Monossacáridos

2-C-Methyl-3,4-O-isopropylidene-L-arabinonic acid d-lactone is a synthetic chemical compound that has been shown to inhibit the growth of bacteria. This compound has been shown to inhibit the growth of bacteria by inhibiting ribulose bisphosphate carboxylase activity and causing cell death. It also inhibits glycosylation reactions in bacteria. 2-C-Methyl-3,4-O-isopropylidene -L-arabinonic acid d -lactone is an oligosaccharide with a complex carbohydrate structure. It contains saccharides and monosaccharides with a methylated C2’ position on the glucose moiety. 2CMOA has a molecular weight of 516.

3-O-Methanesulfonyl-D-glucopyranose is a high purity, custom synthesis sugar that can be modified with fluorination, glycosylation, methylation and modification. It is also synthesized from glycoaldehyde and methanesulfonic acid in the presence of sodium hydroxide and sodium acetate. 3-O-Methanesulfonyl-D-glucopyranose can be used to synthesize saccharides and oligosaccharides. This compound is soluble in water and has a boiling point of 218°C at 760 mmHg. It is slightly soluble in methanol, ethanol and acetone. 3-O-Methanesulfonyl-D-glucopyranose has a CAS number of 40631-95-6.

β,β-Trehalose is a carbohydrate that is synthesized by the expression of a trehalose synthase enzyme from the yeast Saccharomyces cerevisiae. β,β-Trehalose is an acidic sugar with two glucose subunits. It has been shown to have an enzymatic mechanism similar to that of glucose. β,β-Trehalose has been found to increase the solubility and stability of proteins in acidic phs (pHs) by binding to hydroxyl groups on protein surfaces. β,β-Trehalose also binds to alcohols such as ethanol and methanol, which may be due to its ability to form hydrogen bonds between oxygen atoms. This sugar also forms hexamers in solution, which may contribute to its effectiveness as a stabilizer for proteins and other molecules. The optimum ph for β,β-trehalose synthesis is around 5.5-6.0 and it can be used at higher ph

6-O-Acetyl-D-glucose is a natural sugar that is found in Holothuria, a sea cucumber. It has been shown to have anti-cancer and anti-inflammatory properties. 6-O-Acetyl-D-glucose inhibits the production of extracellular Ca2+ and has shown therapeutic effects against colorectal carcinoma. This active substance also exhibits allergenic reactions, which may be due to its ability to bind to IgE antibodies on mast cells and basophils. 6-O-Acetyl-D-glucose is a glycoside that contains an acetate group linked by an O atom to the hydroxyl residue of glucose. The glycosidic bond can be hydrolyzed with the enzyme β glucosidase, releasing the aglycone (sugar) and β glucosidase.

1,2,3,4,6-Penta-O-acetyl-D-mannopyranose is an organic chemical compound that belongs to the group of sugars. It is a synthetic compound that can be used as an analytical reagent in hepg2 cells and chloride. 1,2,3,4,6-Penta-O-acetyl-D-mannopyranose has been shown to have a protective effect against adenosine receptors and phosphotungstic acid in brain cells. This sugar also has a strong affinity for lectins and can be used to study the binding of sugars to proteins by titration calorimetry.

Building block for synthesis of oligosaccharides

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-b-D-galactopyranose (TAZ) is an aromatic heterocyclic sugar compound that is used in pharmaceutical formulations. It has low toxicity and can be synthesized using a number of methods. TAZ has been shown to have antifungal effects against Candida albicans and antitumor effects against cancer cells. TAZ also inhibits the activity of teniposide, which is a drug used for the treatment of leukemia. TAZ may be effective against cancer cells by acting as an amido donor and changing the conformation of the cyclic peptide.

1-Bromo-2,3,4-tri-O-acetyl-a-D-glucuronide methyl ester is a protected D-glucoronic acid with an alpha bromide at the anomeric position ready to undergo glycosylation reactions with suitable glycoside acceptors. Pharmaceutically active compounds have been used as acceptors to form β-linked D-glucuronide prodrugs which can be used to modify pharmacokinetics, improve solubility and lower the toxicity of the drug.

Benzyl 2-deoxy-2-phthalimido-b-D-glucopyranoside is a custom synthesis that belongs to the group of complex carbohydrates. It is an oligosaccharide or polysaccharide that is modified with methylation, glycosylation, and carbamylation, and has a CAS number of 80035-32-1. This compound has been used in the synthesis of saccharides for the preparation of an antibody drug conjugate. Benzyl 2-deoxy-2-phthalimido-b-D-glucopyranoside is also known as 6Fluoro 3 indoxyl beta D galactopyranoside.

Phenyl b-D-thioglucuronide is a synthetic molecule that has been used in studies of the carotid, abdominal and symmetric techniques. It can be used to study water absorption and squamous cell growth. Phenyl b-D-thioglucuronide has been used as a crosslinking agent for optical imaging techniques, such as fluorescence microscopy and confocal microscopy. The basic protein form of phenyl b-D-thioglucuronide is found in the human brain and spinal cord. There have been reports that phenyl b-D-thioglucuronide causes death and teratomas in mice when injected into the sigmoid colon or teratoma. Phenyl b-D-thioglucuronide also causes neuroinflammation, which may be due to its ability to induce matrix metalloproteinase production.

Sorbitan monostearate is a lipid-soluble compound that is used as a surfactant and emulsifier in food products. It has been found to be nontoxic when administered at concentrations up to 5000 mg/kg of body weight for 28 days. Sorbitan monostearate has been shown to be nontoxic in vitro, but the long-term toxicity of this compound has not been established. Sorbitan monostearate also exhibits hydrogen bonding interactions with calcium pantothenate, sodium salts, and coumarin derivatives. The model system used was an artificial membrane composed of chitosan quaternary ammonium and monolaurate. This study found that sorbitan monostearate is able to permeabilize the membrane at an optimum concentration.

3-O-benzyl-D-xylose is a sugar that belongs to the group of dimethyl, diisobutylaluminium, dicarboxylate, malonate, oxygenated, acetylation, cyclopentane. It has been shown to be effective in cleavage and condensation reactions. 3-O-benzyl-D-xylose can be used in the synthesis of pyridinium chlorochromate and chlorochromate. This compound also reacts with pyridinium via hydride reduction and hydroxide cleavage.

Methyl 2,3,5-tri-O-benzoyl-b-D-arabinofuranoside is a custom synthesis of an Oligosaccharide with a molecular formula of C12H22O11. It has CAS No. 1093344-99-0 and Methylation, Glycosylation, Carbohydrate, Click modification, saccharide, sugar. This product is a high purity product that is Fluorination and Synthetic.

Methyl 3-O-benzyl-D-glucopyranoside is a custom synthesis. It is a complex carbohydrate that is an oligosaccharide, polysaccharide, and modified saccharide. Methyl 3-O-benzyl-D-glucopyranoside can be synthesized from glucose with the use of methylation, glycosylation, or carbonylation reactions. The product has been fluorinated to yield a high purity product. This product can be used for click modifications or sugar chemistry experiments.

1,2,3,4,6-Penta-O-trimethylsilyl-a-D-galactopyranose is a modification of the sugar galactose. It is a complex carbohydrate and an oligosaccharide that has been custom synthesized. The molecular weight of 1,2,3,4,6-Penta-O-trimethylsilyl-a-D-galactopyranose is 592.77 g/mol. The purity of this compound is >99%. This compound has been fluorinated and saccharide methylated.

2-O-Acetyl-3,4,6-tri-O-benzyl-a-D-glucopyranosyl trichloroacetimidate is a custom synthesis. It is a modified oligosaccharide with a fluorinated carbon atom in the 2 position of the acetyl group. This chemical has been shown to be effective for click modification and glycosylation reactions. The CAS number for this chemical is 108869-64-3.

Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene-a-D-glucopyranoside is a synthetic compound that has been shown to be an inhibitor of the receptor for the proinflammatory cytokine TNF. It has been proposed as a possible treatment for chronic kidney disease, acute phase, and neurodegenerative diseases such as chronic pain. Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene-a-D-glucopyranoside is an inhibitor of factor receptors and inhibits the activation of NFκB in a dose dependent manner. This inhibition leads to decreased production of proinflammatory cytokines such as TNF.