Monosaccaridi

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.

Myo-inositol-d6 is a stable isotope of myo-inositol. It is used to monitor the biosynthesis of myo-inositol in yeast cells. Myo-inositol is a carbohydrate that has regulatory functions in yeast cells. Myo-inositol-d6 can be used as an extracellular bioassay for determining the uptake and intracellular distribution of myo-inositol in mammalian cells.

Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene-b-D-galactopyranoside is a custom synthesis that belongs to the class of complex carbohydrates. This compound is an oligosaccharide or a polysaccharide that has been modified by methylation and glycosylation. The modification of this saccharide with methyl groups allows for fluorination which is a click modification. Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene b -D galactopyranoside is synthesized via glycosylation followed by fluorination. This product can be used as a research chemical or in other applications.

2-Hydroxyimipramine b-D-glucuronide is a custom synthesis, modification, and fluorination of the drug 2-hydroxyimipramine. The methyl group from the molecule is replaced with a fluoro group. This modification leads to a new compound with improved pharmacokinetic properties. The new compound also has glycosylation sites on the sugar ring that are not present in the parent drug. This modification may lead to an increase in the therapeutic efficacy of 2-hydroxyimipramine b-D-glucuronide as it interacts with other drugs and increases their bioavailability.

Ouabain is a potent inhibitor of the Na+/K+-ATPase pump in cardiac and skeletal muscles. It has been shown to inhibit signal pathways that are involved in the regulation of cellular membrane potentials, such as the michaelis–menten kinetics. Ouabain has also been found to be effective against syncytial virus infection. Ouabain inhibits viral replication by inhibiting cellular protein synthesis and reducing cell number due to its cytotoxic effects on myocardial cells. Ouabain has also been found to inhibit neuronal death induced by α1-adrenergic receptor agonists, such as p2y receptors.

1,2,3,4-Tetra-O-acetyl-D-xylopyranose is a molecule that is derived from D-xylose. It has been shown to inhibit the growth of fungi such as T. rubrum and L. candidum by acetylation of l-threonine at the C2 position. This molecule can be recycled and its inhibitory activity can be increased through acetylation of the hydroxymethyl group on the C4 position. The mechanism of inhibition is not known but it may be due to steric hindrance or peracylation.

Ezetimibe hydroxy-b-D-glucuronide is an oligosaccharide that can be synthesized from the modified sugar, L-glucuronic acid. It has a molecular weight of 536 and is soluble in water and methanol. This compound has been used in the synthesis of glycosides, saccharides, and polysaccharides. The chemical name for this compound is 1-(2-hydroxyethyl)-3-(((4'-carboxybenzyl)oxy)carbonyl)-2,6-diazaoctane glucuronide. Ezetimibe hydroxy-b-D-glucuronide has been shown to increase the absorption of cholesterol and decrease low density lipoprotein (LDL) levels in the blood by inhibiting intestinal cholesterol absorption.

D-ribulose-5-phosphate sodium is a nucleotide sugar that is one of the ribonucleotides, which are fundamental components of RNA. D-ribulose 5-phosphate sodium has been shown to be an intermediate in the metabolism of ribulose and catalyzes the oxidation of d-arabinose. This enzyme also catalyses the synthesis of fatty acids and participates in reactions involving glycerolipids and phospholipids. The reaction mechanism involves a double displacement with simultaneous attack by a water molecule on C2' and C3'. When deuterium is present, it affects the rate of these reactions in a way that depends on the orientation of the substrate to the enzyme.

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.

This product is a custom synthesis. This product is a methylation, click modification, and oligosaccharide. This product is a polysaccharide and saccharide. This product is fluorinated and complex carbohydrate. This product is high purity with modification. This product has monosaccharides and sugar. This product is synthetic and CAS No. 849938-27-8.

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Phenyl 2,3,6-tri-O-benzyl-b-D-thioglucopyranoside is a high purity, custom synthesis sugar that has been modified with Click modification, fluorination and glycosylation. It is a synthetic compound in the form of an oligosaccharide and monosaccharide. Phenyl 2,3,6-tri-O-benzyl-b-D-thioglucopyranoside has CAS No. 97974-20-4 and can be found under Modification.

D-Arabino-5-hexulosonic acid is an intermediate in the pentose phosphate pathway. It is a component of the hexuronate, which is an important precursor for galactitol, 6-phosphate, and acid dehydrogenase. D-Arabino-5-hexulosonic acid is also an important intermediate in the glycolytic pathway for ATP production. The gene product has been shown to be involved in aerobic glycolysis, which is utilized by Staphylococcus aureus to produce energy from glucose fermentation. D-Arabino-5-hexulosonic acid plays a role in ion exchange and mitochondrial metabolism as well.

Methylation is a chemical reaction that transfers a methyl group to an organic molecule. It is one of the most common modifications in organic chemistry and can be used to synthesize saccharides and oligosaccharides, as well as to modify polysaccharides. This compound is a glycosylated benzylidene-N-Boc-1,5-imino-D-glucitol, which has been modified by Click chemistry. It was synthesized from 4,6-O-benzylidene-N-Boc-1,5-imino-D-mannitol with a custom synthesis protocol. The final product has high purity and is available for purchase at CAS No. 133697-16-2.

6-O-Benzyl-D-glucose is an aglycon of 6-O-benzylglycosides, which are synthesized from glucose by alkaline hydrolysis in the presence of silver oxide. The benzyl group can be removed by a variety of methods, including treatment with hydrogen chloride gas. 6-O-Benzyl-D-glucose has been used in research to demonstrate that carbohydrates have a common structural feature that can be identified by looking at their molecular structure. This molecule has also been used to study the synthesis and reactivity of benzyl groups.

1,2,3,4-Tetra-O-acetyl-6-deoxy-6-fluoro-a-D-glucopyranose is a synthetic sugar that contains four acetyl groups and one fluorine atom. It can be used for the synthesis of oligosaccharides and glycosylations. This product is custom synthesized according to customers' requirements, with high purity and good quality.

UDP-2-ketopropyl-a-D-galactose is a synthetic compound that belongs to the group of oligosaccharides. It is an excellent candidate for glycosylation, methylation, and click modification. The product has a CAS number, which provides high purity and custom synthesis. The product is also a complex carbohydrate with a variety of modifications.

Ramipril acyl-b-D-glucuronide is a glycosylated prodrug that is the active form of ramipril, an ACE inhibitor. It is metabolized in the liver to ramipril and excreted in the urine. Ramipril acyl-b-D-glucuronide has been shown to have an increased bioavailability and a longer half-life than ramipril due to its glycosylation. The synthesis of this drug has been modified by methylation, fluorination, and saccharide modification. This compound is also available as a custom synthesis for research purposes with high purity.

2-Acetonyl-1,3,4,6-tetra-O-acetyl-2-deoxy-b-D-galactopyranoside is a synthetic sugar that has been modified to contain an acetyl group at the C2 position. The synthesis of this compound is based on the modification of galactose with acetic anhydride. This product has been shown to be resistant to hydrolysis by esterases or glucuronidases and can also inhibit bacterial growth in culture. It is a monosaccharide with a CAS number of 85583-40-7. It is also used as a precursor for the synthesis of complex carbohydrates.

This chemical is a custom synthesis of (-)-Lyoniresinol 9'-O-glucoside. The chemical is a modification of (-)-Lyoniresinol 9'-O-glucoside and fluorinated at the C2 position. It is also methylated on the C3 position. The chemical is synthesized by click chemistry, which involves the use of copper(II) ions as catalysts to generate covalent bonds between two molecules. This chemical has been shown to be an oligosaccharide with saccharide chains that are linked together by glycosylation. There are six sugar residues in this compound: glucose, galactose, rhamnose, xylose, glucuronic acid, and mannitol. This compound has CAS number 143236-02-6 and molecular weight of 881.5 g/mol (CAS No.).

5-Deoxy-L-lyxono-1,4-lactone is a crystalline solid that belongs to the class of hydroxamic acids. This compound has been shown to react with hydroxylamine in an aldonic reaction and to inhibit the enzyme xanthin oxidase. The monoclinic crystal structure of 5-Deoxy-L-lyxono-1,4-lactone was determined by XRD analysis. This compound is synthesized from glyoxylate and malonitrile in an efficient manner. It also inhibits glucose oxidation and can be used as an additive for food products.

Methyl b-D-thioxylopyranoside is a synthetic sugar that is used in the synthesis of saccharides and oligosaccharides. It is also used to modify saccharides, such as glucosamine, by adding methyl groups to the sugar's hydroxyl group. Methyl b-D-thioxylopyranoside can be used for glycans with high purity and high yield. This product does not contain any other substances except for water and ethanol. The chemical formula for this product is C6H8O6.

Raltegravir b-D-glucuronide is a synthetic, fluorinated analog of raltegravir. It is a potent HIV-1 integrase inhibitor that has been shown to be active against the majority of HIV-1 strains. Raltegravir b-D-glucuronide is less potent than the parent compound and exhibits reduced antiviral activity in vitro. Raltegravir b-D-glucuronide is metabolized to raltegravir and eliminated in urine as the glucuronide conjugate.

2,3,5-Tri-O-p-chlorobenzyl-L-fucopyranoside is a modified sugar and an effective inhibitor of the glycosidase enzymes. It has been shown to inhibit the synthesis of glycogen in vitro. 2,3,5-Tri-O-p-chlorobenzyl-L-fucopyranoside is a major component of commercially available agarose gel electrophoresis buffers and is also used for modification of proteins by click chemistry. The compound can be custom synthesised with a high degree of purity and can be fluorinated for use in mass spectrometry.

1,2-Dichloro-1,2-dideoxy-myo-inositol is a methylated saccharide. It is used in the synthesis of complex carbohydrates and can be modified to include fluorine atoms. 1,2-Dichloro-1,2-dideoxy-myo-inositol has been shown to inhibit the growth of Staphylococcus aureus and Clostridium perfringens.

4-Aminobutyl b-D-galactopyranoside is a methylated saccharide that is also a glycosylation reaction product of 4-aminobutyl b-D-galactopyranoside. It has been modified with Click chemistry and fluorinated for use in carbohydrate research, including glycoprotein synthesis, carbohydrate modification, and oligosaccharide synthesis. 4-Aminobutyl b-D-galactopyranoside has been shown to be a potent inhibitor of the enzyme aminoglycoside adenyltransferase 1 (AGT1), which is involved in the synthesis of bacterial cell wall peptidoglycan. This compound has been used as a model for glycosylation reactions as it contains both an amino and sugar moiety.

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%.

Clofibric acid acyl-b-D-glucuronide is a reactive chemical species that has been shown to have genotoxic effects. It binds to DNA and forms covalent adducts, leading to mutations in the DNA sequence. Clofibric acid acyl-b-D-glucuronide is a metabolite of clofibrate, which is used for the treatment of hyperlipidemia and atherosclerosis. This metabolite can be detected in human blood, serum, and liver samples by GC/MS, with a limit of detection of 0.1 ng/mL (0.0003 µg/L).

Mirabegron is a drug that is used to treat overactive bladder. Mirabegron N-glucuronide is the major metabolite of mirabegron, which has been shown to be excreted in urine. This metabolite can be detected using a validated assay and can be measured using a mass spectrometer. The concentration of mirabegron N-glucuronide in the blood sample was measured at various timepoints after administration of mirabegron. Pharmacokinetic studies were performed in humans and human liver tissue, giving information on how long it takes for the drug to reach its maximum concentration in the body and how long it stays there before being eliminated.

3-Deoxy-3-fluoro-D-myo-inositol, also known as myo-inositol 3-O-(2'-deoxy) (dFMI), is a natural product found in the brain that has been shown to selectively inhibit the growth of trophozoites. It can bind to nonselective cations and block intracellular Ca2+ channels. This causes an increase in cytosolic Ca2+ concentration, which activates a cytosolic Ca2+ signal cascade. These effects show that dFMI is capable of inhibiting the growth of trophozoites by blocking the function of Ca2+ channels and increasing cytosolic Ca2+.

3-Azido-5-O-benzoyl-3-deoxy-1,2-O-isopropylidene a D-ribofuranose (3ABI) is a synthetic monosaccharide that can be synthesized via a custom synthesis. 3ABI is an oligosaccharide that has the ability to modify glycosylation and polysaccharide synthesis. The fluorination of this sugar provides it with high purity and stability. 3ABI has been shown to have a CAS number of 44793-23-2.

5-(β-D-Galactopyranosyloxy)-DL-lysine is a custom synthesized compound that has been modified with 5-(β-D-galactopyranosyloxy) groups. It is an oligosaccharide, polysaccharide, and saccharide that belongs to the category of carbohydrates. This product is available for purchase in high purity and has been fluorinated. The CAS number for this product is 35910-05-5.

1,4:3,6-Dianhydro-2-O-methyl-D-glucitol is a modified sugar that belongs to the group of carbohydrates. It is synthesized by the modification of 1,4:3,6-dianhydro-2,5-diO-methyl D glucitol with methyl iodide and sodium methoxide. The compound is used in pharmaceuticals as an excipient and in cosmetics as a moisturizer. It has been shown to be effective against influenza A virus.

Allyl 4,6-O-benzylidene-b-L-glucopyranoside is a carbohydrate that is synthesized from allyl alcohol and glucose. It is a complex carbohydrate made up of two different saccharides. This product can be custom synthesized to meet your needs. Allyl 4,6-O-benzylidene-b-L-glucopyranoside has been modified by fluorination, methylation and glycosylation. It has the CAS number 133394-02-0 and can be synthesized at high purity levels.

3,4,5,6-Tetra-O-acetyl-D-myo-inositol is a carbohydrate that can be used as a monosaccharide or an oligosaccharide. It is produced by the modification of inositol with acetate and fluoride. The compound has been shown to have anti-inflammatory properties and can be used as a drug target for treating inflammation. 3,4,5,6-Tetra-O-acetyl-D-myo-inositol is also methylated and glycosylated.

1-Deoxy-L-ribose is a metabolite of acetone. It is a monosaccharide that contains one less oxygen atom than its parent compound. 1-Deoxy-L-ribose is found in the urine and blood of humans and animals. In animals, it can be synthesized from glucose by the enzyme ribose 1-phosphate reductase. This reaction requires an energy source such as ATP or NADH to reduce ribose 1,5-bisphosphate to 1,4-dihydroxyacetone phosphate, which then undergoes spontaneous dehydration to form 1-deoxy-D-ribose.

Momordicoside I aglycone is a compound that has been extracted from the roots of Momordica grosvenori. It is a potent inhibitor of the enzyme cyclooxygenase and has been shown to have analgesic, anti-inflammatory, and antipyretic activities in mice.

Glcnacβ(1-3)GalNAc-α-Thr is a polysaccharide that is found in the human body, which is a complex carbohydrate. It is an oligosaccharide modification of galactose and alpha-threonine. Glcnacβ(1-3)GalNAc-α-Thr can be custom synthesized to order with high purity and monosaccharide content. This product is used for research purposes and has not been approved for therapeutic use. The CAS number for this compound is 286959-52-2.

N-Boc-1,5-imino-D-glucitol is a complex carbohydrate that is synthesized by the N-Boc protection group. It is an oligosaccharide with a molecular weight of about 190 daltons and it can be modified at the C1 position to produce various saccharides. N-Boc-1,5-imino-D-glucitol has been shown to be effective as a glycosylation agent for protein modification and for its ability to form stable complexes with other complex carbohydrates. This compound has also been used in the synthesis of polysaccharides and as a fluorination reagent.

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.

L-Sorbosone is an antioxidant that can be used as a food additive or dietary supplement. It has been shown to have antioxidative properties and has the ability to inhibit oxidation reactions. The optimum concentration of L-sorbosone is 0.1 milligrams per liter and it is effective at inhibiting chemical reactions in a wide range of pH levels, from 2 to 8. L-Sorbosone belongs to the genus sorbose, which is a sugar alcohol that does not contain an aldehyde group. It also converts sorbose into dehydroascorbic acid and inhibits the enzyme activities of two important enzymes involved in cell culture, namely glutathione reductase and cytochrome p450, which are necessary for maintaining cellular redox balance.

1,2,3,6-Tetra-O-benzoyl-5-thio-D-glucopyranose is a monosaccharide that can be synthesized by the methylation of 1,2,3,6-tetra-O-(benzoyl) D-glucopyranose. The synthesis of this compound is accomplished by a click modification and the use of a fluoroquinolone to modify the sugar at C1. This compound has been shown to be an excellent substrate for polysaccharide and saccharide synthesis as well as fluorination. Purity levels are high with this product.

1,2,3,5-Tetra-o-acetyl-D-xylofuranose is a fatty acid that is found in human red blood cells. It is used as a biochemical marker to diagnose the activity index of fatty acids in the red cell membrane. The activity index can be used to determine whether an individual has metabolic disorders such as hepatic steatosis or lc-ms/ms method. 1,2,3,5-Tetra-o-acetyl-D-xylofuranose also has antimicrobial effects against bacteria and fungi and can be used for the treatment of infectious diseases.

Benzyl 5-amino-5-deoxy-2,3-O-isopropylidene-6-O-trityl-a-L-gulofuranoside is a custom synthesis of an Oligosaccharide. It is a complex carbohydrate that has been modified by methylation and glycosylation. The saccharide in this compound is a sugar and it has been fluorinated. This product is of high purity and has been synthesized using click chemistry.

P-Coumaroyl-b-D-glucose is a flavanone that belongs to the class of flavonoids. It is an intermediate in the synthesis of many other flavonoids, such as apigenin, labiatae, and rhamnetin. P-Coumaroyl-b-D-glucose has been shown to downregulate the expression of genes encoding proteins involved in the biosynthesis of proanthocyanidins and anthocyanins. This compound also induces apoptosis by binding to the mitochondria membrane and increasing reactive oxygen species production. P-Coumaroyl-b-D-glucose can be used as a marker for phenylpropanoid metabolism in plants.

Mannioside A is a postulated antigen that may be found in the Dracaena genus of plants. This compound has been shown to have an affinity for membranes, which could possibly be used as a strategy for vaccines and other pharmaceutical products. Mannioside A also has hemolytic activity, which may be useful in developing new treatments for autoimmune disorders such as multiple sclerosis.

6-O-Trityl-D-glucose is a sugar derivative that is synthesized by reacting 6,6'-dichloro-1,1'-binaphthyl with D-glucose. It has been used as a model for the stereospecific hydrolysis of polystyrene catalyzed by lipase. The reactive carbonyl group in the molecule allows for substitution reactions to occur at the hydroxyl groups and yields are dependent on the substituent effects.

b-D-Thioglucose sodium salt hydrate is a complex carbohydrate that is used as an intermediate for the synthesis of oligosaccharides and polysaccharides. It is also used in the modification of saccharide chains, such as glycosylation, and for the preparation of fluorinated carbohydrates. b-D-Thioglucose sodium salt hydrate is high purity, with no detectable impurities or degradation products. It has been modified with fluorine to form a new chemical entity that has not been previously described in the literature.

3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranosyl chloride is a modification of the carbohydrate. It is a complex carbohydrate that has been custom synthesized for research purposes. It can be used as a monosaccharide or polysaccharide in glycosylation reactions. This compound has not been fluorinated and the CAS number is 7772-87-4.

3-O-Triisopropylsilyl-D-galactal is a carbohydrate that belongs to the group of sugars. It is an oligosaccharide with a complex structure, which is synthesized from D-galactal by treatment with triisopropylsilyl chloride in pyridine. 3-O-Triisopropylsilyl-D-galactal is used as a reagent for the methylation and glycosylation of proteins and nucleic acids. This compound has been shown to inhibit the enzyme carboxypeptidase A, which may be due to its ability to act as an inhibitor of carbohydrate binding. 3-O-Triisopropylsilyl-D-galactal has also been shown to bind specifically to erythrocyte membranes, suggesting that it could be used as a potential diagnostic marker for glycogen storage diseases.

Glcnacβ(1-2)man-α-ethylazide is a modified oligosaccharide that has been synthesized from the sugar GlcNAcβ(1-2)mannose. It is a complex carbohydrate with a high purity, which can be used as a custom synthesis. The synthesis of this product involves fluorination and saccharide methylation. The CAS number for this product is 1858224-15-3.

4-Epi-daunosamine is a glycopeptide antibiotic that is used to treat infections caused by Gram-positive bacteria. It binds to the cell wall of these bacteria and inhibits the synthesis of new cell walls. This causes the cells to burst and die, which leads to bacterial death. 4-Epi-daunosamine has been shown to be effective against animal pathogens such as Streptococcus pneumoniae, Haemophilus influenzae, and Clostridium perfringens. 4-Epi-daunosamine also has a low level of toxicity in humans, but can cause adverse effects such as nausea and vomiting if taken in large doses.

Glufosfamide is a cytotoxic drug that is used in the treatment of some types of cancer. It is a prodrug that requires conversion to its active form, glufosfamid, by esterase enzymes before it can exert its genotoxic effects. Glufosfamide has shown to be active against platinum-resistant ovarian cancer and solid tumours. This drug also has been shown to inhibit the growth of prostate cancer cells and miapaca-2 cells, which are derived from pancreatic cancer. Glufosfamide has been found to have low toxicity in mice, but there may be adverse reactions when combined with other drugs such as erythromycin or ketoconazole.

3-O-Methyl-D-mannopyranose is a glycosidic compound with immunostimulating properties. It is an intermediate in the synthesis of 3,6-anhydro-N-acetylneuraminic acid and other related carbohydrates. The hydrolysis of this molecule yields silver trifluoromethanesulfonate, chloride, and low molecular weight material. 3-O-Methyl-D-mannopyranose can be used as a reagent for the preparation of high molecular weight material by ion exchange chromatography or by dehydrative coupling.

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.

Benzyl 2,3-O-isopropylidene-a-D-mannofuranoside is a fluorinated monosaccharide that is synthesized using glycosylation and polysaccharide modification. This product has a CAS number of 20689-03-6 and can be used for complex carbohydrate synthesis. It has been shown to have high purity.

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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

Methyl b-D-fructofuranoside is a chemical compound that is used in the production of esters and fatty acids. Methyl b-D-fructofuranoside is produced by a dehydration reaction between two molecules of acetone. The product of this reaction, methyl b-D-fructopyranoside, can be broken down into two molecules of acetone and one molecule each of methyl alcohol and carbon dioxide. This process is called alkylation. Furanocoumarin derivatives are often found in plants such as asperulosidic acid and quinquefasciatus. These compounds are found in many species of plant, but they are most concentrated in the roots of these plants because they are more metabolically active there than other parts of the plant. Environmental pollution can lead to high concentrations of furanocoumarins in plants, which can have toxic effects on organisms that come into contact with them.

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.

1,2,3,4-Tetra-O-acetyl-D-glucuronide methyl ester is a lactone that can be used as a precursor for the synthesis of various types of compounds. The chemical structure was determined by high-resolution x-ray diffraction to be a planar molecule with two conformations: one where the four acetyl groups are on different sides and another where they are all on the same side. The latter conformation is more stable due to the dihedral angle between the hydroxyl group and carbonyl group. This compound is an intermediate in synthesizing 2-(4'-hydroxybenzoyl)-1,2,3,4-tetra-O-acetyl-.alpha.-D-.beta.-D glucopyranoside methyl ester by reacting with 3-(3'-azido)benzaldehyde. The single crystal x-ray diffraction study revealed that this compound has a conformation

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D-Galacturono-6,3-lactone is a fatty acid that is part of the glucuronolactone family and has been shown to have anti-obesity effects in vitro. D-Galacturono-6,3-lactone has been synthesized from sodium citrate and hydrochloric acid in the presence of magnesium salt, and the product was purified by crystallization. It has also been shown to inhibit aminotransferase activity and increase locomotor activity. D-Galacturono-6,3-lactone has a ph optimum of 4.5, which can be determined by an analytical method involving the measurement of hydrogen ion concentration.

Decyl D-glucopyranoside is a sodium salt of decyl D-glucopyranoside that is used as a detergent additive in cleaning compositions. Decyl D-glucopyranoside has shown antimicrobial activity against both Gram-positive and Gram-negative bacteria, including methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. Decyl D-glucopyranoside has also been shown to have chemical stability at high temperatures, making it useful in the manufacture of lacrimal gland preparations and cationic surfactants.

8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35-O-(2,6-dideoxy-L-ribo-hexopyranosyl)amphotericin B is an antifungal drug that belongs to the class of polyene macrolides. It is a potent inhibitor of Candida albicans and Candida glabrata. This compound has been shown to have synergistic effects when used in combination with nystatin against C. albicans. 8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35O-(2,6 - dideoxy - L - ribo - hexopyranosyl)amphotericin B also inhibits toll like receptor 4 (TLR4), which is responsible for the induction of inflammatory cytokines such as IL1B and IL8

D-Sedoheptulose is a sugar that is a member of the pentoses. It has been shown to have a ph optimum of 4.5 and oxidizing potential of -0.18 V. It is also an important intermediate in carbohydrate metabolism and can be used as an energy source by cells. D-Sedoheptulose plays a role in transcriptional regulation and cellular physiology, as well as being involved in the production of acyl chains and disulfide bonds for proteins. D-Sedoheptulose has also been found to have synergic effects with other sugars such as glucose, sucrose, or fructose, which may be due to its ability to act as an inducer of reductive enzymes such as glucose-6-phosphate dehydrogenase (G6PD).

2,4-O-Benzylidene-L-xylose is a white crystalline powder with a melting point of about 125°C. It is an acetate salt that can be used in the synthesis of many natural products. It has been shown to inhibit HMG-CoA reductase and is used in the treatment of hypercholesterolemia. The reaction mechanism for this compound is not well understood, but it is believed to involve an acid catalyst and an organic solvent. The yield for this compound is low and it requires a long reaction time due to its high reactivity.

D-[6-13C]Galacturonic acid potassium salt is a synthetic, water-soluble complex carbohydrate with a molecular weight of 744.2. It is used as a fluorescence probe in magnetic resonance imaging (MRI) and also has applications in the synthesis of oligosaccharides and polysaccharides. D-[6-13C]Galacturonic acid potassium salt is soluble in water and has an average pH of 5.0. This compound is available for custom synthesis with high purity and can be found under CAS number 144561-27-4.

N-Acetylneuraminic acid 9-phosphate is a sugar phosphate

(-)-2,3-O-Isopropylidene-D-threitol is a chiral compound with two stereoisomers. It is a crystalline solid that melts at 71°C and has a population of 50%. (-)-2,3-O-Isopropylidene-D-threitol is an important intermediate for the synthesis of polyethers with chiral centers. The catalytic asymmetric synthesis of (-)-2,3-O-isopropylidene-D-threitol is achieved by alkylation of (+)-2,3-(dimethoxyphosphinyl)propane with isopropanol. This reaction can be used to produce polyethers with chiral centers in high yields and enantioselectivity.

Isosaccharinic acid is a bacterial strain that produces isosaccharinic acid as its main fatty acid. The thermodynamic data for the reaction mechanism of the conversion of glucose to isosaccharinic acid has been determined. Isosaccharinic acid formation is catalyzed by an enzyme called glycosyl-glycerate dehydrogenase, which converts glycerate to 3-hydroxypropanoic acid and then to 3-oxopropanoate before it undergoes decarboxylation and reduction to form isosaccharinic acid. Radionuclides such as TcO4 are used in chemical ionization mass spectrometry for the detection of this compound in samples. Neutral pH, high activation energies, and low binding constants are all factors that affect the stability of this molecule.

5-Thio-N-acetylglucosamine is a microtubule inhibitor that binds to o-glcnac, a posttranslational modification of proteins that regulates the morphology and cycling of stem cells. 5-Thio-N-acetylglucosamine has been shown to inhibit the transcriptional activity of o-glcnacase, an enzyme that catalyzes the conversion of o-glcnac to glucosamine. This drug also inhibits the metabolic activity of neural progenitor cells, which may be due to its ability to regulate subpopulations with concomitant expression of markers such as Oct4 and Sox2.

Daunorubicin-d3 is a fluorinated, monosaccharide, synthetic, oligosaccharide and complex carbohydrate. Custom synthesis of Daunorubicin-d3 is available with glycosylation, methylation and other modifications. Daunorubicin-d3 has CAS No. 1614-68-8 and purity >99%.

ADP-L-glycero-b-D-manno-heptose is a synthetic, fluorinated oligosaccharide that is custom synthesized and modified. It has a high purity level and CAS No., as well as being a complex carbohydrate that can be modified with methylation or click modification to generate desired properties. ADP-L-glycero-b-D-manno-heptose is an Oligosaccharide with a glycosylation and methylation. This compound can be used in the synthesis of saccharides, polysaccharides, or other complex carbohydrates.