Monosaccharides

Mycophenolic acid phenolic b-D-glucoside is a high purity custom synthesis that can be modified to suit customer requirements. It is a complex carbohydrate with a methyl group, fluorine atom, and glycosylation. The chemical name for Mycophenolic acid phenolic b-D-glucoside is CAS No. 55533-52-3. This product is also known as Glycosylation, Oligosaccharide, sugar, Synthetic, Fluorination, Custom synthesis, Methylation, Monosaccharide, Polysaccharide, saccharide. Click modification or Modification.

Phenyl 2,3-di-O-benzyl-6-deoxy-b-D-thioglucopyranoside is a synthetic glycosylated sugar with a fluorinated benzene ring. It is used as an intermediate in the synthesis of oligosaccharides, polysaccharides and saccharides. Phenyl 2,3-di-O-benzyl-6-deoxy-b-D-thioglucopyranoside has an appearance of a white powder and a melting point of around 100°C. This compound has been evaluated for its purity and quality by analytical methods such as high performance liquid chromatography (HPLC), gas chromatography (GC) and nuclear magnetic resonance (NMR).

2-Methoxycarbonylphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside is a high purity and custom synthesis sugar that can be fluorinated and glycosylated. This molecule has been modified with methyl groups and is an oligosaccharide. It is a complex carbohydrate with saccharide units, which are monosaccharides or polysaccharides. CAS No. 7791-66-4

3-O-Acetyl-1,2-O-isopropylidene-a-D-galactofuranose is a modification of the carbohydrate structure galactofuranose. It has been custom synthesized and is available in high purity with a monosaccharide content of >99%. 3-O-Acetyl-1,2-O-isopropylidene-a-D-galactofuranose can be methylated or glycosylated and is used as a building block for the synthesis of complex carbohydrates. 3-O-Acetyl-1,2,3,4,6,7,8,-octahydrobenzo[b]naphtho[2,1b][1]benzopyran (CAS No. 109680) is also known as 3-(acetamido)-1,2:3',4'-diisopropyl

N6-Benzyladenine-3-glucoside is a carbohydrate that is modified with a click chemistry reaction. It is synthesized from D-mannose and 6-benzylaminopurine and has been glycosylated with 2,3,4,6-tetra-O-acetyl glucosamine. N6-Benzyladenine-3-glucoside is an important component of the bacterial cell wall. The compound consists of a single sugar chain and is fluorinated at the C2 position.

Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene-b-D-glucopyranoside is a carbohydrate with a saccharide structure that has been modified by fluorination and methylation. The sugar is an oligosaccharide containing sugar monomers of glucose and galactose. This compound is available for custom synthesis to order. It can be synthesized in high purity and with a high degree of modification, such as glycosylation, click modification, and methylation.

Mannostatin A is a prodrug that is activated in the body by cleavage of the ester linkage. It has been shown to be a specific inhibitor of feedback inhibition of protein synthesis and cleavage at the carboxyl-terminal end. Mannostatin A has also been shown to inhibit, selectively, the synthesis of proteins in bacteria. In addition, it is possible that this drug may be converted into an inactive form by conjugation with glucuronic acid or by oxidation.

1,2-Dideoxy-2-fluoro-galactonojirimycin is a synthetic glycoside derived from galactonojirimycin. It has been modified to include fluorine and methyl groups. 1,2-Dideoxy-2-fluoro-galactonojirimycin is an oligosaccharide with a complex carbohydrate structure. It can be synthesized by Click modification of the sugar moiety with fluoroacetate followed by glycosylation and methylation of the saccharide chain.

a-D-Glucosyl hesperidin is a water-soluble drug that has been shown to have antioxidant properties. It inhibits the activity of certain enzymes, such as phospholipase A2 and lipoxygenase, which are involved in inflammation. The compound has also been shown to inhibit cancer cells in vitro by inducing apoptosis and inhibiting cell proliferation. Glibenclamide, the active form of a-D-glucosyl hesperidin, is an orally active hypoglycemic agent used to treat diabetes mellitus type 2 and gestational diabetes. It works by stimulating insulin release from beta cells in the pancreas and promoting insulin sensitivity in peripheral tissues. This compound also inhibits annexin V binding to phosphatidylserine, which leads to apoptosis.

The 4-Toluoyl-a-D-thiomannopyranoside is a six-membered ring with a hydrogen atom at the center. The structure of this molecule is composed of two chains, each of which has four atoms in their backbone. There are also two conformations to the molecule, one that can be observed as a chair conformation and one that can be seen as a boat conformation. In the chair conformation, there are three bonds that form from the central carbon atom to other carbons on the same chain. These bonds are called alpha bonds, and they connect in a linear fashion. In the boat conformation, these three bonds form an angle of 120 degrees with each other and have staggered geometry. The alpha bonds in this case form an angle of 180 degrees with each other.

1,2,3,4-Tetra-O-acetyl-L-xylopyranose is a custom synthesis product. It is a sugar that is found in glycosaminoglycans and proteoglycans. This product can be customized through the modification of the sugar with fluorination, methylation, acetylation or other modifications. This product has a CAS number of 142130-89-0 and can be synthesized from sucrose using Click chemistry. The chemical name for this compound is 1,2,3,4-Tetra-O-[(trimethylsilyl)acetyl]-L-xylopyranose.