Monosaccaridi

<p>Hesperetin 7,3'-O-b-D-glucuronide is a custom synthesis that can be synthesized with a variety of modifications including the addition of fluorine atoms. It is an oligosaccharide or polysaccharide consisting of saccharides. Hesperetin 7,3'-O-b-D-glucuronide is a white crystalline powder that has high purity and low impurities. It is an effective topical treatment for acne vulgaris and other skin conditions.</p>

2,3,5-Tri-O-benzyl-L-lyxofuranose is an acetal that is prepared by hydrolysis of 2,3,5-tri-O-benzylglycol with sodium methoxide in methanol. It can be made from the dimethyl acetal by displacement with sulphonate. The aldehyde group can be converted to an acetal by reaction with ethylene glycol and hydrochloric acid. The displacement of the aldehyde group with methoxide produces the acetal. Dimethyl acetals are also displaced by methyl iodide to produce aldehydes. Acetals are readily hydrolysed and acidic hydrolysis produces the corresponding alcohols.

Hesperetin-d3 7-O-beta-D-glucuronide is a novel glycosylated hesperetin derivative that has been synthesized for the first time. It is a synthetic sugar with an Oligosaccharide structure, which is a saccharide composed of three to nine monosaccharides. Hesperetin-d3 7-O-beta-D-glucuronide has been fluorinated and methylated on the sugar moiety. It has been prepared in high purity and it is available at CAS No. 1407813-41-5. This product can be custom synthesized according to your specifications and needs.

<p>Starting material for chiral-pool based synthesis of modified nucleosides</p>

Donor for Koenigs-Knorr type galactosylation and other anomeric substitutions

1,3,4,6-Tetra-O-acetyl-a-D-glucopyranose is a synthon that is used as a synthetic intermediate for the synthesis of other compounds. It is also a reactive compound that can be used to synthesize carboxylic acids and hydroxy ketones by reaction with water or alcohols. 1,3,4,6-Tetra-O-acetyl-a-D-glucopyranose can also be converted into esters by reaction with alcohols.

1,2,3,4-Tetra-O-pivaloyl-6-O-trityl-b-D-glucopyranose is a trityl derivative of glucose that can be used as a diagnostic agent for the assessment of cancer. When labeled with radioactive iodine, 1,2,3,4-Tetra-O-pivaloyl-6-O-trityl-b-D-glucopyranose has been shown to accumulate in bile and esophageal cancer cells. Magnetic resonance imaging (MRI) was used to evaluate the distribution of 1,2,3,4 tetra O pivaloyl 6 O trityl b D glucopyranose in patients with cirrhosis. The results suggest that this compound can be used as an indicator for the diagnosis of liver disease.

<p>fucosylation inhibitor</p>

2,3,4,6-Tetra-O-benzyl-D-galactopyranose is a building block which can be used as both a galactosyl donor and acceptor in the synthesis of saccharides. The benzyl protecting groups can be readily and selectively cleaved but are stable to a variety of reaction conditions allowing chemical manipulations to be carried out on the rest of the saccharide. 2,3,4,6-Tetra-O-benzyl-D-galactopyranose has been used in the synthesis of potential cholera toxin inhibitors, analogues of α-galactosyl ceramide (iNKT agonist) and more recently in the synthesis of Scleropentaside A.

4-Aminophenyl a-D-glucopyranoside is an alkoxycarbonyl analog that can be used in the preparation of antigens. It is a small, water-soluble molecule that can be used to induce antibody production and to identify antigenic determinants. 4-Aminophenyl a-D-glucopyranoside has been shown to react with glutamicum and corynebacterium cells in vitro. The compound binds to the bacterial cell surface by reacting with amino groups, inducing the production of acid molecules, which leads to bacterial death. 4-Aminophenyl a-D-glucopyranoside also reacts with methoxy residues on the ribosomal RNA molecule and corynebacterium DNA molecules. This allows it to be used as an expression vector for proteins and nucleic acids in Corynebacterium glutamicum (a bacterium commonly found in soil). Spectrosc

<p>4-Deoxy-4-fluoro-D-glucose is a biochemical compound that is used to bind to the carbon source in target tissues. It has a fluorine atom and two hydroxy groups, which are responsible for its biological properties. 4-Deoxy-4-fluoro-D-glucose binds to the 6 phosphate in bacterial enzymes and inhibits their activity, leading to cell death. It also binds to the hydroxyl group of proteins and alters their function. 4-Deoxy-4-fluoro-D-glucose is an inhibitor of bacterial enzymes, but has no effect on eukaryotic cells due to its inability to bind with these types of enzymes.</p>

<p>Butyl a-D-glucopyranoside is an antimicrobial agent that inhibits the growth of photosynthetic organisms. It has been shown to have high cytotoxicity against Gram-positive bacteria, including Enterobacter and Bacillus. Butyl a-D-glucopyranoside also exhibits strong antimicrobial activity against Gram-negative bacteria such as Escherichia coli, Salmonella enterica, Klebsiella pneumoniae, and Pseudomonas aeruginosa. This compound also has potent activity against fungi and yeast. The mechanism of action is not known but may involve the inhibition of tyrosol synthesis or the disruption of microbial membranes.</p>

1,2,3,4,6-Penta-O-benzoyl-D-mannopyranose is a high purity sugar that is custom synthesized to be used in glycosylation reactions. It has been shown to be effective for Click chemistry and can be fluorinated or methylated. 1,2,3,4,6-Penta-O-benzoyl-D-mannopyranose is a synthetic sugar that can be modified by glycosylation reactions. This sugar has the CAS No. 96996-90-6 and is known as Methyl 1-(1'-methylpropyl)-1H-[1',2',3',4',5',6']pentaoxacyclohexane.

<p>Chiral-pool resource for organic synthesis</p>

Allyl α-D-galactopyranoside is a colorimetric reagent that reacts with the polysaccharides to form a colored product. The reaction is based on the transfer of an allyl group from the reagent to the polysaccharide. This reaction can be performed using atomic force microscopy and microscopy techniques, as well as using light and UV-visible spectroscopy. The reaction can also be used to measure glycopolymer concentrations. A titration procedure has been developed for this purpose, in which an excess of allyl α-D-galactopyranoside is added to a solution containing galactose and ammonium sulfate. Allyl α-D-galactopyranoside reacts with galactose to produce an insoluble precipitate that can be measured by weighing or using optical density measurements at a certain wavelength.

4-Acetamidophenyl b-D-glucuronide sodium salt is a pharmaceutical drug that is a metabolite of acetaminophen. It can be detected in the urine by biochips, which are microarrays that contain immobilized binding sites for specific analytes. The analysis of 4-acetamidophenyl b-D-glucuronide sodium salt in urine is used to screen for the use of acetaminophen and to identify cytochrome P450 2C19 (CYP2C19) activity. This drug can also be detected by spectrometric methods using biochemical assays on plates or hepatocytes and mass spectrometric detection methods using liquid chromatography/mass spectrometry (LC/MS). Acetaminophen has been shown to have toxic effects on the liver, kidneys, and lungs in humans, as well as on diode photoluminescence.

Propyl b-D-glucuronide is a synthetic compound that belongs to the family of carbohydrates. It has a fluorinated hydroxyl group at the C3 position and an esterified carboxylic acid at the C1 position. This compound can be used as a building block for oligosaccharides and polysaccharides, which are complex carbohydrates. Propyl b-D-glucuronide is soluble in water and has a molecular weight of 176.

L-Galactose is a glycol ether that has been shown to have antibacterial efficacy against Gram-positive bacteria. It acts by inhibiting the synthesis of p-hydroxybenzoic acid, which is required for the synthesis of bacterial cell walls and their components. L-Galactose also has an inhibitory effect on the growth of Gram-negative bacteria by preventing methyl glycoside formation. L-Galactose has been used in polymerase chain reaction assays as a competitive inhibitor in analytical methods. It can be used at concentrations up to 5% and does not affect x-ray diffraction data or pluripotent cells. L-galactose can be used as a preservative in cosmetics such as lotions, creams, and ointments due to its mildness and lack of toxicity. The use of L-galactose in these products may prevent spoilage due to microbial contamination.

<p>Neu5Ac a(2-3)-Gal-b(1-3)-GalNAc)SL-OH is an Oligosaccharide that is a complex carbohydrate with a Methylation modification. It is the product of Click chemistry and has been Fluorinated and saccharide, Modification, sugar, Oligosaccharide, Synthetic, CAS No., Monosaccharide, Custom synthesis, High purity.</p>

2,7-Anhydro-D-sedoheptulose-2,3,4,5,6,7-13C6 is a custom synthesis of a complex carbohydrate. It is an oligosaccharide that is modified with methylation and glycosylation. This compound has been synthesized by Click modification and fluorination. 2,7-Anhydro-D-sedoheptulose-2,3,4,5,6,7-13C6 is water soluble and has a high purity. It is used as a research tool in the field of saccharides and carbohydrates.

<p>1,2,3,4,6-Penta-O-acetyl-5-thio-D-galactose is a fluorinated monosaccharide that is synthesized by the reaction of 1,2,3,4,6-penta-O-acetyl-D-galactose with sodium hypochlorite in the presence of sodium bicarbonate. This compound has been shown to be an excellent substrate for glycosylation reactions and can be used as a sugar donor in polysaccharide synthesis. 1,2,3,4,6 penta O acetyl 5 thio D galactose can also be methylated with dimethylsulfoxide and trimethylsilyl chloride to form the corresponding methylated derivative. This product is available at high purity levels and CAS No. 68713-89-1.END&gt;</p>

Vitamin added to plant cell culture medium to promote growth. Used to differentiate microorganisms based on their metabolic properties.

4-Methoxyphenyl 2-deoxy-4,6-O-(4-methoxybenzylidene)-2-phthalimido-b-D-glucopyranoside is a complex carbohydrate that has been modified with methylation and glycosylation. This product can be used for custom synthesis and is a high purity product. It is soluble in water. The CAS number for this compound is 57810-97-0. The molecular weight of this product is 576. The chemical formula for this compound is C24H28N2O8F3O7, which corresponds to an empirical formula of C24H28N2O8F3O7.

Resource for the synthesis of Clofarabine and other bioactive arabinosides

<p>4-O-Acetyl-N-acetyl-neuraminic acid is a derivative of sialic acid, which is an important component of the human cell membrane. It has been found to have inhibitory properties against influenza virus and other viruses. 4-O-Acetyl-N-acetyl-neuraminic acid inhibits viral activity by irreversible inhibition of the α subunit on the surface glycoprotein, preventing it from binding to host cells. This compound has been shown to be effective against hepatitis B virus and galleria mellonella (a type of wax moth). 4-O-Acetylneuraminic acid has also been shown to be effective in inhibiting the replication of Influenza A virus strains that are resistant to neuraminidase inhibitors such as zanamivir and oseltamivir.</p>

Dihydrozeatin-O-glucoside riboside is a plant hormone that is found in the roots of Eucomis species. It has been shown to interact with indole-3-acetyl-L-aspartic acid and inhibit the growth of plantlets. The interaction between dihydrozeatin and indole-3-acetyl-L-aspartic acid has been shown to be due to the formation of an intermediate, which is also metabolized by rhizobia. Dihydrozeatin also interacts with ammonium formate and profiles have been obtained for its metabolic products. This molecule also inhibits the production of growth regulators such as abscisic acid, alnifolia, and salicylic acid.

<p>The compound 1,7,7a-Triepialexine is an alkaloid that is found in plants of the genus Trientalis. It has been shown to have anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis. The compound also has a stereoselective synthesis and a stereoselective syntheses.</p>

<p>L-Rhamnose diethyl mercaptal is an antiperspirant and deodorant that is used in combination with other ingredients to reduce or eliminate body odor. It is a supplement, often found in combinations with other compounds such as neodymium and radium. This compound works by preventing the formation of sweat from the apocrine glands, which reduces underarm wetness and body odor. L-Rhamnose diethyl mercaptal also has antimicrobial properties that help prevent bacterial growth on the skin surface.</p>

<p>Allyl alpha-D-glucopyranoside is an optical isomer of D-glucose that is used in the synthesis of a number of synthetic trisaccharides, including maltotriose. Allyl alpha-D-glucopyranoside is also a potent antibacterial agent and has been shown to be active against Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. Allyl alpha-D-glucopyranoside has hydrophilic and hydrophobic properties, which makes it soluble in both water and organic solvents. This compound can also form stable complexes with metal cations such as sodium and potassium, making it useful for tissue culture experiments.</p>

Isosaccharinic acid-1,4-lactone is an organic compound that is found in human urine. It has been shown that the concentration of this compound can be used as a marker for renal health. The hydrated form of isosaccharinic acid-1,4-lactone can be prepared by heating with acetic anhydride, and it has been shown to have potential applications as a buffer in diagnostic tests for human serum or as a stabilizer for x-ray structures. The 1H NMR spectrum of isosaccharinic acid-1,4-lactone reveals two distinct signals at 1.6 and 2.0 ppm, which are assigned to the two isomers of this compound. The second order rate constant was measured to be 0.025 s−1 at pH 7 and 22 °C using acetate extract from human urine. This technique was also applied to measure rates constant for other organic acids such as formic acid

<p>N-Acetyl-L-talosaminuronic acid is a natural product that has been shown to have anti-inflammatory activity in experimental models of inflammatory bowel disease. N-Acetyl-L-talosaminuronic acid inhibits the production of proinflammatory cytokines, such as tumor necrosis factor alpha (TNFα), by binding to TNFα receptors on the surface of cells. This can be attributed to its ability to inhibit ATP levels and reduce oxidative stress, which are both factors that contribute to inflammation. N-Acetyl-L-talosaminuronic acid also has been shown to inhibit inflammatory responses in human monocytes and neutrophils. It binds specifically to her2+ breast cancer cells and inhibits their growth in culture. Furthermore, it has been shown to have cytotoxic effects on bladder cancer cells and can be used for the treatment of bladder cancer.</p>

<p>Methyl 4,6-O-isopropylidene-a-D-glucopyranoside is a glycosylation reagent that is used in the synthesis of oligosaccharides and polysaccharides. It is used as an intermediate for the production of active pharmaceutical ingredients and in the production of modified sugars. Methyl 4,6-O-isopropylidene-a-D-glucopyranoside can be custom synthesized to meet specific requirements such as purity, fluorination, and complex carbohydrate. This product is available with high purity and has been shown to be stable under a wide range of conditions.<br>Methyl 4,6-O-isopropylidene-a-D-glucopyranoside is not compatible with strong acids or bases.</p>

Methyl 4,6-O-benzylidene-a-D-mannopyranoside is a hexadecanoic acid that is mediated by the target cell. It has been shown to inhibit the growth of bacteria and cancer cells in vitro. Methyl 4,6-O-benzylidene-a-D-mannopyranoside also possesses an antibacterial activity with a low mammalian toxicity. This compound is hydrolyzed by esterases or glucuronidases, oxidized by cytochrome P450 enzymes, reduced by glutathione reductase, or conjugated with glucuronic acid. The residue of this compound has been shown to be carcinogenic in vivo and in vitro. Anticancer activity of this compound may be due to its ability to disrupt DNA synthesis and induce apoptosis of cancer cells.

L-Erythrose is a monosaccharide that contains an hydroxyl group on the second carbon atom. It can be synthesized by a synthetic scheme involving glycolaldehyde and hydroxylamine. L-Erythrose has been shown to inhibit the enzyme phosphoglycerate kinase, which converts 2-phosphoglycerate into phosphoenolpyruvate. L-Erythrose has also been shown to inhibit dehydroascorbic acid reductase, which converts dehydroascorbic acid into ascorbic acid, and galactitol reductase, which converts galactitol into D-tagatose. The mutant strain of Escherichia coli K12 that was engineered to produce L-erythrose showed a decreased susceptibility to phage infection and an increased resistance to oxidative stress. In addition, the polyol pathway in E. coli was induced by L-erythrose treatment.

<p>D-myo-Inositol 1,4,5,6-tetraphosphate sodium salt is a colony-stimulating factor that is involved in the regulation of metabolism and growth. It has been shown to increase the number of blood cells in rats with myeloid leukemia by acting on stem cells. D-myo-Inositol 1,4,5,6-tetraphosphate sodium salt binds to stem cell factor receptors on cell membranes to activate the receptor activity and initiate protein synthesis. This leads to increased production of hematopoietic cells and monoclonal antibodies. D-myo-Inositol 1,4,5,6-tetraphosphate sodium salt also stimulates erythropoiesis by regulating red blood cell production through its interaction with epidermal growth factor (EGF).</p>

<p>A protected thioglucose sugar</p>

<p>L-Rhamnose monohydrate is a sugar that is found in plants, animals, and bacteria. It is a component of polysaccharides like cellulose and hemicellulose. L-Rhamnose monohydrate has been shown to stimulate the growth of probiotic bacteria like Lactobacillus acidophilus in vitro. It also has antiviral properties against the herpes simplex virus type 1 (HSV-1). The antiviral activity may be due to its ability to inhibit viral replication by interfering with the synthesis of viral DNA and RNA. L-Rhamnose monohydrate may also have anti-inflammatory effects due to its ability to inhibit prostaglandin synthesis through inhibition of cyclooxygenase enzyme activity. This product has applications as a dietary supplement and ingredient in functional foods or beverages.</p>

<p>Resource for the industrial synthesis of ascorbic acid alias Vitamin C</p>

<p>Flurbiprofen is an anti-inflammatory drug that belongs to the group of non-steroidal anti-inflammatory drugs. It is a prodrug that is converted to the active form, flurbiprofen acid, in the liver. Flurbiprofen is used to reduce inflammation and relieve pain. The synthesis of this compound starts with the fluorination of 2,3-dihydroxybenzoic acid using N-fluorobenzenesulfonimide as a reagent. This reaction produces an alkylating agent, which reacts with sucrose in the presence of sodium methoxide to produce methylated sucrose ester. This is then oxidized with potassium permanganate to produce methylated sucrose ester oxide, which undergoes a click modification reaction with tetramethyl orthosilicate and triethylamine to produce flurbiprofen sorbitol ester (FSE).</p>

<p>1,2,3,4-Tetra-O-acetyl-6-S-acetyl-6-deoxy-6-thio-b-D-glucopyranose is a synthetic compound that is used as a building block for the synthesis of other compounds. It is an acetylated oligosaccharide that can be modified with fluorine atoms to form 1,2,3,4-tetra-[F]fluoro-[F]deoxy-[F]thio-[F]hexose. This product has high purity and can be used in glycosylation reactions.</p>

This is a custom synthesis of a carbohydrate. It is a methylated, glycosylated, fluorinated, complex carbohydrate that can be synthesized to any desired degree of substitution. This product has been designed for use as a fluorescent tag or label in biochemistry and cell biology research. It is modified at the anomeric position with an acetyl group and an azide group. The acetyl group confers solubility in water, while the azide group confers fluorescence. The modifications also allow for click chemistry reactions, which are used in protein labeling and activation studies.

1-Deoxy-1-(hydroxyethylamino)-D-glucitol (DEG) is a sugar alcohol that has been used as a transport inhibitor for the efflux of galactitol. It competitively inhibits the uptake of galactitol in the cell, resulting in a decrease in intracellular levels of this sugar. The uptake of other sugars is not affected by DEG, which makes it an effective tool for studying the transport mechanisms for these sugars. DEG is also chiral and has been used to study the uptake of chiral molecules. This research was done by using Drosophila melanogaster as an animal model, showing that DEG can be used to investigate how cells take up different molecules. These studies have led to insights into how cells metabolize different sugars and fats.

2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-thioglucopyranose is a synthetic monosaccharide that belongs to the group of complex carbohydrates. It has CAS No. 10043-46-6 and is used in glycosylation reactions. The fluorination of the sugar can be done by using a Click modification or methylation reaction. This product has been custom synthesized and can be ordered with high purity.

<p>2,3,4,6-Tetra-O-acetyl-b-D-thiogalactopyranose is a synthetic sugar that is prepared by the fluorination of D-galactopyranose and subsequent acetylation. This compound can be used for glycosylation reactions and as a substrate for click chemistry. It is an oligosaccharide with four monosaccharides in its backbone. The CAS number of 2,3,4,6-Tetra-O-acetyl-b-D-thiogalactopyranose is 50615-66-2.</p>

<p>5-O-Lauryl-D-xylofuranose is a lipase that can hydrolyze pentoses and hexoses. This enzyme has been shown to be active at temperatures between 0°C and 40°C, with optimal activity at 30°C. 5-O-Lauryl-D-xylofuranose is also thermostable and can be immobilized on silica gel or alumina. It is used in the manufacture of lysine, L-arabinose, and D-xylose. The enzyme catalyzes the reaction by removing a hydroxyl group from the pentoses or hexoses through an ester linkage with a dodecanoate group. The aliphatic chain of 5-O-lauryl dodecanoate is attached to the pentose or hexose molecule in an ester linkage by a thioether bond.</p>

D-Maltose 1-phosphate dipotassium salt is a disaccharide that can be used in the synthesis of oligosaccharides and polysaccharides. It is also an excellent candidate for further modification.

2-Acetamido-2-deoxy-3-O-(a-D-galactopyranosyl)-D-galactopyranose is a high purity synthetic oligosaccharide. It is an off white to light yellow powder with a molecular weight of 514.06 and a melting point of >200 degrees Celsius. The chemical formula for this product is C12H24O11N2. This product has been fluorinated, methylated, glycosylated, and click modified to create a complex carbohydrate that can be used in the synthesis of other molecules.

<p>Chromogenic substrate targeting beta-glucuronidase</p>

<p>1,2:5,6-Di-O-isopropylidene-alpha-D-glucofuranose, also known as diacetone-D-glucose (DAG), is a partially protected D-glucose sugar locked in the furanose form with isopropylidene protecting groups on the 1,2 and 5,6 positions. The unprotected 3 position is ready for a variety of chemical manipulations, such as alkylation, acylation or stereo-inversion. An orthogonal protecting group could be added to the 3 position to allow deprotection of an isopropylidene and therefore manipulations of the other hydroxyl groups. Diacetone-D-glucose has been used to make fluorinated hexopyranose glycolysis inhibitors useful in the treatment of brain tumours.</p>

4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside is a white crystalline powder. It is soluble in water and ethanol. This chemical has been used as a reagent for the methylation of saccharides and oligosaccharides with 4-methoxybenzene sulfonate. It is also an excellent substrate for click chemistry reactions.

2,3,4,6-Tetra-O-pivaloyl-D-glucopyranosyl amine is a monosaccharide that is custom synthesized and modified with fluorination. It also has saccharide properties such as methylation and glycosylation. This product can be used in the synthesis of complex carbohydrates or polysaccharides. It is a high purity compound with CAS No. 888963-33-5.

<p>1,2-Isopropylidene-D,L-myo-inositol is a modification of the natural product myo-inositol. It is synthesized by methylation and glycosylation of inositol with methanol. This chemical compound has been modified to include fluorination and saccharide.</p>

<p>D-Galactono-1,4-lactone is an intermediate in the galactose catabolism pathway. It is an acidic compound that can be found in plants and bacteria. D-Galactono-1,4-lactone has been shown to inhibit enzyme activities when it is present at high concentrations. This compound also inhibits the enzyme carbon source, which is involved in the conversion of glucose to energy. The deuterium isotope effect on the inhibition of enzyme activity by D-galactono-1,4-lactone has been studied extensively using plant phytochemicals such as triticum aestivum.</p>

Glucose metabolite

1-(2,2,2-Trifluoro-N-phenylethanimidate)-2,3,4-tri-O-acetyl-D-glucopyranuronic acid methyl ester is a methylated variant of an oligosaccharide. It has been synthesized by the click modification of an oligosaccharide with a monosaccharide and a fluorinated saccharide. This compound has been shown to have antiviral activity against the influenza virus in vitro. The antiviral activity may be due to its ability to inhibit the viral polymerase and RNA synthesis or to prevent virus assembly and release.

Xylose (Xyl) is an aldopentose also known as wood sugar (Collins, 2006). The main sources of xylose are hemicelluloses found in hardwood and perennial plants, such as, grasses, cereals, and herbs (Petzold-Welcke, 2014) and some algae. Xylose is used in the production of xylitol, a low calory sugar substitute. Xylose is used in glycosaminoglycan (GAG) biosynthesis, which is initiated by peptide O-xylosyltransferases, which transfer xylose onto selected serine residues in the core proteins. The first enzyme in the pathway, peptide O-xylosyltransferase, catalyzes the transfer of xylose from uridine diphosphate (UDP)-α-D-xylose onto serine and thus determines the site(s) of GAG attachment on the core protein (Briggs, 2018).

2,3-O-Isopropylidene-2-C-methyl-D-ribono-1,4-lactone is a crystalline compound that is obtained by the reaction of dimethylamine with epichlorohydrin. The compound has an asymmetric carbon atom and exists in two enantiomeric forms. It can be used as an acceptor in crystallographic analysis. The chemical structure of 2,3-O-Isopropylidene-2-C-methyl-D-ribono-1,4 -lactone is a lactone form of episulfide. Episulfides are lactones with episulfide groups attached to the C2 and C3 positions on the D ring. The episulfide group is formed by the reaction between the alcohol and sulfhydryl group from cysteamine with sulfur trioxide. The chemical formula for this compound is C13H20N2O8S

Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside (ABTS) is a synthetic sugar derivative that is used in the modification and synthesis of saccharides. ABTS can be modified by fluorination, glycosylation, methylation, or other modifications to produce new compounds. ABTS has a CAS number of 940274-22-6.

3-O-Benzyl-D-glucopyranose is a molecule that has been optimized for its autodock score. It binds to the active site of peptidases, which are enzymes that break down proteins in the body. 3-O-Benzyl-D-glucopyranose is a nauclea that can be used as a pharmacokinetic (PK) or pharmacodynamic (PD) inhibitor. Nauclea have shown effectiveness against diabetes by preventing the breakdown of glucose, which is an important energy source for cells. 3-O-Benzyl-D-glucopyranose has also been found to be an effective inhibitor of DPPIV, which is an enzyme involved in breaking down insulin and other hormones in blood circulation. In vitro studies have shown that it may also have antiaging properties due to its ability to inhibit production of inflammatory cytokines such as IL1β, IL6, and TNFα.

<p>Mannose (Man) is the C2 epimer of glucose with one hydroxyl group axial which by Hudsons rules makes it slightly less stable than glucose (Hudson, 1948). However, mannose is very common in plants and animals, and occurs in many polysaccharides, such as, galactomannans (e.g. Guar, Locust Bean Gum), mananns (e.g. Ivory Nut Mannan), Spruce Galactoglucomannan, Gum Ghatti (Whistler, 1993) and baker’s yeast (Saccharomyces cerevisiae) (Manners, 1973). Mannose is one of the key mammalian monosaccharides (Glucose, Galactose, Mannose, Fucose, N-Acetyl Glucosamine, N-Acetyl galactosamine and Sialic acid) and occurs in N-linked glycans where it is a core oligosaccharide (Gabius, 2009).</p>

3,5-((R)-Benzylidene)-6-deoxy-L-glucono-1,4-lactone is a synthesized sugar that can be modified to include fluorination, glycosylation, methylation and other modifications. It is an oligosaccharide with a saccharide backbone made up of glucose units. The monosaccharides are galactose and glucuronic acid. 3,5-(R) Benzylidene)-6-deoxy-L-glucono-1,4-lactone is used in the synthesis of complex carbohydrates for research purposes.

<p>2,3,4,6-Tetra-O-pivaloyl-D-mannopyranosyl fluoride is a carbohydrate that is synthesized by the modification of D-mannose with 4,6-dichlorohexanoic acid. It is a white powder with a melting point of 170°C. 2,3,4,6-Tetra-O-pivaloyl-D-mannopyranosyl fluoride can be used as a monosaccharide for glycosylation reactions or as an intermediate for custom synthesis. This product has been methylated and glycosylated before the final purification process. It has a high purity level and can be used in Click chemistry reactions.</p>

<p>Constituent of RNA; important resource for RNA- and DNA-related syntheses</p>

Fluorinated glucose analog

3,6-Di-O-acetyl-5-S-acetyl-5-deoxy-1,2-O-isopropylidene-a-D-glucofuranose is an acetal sugar. It is custom synthesized for research purposes. The sugar has a purity of >99% and was synthesized by click chemistry as well as fluorination and glycosylation. This product is offered in a variety of modifications including methylation, modification, and oligosaccharide. 3,6 Di O Acetyl 5 S Acetyl 5 Deoxy 1 2 O Isopropylidene A D Glucurono Furanose can be used to produce saccharides or complex carbohydrates in the laboratory setting.

2C-Hydroxymethyl-2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone is a synthetic monosaccharide with a CAS number of 70147-48-7. This compound has been modified to include the hydroxymethyl group and the 2C designation. It is used as an ingredient in the synthesis of complex carbohydrates.

Chenodeoxycholic acid 24-acyl-b-D-glucuronide (CDCA) is a drug that is used to treat gallstones and primary biliary cirrhosis. CDCA has been shown to be effective in treating gallstones by reducing the amount of cholesterol and other bile salts in the bile. It is also prescribed for patients with primary biliary cirrhosis, which is an autoimmune disease that causes inflammation of the small intestine. CDCA has been shown to decrease cholesterol levels and improve liver function in clinical studies. It also has a low toxicity profile, making it safe for long-term treatment. The major side effects are nausea, vomiting, headache, and diarrhea. CDCA binds to fatty acids in the liver cells and prevents their uptake into the cells by blocking fatty acid transporters such as LPL or FATP4 receptors. This increases the amount of free fatty acids available for oxidation by increasing β-oxidation rates within the cell

1,6-Bis-O-tert.butyldimethylsilyl-3,4-O-isopropylidene)-2,5-O-methanesulfonyl-D-mannitol is a sugar that is used as a starting material for the synthesis of glycosides. This compound has been shown to react with click chemistry and undergo fluorination, glycosylation, methylation, and modification reactions. It has been shown to be useful in the synthesis of oligosaccharides and monosaccharides. The chemical formula for 1,6-Bis-O-tert.butyldimethylsilyl-3,4-O-[isopropylidene)-2,5 - O]-methanesulfonyl--D--mannitol is C14H30OSiMesO8S2.

Allyl 3-O-benzyl-a-D-glucopyranoside is a synthetic, monosaccharide carbohydrate. The product is a modification of the natural polysaccharide allyl 3-O-benzyl-a-D-glucopyranoside. Allyl 3-O-benzyl-a -D glucopyranoside is an Oligosaccharide with CAS No. 145454-72 -4 and has the molecular formula C14H20O6 and molecular weight of 312.32 g/mol. The product is available in high purity and can be synthesized to order. Allyl 3-O -benzyl -a D glucopyranosides are useful as a Fluorination, saccharide for use in glycosylation or methylation reactions or as a complex carbohydrate in the synthesis of oligosaccharides, polysaccharides, or sugar chains.

<p>Substrate for UDP-3-O-acyl-GlcNAc deacetylase</p>

<p>Glucosyl-C18-sphingosine is a sphingolipid that has been shown to inhibit the activity of Gaucher's enzyme, which is responsible for the synthesis of glucosylceramide. It has been demonstrated in a model system that glucosyl-C18-sphingosine inhibits mitochondrial membrane potential and decreases ATP levels, leading to cell death. The molecular pathogenesis of Gaucher disease is not well understood but it is believed to be related to defective lysosomal function. Glucosyl-C18-sphingosine may be used as a diagnostic agent for Gaucher disease and other metabolic disorders involving glucosylceramide accumulation.</p>

4-Methoxyphenyl 2,3:4,6-di-O-benzylidene-a-D-mannopyranoside is a water soluble polysaccharide that is a methylated derivative of mannose. It has been fluorinated at the 4 position and modified with benzyl groups at the 2, 3, and 6 positions. This compound is used in custom synthesis to synthesize oligosaccharides or polysaccharides.

<p>Hesperetin 3'-O-b-D-glucuronide is a natural product that is synthesized by glycosylation of hesperidin with 3,4,5-trihydroxybenzoic acid. It is a synthetic and complex carbohydrate that can be modified to include fluorination, monosaccharide, oligosaccharide, methylation, and click modification. Hesperetin 3'-O-b-D-glucuronide can also be used in the synthesis of polysaccharides with glycosylations. This product has high purity and can be custom synthesized for customers.</p>

Perseitol is a nutrient solution that contains fatty acids and is used in tissue culture to supplement the growth of cells. It can be used as a substitute for animal serum, which is usually derived from bovine or porcine sources. Perseitol provides all essential components required for cell growth, including amino acids, vitamins, minerals, and lipids. Perseitol is also used in vitro assay systems to determine the redox potential of substances. This solution has been shown to have anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis.

Quercetin-3-O-b-D-glucose-7-O-b-D-gentiobioside is a flavonoid that is found in fruits and vegetables. Quercetin has been shown to have antioxidative activity and can be used as a dietary supplement for the prevention of cardiovascular disease. Quercetin has also been shown to inhibit the oxidation of cholesterol, which may help prevent atherosclerosis. Quercetin has been shown to have antiinflammatory properties in women with symptoms of premenstrual syndrome (PMS). Quercetin inhibits the production of prostaglandins, which are inflammatory mediators that are associated with PMS. Quercetin also blocks the inflammatory effects of methyl linoleate, a fatty acid found in meat, dairy products, and vegetable oils. Quercetin has also been shown to bind with specific proteins on white blood cells called immunoglobulins or antibodies. The

<p>Dodecyldeoxynojirimycin is a polyketide natural product that has been shown to be a potent inhibitor of the synthesis of mannose-containing glycoproteins, including glucans and chitooligosaccharides. It binds to the active site of glucan synthetase and prevents the formation of glucose residues, which blocks glucan biosynthesis. Dodecyldeoxynojirimycin has also been shown to have anti-inflammatory properties.</p>

2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-a-D-glucopyranose (2AAT) is a synthetic nucleoside that binds to the same sequence of n-acetylgalactosamine in the cell wall of Gram positive bacteria. It was found to be effective against bacterial strains that produce beta lactamase enzymes. 2AAT has been shown to inhibit the growth of Gram positive bacteria and is able to penetrate tissues. It also prevents bacterial DNA gyrase and topoisomerase IV from binding with their respective substrates. 2AAT is made up of four parts: two ribose molecules, one deoxyribose molecule and one acetamido group. This last part is what makes it bind to the bacterial cell wall and inhibits protein synthesis by preventing mRNA from being translated into proteins.

3,5-Di-O-benzoyl-2-deoxy-2,2-difluoro-D-ribonic acid-1,4-lactone (3DBR) is a nucleoside that has been shown to have antiaging properties. It has been found to be an effective scavenger of peroxyl radicals and reactive oxygen species (ROS). 3DBR also inhibits the formation of aluminum oxide and styrene by catalyzing the salt formation reaction. This compound also has anti-tumour activity and can be used as a chemotherapeutic agent for the treatment of cancer. It is heat resistant and can be combined with gemcitabine hydrochloride in chemotherapy.

Methyl 2,3,6-tri-O-benzoyl-4-deoxy-4-fluoro-a-D-glucopyranoside is a sugar that is synthetically modified. This product has been fluorinated and glycosylated with a benzoyl group at C2 position. It contains methyl groups attached to the ring carbons at C1 and C6 positions. The product is also an oligosaccharide that contains two monosaccharides (sugar units) linked by an alpha (1→4) glycosidic bond. Methyl 2,3,6-tri-O-benzoyl-4-deoxy-4-fluoro-a-Dglucopyranoside can be used as a synthetic building block for the synthesis of complex carbohydrate structures.

beta-glucuronidase substrate

6-Azido-6-deoxy-1,2:3,4-di-O-isopropylidene-a-D-galactopyranose is a copper complex that is soluble in water. It is used as an initiator for the polymerization of galactose monomers. 6AIDOGAL reacts with azide or diazo compounds to form a cycloaddition reaction and can be used to prepare copolymers by reacting with other monomers such as D-glucose. The temperature range for this reaction is between 20°C and 100°C. This compound has been shown to form stable complexes with Cu(II) ions at temperatures below 0°C.

<p>2-Acetamido-2-deoxy-D-mannono-1,4-lactone is a chemical compound that is an aldonic acid and is classified as an ester. It has a molecular formula of C8H10O5 and it has the following structural formula:<br>This product can be synthesized from benzoic acid and glyceraldehyde. 2-Acetamido-2-deoxy-D-mannono-1,4-lactone is also known as benzoylated mannose. It has been reconfirmed to have high yield in acetylation reactions with molybdate. 2-Acetamido-2deoxy-Dmannono1,4lactone can also undergo epimerization to form the optical antipode of 2,3,4,6tetraacetyloxybenzoic acid (2,3,4,6tetraacetyl</p>

This product is custom synthesized. The synthesis of this product was accomplished by modification, fluorination, methylation and monosaccharide synthesis. It is a synthetic oligosaccharide that has been modified with click chemistry. This product is made up of saccharides in a glycosylation configuration. It is a complex carbohydrate that contains sugar units in various configurations. This product has high purity and can be used as an intermediate for the synthesis of other products.

Febuxostat is a drug that inhibits the enzyme xanthine oxidase, which is involved in the production of uric acid. The chronic use of this drug can lead to a decrease in serum uric acid levels, which is associated with lowering of blood pressure and prevention of kidney stones. Febuxostat has been shown to be effective in patients with polyarticular rheumatoid arthritis and allopurinol-induced gout. Side effects may include gastrointestinal discomfort, low dose-related hypertension, and cardiovascular complications. Febuxostat interacts with colchicine and other drugs that are metabolized through cytochrome P450 enzymes. This interaction may reduce the effectiveness of these drugs or increase their toxicity.

D-Erythrulose is a sugar that can be synthesized from the chemical structures of glycolaldehyde and carbonyl group. It can also be produced by hydrolysis of erythritol, which is found in plant cell walls. D-Erythrulose has been used as an alternative to glucose for fermentation processes because it does not inhibit the growth of most bacteria. D-Erythrulose has been shown to increase ATP levels in Escherichia coli K-12 cells and to affect the activities of enzymes involved in glycolysis, such as glyceraldehyde 3-phosphate dehydrogenase, phosphoglycerate kinase, and enolase. The metabolic pathways that produce D-erythrulose are found in many organisms, including Corynebacterium glutamicum, Brucella melitensis, and Brucella suis.

2-O-Methyl-D-glucose is an aldohexose that is used in the synthesis of a number of biological compounds. It has been shown to inhibit the growth of cancer cells by interfering with the synthesis of fatty acids and proteins.