Monossacáridos

<p>The 4-methoxyphenyl 2,3,6-tri-O-benzoyl-b-D-galactopyranoside (4MP) is a coagulation factor that inhibits the activity of coagulation factors Xa and IIa. The compound has been shown to be reactive with the detection methods used for other coagulation factors. The sensitivity of 4MP to detection was assessed using a battery of detection methods. 4MP was found to be more reactive than other compounds studied with regard to the use of an immunoassay for detection. This compound has hepatotoxic effects and can cause cell death in vitro. Cell culture studies show that 4MP causes membrane permeabilization and cellular uptake by bacteria.</p>

2,3,5-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-D-arabinofuranose is an organic compound that belongs to the group of furan derivatives. The configuration of this molecule was determined to be (2S,3S) by the use of stereoselective synthesis. It can be synthesized from a benzaldehyde and a ribofuranosyl chloride with a yield of about 95%. This compound has been shown to react with azides in a catalytic transfer reaction yielding yields of up to 100%.

Mucic acid is a metal chelate that stimulates the metabolism of carbohydrates, fats and proteins. It also plays a role in the production of energy in the body. Mucic acid has been shown to have a protective effect against infectious diseases, as it activates toll-like receptor 2 (TLR2) and TLR4, which are molecules involved in innate immunity. Mucic acid has been shown to protect against influenza virus infection by increasing the expression of interferon-gamma (IFN-γ) and IL-12, which are cytokines that inhibit viral replication. Mucic acid can be used as a fluorescence probe for detection of polymorphonuclear leucocytes in blood samples.

<p>Glycogen phosphorylase inhibitor</p>

<p>Antioxidant; antibacterial; suppresses LPS-induced inflammatory response</p>

<p>1,3,4,6-Tetra-O-benzyl-b-D-galactopyranoside is a custom synthesis that has been modified with methylation and fluorination. It is an oligosaccharide composed of saccharides linked by glycosidic bonds. Carbohydrates are polymers of monosaccharides, which can be classified as either simple sugars or complex carbohydrates. This product is a high purity, synthetic sugar that is suitable for use in the synthesis of complex carbohydrate polymers.</p>

<p>1,2,3,4,6-Penta-O-benzyl-b-D-thiogalactopyranoside is a custom synthesis that is a complex carbohydrate. It has a CAS number of 210358-01-3 and a molecular weight of 603. It is modified with saccharide, methylation, glycosylation, and carbonyl groups. This product is available in high purity and without fluorination or synthetic modification.</p>

<p>a-Homonojirimycin is a chaperone that is effective in inhibiting HIV infection. It has been shown to inhibit the activity of chymotrypsin, carboxypeptidase A, and aminopeptidase B. The model system used for this compound was the human liver, which showed that a-homonojirimycin had a potent inhibitory activity against these enzymes. This drug also has a dry weight of 1,520 g/mol and an effective dose of 0.01 mg/mL. In vitro studies have shown that a-homonojirimycin inhibits influenza virus by binding to the hemagglutinin protein on the surface of the virus and preventing its attachment to host cells.</p>

<p>Synthetic carbohydrate building block</p>

<p>Ginsenoside F1 is a natural compound found in ginseng. It is believed to have anti-cancer properties. Ginsenoside F1 has been shown to inhibit the proliferation of HL-60 cells and have an apoptotic effect by regulating mitochondrial membrane potential and activating the apoptotic pathway. The mechanism of action for the anti-cancer activity of Ginsenoside F1 may be due to its ability to inhibit angiogenesis, which is needed for cancer cell proliferation. Ginsenoside F1 also inhibits the growth of skin cancer cells in mice by regulating microvessel density. This compound has been found in foods such as soybeans, rice, peanuts, and kiwifruit.</p>

<p>Tert-butyl 2-deoxy-L-ribopyranoside is a synthetic monosaccharide that can be used in the synthesis of polysaccharides and oligosaccharides. It is also used for fluorination reactions, such as click modification. This compound can be custom synthesized to order, and it is available in high purity. Tert-butyl 2-deoxy-L-ribopyranoside can be modified with a variety of different functional groups, including methylation. It has an CAS number of 1032153-57-3.</p>

Phenyl α-D-thiomannopyranoside is a saccharide that can be modified to produce various derivatives. Phenyl α-D-thiomannopyranoside is a high purity, custom synthesis carbohydrate. This product is synthesized by the methylation and glycosylation of phenyl α-D-mannopyranoside. The carbohydrate has been fluorinated for the production of fluorinated derivatives. Phenyl α-D-thiomannopyranoside is an oligosaccharide and sugar that belongs to the class of carbohydrates. It can be used in protein modification and complex carbohydrate synthesis.

<p>N-Acetyl-2-O-methyl-b-D-neuraminic acid (AOMBNA) is a modification of sialic acid. It is an N-acetylated, O-methylated analogue of b-D-neuraminic acid. AOMBNA is synthesized by the chemical modification of D,L -erythro -2,3,4,6 tetra hydro sialic acid with methyl bromo acetate in the presence of sodium methoxide. The product can be purified by crystallization from dichloromethane and methanol mixture. AOMBNA has been used in complex carbohydrate synthesis and glycosylation reactions.</p>

<p>D-Glucono-1,5-lactone is a chemical compound that is a member of the class of compounds known as diketones. It can be used in chemical biology and polymer chemistry to probe hydrogen bonding interactions, polymer compositions, and redox potentials. D-Glucono-1,5-lactone has been shown to inhibit the growth of cells in culture by inhibiting DNA synthesis. This inhibition is due to its ability to bind with high affinity to nucleic acids and prevent the formation of the enzyme complexes required for transcription and replication. The effects are reversible.</p>

<p>Phenyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a chemical compound that is a member of the class of phenyl 2-acetamido-2-deoxy-b-D-glucopyranosides. This compound has been shown to be anomeric, substituent and phenyl.</p>

<p>D-Xylulose is a sugar monomer found in the cell walls of bacteria. It is also present in human blood, where it is converted to xylitol. D-Xylulose has been shown to be an important component of bacterial cell wall synthesis and can be used as a probiotic for humans. The enzyme xylitol dehydrogenase catalyses the conversion of D-xylulose to xylitol. The reaction mechanism is thought to be similar to that of other enzymes in the glycolysis pathway, such as ribitol dehydrogenase, which converts ribitol to ribose 5-phosphate. This conversion can be achieved through two different methods: hydrogen fluoride or sodium hydroxide. D-Xylulose can also be used for analytical purposes, such as in the detection of trifluoroacetic acid (TFA) by gas chromatography and mass spectrometry.</p>

<p>Chloramphenicol glucuronide is an active metabolite of chloramphenicol. It can be detected in human serum and urine, as well as rat liver microsomes. Chloramphenicol glucuronide binds to the cytosolic protein, cytochrome b5 reductase, which inhibits protein synthesis and cell growth. This compound has been shown to be effective for treating infectious diseases such as typhoid fever, pelvic inflammatory disease, and pneumonia. The chloramphenicol glucuronide group also includes a number of other metabolites that are formed from chloramphenicol by conjugation with glucuronic acid.</p>

2,5-Di-O-acetyl-3-deoxy-D-threo-pentono-1,4-lactone is a monosaccharide with the molecular formula C5H8O4. It is a carbohydrate that can be found in natural products such as honey and sugar cane. 2,5-Di-O-acetyl-3,6,-dideoxyhexose can be custom synthesized to order. Carbohydrates are polymers of glycosidic bonds between monosaccharides. Glycosylation refers to the attachment of a sugar molecule (glycosyl donor) to another molecule (glycosyl acceptor). This process is often catalyzed by enzymes called glycosyltransferases. The modification of carbohydrates can be achieved through glycosylation, which results in the formation of an oligosaccharide or a complex carbohydrate. 2,5 Di-O acetyl 3,6 -

Donor for Koenigs-Knorr type galactosylation and other anomeric substitutions

<p>D-Altrose is an alpha-hydroxy acid that is synthesized from D-arabinose and trifluoroacetic acid. It has been shown to be a substrate for the synthesis of oligosaccharides, which are important in carbohydrate chemistry. This molecule can also be used as a reagent in the preparation of carbohydrates with a specific configuration at C2. One use of this product is in generating analytical methods that can distinguish between D-altrose and D-arabinose by monitoring the ratio of hydrogen fluoride to carbonyl group signals. D-Altrose may also be used in asymmetric synthesis, where it is a useful chiral building block for the construction of galacturonic acid derivatives.</p>