Monosaccharides

Used as source of carbon in culture medium.

Methyl 2,3-di-O-acetyl-4,6-O-(4-methoxybenzylidene)-a-D-mannopyranoside is a custom synthesis that contains a fluorinated sugar with a methyl group attached to the 4 position. The oligosaccharide is synthesized through click chemistry and has been modified with an acetate at the 6 position. The CAS number is 108739-53-0. The carbohydrate is a complex carbohydrate that can be found in nature or synthesized in the laboratory.

A metabotoxin, a neurotoxin, and a hepatotoxin at high levels

(-)-isolariciresinol-2a-O-b-D-xylopyranoside is a methylated saccharide that is used in the synthesis of complex carbohydrates. It is synthesized by reacting an aldehyde with an alcohol, and it has been modified using click chemistry. The product is purified to be at least 98% pure, and it can be custom synthesized to order. (-)-isolariciresinol-2a-O-b-D-xylopyranoside can be fluorinated for use as a fluorescent probe for various applications. It has a CAS number of 564964-92-1.

D-Arabinose is a dinucleotide phosphate that is an important metabolic intermediate in the pentose phosphate pathway. It has been shown to have pharmacological effects, such as enzyme inhibition and binding to DNA. D-Arabinose has been used in biochemical studies of energy metabolism and related areas. D-Arabinose is converted to ribitol by ribitol dehydrogenase, which can be oxidized to ribulose 5-phosphate by ribulose 5-phosphate dehydrogenase. The conversion of D-arabinose to ribitol requires NAD(P)H, which provides the reducing power for this reaction. The conversion of ribitol to ribulose 5-phosphate also requires NAD(P)H, but does not produce any reducing power. A redox potential measurement was used to determine the relative reduction potentials of the two reactions and found that they are equal at -0.5 volts (V).

2-Amino-b-D-arabinofurano[1,2;4,5]oxazoline is an organic compound that can be used in the synthesis of saccharides. It is also a fluorescent probe for amino acids and sugars. 2-Amino-b-D-arabinofurano[1,2;4,5]oxazoline has been shown to be a high purity product and can be custom synthesized. This compound is often used in glycosylation reactions with sugar or saccharide donors. The synthesis of 2-amino b D arabinofurano [1,2;4,5] oxazoline is not complicated and can be achieved by modifying the methyl group on the ring at C2 position. The CAS number for this compound is 27963-98-0.

(2R,3R,4R,5R)-2-(3-hydroxy-4-methoxyphenyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol is an imino-sugar

Amiprilose hydrochloride is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits the production of prostaglandins. It has been shown to have antimicrobial properties against skin cells and has been used as a topical treatment for wounds. Amiprilose may also be effective in treating inflammatory diseases, such as rheumatoid arthritis and ulcerative colitis, by inhibiting the production of IL-2 receptors. This drug is also used as a diagnostic tool in infectious diseases and has been found to be active against various bacteria, including Staphylococcus aureus and Escherichia coli; fungi including Candida albicans, Saccharomyces cerevisiae, and Aspergillus niger; protozoa such as Entamoeba histolytica; and viruses such as herpes simplex virus type 1. Amiprilose can inhibit inflammation by blocking the activity of leukotrienes. It is also

2,3:4,5-Di-O-isopropylidene-b-D-fructopyranose (IDFP) is a natural compound that has been shown to have pharmacological properties. It is an inhibitor of the enzyme alpha-glucosidase and may be used as a treatment for diabetes mellitus type II. IDFP binds to the active site of the enzyme α-glucosidase, preventing access of the substrate glucose. This causes a decrease in blood glucose levels and has also been shown to reduce cholesterol levels in mice. IDFP is synthesized by reacting ethylene diamine with 2,3:4,5-di-O-isopropylidene b -D -fructofuranose. This reaction produces a heterocycle that undergoes asymmetric synthesis using sodium hydroxide solution and hydrogen fluoride as catalysts.

(2R, 3S, 4S) -3-Fluoro-4-(fluoromethyl)-1-(phenylmethyl)-2-azetidinecarboxylic acid methyl ester is a synthetic compound that is used in the preparation of modified saccharides and oligosaccharides. These compounds are used in the synthesis of complex carbohydrates. This product also has fluoroquinolone resistance and has been shown to be an inhibitor of RNA polymerase II transcription and DNA topoisomerase I.

Chromogenic substrate targeting beta-glucuronidase

4,6-O-Benzylidene-D-galactose is an anomer of D-galactose. It is a lectin that has been shown to inhibit the binding of amyloid beta to the cerebroside in the brain tissue. This activity may be due to its ability to form an amide bond with galactose, which is present in amyloid beta. 4,6-O-Benzylidene-D-galactose also has a coronary heart disease prevention effect and can help reduce cholesterol levels. Furthermore, it has been found to have anti-cancer properties and can help prevent the growth of cancerous cells by inhibiting protein synthesis. In addition, 4,6-O-Benzylidene-D-galactose can be used as a cationic surfactant or detergent composition for cleaning or treating surfaces.

(2R, 3R, 3aS, 9aR) -3- (Benzoyloxy) - 2- [(benzoyloxy) methyl] - 2, 3, 3a, 9a- tetrahydro- 3a- methyl-6H- Furo[2', 3':4, 5] oxazolo[3,2- a]pyrimidin- 6- one is a custom synthesis of Methylation. It is only available in the form of a white solid and has a purity of 99.9%. It is soluble in methanol and ethanol.

1,2:5,6-Di-O-isopropylidene-alpha-D-glucofuranose, also known as diacetone-D-glucose (DAG), is a partially protected D-glucose sugar locked in the furanose form with isopropylidene protecting groups on the 1,2 and 5,6 positions. The unprotected 3 position is ready for a variety of chemical manipulations, such as alkylation, acylation or stereo-inversion. An orthogonal protecting group could be added to the 3 position to allow deprotection of an isopropylidene and therefore manipulations of the other hydroxyl groups. Diacetone-D-glucose has been used to make fluorinated hexopyranose glycolysis inhibitors useful in the treatment of brain tumours.

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