Monossacáridos

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.

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-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.

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.

1,4-Anhydro-3-deoxy-D-threo-pentitol is a custom synthesis of a monosaccharide. The structure consists of a hydrogen attached to the oxygen on the anomeric carbon which is then substituted with fluorine. The hydroxyl group on C1 is methylated and then reduced to form a hemiacetal linkage with the C6 hydroxyl group. This product can be used in glycosylation reactions to produce complex carbohydrates.

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.

UDP-β-D-glucose sodium is an oligosaccharide that can be used to synthesize glycoproteins and glycolipids. UDP-β-D-glucose sodium is a synthetic compound that contains one β-D-glucose moiety, which is attached to the molecule via a β-(1→4) linkage. This product can be custom synthesized and modified to suit customer needs. It has been shown to have high purity, chemical stability, and good solubility in water. The synthesis of UDP-β-D-glucose sodium has been modified by click chemistry to produce a variety of different products with new properties.

Palatinose monohydrate is a hydrogenated form of the natural disaccharide palatinose. It is often used as a solid catalyst in pharmaceutical preparations and has been shown to have a lower molecular weight than sucrose. Palatinose monohydrate may have beneficial effects on postprandial plasma glucose, protein data, and lipid metabolism. The hydrogenation process also produces fatty acids that are less reactive than those found in other sugars. Amine groups are also reduced in palatinose monohydrate, which may improve its taste. Palatinose monohydrate is not toxic at high doses and has been shown to be safe for use in toxicity studies. Surface methodology has been used to characterize the surface properties of palatinose monohydrate crystals, which can be used as a model for other sugar crystals.

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.

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.

1,3,4,6-Tetra-O-acetyl-N-(4-methoxybenzylidene)-b-D-glucosamine is a high purity custom synthesis sugar that has been fluorinated and glycosylated. It is synthesized from the methylation of 4-(1,3,4,6-tetra-O-acetyl)-N-(4-hydroxybenzylidene)-b-D-glucosamine and can be used for the modification of saccharides or oligosaccharides. This compound has CAS No. 7597-81-1 and is known as a carbohydrate.

Ethyl D-thioglucuronide is a modification of an oligosaccharide, carbohydrate, complex carbohydrate or sugar. It can be synthesized by custom synthesis or by synthetic methods. The product is highly pure and monosaccharide methylated. The product can be glycosylated, polysaccharide, sugar fluorinated and saccharides click modified.

4,6-O-Benzylidene-a-D-galactopyranoside is an artificial sweetener that has a high purity and can be custom synthesized. This compound is also known as an oligosaccharide or complex carbohydrate. It is a member of the saccharide family, which includes monosaccharides and disaccharides. 4,6-O-Benzylidene-a-D-galactopyranoside is a sugar that has been modified by glycosylation and methylation. This product has CAS No. 57783-86-5 and can be found in the Glycosides section of the Chemical Directory.

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.

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.

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.

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.

Tetra-O-acetyl-2-acetamido-2-deoxy-b-D-mannose is a modified sugar that is synthesized by the methylation of 2,4,6-trichloroacetimidate. This compound has been used in the synthesis of glycosylations and other modifications. Tetra-O-acetyl-2-acetamido-2-deoxy-b-D mannose can be custom synthesized to your specifications with high purity.

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.

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

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.

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.

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.

2,3,4-Tri-O-acetyl-b-D-xylopyranosyl azide is a compound that has a linear range of 10 to 500 μM. It has been shown to inhibit the growth of bacteria such as C. perfringens and S. aureus. This compound inhibits the production of toxins in these bacteria by binding to the ribosomes and inhibiting protein synthesis. In addition, this compound has been shown to have high activity at salinity levels up to 15% NaCl and diffraction data was obtained from 2,3,4-tri-O-acetyl-b-D-xylopyranosyl azide crystals using XRD in order to quantify its molecular structure.

Iminosugar 2 is a custom synthesis that is modified with fluorination, methylation, and click modification. This product is a monosaccharide and an oligosaccharide that has glycosylation. It is a saccharide that has polysaccharides as complex carbohydrates. Iminosugar 2 can be used in the production of polymers and pharmaceuticals.

D-Glucose 6-phosphate, disodium salt is an antibiotic that is used to treat gram-negative bacterial infections. It binds to the bacterial ribosome and inhibits protein synthesis, which leads to cell death by inhibiting the production of proteins vital for cell division. This drug has been shown to be active against a wide range of bacteria, including resistant strains such as Escherichia coli and Salmonella typhimurium. D-Glucose 6-phosphate, disodium salt also has anti-inflammatory properties and can be used as an anti-bacterial agent in the treatment of typhoid fever.

Phenyl a-L-thiorhamnopyranoside is a monosaccharide that is synthesized by the methylation of alpha-D-glucose. It is a custom synthesis that is used in the synthesis of oligosaccharides, polysaccharides, and sugar drugs. Phenyl a-L-thiorhamnopyranoside can be fluorinated to create an active form that has antibacterial activity. This compound has shown no signs of toxicity in animal studies and has been used as a food additive.

Methyl 1-(5-fluoro-1H-2-oxopyrimidin-4-yl)-b-D-glucopyranuronate is an anticancer drug that inhibits β-glucuronidase. Methyl 1-(5-fluoro-1H-2-oxopyrimidin-4-yl)-b-D-glucopyranuronate is a colorless solid that has been recrystallized, purified, and analyzed for its chloride content. The function of this compound has been tested in vitro using tissue cultures and animal models. The reaction vessel used for the test was an acetonitrile solution with a pH between 7 and 8. The methylester form of methyl 1-(5-fluoro-1H--2--oxopyrimidin 4--yl)-b--D--glucopyranuronate reacts with sulphite to produce a green product with a colorimetric method

3-Pyridinylmethylbeta-D-glucopyranoside is a sugar that can be custom synthesized. It is a white to off-white crystalline powder with an odorless taste and is soluble in water. 3-Pyridinylmethylbeta-D-glucopyranoside is used in the synthesis of glycosides, saccharides, oligosaccharides, and monosaccharides. This compound can also be modified with fluorination or methylation reactions. The use of this product has been shown to produce high purity compounds for use in pharmaceuticals, agrochemicals, and other chemical industries.

Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is a synthetic compound that belongs to the class of carbohydrates. It is used as a reagent in sugar chemistry and glycosylation reactions. Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is also used for the modification of polysaccharides and fluorination reactions. This product has been shown to be effective as a substrate for site specific methylation reactions. Allyl 2 acetamido 4,6 O benzylidene 2 deoxy b D glucopyranoside has been tested in vitro against methicillin resistant Staphylococcus aureus (MRSA) with promising results.

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.

SN-38 glucuronide is a metabolite of irinotecan that inhibits the growth of cancer cells by binding to the DNA polymerase, blocking the synthesis of DNA. SN-38 glucuronide has potent antitumor activity and high values for inhibiting tumor metastasis. It is mainly excreted in urine as a conjugate with glucuronic acid, which may be why urine samples are often used to measure its concentration. SN-38 glucuronide also interacts with other drugs, including chemical inhibitors and ATP-binding cassette transporters, which can affect its pharmacological properties.

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.

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.

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.

Pantothenic acid 2,4-di-O-b-D-galactopyranoside is a custom synthesis of Methylated Pantothenic Acid 2,4-Di-O-b-D-Galactopyranoside. The compound is an oligosaccharide composed of two glucose molecules and one galactose molecule. It contains a fluorine atom at the 4th position of the sugar chain. This modification was made to increase the solubility in water. Pantothenic acid 2,4-di-O-b-D-galactopyranoside can be used in industry as a food additive or pharmaceutical intermediate.

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.

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.

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.

3-Amino-2,3-dideoxy-D-myo-inositol (3ADMI) is a gene product that belongs to the class of chemical biology. It is an actuator that has been shown to be able to bind and activate enzymes. 3ADMI is used as a substrate in the calibration of enzyme kinetics and as an analog for aminoglycosides. The conjugates of 3ADMI have been shown to prevent viral replication by inhibiting the synthesis of DNA or RNA.

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.

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.

L-Idaric acid is a novel anti-inflammatory agent that is a derivative of the endogenous compound d-glucuronic acid. It has been shown to have anti-inflammatory effects in animal studies as well as in human cell cultures and it has been shown to be safe for use in humans. L-Idaric acid inhibits the production of inflammatory mediators, such as prostaglandins, leukotrienes, and cytokines. L-Idaric acid also inhibits the activity of β-glucuronidase, which may be responsible for its ability to prevent the degradation of glucuronic acid derivatives.

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).

2-Amino-2,3,5-trideoxy-3-methyl-L-arabinonic acid-gamma-lactone hydrochloride is a lipid biosynthesis inhibitor that blocks the first step of this pathway by inhibiting the enzyme d-arabinose 4,5-diphosphate aldolase. This compound inhibits bacterial growth and leads to cell lysis. It has been shown to be active against cryptococcus neoformans and Candida neopformans. 2AADL has also been shown to inhibit the production of cell wall polysaccharides in C. neoformans and other fungi. 2AADL is thought to bind to the cell membrane through its alcohol group, which may lead to changes in the redox potential of the cells.

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.