Glicoscienza

Tetradecyl b-D-maltopyranoside is a crystalline polymer of high molecular weight that is made up of repeating units of tetradecyl b-D-maltose. It has a lamellar morphology and can be sectioned with techniques such as electron microscopy, X-ray diffraction, and differential scanning calorimetry. Tetradecyl b-D-maltopyranoside is a metastable form of the compound. It has been found in nature in the form of the monomer unit, tetradecyl maltosyl (tetramethyleneglycol) b-d-maltoside. In order to produce this compound as a polymer, it must first be heated to about 160°C for several hours, which causes the monomers to assemble into chains of tetrahedrons. The properties of tetradecyl b-D-maltopyranoside depend on its environment

Irbesartan N-b-D-glucuronide is a complex carbohydrate that is a synthetic saccharide. It is an intermediate in the synthesis of irbesartan, which is an angiotensin II receptor antagonist. Irbesartan N-b-D-glucuronide has been shown to have antihypertensive properties, inhibiting the activity of the renin-angiotensin system and increasing blood flow to the kidneys. It also inhibits the growth of cancer cells. This compound can be custom synthesized for your specific needs and purities can be controlled to meet your specifications.

Welan gum is a microbial polysaccharide produced by a species of Alcaligenes and shows interesting rheological properties of use in the oil and agricultural industries. The structure is similar to gellan based on repeating glucose, rhamnose and glucuronic acid units but with a single side chain of either an α-L-rhamnopyranosyl or an α-L-mannopyranosyl unit linked (1,3) to the 4-O-substituted β-D-glucopyranosyl unit in the backbone.

Metabolite of Mycophenolic acid

1,2,3,4,6-Penta-O-acetyl-D-galactopyranose is an analog of the natural pentoses that binds to the mitochondrial membrane and inhibits the production of pro-inflammatory cytokines. This drug has been shown to inhibit the binding of lysophosphatidic acid (LPA) to its receptor by substituting for LPA in this binding site. 1,2,3,4,6-Penta-O-acetyl-D-galactopyranose also inhibits the expression of proinflammatory cytokines such as interleukin 6 (IL6) and IL1β in a dose dependent manner. This drug is also capable of inhibiting phosphotungstic acid from binding to a monolayer surface and can be used as a glycopolymer for cell culture. It has been shown that 1,2,3,4,6-Penta-O-acetyl

1,2,3-Tri-O-methyl-D-glucopyranoside is a custom synthesis and modification of the natural product 1,2,3-tri-O-methyl-D-mannopyranoside. The compound was synthesized by fluorination of the 3' hydroxyl group followed by methylation of the 2', 3' hydroxyl groups to form a triol. This sugar was then glycosylated with D-glucose to produce an oligosaccharide. 1,2,3 - Tri -O - methyl - D - glucopyranoside is a natural product that can be found in plants such as barley and wheat. It has been shown to have antiinflammatory properties.

2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl chloride is a carbohydrate that has been modified by fluorination. It is used as an ingredient in the synthesis of saccharides and oligosaccharides. This product is synthesized by the reaction of 2,3,4,6-tetra-O-acetylmannose with chlorodifluoromethane in the presence of a base.

Difucosyl-para-lacto-N-hexaose II is a blood group oligosaccharide

UDP-b-L-arabinofuranose is a custom synthesis product that is used to modify polysaccharides. It is a high purity sugar nucleotide. UDP-b-L-arabinofuranose has CAS number 331001-44-6.

6-Deoxy-6-mercapto-gamma-cyclodextrin, octakis (Methyl 6DG) is a novel and unique sugar with two methyl groups on the C6 hydroxyl position. It has been synthesized from glucose by a click modification reaction and can be used as an alternative to 6DG for the production of oligosaccharides and polysaccharides. The high purity of Methyl 6DG makes it suitable for use in analytical research, such as fluorescence resonance energy transfer measurements.

4-Methoxyphenyl 3-O-allyl-b-D-galactopyranoside is an antigen that is found on the surface of chronic lymphocytic leukemia cells. It is a highly reactive antibody that has been shown to be able to induce monoclonal antibody production in animals and humans. The antigen was first discovered in tissues from patients with chronic lymphocytic leukemia, but it has also been identified in tissues from other animals, including rabbits, rats, guinea pigs, and mice. 4MP3AG binds to the CD20 surface antigen on B cells. This binding leads to a conformational change in the antigen and exposes a new epitope on the molecule for binding by antibodies. The resulting antibodies are then used as diagnostic tools for chronic lymphocytic leukemia.

1,3,4,6-Tetra-O-acetyl-2-O-benzyl-a-D-mannopyranose (1) is a high purity monosaccharide that can be custom synthesized to meet the needs of your research. 1 is a synthetic compound that is fluorinated and glycosylated. It has been shown to be an efficient methylation and modification agent for saccharide synthesis. It also acts as a building block for oligosaccharides and complex carbohydrates.

Safflor Yellow A is a natural drug that has been shown to have hypoglycemic effects. It is a potent inhibitor of glucose-6-phosphatase and glucose-6-phosphate dehydrogenase, which are enzymes involved in the conversion of glucose to glycogen. Safflor Yellow A also inhibits neuronal death, as it blocks the enzyme activities that lead to neuronal cell death. This drug has also shown antitumor activity, as it induces apoptosis in tumor cells. Safflor Yellow A also has antihyperlipidemic effects and can be used for the treatment of coronary heart disease. Low doses of this drug have been shown to reduce systolic pressure in rats and improve blood coagulation. The mechanism of action for this drug is not yet known but may involve toll-like receptor 4 signaling pathways or polymerase chain reaction (PCR).

Intermediate in the synthesis of empagliflozin

D-Arabinose-5-phosphate is an intermediate in the pentose phosphate pathway. It is synthesized from D-xylulose-5-phosphate by xylitol dehydrogenase. D-Arabinose-5-phosphate inhibits the enzyme xylitol dehydrogenase, which converts xylulose to d-xylulose, and thus prevents the formation of 5-hydroxyisoxazole phosphate, a precursor to the synthesis of NADPH. In this way, it blocks the synthesis of NADPH, which is essential for aerobic metabolism. This inhibition leads to a decrease in ATP production and consequently cell death.

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

Neutral difucosylated hexasasaccharide naturally present in human breast milk