,5-Anhydro-D-glucitol-1,6-diphosphate is a cell signaling molecule that is involved in the regulation of glycolysis and the phosphofructokinase enzyme. It binds to platelets and regulates platelet aggregation. This enzyme has been shown to be a potential drug target for cancer. Cancer cells have been found to contain higher concentrations of 2,5-Anhydro-D-glucitol-1,6-diphosphate than their normal counterparts. The increased concentration of this enzyme in cancer cells is due to an allosteric change in the enzyme’s activity. The increased activity leads to a more rapid metabolism of glucose, which provides energy for tumor growth and metastasis. This enzyme can be used as a marker for malignancy in human diseases such as breast cancer or prostate cancer.</p>

<p>Tetra-O-galloyl glucose is a pentagalloyl glucose that is found in the Chinese herb Paeonia lactiflora. It has been shown to inhibit the replication of hepatitis B virus, and can be used for the treatment of hepatitis B infection. Tetra-O-galloyl glucose also has anti-inflammatory activities, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>1-Deoxy-1-nitro-L-glucitol is a potent apoptosis-inducing compound that has shown promising results in cancer research. It is an analog of vanillin and nintedanib, two well-known cancer cell inhibitors. 1-Deoxy-1-nitro-L-glucitol has been shown to inhibit the activity of several kinases, including those involved in tumor growth and progression. In addition, it has been found to be effective against various types of cancer cells, including Chinese hamster ovary cells and human bladder cancer cells. This compound also exhibits synergistic effects with other anti-cancer drugs such as glimepiride and apomorphine. The presence of 1-Deoxy-1-nitro-L-glucitol in urine may serve as a potential biomarker for the diagnosis and monitoring of certain cancers.</p>

<p>Inducer of cytochine and chemochine production in blood cells</p>

<p>A thio-sugar</p>

<p>D-Fructose 1-phosphate barium salt trihydrate is a custom synthesis, high purity sugar. It has been modified with fluorination, glycosylation, and methylation. D-Fructose 1-phosphate barium salt trihydrate is made from the modification of various sugars such as oligosaccharides and monosaccharides to form complex carbohydrates. It can be used for Click modification or in the synthesis of glycoconjugates. D-Fructose 1-phosphate barium salt trihydrate is also known as saccharide.</p>

<p>5-Deoxy-D-ribose is a molecule that is an intermediate in the shikimate pathway, which produces the aromatic amino acids. 5-Deoxy-D-ribose can be synthesized from D-ribose and shikimic acid. The biosynthesis of 5-deoxy-D-ribose is catalyzed by the enzyme ribose 5'-phosphate kinase, which converts ribose 5'-phosphate to 5-deoxy--D--ribose phosphate. This reaction requires ATP as a source of energy, and it is inhibited by phosphoribosyl pyrophosphate (PRPP). The asymmetric synthesis of 5-deoxy--D--ribose has been achieved with a chiral Lewis acid catalyst. The molecular structure of 5-deoxy--D--ribose has been determined by NMR spectroscopy. Shikimate pathways are present in mammalian cells, but not in plants or bacteria.</p>

<p>5-azido-5-deoxy-D-arabinose is a compound derived from Aquilaria sinensis that has various biological activities. It has been shown to modulate transmembrane conductance by interacting with fatty acid-binding proteins and divalent metal ions. Additionally, it can regulate the activity of potassium channels, which play a crucial role in cellular function. 5-azido-5-deoxy-D-arabinose is known for its reactive properties and can form covalent adducts with nucleophilic residues in proteins, affecting their structure and function. This compound has also been studied for its potential therapeutic applications, such as enhancing the delivery of iron sucrose through electrode-based systems or improving the bioavailability of drugs like ketorolac or creatine. Furthermore, 5-azido-5-deoxy-D-arabinose exhibits interesting carbohydrate chemistry, making it a valuable tool for carbohydrate synthesis and modification. Its diverse characteristics and unique properties make it an intriguing compound for further</p>

<p>Phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside is a fluorinated synthetic monosaccharide that has been synthesized to serve as a glycosylation and polysaccharide modification agent. Phenyl 3,4,6-tri-O-acetyl-2-deoxy-2--phthalimido--b--D--glucopyranoside is an effective methylation agent for the synthesis of complex carbohydrates. It can be used for click modifications on the sugar moiety of oligosaccharides and polysaccharides. Phenyl 3,4,6 -tri -O -acetyl -2 -deoxy -2 -phthalimido -b -D--glucopyranoside is soluble in water as well as many organic solvents. The CAS No. 120498 97 7 is assigned to</p>