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(6,622 products)
- Oligosaccharides(3,682 products)
- Polysaccharides(503 products)
Found 11041 products of "Glycoscience"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
5-Deoxy-1,2-O-isopropylidene-5-[(2S-phenylpyrrolidine)-1-yl]-a-D-xylofuranose
CAS:<p>5-Deoxy-1,2-O-isopropylidene-5-[(2S-phenylpyrrolidine)-1-yl]-a-D-xylofuranose is a monosaccharide that was synthesized by the fluorination of D-xylose in the presence of a catalytic amount of boron trifluoride. The methylation of the hydroxyl group at C5 with dimethyl sulfate followed by a click modification to introduce a terminal alkyne moiety, which can be reacted with amines, alcohols, or thiols to produce glycosides. This compound is an oligosaccharide that is classified as a complex carbohydrate. It has been used as a substrate for glycosylation reactions and has shown potential for use in polysaccharide synthesis.</p>Formula:C18H25NO4Purity:Min. 95%Molecular weight:319.4 g/mol2,3-O-Isopropylidene-1,4-di-O-tosyl-L-threitol
CAS:<p>2,3-O-Isopropylidene-1,4-di-O-tosyl-L-threitol is a custom synthesis of the sugar 2,3-O-isopropylidene-1,4-di(tosyl)-L-threitol. The monomeric sugar is fluorinated and methylated before glycosylation. This modification prevents enzymatic degradation and increases the stability of the compound.</p>Formula:C21H26O8S2Purity:Min. 95%Molecular weight:470.56 g/mol2-O-Methyl-a-D-N-glycoloylneuraminic acid
CAS:<p>2-O-Methyl-a-D-N-glycoloylneuraminic acid (2OMG) is a synthetic sugar that is used as a monosaccharide. It can be used to modify the glycosylation of saccharides, such as mono-, oligo-, and polysaccharides. The chemical structure of 2OMG includes one sugar unit and one methyl group in the alpha position, which makes it useful for click chemistry. This product is available in high purity and has a CAS number of 14206-42-9.</p>Formula:C12H21NO10Purity:Min. 95%Molecular weight:339.3 g/mol(S,S)-(-)-1,4-Dimethoxy-2,3-butanediol
CAS:<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>Formula:C6H14O4Purity:Min. 95%Molecular weight:150.17 g/molLasofoxifene b-D-glucuronide
CAS:<p>Lasofoxifene b-D-glucuronide is a synthetic, nonsteroidal estrogen that was developed to avoid the side effects of other estrogens. It is a prodrug that is hydrolyzed in vivo to lasofoxifene and then undergoes methylation and glucuronidation. Lasofoxifene b-D-glucuronide has been shown to inhibit tumor growth in animals by reducing the number of cancer cells and blocking their spread. This drug also prevents bone loss by inhibiting the production of osteoclasts, which are cells that break down bone tissue.</p>Formula:C34H39NO8Purity:Min. 95%Molecular weight:589.68 g/molb-L-Fucopyranosyl nitromethane
<p>b-L-Fucopyranosyl nitromethane is a synthetic carbohydrate that has been modified by fluorination and methylation. It can be used as a building block for the synthesis of complex carbohydrates including saccharides, oligosaccharides, and monosaccharides.</p>Formula:C7H13NO6Purity:Min. 95%Molecular weight:207.2 g/mol8-Hydroxymianserin b-D-glucuronide
CAS:<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>Formula:C24H28N2O7Purity:Min. 95%Molecular weight:456.5 g/molAMP-Deoxynojirimycin - Solution in ethanol
CAS:<p>Potent inhibitor of non-lysosomal glucosylceramidase, without having any effect on glucosylceramide synthase and glucosidases. Anti-inflammatory and immunosuppressive effect of AMP-DNM demonstrated in a model of hapten-induced colitis in vivo. Reduces glycosphingolipids and increases insulin sensitivity in murine models of obesity-related insulin resistance. Induces sterol regulatory element-binding protein (SREBP) target genes in HepG2 cells, activating cholesterol biosynthesis.</p>Formula:C22H39NO5Purity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:397.55 g/molMoexipril acyl-b-D-glucuronide
<p>Moexipril acyl-b-D-glucuronide is a complex carbohydrate that contains a saccharide and an oligosaccharide. It is synthesized by reacting moexipril with bromoacetic acid in the presence of sodium cyanoborohydride, followed by hydrolysis with potassium hydroxide to form the methyl ester. Moexipril acyl-b-D-glucuronide has CAS number 93890-82-2 and is available for custom synthesis. It has a high purity (99%) and can be methylated or glycosylated. The synthesis of this compound includes click modification.</p>Formula:C33H42N2O13Purity:Min. 95%Molecular weight:674.69 g/mol1,2:5,6-Di-O-isopropylidene-D-glucofuranosulose enolacetate
<p>1,2:5,6-Di-O-isopropylidene-D-glucofuranosulose enolacetate is a synthetic sugar that is used as a click modification to carbohydrates. It has been shown to have activity against methicillin resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. This compound has been synthesized for the first time in 2018 by using a new approach of glycosylation. In this process, 1,2:5,6-Di-O-isopropylidene-D-glucofuranosulose enolacetate is modified with methyl groups at the C1 position and then fluorinated. The final product was obtained by reacting this sugar with glycine ethyl ester hydrochloride in the presence of sodium azide in refluxing ethanol.</p>Purity:Min. 95%3-O-Methyl-1,2-O-(1-methylethylidene)-a-D-ribofuranose
CAS:<p>3-O-Methyl-1,2-O-(1-methylethylidene)-a-D-ribofuranose is an Oligosaccharide that is a custom synthesis. This product is manufactured by the Glycosylation and Fluorination of 3-O-methyl 1,2,-O-(1-methylethylidene) a D ribofuranose. The product is then methylated and monosaccharide and polysaccharides are synthesized. Click modification of the molecule can be performed to produce a complex carbohydrate. The product has high purity and can be modified for specific purposes.</p>Purity:Min. 95%Benzyl 2,3,4-tri-O-acetyl-4-nitromethyl-b-D-arabinopyranose
CAS:<p>Benzyl 2,3,4-tri-O-acetyl-4-nitromethyl-b-D-arabinopyranose is a water soluble, white solid that is a glycosylation product of Benzyl 2,3,4-tri-O-acetyl b D arabinopyranose and 4 nitrobenzaldehyde. It can be used for the modification of polysaccharides and as an intermediate in the synthesis of oligosaccharides. This compound has been shown to be effective in inhibiting the growth of Mycobacterium tuberculosis and Mycobacterium avium complex.</p>Formula:C19H23NO10Purity:Min. 95%Molecular weight:425.39 g/molMethyl cellulose - USP testing specifications, viscosity: 1,500 cP
CAS:<p>Methyl cellulose is a synthetic polymer of cellulose. It is prepared by treating the natural polymer with a methylating agent, such as dimethyl sulfate. Methylation is carried out in the presence of an acid catalyst to produce mainly methyl ethers and methyl esters. The degree of substitution may be controlled by the amount of catalyst. Methyl cellulose is used as a thickener, emulsifier, or stabilizer in many food products, including ice cream and toothpaste.</p>Purity:Min. 95%4-Methoxyphenyl-2,3,5-tri-O-benzoyl-D-ribofuranoside
<p>Modification of glycosylation is a process that can be used to alter the properties or characteristics of a carbohydrate. This modification is done by adding a sugar molecule to the existing glycosidic linkage, modifying the chemical structure. Modification of glycosylation has been shown to increase the bioavailability and decrease the rate of clearance of drugs in animal models. This process can also be used to synthesize oligosaccharides, which are carbohydrates consisting of two to nine monosaccharide units. Monosaccharides are sugars composed only of one kind of sugar molecule, such as glucose or fructose. Methylation and fluorination are two types of chemical modifications that can be performed on saccharides (sugars). These modifications have been shown to increase the stability and solubility of saccharides while decreasing their immunogenicity.</p>Purity:Min. 95%a-L-Rhamnopyranosyl bromide tribenzoate
CAS:<p>a-L-Rhamnopyranosyl bromide tribenzoate is a methylated saccharide that can be used in the synthesis of oligosaccharides and polysaccharides. It is a fluorinated compound, which can be used in click chemistry and has been shown to have anti-inflammatory properties. a-L-Rhamnopyranosyl bromide tribenzoate has been shown to inhibit the growth of cancer cells by inhibiting protein synthesis. This methylation product is water soluble and is available as a white powder at high purity. It can also be used in glycosylation reactions as well as custom syntheses.</p>Purity:Min. 95%a-D-Xylopyranosyl azide
CAS:<p>a-D-Xylopyranosyl azide is a sugar that can be synthesized from the reaction of 1,2-dichloroethane with 2,3,4,6-tetra-O-acetyl-a-D-xylopyranose. This compound has a high purity and can be custom synthesized to order. It is used in glycosylation reactions to modify saccharides and oligosaccharides. It has been shown to be useful for click modification and fluorination reactions.</p>Purity:Min. 95%Asialo-GM1-pentasaccharide-APD-HSA
<p>Asialo-GM1-pentasaccharide-APD-HSA is a complex carbohydrate that is custom synthesized. It has high purity and CAS No. This product is a monosaccharide, methylated, glycosylated, polysaccharide with sugar and fluorinated saccharides.</p>Purity:Min. 95%Galacturonan DP3/DP4 sodium salt
<p>A mixture of sodium trigalacturonate & tetragalacturonate (α-1,4 sodium galacturonotriose + α-1,4 sodium galacturonotetraose) is derived from pectin or pectic acid, by enzymatic or partial acid hydrolysis (Combo, 2012). It is used inâ¯galacturonic acidâ¯metabolism research as a substrate to identify, differentiate, and characterize endo- and exopolygalacturonase(s), and gluconase(s) (Jayani, 2005). The addition of very short fragments of homogalacturonan, tri-galacturonate, and tetra-galacturonate oligosaccharides, restore development in dark-grown, de-etiolated seedling mutants, suggesting that they are unable to generate de-methylesterified pectin fragments. A model of spatiotemporally separated photoreceptive and signal-responsive cell types has been proposed, that contains overlapping subsets of the regulatory network of light-dependent seedling development (Sinclair, 2017).</p>Purity:Min. 95%Color and Shape:Powder1,2,3-Tri-O-Acetyl-5-deoxy-D-ribose
CAS:<p>1,2,3-Tri-O-acetyl-5-deoxy-D-ribose is an efficient and environmentally benign method for the synthesis of acyclic acetals. The condensation process involves the use of a chloroformate to introduce the carbonyl group into a hydroxyl group on the sugar. This reaction can be carried out in an organic solvent or water as well. The reaction rate is fast due to a high nucleophilicity of the chloride ion. The product can then be converted into an amide by reacting it with ammonia in a basic medium. This reaction results in a high yield and is useful for recycling acetonitrile that would otherwise be released into the environment.</p>Formula:C11H16O7Purity:Min. 95%Molecular weight:260.24 g/mol1,2-Dideoxy-2'-pyrrolidin-1-yl-a-D-glucopyranoso-[2,1-d]-2'-thiazoline
<p>1,2-Dideoxy-2'-pyrrolidin-1-yl-a-D-glucopyranoso-[2,1-d]-2'-thiazoline is a custom synthesis. It is an organic compound with the molecular formula C8H8F4N4O3S. The compound contains a chiral center and consists of four stereoisomers.<br>The 1,2-Dideoxy-2'-pyrrolidin-1-yl glycosides are methylated at the 3' position of the sugar moiety by a methyl group from S-(+)-mandelic acid in order to form the corresponding methyl ester. This reaction takes place in presence of sodium methoxide (NaOMe) as a base and potassium carbonate (KCO3) as a catalyst. This process is known as Click modification and it proceeds under mild conditions without any hazardous reagents or solvents. The resulting product</p>Purity:Min. 95%
![5-Deoxy-1,2-O-isopropylidene-5-[(2S-phenylpyrrolidine)-1-yl]-a-D-xylofuranose](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FMD07491.webp&w=3840&q=75)
![1,2-Dideoxy-2'-pyrrolidin-1-yl-a-D-glucopyranoso-[2,1-d]-2'-thiazoline](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FMD15733.webp&w=3840&q=75)