Monossacáridos

<p>1-Octylamino-1-deoxy-D-glucitol is a natural product that is extracted from the bark of the tree Streptomyces griseorubens. It has been shown to have a diastereomeric ratio of 97:3 and an optical purity of 98%. The thermodynamic properties of this compound are determined by the reaction time, which can vary from 1 to 24 hours. The enantiomers are separated by chromatography or crystallization, and the solubility data is determined at 25°C.</p>

<p>Used for the synthesis of 1β-O-acyl glucuronides</p>

<p>Thymol-b-D-glucopyranoside is a bactericidal agent that is resistant to encapsulation. It has been shown to be effective against animals and typhimurium in an incubated population and endogenous deaminase inhibitor strategy. The porcine activated food chemistry and abattoir experiments show that thymol-b-D-glucopyranoside has the potential to reduce populations of bacteria in the gastrointestinal tract by inhibiting protein synthesis.</p>

<p>3,4,6-Tri-O-acetyl-D-galactal is a versatile building block used for the synthesis of mono- and oligosaccharides. The galactal double bond affords a ready means through which to introduce new functionality or introduce deoxy positions at the C1 and C2 positions to afford functionalised monosaccharides and also allows galactals to be used as glycosylation donors.</p>

<p>UDP-6-azido-6-deoxy-D-glucose is a chemical building block that is used for saccharide synthesis. The azide group can be reduced to give the amine which has been used to make a fluorescent tag for 5-(hydroxymethyl)cytosine in DNA. UDP-6-azido-6-deoxy-D-glucose has also been used to synthesise siderophore conjugates which can be used to deliver functional reagents across bacterial cell membranes.</p>

<p>D-Glucono-1,5-lactone is a chemical compound that is a member of the class of compounds known as diketones. It can be used in chemical biology and polymer chemistry to probe hydrogen bonding interactions, polymer compositions, and redox potentials. D-Glucono-1,5-lactone has been shown to inhibit the growth of cells in culture by inhibiting DNA synthesis. This inhibition is due to its ability to bind with high affinity to nucleic acids and prevent the formation of the enzyme complexes required for transcription and replication. The effects are reversible.</p>

<p>Ginsenoside F1 is a natural compound found in ginseng. It is believed to have anti-cancer properties. Ginsenoside F1 has been shown to inhibit the proliferation of HL-60 cells and have an apoptotic effect by regulating mitochondrial membrane potential and activating the apoptotic pathway. The mechanism of action for the anti-cancer activity of Ginsenoside F1 may be due to its ability to inhibit angiogenesis, which is needed for cancer cell proliferation. Ginsenoside F1 also inhibits the growth of skin cancer cells in mice by regulating microvessel density. This compound has been found in foods such as soybeans, rice, peanuts, and kiwifruit.</p>

<p>Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an enzyme that catalyzes the conversion of glyceraldehyde-3-phosphate to 1,3 bisphosphoglycerate. GAPDH is involved in glycolysis and the pentose phosphate pathway. It has been shown to be an important player in mediating cellular responses to hypoxia, inflammation, and oxidative stress. The glyceraldehyde-3-phosphate dehydrogenase gene has been found to be mutated in a number of cancers including breast cancer and colon cancer. This gene also has a role in inflammatory lesion development as well as energy metabolism. GAPDH also participates in the biochemical reactions that lead to neuronal death during neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease.</p>

<p>Propargyl a-D-glucopyranoside is a high purity custom synthesis sugar. It is synthesized by Click modification, fluorination, and glycosylation followed by methylation. Propargyl a-D-glucopyranoside can be used for the modification of oligosaccharides and monosaccharides to produce complex carbohydrates.</p>

<p>D-Arabinaric acid dipotassium salt is a custom synthesis with complex carbohydrate, which can be modified by methylation, glycosylation, and carbonylation. It has CAS number 6703-05-5 and a high purity. This product is also fluorinated, which makes it an excellent synthetic reagent.</p>

<p>D-Glucose 3-sulfate sodium salt is a fluorinated, monosaccharide that can be used as a synthetic, oligosaccharide or complex carbohydrate. It is custom synthesized with glycosylation and polysaccharides and has been shown to be useful in click modification. D-Glucose 3-sulfate sodium salt is also methylated and sugar modified. The CAS number for this product is 89830-83-1. It has high purity and can be purchased at any lab supply store.</p>

<p>Phloridzin is a phenolic acid that is found in the cell walls of plants. It has been shown to be a potent antioxidant, with anti-inflammatory and anti-tumour properties. Phloridzin is also an inhibitor of the divalent metal ion-dependent diphenolase activity that causes oxidative DNA damage. The dihydrate form of phloridzin has been shown to inhibit cisplatin-induced nephrotoxicity in mice by reducing oxidative stress.</p>

<p>1,2,3,4,5-Penta-O-acetyl-β-D-fructose is a synthetic oligosaccharide that is modified with fluorine to produce a variety of products. This product is used in the synthesis of complex carbohydrates and has been shown to have high purity. It is used for methylation reactions and can be found in saccharides and polysaccharides. The CAS number for this compound is 20764-61-8.</p>

<p>Methyl 2,3-O-isopropylidene-β-D-ribofuranoside is a heterocycle that is classified as a furanose. It reacts with reactive compounds such as nitro groups to form nitrofurans. This compound also has carcinogenic properties and has been shown to be an animal carcinogen. Methyl 2,3-O-isopropylidene-β-D-ribofuranoside is also capable of forming conformationally constrained derivatives in which the carbonyl group adopts an α,α'-diaxial orientation with the adjacent nitrogen atom and can be used for synthesis of phenalenes.</p>

<p>N6-Benzyladenine-7-glucoside is a benzyladenine derivative that is the major precursor of dihydrozeatin, an important plant growth regulator. N6-Benzyladenine-7-glucoside has been shown to be a potent inhibitor of the uptake of radioactive n6-benzyladenine in tobacco leaves. It also inhibits the uptake of radioactive adenine and guanine in tabacum l. explants and tissues. The compound can inhibit cell division by interfering with hormonal treatments that promote growth and development. The inhibition of cell division may be due to interference with the auxin transport system in plants, which leads to decreased levels of endogenous auxins and growth regulators, such as cytokinins, gibberellins, abscisic acid, and ethylene.</p>

<p>1,2,3,4-Tetra-O-benzyl-β-D-glucopyranoside is a prodrug that becomes active after acetylation. It is an endogenous compound that has been shown to inhibit the synthesis of myelin and lipid peroxidation in rat brains. This drug has also been found to be effective in the treatment of amyotrophic lateral sclerosis (ALS). 1,2,3,4-Tetra-O-benzyl-β-D-glucopyranoside is unmodified and does not have any side effects on the nervous system. It can be used for the treatment of Parkinson's disease when combined with levodopa.</p>

<p>Muco-Inositol is a compound that is involved in the metabolism of glucose, lipid and protein. It can be synthesized from myo-inositol and plays an important role in the synthesis of phosphatidylinositols. Muco-Inositol has been shown to inhibit enzyme activities in a wild type strain of E. coli. This inhibition may be due to its ability to bind to the active site of these enzymes, thereby inhibiting their activity. Muco-Inositol also inhibits the growth of ovarian cancer cells, as well as myo-inositol levels in maternal blood.</p>

<p>Building block for galectin-3 inhibitors based on 3’-modified LacNAc</p>

<p>L-Gulonic acid-1,4-lactone is an ascorbic acid derivative that inhibits the production of matrix metalloproteinases (MMPs) and other enzymes. L-Gulonic acid-1,4-lactone has been shown to inhibit the activity of MMPs in hl-60 cells, which may be due to its ability to chelate metal ions, such as zinc and copper. This molecule also has a stabilizing effect on collagen type I because it prevents cross linking between lysine amino acids. The discovery process for this molecule was found by screening clones from a cDNA library with biochemical properties similar to those of ascorbic acid. This molecule has been shown to inhibit the activation of protein kinase C (PKC) and phosphorylation of extracellular signal regulated kinase (ERK). L-Gulonic acid-1,4-lactone is metabolized through plant metabolism</p>

<p>2-Hydroxydesipramine glucuronide is a metabolite of desipramine, which is a tricyclic antidepressant that inhibits the uptake of noradrenaline and 5-hydroxytryptamine. 2-Hydroxydesipramine glucuronide is formed by conjugation with glucuronic acid. It has been found in human urine and has been proposed as a biomarker for the clinical monitoring of patients taking desipramine. The pharmacological effects of 2-hydroxydesipramine glucuronide are similar to those of desipramine, but it is less potent and selective than its parent compound. This metabolite also has biliary excretion properties, which may be due to its small molecular size.</p>

<p>3-Deoxy-D-galactopyranose is a galectin that has been synthetically produced. It has shown to be an antagonist of galactoside, which may be useful in the treatment of type 2 diabetes. The synthetic method for this molecule is still being developed.</p>

<p>The chemical profile of the methyl ester (Z)-3-hexen-1-yl b-D-glucopyranoside has been determined using high performance liquid chromatography. The compound is an anti-fungal agent and its main pharmacological effects are related to radical scavenging activity. It shows possible neuropharmacological activity, but further studies are required to confirm this. The chemical profile of Z)-3-hexen-1-yl b-D-glucopyranoside was found to be different from that of other compounds in the genus. This compound belongs to a group of compounds called aldehydes, which is characterized by methoxy and dimethoxy substitutions on the benzene ring. The compound is used in traditional Chinese medicine for the treatment of scopolin or codonopsis radix, which are two types of chinese medicinal herbs.</p>

<p>4-Methoxyphenyl 3-O-allyl-2-azido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside (MPA) is a glycosylated antigen that has been shown to be specific for mycobacterium avium. It is a cytosolic calcium ionophore and can induce platelet membrane activation and coagulation. MPA has also been found to be chemoprotective in animal models of cancer. MPA can be used as an indicator of the body mass index (BMI).</p>

<p>Hexadecyl-D-xylopyranoside is a synthetic sugar that has been fluorinated and methylated. It is a complex carbohydrate that belongs to the group of modified sugars. This product has many applications in the synthesis of oligosaccharides and saccharides, as well as in glycosylation reactions. Hexadecyl-D-xylopyranoside can be used in custom syntheses, and has been shown to have high purity with a CAS No. 115211-19-3.</p>

<p>Keratin-reducing component in cosmetic applications; used in Glc conjugation</p>

<p>2,4-Di-O-methyl-D-glucose is a partially O-methylated glucose sugar.</p>

<p>Xylitol is a sugar alcohol that has been shown to have antimicrobial properties. It is also used as a sweetener in chewing gum and toothpaste. Xylitol inhibits the growth of bacteria by binding to the enzyme adenosine triphosphate (ATP) synthase, which is required for energy metabolism. The binding of xylitol to ATP synthase prevents the formation of ATP and blocks bacterial growth, leading to cell death. Xylitol can be produced from xylose, a sugar found in plants and animals, through biochemical reactions that are catalyzed by enzymes such as xylitol dehydrogenase and xylulokinase. This process is anaerobic and does not require oxygen or organic nutrients. Xylitol has been shown to have physiological effects on wild-type strain bacteria such as Aerobacter aerogenes.</p>

<p>Methyl a-L-fucopyranoside is a natural product that has been shown to have many biological effects, including antioxidant and anti-inflammatory properties. It has been shown to inhibit the growth of bacteria by binding to the ribosome, preventing protein synthesis and cell division. The compound has also been shown to have anti-inflammatory effects in mice with inflammatory bowel disease. Methyl a-L-fucopyranoside inhibits the production of pro-inflammatory cytokines, such as interferon alfa-2b (IFNα2β), which is induced by IFNγ. This inhibition of IFNα2β activity may be due to methyl a-L-fucopyranoside's ability to bind to cytosolic calcium and inhibit its transport into the nucleus. Methyl a-L-fucopyranoside also blocks the production of antimicrobial peptides, such as defensins or cathelicidins.</p>

<p>Diethoxy phosphonyl 4,7,8,9-tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is a glycosylation agent that is used in the synthesis of complex carbohydrates. It is a methylated derivative of 4,7,8,9 tetra-O-acetyl neuraminic acid and can be used to modify the polysaccharide structure. This product has been shown to react with saccharides and oligosaccharides in a click reaction to produce fluorinated derivatives. Diethoxy phosphonyl 4,7,8,9 tetra-O-acetyl neuraminic acid methyl ester is also available as a custom synthesis.</p>

<p>2-Azido-2-deoxy-L-glucopyranose is a Custom synthesis, modification and fluorination of methylated glucopyranosides. This compound has been shown to be effective in the synthesis of mono-, oligo-, and polysaccharides. 2-Azido-2-deoxy-L-glucopyranose is used for the preparation of glycosylation reagents. It can also be used to modify saccharide chains with azide or alkyne functionalities. 2-Azido-2-deoxy-L-glucopyranose is an important building block for the synthesis of complex carbohydrates, such as polysaccharides, glycosylation reagents, and click chemistry compounds.</p>

<p>1,2,3,4,6-Penta-O-acetyl-b-D-glucopyranose, also known as beta-D-glucose pentaacetate, has high chemical stability and long shelf life. This protected form of glucose is a key building block of any chemical synthesis of glucose-containing oligosaccharides or glycoconjugates. In the presence of Lewis acids it can be used as a glycosyl donor to make simple glycosides. In order to perform more complex glycosylations, it can be converted into more reactive donors, such as glycosyl halides or thioglycosides. Beta-D-glucose pentaacetate is also used as a food additive and flavouring agent.</p>

<p>N-Methyldeoxynojirimycin is a monoclonal antibody that is a competitive inhibitor of the melanoma antigen gp75. It is also an inhibitor of oligosaccharide synthesis and has been shown to have anti-inflammatory properties. N-Methyldeoxynojirimycin binds to the golgi alpha-mannosidases, preventing them from processing high-mannose type oligosaccharides. This leads to decreased chemoattractant protein production by neutrophils, which are important in the inflammatory process. N-Methyldeoxynojirimycin has also been shown to inhibit myocardial infarct size and glomerular filtration rate in rats, as well as increase biochemical markers for inflammation, such as α subunit of α1 acid glycoprotein and basic fibroblast growth factor.</p>

<p>Genistin is an isoflavone found in soybeans and other plants. It has antioxidative properties, which may be due to its ability to scavenge free radicals. Genistin also has protein-binding activity, and it can inhibit the growth of certain insects by binding to their DNA. Genistin can also bind to a number of enzymes and affect their activities, including amylase, chymotrypsin, trypsin, and lipase. It is also involved in energy metabolism and protein synthesis. The physiological effects of genistin are not well understood but may be related to its ability to act as a phytoestrogen or mimic estrogen.</p>

<p>Methyl 3,5-di-O-(p-chlorobenzoyl)-a-D-ribofuranoside is an organic compound. It is a synthetic product that is used in the synthesis of saccharides and polysaccharides. This chemical can be modified with Click chemistry to create a glycosylate or fluorinated complex carbohydrate. The compound has CAS number 62700-92-3 and can be custom synthesized to meet customer specifications.</p>

<p>2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-Fmoc serine is a protein that belongs to the group of bifunctional glycosides. It is used in recombinant virus production as a component of the viral coat protein (VP). 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-Fmoc serine binds to tyrosine kinase receptors and inhibits their activity. This inhibition prevents cell adhesion and migration and can cause tumor regression in some cancers. 2,3,4,6-Tetra-O-acetyl-b-D--glucopyranosyl--Fmoc serine also has antiviral activity due to its ability to inhibit the replication of viruses containing RNA genomes.</p>

<p>Substrate for glucuronosyltransferases</p>

<p>3,5,6-Trichloro-2-pyridinol b-D-glucuronide is a synthetic glycosylate that has been modified by fluorination and methylation. It is used as an intermediate in the manufacture of a variety of saccharides and oligosaccharides. The sugar has been synthesized to have a high purity. 3,5,6-Trichloro-2-pyridinol b-D-glucuronide is a complex carbohydrate that can be modified using click chemistry. Click chemistry is a modification technique that uses copper (II) ions as catalysts for the formation of carbon–carbon bonds. This process can be used to modify saccharides and oligosaccharides with functional groups such as amines, thiols, alcohols, carboxylic acids, or nitriles.</p>

<p>6-Chloro-6-deoxy-D-glucose is a sugar that is used as a carbon source in the process of spermatozoa production. It has been shown to increase the fertility of animals by increasing the uptake of phosphorus pentachloride and ganglion cells in the testes. This drug also has contraceptive and antifertility effects, which may be due to its ability to inhibit the uptake of adenine nucleotide in cells. 6-Chloro-6-deoxy-D-glucose may have a role in ATP levels, with intracellular levels being higher than those in control analysis.</p>

<p>3-Deoxypentulose is a kinetic, reactive and chromatographic compound that belongs to the family of glycolysis. It is present in small amounts in the blood and is derived from pentose sugars. The reaction mechanism of 3-deoxypentulose can be divided into two steps: glyoxal formation and hydroxide solution modification. In the first step, 3-deoxypentulose reacts with glucose to form glyoxal. In the second step, 3-deoxypentulose reacts with hydroxide solution to form galactose, which can further react with other compounds or be modified by enzymatic reactions. This compound has been used as a tagatose substitute in food products and as an oligosaccharide modifier. Recently, it has been shown that 3-deoxypentulose may be used as a chemical probe for studying glycolic acid synthesis in bacteria.</p>

<p>3,4,6-Tri-O-benzyl-D-galactal is a hydrogen bond donor and has been shown to have physiological activities. It was found to increase the number of lymphocytes in unimmunized mice. It also inhibits the growth of psoralea virus. The glycosidic bond between 3,4,6-tri-O-benzyl-D-galactal and glucose produces a product with an acetylated hydroxyl group and an aldehyde group. This type of bond is stereoselective and benzofuran derivatives are formed from the reaction. 3,4,6-Tri-O-benzyl-D-galactal has been shown to have anticancer activity against cancer cells in laboratory experiments.</p>

<p>1,3,6-Tri-O-galloylglucose is an extract of the fruit of Terminalia catappa and Terminalia citrina. It has been shown to have antimicrobial activity against a variety of bacteria and fungi. The antimicrobial activity may be due to its ability to chelate metal ions or inhibit their activities. Punicalagin also has tannin content, which may contribute to its antimicrobial properties.</p>

<p>DNA-binding agent</p>

<p>2,3,4-Tri-O-benzyl-D-glucopyranose is a thioglucoside that can be synthesized from D-glucose and benzyl bromide. This compound is a protonated nucleophile with a hydroxyl group that can interact with the sulfur of a thiol or disulfide group. The interaction between 2,3,4-tri-O-benzyl-D-glucopyranose and S. aureus has been shown to be dependent on the concentration of 2,3,4 tri O benzyl glucopyranose. The reaction between this compound and oligosaccharides led to the formation of dioxane ring structures that were hydrophobic.</p>

<p>UDP-2-deoxy-2-fluoro-D-galactose is a methylated and fluorinated saccharide that is used in click chemistry. It is a synthetic compound that can be custom synthesized to create polysaccharides or oligosaccharides. This product has high purity and can be modified with glycosylation, methylation, and other modifications.</p>

<p>4-Methoxyphenyl a-D-mannopyranoside is a fluorinated monosaccharide. It is synthesized by the reaction of 4-methoxyphenol with an aldose in the presence of sodium hydroxide and sulfuric acid. The product is purified by chromatography with silica gel and eluted with methanol. This compound is also used to produce polysaccharides, glycosyls, oligosaccharides, or complex carbohydrates through glycosylation or polysaccaride synthesis. 4-Methoxyphenyl a-D-mannopyranoside can be modified to produce methylated, acetalized, or deoxygenated derivatives for use in click chemistry reactions.</p>

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

<p>3,4,6-Tri-O-acetyl-2-O-trifluoromethanesulfonyl-b-D-mannopyranosyl azide is a chemically synthesized compound that can be used for methylation reactions. It is an Oligosaccharide with a molecular weight of 597.5 and contains the following structural features: A saccharide composed of three monosaccharides (D-glucose, D-mannose, and D-galactose), which is bonded by alpha 1,6 linkages. The chemical formula is C12H14F3N3O8. The CAS number is 1159265-99-2.</p>

<p>D-Ribopyranosyl amine is a heterocyclic compound that can be synthesized from ethyl formate and thiourea. The synthesis of this compound has been studied using techniques such as hydrogen bonding, high yield, and optical rotation. D-Ribopyranosyl amine is an aminoimidazole derivative with a decarboxylation reaction to produce uridine. This process can be carried out in acetone or dimethylformamide solvent, which produces the α-form of the molecule. The 1H NMR spectra of D-ribopyranosyl amine have peaks at 3.8 ppm, 2.5 ppm, and 2.0 ppm, while the 13C NMR spectrum peaks are found at 79.2 ppm and 131.9 ppm</p>

<p>Methyl L-fucopyranoside is a saponin glycoside that has been shown to have anti-tumor effects. It acts by binding to the nucleophilic sites on the cancer cells and inhibits their growth. The molecule is chiral, which means that it can exist in two different forms, or enantiomers. The structure of this compound has been determined using vibrational spectroscopy and nuclear magnetic resonance (NMR) spectroscopy. It is also a synthetic product that can be made from an acid catalyst and an oligosaccharide molecule. Methyl L-fucopyranoside has been shown to inhibit glycoconjugates and muscari alkylation, as well as having liquid chromatographic properties.</p>

<p>1,3,5-Tri-O-benzoyl-2-O-(1H-imidazole-1-sulfonate) a-L-arabinofuranose is a methylated and modified arabinofuranose. It is one of the most common monosaccharides in nature. This compound is an important component of polysaccharides such as cellulose and starch. 1,3,5-Tri-O-benzoyl-2-O-(1H-imidazole-1-sulfonate) aL arabinofuranose is used to create saccharide derivatives that are widely used in the pharmaceutical industry.</p>

<p>Substrate for N-acetylgalactosaminyltransferases</p>

<p>2,3,4,6-Tetra-O-benzyl-D-mannopyranose is a trisaccharide that consists of two covalently linked glycosyl acceptors and one galacto moiety. This molecule is synthesized by chemoenzymatic synthesis and can be found in the biosynthesis of trehalose. 2,3,4,6-Tetra-O-benzyl-D-mannopyranose is an anomeric form of D-glucopyranose. The anomeric form is determined by the orientation of the hydroxyl group at C1' with respect to the anomeric carbon atom at C2'. This molecule has been isotopically labelled with 13C and 15N for use in studies on carbohydrate metabolism.</p>

<p>L-Arabinaric acid dipotassium salt is a custom synthesis of an L-arabinaric acid, which is a monosaccharide that is found in the cell wall of bacteria. This compound has been modified to be resistant to fluorination, methylation, and click chemistry. The modification process includes the use of Oligosaccharides, saccharides, and polysaccharides as well as glycosylation and sugar. L-Arabinaric acid dipotassium salt can also be used for the synthesis of complex carbohydrates.</p>

<p>N-Propanoyl mannosamine is a biochemical that belongs to the group of glycoconjugates. It is an intracellular messenger that modulates the concentration of intracellular calcium and controls the release of gamma-aminobutyric acid (GABA). N-Propanoyl mannosamine has been shown to stimulate axonal growth in cell culture, which is mediated by the polysialic acid receptor. This molecule also has a role in human osteoblast differentiation and bone formation.<br>N-Propanoyl mannosamine can be synthesized from dopamine and erythrose via a series of reactions involving acidification, oxidation, reduction, and decarboxylation. The synthesis of this molecule requires blood group O as an acceptor.</p>

<p>D-Sorbose is a monosaccharide that belongs to the group of sugar alcohols. It is a reducing sugar that can be used as an alternative for sugar in food and pharmaceutical industries. D-Sorbose has been shown to have potential industrial applications due to its high solubility, low melting point, and resistance to crystallization. The enzyme ribitol dehydrogenase from Escherichia coli was found to be active with D-sorbitol, but not with l-sorbitol. This indicates that D-sorbitol is a better substrate for this enzyme than L-sorbitol.</p>

<p>3-O-Acetyl-4-O-methyl-D-glucuronic acid is a custom synthesis that is used in the preparation of oligosaccharides and polysaccharides. It has been modified by fluorination, which increases its stability. 3-O-Acetyl-4-O-methylglucuronic acid can be used to synthesize saccharides and carbohydrates as well as to modify monosaccharides and sugars. This product is available at high purity with a CAS number.</p>

<p>2,3,5-Tri-O-benzyl-b-D-arabinofuranose is a stereoselective analog that inhibits human maltase glucoamylase and acetylation. It is also a potent nucleophile that reacts with the hydroxyl group of dimethyl fumarate to form an acetal linkage. This compound is used in the stereoselective synthesis of oligosaccharides and carbohydrates.</p>

<p>Ginsenoside Ft1 is a saponin and bioactive compound, which is derived from the roots of Panax notoginseng, a plant known for its traditional medicinal uses. The mode of action of Ginsenoside Ft1 involves multiple biochemical pathways, including the modulation of signaling pathways related to inflammation, apoptosis, and angiogenesis. Its ability to influence these pathways underpins its potential therapeutic applications.</p>

<p>Inhibitor of Gal-dependent lectin binding; used in synthesis of galactoses</p>

<p>D-Idose is a single-enantiomer sugar with a pyranose ring and an enantiomeric configuration. It is used in the treatment of bacterial infections and has been shown to be effective at inhibiting the growth of bacteria that are resistant to beta-lactam antibiotics, such as methicillin-resistant Staphylococcus aureus (MRSA). D-Idose is active against bacteria that do not produce beta-lactamase enzymes, such as Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>Intracellular form of GlcNAc; substrate for GlcNAc-phosphate deacetylase</p>

<p>Benzyl 2-acetamido-2-deoxy-6-O-trityl-a-D-glucopyranoside is a glycosylation of benzyl 2,3,4,6-tetraacetamido-2,3,4,6-tetra deoxyglucopyranoside. It is a complex carbohydrate that can be modified with methyl groups or fluorine atoms. This product is often used in Click chemistry and as a building block for oligosaccharides and polysaccharides. Benzyl 2-acetamido-2-deoxy 6O trityl a D glucopyranoside has CAS number 33493 71 9 and can be custom synthesized to meet individual requirements.</p>

<p>3-Deoxy-D-glucosone is a compound that belongs to the group of monosaccharides and has a basic structure. It can be found in many types of biological samples, including blood. The x-ray diffraction data for 3-deoxy-D-glucosone shows an asymmetric unit of two molecules with a coordination geometry of 2.3. This compound is known to have high protein oxidation rates, which are caused by dna binding activity. 3-Deoxyglucosone has been shown to be involved in the pathogenic mechanism of many types of cancers.</p>

<p>Mycophenolic acid acyl-b-D-glucuronide is a prodrug of mycophenolic acid that is metabolized by esterases to its active form. This compound has been shown to inhibit the activity of drug receptors, including those for immunosuppressants and anticonvulsants. Mycophenolic acid acyl-b-D-glucuronide has also been found to have a matrix effect on the concentration–time curve of other drugs in human serum. This drug is used for the treatment of bowel disease, autoimmune diseases, and for the prevention of organ transplant rejection. It can be administered orally or intravenously and has been shown to be well tolerated with few adverse effects.</p>

<p>Methyl 3,5-di-O-benzyl-D-xylofuranoside can also be used as an intermediate in the synthesis of other xylo or oligo related compounds.</p>

<p>Penta-O-benzoyl-D-glucopyranoside is a carbohydrate that has been prepared in a preparative scale. It is an organic compound and the structural formula is C12H22O11. The diameter of this molecule is around 1.5 nm, which makes it mesoporous. Penta-O-benzoyl-D-glucopyranoside has been analysed by high performance liquid chromatography (HPLC) and mass spectrometry (MS). The tree ring processability of this product is good and can be processed thermally.</p>

<p>a-D-Mannose-1-phosphate dipotassium salt (DMDK) is a synthetic oligosaccharide that was designed and synthesized for use as a potential drug in the treatment of cancer. DMDK has been shown to be an inhibitor of protein glycosylation, which may lead to the prevention of tumor formation. It also has anti-inflammatory properties and can inhibit the growth of bacteria by binding to bacterial 16S ribosomal RNA and inhibiting protein synthesis.</p>

<p>1,2,3,6-Tetra-O-benzyl-β-D-glucopyranoside is a synthetic compound that is produced by the modification of natural sugars. It was first synthesized by a team of chemists led by Professor Robert Burns Woodward. This molecule has been modified with methyl groups and fluorine atoms to improve its stability and to provide a more convenient method for its analysis. 1,2,3,6-Tetra-O-benzyl-β-D-glucopyranoside can be used in the synthesis of oligosaccharides and polysaccharides.</p>

<p>1,3,5-Tri-O-benzoyl-2-deoxy-2-bromo-alpha-L-arabinofuranose is a complex monosaccharide that can be used as a building block in the synthesis of various compounds. It is a derivative of the sugar arabinose, with the addition of benzoyl and bromo groups at specific positions. The compound has potential applications in the fields of organic chemistry and medicinal chemistry and is available for research.</p>

<p>N-Acetyl-2,3-dehydro-2-deoxyneuraminic acid methyl ester (NAD) is a natural product that is produced by the human body. NAD has been shown to induce apoptosis in cancer cells and modulate gene expression. This compound also plays a role in the development of stem cells, which are important for tissue regeneration. NAD has been shown to have therapeutic effects on paraplegia and angiogenesis. It also has anti-inflammatory properties that may be related to its ability to regulate mesenchymal stem cells.</p>

<p>Lumiracoxib acyl-b-D-glucuronide is a synthetic compound that is a derivative of the nonsteroidal anti-inflammatory drug lumiracoxib. It has been shown to be effective as an inhibitor of inflammation and pain in animal models, with no significant toxic effects on the liver or kidney. Lumiracoxib acyl-b-D-glucuronide is a white powder that can be synthesized by glycosylation and modification of lumiracoxib. This compound is soluble in water and ethanol, but insoluble in ether.</p>

<p>Inhibitor of β-galactosidase</p>

<p>L-Fucitol is a sugar that is found in the form of D-arabinose and D-xylitol. It is used in flow systems for the detection of herpes simplex virus type 1 (HSV1) glycoproteins and can be used to measure xylitol dehydrogenase activity. L-Fucitol has been shown to inhibit the growth of bacteria that are resistant to penicillin, ampicillin, and erythromycin. L-Fucitol also inhibits enzymes such as galactocerebrosidase, which breaks down galactocerebroside, a myelin constituent. This inhibition leads to accumulation of galactitol, an inhibitor of oligosaccharide synthesis. L-Fucitol also inhibits enzyme activities such as glycosidases and glycosyltransferases, which affect metabolic profiles by inhibiting the breakdown or synthesis of sugars. L-Fucitol is a monosac</p>

<p>L-Gluconic acid calcium salt is a white crystalline powder. It is soluble in water and slightly soluble in alcohol. The structure of this compound has not been fully elucidated, but it is known to be a modification of L-gluconic acid, which is a monosaccharide. This product can be used as a biochemical reagent for the synthesis of oligosaccharides and polysaccharides.</p>

<p>2,3,4,6-Tetra-O-benzyl-1-deoxynojirimycin hydrochloric acid salt is a synthetic monosaccharide. It was originally synthesized by the methylation of a native oligosaccharide before being subjected to click chemistry. The resulting product is a complex carbohydrate with an aromatic ring in place of the sugar alcohol moiety. 2,3,4,6-Tetra-O-benzyl-1-deoxynojirimycin hydrochloric acid salt has CAS number 72983-76-7 and is soluble in water. This product is also available as a custom synthesis service and can be modified to meet your needs.</p>

<p>Isorhamnetin 3-O-galactoside is a flavonoid derivative that is found in plant tissue. It has antioxidant properties and has been shown to inhibit leucaena seed germination, growth, and the production of reactive oxygen species (ROS). Isorhamnetin 3-O-galactoside can be extracted from fruit by using an aqueous solution of potassium hydroxide. It is also used as a dietary supplement for its potent inhibitory activity on ROS. Isorhamnetin 3-O-galactoside is found in plants with other flavonoids such as quercetin and kaempferol. The chemical structure of this compound consists of a hydroxyl group at the C3 position and an O-glycosidic linkage to galactose at the C2 position. This compound can be detected by mass spectrometric methods such as electron ionization or electrospray ionization because it</p>

<p>Important resource for RNA- and DNA-related syntheses including ribosylation</p>

<p>Streptamine derivative; antibiotic agent</p>