Glycoscience
Glycoscience is the study of carbohydrates and their derivatives, as well as the interactions and biological functions they participate in. This field of research is crucial for understanding a wide variety of biological processes, including cell recognition, signaling, immune response, and disease development. Glycoscience has important applications in biotechnology, medicine, and the development of new drugs and therapies. At CymitQuimica, we offer a wide selection of high-quality, high-purity products for glycoscience research. Our catalog includes monosaccharides, oligosaccharides, polysaccharides, glycoconjugates, and specific reagents, designed to support researchers in their studies on the structure, function, and applications of carbohydrates in biological systems. These resources are intended to facilitate scientific discoveries and practical applications in various areas of bioscience and medicine.
Subcategories of "Glycoscience"
- Aminosugars(108 products)
- Glyco-Related Antibodies(282 products)
- Glycolipids(46 products)
- Glycosaminoglycans (GAGs)(55 products)
- Glycosides(419 products)
- Monosaccharides(6,624 products)
- Oligosaccharides(3,682 products)
- Polysaccharides(503 products)
Found 11046 products of "Glycoscience"
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Allitol
CAS:<p>Allitol is a sugar alcohol that is used as a sweetener. It can be found naturally in some fruits and vegetables, but it can also be produced by hydrogenation of xylose. Allitol is metabolized by the liver and has been shown to inhibit fatty acid synthesis. It also has insulin-resistance effects, which may be due to its ability to inhibit the conversion of glucose into fatty acids. Allitol has been shown to decrease the levels of hydrochloric acid in the stomach, which may lead to an increase in gastric pH. Allitol will react with strong bases such as sodium hydroxide or potassium hydroxide to form d-talitol and polycarboxylic acid, respectively. Magnetic resonance spectroscopy (MRS) can be used to study the biochemical properties of allitol because it has a unique magnetic resonance spectrum (MRS).</p>Formula:C6H14O6Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:182.17 g/mol3,5,6-Trichloro-2-pyridinol β-D-glucuronide
CAS:<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>Formula:C11H10Cl3NO7Purity:Min. 95%Color and Shape:White PowderMolecular weight:374.56 g/mol6-Chloro-6-deoxy-D-glucose
CAS:<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>Formula:C6H11ClO5Purity:Min. 95%Color and Shape:White Off-White PowderMolecular weight:198.6 g/mol3-O-Benzyl-1,2-O-isopropylidene-a-D-xylopentodialdo-1,4-furanose
CAS:3-O-Benzyl-1,2-O-isopropylidene-a-D-xylopentodialdo-1,4-furanose is a synthetic sugar that can be used as a building block for the synthesis of glycoproteins, polysaccharides and other complex carbohydrates. It is also used for the modification of saccharide chains by methylation and fluorination. 3Bz DAPF was custom synthesized using high purity chemicals and has been shown to have an excellent level of purity.Formula:C15H18O5·xH2OPurity:Min. 95%Color and Shape:Colourless LiquidMolecular weight:278.3Methyl 2-deoxy-b-D-ribopyranoside
CAS:<p>Methyl 2-deoxy-b-D-ribopyranoside is a synthetic monosaccharide that has been modified by fluorination, monosaccharide, and methylation. It is an oligosaccharide that belongs to the group of complex carbohydrates. This compound can be used for glycosylation reactions or as a sugar donor in click chemistry. Methyl 2-deoxy-b-D-ribopyranoside has CAS No. 17676-20-9 and it's purity is greater than 99%.</p>Formula:C6H12O4Purity:Min. 95%Molecular weight:148.16 g/molPhenyl 4,6-O-benzylidene-a-D-thiomannopyranoside
CAS:<p>Phenyl 4,6-O-benzylidene-a-D-thiomannopyranoside is a custom synthesis that is modified with fluorination, methylation and click modification. It is a monosaccharide that is used in the preparation of polysaccharides and glycosylations. Phenyl 4,6-O-benzylidene-a-D-thiomannopyranoside also has saccharide and carbohydrate properties.</p>Formula:C19H20O5SPurity:Min. 95%Color and Shape:White PowderMolecular weight:360.43 g/molD-[UL-13C6]Fructose 6-phosphate disodium salt hydrate
CAS:D-[UL-13C6]Fructose 6-phosphate disodium salt hydrate is a compound that inhibits sperm motility by binding to the transmembrane proteins of the plasma membrane. This inhibition leads to an increase in spermatozoa's mitochondrial transmembrane potential, which is necessary for fertilization. D-[UL-13C6]Fructose 6-phosphate disodium salt hydrate also has been shown to significantly increase the fertility of cryopreserved semen samples and can be used as an extender for animal spermatozoa.Formula:C6H11Na2O9P•(H2O)xPurity:Min. 95 Area-%Color and Shape:PowderMolecular weight:310.1 g/mol(1R) -1- [(2R, 3R,4S) -N-Benzyl-3- benzyloxy- 4-hydroxymethyl-1- azetidinyl] -1, 2- ethanediol
(1R) -1- [(2R, 3R,4S) -N-Benzyl-3- benzyloxy- 4-hydroxymethyl-1- azetidinyl] -1, 2- ethanediol is a modification of the oligosaccharide glycogen. It is a synthetic compound that has been modified by methylation and glycosylation. This compound is soluble in water and ethanol, but insoluble in ether. It has a CAS number of 55634-00-2.Purity:Min. 95%3-Deoxypentulose
CAS:<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>Formula:C5H10O4Purity:Min. 95%Color and Shape:PowderMolecular weight:134.13 g/molSodium alginate, Laminaria Hyperborea
CAS:<p>Sodium alginate is a biocompatible polymer that is used in the treatment of wastewater. It is a water-soluble substance that forms a viscous solution when dissolved in water. Sodium alginate has been shown to inhibit the growth of bacteria and fungi, as well as to reduce the number of coliforms and other microorganisms in water. The potential for an alginate to be biocompatible depends on its chemical structure, with Laminaria Hyperborea being the most biocompatible. Alginates have been shown to have surface properties that are similar to those of natural tissue, making them useful for wound dressings.</p>Formula:C6H9NAO7Color and Shape:PowderMolecular weight:216.12 g/molPhenyl 4,6-O-benzylidene-β-D-glucopyranoside
CAS:<p>Phenyl 4,6-O-benzylidene-b-D-glucopyranoside is a white crystalline powder that belongs to the group of glycoconjugates. It has been made by the modification of glycosides and saccharides. This product can be used as a fluorination agent in organic synthesis, or as a click modification in carbohydrate chemistry. Phenyl 4,6-O-benzylidene-b-D-glucopyranoside can also be used for glycosylation reactions and methylation reactions.</p>Formula:C19H20O6Purity:Min. 95%Color and Shape:White to off-white solid.Molecular weight:344.36 g/mol1,2,3,6-Tetra-O-acetyl-4-O-(2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-a-D-glucopyranosyl)-a-D-glucopyranosyl)-b-D-thioglucopyra nose
<p>1,2,3,6-Tetra-O-acetyl-4-O-(2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetylaDglucopyranosyl)-aDglucopyranosyl)-bDthioglucopyra nose is a sugar with the chemical formula C27H42O14. This compound is synthesized by the glycosylation of 1,2,3,6 tetra O acetyl 4 O (2 3 6 tri O acetyl 4 O (2 3 4 6 tetra O acetyl a D glucopyranosyl) a D glucopyranosyl) b D thioglucopyrazine with 2 3 6 tri O acetate 4 O (2 3 4 6 tetra O acetate a D glucopyranoside a D glucopyranoside</p>Formula:C40H54O26SPurity:Min. 95%Molecular weight:982.91 g/mol3,4,6-Tri-O-benzyl-D-galactal
CAS:<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>Formula:C27H28O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:416.51 g/mol2,3,5-Tri-O-benzhydryloxybis(trimethylsilyloxy)silyl-2-C-methyl-D-ribono-1.4-lactone
2,3,5-Tri-O-benzhydryloxybis(trimethylsilyloxy)silyl-2-C-methyl-D-ribono-1.4-lactone is a custom synthesis that is used as a building block for saccharides and polysaccharides due to its high purity. It is also used for the modification of saccharides and polysaccharides. It is synthesized using Click chemistry, which has been shown to be effective in glycosylation reactions. This product has fluorination at C2 and C3 positions, which provides resistance against hydrolysis by esterases and glucuronidases. It also has methylation at the 3' position of the sugar moiety, which makes it resistant to hydrolysis by phosphodiesterases. The CAS number of this product is 549299-05-5.br>br> br>br> ThisPurity:Min. 95%3-Deoxy-3-fluoro-D-galactose - Aqueous solution
CAS:<p>3-Deoxy-3-fluoro-D-galactose (3DFGal) is a potential drug that has been shown to shift the metabolic pathway of gram-positive pathogens from glycolysis to gluconeogenesis. This compound may be used as a tool for studying the enzymatic reaction catalyzed by galactokinase, which is involved in the conversion of 3DFGal to D-galactose. 3DFGal is a stereospecific carbohydrate and can be used as a substrate for biochemical studies. The bacterial surface profile of 3DFGal has been investigated and it has been found that 3DFGal is not significantly toxic to Gram-negative bacteria. The kinetics of 3DFGal hydrolysis have been studied and it was found that the hydrolysis rate was increased when the solution was acidified with hydrofluoric acid.</p>Formula:C6H11FO5Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:182.15 g/mol5-Deoxy- 5- iodo- 2, 3- O- isopropylidene -D- ribonic acid γ-lactone
<p>5-Deoxy-5-iodo-2,3-O-isopropylidene-D-ribonic acid gamma-lactone is a sugar molecule that has been modified and synthesized. It is a glycosylation product of 5'-deoxy-5'-iodoarabinose with 3,4,6-trihydroxybenzoic acid. It can be used for the synthesis of oligosaccharides and saccharides. This compound has been shown to inhibit the growth of Mycobacterium tuberculosis in culture.</p>Purity:Min. 95%1,2,3-Tri-O-benzyl-4,6-O-(4-methoxybenzylidene)-b-D-galactopyranoside
<p>1,2,3-Tri-O-benzyl-4,6-O-(4-methoxybenzylidene)-b-D-galactopyranoside is a synthetic compound that has been synthesized as an example of a fluorinated sugar. This compound is an oligosaccharide with a molecular weight of 839.</p>Formula:C35H36O7Purity:Min. 95%Molecular weight:568.66 g/mol2-Azido-2-deoxy-3,4:5,6-di-O-isopropylidene-L-gulonic acid methyl ester
<p>This product is a custom synthesized and modified monosaccharide. It is an oligosaccharide, which is made up of two or more sugars that are linked together by glycosidic bonds. The sugar in this product is a glycosylation, which is a type of sugar that has been modified by adding a new chemical group to it. This modification can be done by fluorination, methylation, or click modification. This product also contains a saccharide, which is a large carbohydrate molecule that consists of many sugar molecules. This type of carbohydrate can be either polysaccharides or complex carbohydrates. This product has high purity and CAS number (CAS No.).</p>Purity:Min. 95%1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-b-D-galactopyranose
CAS:1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-b-D-galactopyranose (TAZ) is an aromatic heterocyclic sugar compound that is used in pharmaceutical formulations. It has low toxicity and can be synthesized using a number of methods. TAZ has been shown to have antifungal effects against Candida albicans and antitumor effects against cancer cells. TAZ also inhibits the activity of teniposide, which is a drug used for the treatment of leukemia. TAZ may be effective against cancer cells by acting as an amido donor and changing the conformation of the cyclic peptide.Formula:C14H19N3O9Purity:Min. 95%Color and Shape:PowderMolecular weight:373.32 g/molL-Glucono-1,4-lactone
CAS:<p>L-Glucono-1,4-lactone is a substance that belongs to the group of compounds known as alpha hydroxy acids. It is produced in the body by an enzyme called l-gluconolactonase and is present in small quantities in many fruits and vegetables. L-Glucono-1,4-lactone has been shown to prevent skin aging and protect against UV light damage through its antioxidant properties. This compound can be found in sunscreens or it can be taken orally to provide protection from the sun. Clinical data on L-Glucono-1,4-lactone treatments are not yet available.</p>Formula:C6H10O6Purity:Min. 95%Color and Shape:PowderMolecular weight:178.14 g/mol
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