Glycoscience

GD1b ganglioside (shown as ammonium salt) is one of the major gangliosides in neuronal and glial membranes. It has a core tetrasaccharide structure (Galβ1,3GalNAcβ1,4Galβ1,4Glc) with its two sialic acids linked α2,3/α2,8 to the inner galactose residue, and ceramide linked β to position 1 on the reducing terminal glucose residue (Ledeen, 2009). GD1b ganglioside acts as a receptor for BK virus, as well as for heat-labile LTII-a toxin, produced by enteropathogenic E. coli. GD1b ganglioside also interacts with tetanus neurotoxin (TeNT) and is crucial for its entry into cells (Kolter, 2012). The functional significance of ammonia in the brain is not yet fully understood: see (Modi 1994).

An anhydro thio sugar

13-cis-Retinoyl b-D-glucuronide is a synthetic compound that can be modified to create a wide range of potential products. 13-cis-Retinoyl b-D-glucuronide is an oligosaccharide with a carbohydrate that may be glycosylated or polysaccharided. It has been custom synthesized and fluorinated, methylated, and monosaccharided. This product is extremely pure and can be used for many applications in the biomedical field.

1,4-Anhydro-D-mannitol is a sugar alcohol that belongs to the group of alditols. It is a tautomer of galactitol, which is found in fetal bovine serum. The dehydrated form of this compound has been shown to have an inhibitory effect on tyrosinase activity. 1,4-Anhydro-D-mannitol may be used as an intermediate in the production of polymers or as a cosmeceutical agent due to its high water solubility and low toxicity.

Tetrasaccharide; tumor-associated antigen; prognostic factor

The enzyme alcohol dehydrogenase, which is located in the cytosol of cells, catalyzes the conversion of ethanol to acetaldehyde. In this reaction, a hydrogen ion (H+) is abstracted from ethanol and two electrons (e-) are added to the molecule. The addition of these electrons results in the formation of a hydrogen bond between the alcohol and an electron-donating species such as water or octyl glucopyranoside. Octyl glucopyranoside is a detergent that has been used as a substrate for measuring rates of alcohol dehydrogenase. This detergent also has been shown to be effective at removing glycol ethers from biological samples.
The biochemical research on octyl glucopyranoside includes its use as an equilibrative nucleoside and its effect on bowel disease.

2-Hydroxypropyl-b-cyclodextrin is a water-soluble drug that is chemically stable in aqueous media. It has been shown to be safe for use in the eye, with no significant side effects. 2-Hydroxypropyl-b-cyclodextrin has been shown to have anti-inflammatory properties and will not cause hemolytic activity. 2-Hydroxypropyl-b-cyclodextrin binds to retinoic acid receptors, which are found on cells of the corneal surface and in human spermatozoa. The binding of retinoic acid inhibits the production of enzymes that break down retinoids and prevents cell proliferation. This agent also interacts with other cellular components such as proteins, lipids, carbohydrates, nucleic acids, and hormones.

Rengasin-4'-O-glucoside (RG4G) is a natural glycoside that belongs to the category of sugar derivatives. It has versatile uses and can be used as a building block for complex compounds, as well as in research chemicals, pharmaceuticals, and cosmetics. RG4G also has many applications in chemistry, including being used as a reagent or speciality chemical. RG4G is also an important intermediate in organic synthesis, which can be used to synthesize many useful compounds. The compound is often used as a scaffold for larger molecules.

Rengasin-3'-O-glucoside is a fine chemical, useful building block, and research chemical. It is a versatile building block that can be used in the synthesis of complex compounds. Rengasin-3'-O-glucoside is also a useful intermediate or scaffold for reactions. This compound has been shown to react with 1,2-ethanediol and form an ester, which can be hydrolyzed to release glycerol and the original rengasin-3'-O-glucoside.

This beta-cyclodextrin (β-CD) derivative is a functionalized cyclic oligosaccharide composed of seven glucose units, characterized by a hydrophilic exterior and a lipophilic cavity (bigger than α-CD and smaller than γ-CDs), which allows it to encapsulate various guest molecules. This structural feature facilitates its use in multiple applications, including pharmaceuticals, food enhancement, and cosmetics. In the pharmaceutical industry, it enhances the solubility and stability of poorly water-soluble drugs, improving their bioavailability and efficacy while also masking unpleasant tastes. The food sector utilizes it as a stabilizer for flavors, colors, and nutrients, extending shelf life by protecting sensitive ingredients from degradation. In cosmetics, it serves as a complexing agent for fragrances and active components, ensuring their stability and controlled release. Its use expands to many other fields, including nanotechnology for drug delivery systems, environmental remediation for extracting organic pollutants, textiles for slow-release fragrances, and analytical chemistry for chiral separation.

GD1b oligosaccharide (shown as ammonium salt) is the carbohydrate moiety in one of the major gangliosides in neuronal and glial membranes; it has a core tetrasaccharide structure (Galβ1,3GalNAcβ1,4Galβ1,4Glc) with its two sialic acids linked α2,3/α2,8 to the inner galactose residue (Ledeen, 2009). GD1b ganglioside acts as a receptor for BK virus as well as for heat-labile LTII-a toxin, produced by enteropathogenic E. coli. GD1b ganglioside also interacts with tetanus neurotoxin (TeNT) and is crucial for its entry into cells (Kolter, 2012). The functional significance of ammonia in the brain is not yet fully understood. However, NH4 + stimulates Na+, K+ activated ATPase causing stabilization of the neuronal membranes of which gangliosides are major structural components. Further, ammonia is known to inhibit lysosomal enzymes which include enzymes degrading gangliosides (Modi, 1994).

Please enquire for more information about Benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside including the price, delivery time and more detailed product information at the technical inquiry form on this page

This beta-cyclodextrin (β-CD) derivative is a functionalized cyclic oligosaccharide composed of seven glucose units, characterized by a hydrophilic exterior and a lipophilic cavity (bigger than α-CD and smaller than γ-CDs), which allows it to encapsulate various guest molecules. This structural feature facilitates its use in multiple applications, including pharmaceuticals, food enhancement, and cosmetics. In the pharmaceutical industry, it enhances the solubility and stability of poorly water-soluble drugs, improving their bioavailability and efficacy while also masking unpleasant tastes. The food sector utilizes it as a stabilizer for flavors, colors, and nutrients, extending shelf life by protecting sensitive ingredients from degradation. In cosmetics, it serves as a complexing agent for fragrances and active components, ensuring their stability and controlled release. Its use expands to many other fields, including nanotechnology for drug delivery systems, environmental remediation for extracting organic pollutants, textiles for slow-release fragrances, and analytical chemistry for chiral separation.