Monosacáridos

<p>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.</p>

<p>Butyl b-D-glucopyranoside is a fluorinated monosaccharide that is used in the synthesis of oligosaccharides and polysaccharides. It is also used as a synthetic sugar for glycosylation, methylation, and click modification reactions. Butyl b-D-glucopyranoside has been shown to be stable under both acidic and basic conditions and has a CAS number of 5391-18-4.</p>

<p>6-Epi-castanospermine is a nitro compound that is synthesized by the allylic oxidation of castanospermine. It has been shown to inhibit glycosidases and glycosidase inhibitors in vitro, including those from the families of α-amylase, α-L-arabinofuranosidases, β-hexosaminidases, α-glucuronidases, and phytases. 6-Epi-castanospermine has also been used as an intermediate for the synthesis of chiral polyhydroxylated compounds. The 13C NMR spectrum of this compound was found to be diagnostic for its structural assignment.</p>

<p>β-Xylobiose hexa-O-acetate is an acetyl protected xylobiose</p>

<p>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.</p>

<p>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.<br>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.</p>

<p>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.</p>

<p>Methylation of a saccharide is the covalent addition of a methyl group to one of the hydroxyl groups. This process may be achieved through an electrophilic substitution reaction with a methylating agent such as dimethyl sulfate. In the case of polysaccharides, this process can be carried out in vitro using enzymes called glycosyltransferases. The mechanism for glycosyltransferase-mediated methylation was elucidated by Michaelis and Menten in 1913.</p>

<p>UDP-N-acetyl-D-mannosaminuronic acid is a monosaccharide that is synthesized from UDP and N-acetyl-D-mannosamine. It is an important precursor for the synthesis of glycoproteins, lipopolysaccharides, and proteoglycans in bacteria. Mutants have been identified in Escherichia coli and Staphylococcus aureus that lack the enzyme UDP-N-acetylglucosamine 2’:3’ phosphotransferase, which is required for the biosynthesis of UDP-N-acetylglucosamine. The enzyme responsible for this reaction is acetamidase/uridine diphosphate mannosyltransferase. This enzyme catalyzes the transfer of mannose from uridine diphosphate (UDP) to N acetylglucosamine to form UDP N acetyl D mannosaminuronic acid</p>

<p>Isopropyl 2,3,4,6-tetra-O-acetyl-b-D-thiogalactopyranoside is a carbohydrate that is a modification of the sugar galactose. It is a synthetic monosaccharide with a high purity and custom synthesis. The chemical modification includes fluorination and methylation. This compound has been shown to be effective in inhibiting bacterial growth and is used in the treatment of tuberculosis.</p>

<p>Methyl alpha-D-mannopyranoside is a methylated sugar used as an inhibitor of lectin-conjugate binding. It is commonly used in protein purification for eluting glycoproteins and other glycoconjugates from affinity chromatography columns of agarose lectin. In addition, Methyl alpha-D-mannopyranoside can be used in the mannosylation of lipid nanoparticles (LNPs) for vaccine or drug delivery which targets Antigen Presenting Cells (APCs) through mannose receptors. Methyl alpha-D-mannopyranoside is also known as Methyl alpha-D-mannoside or alpha-Methyl-D-mannoside.</p>

<p>Tiazofurin is a novel anticancer agent that inhibits the activity of various enzymes, including dehydrogenase and acetyl-CoA carboxylase. Tiazofurin shows significant cytotoxicity against human leukemia cells in vitro. It also has an anti-infectious effect on hl-60 cells and k562 cells, which are carcinoma cell lines. Tiazofurin has been shown to have a higher inhibitory effect on dextran sulfate than on basic protein in vitro, suggesting that it may be more effective as an anticancer compound against cancerous tumors with high levels of glycolipids.</p>

<p>Methyl 6-deoxy-α-D-glucopyranoside is a synthetic monosaccharide. It is an important building block in the synthesis of glycosides, polysaccharides, and oligosaccharides. The product also has many applications in click chemistry, fluorination, and polysaccharide modification. Methyl 6-deoxy-α-D-glucopyranoside is available for custom synthesis to suit your specifications.</p>

<p>1,2:5,6-Di-O-isopropylidene-D-mannitol (IDM) is a chemical compound that has been shown to have physiological activities. It has been studied for its potential use as an antimicrobial agent against bacteria and fungi. IDM is structurally similar to 2,3:5,6-Tri-O-methylenetetrahydrofolate (THF), which can be used in the synthesis of polysaccharides and DNA bases. IDM also has properties that may be beneficial in treating congenital heart disease.</p>

<p>2-Deoxy-L-fucose is a sugar that is found in the human body. It has been shown to have anti-tumour properties and can be used as a chemotherapeutic agent in the treatment of solid tumours. 2DFL binds to the receptor for fucose, which is expressed in many types of cancer cells. It also inhibits DNA synthesis by stabilizing a complex between the sugar and dna template, inhibiting the binding of monoclonal antibodies to cancer cells, and preventing glycosidic bond formation on cancer cells. 2DFL has also been shown to inhibit microbial biotransformation and cell culture.</p>

<p>Methyl 3-O-benzyl-b-D-xylopyranoside is a modified oligosaccharide that is used in the synthesis of complex carbohydrate structures. It has been shown to be a good substrate for glycosylation. Methyl 3-O-benzyl-b-D-xylopyranoside is also a monosaccharide, and can be fluorinated to produce a saccharide with potential antiholistic properties.</p>

<p>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.</p>

<p>Ethyl 2,3-di-O-benzyl-4,6-O-benzylidene-b-D-thioglucopyranoside is a glycosylated monosaccharide. It is synthesized by the reaction of 1,2,3,4,6-pentaacetyl bromohexose with benzaldehyde and thioglycolic acid. The product is purified by recrystallization. This compound has a CAS number of 141263-01-6 and can be custom synthesized to meet your needs.</p>

<p>D-Mannonic acid-1,4-lactone is a recombinant carbohydrate that is synthesized from l-ribose and l-arabinose. It has lysozyme inhibitory activity. D-Mannonic acid-1,4-lactone can be used to study the synthesis of lactones by escherichia coli and their inhibitory effects on lysozyme. The compound consists of two stereoisomers: dl-mannonic acid and ldl-mannonic acid. It can be detected by liquid chromatography (LC) and electrophoresis.</p>

<p>1,2,3,4-Tetra-O-acetyl-D-galacturonic acid is a carbohydrate that belongs to the group of oligosaccharides and sugars. It is used as a synthetic intermediate in the production of complex carbohydrates and glycosylations. 1,2,3,4-Tetra-O-acetyl-D-galacturonic acid is also used as an active ingredient in some topical medications. The fluorination of this product leads to increased solubility and stability. It has been shown to be resistant to degradation by enzymes such as alpha amylase or beta amylase. This product can be customized for customers requirements with high purity and custom synthesis services.</p>