Monosaccaridi

Norfluoxetine is a selective serotonin reuptake inhibitor (SSRI) that is metabolized to the active metabolite, norfluoxetine b-D-glucuronide. The metabolism of norfluoxetine b-D-glucuronide has been shown to be inhibited by estradiol. Norfluoxetine b-D-glucuronide also exhibits antioxidant activity, which may be related to its ability to modulate expression of genes encoding antioxidant proteins. Norfluoxetine b-D-glucuronide has been found in wastewater and wastewater treatment plant effluents, suggesting this drug may have an environmental impact. The transcriptome of organisms exposed to norfluoxetine b-D-glucuronide has been studied and it was found that there are some genes that are responsive to this drug.

2-Acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranosyl azide is a synthetic carbohydrate that has been modified with an azide group. This modification allows for the introduction of a variety of different functional groups to be incorporated into the carbohydrate. This synthetic carbohydrate can be used as a sugar or glycosylation acceptor in chemical synthesis, and it is soluble in water. The CAS number for this compound is 168397-51-1.

Tri-O-benzyl-isofagomine hydrochloride is a modification of an oligosaccharide and a carbohydrate. It is synthesized by the methylation and glycosylation of isofagomine. Tri-O-benzyl-isofagomine hydrochloride has been shown to have high purity and can be used in the treatment of cancer, as well as being a potential drug for diabetes mellitus. This drug also prevents the formation of glycosaminoglycan polymers, which are responsible for cartilage rigidity. The CAS number for this drug is 569287-73-2.

N-Valeryl-D-glucosamine is an aldol product of the condensation of acetone and formaldehyde. N-Valeryl-D-glucosamine is a bioactive molecule that has been shown to be synthesized by the c-glycosidic linkage of D-glucose molecules in bacteria and fungi. It is also found in plants, such as sugar cane and sugar beet. The synthesis of this molecule occurs through the aldol reaction, which involves the unactivated ketones (acetone). This compound can also be found in biomolecular chemistry, where it is used as a substrate for condensation reactions.

Phenyl-alpha-D-glucopyranoside is a molecule that is found in the β-cell of the pancreas. It is thought to be involved in the biosynthesis of oligosaccharides and interacts with other molecules to form glycosidic bonds. The interaction between phenyl-alpha-D-glucopyranoside and other molecules has been analysed by gas chromatography, which showed that it was hydrophobic, but also interacted with carbohydrates. Phenyl-alpha-D-glucopyranoside has also been shown to inhibit gram negative bacteria, such as Escherichia coli or Salmonella enterica.

Phenyl 4,6-O-benzylidene-2,3-di-O-(4-methoxybenzyl)-a-D-thiomannopyranoside is a synthetic glycosylated mannose oligosaccharide. It has a molecular weight of 756.85 and the chemical formula C36H43NO14. Phenyl 4,6-O-benzylidene-2,3-di-O-(4-methoxybenzyl)-a-D-thiomannopyranoside has been shown to be effective against fungus infections in mice models. This product is custom synthesized for research purposes only and does not contain any hazardous or toxic chemicals.

2-Deoxy-a-L-ribofuranose is a monosaccharide that can be modified by either fluorination or methylation. It is an important building block in the synthesis of complex carbohydrates and saccharides, such as oligosaccharides and polysaccharides. 2-Deoxy-a-L-ribofuranose has been shown to have excellent purity, high quality, and custom synthesis for use in pharmaceuticals.
2-Deoxy-a-L-ribofuranose can be used in the production of nucleotides, which are essential for DNA replication and transcription. These nucleotides are also involved in protein synthesis, as they contain nitrogenous bases which provide the amino acids needed for proteins.

p-Methoxytopolin-9-glucoside is a Glycosylation product that is used in the synthesis of glycoproteins. It is synthesized by methylation and fluorination of p-methoxyphenol, followed by glycosylation with glucosamine. The monosaccharide units of this product are then modified to give a variety of oligosaccharides. This product can be custom synthesized for different customers, depending on their specifications. The final purity of this product is at least 98%.

2-O-Benzyl-D-glucose is a disaccharide that is an intermediate in the synthesis of benzoic acid. It is benzylated with benzaldehyde and then reacted with sodium hydroxide to form 2-O-benzylidene-D-glucose. Spectroscopy has shown that this product has an anomeric proton at δH 7.1 to 7.4 and a pyranoside group at δH 4.2 to 4.6, which are characteristic of 2-O-benzylidene-D-glucose. The sugar's molecular formula is C9H12O5, and its molecular weight is 230. The sugar has been shown to be acylated with acetate or benzoic acid as well as undergo glycosidation reactions in the presence of sulfuric acid or sodium hydroxide.

UDP-a-D-Xylose disodium is a fluorinated synthetic monosaccharide that has been synthesized to produce an oligosaccharide. It is a complex carbohydrate with glycosylation and polysaccharide modifications, which can be modified by methylation or click chemistry. This product is usually used as a custom synthesis for research purposes.