Monossacáridos

2,3,4,6-Tetra-O-acetyl-β-D-thiogalactopyranose sodium salt is a high purity custom synthesis sugar with a click modification. The fluorination and glycosylation are carried out to give the desired product. It has CAS No. 73962-00-2 and is a synthetic carbohydrate that can be used in oligosaccharides, monosaccharides, saccharide and complex carbohydrates.

Methyl 2,6-dideoxy-a-D-glucopyranoside is a custom synthesis of an oligosaccharide that is modified with fluorination. It is a saccharide, or carbohydrate, that has been methylated and glycosylated. The modification of this complex carbohydrate has been achieved through the use of the Click reaction. This product has been purified to high purity and is ready for use in research and development.

O-(D-glucopyranosylidene)amino N-phenylcarbamate is a synthetic monosaccharide that is used in our laboratory as an intermediate for the synthesis of complex carbohydrates. It is also used in the modification of polysaccharides and glycosylations. This compound has been shown to be stable to hydrolysis, methylation, and oxidation. O-(D-glucopyranosylidene)amino N-phenylcarbamate has been shown to be a high purity product with a CAS number of 104012-84-2.

1’,2’-Di-O-acetyl-5’-O-benzoyl-3’-deoxy-3’-fluoro-D-ribofuranose is a glycosylated monosaccharide that is custom synthesized for use as a fluorinated probe in the detection of protein glycosylation. This compound has been shown to react with Methyl groups to form a complex carbohydrate. 1’,2’-Di-O-acetyl-5’-O-benzoyl-3’ -deoxy -3’ -fluoro D ribofuranose is soluble in water and organic solvents such as ethanol or methanol. The CAS number for this compound is 522611–41–0.

2,3,5-Tri-O-benzyl-b-D-ribofuranose is a synthetic monosaccharide that is used in the synthesis of complex carbohydrates such as glycosylation and polysaccharides. One use for this chemical is to modify the sugar moiety with methyl groups, yielding 2,3,5-tri-O-methyl b-D-ribofuranose. This modification helps prevent the sugar from being metabolized by enzymes in the body. The chemical can also be fluorinated to yield 2,3,5-trifluoro b-D-ribofuranose.

2,3,4-Tri-O-benzyl-L-rhamnopyranose is a chemical compound that belongs to the family of carbohydrates known as rhamnopyranoses. It is a derivative of L-rhamnose, which is a naturally occurring aldohexose sugar. The compound is often used as a glycosyl donor in the synthesis of oligosaccharides and glycoconjugates. The three benzyl groups in the molecule provide protection for the hydroxyl groups, allowing for selective deprotection and glycosylation. 2,3,4-Tri-O-benzyl-L-rhamnopyranose is also used as a precursor in the synthesis of various natural products.

D-ido-Heptono-1,4-lactone is a glycosylation product of heptose with d-ido-D-glucofuranose and is a synthetic sugar. It has an Oligosaccharide, sugar, Synthetic, Fluorination, Custom synthesis, Methylation, Monosaccharide, Polysaccharide, saccharide Click modification. It has CAS No., Modification.

3,4-Di-O-acetyl-L-arabinal is a synthetic compound that belongs to the class of monofluorides. It has been synthesized from l-arabinose by a stereoselective process, with triflic acid as the catalyst and propargylation as the key step. The synthetic pathway starts from an acid hydrolysis of L-arabinose to yield 3,4-di-O-acetyl-L-arabinonic acid. This acid is then converted to 3,4 diacetyl L arabinonic acid with acetic anhydride and acetic acid in the presence of triethylamine. The final product is then obtained by reacting this intermediate with 1 equivalent of sodium fluoride in tetrahydrofuran (THF) using catalytic reduction with sodium borohydride at 0 °C. The major advantage of this synthetic process is that it provides two stereoisomers: (

Specific and potent inhibitor of lysosomal α-galactosidase with IC50 in nanomolar range. It acts as pharmacological chaperone and assists folding of the wild type and mutant versions of the enzyme. It places itself in the instable active site and prevents the damage to the enzyme during the passage through Golgi apparatus, endoplasmatic reticulum and lysosome axis. The exposure to this compound leads to increased levels of functional α-galactosidase in models for lysosomal storage disorders and brings therapeutic benefits to patients with Fabry disease.

Allyl 2,3,4-tri-O-acetyl-b-D-galacturonide methyl ester is a synthetic monosaccharide that is custom synthesized for use in modifying complex carbohydrates. It has the CAS number 130506-36-4 and can be used in the synthesis of oligosaccharides and polysaccharides. This chemical may be fluorinated to give a fluorinated carbohydrate, which may then be methylated to produce an allyl 2,3,4-tri-O-acetyl-b-D-galacturonide methyl ester. Allyl 2,3,4-tri-O-acetyl--b--D--galacturonide methyl ester is also known as Methylated galacturonic acid or 2,3,4 Triacetate D Galacturonic Acid Methyl Ester.

3,5-Dimethyl-D-fructose is a glycosylation product of 3,5-dimethoxy-4-hydroxybenzoic acid and D-glucose. It can be synthesized by the reaction of 3,5-dimethoxy-4-hydroxybenzoic acid with D-glucose in the presence of sodium cyanoborohydride. This product has been used as a reactant in click chemistry and as a fluorinating agent for saccharides. 3,5-Dimethyl-D-fructose is a custom synthesis that can be ordered in high purity at CAS No. 52674-57-6.br>br>
3,5 - Dimethyl - D - fructose
is an oligosaccharide that is used as an intermediate in the synthesis of other sugars. This product has been shown to have antiinflammatory properties due to its inhibition of prostaglandin synthesis.br

D-Lyxonic acid potassium salt is a pentitol that is a stereospecific, aldonic, and nature D-glycosylamine. It can be synthesized by reacting phenylhydrazine with glycolic acid chloride in the presence of catalytic amounts of sodium hydroxide. The yield is about 98%. This compound has been shown to have anti-inflammatory properties when it reacts with hydrogen chloride to form D-lyxonic acid chloride. It also has been shown to inhibit the growth of bacteria and fungi by binding to the cell wall and inhibiting protein synthesis.

Building block for polymers synthesis, ionic liquids and chiral auxiliaries

4-Acetylphenyl-β-D-glucopyranoside (4APG) is a natural compound that belongs to the group of p-hydroxybenzoic acid. It has been shown to have antibacterial properties, with an optimum pH of 5.0 and an MIC of 1.0 μg/mL. 4APG was found to be active against Gram-positive bacteria, including Staphylococcus aureus, Bacillus subtilis, and Clostridium perfringens. This compound also inhibits the growth of Gram-negative bacteria such as Escherichia coli, Salmonella enteritidis, and Shigella dysenteriae. The chemical structure of 4APG was determined by NMR spectroscopy analysis and HPLC analysis. Analysis by GCMS revealed that 4APG contains protocatechuic acid, 5-caffeoylquinic acid, and other unknown compounds.

1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldimethylsilyl-b-D-glucopyranose is a custom synthesis. It is an oligosaccharide that is glycosylated with methyl groups and fluorinated. This product has a purity of >99% and can be used as a substitute for natural glycosides in pharmaceuticals or other applications.

Methyl 2,3,4,6-tetra-O-benzyl-D-galactopyranoside is a trisaccharide that binds to the fluorescent chromophore. It has been shown to have strong binding activity and can be used for the labeling of carbohydrates. Methyl 2,3,4,6-tetra-O-benzyl-D-galactopyranoside is also used in assays to detect toxins or as a fluorescent label for polymers. This compound can be synthesized by reacting methyl 4,6-dibenzyloxybenzoate with glucose in methanol.

2,3,4,6-Tetra-O-acetyl-D-glucopyranose is a carbohydrate that is used in the synthesis of besifloxacin. This compound has been studied as an analog for many other natural compounds and its derivatives have shown to be effective against bacteria such as Staphylococcus aureus and Clostridium perfringens. The acetyl groups on this molecule allow it to be easily converted into other compounds with desired properties. This compound has been found to be acidic and can be used as a medicinal preparation or analytical chemistry reagent. The hydroxyl group on the 2 carbon atom allows the molecule to form glycoside derivatives. The halides on this molecule are also important for making new molecules by replacing one of the hydrogen atoms with another halogen atom. The phenylpropanoid glycosides are found in plants and may contain an enantiomeric form of 2,3,4

Glucal is a carbohydrate that is used as a synthon in organic synthesis. It has been shown to be anomeric and can be synthesized by acetylation of the corresponding aldose, or by the glycosidic bond reaction with borohydride reduction. Glucal is not stable at high pH and can undergo ring-opening reactions with nucleophiles such as sodium borohydride. Glucal also reacts with glycoconjugates to form new molecules, which are called glycosidic products.

1,5-Anhydro-2,3,4-tri-O-benzoyl-D-threo-pent-1-enitol is a high purity compound that is synthesized from D-threo pent 1 enitol. It is a sugar that belongs to the category of complex carbohydrates. This product can be custom synthesized and modified according to customer requirements.

Isosorbide dinitrate is used to treat chronic bronchitis and congestive heart failure. It dilates blood vessels, allowing more oxygen-rich blood to reach the heart. Isosorbide dinitrate is also used to relieve chest pain (angina) and reduce complications after a heart attack. Isosorbide dinitrate is a prodrug that is converted in vivo to its active form, isosorbide mononitrate, by the enzyme nitric oxide synthase in response to hypoxia. In addition, it has been shown that this drug reduces levels of low-density lipoprotein cholesterol (LDL-C) and may be useful for the treatment of high cholesterol.
The mechanism of action for reducing LDL-C levels is not known but may be due to increased clearance of LDL-C from plasma or decreased production of very low density lipoproteins (VLDL). This medication does not affect triglycerides or high density lip