Monosacáridos

D-Galacturonic acid benzyl ester is a donor of d-galacturonic acid that is used to regulate the growth of bacterial cells. It has been shown to be an acceptor for oligosaccharides, which are substrates for glycosidases. D-Galacturonic acid benzyl ester has been shown to have anti-inflammatory effects in animal models and may be useful in the treatment of heart diseases, such as cardiac hypertrophy.

Caffeic acid 3-O-b-D-glucuronide (3BGA) is a phenolic compound that is found in plants. It has been shown to inhibit the growth of viruses, including influenza virus, and chlorogenic acid isomers have been shown to inhibit the growth of bacteria. The highest concentration of 3BGA was found in the heartwood of the plant. Recent pharmacokinetic studies have shown that caffeic acid 3-O-b-D-glucuronide is metabolized by gut bacteria and excreted in human urine.

D-Glucarate monopotassium is a pharmaceutical preparation that is used to inhibit the growth of bacteria. It inhibits the proliferation of cells by inhibiting fatty acid synthesis, which leads to decreased levels of cholesterol, and reduces the uptake of glucose. D-Glucarate monopotassium is also an oxidizing agent that converts uridine into uric acid and has been shown to have inhibitory properties against human cancer cells. D-Glucarate monopotassium can be used as an antioxidant for the prevention or treatment of chronic diseases such as atherosclerosis, diabetes, and cancer. This compound acts as an inhibitor for trypsin treatment on carbohydrates, preventing hydrolysis by this enzyme.

D-Gluconic acid manganese salt is a wild-type strain that is used to treat infectious diseases. The mechanism of action is not yet fully understood, but it has been shown to inhibit the growth of bacteria by binding to the cell wall and disrupting bacterial enzymes. It also has been shown to bind to calcium ions, which can lead to cardiac problems. The drug can be used in combination with other antimicrobial agents, such as malonic acid, for the treatment of infections caused by methicillin resistant Staphylococcus aureus (MRSA).

L-Glucurono-3,6-lactone is an acetonide that is a derivative of L-glucose. L-Glucurono-3,6-lactone can be used as a precursor for the synthesis of polyhydroxybutyrate (PHB).

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.

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).

Used as source of carbon in culture medium.

Please enquire for more information about N-Acetyl-D-glucosamine - plant source including the price, delivery time and more detailed product information at the technical inquiry form on this page

Substrate for UDP-3-O-acyl-N-acetylglucosamine deacetylase (LpxC)

The chemical structure of Astragalus polysaccharide is complex and consists of an α-D-(1,4)-Glc and (1,6)-α-D-Glcp backbone, and a branch point at O-6. The molecular weight is approximately 3.01 × 105 Da from Mongolian Astragalus using low concentration of ethanol for precipitation and gel chromatography for purification. Spectral analysis results of 1H NMR and 13C NMR showed that the polysaccharide backbone has a 1,3-linked β-D-Gal residue and the branched portion has β-Glc, 1,6-linked α-Gal; 1,5-linked β-Xyl; 1,4-linked β-Gal; β-D-Gal, 1,2-linked α-Rha; and 1,2,4-linked α-Rha residues.

3,5-Di-O-lauryl-D-xylofuranose is a custom synthesized monosaccharide that is used as a raw material for the synthesis of complex carbohydrates. It has been modified with fluorine and methyl groups to produce 3,5-di-O-lauryl-D-xylofuranose. This compound can be used in the production of polysaccharides or saccharides. The chemical name for this compound is 3,5-di-O-[(9Z)-hexadecenyl]-2-(1E,3E)-dioxaheptalene.

N-2,4-Dinitrophenyl-deoxynojirimycin (DNPDNJ) is a methylated derivative of deoxynojirimycin. It is an inhibitor of glycosylation that can be used to study the structure and function of carbohydrates. DNPDNJ is a synthetic saccharide that can be custom synthesized. Click modification and modification with Oligosaccharides are common modifications for DNPDNJ. DNPDNJ is available in high purity and has been fluorinated for use in fluorescence studies.

2-C-Hydroxymethyl-D-ribose is a sugar that has been found in the cell wall of Mycobacterium tuberculosis. It is also found in some other bacteria, such as Streptomyces coelicolor. 2-C-Hydroxymethyl-D-ribose may be involved in the synthesis of glycan and may have a role in the molybdenum cofactor biosynthesis pathway. This molecule has been shown to have acidic properties, which are most likely due to its hydroxyl groups. The 13C NMR spectrum for this compound shows three peaks at δ H = 138.2, 144.3, and 154.5 ppm corresponding to the ribofuranoside moiety. The skeleton of this molecule was rationalized by attaching an acetaldehyde group to the 2'-hydroxyl group on position C2 of ribose, which is consistent with the observed 13C NMR spectrum. This molecule has

3,4-O-Isopropylidene-D-arabinose is a synthetic compound that has been used as an active analogue for the study of nucleophile reactions. 3,4-O-Isopropylidene-D-arabinose undergoes nucleophilic addition with potassium azide to form a thiazolidine intermediate. The stereospecificity of this reaction was shown by the chemists and biochemists who synthesized it. It has also been shown to react with an anion in a similar manner. This chemical is used in the synthesis of d-arabinose, which can be used for the production of other compounds.

Methyl 2-deoxy-D-ribofuranoside is a methylglucoside that is synthesized by the reaction of thiourea with chloroacetic acid. The anomers of this compound are atypical and the product can be obtained in high yield (70%) by the use of chromatographic purification. This chemical has been used to produce a variety of compounds including carbamates, chloroacetamides, sulfonamides and others. Methyl 2-deoxy-D-ribofuranoside is also an intermediate for asymmetric synthesis. It can act as a catalyst for reactions involving alkali metals and nucleophiles such as chloride, hydantoin and dimethylformamide. The structure of this molecule has been determined by nmr spectroscopy and its 1H NMR spectrum is consistent with that predicted from its molecular formula.

Monogalactosyldiacylglycerol (MGDG) is a polyunsaturated fatty acid, specifically a galactolipid. MGDG is synthesized by plants and plays an important role in plant physiology. MGDG is involved in the regulation of transcription and translation and also has anti-cancer properties. It has been shown that MGDG can inhibit the proliferation of breast cancer cells such as MDA-MB-231 cells through its interactions with miR-205, a microRNA that regulates cellular growth, differentiation, and apoptosis. The biochemical properties of MGDG are similar to those of diacylglycerol (DAG), which is also involved in transcriptional regulation. It has also been shown that MGDG inhibits the growth of MDA-MB-231 cells when exposed to high salt concentrations.

1-Octen-3-ol glucoside is a synthetic, fluorinated sugar that is modified with glycosylation, methylation, and click chemistry. It contains a high degree of purity and is custom synthesized to order. This product can be used as a substitute for other sugars in the production of oligosaccharides, saccharides, and polysaccharides.
1-Octen-3-ol glucoside has been shown to have various modifications including glycosylation, methylation, and click chemistry. It is often used when there are restrictions on the types of sugars that can be used in the synthesis of complex carbohydrates.

Ethyl maltol glucoside is a methylated and fluorinated sugar that is used as an intermediate in the synthesis of oligosaccharides or polysaccharides. It has been shown to be an efficient and selective substrate for glycosyltransferases. Ethyl maltol glucoside has been modified with click chemistry, which enables it to be incorporated into complex carbohydrates. This modification also allows for the synthesis of monosaccharides, which are common building blocks of many other types of sugars. Ethyl maltol glucoside is soluble in water and can be purified by recrystallization. It is also available in high purity, with a CAS number of 1838567-35-3.

Fuculose is a monosaccharide that is a constituent of fucose-containing glycoproteins. It is found in the blood and urine, as well as in various tissues, such as liver, lung, kidney, and spleen. The biological properties of L-fuculose are related to its ability to form hydrogen bonds with other molecules. Fuculose has been shown to be an effective activator for cutaneous lesions in mice models. The structural analysis of L-fuculose has revealed that it contains a reactive site for the synthesis of glycosaminoglycans and polysaccharides. Fuculose has also been shown to increase the proliferation of some cells, including corynebacterium glutamicum and human umbilical vein endothelial cells (HUVECs). This property may be due to its ability to activate growth factors or interfere with cell signaling pathways.

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

Competitive inhibitor of ceramide-glycosyltransferase used for substrate reduction therapy in lysosomal storage disorders. It inhibits glucosylceramide synthase, which catalyses the initial step in glycosphingolipid biosynthetic pathway. This compound delays the onset of symptoms in type 1 Gaucher disease, Sandhoff disease and Tay-Sachs disease. It also reduces brain abnormalities in mucolipidosis type IV.