Glycosciences

Heptyl b-D-glucopyranoside is a natural product that belongs to the class of 5HT agonists. It was originally isolated from plants and has been shown to have antiinflammatory activity. It has also been observed to have effects on human serum, lymphocyte transformation, high salt, polymerase chain reaction (PCR), and kinetic energy. Heptyl b-D-glucopyranoside is synthesized by reacting heptanol with 5-hydroxybenzaldehyde in the presence of an acid catalyst.

Lewis Y tetrasaccharide-BSA is a synthetic oligosaccharide that contains Lewis Y, a sugar that is naturally found in human blood. It is used in glycoprotein research and can be modified with fluorination, methylation, or click chemistry to suit the needs of the researcher. This product has high purity and can be custom synthesized to meet specific requirements.

2,3,5-Tri-O-p-chlorobenzoyl-a-D-ribofuranosyl chloride is a sugar derivatized with chlorine. It is a high purity product that can be custom synthesized to meet your needs. This compound has been used in the synthesis of saccharides and oligosaccharides with click modification, fluorination, glycosylation, methylation, and modification.
2,3,5-Tri-O-p-chlorobenzoyl-a-D-ribofuranosyl chloride is an important intermediate for the synthesis of complex carbohydrates. The chemical structure of this molecule consists of three parts: an aromatic ring (benzene), a glycosylation site (glycine), and a carboxylic acid group (carboxylic acid). The aromatic ring allows 2,3,5-Tri-O-p-chlorobenzoyl-a-D

3,4-Di-O-acetyl-D-xylal is a sterically hindered substrate analogue of the natural L-xylal. It can be used to synthesize stereoselective reaction products with carbohydrate derivatives, such as vitamin B12 and magnesium. 3,4-Di-O-acetyl-D-xylal has been shown to react with azides and hydroxymethyl groups to produce formyl and formate groups. The nmr spectra of this compound show strong signals for the acetoxy group at 2.2 ppm and the hydroxymethyl group at 2.6 ppm. Treatment of 3,4-Di-O-acetyl-D-xylal with borohydride yields chloride and acid catalyst, respectively.

2,3,4,6-Tetra-O-acetyl-D-glucopyranose is a carbohydrate that is used in the synthesis of besifloxacin. This compound has been studied as an analog for many other natural compounds and its derivatives have shown to be effective against bacteria such as Staphylococcus aureus and Clostridium perfringens. The acetyl groups on this molecule allow it to be easily converted into other compounds with desired properties. This compound has been found to be acidic and can be used as a medicinal preparation or analytical chemistry reagent. The hydroxyl group on the 2 carbon atom allows the molecule to form glycoside derivatives. The halides on this molecule are also important for making new molecules by replacing one of the hydrogen atoms with another halogen atom. The phenylpropanoid glycosides are found in plants and may contain an enantiomeric form of 2,3,4