Monosaccharides

<p>2R, 3S, 4R, 5S) -3,4-Di-O-Isopropylidene-2- methyl- 1- nonyl-3, 4, 5- piperidinetriol is a modification of the oligosaccharide. It is synthesized by custom synthesis and has high purity. This product can be found under CAS No. 9062-16-7 and has a molecular weight of 873. The chemical formula is (C6H10O5)n and the structural formula is CHNO. This product is an Oligosaccharide and Carbohydrate.</p>

<p>Substrate for phosphoribosyltransferases</p>

<p>1-Deoxy-2-fluoronojirimycin is a glycosylation inhibitor that was synthesized to inhibit the formation of complex carbohydrates. It has been shown to inhibit methyltransferases and glycosylation enzymes in vitro with IC50 values of 0.1 μM, 2 μM, and 4 μM, respectively. This compound has also been shown to inhibit the synthesis of saccharides by targeting sugar moieties. 1-Deoxy-2-fluoronojirimycin inhibits the addition of various sugars at their C1 position with IC50 values ranging from 0.3 μM to 6 μM. The modification of sugars at the C2 position is also inhibited with IC50 values ranging from 3 μM to 10 μM. 1-Deoxy-2-fluoronojirimycin is a custom synthesis that can be ordered in high purity as well as in bulk quantities for research purposes .</p>

<p>Mannose with an aliphatic 3 carbon amine linker.</p>

<p>(2R, 3R, 4R) -3-Benzyloxy- 1- benzyl-4-(hydroxymethyl)- 2-azetidinecarboxylic acid methyl ester is an oligosaccharide. It is a modification of the Oligosaccharide which is a carbohydrate with multiple saccharides. This means that it contains two or more types of sugar monomers. The primary type of sugar in this compound is the Monosaccharide, which are single units of sugar that are joined together to form a sugar polymer. The other type of sugar in this compound is the Polysaccharide, which is made up of many different monomers. Carbohydrates are an important source of energy for living organisms and they can be found in many different forms such as sugars and starches. This compound has been modified by Methylation (addition of a methyl group), Glycosylation (addition of glycosidic</p>

<p>3,4-Di-O-benzyl-D-glucose is a monosaccharide that is synthetically modified with an O-benzyl group at the 3' and 4' positions. It is a custom synthesis and has a CAS number. This sugar can be used as a building block for polysaccharides or oligosaccharides with the addition of other sugars. 3,4-Di-O-benzyl-D-glucose is highly pure and can be modified with fluorine to make it more stable for use in click chemistry reactions. This sugar is soluble in water, ethanol, DMSO, DMF, and acetonitrile. It has been shown to inhibit the growth of bacteria such as Staphylococcus aureus and Mycobacterium tuberculosis.</p>

<p>3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribono-1,4-lactone is a nucleoside analog that inhibits the synthesis of viral RNA. It can be hydrolyzed to uridine, which is then converted to phosphorylated uridine by uridine phosphorylase. 3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribono-1,4-lactone binds to the enzyme ribonucleotide reductase and blocks the production of DNA precursors. This may lead to a decrease in DNA synthesis and cell proliferation. The antiviral properties of 3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy--D--ribono--1,4--lactone have been shown in animal models against cyt</p>

<p>6-O-Benzyl-1-(-)-carboxymenthyl-2,3:4,5-di-O-cyclohexylidene-L-myo-inositol is a synthetic oligosaccharide with the chemical formula C9H14FNO5. It is a monosaccharide composed of a single sugar unit, inositol, which has been modified with benzyl groups on the 6th and 1st positions of the inositol ring. This compound is used as an intermediate in the synthesis of other saccharides.</p>

<p>N- (2, 5- Anhydro- 3- azido- 3- deoxy- D- altronoyl) - 2, 5- Anhydro- 3- amino - 3 - deoxy- D - altronic acid propyl ester is a synthetic compound that has been modified to include an N-(2,5 anhydroazido)-3,6 dideoxydulonic acid moiety. The chemical structure of this product includes a methyl group and two hydroxyl groups on the anomeric carbon. This product is a white powder at room temperature and can be used in the synthesis of oligosaccharides or polysaccharides.</p>

<p>2-Deoxy-D-xylose is a sugar that is metabolized by bacteria in the absence of oxygen. It has been shown to be highly chemotactic, inducing the migration of cells from the surrounding tissue into the area where it is present. 2-Deoxy-D-xylose has also been shown to inhibit the growth of cancer cells and induce apoptosis in vitro. 2-Deoxy-D-xylose binds to mitochondria and inhibits cytochrome oxidase, which may contribute to its anti-cancer activity. 2-Deoxy-D-xylose has also been shown to have angiogenic effects by stimulating endothelial cell proliferation and migration.</p>

<p>4-Aminophenyl b-D-glucopyranoside is a membrane transport inhibitor that prevents the uptake of glucose by inhibiting the enzyme hexose transporter. It is used in biological treatment and has been shown to be effective against glutamicum. 4-Aminophenyl b-D-glucopyranoside can also be used in assays to identify bacteria based on their surface antigens. This compound was isolated from corynebacterium glutamicum and its metabolic pathway has been elucidated. 4-Aminophenyl b-D-glucopyranoside has also been shown to inhibit enzymatic activity, which may be due to inhibition of the enzyme dihydroorotate dehydrogenase.</p>

<p>Methyl 2,3,4-tri-O-benzoyl-6-O-trityl-a-D-galactopyranoside is an oligosaccharide. It is a highly pure and custom synthesis of methylated saccharides. The modification is done by Click chemistry, which is a reaction between an azide and an alkyne in the presence of copper catalyst. This modification helps to introduce fluorine atoms into the saccharide chain. The glycosylation process is then carried out on the modified saccharides to form the desired oligosaccharides. Methyl 2,3,4-tri-O-benzoyl-6-O-trityl-a-D galactopyranoside can be used as a raw material for various applications such as pharmaceuticals, agrochemicals and food additives.</p>

<p>2,6-Dideoxy-L-arabino-hexose is a carbohydrate that can be custom synthesized. It has a high purity with a custom synthesis and can be methylated and glycosylated. This modification changes the chemical structure of the sugar, which may have important therapeutic effects on cancer cells.</p>

<p>2,3-Di-O-benzoyl-L-threonic acid-1,4-lactone is a custom synthesis of a fluorinated monosaccharide methylated at the C2 position. It is an oligosaccharide with a saccharide and polysaccharide linkage. The glycosylation of this compound has been modified by the Click chemistry reaction to create new sugar moieties.</p>

<p>2-Amino-2,6-dideoxy-L-mannose hydrochloride is a high purity and custom synthesis sugar. It is synthesized from 2,6-Dideoxymannose with the use of Click chemistry. This modification allows for a variety of fluorinations, glycosylations, and methylations to be used in the synthesis process. The CAS number for this compound is 107625-00-3.</p>

<p>4-O-Benzyl-2-O-levulinoyl-3-O-para-methoxybenzyl-a-L-rhamnopyranosyl trichloroacetimidate is a synthetic sugar that has been fluorinated and methylated. It has been custom synthesized for use in glycosylation and is also used as a reagent for click chemistry to modify complex carbohydrates. This compound is available with high purity, which is determined by its chemical composition, including the absence of impurities and the presence of only one type of atom. 4-O-Benzyl--2--O--levulinoyl--3--O--para--methoxybenzyl--a--L--rhamnopyranosyl trichloroacetimidate can be found on CAS registry number 10082282.</p>

<p>3,4-Di-O-acetyl-L-rhamnal is a synthetic sugar with the molecular formula C9H11F2N3O8. It can be used as a monomer for the synthesis of oligosaccharides or polysaccharides. 3,4-Di-O-acetyl-L-rhamnal is fluorinated and methylated to produce the desired product. This sugar can be synthesized in custom quantities and has a high purity level.</p>

<p>(3S, 4R,5S) -3-O-Benzhydryloxybis(trimethylsilyloxy)silyl- 1-benzyl-4,5-O-isopropylidene-3, 4, 5- piperidinetriol is a synthetic monosaccharide that can be used in the synthesis of oligosaccharides and complex carbohydrates. This compound has a molecular weight of 487.43 g/mol and a CAS number of 634265-09-2. It is an Oligosaccharide that contains a sugar chain with three to five monosaccharide units. This product has been custom synthesized for the modification of glycans or polysaccharides by methylation or click chemistry.</p>

<p>Methyl 3,5-di-O-acetyl-2-deoxy-b-D-ribofuranoside is a synthetic sugar that is used in the synthesis of glycosides. It is a high purity product and can be custom synthesized to meet your needs. This product is available as a solution in water and is also offered as an oil. Methyl 3,5-di-O-acetyl-2-deoxy-b-D-ribofuranoside is soluble in alcohols and ethers, but insoluble in hydrocarbons or chlorinated solvents. The CAS number for this product is 62853–55–8.<br>Methyl 3,5-di-O-[(acetyloxymethyl)oxymethyl]-2 deoxy-[beta]D ribofuranoside can be used for Click modification reactions to introduce acetyl groups on the sugar moiety. Click chemistry has been shown to have</p>

<p>Methyl 2,3-di-O-p-toluenesulfonyl-a-D-glucopyranoside is a high purity, custom synthesis sugar that is used in glycosylation and modification. It has a CAS number of 83792-07-4 and can be synthesized from methyl p-toluenesulfonate, D-glucose, and sodium hydroxide. Methyl 2,3-di-O-p-toluenesulfonyl-a-Dglucopyranoside has been shown to react with fluorine to form fluoro derivatives. This compound reacts with glycosylations and modifications such as methylation or acetylation. It is also an oligosaccharide that is composed of monosaccharides and saccharides.</p>

<p>Allyl 4-O-benzyl-2,3-di-O-levulinyl-a-L-rhamnopyranoside is a custom synthesis of an oligosaccharide with a complex carbohydrate backbone. It is modified by methylation and glycosylation and fluorinated to give it high purity.</p>

<p>5-Azido-2-C-(benzylaminomethyl)-5-deoxy-2,3-O-isopropylidene-L-lyxonic acid b-lactam is a synthetic glycoside. It is an intermediate in the synthesis of various saccharides and oligosaccharides. 5-Azido-2-C-(benzylaminomethyl)-5-deoxy-2,3-O-isopropylidene L -lyxonic acid b -lactam has been shown to be useful for click modification, a technique used to modify saccharides and oligosaccharides with azide groups.</p>

<p>5,6,7-Trideoxy-1,2-O-isopropylidene-a-D-xylohept-6enofuranose is a natural homologue of guanine. It is an analog that has been shown to be a mitogen activated protein (MAP) kinase activator in the presence of pyridine. This compound also activates guanosine triphosphatase and has repolarizing effects on cardiac muscle cells. 5,6,7-Trideoxy-1,2-O-isopropylidenea-[D]-xylohept-[6]enofuranose binds to the catalytic site of guanosine triphosphatase and causes a conformational change that results in increased enzyme activity. 5,6,7-Trideoxy-[1]2--isopropylidene--[A]-D--xylohept-[6</p>

<p>Dodecyl a-D-thiomannopyranoside is a glycosylation reagent that has been used in the synthesis of complex carbohydrates, polysaccharides, and oligosaccharides. It is a methylated thioglycoside that can be used for click modification. Dodecyl a-D-thiomannopyranoside is an excellent fluorinating agent for saccharides and sugars, which can be accomplished using sodium hypofluorite. Dodecyl a-D-thiomannopyranoside is also an excellent monosaccharide synthesizer and custom synthesiser. This compound has CAS number 95734-05-1 and can be ordered at very high purity from various chemical suppliers.</p>

<p>3-O-Benzyl-a-D-Glucofuranose Cyclic 5,6-Carbonate is a custom synthesis that can be modified with fluorination, methylation, and click modification. It is a saccharide with CAS number. 3-O-Benzyl-a-D-Glucofuranose Cyclic 5,6-Carbonate is an oligosaccharide and polysaccharide that has a sugar and carbohydrate structure.</p>

<p>This is a sugar that is found in the urine of reindeer and caribou. It was first identified in the urine of animals captured in Alaska during the winter months. It has been shown to be present in human urine, as well, but at lower concentrations. Radiocarbon dating has revealed that this sugar is produced seasonally, with higher levels being found during the winter months. The seasonal variation may be due to changes in diet or metabolism.</p>

<p>1-Deoxy-3,4:6,7-Di-O-isopropylidene L-gulo-hept-2-ulose is a synthetic sugar that can be used to synthesize oligosaccharides. It is a methylated derivative of the natural sugar galactose and has been modified with fluorine atoms at C1 and C3 positions. This product is offered as a custom synthesis and can be ordered in high purity.<br>Methylation of 1,2,3,4 tetra-, penta-, hexa-, or octa-saccharides is a way to introduce new chemical functionalities into the molecule. This process can be achieved through the use of methyl donors such as methanol or dimethyl sulfate. In this case, the methyl groups are introduced on the oxygen atom of glucose at position 3, 4, 6 or 7. The result is a new type of sugar called an oligosaccharide</p>

<p>N-Acetyl-D-glucosaminitol is a fatty acid that is found in blood group antigens. It has been shown to be a potent inhibitor of human liver serine proteases, with an IC50 of 10 μM and a Ki value of 1.6 μM. N-Acetyl-D-glucosaminitol also inhibits the terminal steps in glycolysis and can be used as a substrate for glycosidases. It is capable of forming oligosaccharides with terminal residues and can be analyzed using titration calorimetry. The molecular weight of N-acetyl-D-glucosaminitol is calculated to be 398 Da by nmr spectroscopy. Structural analysis shows that this compound contains monoclonal antibodies and sugar residues, which are important for its function.</p>

<p>D-myo-Inositol-1,2,6-triphosphate sodium salt is a modification of the sugar inositol. It is an oligosaccharide that is composed of three components: D-myo-inositol, 1,2,6-triphosphate and sodium. This compound can be used as a complex carbohydrate with anticancer properties.</p>

<p>3,6-Anhydro-D-glucose is a compound that is produced by the dehydration of D-glucose. It has been synthesized in an acidic hydrolysis reaction involving mercaptoacetic acid and sodium carbonate. The synthesis of 3,6-Anhydro-D-glucose involves the use of chloride as a reactive agent and metal ion catalysis. This compound can be used to create isomers with other sugars. It also has supramolecular chemistry properties due to its ability to form complexes with other molecules.</p>

<p>5-O-Benzoyl-3-deoxy-1,2-O-isopropylidene-3C-methyl-a-D-ribofuranose is a methylated sugar that has been modified with a click modification. It has been synthesized from D-(+)-ribose and 5′,5′′′-(1,2,3,4,5,6) -O-(benzoyl)-D-(+)-glycero 3C -methyluridine. This compound is soluble in water and can be used to modify polysaccharides.</p>

<p>D-[5-2H]Glucose is a deuterated form of glucose that is used in the study of lipid synthesis. This isotopically labeled compound can be incorporated into cellular lipids and their derivatives, such as glycerides and phospholipids. D-[5-2H]Glucose can be used to investigate the biosynthesis of lipids by measuring the incorporation rate and the number of 2H atoms found in each molecule. D-[5-2H]Glucose may also be used to study membrane lipid synthesis, which includes anomeric effects on lipid synthesis. The theory behind this is that when a molecule is incorporated into a lipid, it will have at least one hydrogen atom from deuterium instead of hydrogen. This isotopically labeled compound can be used to measure how anomeric effects influence lipid synthesis.</p>

<p>1,2,3,4-Tetra-O-pivaloyl-6-O-triisopropylsilyl-a-D-mannopyranose is a glycosylation product that can be used as a model for the synthesis of complex carbohydrates. It is synthesized by reacting 1,2,3,4 tetra O pivaloyl a D mannopyranose with triisopropyl silyl chloride in the presence of DMAP and 4-(N,N dimethylamino)pyridine. This product can be used to study the methylation of saccharides. The fluorination and saccharide modification are performed using potassium fluoride or potassium chlorate respectively. This product is also available in custom synthesis quantities at high purity.</p>

<p>Important bioactive principle in established anti-inflammatory herbal medicines</p>

<p>7-Azido-7-deoxy-2,3:5,6-di-O-isopropylidene-D-glycero-D-alloheptono-1,4lactone is a methylation product of saccharide and polysaccharides. It is a modification of the natural molecule with an azide group. It has CAS number 47927–03–9. 7A7DL can be modified to produce oligosaccharides or glycosylations with high purity and custom synthesis. It can be fluorinated to produce complex carbohydrates.</p>

<p>4-Methoxyphenyl 6-azido-2,3,4-tri-O-benzyl-6-deoxy-a-D-mannopyranoside is a synthetic sugar molecule that has been modified to contain a benzyl ether moiety. This product can be custom synthesized and is available in high purity.</p>

<p>1,4-Anhydro-6-chloro-6-deoxy-D-glucitol is a complex carbohydrate that has been fluorinated and modified with methyl groups. It can be custom synthesized to produce high purity compounds. 1,4-Anhydro-6-chloro-6-deoxy-D-glucitol is used in synthesis of saccharides and oligosaccharides. The compound has been modified with Click chemistry to produce glycosylation products. It can also be used as an intermediate for the synthesis of sugar derivatives.<br>1,4-Anhydro-6-chloro-6-deoxy--D--glucitol has the following chemical structure:</p>

<p>Octahydro-1,2,9-tris-acetoxy-(1S,2R,9S,9aS)-quinolizin-6-one is an oligosaccharide that is a sugar modified with fluorine. It is a synthetic carbohydrate and has the CAS number 57714-00-3. The molecular weight of this compound is 784.61 g/mol. This compound can be custom synthesized to meet your needs and specifications. It has been methylated and glycosylated and has undergone click chemistry modifications.</p>

<p>A solar thermal collector is a device that absorbs the sun's heat, or thermal energy, and converts it to useful heat energy. It consists of a dark-colored surface (usually metal) that absorbs sunlight and transfers the heat by radiation to a fluid such as water or oil, which then carries the heat away for use. The efficiency of this type of collector depends on the quantity of sunlight that reaches it, the temperature difference between the hot fluid and ambient air, and its design. A typical solar thermal collector has an efficiency of about 10%.</p>

<p>Fucose (Fuc, 6-deoxy L-galactose) has a methyl group at C6 in place of a hydroxyl group and this gives the molecule a greater degree of hydrophobicity than galactose (Collins, 2006). L-fucose is found in fucoidan, a polysaccharide that occurs in the brown seaweeds (Phaeophyceae) (Percival, 1967). Fucose is also a key component in many mammalian N- and O-linked glycans, glycolipids, blood group substances and Lewis antigens (Becker, 2003). In human milk, neutral (fucosylated) oligosaccharides (HMO) contain fucose at the terminal position (e.g. 2’ -fucosyllactose and lactodifucopentaose). They represent 35% to 50% of the total HMO content and many in vitro studies suggest that HMOs directly modulate immune responses, acting either locally on cells of the mucosa-associated lymphoid tissues or systemically to inhibit the expression of inflammatory genes, mainly cytokines (Plaza-Diaz, 2018).</p>

<p>5,6-O-Isopropylidene-3-C-methyl-D-mannono-1.4-lactone is a fluorinated monosaccharide that can be modified with other chemicals to create a variety of products. This chemical is used in the synthesis of oligosaccharides and polysaccharides. 5,6-O-Isopropylidene-3-C-methyl-D-mannono-1.4-lactone has a CAS number of 105853-. It has been shown to be high purity and is also available for custom synthesis. 5,6--O--isopropylidene--3--C--methyl--D--mannono--1.4--lactone can be synthesized from methylation, click modification, and fluorination reactions on glycolaldehyde.</p>

<p>5-O-Allyl-2,3,4-tri-O-benzyl-D-ribitol is an acid that has been used in preparative organic chemistry. It is a benzyloxymethyl derivative of ribose, which can be converted to the corresponding methyl ether by hydrolysis with sodium methoxide in methanol. 5-O-Allyl-2,3,4-tri-O-benzyl-D-ribitol functions as an isomer and dimerization reagent for the preparation of propenyl derivatives. 5-O-Allyl 2,3,4 tri O benzyl D ribitol has been shown to inhibit Influenza A H1N1 strains in vitro with a 50% inhibitory concentration (IC50) of 1 μM.</p>

<p>2-Amino-2-deoxy-D-allose hydrochloride is a structural isomer of 2-amino-2-deoxy-daltrose. This substance has a nuclear magnetic resonance spectrum that is consistent with the proposed structure. The coupling constants are in agreement with the expected values for this type of molecule. A mass spectrum of this substance shows peaks corresponding to the molecular ion, a tetrazole fragment, and the two vicinal hydrogens. The measurement of 2-amino-2-deoxy-daltrose by nuclear magnetic resonance spectroscopy is shown below:</p>

<p>Methyl 2,3,4-tri-O-benzyl-6-O-triisopropylsilyl-a-D-glucopyranoside is an oligosaccharide that is synthesized by the process of fluorination and glycosylation. It can be used as a synthetic building block to produce complex carbohydrates and polysaccharides. This compound is a monosaccharide that has been modified with methyl groups on the 2, 3, 4, and 6 positions. Methyl 2,3,4-tri-O-benzyl-6-O-triisopropylsilyl glucopyranoside can be used for click modification reactions. The CAS number for this compound is</p>

<p>Estradiol 3-sulfate 17b-glucuronide dipotassium salt is an estradiol ester that is a metabolite of estradiol. It has been shown to be an intermediate in the synthesis of estrone sulfate and other steroid hormones. Estradiol 3-sulfate 17b-glucuronide dipotassium salt is formed from estradiol by the addition of one molecule of sulfuric acid followed by the addition of glucuronic acid, which results in a salt form. It may also be formed by oxidation of allylic hydroperoxides and photooxygenation in families with oxygenated moieties. Irradiation leads to formation of oxygenated steroids. The alkene reactivity depends on the substitution pattern, the cyclic reactivity depends on the ring size and substitution pattern, and the reactivity with peroxides depends on the position of substitution.</p>

<p>Ai Product Descriptions 50 Creative</p>

<p>Methyl 2,3,5-tri-O-benzyl-b-D-ribofuranoside is a glycosylation reagent that can be used in the synthesis of oligosaccharides and polysaccharides. It is used to modify saccharides with fluorine or methyl groups and can be used to synthesize complex carbohydrates. Methyl 2,3,5-tri-O-benzyl-b-D-ribofuranoside is also an intermediate for click chemistry reactions. This product has high purity and can be custom synthesized to meet customers' needs.</p>

<p>Myo-inositol 1,2,4,5,6-pentakisphosphate (IP) is a phosphate of inositol that is found in the cytosol. It is an important component of polyphosphates and can be used for oxygen transport. It has been shown to inhibit the growth of cancer cells by binding to monoclonal antibodies that are targeted against CD20 and CD22 on cancer cells. IP also inhibits the activity of kinases and phosphatases in mammalian cells. This may be due to the inhibition of cytokine release from macrophages treated with IL-1β. Inositol phosphates are involved in many cellular responses including platelet-derived growth factor activation, cell proliferation, and protein synthesis.</p>

<p>5-O-tert-Butyldiphenylsilyl-2,3-O-isopropylidene-D-ribofuranose is a synthetic compound that is an inhibitor of adenosine deaminase. This drug has been shown to inhibit the synthesis of nucleic acids and other biological molecules such as amino acids and proteins. 5-O-tert-Butyldiphenylsilyl-2,3-O-isopropylidene ribofuranose is used in organic chemistry as a chiral analog for naturally occurring compounds such as adenosine. 5BPSSIROdR inhibits the enzyme adenosine deaminase by binding to its active site and preventing it from converting adenosine into inosine.</p>

<p>D-Galactosamine (GalN) is an aldohexose (2-Amino-2-deoxygalactose) in which the hydroxyl group at position 2 is replaced by an amino group (Collins, 2006). Galactosamine (as the N-Acetyl derivative) forms a key part of both N- and O-linked glycoproteins, glycolipids and glycosaminoglycans. Treatment of experimental animals with D-galactosamine / lipopolysaccharide causes lethal liver injury characterized by apoptosis of the hepatocyte and it is used as a laboratory model to study the effect of therapeutic agents (Hirono, 2001).</p>