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3-Deoxy-3-fluoro-D-mannose (3DFM) is a synthetic sugar molecule that acts as an inhibitor of bacterial growth. It binds to the 6-phosphate group of nucleic acids, which prevents the addition of sugar molecules to ribose or deoxyribose groups. 3DFM also inhibits the synthesis of proteins and RNA, which are necessary for bacterial growth. 3DFM is a structural analog of mannose and glucose, and has been shown to be effective against chronic infections caused by bacteria that produce lectins, such as C. difficile. This drug can be used in combination with other antibiotics to enhance their effectiveness.

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-D-fucopyranose is a glycosylation agent that can be used in the synthesis of complex carbohydrates or in the modification of natural polysaccharides. It can be fluorinated to produce 1,2,3,4-tetra-O-fluoro-D-fucopyranose or modified with a click reagent to produce 1,2,3,4-tetra-[5-(N'-diethylamino)pentyl]-D-fucopyranose. The CAS number for this product is 109712-63-7. This product is available for custom synthesis and is sold at a purity of >99%.

Phenyl 4,6-O-benzylidene-2,3-di-O-(4-methoxybenzyl)-a-D-thiomannopyranoside is a synthetic glycosylated mannose oligosaccharide. It has a molecular weight of 756.85 and the chemical formula C36H43NO14. Phenyl 4,6-O-benzylidene-2,3-di-O-(4-methoxybenzyl)-a-D-thiomannopyranoside has been shown to be effective against fungus infections in mice models. This product is custom synthesized for research purposes only and does not contain any hazardous or toxic chemicals.

N-Acetyl-L-neuraminic acid is a glycosylation compound that is an important component of the cell wall of Gram negative bacteria. It is used in the synthesis of polysaccharides and in the formation of complex carbohydrates. N-Acetyl-L-neuraminic acid has been studied for its potential use as a drug delivery agent due to its ability to inhibit the activity of enzymes such as α-mannosidase, which can lead to tumor metastasis. This compound can be synthesized using methylation, fluorination, and click chemistry, or custom synthesized by ordering specific monosaccharides. N-Acetyl-L-neuraminic acid can also be modified with acetate groups to create an acetylated form for use in chemical analysis or as a substrate for enzymatic reactions.

N-Acetyl-glucosaminyl thiazoline triaacetate is a custom synthesis that is fluorinated. It has been modified for methylation and Click chemistry. This chemical is an oligosaccharide, polysaccharide, saccharide, carbohydrate, or sugar. It is purified with high purity and has a monosaccharide modification. N-Acetyl-glucosaminyl thiazoline triaacetate is used in the modification of complex carbohydrates and can be synthesized from methylated glucosamine and acetamidomethylthiazoline.