Monossacáridos

Please enquire for more information about 4-Methylphenyl 4,6-o-benzylidene-2,3-di-o-(4-methoxybenzyl)-β-D-thiogalactopyranoside including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about D-Glucose-1,3-13C2 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Heptamaloxyloglucan is an analog of marbofloxacin that has been shown to inhibit tumor growth and induce apoptosis in cancer cells. This compound acts as a kinase inhibitor, blocking the activity of enzymes involved in cell division and proliferation. Heptamaloxyloglucan has also been found to have anticancer properties, inhibiting the growth of cancer cells and inducing apoptosis through various mechanisms. In addition, this compound has been shown to be effective in treating urinary tract infections caused by gram-negative bacteria such as Escherichia coli and Proteus mirabilis. Heptamaloxyloglucan may also have potential therapeutic applications for other diseases such as hypertension, as it has been found to be a potent inhibitor of ACE (angiotensin-converting enzyme) activity.</p>

<p>Methyl a-L-arabinopyranoside is an organic compound that has resonance configurations and can exist in two different stereoisomers. It can be synthesized by reacting 1,2-dichloroethane with glycerol and aqueous sodium hydroxide. The ethers of methyl a-L-arabinopyranoside are catalytic oxidation epoxides. Magnetic resonance analysis of the molecule has been done using nuclear magnetic resonance (NMR).<br>Methylation of the compound will yield methyl ethers, which are obtained by reacting methyl a-L-arabinopyranoside with methanol and sodium methoxide in methanol.</p>

<p>4-Methylphenyl 2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is a synthetic saccharide set up to be an oligo-saccharide building block.</p>

<p>2,3,4,6-Tetra-O-benzoyl-D-galactopyranosyl trichloroacetimidate is a fluorinated carbohydrate that can be used for synthesis of complex carbohydrates. It is a monosaccharide with an O-benzoyl group at the 2 position and a glycosylation at the 4 position. The chemical structure has been modified by a reaction with trichloroacetimidate to form an acetal linker. This product is available in both custom synthesis and high purity.</p>

<p>Please enquire for more information about D-Xylose-1-C-D including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,6, 2,3-Dianhydro-beta-D-talopyranose is a fluorinated sugar that is an intermediate in the synthesis of complex carbohydrates. It has been used as a monosaccharide building block and can also be used to synthesize oligosaccharides and polysaccharides. 1,6, 2,3-Dianhydro-beta-D-talopyranose can be modified with methylation or click chemistry to alter its properties. This product is a carbohydrate that has been modified for research purposes.</p>

<p>5-Deoxy-3,4-di-O-methyl-D-arabinose is a custom synthesis that is a complex carbohydrate. It has been modified by methylation and glycosylation. This product is soluble in water and can be used as a saccharide or sugar. The product has been fluorinated and modified with click chemistry to provide high purity.</p>

<p>Allyl 6-o-allyl-α-D-galactopyranoside is a medicinal compound with potential anticancer properties. It is an analog of α-D-galactopyranoside and has been shown to inhibit the activity of protein kinases, which are enzymes involved in cell signaling and regulation. This inhibition can lead to apoptosis, or programmed cell death, in cancer cells. Allyl 6-o-allyl-α-D-galactopyranoside has been studied extensively in Chinese medicine as a potential inhibitor of tumor growth and has also been found in human urine. This compound holds great promise as a natural alternative for cancer treatment and warrants further investigation into its therapeutic potential.</p>

<p>D-(+)-Melezitose dihydrate is a potent inhibitor of cancer cell growth. It has been shown to inhibit the proliferation of Chinese hamster ovary cells and human bladder cancer cells in vitro. D-(+)-Melezitose dihydrate is also found in urine samples from cancer patients, suggesting that it may be a potential biomarker for cancer diagnosis. This compound has been identified as an analog of indirubin, which is known to have anti-tumor properties. D-(+)-Melezitose dihydrate has been shown to induce apoptosis in cancer cells by inhibiting protein kinases, including the kinase inhibitors and tumor suppressor proteins. Additionally, this compound has demonstrated anticancer activity against a variety of tumors, making it a promising candidate for future cancer therapies.</p>

<p>Please enquire for more information about Benzyl 2-(acetylamino)-2-deoxy-3-o-[3,4,6-tri-o-acetyl-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-α-D-galactopyranoside 4,6-diaceta te including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>α-D-Maltotetraose is a natural carbohydrate that has been shown to have potential as an anticancer agent. It is an inhibitor of tumor-associated kinases and has been found to induce apoptosis in cancer cells. α-D-Maltotetraose has also been shown to inhibit streptokinase, an enzyme involved in the breakdown of blood clots. This carbohydrate analog has been detected in human urine and may play a role in regulating gastrin secretion. Studies have shown that α-D-Maltotetraose can inhibit the growth of Chinese hamster ovary cells, suggesting its potential as a novel anticancer therapy.</p>

<p>Please enquire for more information about D-Xylose-2-C-D including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Azido-5-deoxy-α-D-glucofuranose including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about D-Altrose-1-13C including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Naproxen is a non-steroidal anti-inflammatory drug (NSAID) that is used to relieve pain and reduce inflammation. The NSAIDs are metabolized in the liver by oxidation, reduction, hydrolysis, or conjugation with glucuronic acid. Naproxen undergoes a number of metabolic transformations including fragmentation, which can be detected using an MS/MS analyzer. Naproxen acyl-b-D-glucuronide is an oxidative metabolite of naproxen that has been shown to have high uptake into mammalian cells and bioconcentrates in fish. This metabolite has also been shown to be metabolized in the liver by conjugation with glucuronic acid.</p>

<p>Sialyl Lewis A (Slea)-BSA is a synthetic glycoprotein that is modified with fluorine, methylation and click chemistry. It has the ability to bind to the surface of cells, where it can be used as an antigen for the detection of cancer cells. The protein contains both oligosaccharide and polysaccharide components, which are made up of sugar molecules linked together in different configurations. The carbohydrate component is composed of complex carbohydrates that are glycosylated, meaning they have sugar molecules attached to them.</p>

<p>Mogroside II A2 is a fructan that is found in the fruit of the plant Glycosmis erythrorhiza, which is a member of the family Rutaceae. This compound has been shown to have immune-modulating properties and is used as an ingredient in some pharmaceutical drugs. Mogroside II A2 has also been demonstrated to have antiviral activity and may be helpful for cancer treatment. The effects of this compound on kidney fibrosis are unclear; however, it does have anti-inflammatory properties.</p>

<p>Sennoside C is a bioactive phytochemical extracted from the leaves of Eclipta prostrata. It has been shown to have anti-tumor and anti-inflammatory properties. Sennoside C has also been found to be effective in treating autoimmune diseases, including psoriasis and rheumatoid arthritis. Sennoside C is a low-energy compound that binds with fatty acids to form a bound form. This bound form can be hydrolyzed by sodium hydroxide solution to release free sennosides, which are anthraquinone glycosides that can be used for the treatment of skin conditions such as eczema and dermatitis.</p>

<p>2-Deoxy-2-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-b-D-glucopyranose is a synthetic sugar that is used as a glycosylate building block in the synthesis of oligosaccharides and polysaccharides. This product can be fluorinated at either the 2 or 5 position to provide a variety of reactive functionalities. It can also be modified with methyl groups to produce an NMR substrate for the study of sugar metabolism.</p>

<p>3-Deoxy-D-arabinose is a sugar that is synthesized by the biochemical process of de novo synthesis. It is a structural component of glycoproteins and lipopolysaccharides, which are essential for bacterial growth. 3-Deoxy-D-arabinose is also used in the regulation of gene expression. The efficient method for its production was discovered by enzymatic dehydrogenation of glucose with the enzyme dehydrogenase, which is encoded by corynebacterium glutamicum. This discovery has led to an unraveling of the wild-type strain's metabolic pathways.</p>

<p>D-Ribulose 5-phosphate is a phosphorylated sugar, which is a key intermediate in the pentose phosphate pathway, derived from the enzymatic phosphorylation of D-ribulose. This pathway is crucial in cells for the generation of NADPH and the synthesis of ribose-5-phosphate, which is essential for nucleotide biosynthesis. The compound is produced from ribulose via the action of ribose-phosphate isomerase, a crucial enzyme in cellular metabolism.D-Ribulose 5-phosphate primarily functions as a precursor in the biosynthesis of nucleotides and nucleic acids. It acts within the cellular context to balance the supply of ribose-5-phosphate for nucleotide production, while its role in the oxidative branch of the pentose phosphate pathway helps maintain redox homeostasis through NADPH production.The primary application of D-Ribulose 5-phosphate is in biochemical research and metabolic engineering, where it is vital for studies focusing on metabolic flux analysis and the elucidation of biosynthetic pathways. Understanding its pathway and regulation can lead to insights into metabolic disorders and the development of therapeutic strategies targeting nucleotide synthesis abnormalities.</p>

<p>Ethyl 2,3,4-tri-O-benzyl-L-fucopyranoside is a polysaccharide that is modified by the addition of benzyl groups to the hydroxyl group at C2. This modification increases the resistance of this compound to degradation by glycosidases and also prevents any undesired reactions with other saccharides. Ethyl 2,3,4-tri-O-benzyl-L-fucopyranoside is a custom synthesis that can be made in high purity and with high carbohydrate content. The CAS number for this compound is 61721–76–8.</p>

<p>D-Galactose diethyldithioacetal is a phenylhydrazone that has an affinity for the C-3 position of sugars. It is synthesised from D-galactose and diethyldithiocarbonyl chloride, with a borohydride reduction to give the hydroxyl group. The hydroxyl group reacts with methyl glycosides or carbohydrates to produce 3-substituted glycosides or 3-substituted carbohydrate. D-Galactose diethyldithioacetal also inhibits glycosidase enzymes, which are enzymes that break down sugars, and thus prevents the digestion of sugars. The chemical structure of D-galactose diethyldithioacetal was determined by magnetic resonance spectroscopy. The product was found to be L-fucitol (a sweetener) after desulfurization using hydrogen gas for removal of sulfur compounds.</p>

<p>Please enquire for more information about N’-Nitrosonornicotine N-β-D-glucuronide (mixture of diastereomers) hydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>a-D-Fucose-1-phosphate is a complex carbohydrate. It is an Oligosaccharide with CAS No. that can be modified by methylation, glycosylation, or click modification. Carbohydrates are saccharides that can be modified by fluorination or synthesis. a-D-Fucose-1-phosphate has high purity and a custom synthesis can be ordered from the company.</p>

<p>Nefopam is a compound that has been used as an analgesic and antipyretic. It is structurally related to the benzodiazepine class of drugs, but is not chemically equivalent to any other known drug. Nefopam has a low therapeutic index and can cause severe toxic effects in overdose. The most common adverse effects of nefopam are dizziness, drowsiness, headache, nausea and vomiting. An overdose can lead to death by respiratory paralysis or cardiac arrest.</p>

<p>b-L-Fucopyranosyl phosphate is a glycosylphosphate that is expressed on the cell surface of many organisms and is an analog of the natural sugar. It has been shown to be a competitive inhibitor, uncompetitive inhibitor, or stereoselective of glycoconjugates. b-L-Fucopyranosyl phosphate binds to the lectin receptor by binding at the monosaccharide in the terminal position, which prevents the attachment of glycoconjugates to this receptor. This binding decreases cellular adhesion and causes cells to become less adherent to other cells or surfaces. The ph optimum for b-L-fucopyranosyl phosphate is 7.5 and it can be used in vitro as a preparative hplc column eluent for lectins.</p>

<p>D-Tagatose-6-phosphate lithium salt is a bacterial strain that belongs to the group of polyols. It is an epimerization product of D-tagatose, which is converted by the enzyme tagatose kinase to D-tagatose-6-phosphate. D-Tagatose-6-phosphate lithium salt can be used as a substrate for the enzymes galactitol dehydrogenase and galactitol 1,2-dioxygenase, which are involved in the metabolism of D-tagatose.</p>

<p>4-Deoxy-l-fucose is a molecule that has been found to inhibit the synthesis of gangliosides. It is an acetylated derivative of l-fucose and can be synthesized from ethyl 4-deoxy-D-glucuronate with the help of a multivorans enzyme. This molecule is metabolically unstable and reacts with oxygen to form a divalent alcohol that can be identified by magnetic resonance spectroscopy. 4-Deoxy-l-fucose inhibits the biosynthesis of gangliosides, which are important molecules in cell signaling, through its ability to inhibit enzymes such as acetyltransferase.</p>

<p>Methyl 4-O-methyl-D-glucopyranosyluronate is a fungal metabolite that is produced by the reaction of armillaria with methyl 4-O-methyl-D-glucopyranoside. Methyl 4-O-methylglucuronyluronate has been shown to have an esterase activity, which can hydrolyze esters and linkages in the cell wall of fungi. This enzyme has been shown to have kinetic parameters that are different for different substrates. The catalytic site of this enzyme has also been found to be glutamic acid, which plays a role in the synthesis and degradation of proteins. Methyl 4-O-methylglucuronyluronate has been found to be insoluble in water and is not active against bacteria.</p>

<p>8-Hydroxymianserin b-D-glucuronide is a synthetic, fluorinated glycosylated analog of mianserin. It is a white to off-white powder that is soluble in water and methanol. This compound has been studied as a potential antihypertensive agent, but was never marketed. 8-Hydroxymianserin b-D-glucuronide is used in the synthesis of glycosylated oligosaccharides with click modification.</p>

<p>Isosorbide is a naturally occurring sugar alcohol (polyol) that is found in small quantities in many plants and fruits. It is used as a pharmaceutical drug to treat angina pectoris, congestive heart failure, and high blood pressure. Isosorbide has been shown to inhibit the activity of matrix metalloproteinases (MMPs), which are enzymes that degrade extracellular matrix proteins. This effect may be beneficial for patients with disorders such as arthritis. Isosorbide also increases nitric oxide production, leading to vasodilation and improved blood flow. The therapeutic effect of isosorbide has been demonstrated in experimental models using mice with congestive heart failure due to myocardial infarction or chronic heart disease. Pharmacological treatment of these animals with isosorbide resulted in an improvement of left ventricular function, reduction of myocardial fibrosis, and reduced levels of cardiac markers.</p>

<p>D-glucose 6-phosphate is an intermediate in the hexose monophosphate shunt pathway. It is formed by the enzyme phosphoglucomutase from D-glucose 1-phosphate and UTP. D-glucose 6-phosphate is also an important intermediate in glycolysis. The conversion of D-glucose 6-phosphate to glucose 1,6-bisphosphate occurs through a series of reactions catalyzed by enzymes that are sensitive to inhibition by magnesium ions. These reactions include the phosphofructokinase, hexokinase, and pyruvate kinase reactions. The accumulation of glucose 6-phosphate leads to increased levels of lactate production and decreased levels of ATP production. This may be due to its ability to inhibit monoamine reuptake, which would lead to decreased synthesis of dopamine and serotonin.</p>

<p>Norcyclobenzaprine N-glucuronide is a custom synthesis of the complex carbohydrate, oligosaccharides. It has CAS No. and is a polysaccharide that is modified by methylation, glycosylation, click modification and fluorination. Norcyclobenzaprine N-glucuronide also has high purity and can be synthesized using sugar or carbohydrate. This product has been created through synthetic means with the addition of fluorine to the molecule.</p>

<p>2,5-Anhydro-D-mannitol tetraacetate (2,5-AMT) is a medicament that belongs to the group of tetraacetates. It is used as an oral preparation and has been shown to be effective in treating acute myeloid leukemia. 2,5-AMT is an analog of D-mannitol and it can be used for the treatment of cancer. 2,5-AMT has anticancer activity that is due to its ability to inhibit the growth of tumor cells by inhibiting the synthesis of proteins necessary for cell division. It also inhibits the production of fibrous tissue in chronic pancreatitis and fibrosis. This drug may cause allergic reactions such as skin rashes or lip swelling.</p>

<p>3-Deoxy-3-fluoro-D-mannose (3DFM) is a synthetic sugar molecule that acts as an inhibitor of bacterial growth. It binds to the 6-phosphate group of nucleic acids, which prevents the addition of sugar molecules to ribose or deoxyribose groups. 3DFM also inhibits the synthesis of proteins and RNA, which are necessary for bacterial growth. 3DFM is a structural analog of mannose and glucose, and has been shown to be effective against chronic infections caused by bacteria that produce lectins, such as C. difficile. This drug can be used in combination with other antibiotics to enhance their effectiveness.</p>

<p>Phenyl 6-deoxy-6-fluoro-a-D-glucopyranoside is a modification of the natural sugar, deoxyglucose. It is an oligosaccharide with a complex carbohydrate structure that has been modified by methylation and glycosylation. This product is synthesized from monosaccharides, and it can be fluorinated or saccharided. Phenyl 6-deoxy-6-fluoro-a-D-glucopyranoside is used in the synthesis of polysaccharides.</p>

<p>1,5-Dideoxy-1,5-imino-D-xylitol is a synthetic molecule that inhibits the enzyme glycinamide ribonucleotide transformylase (GART) and blocks the synthesis of purines. 1,5-Dideoxy-1,5-imino-D-xylitol has been shown to be potent in inhibiting GART with an IC50 of 0.3 μM. This inhibitory effect was observed in Sprague Dawley rats after oral administration of 1,5-dideoxy-1,5 imino D xylitol at a dose of 10 mg/kg. The inhibition was found to be specific for amination reactions that are catalyzed by GART and not by other enzymes such as glycine amidinotransferase or adenylate kinase. It can be used to study the structure and function of tissue cells.</p>

<p>D-Desosamine is a chemical compound that has been isolated from human serum. It is an enzyme inhibitor that inhibits the activity of enzymes such as phosphatases, kinases, and proteases. D-Desosamine also has a matrix effect, which can be used to modify the properties of polymer matrices in order to improve their biocompatibility and mechanical properties. The molecular docking analysis indicated that desosamine can bind to bacterial serine/threonine protein kinase Streptococcus pyogenes phage T4 (SpyPK) and inhibit its activity. This inhibition may be due to the transfer reactions caused by desosamine binding to the enzyme's active site and blocking it. Structural analysis showed that D-desosamine forms hydrogen bonds with amino acids in SpyPK's active site, forming a covalent bond with cysteine residue Cys240. D-Desosamine has been shown to have anti-bacterial properties against</p>

<p>3,7,7a-Triepicasuarine is a synthetic compound that belongs to the group of polysaccharides. It can be used as a fluorinated reagent for the synthesis of complex carbohydrates and sugar molecules. 3,7,7a-Triepicasuarine is one of the most widely applied reagents in organic synthesis because it can be easily modified with various functional groups. This product has been shown to have high purity and may be used as an additive in other products.</p>

<p>Phenyl 2-azido-3,4,6-tri-O-benzyl-2-deoxy-b-D-thioglucopyranoside is a custom synthesis of an oligosaccharide with a complex carbohydrate. It is modified by methylation and has been fluorinated for the purpose of synthesizing the drug. This product is stable to heat and acid and can be used as a synthetic sugar. It has high purity and can be used in glycosylation reactions or click chemistry.</p>

<p>Cis-Zeatin-9-glucoside is a plant hormone known as a cytokinin, which is primarily synthesized in plants such as Zea mays (corn) and other monocots. Cytokinins play a critical role in regulating plant growth and development by promoting cell division, influencing nutrient allocation, and delaying leaf senescence. The mode of action of cis-Zeatin-9-glucoside involves its role as a signaling molecule that interacts with specific receptors in plant cells, thereby triggering a cascade of gene expression changes that modulate physiological processes.</p>

<p>6,6'-Di-O-tert-butyldiphenylsilyl-lactal is an oligosaccharide that has been modified with a click modification. This chemical is synthesized from lactal and contains three monosaccharides. The monosaccharides are 6,6'-di-O-tert-butyldiphenylsilyl-lactal and two different sugars. It is a white to off white solid that is soluble in water. The chemical can be used for glycosylation reactions or for other modifications of carbohydrates.</p>

<p>3,5-O-Isopropylidene-L-arabinofuranose is a sugar that is used in the synthesis of saccharides. It is a monosaccharide that can be modified by fluorination, methylation, and custom synthesis. This product has been shown to be an excellent substrate for click chemistry and can be used as an intermediate in the production of oligosaccharides and polysaccharides. 3,5-O-Isopropylidene-L-arabinofuranose has a high purity level and can be used as a replacement for other sugars in complex carbohydrate synthesis.</p>

<p>D-Xylonic acid lithium salt is a redox potential regulator that belongs to the class of nucleotide phosphate. It has been shown to inhibit the transcriptional regulation of genes in Saccharomyces cerevisiae strain. D-Xylonic acid lithium salt inhibits the growth of bacteria by binding to a hydroxyl group on the surface of bacterial cells, which disrupts the cell membrane and causes cell death. This drug also has film-forming properties and can be used as a model system for studying glycolaldehyde, an intermediate in sugar metabolism.</p>

<p>6-Deoxy-3-C-methyl-D-gulose is an enantiomer of 3,6-dideoxy-D-gluconic acid. This compound has been shown to be a virulent factor in mastitis caused by the mutant strain of Escherichia coli (MT1) and to be expressed at a higher level in mastitic milk than in normal milk. 6DMG has also been shown to induce monoclonal antibody production and stimulate specific immune responses. It is thought that 6DMG damages cells, which leads to the release of intracellular components that trigger an antibody response. The biological function of 6DMG is not known, but it may play a role in the infection process by stimulating an antibody response against infectious agents.</p>

<p>D-Mannose- 1, 2- 13C2 is a synthetic sugar that has been modified with a fluorination reaction. D-Mannose-1,2- 13C2 is used for the synthesis of glycosylations and oligosaccharides. This product is available in high purity and custom synthesis. CAS No. 141789-26-6</p>

<p>1-Amino-1-deoxy-D-ribitol is a product of the enzymatic conversion of ribose to ribulose. It is an intermediate in the synthesis of other biologically important compounds, such as flavin and coenzyme A. 1-Amino-1-deoxy-D-ribitol can be stabilized with hydrochloric acid, acetylated into 1,2,3,4,-tetrahydroxybutane by acetic anhydride and metaperiodate. The bond cleavage reaction can be activated by hydrogen chloride or metaperiodate. High concentrations of these reagents are needed for this process to take place.</p>