Monosaccaridi

3,4-O-Isopropylidene-D-galactal is a modified form of galactal. This compound is a methylated derivative of D-galactal that has been synthesized by the click reaction. It can be used in the synthesis of oligosaccharides and polysaccharides. 3,4-O-Isopropylidene-D-galactal is a high purity compound with a CAS number of 124477-12-9.

2,3,4-Tri-O-acetyl-1-azido-1-deoxy-b-D-arabinopyranosyl cyanide is a synthetic carbohydrate that can be modified with fluorination, methylation and glycosylation. It is modified with acetyl groups at the 2, 3 and 4 positions of the sugar ring. This carbohydrate has been used to synthesize oligosaccharides and polysaccharides. The modification of this carbohydrate has been shown to improve its solubility in water.

α-GalCer analog 8 is a high purity, custom synthesis, synthetic α-galactocerebrosidase enzyme that has been modified to include 8 fluorine atoms. The enzyme is glycosylated at the N-terminal and methylated at the C-terminal. The modification of this enzyme with an oligosaccharide and monosaccharide moiety improves its stability in vivo. α-GalCer analog 8 is used for the treatment of Gaucher's disease, which is caused by the accumulation of complex carbohydrates in the body. This condition can be managed using α-GalCer analog 8 because it hydrolyzes these complex carbohydrates into their monosaccharides.

2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-N-Fmoc-L-threonine pentafluorophenyl ester is a custom synthesis. This product is a complex carbohydrate that belongs to the group of polysaccharides. It has been modified by methylation and glycosylation. 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-N-Fmoc-L--threonine pentafluorophenyl ester has a CAS number and is available in high purity. This product can be used as an additive for food products or as a starting material for the synthesis of other saccharides.

3-O-Toluoyl decitabine is a synthetic, high purity drug that is custom synthesized to order. The synthesis of 3-O-Toluoyl decitabine involves the modification of sugar molecules with fluorination, glycosylation, and methylation. This compound has CAS No. 183016-21-9 and is used in the treatment of cancer by inhibiting ribonucleic acid (RNA) synthesis. 3-O-Toluoyl decitabine inhibits RNA polymerase II and III, which are enzymes that catalyze the transcription of DNA into RNA. It also inhibits protein kinase C, which leads to cell death and tumor shrinkage.

3-O-Methyl-D-mannopyranose is a glycosidic compound with immunostimulating properties. It is an intermediate in the synthesis of 3,6-anhydro-N-acetylneuraminic acid and other related carbohydrates. The hydrolysis of this molecule yields silver trifluoromethanesulfonate, chloride, and low molecular weight material. 3-O-Methyl-D-mannopyranose can be used as a reagent for the preparation of high molecular weight material by ion exchange chromatography or by dehydrative coupling.

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.

6-O-Benzoyl-3-O-tert-butyldimethylsilyl-D-glucal is a custom synthesis that is used in the modification of monosaccharides and oligosaccharides. It is a synthetic molecule that has been modified with fluorination, methylation, and click chemistry. This product is a saccharide with a CAS number.

O-(A-D-Galactopyranosyl)-D-galactose is a sugar that is used in the synthesis of complex carbohydrates. O-(A-D-Galactopyranosyl)-D-galactose can be fluorinated and methylated to produce o-(A-D-Galactopyranosyl)-2,6-dideoxy--glucose. This sugar has been shown to inhibit the growth of bacteria such as Mycobacterium tuberculosis and Mycobacterium avium complex. Synthesis of this sugar is done through a custom synthesis process with high purity and quality.

D-Arabinopyranosyl thiosemicarbazide is a synthetic compound. It has been shown to be effective in the synthesis of oligosaccharides and sugars, as well as glycosylation reactions. This product can be used in fluorination, methylation, and other custom synthesis reactions. D-Arabinopyranosyl thiosemicarbazide is also useful for click modification of complex carbohydrates. The purity of this product is high and it can be modified with various functional groups.

Inositol nicotinate is a combination of two substances, inositol and nicotinate. It is used to reduce the risk of heart disease by lowering low-density lipoprotein-cholesterol (LDL) levels. Inositol nicotinate has been shown to increase the surface area of mitochondria, which may be due to its ability to inhibit the release of fatty acids from fat cells. Inositol nicotinate also increases magnesium levels in cells and induces mitochondrial functions. This drug has been tested in cell culture for its effects on skin cells and found that it can reduce the amount of x-linked adrenoleukodystrophy protein (XALD), a substance that accumulates in patients with X-linked adrenoleukodystrophy, an inherited disorder that causes progressive damage to the nervous system. The drugs also have been shown to have beneficial effects on cholesterol metabolism, reducing LDL cholesterol levels, as well as inhibiting platelet aggregation.

Losartan N1-glucuronide is a glucuronidated metabolite of losartan that is produced naturally in the human body. It is converted from losartan by the enzyme UDP-glucuronosyltransferase, which is found in humans and other animals. The rate of glucuronidation varies between individuals and is determined by genetic factors. Losartan N1-glucuronide has shown to be an effective inhibitor of angiotensin II, with an IC50 value of 1.4 μM. This inhibition can be reversed by dobutamine or recombinant human UGT2B7 enzyme, which are both competitive inhibitors of the enzyme UGT2B7. Magnetic resonance spectroscopy has been used to study the kinetic properties of this inhibitor and its effect on dobutamine-induced changes in cardiac function.

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.

The 4-Toluoyl-a-D-thiomannopyranoside is a six-membered ring with a hydrogen atom at the center. The structure of this molecule is composed of two chains, each of which has four atoms in their backbone. There are also two conformations to the molecule, one that can be observed as a chair conformation and one that can be seen as a boat conformation. In the chair conformation, there are three bonds that form from the central carbon atom to other carbons on the same chain. These bonds are called alpha bonds, and they connect in a linear fashion. In the boat conformation, these three bonds form an angle of 120 degrees with each other and have staggered geometry. The alpha bonds in this case form an angle of 180 degrees with each other.

Synthetic building block for nucleic acid research