Monosaccharides

<p>4-Methoxyphenyl 3-O-allyl-b-D-galactopyranoside is an antigen that is found on the surface of chronic lymphocytic leukemia cells. It is a highly reactive antibody that has been shown to be able to induce monoclonal antibody production in animals and humans. The antigen was first discovered in tissues from patients with chronic lymphocytic leukemia, but it has also been identified in tissues from other animals, including rabbits, rats, guinea pigs, and mice. 4MP3AG binds to the CD20 surface antigen on B cells. This binding leads to a conformational change in the antigen and exposes a new epitope on the molecule for binding by antibodies. The resulting antibodies are then used as diagnostic tools for chronic lymphocytic leukemia.</p>

<p>1,2,3,4-Tetra-O-benzyl-6-O-trityl-a-D-mannopyranose is a methylated form of mannopyranose. It can be custom synthesized and modified with various functional groups to produce a wide range of saccharide derivatives and oligosaccharides. The 1,2,3,4-tetra-O-benzyl group is commonly used for glycosylation reactions because it can be easily removed by acid hydrolysis. The methylation of the sugar molecule also increases its stability and prevents further reactions from occurring. This product is available in high purity and has been fluorinated on one or more hydroxyl groups to make it resistant to hydrolysis.</p>

<p>Forodesine is a purine nucleoside that inhibits the nucleoside phosphorylase enzyme and prevents the synthesis of purines. It has minimal toxicity and is effective against intracellular targets such as mitochondria, which are important for apoptosis induction. Forodesine also inhibits the mcl-1 protein, which is an inhibitor of t-cell lymphomas. This drug has been shown to be effective in animal models of human lymphoma and leukemia.</p>

<p>D-Fructose-1,6-diphosphate trisodium salt (D-FDP) is an ATP precursor that is used to study the effects of D-FDP on energy metabolism in rat cardiomyocytes. The results from this study showed that D-FDP increased ATP levels and inhibited the accumulation of intracellular lactate. This compound also inhibits ventricular myocardial hypertrophy induced by pressure overload in animal experiments. In addition, D-FDP has been shown to inhibit the polymerase chain reaction (PCR) process and to be active at a concentration of 25 mM.</p>

<p>Methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-D-glycero-D-galacto-non-2-enonate is a synthetic oligosaccharide that is used in the synthesis of glycosides. The carbohydrate has been modified to include fluorination and glycosylation. This product can be custom synthesized to meet your specifications.</p>

<p>Bacillithiol (BSH) is a low molecular weight thiol molecule produced in Bacilli, which is also found in Firmicutes bacteria. It plays an important role in maintaining the balance of reactive oxygen species within cells and detoxifying certain harmful compounds. It is the α-anomeric glycoside of L-cysteinyl-D-glucosamine with L-malic acid and it seems to have antioxidant properties. Bacillithiol plays an important role in bacterial redox homeostasis and plays an important role in the detoxification of electrophiles as it is a cofactor for FosB (thiol transferase). <br>This is the salt form (trifluoroacetic acid salt, TFA) of Bacillithiol.</p>

<p>Dipyridamole di-O-b-D-glucuronide is a fluorinated oligosaccharide that has been synthesized using the click chemistry reaction. It is a monosaccharide that has been glycosylated and modified with methyl groups to produce a high purity product. The carbohydrate consists of one or more sugar units linked by glycosidic bonds. Carbohydrates are classified by their number of sugar units and by the presence of other chemical groups such as phosphate, sulfate, or hydroxyl. This product is also used in the synthesis of complex carbohydrates and polysaccharides.</p>

<p>4-Nitrobenzyl b-D-thiogalactopyranoside is a synthetic glycosylation agent that can be used for the modification of saccharides and oligosaccharides. The product is available in different purity grades, custom synthesis, and custom modifications.</p>

<p>Mefenamic acid-acyl-b-D-glucuronide is a synthetic drug that binds to albumin and human serum albumin. It has been shown to irreversibly inhibit human UDP-glucuronosyltransferase, an enzyme in the human liver that catalyzes the addition of glucuronic acid to drugs and other xenobiotics. Mefenamic acid-acyl-b-D-glucuronide has also been shown to inhibit the activity of a wide range of enzymes in humans, including isoenzyme UGT1A6, which is found in the liver and kidney. This drug has been studied as a potential treatment for pain and inflammation in humans.</p>

<p>1,3,4,6-Tetra-O-acetyl-2-O-benzyl-a-D-mannopyranose (1) is a high purity monosaccharide that can be custom synthesized to meet the needs of your research. 1 is a synthetic compound that is fluorinated and glycosylated. It has been shown to be an efficient methylation and modification agent for saccharide synthesis. It also acts as a building block for oligosaccharides and complex carbohydrates.</p>

<p>3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-b-D-mannopyranose is a synthetic monosaccharide that is used as a substrate for the production of various oligosaccharides and polysaccharides. This substance can be fluorinated to produce 3,4,6-tri-O-(3′,5′ -difluoro) acetyl-1,2:5′,6′ -di(O—ethoxyethylidene)-b-D mannopyranose. It has been shown that methylation of the C1 position in this compound results in a variety of different compounds with different properties. In addition to its use as a substrate in organic synthesis, 3,4,6 triacetyl 1,2:5', 6'-di(O—ethoxyethylidene)-b D mannopyranose is also</p>

<p>N-5-Carboxypentyl-1-deoxygalactonojirimycin is an inhibitor of glycolipid hydrolase and a potential drug for the treatment of lysosomal storage disorders. N-5-Carboxypentyl-1-deoxygalactonojirimycin is derived from the natural product galactonojirimycin, which has been shown to inhibit glycolipid hydrolase in vitro. The compound was developed by modifying the peptide sequence to increase its affinity for the enzyme. N-5-Carboxypentyl-1-deoxygalactonojirimycin displays a higher affinity for glycolipid hydrolase than galactonojirimycin, and it also has a greater inhibitory effect on this enzyme.<br>N-5-Carboxypentyl-1-deoxygalactonojirimycin is</p>

<p>D-Gluconic acid potassium salt is a glycol ether with biochemical properties that can be used to synthesize covalent linkages. It has been shown to have antimicrobial properties in wild-type strains of Escherichia coli and Salmonella typhimurium. D-Gluconic acid potassium salt has been shown to exhibit inhibitory effects on the synthesis of DNA, RNA, and protein, as well as enzyme activities. The matrix effect is an analytical method that measures the inhibition of bacterial growth in agar plates. Electrochemical impedance spectroscopy (EIS) is a technique that measures changes in electrical resistance when bacteria are placed on an electrode surface. This technique has been used to show that D-gluconic acid potassium salt exhibits inhibitory effects against group P2 enzymes, such as polymerase chain reaction (PCR), which is used for DNA replication and amplification.</p>

<p>a-D-Mannopyranosyl amine is a synthetic product that is used as a sugar donor in glycosylation reactions. It can be custom synthesized to suit the needs of the customer. The chemical structure contains a methyl group and an oxygen atom, which are both in their highest oxidation state. This product is not intended for use as a food additive or dietary supplement.</p>

<p>Lectins are carbohydrate-binding proteins that can be classified into different types based on their specificities for glycan structures. One of the most common types is the N-acetyl-D-glucosamine (NAG) lectin, which binds to oligomers of NAG and related sugars. Lectins are used to activate cells and induce cell death. The dodecyl NAG lectin has been shown to bind to glucocerebrosides in a reductively irreversible manner and has been used as a model for such interactions. This lectin is also inexpensively produced from a synthetic benzylidene acetal, which can be made from commercially available materials. It has been shown that this lectin binds to polyacrylamide gels in an SDS-polyacrylamide gel electrophoresis, with a pH optimum at 7.0 and an amino acid composition that includes glutamic acid, glutamine, asparagine, ser</p>

<p>Beta-rutinose is a potent kinase inhibitor that has shown anti-tumor activity in Chinese hamster ovary (CHO) cells. It inhibits the activity of cyclin-dependent kinases, which are essential for cell division and proliferation. Beta-rutinose has been shown to induce apoptosis in human cancer cells, making it a promising candidate for anticancer therapy. This compound is an analog of rutin, a flavonoid found in many plants, and has been shown to have potent anticancer effects in vitro and in vivo. Beta-rutinose inhibits the growth of cancer cells by blocking the activity of specific kinases involved in tumor progression, making it an attractive target for developing new cancer therapies. Additionally, this compound has been found to be effective at reducing protein levels associated with cancer cell growth and proliferation.</p>

<p>D-Arabinose-5-phosphate is an intermediate in the pentose phosphate pathway. It is synthesized from D-xylulose-5-phosphate by xylitol dehydrogenase. D-Arabinose-5-phosphate inhibits the enzyme xylitol dehydrogenase, which converts xylulose to d-xylulose, and thus prevents the formation of 5-hydroxyisoxazole phosphate, a precursor to the synthesis of NADPH. In this way, it blocks the synthesis of NADPH, which is essential for aerobic metabolism. This inhibition leads to a decrease in ATP production and consequently cell death.</p>

<p>Corchoionoside C is a natural compound classified as an iridoid glycoside. This compound is isolated from various plant species, particularly those within the Boraginaceae family. The mode of action of Corchoionoside C involves modulation of biological pathways, likely through its interaction with cellular enzymes and receptors, contributing to its potential therapeutic effects.</p>

<p>Irbesartan N-b-D-glucuronide is a complex carbohydrate that is a synthetic saccharide. It is an intermediate in the synthesis of irbesartan, which is an angiotensin II receptor antagonist. Irbesartan N-b-D-glucuronide has been shown to have antihypertensive properties, inhibiting the activity of the renin-angiotensin system and increasing blood flow to the kidneys. It also inhibits the growth of cancer cells. This compound can be custom synthesized for your specific needs and purities can be controlled to meet your specifications.</p>

<p>1,2,3,4,6-Penta-O-acetyl-D-galactopyranose is an analog of the natural pentoses that binds to the mitochondrial membrane and inhibits the production of pro-inflammatory cytokines. This drug has been shown to inhibit the binding of lysophosphatidic acid (LPA) to its receptor by substituting for LPA in this binding site. 1,2,3,4,6-Penta-O-acetyl-D-galactopyranose also inhibits the expression of proinflammatory cytokines such as interleukin 6 (IL6) and IL1β in a dose dependent manner. This drug is also capable of inhibiting phosphotungstic acid from binding to a monolayer surface and can be used as a glycopolymer for cell culture. It has been shown that 1,2,3,4,6-Penta-O-acetyl</p>