Monosaccharides

M-topolin-9-glucoside is a synthetic sugar that has been modified by the introduction of fluorine atoms at C-2, C-3, and C-4. This sugar is used to study the interactions between carbohydrates and proteins. It is also used for the synthesis of oligosaccharides as well as for glycosylation and methylation reactions. M-topolin-9-glucoside is a monosaccharide that has been glycosylated and methylated. It can be used as a replacement for glucose in some reactions due to its stability and low cost.

2-Acetamido -1,3,4,6-tetra-O-acetyl-2-deoxy-5-thio-a-D-glucopyranose is a custom synthesis. It is an oligosaccharide and polysaccharide. It is a carbohydrate that has been modified by fluorination and a click modification. The complex carbohydrate contains one monosaccharide sugar. 2AATG can be used in the synthesis of other carbohydrates.

Methyl 2,3,4-tri-O-acetyl-b-L-thiofucopyranoside is a ferrite that is important for the growth of cells. It can be used as a growth factor to promote the growth of cells. Covid®-19 pandemic A/Aureus strain is resistant to this drug and it has been shown to inhibit cellular transformation in human epidermal cells. The drug also reduces the size and number of cancerous lesions in mice by inhibiting tumor angiogenesis. Methyl 2,3,4-tri-O-acetyl-b-L-thiofucopyranoside can cause an overload of Ca2+ ions in the cell, which may lead to apoptosis or necrosis.

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.

4-Aminophlorizin is a chemical compound that inhibits the uptake of azide by red blood cells. It has been shown to be effective against intestinal parasites and trophozoites. 4-Aminophlorizin is a potent inhibitor of the membrane system, which may be due to its interaction with the semenza, or membrane protein.

O-topolin-9-glucoside is a custom synthesis of a sugar. It can be modified with fluorination, methylation, and click modification. O-topolin-9-glucoside is an oligosaccharide sugar that can be glycosylated or polysaccharided.

3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-a-D-fructopyranose is a modified carbohydrate with the chemical formula C 12 H 20 O 8 . It is a white crystalline solid that is soluble in water. 3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-a-Dfructopyranose can be used as a monosaccharide or an oligosaccharide. This compound has been synthesized by methylation and glycosylation of glucose.

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.

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.

Nicotine-N-b-D-glucuronide hydrate is a metabolite of nicotine that is excreted in the urine as an organic anion. It has been shown to have anticancer activity against a variety of human cancer cell lines, including lung, stomach, colon, and prostate. Nicotine-N-b-D-glucuronide hydrate has also been shown to inhibit protein synthesis in vitro by interfering with the ability of cells to import amino acids such as tryptophan and phenylalanine. The same study also showed that this metabolite can cause symptoms similar to those caused by nicotine withdrawal.

4-Aminophenyl b-D-thioglucopyranoside is a compound that belongs to the group of small molecules and has been studied for its potential use as a drug to treat brain tumours. It has been shown that 4-Aminophenyl b-D-thioglucopyranoside binds to centromeric DNA sequences in mammalian cells, which can lead to inhibition of transcription and replication. This inhibitory effect on transcription and replication is due to the inhibition of acetyltransferase enzymes by 4-Aminophenyl b-D-thioglucopyranoside.

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.

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.

(2R,3R,4S,5R,6S)-3,4,5-Trihydroxy-2-hydroxymethyl-7,9-diaza-1-oxa-spiro[4,5]decane-10-one-8-thione is a custom synthesis of a polysaccharide. It has been modified to include fluorination and methylation. The monosaccharides present are glucose and galactose. This polysaccharide also has a saccharide linkage to an oligosaccharide that contains glycosylation sites for sugar groups.

1,2,3,5-Tetra-O-acetyl-D-ribofuranose is a dietary supplement that can be found in the form of palladium complexes. This compound has been shown to have anti-inflammatory properties and may be effective against cancer cells. 1,2,3,5-Tetra-O-acetyl-D-ribofuranose is an acetylated pyridazine derivative with antimicrobial and antibacterial effects. It has also been shown to inhibit the synthesis of purines and pyrimidines by cleaving the 6th carbon from ribose. 1,2,3,5-Tetra-O-acetyl-D-ribofuranose is synthesized by chlorination of 2,6-, 3-, 5-, or 7-(chloropurinomethyl)pyridine with mercuric chloride or nitrosyl chloride. The cleavage products are hydroxyl group

MW of BSA approx 65000

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

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.

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.

Trimethylsilyl-2,3,4,6-tetra-O-benzyl-b-D-glucopyranoside is a modified carbohydrate that has been fluorinated and silylated. It is used as an intermediate in the synthesis of glycosylated compounds. Trimethylsilyl-2,3,4,6-tetra-O-benzyl-b-D-glucopyranoside can be custom synthesized to meet your needs. It is a white powder that is soluble in water and alcohols. The CAS number for this compound is 89825-08-1.

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.

(S)-Propranolol glucuronide is a custom-synthesized sugar that has been modified with fluorination and methylation. It is also a polysaccharide that has been glycosylated and carbamoylated. This compound is a white crystalline solid that can be used as an intermediate in the synthesis of saccharides, oligosaccharides, and polysaccharides.

a-D-Xylopyranosyl azide is a sugar that can be synthesized from the reaction of 1,2-dichloroethane with 2,3,4,6-tetra-O-acetyl-a-D-xylopyranose. This compound has a high purity and can be custom synthesized to order. It is used in glycosylation reactions to modify saccharides and oligosaccharides. It has been shown to be useful for click modification and fluorination reactions.

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.

Please enquire for more information about D-Lyxose-1-C-D including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

4-O-Acetyl-3,6-di-O-benzyl-D-glucal is a custom synthesized compound with high purity. This product is a complex carbohydrate that can be used as a monosaccharide or sugar. It has been modified with fluorination and methylation to produce a compound that is resistant to degradation by enzymes and oxidation. The CAS number for this product is 165524-87-8.

4'-O-(b-D-2,3,4,6-Tetra-O-acetyl-glucopyranosyl)-4-nitrophloretin is a custom synthesis with Modification. This product was prepared by fluorination and methylation of 4'-O-(b-D-2,3,4,6-tetra-O-[1,2:1,3]triazolium chloride)-4' nitrophloretin. The molecular formula is C21H18N8O12 and molecular weight is 524.32. CAS No. 82628-87-3.

2-Amino-2-deoxy-D-altrose (2AD) is a molecule with the chemical formula C6H14N2O4. It belongs to the class of compounds known as uronic acids. 2AD is an acetylated molecule that has been structurally studied by X-ray crystallography and NMR spectroscopy. The molecule contains a ring of six carbon atoms, two of which are epoxide groups. The nature of this compound is glycosidic, with focus on hexamethylphosphoramide and diamino oligosaccharides. 2AD has been shown to have anti-inflammatory activities in animals, but its exact mechanism of action remains unknown. This compound may act through a ring-opening reaction or by inhibiting prostaglandin synthesis.

Allyl 2-acetamido-4,6,-O-benzylidene-2-deoxy-a-D-glucopyranoside is a sugar that is used as a custom synthesis or modification. It is also called allyl 2-(1,3-dioxo-1,3,4,-thiadiazolidinium)acetamido 4,6,-O-(benzylidene)-2 deoxy erythro -a D glucopyranoside. Allyl 2 acetamido 4,6,-O -benzylidene -2 deoxy erythro -a D glucopyranoside is used in the glycosylation of proteins and oligosaccharides and in the synthesis of saccharides. This compound has been shown to be useful in identifying glycosaminoglycan chains in complex carbohydrates.

(2R,4R)-2-[D-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid is a methylated saccharide that has been modified by the click chemistry method. It is a synthetic product with high purity and good quality. This compound can be used for glycosylation and oligosaccharide synthesis. (2R,4R)-2-[D-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid has CAS No. 110270-19-4 and can be found in complex carbohydrates in nature.

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.

Methyl D-arabinofuranoside is an antimycobacterial agent that inhibits the synthesis of mycolic acids, which are important components of the cell wall of Mycobacterium tuberculosis. Methyl D-arabinofuranoside has been shown to be active against drug-resistant strains and has been well tolerated by animals. This compound can be synthesized from 2,4-dichlorophenylacetic acid and arabinose in two steps. The first step involves a three-component condensation reaction with sodium hydroxide, hydrochloric acid, and 2,4-dichlorophenylacetic acid. The second step is a nucleophilic attack on the pyran ring of methyl D-arabinofuranoside with hypophosphorous acid. Methyl D-arabinofuranoside can also be prepared by reacting sodium nitrosobenzene with sodium benzene sulfinate in alcoholic solution

D-Ribose-2,3,4,5-13C4 is a complex carbohydrate with saccharide units. It is synthesized by the chemical modification of D-ribose. This product can be used to modify or methylate glucose and other carbohydrates. It has been shown to inhibit the formation of amyloid plaques in Alzheimer's disease, which may be due to its ability to reduce nitric oxide and reactive oxygen species levels. The purity of this product is at least 98%.

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.

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.

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.

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.

1,2,3,5,6-Penta-O-propanoyl-b-D-glucofuranose is a methylated sugar. It is a polysaccharide consisting of 1,2,3,5,6-penta-O-propanoyl-b-D-glucopyranosyl units linked by β-(1→4)-glycosidic bonds. This carbohydrate can be used in the synthesis of oligosaccharides and glycosylation reactions. 1,2,3,5,6-Penta-O-propanoyl b -D -glucofuranose has been fluorinated to give pentafluorobenzoyl b -D -glucofuranose which is used for click 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.

Methyl L-rhamnopyranoside is a sugar that is the product of the reaction between l-rhamnose and acetone. This compound has been used as a chiral building block for the synthesis of other sugars, such as D-arabinose and D-lyxose. The yield of this reaction depends on the concentration of potassium thioacetate and temperature. This compound can be obtained in two forms: (1) anomeric form, which is an intermediate in the synthesis of carbohydrates and (2) crystalline form, which is a white solid with melting point at 157.3°C. The anomeric form has a stereogenic center at carbon atom 3, whereas the crystalline form does not have any stereogenic centers. Methyl L-rhamnopyranoside also reacts with chlorination reagents to produce chlorinated derivatives, such as 2-chloro-3-(3′,4′-dimeth

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.

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.

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.

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.

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-Allose is a sugar that is modified with a fluorine atom at position 6. This modification can be used to trace the origin of D-allose in complex carbohydrates such as glycogen and glycosylated proteins. The addition of a 13C6 atom allows for the identification of this sugar through mass spectrometry and nuclear magnetic resonance (NMR) analysis.

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.

3,2',3',4'-Tetra-O-acetyl-6,6'-di-O-tert-butyldimethylsilyl-lactal is a glycosylation agent that can be used in the synthesis of oligosaccharides and polysaccharides. It can be fluorinated to create a reactive site for methylation and click modification. 3,2',3',4'-Tetra-O-acetyl-6,6'-di-O-tert-butyldimethylsilyl-lactal is an acetylated lactal with a silyl ether protecting group. This product has been custom synthesized and is available in high purity.

Sertraline is a selective serotonin reuptake inhibitor (SSRI) that is used primarily in the treatment of depression and anxiety. It inhibits the serotonin transporter protein, making more serotonin available for binding to postsynaptic receptors. Sertraline also has a minor inhibitory effect on norepinephrine and dopamine reuptake, but its primary function is as a selective serotonin reuptake inhibitor. The major metabolite of sertraline is sertraline carbamoyl glucuronide, which is formed through glucuronidation by UGT2B7. This metabolite has been found to be bifurcated with one half being excreted in urine and the other half being excreted in faeces. The half that undergoes urinary excretion has been shown to have a half-life of 24 hours whereas the other half has a much shorter half-life of 2 hours. Carbamoylation of sertraline may

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+.

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.

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.

3-Deoxy-3-fluoro-D-fructose is a monosaccharide that has been used as an inhibitor of glucose uptake and metabolism in the lymphocytic leukemia cell line. This compound has been shown to inhibit the glucose transporter GLUT1, which is responsible for the transport of glucose across the plasma membrane. 3-Deoxy-3-fluoro-D-fructose inhibits cancer cells by inhibiting galactitol production through inhibition of gluconeogenesis. It also inhibits oxidative phosphorylation in lymphocytic leukemia cells, leading to apoptosis. 3-Deoxy-3-fluoro-D-fructose has been shown to inhibit cancer growth by blocking glucose uptake in xenopus oocytes.

Fucose 2-nitrophenylhydrazone is a custom synthesis that is a modification of fucose. It has been used in methylation, click modification, and fluorination. This compound has been shown to be effective in the synthesis of oligosaccharides and polysaccharides. Fucose 2-nitrophenylhydrazone has also been used as an intermediate for the synthesis of saccharides such as monosaccharide and sugar.

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.

D-Ribopyranosyl thiosemicarbazide is a glycosylation agent that can be used in the synthesis of complex carbohydrates. It also has the ability to modify sugar structures, such as methylation, click modification, and fluorination. This reagent can be used for the modification of saccharides, oligosaccharides, and monosaccharides. D-Ribopyranosyl thiosemicarbazide is synthesized from d-ribose and thiosemicarbazide. The CAS number for this product is 95352-77-5.

Muraglitazar acyl-b-D-glucuronide is a complex carbohydrate that has been modified with fluorination. The compound is synthesized from methylation, glycosylation, and carbamylation reactions with saccharides. The saccharide modification includes the attachment of various sugars such as glucose, galactose, and mannose. Muraglitazar acyl-b-D-glucuronide can be used in the synthesis of oligosaccharides and polysaccharides. It is also used for Click modification of sugar molecules.

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.

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

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.

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.

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.

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).

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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

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.

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.

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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

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.

(-)-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.

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

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%.

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.

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.