Monosaccaridi

1,2,3,4-Tetra-O-acetyl-D-[6-13C]glucuronide methyl ester is a custom synthesis that can be used for the methylation of saccharides and polysaccharides. It is also used to modify glycosides and oligosaccharides. This compound has a CAS number and can be modified with click chemistry. It is a high purity product that can be synthesized with fluorination or complex carbohydrates.

2,3-O-Isopropylidene-5-O-trityl-D-ribofuranose is a metal complex that can be used as an antitumor agent. It has been shown to have antimicrobial activity against Gram positive and Gram negative bacteria and fungi. 2,3-O-Isopropylidene-5-O-trityl-D-ribofuranose is also active against Gram negative bacteria such as Escherichia coli and Pseudomonas aeruginosa. This compound is easily synthesized from acetoacetic acid by the reaction with trifluoroacetic anhydride followed by ammonolysis or azide coupling. The product is then amidated or tosylated to give the desired product.
2,3-O-Isopropylidene - 5 - O - trityl - D - ribofuranose has also been shown to inhibit tumor growth in

b-Core-APE-HSA is a custom synthesis of an oligosaccharide. This product is a complex carbohydrate with a CAS number and the molecular weight range of 500 to 10,000 Daltons. It is a polysaccharide that has been modified by methylation or glycosylation. The saccharide in this product is either glucose or mannose and it can be modified using click chemistry, fluorination, or other modifications. This product has high purity and can be synthesized using synthetic techniques such as glycosylation or Methylation.

D-Tagatose-6-phosphate lithium salt is a bacterial strain that belongs to the group of polyols. It is an epimerization product of D-tagatose, which is converted by the enzyme tagatose kinase to D-tagatose-6-phosphate. D-Tagatose-6-phosphate lithium salt can be used as a substrate for the enzymes galactitol dehydrogenase and galactitol 1,2-dioxygenase, which are involved in the metabolism of D-tagatose.

2-C-Methyl-D-arabono-1,4-lactone is a synthetic sugar that can be custom synthesized to order. This product is fluorinated and methylated, which allows for the modification of any desired position. The product is also an oligosaccharide with a high purity and can be modified using click chemistry. 2-C-Methyl-D-arabono-1,4-lactone can be used as a sugar in glycosylation reactions or as a polysaccharide in complex carbohydrate synthesis.

4-Deoxy-l-fucose is a molecule that has been found to inhibit the synthesis of gangliosides. It is an acetylated derivative of l-fucose and can be synthesized from ethyl 4-deoxy-D-glucuronate with the help of a multivorans enzyme. This molecule is metabolically unstable and reacts with oxygen to form a divalent alcohol that can be identified by magnetic resonance spectroscopy. 4-Deoxy-l-fucose inhibits the biosynthesis of gangliosides, which are important molecules in cell signaling, through its ability to inhibit enzymes such as acetyltransferase.

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.

O-Desmethyl-N,N-desmethyl-venlafaxine D-gluronide is a custom synthesis, modification and fluorination of venlafaxine. It is a polysaccharide that is synthesized from saccharides with a glycosylation process. The carbohydrate has a complex structure made up of oligosaccharides and monosaccharides.

Fluconazole D-glucuronide is a synthetic, fluorinated sugar that has been modified with a glycosylation. It is synthesized by reacting fluconazole with the sugar glucuronic acid in the presence of an enzyme called glycosyltransferase. Fluconazole D-glucuronide is a custom synthesis, and it can be used as a pharmaceutical intermediate to produce other compounds. Fluconazole D-glucuronide is also used as an analytical standard for quantifying fluconazole in biological samples.

D-tagatose 1-phosphate is a cytosolic intermediate of tagatose, which is found in many dietary sources. It has been shown to have regulatory effects on mitochondrial membrane potential and peroxisome proliferation in human cells. D-tagatose 1-phosphate also has been shown to have clinical relevance for humans with liver disease, as it enhances aerobic glycolysis and increases adenine nucleotide levels.

Iminosugar 1 is a fluorinated saccharide that belongs to the group of carbohydrates. It is synthesized by the modification of glucose with a fluorine atom. This modification prevents crystallization and increases solubility in water. Iminosugar 1 has been modified by methylation and glycosylation to increase its stability. This product is available as a custom synthesis, and has high purity.

Olmesartan acid O-b-D-glucuronide is a synthetic, high purity, and custom synthesis oligosaccharide. It can be fluorinated in the presence of a base to give a fluorinated compound with the following CAS number: 369395-57-3. Olmesartan acid O-b-D-glucuronide is an oligosaccharide that has been modified by click chemistry. This modification results in a polysaccharide that contains saccharides connected through ether linkages. The saccharides are made up of monosaccharides and disaccharides, which are all sugars.

L-altronojirimycin is a diterpene glycoside that belongs to the group of natural products that have inhibitory properties against lipid peroxidation. It has been shown to decrease the concentration of 1,2-dipalmitoylglycerophosphocholine (DPPC) in primary cells and reduce the rate of lipid peroxidation in a concentration-dependent manner. L-altronojirimycin inhibits the activity of enzymes such as acetylcholinesterase and phospholipase A2, which are involved in inflammation. This drug has also been shown to have cardioprotective effects and inhibit mutations in cardiac muscle cells. L-altronojirimycin has been tested for its long-term efficacy and shown to be effective against both bowel disease and cardiac effects.

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.

a-L-Fucose-1-phosphate is a Glycosylation, complex carbohydrate, Methylation, Click modification, Polysaccharide, Fluorination, saccharide, Modification, sugar, Oligosaccharide and Synthetic product. a-L-Fucose-1-phosphate is available for custom synthesis and can be ordered with high purity.

6-O-tert-Butyldiphenylsilyl-3,4-O-isopropylidene-D-galactal is a synthetic monosaccharide that is used as a building block for the synthesis of complex carbohydrates. This product is also used in glycosylation reactions and click modification. It is available in high purity and can be custom synthesized to meet customer needs.

2,5-Anhydro-D-mannofuranose oxime is a glycosylation inhibitor that prevents the formation of glycosidic bonds. It is used in the synthesis of complex carbohydrates, such as polysaccharides and oligosaccharides. This compound can be fluorinated or methylated to produce 2,5-anhydro-D-mannofuranose oxime derivatives that are useful for click chemistry. 2,5-Anhydro-D-mannofuranose oxime has been shown to inhibit the enzymatic conversion of mannitol to mannose and fructose by blocking the enzyme alpha mannosidase. The high purity of this compound makes it suitable for use in a variety of reactions, including glycobiology studies and carbohydrate modifications.

1,4-Dideoxy-1,4-imino-D-xylitol HCl (DDX) is a potent inhibitor of the enzyme carboxypeptidase A2. DDX has been shown to inhibit the growth of HIV in vitro and in vivo. DDX also inhibits the production of proinflammatory cytokines and neurotrophic factors from HL60 cells. It has been shown to be a potential drug target for the treatment of infectious diseases such as alphaviruses, which produce a severe neuroinvasive disease in humans. DDX binds to dna with high affinity and specificity, but does not bind to RNA or proteins. DDX inhibits mitochondrial membrane potential by binding to ATP synthase and blocking the synthesis of ATP. DDX has also been shown to have an anti-oxidative injury effect on mitochondria, which may contribute to its inhibition of viral replication.

2-epi-(-)-emtricitabine is an analog of the nucleoside cytidine, which inhibits the phosphorylation and subsequent degradation of deoxycytidine kinase, thereby blocking the production of the viral DNA polymerase. The compound also inhibits tyrosine kinases, which are enzymes that play a vital role in cell signaling. This inhibition may contribute to its antiviral activity. 2-epi-(-)-emtricitabine has been shown to inhibit human immunodeficiency virus (HIV) replication in vitro and in vivo. It is a prodrug that is converted to emtricitabine, its active form, by deoxycytidine kinase and then hydrolyzed by esterases. 2-epi-(-)-emtricitabine has been shown to be effective against hepatitis B virus and cancer cells.

Glucose covalently bound to BSA through a 3 atom spacer.

1,2-O-Isopropylidene-5-O-p-toluoyl-a-D-xylofuranose is a glycosylation product of orotic acid with 5,6-dihydroxybenzoic acid. It is a white solid that can be used for the synthesis of various saccharides. 1,2-O-Isopropylidene-5-O-p-toluoyl-a-D -xylofuranose is an effective reagent for the methylation of carbohydrates and also shows high reactivity with fluorine. This compound has a CAS number of 7509660 and has been modified with click chemistry to form an oligosaccharide. 1,2 -O -Isopropylidene -5 -O p -toluoyl -a D xylofuranose is synthesized by custom synthesis and has a purity

5-Fluorouracil N-b-D-glucuronide is the major metabolite of 5-fluorouracil. It is mainly excreted in urine and bile, and has a high blood level. The glucuronide conjugate of 5-fluorouracin is hydrolyzed by beta-glucuronidase to generate 5-fluorouridine, which can be reabsorbed into the cell to form cytotoxic 5-fluoro uridine triphosphate. This process inhibits protein synthesis, leading to cell death. The half life of 5FU glucuronide is short and it needs to be constantly replaced with new doses. It has also been shown that levels of 5FU glucuronide are higher in tissues than in plasma, which may explain its inhibitory effect on tumors.

Allyl 3-O-benzyl-a-L-rhamnopyranoside is an oligosaccharide that is a modification of the disaccharide, allyl 3-O-benzyl-a-D-galactopyranoside. Allyl 3-O-benzyl-a-L-rhamnopyranoside has been synthesized from D-(+)-glucose and L-(+)-rhamnose. The compound has a molecular weight of 756.40 g/mol. It is a white to off white powder that is soluble in water, but insoluble in ethanol at low concentrations. It can be used as a carbohydrate or sugar for research purposes.

2-Deoxy-2-fluoro-L-[UL-13C]fucose is a modified sugar molecule used in various scientific applications, particularly in glycobiology and drug development.  It's used to study fucose-containing glycans, enzyme interactions, metabolic pathways, and glycoengineering. For instance, it can be incorporated into proteins to investigate the effects of fucose modifications on their function or used to develop drugs targeting fucose-metabolizing enzymes

1,5-Dideoxy-1,5-imino-D-xylitol is a synthetic molecule that inhibits the enzyme glycinamide ribonucleotide transformylase (GART) and blocks the synthesis of purines. 1,5-Dideoxy-1,5-imino-D-xylitol has been shown to be potent in inhibiting GART with an IC50 of 0.3 μM. This inhibitory effect was observed in Sprague Dawley rats after oral administration of 1,5-dideoxy-1,5 imino D xylitol at a dose of 10 mg/kg. The inhibition was found to be specific for amination reactions that are catalyzed by GART and not by other enzymes such as glycine amidinotransferase or adenylate kinase. It can be used to study the structure and function of tissue cells.

6-Deoxy-3-C-methyl-D-gulose is an enantiomer of 3,6-dideoxy-D-gluconic acid. This compound has been shown to be a virulent factor in mastitis caused by the mutant strain of Escherichia coli (MT1) and to be expressed at a higher level in mastitic milk than in normal milk. 6DMG has also been shown to induce monoclonal antibody production and stimulate specific immune responses. It is thought that 6DMG damages cells, which leads to the release of intracellular components that trigger an antibody response. The biological function of 6DMG is not known, but it may play a role in the infection process by stimulating an antibody response against infectious agents.