Monossacáridos

1,2-Dideoxy-5-O-DMT-D-ribose is a methylation inhibitor that inhibits the transfer of a methyl group from S-adenosylmethionine to a substrate. This modification can be found in many biological systems, including DNA and RNA. It is also used as an intermediate in the synthesis of other compounds such as oligosaccharides and polysaccharides. 1,2-Dideoxy-5-O-DMT-D-ribose has been shown to inhibit the growth of bacteria by inhibiting bacterial cell wall synthesis. It is believed to work by binding to glycosidic bonds in bacterial cell walls, preventing the formation of new bonds and therefore inhibiting cell wall biosynthesis.
1,2 - Dideoxy - 5 - O - DMT - D - ribose can be used for fluorination reactions with various types of compounds, including sugars and other complex carbohydrates.

Inhibitor of β-galactosidase

1-Deoxy-1-nitro-L-mannitol is an irreversible inhibitor of the enzyme mannitol dehydrogenase. It also inhibits other enzymes, such as L-arabinose isomerase and L-azide amidohydrolase, which are involved in the biosynthesis of arabinose and azide. The synthesis of 1-deoxy-1 nitro mannitol can be achieved through a one step reaction with hydroxide and l-arabinose (or l-xylose) in the presence of carbonate or sulfate. This product can be used in syntheses of amphoteric compounds.

3,4-O-Isopropylidene-L-arabinose (3,4-OIRA) is an isopropylidene derivative of L-arabinose. 3,4-OIRA has been shown to be a substrate for glycosylation reactions with various other sugars. It can also undergo methylation reactions and has been modified by fluorination. 3,4-OIRA is a food additive that belongs to the category of complex carbohydrates.

2-Azido-2-deoxy-3,5-O-benzylidene-D-lyxono-1,4-lactone is a custom synthesis that is methylated with an azide group. It has been modified with a click reaction to attach an oligosaccharide or polysaccharide and then fluorinated. The modification of this product is not limited to methylation, but includes many other modifications such as fluoroquinolone resistance. 2-Azido-2-deoxy-3,5-O-benzylidene -D-lyxono--1,4--lactone can be used for the preparation of complex carbohydrates. This product can also be used in the synthesis of monosaccharides and sugars.

(5S, 8S, 9S) -8- [(4S) - 2, 2-Dimethyl- 1, 3- dioxolan- 4- yl] - 9- hydroxy- 2, 2- dimethyl- 1, 3, 7- trioxaspiro[4.4] nonan- 6- one is a synthetic molecule that has been modified to include fluorine atoms at the C3 and C4 positions. It is a sugar that is found in many plants and animals. This sugar can be methylated or modified with other molecules to form complex carbohydrates. The ability of this sugar to form oligosaccharides and polysaccharides makes it an important part of carbohydrate metabolism.

Methyl N-benzyl-4,6-dideoxy-4,6-imino-2,3-O-isopropylidene-b-D-talopyranoside is a fluorinated monosaccharide with a custom synthesis. It is a synthetic oligosaccharide that has undergone glycosylation and polysaccharide modification. This compound has been modified by methylation, click chemistry, and sugar formation. It is available in high purity with a CAS number of 29059-07-1.

Iron sucrose is a sucrose-iron complex that is administered intravenously for the treatment of bowel disease and iron deficiency. Iron sucrose has been shown to have potent inducers of oxidative injury, which may be due to the formation of reactive oxygen species. Iron sucrose has also been shown to increase cellular transformation and congestive heart failure in mice. Long-term toxicity studies have not been conducted.

Allyl 2-O-acetyl-3-O-benzyl-a-L-rhamnopyranoside is a synthetic monosaccharide that is used in the synthesis of complex carbohydrates. It has a CAS number of 940274-20-4 and may be modified with fluorine or methyl groups. Synthetic allyl 2-O-acetyl-3-O-benzyl-a -L -rhamnopyranoside is also known as "Methylated, Custom synthesis, Click modification, Oligosaccharide, Polysaccharide, saccharide, sugar."

Ethyl 4,6-O-benzylidene-b-D-thiogalactopyranoside is a synthetically produced carbohydrate typically used as a building block in oligo-saccharide synthesis.