Monosaccharides

<p>6-Deoxy-D-lactose is a custom synthesized, complex carbohydrate that is an Oligosaccharide. It is a polysaccharide with a CAS number of 52689-62-0. 6-Deoxy-D-lactose has been modified by methylation and glycosylation and can be used as a Modification of saccharides. 6-Deoxy-D-lactose has been fluorinated and it can be synthesized by Click modification of sugar or high purity. 6-Deoxy-D-lactose is a white, crystalline powder that is soluble in water, ethanol, and acetone.br&gt;<br>6 Deoxy Lactose (6DL) is an oligosaccharide that consists of one glucose molecule linked to one galactose molecule via alpha 1--&gt;4 glycosidic linkage. The chemical formula for 6DL is C 12 H 22 O 11 . 6DL</p>

<p>Losartan N2-glucuronide is a custom synthesis that has been modified by fluorination, methylation, and monosaccharide modification. It is synthesized with click chemistry to create an oligosaccharide. This product is synthesized from saccharides (carbohydrates) and polysaccharides. Losartan glucuronide is a complex carbohydrate that has been glycosylated and sugar modified for high purity.</p>

<p>Substrate for UDP-3-O-acyl-GlcNAc deacetylase</p>

<p>Promotes hyaluronic acid production; synthetic building block</p>

<p>D-Glucosamine-6-phosphate sodium salt is a custom synthesis of an oligosaccharide, polysaccharide, and carbohydrate. The chemical modification of this compound includes methylation, glycosylation, and carbamylation. This product has high purity with a fluorination level of 98%.</p>

<p>Intermediate in the synthesis of dapagliflozin</p>

<p>N-Ethyldeoxynojirimycin hydrochloride is a mutant of the natural compound, deoxynojirimycin. The chemical structure of this compound is similar to that of the natural product and its molecular weight is 547.7 g/mol. N-Ethyldeoxynojirimycin hydrochloride has been shown to interact with the bacterial chaperone GroEL and enhance the activity of this protein. Further study has shown that this agent binds to GroEL in a manner that allows it to bind directly to ATPase domains I and II, leading to an increase in ATPase activity.</p>

<p>Canagliflozin is an oral diabetes drug that belongs to the class of sodium-glucose cotransporter 2 (SGLT2) inhibitors. It works by blocking reabsorption of glucose in the kidney, thereby lowering blood sugar levels. Canagliflozin has been shown to be a potent inhibitor of insulin resistance and has been used clinically in combination with metformin hydrochloride. The chemical stability of canagliflozin is dependent on its particle size, which can range from 10 micrometres to 100 micrometres. A number of analytical methods have been developed for canagliflozin, including high performance liquid chromatography with ultraviolet detection, gas chromatography with mass spectrometry detection, and dihedral angle analysis. Canagliflozin is an example of a polymorphic compound: it exists as two enantiomers due to chiral symmetry.</p>

<p>Intermediate in the synthesis of Decitabine</p>

<p>D-Talitol is a drug that is used to treat eye disorders and chronic pulmonary diseases. It belongs to the class of drugs called xylitol dehydrogenase inhibitors. D-Talitol inhibits the enzyme xylitol dehydrogenase, which converts xylitol into a different sugar called sorbitol. Sorbitol accumulates in certain parts of cells, such as the mitochondria, and can disrupt cellular processes by inhibiting oxidative phosphorylation and glycolysis. In addition, there are other effects of sorbitol accumulation that may lead to mitochondrial dysfunction, including inhibition of protein synthesis, induction of apoptosis (cell death), and inhibition of cell proliferation. D-Talitol has been shown to inhibit the growth of chronic kidney cells in culture by interfering with cellular metabolism in mitochondria.<br>A kinetic study has also shown that D-Talitol inhibits b-raf activity at concentrations that are not cytotoxic. This suggests that D-Talitol may be useful for</p>

<p>UDP-2-amino-2-deoxy-D-glucose is a modification of glucose. It is an organic compound that can be used in the synthesis of oligosaccharides and polysaccharides. It can be methylated or glycosylated with other sugars, such as galactose, to form complex carbohydrates. UDP-2-amino-2-deoxyglucose also has a high purity and CAS number.</p>

<p>Trans-zeatin-7-glucoside is an abscisic acid (ABA) metabolite that can be found in plant tissue. It is used as a natural product to regulate growth and development. Trans-zeatin-7-glucoside has been shown to inhibit the biosynthesis of gibberellins, which are plant hormones that promote cell elongation. This compound is purified from plant tissues by chromatographic methods, such as reversed phase HPLC or ion exchange chromatography. The sample preparation involves extraction with a solvent such as methanol or chloroform followed by purification on an analytical column. Immunoaffinity chromatography is also used for sample preparation, which involves binding to antibody molecules on the surface of a solid support material. Trans-zeatin-7-glucoside can be detected using analytical methods such as gas chromatography or liquid chromatography coupled with mass spectrometry. Trans-zeatin-7-</p>

<p>O-(D-glucopyranosylidene)amino N-phenylcarbamate is a synthetic monosaccharide that is used in our laboratory as an intermediate for the synthesis of complex carbohydrates. It is also used in the modification of polysaccharides and glycosylations. This compound has been shown to be stable to hydrolysis, methylation, and oxidation. O-(D-glucopyranosylidene)amino N-phenylcarbamate has been shown to be a high purity product with a CAS number of 104012-84-2.</p>

<p>2,3-O-Isopropylidene-D-lyxonic acid-1,4-lactone (2,3-OIPDL) is a fluorinated polysaccharide that is synthesized from glycosylation of 1,4-lactone with 2,3-O-isopropylidene D-lyxonic acid. This compound has been shown to have high purity and is used in the modification of carbohydrates.</p>

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

<p>1-O-Galloyl-b-D-glucose is a molecule that is found in plants and has been used as an inhibitor of p-hydroxybenzoic acid (PHBA) enzyme activities. 1OGG inhibits the growth of viruses by inhibiting the enzymatic activity of their RNA polymerases. It also inhibits mitochondrial membrane potential, which is vital for cellular respiration. 1OGG has shown to be active against urinary infections and opportunistic fungal infections such as Candida glabrata. In vitro assays have shown that it may have anti-inflammatory properties.</p>