Monossacáridos

<p>Methyl 7,8,9-Tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-S-phenyl-2-thio-D-glycero -b-(1→4)-D-(1→3)-galacto-(1→4)-2-[N-[(1R,2R)-2-(methoxyimino)ethoxy]acetamido]-nonulopyranosylonate is a synthetic carbohydrate. It has been modified with methylation at position 7 and 8 of the sugar and click modification. Methyl 7,8,9 -triacetyl 5 -N, 4 -O carbonyl 3 , 5 -dideoxy 2 -S phenyl 2 -thiophenediol glycero b D galacto 2 nonulopyranoside is a complex carbohydrate.</p>

<p>Ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a compound with a molecular mass of 536.35 Da. It is an inhibitor of the enzyme catalase and has been shown to bind to monoclonal antibodies that are specific for human vascular endothelial growth factor (VEGF). This inhibition prevents the binding of VEGF to its receptor, which blocks the activation of the VEGF pathway. Ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy--b D glucopyranoside has also been shown to inhibit HIV replication in vitro.</p>

<p>2,3,4,6-Tetra-O-pivaloyl-β-D-glucopyranoside is a carbohydrate modified with fluorination and methylation. It is also a synthetic oligosaccharide that has been glycosylated. This product can be custom synthesized to meet your needs. We offer high purity and custom synthesis for this product.</p>

<p>Sunitinib N-glucuronide is a synthetic small molecule with a molecular weight of 517.63 Da and a chemical formula of C14H18F3N5O6S. Sunitinib N-glucuronide is a monosaccharide sugar that is modified with fluorine. It is one of the products of the methylation, custom synthesis, and click modification reactions. The CAS number for this product is 70698-74-7. Sunitinib N-glucuronide has a purity level of 98%, which means that it has less than 2% impurities. This product can be used in oligosaccharides, polysaccharides, or saccharides as a complex carbohydrate or high purity carbohydrate. It can also be used as an additive to modify the properties of monosaccharides and sugars.</p>

<p>Iron sucrose is a form of iron that is used in the treatment of iron deficiency anemia. Iron sucrose is administered orally and absorbed in the small intestine. The amounts of iron absorbed are not sufficient to correct the underlying cause of iron deficiency anemia, but can be used as a substitute for oral iron therapy. Iron sucrose has been shown to be safe and effective in treating chronic bowel disease and may be useful in other diseases with inflammatory components, such as infectious diseases and inflammatory bowel disease. Iron sucrose may also be helpful for patients with congestive heart failure or nephrology dialysis who require supplemental erythropoietin.</p>

<p>L-Gulono-gamma-lactone is a natural vitamin C metabolite that is synthesized from L-ascorbic acid in the liver. It has been shown to inhibit the oxidase and other enzymes involved in ascorbic acid metabolism, which may be due to its ability to bind to iron. L-Gulono-gamma-lactone also inhibits polymerase chain reactions in rat liver microsomes and inhibits the activities of ascorbic acid and glutathione reductase in rat hepatic tissues. This compound is not active against humans, but it has been shown to have antioxidation properties.</p>

<p>1,2,3,5,6-Penta-O-acetyl-D-galactofuranose is a condensation product of a 4-methylumbelliferone with the anomeric form of D-galactose. It is a white crystalline solid that can be obtained in yields up to 200 g per multigram of reactants. This compound has been shown to react with chloride ion and zinc chloride at elevated temperatures to yield the corresponding chloride or zinc salt. The crystal structure of this compound has been studied by x-ray diffraction and found to have an anomeric configuration and a space group P2(1)22(1). Carbohydrates are polyhydroxyaldehydes or polyhydroxyketones containing at least one hemiacetal or hemiketal group in their structure. The general formula for carbohydrates is (Cx(H2O)y)z where x is usually 2 or 3, y is</p>

<p>1-O-Acetyl-3,5-bis(4-chlorobenzoyl)-2-deoxy-D-ribose is a methylated saccharide that can be synthesized from D-ribose and 4-(chloromethyl)benzaldehyde. It has been used for the modification of polysaccharides with click chemistry to produce oligosaccharides. This compound has also been used in the synthesis of glycosyls such as N,N'-diacetylchitobiose and N,N'-diacetylchitotriose. 1-O-Acetyl 3,5 bis (4 chlorobenzoyl)-2 deoxy D ribose is an Oligosaccharide that is soluble in water and is stable at high temperatures. The purity of this compound exceeds 99% and it's CAS number is 1207459-15-1.</p>

<p>D-Galactose is a monosaccharide that is found in the cells of plants and animals. It can be synthesized from D-glucose by adding a D-galactose molecule to the alpha carbon of an existing glucose molecule. The resulting bond is called a glycosidic linkage. This process is called glycosylation. Glycosylation occurs when a sugar molecule reacts with another molecule, such as an amino acid, lipid, or nucleotide, to form what is known as a glycoside linkage. In this case, the sugar is D-galactose and the other molecules are either amino acids or lipids. The reaction between D-galactose and other molecules often results in polysaccharides and complex carbohydrates such as cellulose, chitin, and glycogen.<br>Methylation of D-galactose can produce methyl galactoside (CAS No. 1881-42-7), which</p>

<p>ADP-D-glucose disodium salt is a synthetic saccharide with the chemical formula C6H14N2O8. It is used as a building block for the synthesis of complex carbohydrates, such as polysaccharides and oligosaccharides. ADP-D-glucose disodium salt can be modified to create methylated, glycosylated, and fluorinated derivatives. These modifications allow ADP-D-glucose disodium salt to be used in Click chemistry and other advanced applications.br&gt;br&gt;ADP-D-glucose disodium salt is also known by its CAS number 102129-65-7.br&gt;br&gt; br&gt;br&gt;</p>

<p>6-Azido-6-deoxy-L-galactose is an analog of the natural L-galactose. It has been shown to inhibit the growth and survival of a number of human pathogens, including those that cause tuberculosis, staphylococcal infections, and meningitis. 6-Azido-6-deoxygalactose is reactive with cellular structures and glycoconjugates, which may have contributed to its antimicrobial activity in tissue culture. 6A6DG blocks fatty acid synthesis by inhibiting enzymes called acyltransferases. It also inhibits glycolysis by interfering with the conversion of glucose into glycogen through inhibition of glycogen synthase kinase 3β (GSK3β), which leads to decreased levels of ATP in cells. This compound also inhibits glutaminase activity in the brain, leading to impaired neurotransmitter release and subsequent neuronal cell death.</p>

<p>2-C-(Hydroxymethyl)-2,3-O-isopropylidene-L-lyxono-1.4-lactone is a synthetic modification of the oligosaccharide, 2,3-O-isopropylidene L-lyxonic acid lactone. It is a white to off-white crystalline powder that is soluble in water. This product has been custom synthesized and can be used as a monosaccharide or methylated in the glycosylation step. The CAS number for this product is 72893-21-6 and it has a molecular weight of 252.24 g/mol.</p>

<p>2,3-O-Isopropylidene-D-lyxofuranose is a synthetic disaccharide that is used as an antiinflammatory agent. It has been shown to inhibit the production of e-selectin, a protein that mediates inflammation by binding to cells in the vicinity of the site of injury. This compound has also been shown to inhibit diacetate formation from oxocarbenium ions and glycosidic linkage formation. 2,3-O-Isopropylidene-D-lyxofuranose may be synthesized via a Wittig reaction with phytosphingosine or wittig reaction with acetone.</p>

<p>3,4-O-(1',1',3',3'-Tetraisopropyl-1,3-disiloxanediyl)-L-rhamnal is a synthetic sugar that is used as a building block for the synthesis of glycoproteins and other polymers. It can be methylated to give 3,4-O-(1',1',3',3'-tetramethyl-1,3-disiloxanediyl)-L-rhamnal, which is an inhibitor of protein glycosylation. 3,4-O-(1',1',3',3'-Tetraisopropyl-1,3-disiloxanediyl)-L-rhamnal has been fluorinated to give 3,4-O-(2'-fluoroethylidene) -L-rhamnal and used in Click chemistry reactions.</p>

<p>Methyl 2,3,4-tri-O-benzoyl-6-O-trityl-a-D-glucopyranoside is a synthetic compound that has been modified. This modification includes the addition of fluorine at the 6th carbon on the right side of the molecule. The methylation and tritylation of the molecule have also been performed to create a new product with a better stability. Methyl 2,3,4-tri-O-benzoyl-6-O-trityl-aDglucopyranoside can be used as a monosaccharide or oligosaccharide in glycosylation reactions. It can also be used as an intermediate in the synthesis of complex carbohydrate molecules.</p>

<p>(1R,4R,5S)-4-tert-Butyldimethylsiloxymethyl-5-tert-butyldimethylsilyloxycyclohex-2en-1-ol is a custom synthesis of a monosaccharide with a fluorine atom at the 4 position. The monosaccharide has been modified by methylation and click modification. It has also been synthesized from an oligosaccharide or polysaccharide through glycosylation.</p>

<p>Ducheside A pentaacetate is a fluorescent sugar that can be used as a fluorescent probe to study the glycosylation of proteins. This compound has been shown to be effective in inhibiting the growth of Gram-positive bacteria such as Mycobacterium tuberculosis, Clostridium perfringens, and Streptococcus pyogenes. Ducheside A pentaacetate is synthesized from duchesidin I and an acetyl group, which is then fluorinated with N-fluorobenzenesulfonamide. The product can be modified through methylation or click chemistry reactions. Ducheside A pentaacetate is soluble in water and has a molecular weight of 585.5 g/mol. It has CAS number 314965-07-8 and purity greater than 99%.</p>

<p>1,3,5-Tri-O-benzoyl-a-L-ribofuranose is a synthetic sugar with a complex carbohydrate structure. It is synthesized by the sequential addition of benzoyl groups to the alditol acetal of ribose. The molecular weight of this compound is 598.6 g/mol and its CAS number is 171866-30-1. 1,3,5-Tri-O-benzoyl-a-L-ribofuranose has been shown to be an excellent substrate for glycosylation and methylation reactions due to the presence of three reactive hydroxyl groups that can react with nucleophiles such as amines or thiols. Methylation reactions are typically carried out in the presence of sodium methoxide in methanol at room temperature for several hours. Glycosylation reactions require the use of activated glycosyl donors such as UDP glucose, UDP galactose</p>

<p>Deferiprone 3-O-b-D-glucuronide is a modification of deferiprone. It is synthesized by methylation, glycosylation, and polysaccharide modification with fluorine. Deferiprone 3-O-b-D-glucuronide is monosaccharide in nature and has high purity and custom synthesis.</p>

<p>3,4-O-Isopropylidene-L-arabinose (3,4-OIRA) is an isopropylidene derivative of L-arabinose. 3,4-OIRA has been shown to be a substrate for glycosylation reactions with various other sugars. It can also undergo methylation reactions and has been modified by fluorination. 3,4-OIRA is a food additive that belongs to the category of complex carbohydrates.</p>