Monosaccharides

<p>3,6-Di-O-benzoyl-D-galactal is a complex carbohydrate with CAS No. 130323-36-3 and a molecular weight of 538. It is an oligosaccharide that can be modified by methylation, glycosylation, or carbamylation. This product can also be fluorinated to form 3,6-di-O-(4'-fluoro)benzoyl-D-[2]galactal.</p>

<p>3,5-O-Benzylidene-L-lyxono-1,4-lactone is a custom synthesis that has been modified with fluorination, methylation and monosaccharide. This product is also synthesized from a saccharide and may be modified with glycosylation. These modifications will create an oligosaccharide or complex carbohydrate. 3,5-O-Benzylidene-L-lyxono-1,4-lactone can be found in the CAS registry number 177538-08-3.</p>

<p>2,3,4-Tri-O-acetyl-D-xylopyranose is a lactide sugar that is found in the cell walls of many plants. It is synthesized from D-xylose by enzymatic condensation with acetylated L-malic acid and has been shown to be biodegradable. 2,3,4-Tri-O-acetyl-D-xylopyranose has been shown to have physical properties that are similar to those of cellulose, such as crystallization and solubility in water. The compound also has an NMR spectrum that contains peaks at δ = 0.8 (triplet), 1.1 (singlet) and 1.5 ppm (doublet). The hydrophobic group on the molecule is thought to contribute to its hydrophilicity.</p>

<p>9,10-Dimethoxy-pterocarpane-3-O-b-D-glucoside is a custom synthesis that is a polysaccharide with a complex carbohydrate structure. The chemical name for this compound is 9,10-dimethoxy-pterocarpane-3-O-[4′″-(1″″′′)-b′″'-D-glucopyranosyl]-3′′′,4′″’,6′"’] bibenzyl. This compound has been modified by methylation and glycosylation. It can be used in the treatment of cancer and diabetes due to its high purity and fluorination. 9,10-Dimethoxy pterocarpane 3β O glucoside is a sugar or saccharide that can be found in plants such as the roots of tobacco plants. The modification of this sugar by methylation and glycosylation makes it more</p>

<p>6-Deoxy-L-glucose (6DG) is a glucose analogue that has been extensively studied for its effect on the metabolism of other sugars. It is an inhibitor of glycolysis and the pentose phosphate pathway in both wild-type and mutant strains of yeast, as well as in mammalian cells. 6DG inhibits the activity of enzymes such as gamma-aminobutyric acid (GABA) transaminase and phosphoglycerate kinase, which are involved in the synthesis of GABA and glycogen respectively. 6DG also inhibits the transport of sugar molecules into cells. The hydrochloric acid (HCl) concentration required to activate 6DG varies with pH, with a pKa near 7.5 at physiological pH. 6DG is activated by HCl when the pH falls below this value. The hydroxyl group on 6DG can react with HCl to form a chlorohydrin intermediate, which reacts further to yield</p>

<p>Phenyl a-L-thioglucopyranoside is an intermediate in the synthesis of glycosides. It is used as a fluorinating or methylating agent, and as a glycosylating or modifying agent. Phenyl a-L-thioglucopyranoside can be synthesized by the click modification of thioglycolic acid with phenol, followed by glycination. It has been shown to react with monosaccharides to form oligosaccharides and polysaccharides. Phenyl a-L-thioglucopyranoside can also react with saccharides to form complex carbohydrates.</p>

<p>Perindopril acyl-a-D-glucuronide is a synthetic small molecule that has been modified with fluorination, methylation, and click modification. It can be used for the synthesis of oligosaccharides and saccharides. Perindopril acyl-a-D-glucuronide is a highly reactive compound that is useful in glycosylation reactions, including Click chemistry. The CAS number for this compound is 217917-05-8. The molecular weight of perindopril acyl-a-D-glucuronide is 284.36 g/mol and the molecular formula is C14H24N2O6•C2H3O2•1/2 H2O.</p>

<p>2,3,6-Tri-O-carboxymethyl-D-glucose (TCMG) is a potent polyelectrolyte that can be used as an additive to cellulose. TCMG is synthesized by the reaction of 2,3,6-tri-O-carboxymethylcellulose with potassium bitartrate in acidic medium. TCMG has been shown to interact with cellulose and form a gel matrix. This reaction is due to the ionic interactions between the carboxyl groups in TCMG and the hydroxyl groups in cellulose. The conductimetric titration measurement shows that TCMGs have a constant value at pH 5.5, indicating that they are anionic polyelectrolytes. Potentiometric titration indicates that TCMGs are nonionic polyelectrolytes and the interaction between these two polymers is due to electrostatic forces.</p>

<p>D-Glucose-4-D is a deuterated form of glucose. It is a halophilic sugar that is used in the biosynthesis of lipids. D-Glucose-4-D can be synthesized chemically or by isotope effect by using d-glucose as the starting material. This compound can be used to study lipid synthesis and lipid metabolism in bacteria, such as E. coli, because it has been shown to inhibit the enzyme glycerol dehydratase, which catalyzes the conversion of glycerol to dihydroxyacetone phosphate, an intermediate in lipid biosynthesis. D-Glucose-4-D also inhibits the enzyme phosphatidate phosphohydrolase, which converts phosphatidic acid to diacylglycerol. These compounds are important for membrane lipid formation and are involved in cellular signalling pathways.</p>

<p>Propylbeta-D-glucopyranoside is a sugar transport inhibitor that is used to inhibit bacterial growth. It has been shown to bind to the glucose transporter and quench tryptophan fluorescence in plant cells. This active form of Propylbeta-D-glucopyranoside also inhibits bacterial growth by binding to fatty acid esters and cytochalasin, modifiers of cell membrane permeability, which inhibit the synthesis of fatty acids. Microcapsules containing this drug have been shown to be effective against staphylococci and other bacteria. The activity of Propylbeta-D-glucopyranoside can be increased by hydrochloric acid or sodium hydroxide, which increase the solubility of its salts.</p>

<p>3,4-O-Isopropylidene-D-galactal is a modified form of galactal. This compound is a methylated derivative of D-galactal that has been synthesized by the click reaction. It can be used in the synthesis of oligosaccharides and polysaccharides. 3,4-O-Isopropylidene-D-galactal is a high purity compound with a CAS number of 124477-12-9.</p>

<p>Methyl 2,3,5-tri-O-benzyl-a-D-arabinofuranoside is a methylated sugar that belongs to the group of saccharides. It is often used as a Click modification and in custom synthesis of oligosaccharides. This product is also used for glycosylation and high purity modifications. Methyl 2,3,5-tri-O-benzyl-a-D-arabinofuranoside can be synthesized from arabinose and benzaldehyde with fluorination. The CAS number for this product is 51469-61-1.</p>

<p>2-Deoxy-scyllo-inosose is a biochemical with an unknown function. It is not a substrate for any known enzyme, but has been shown to be a substrate for the synthesis of corynebacterium glutamicum. The reaction mechanism of 2-deoxy-scyllo-inosose is still unclear, but it has been proposed that this molecule undergoes dehydration and then undergoes an acid catalyzed aldol cyclization to form 3-aminohexanol. This reaction produces fluorescence resonance energy transfer in group p2 subtilisin.<br>2DOS is also an antimicrobial agent which exhibits activity against Gram positive bacteria such as Streptococcus pyogenes, Enterococcus faecalis, and Bacillus subtilis.</p>

<p>MW of BSA approx 65000</p>

<p>2-Deoxy-b-L-erythro-pentofuranose is an experimental drug that is a protonation product of 2,3-dideoxyproline. It is the result of conformational changes in the deoxyribose ring and puckering of the ribose units. The puckering motion also results in a change in the orientation of the hydrogen atoms on the carbons. This has led to analogous carbon configurations with different numbers of hydrogens, which can lead to different solutions. 2-Deoxy-b-L-erythro-pentofuranose binds to ribosomes and inhibits protein synthesis, which may be due to its pyrrolidine ring or membered ring structure.</p>

<p>1-Deoxy-L-idonojirimycin hydrochloride is a chaperone that is structurally related to the natural substrate, L-idonojirimycin. It has been found to interact with recombinant human Hsp70 and Hsp90. 1-Deoxy-L-idonojirimycin hydrochloride enhances the kinetic and thermodynamic parameters of these chaperones in vitro. The structural analysis of this compound revealed that it binds to both Hsp70 and Hsp90, which may be due to its ability to mimic the natural substrate's binding site on these chaperones.</p>

<p>Fluorescent substrate used to monitor fructose uptake</p>

<p>Methyl b-D-altropyranoside is a methylated saccharide that can be used as a sugar substitute. It has the same sweetness as sugar and is also resistant to browning. Methyl b-D-altropyranoside is synthesized by treating an aldose or ketose with formaldehyde in the presence of sulfuric acid and an alkali. This product is water soluble, heat stable, and free from impurities such as glucose or fructose. Methyl b-D-altropyranoside can be used to modify polysaccharides and oligosaccharides, adding a methyl group to the carbon 2 position. In addition, it has been shown to have antioxidant properties due to its ability to quench reactive oxygen species (ROS).</p>

<p>1,2,6-Tri-O-methyl-D-glucopyranoside is a synthetic sugar that has been modified by fluorination and glycosylation. This product is a white crystalline powder with a melting point of 185°C. The chemical formula for this product is C5H12O5.</p>

<p>3-O-Toluoyl decitabine is a synthetic, high purity drug that is custom synthesized to order. The synthesis of 3-O-Toluoyl decitabine involves the modification of sugar molecules with fluorination, glycosylation, and methylation. This compound has CAS No. 183016-21-9 and is used in the treatment of cancer by inhibiting ribonucleic acid (RNA) synthesis. 3-O-Toluoyl decitabine inhibits RNA polymerase II and III, which are enzymes that catalyze the transcription of DNA into RNA. It also inhibits protein kinase C, which leads to cell death and tumor shrinkage.</p>

<p>Cladinose is a natural compound that has been shown to have potent inhibitory properties against microorganisms, such as bacteria and fungi. Cladinose has been shown to inhibit the growth of bacteria by reacting with the ribosomes of cells in the bacterial cytoplasm. It inhibits bacterial protein synthesis by binding to the ribosomal RNA and blocking access to the mRNA template. Cladinose also inhibits fungal growth by inhibiting ergosterol biosynthesis, which prevents fungal cell membrane formation. Cladinose has been shown to have antiinflammatory activity in mice with induced inflammation. This is due to its ability to bind to cyclooxygenase-2 (COX-2) and prevent its activation, thereby preventing prostaglandin synthesis.</p>

<p>(S,S)-(-)-1,4-Dimethoxy-2,3-butanediol is an organic compound with the chemical formula CH(OCH)CHOH. This colorless liquid is a chiral molecule that can exist in two enantiomeric forms. The asymmetric carbon atom (C-1) is of high stereoselectivity and has been shown to undergo nucleophilic attack by a wide variety of nucleophiles. The reaction product can be either the corresponding enolate or enolates depending on whether the nucleophile is a base or acid. In addition, this compound yields a stereoselective synthesis of chiral products when reacted with carbonyls.</p>

<p>D-Galactose-BSA is a modified carbohydrate that is synthesized by the selective substitution of the hydroxyl group on the beta-carbon of D-galactose. This modification enhances the binding affinity of D-galactose to bovine serum albumin (BSA), which is used as a carrier protein for many biological assays. The fluorination step in this synthesis creates reactive sites on the molecule, which are then available for chemical modifications such as methylation or glycosylation. D-Galactose-BSA can be custom synthesized to meet your specifications for purity, stability, and activity.</p>

<p>5-O-Trityl-D-ribose is a sugar derivative that is used in the chemical synthesis of pharmaceuticals, natural products, and other compounds. It is an important intermediate in the synthesis of various nucleosides and nucleotides.</p>

<p>1-13C-L-Arabinose is a metabolite of the sugar, L-arabinose. This compound is formed by escherichia bacteria and can be found in the urine of mice. 1-13C-L-Arabinose has been shown to inhibit the growth of escherichia coli and has a six membered ring structure.</p>

<p>Glycerone phosphate lithium salt is a reactive molecule that serves as an intermediate in the synthesis of rapamycin, a complex of glycerone phosphate and rapamycin. Glycerone phosphate lithium salt is used to detect the presence of glutamate dehydrogenase and to purify monoclonal antibodies. Glycerone phosphate lithium salt has been shown to react with platinum-based chemotherapy, which may be due to its ability to bind to active sites on cancer cells. This molecule also has been shown to reduce high cholesterol levels in mice and inhibit skin cancer tumor growth. Glycerone phosphate lithium salt's physiological effects have not been fully determined, but it may have some anticancer activity.</p>

<p>B-D-glucofuranose is a natural compound with the molecular formula C6H12O6. It is found in plants, specifically in the seeds of the granatum tree. The calibration of this compound can be done using anions and ion chromatography. B-D-glucofuranose has antibacterial activity against Gram-positive bacteria, but not against Gram-negative bacteria or fungi. It also inhibits fatty acid synthesis and may have nutritional value for humans as a source of 5-hydroxymethylfurfural (HMF). HMF has been shown to inhibit the growth of cancer cells in vitro and induce apoptosis in cancer cells by uv irradiation. Mass spectrometric analysis and spectrometric methods are used to identify this compound.</p>

<p>Luteolin 7,3'-di-O-glucuronide is a flavonoid that is structurally similar to luteolin. It has been characterized by deglycosylation and the technique of fluitans. The deglycosylation step was carried out using glycosidase from liverwort, which cleaves the glycosidic linkage between the sugar and the aglycone. Luteolin 7,3'-di-O-glucuronide has been found in Chrysoeriol and Fluitans, which are flavonoid glycosides from Liverwort. Luteolin 7,3'-di-O-glucuronide also exhibits antiplatelet activity due to its ability to inhibit platelet aggregation and thrombus formation.</p>

<p>Inositol nicotinate is a combination of two substances, inositol and nicotinate. It is used to reduce the risk of heart disease by lowering low-density lipoprotein-cholesterol (LDL) levels. Inositol nicotinate has been shown to increase the surface area of mitochondria, which may be due to its ability to inhibit the release of fatty acids from fat cells. Inositol nicotinate also increases magnesium levels in cells and induces mitochondrial functions. This drug has been tested in cell culture for its effects on skin cells and found that it can reduce the amount of x-linked adrenoleukodystrophy protein (XALD), a substance that accumulates in patients with X-linked adrenoleukodystrophy, an inherited disorder that causes progressive damage to the nervous system. The drugs also have been shown to have beneficial effects on cholesterol metabolism, reducing LDL cholesterol levels, as well as inhibiting platelet aggregation.</p>

<p>O-Methoxytopolin-9-glucoside is a sugar that is used in the synthesis of glycoproteins, glycosaminoglycans, and glycoconjugates. It can be used as a fluorinated sugar probe to study glycosylation. This compound has been synthesized with a variety of modifications such as methylation, fluorination, and click chemistry. O-Methoxytopolin-9-glucoside is an oligosaccharide with a monosaccharide at its reducing end. The saccharides are linked through beta 1→4 glycosidic bonds with alpha 1→2 glycosidic bonds at their other ends.<br>O-Methoxytopolin-9-glucoside has been shown to be stable under acidic conditions and can act as both an antioxidant and prooxidant depending on the pH level.</p>

<p>Losartan N1-glucuronide is a glucuronidated metabolite of losartan that is produced naturally in the human body. It is converted from losartan by the enzyme UDP-glucuronosyltransferase, which is found in humans and other animals. The rate of glucuronidation varies between individuals and is determined by genetic factors. Losartan N1-glucuronide has shown to be an effective inhibitor of angiotensin II, with an IC50 value of 1.4 μM. This inhibition can be reversed by dobutamine or recombinant human UGT2B7 enzyme, which are both competitive inhibitors of the enzyme UGT2B7. Magnetic resonance spectroscopy has been used to study the kinetic properties of this inhibitor and its effect on dobutamine-induced changes in cardiac function.</p>

<p>D-[6,6'-2H2]Glucose is a carbohydrate that is present in many foods and also produced by the cells of the human body. It can be used as a biomarker for cancer cells because it is taken up by malignant cells at a higher rate than normal cells. D-[6,6'-2H2]Glucose is often used to assess the response of patients to chemotherapy treatment. The uptake of D-[6,6'-2H2]Glucose by malignant cells can be measured using vibrational spectroscopy or chromatographic science. The deformation of glucose molecules can be quantified using nuclear magnetic resonance (NMR) spectroscopy and this data can then be used to estimate the degree of glycolysis in specific tissues.</p>

<p>1-Deoxy-D-glucitol is a sugar alcohol that is a reduction product of glucose. It can be produced by the reduction of glucose 6-phosphate in muscle cells. The enzyme dehydrogenase catalyzes this reaction, which is influenced by the presence of gemini surfactants such as DMSO. 1-Deoxy-D-glucitol has been shown to have anti-fungal properties against Aspergillus parasiticus and other organisms. This activity may be due to its ability to inhibit phosphofructokinase, hexokinases, or other enzymes that are involved in the metabolism of glucose by these organisms.</p>

<p>Amiprilose is a nonsteroidal anti-inflammatory drug that inhibits the production of IL-2. Amiprilose has been shown to inhibit IL-17a, which is an inflammatory cytokine, in skin cells and mononuclear cells. It also inhibits cell proliferation by binding to the il-2 receptor on muscle cells. Amiprilose has been shown to be effective as a pharmacological agent for treating autoimmune diseases such as rheumatoid arthritis and psoriasis.</p>

<p>R-Phenyleprine-3-D-glucuronide is a synthetic compound that is used for the modification of saccharides. It has fluoro groups and has been shown to be active in glycosylation reactions. R-Phenyleprine-3-D-glucuronide can also be used as a methylating agent, or as an intermediate in the synthesis of oligosaccharides and monosaccharides. The molecular weight of this compound is 594.</p>

<p>4-Deoxy-4-fluoro-D-galactopyranose is a custom synthesis that is an oligosaccharide, polysaccharide, saccharide, and carbohydrate. It is fluorinated with a methyl group on the 4th carbon atom and has been modified to include a fluoro group at the 4th position of the molecule. 4-Deoxy-4-fluoro-D-galactopyranose can be used in research as it is high purity and has been modified into a monosaccharide sugar.</p>

<p>Phenyl 2,3,4-tri-O-benzoyl-b-D-thiogalactopyranoside is a methylation product of b-D-thiogalactopyranoside. It has CAS No. 139608-11-0 and a molecular weight of 536.2. This compound is an Oligosaccharide with a molecular formula of C8H8O7 and a molecular weight of 432.1. Phenyl 2,3,4-tri-O-benzoyl-b-D-thiogalactopyranoside is also known as Methyl 3,4-(Benzoyloxy)galactoside or Methyl 3,4-(Benzoic acid)galactoside. This compound is soluble in water and ethanol and has the appearance of a white to off white powder at room temperature.</p>

<p>4-Aminophlorizin is a chemical compound that inhibits the uptake of azide by red blood cells. It has been shown to be effective against intestinal parasites and trophozoites. 4-Aminophlorizin is a potent inhibitor of the membrane system, which may be due to its interaction with the semenza, or membrane protein.</p>

<p>Neosamine is an antimicrobial agent that is activated by the addition of fatty acids. It has a low potency and is used to diagnose infections caused by bacteria. Neosamine has been shown to inhibit the growth of bacteria, fungi, and parasites on electron microscopy. Neosamine also inhibits protease activity and may be useful in detergent compositions for removing fats, oils, and greases from surfaces. This chemical is stable in acidic solutions and does not react with carbostyril or other diagnostic agents.</p>

<p>Secoxyloganin is a 4-hydroxycinnamic acid that belongs to the group of caffeic acids. It is an iridoid, which is a type of monoterpene indole alkaloid that has been found in various plants. Secoxyloganin can be found in the roots, stems, and leaves of plants such as Securigera varia and Digitalis purpurea. Secoxyloganin has shown antimicrobial activity against Gram-positive bacteria such as Staphylococcus aureus and Gram-negative bacteria such as Pseudomonas aeruginosa. It also has antiviral properties, which may be due to its ability to inhibit RNA synthesis and protein synthesis.<br>Secoxyloganin has been shown to have physiological effects in vitro assays, including an increase in glucose uptake by cells after injection of glucose into the cell culture medium.</p>

<p>Raltegravir is an HIV protease inhibitor that belongs to the class of glycosylated polymers. This compound is synthesized by a click modification of d-glucose with a methyl group and then fluorinated. The sugar moiety is attached to the backbone through a glycosyl linkage, which results in the formation of a complex carbohydrate. Raltegravir b-D-glucuronide methyl ester is soluble in water, alcohols, and organic solvents. It has been shown to be active against HIV type 1 strains resistant to other drugs. The synthesis of this compound was custom designed for high purity and high yield.</p>

<p>3-hydroxy-L-aspartic acid is a non-protein amino acid that is found in mammalian tissue and has been shown to have structural and functional similarities to glutamate. It is involved in the metabolism of energy, such as the synthesis of fatty acids and epidermal growth factor. 3-Hydroxy-L-aspartic acid also binds to calcium ions, which may be due to its carboxylate group. This compound does not have a disulfide bond, unlike many other amino acids.<br>3S)-3-Hydroxy-L-aspartic acid can be used as a monoclonal antibody for the detection of pseudobactin, an antibiotic secreted by Pseudomonas bacteria that inhibits protein synthesis in eukaryotes.</p>

<p>6-Chloro-6-deoxy-D-glucitol is a synthetic sugar, in which the D-glucose moiety has been substituted with a 6-chloro group. It is an important precursor for the synthesis of many complex carbohydrates and polysaccharides. The product can be used as a methylating agent to modify saccharides, oligosaccharides, and polysaccharides. The product is also used to modify sugars by glycosylation, fluorination, or click chemistry. In addition, this product can be used as a starting material for the synthesis of other sugars via glycosylation or fluorination.</p>

<p>2-Amino-2-deoxy-D-lyxose is a sugar that is commonly found in nature. It is an isomaltose and a galactitol, which are both forms of sugar alcohols. 2-Amino-2-deoxy-D-lyxose can be found in acid hydrolysates and arabinitol, which are the products of the hydrolysis of starch. It has been shown to have inhibitory effects on the metabolism of glucose and to regulate the blood glucose levels due to its ability to stimulate insulin secretion. This compound also has an effect on logarithmic growth phase in bacteria, as it inhibits cell growth. 2-Amino-2-deoxy-D-lyxose can be used as a chromatographic stationary phase with glycolaldehyde, which is another sugar alcohol that binds strongly to the column matrix. This compound also has an effect on galacturonic acid, ion exchange</p>

<p>a-Glucametacin is a methylation of glucosamine. It is a polysaccharide that consists of glycosylated and non-glycosylated saccharides. The glycosylation pattern can be customized to suit the needs of the customer, as well as being synthesized to have no glycosylation at all. This compound also has fluorination on its sugar ring, which may be beneficial for certain applications.</p>

<p>Isopropyl-β-D-thioglucopyranoside is a hydrogen bond donor that has been shown to inhibit the glyceraldehyde-3-phosphate dehydrogenase enzyme, which is involved in lipid biosynthesis. It has been used for the diagnosis of malariae and has potential as a biomarker for diagnosing human tissues. Isopropyl-β-D-thioglucopyranoside may be useful in the study of protein synthesis, due to its ability to bind to recombinant proteins and block the formation of intermolecular hydrogen bonds. Isopropyl-β-D-thioglucopyranoside is also expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell growth in culture.</p>

<p>Colitose is a sugar that has antimicrobial properties. It is a monosaccharide, which means it contains six carbon molecules. Colitose has been shown to inhibit bacterial growth and to prevent the development of resistant mutants in human serum. Colitose has also been shown to have therapeutic potential for infectious diseases such as bowel disease and other inflammatory bowel diseases. The structural analysis of colitose revealed that it contains terminal residues at the end of each chain, which are composed of glucose, galactose, and mannose. The glycan chains are linked together by alpha-1,6-glycosidic bonds. These terminal residues serve as a receptor for Toll-like receptors (TLRs), which are found on cells in the bowel wall and help regulate inflammation.</p>

<p>α-D-Glucosamine 1-phosphate is a methylated and glycosylated carbohydrate that is synthesized from glucose. It can be used as a building block for the synthesis of polysaccharides, such as chitin and cellulose. α-D-Glucosamine 1-phosphate can also be modified by fluorination to produce an active form with potent anticancer activity.</p>

<p>L-Glucuronic acid sodium salt is a natural product that is used as an excipient and additive in pharmaceuticals. L-Glucuronic acid sodium salt is the sodium salt of L-glucuronic acid, which is a natural compound found in plants, animals and humans. It is used as a protective agent for drugs because it can be easily metabolized by the liver and has low toxicity. L-Glucuronic acid sodium salt inhibits the uptake of radioactive isotopes into cells, which may be due to its ability to bind to cytosolic proteins. The binding of L-glucuronic acid sodium salt to these proteins blocks the binding sites for radioactive isotopes on these proteins. This inhibition leads to reduced uptake of radioactive isotopes by cells.</p>

<p>Topiramate dimer impurity is a Glycosylation, Oligosaccharide, sugar, Synthetic, Fluorination, Custom synthesis, Methylation, Monosaccharide that is custom synthesized and is available as a high purity and complex carbohydrate. It has a CAS No. 35405-70-0 and is available in Click modification. This product is used to modify polysaccharides or saccharides by click chemistry reactions.</p>