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"
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2,3,5-Tri-O-benzyl-1-a-D-arabinofuranosyl chloride
CAS:<p>2,3,5-Tri-O-benzyl-1-a-D-arabinofuranosyl chloride is a patent antibiotic produced by Streptomyces antibioticus. It has potent anticancer activity and is being developed as an antitumor agent. 2,3,5-Tri-O-benzyl-1-a-D-arabinofuranosyl chloride inhibits cell proliferation by inhibiting DNA synthesis and protein synthesis. This compound also induces programmed cell death (apoptosis) in tumor cells. Vidarabine is a nucleoside analog that can be used to treat herpes virus infections of the eye or genital tract. Vidarabine is chemically synthesized from 2,3,5 tri O benzyl d arabinofuranosyl chloride and has been shown to have potential antitumor activity.</p>Formula:C26H27ClO4Purity:Min. 95%Molecular weight:438.94 g/mol6-α-D-Glucopyranosyl maltotriose-13C6
CAS:<p>Please enquire for more information about 6-α-D-Glucopyranosyl maltotriose-13C6 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C6C18H42O21Purity:Min. 95%Molecular weight:672.53 g/mol4,7-Anhydro-1,2,3-trideoxy-D-allo-oct-1-enitol
CAS:<p>4,7-Anhydro-1,2,3-trideoxy-D-allo-oct-1-enitol is a modified sugar that has been synthesized for use in glycosylation reactions. It is a high purity product with no detectable impurities. Click modification of this product has been shown to be useful for glycosylation reactions. 4,7-Anhydro-1,2,3-trideoxy-D-allo-oct-1-enitol is also fluorinated and glycosylated. This product can be used in the synthesis of oligosaccharides and monosaccharides.</p>Formula:C8H14O4Purity:Min. 95%Molecular weight:174.19 g/molD-Glycero-D-manno-heptose
CAS:<p>A seven carbon sugar</p>Formula:C7H14O7Purity:Min. 98 Area-%Color and Shape:Colorless Clear LiquidMolecular weight:210.2 g/mol1,3-Di-O-acetyl-5-O-benzoyl-2-deoxy-D-xylofuranose
CAS:<p>1,3-Di-O-acetyl-5-O-benzoyl-2-deoxy-D-xylofuranose is a complex carbohydrate that has been custom synthesized. It is a monosaccharide with a methyl group at the C1 position and an acetyl group at the C3 position. The chemical formula for 1,3 Di-O-acetyl 5 O benzoyl 2 deoxy D xylofuranose is C11H21NO6. The molecular weight of 1,3 Di O acetyl 5 O benzoyl 2 deoxy D xylofuranose is 277.27 g/mol. 1,3 Di O acetyl 5 O benzoyl 2 deoxy D xylofuranose may have glycosidic bonds and be used in the synthesis of other carbohydrates or as a reagent in organic chemistry reactions.</p>Formula:C16H18O7Purity:Min. 95%Molecular weight:322.31 g/molDigalactosylceramide
CAS:<p>Digalactosylceramide is a bioactive glycosphingolipid, which is derived from the cellular membranes of certain bacteria and plants. This compound plays a significant role in modulating immune responses through its interaction with the immune system. Its mode of action involves binding to specific receptors on immune cells, influencing cell signaling pathways that are crucial for the regulation of the immune response, including the modulation of cytokine production and immune cell activation.</p>Formula:C46H87NO13Purity:Min. 95%Color and Shape:PowderMolecular weight:862.18 g/mol2,4-Bis(acetylamino)-2,4,6-trideoxy-D-galactose
CAS:<p>2,4-Bis(acetylamino)-2,4,6-trideoxy-D-galactose (BTDG) is a nitro derivative of L-threonine that has been derivatized with an acetyl group and a molecule of 2,4,6-trideoxygalactose. BTDG has been shown to be safe in clinical trials for vaccine development against life-threatening diseases. It is the first glycopolymer approved by the FDA for clinical use in humans. This drug has been shown to increase the antibody response and improve protection against influenza virus infection. BTDG also inhibits bacterial replication by blocking protein synthesis in some bacteria and inhibiting glycolysis in others.</p>Formula:C10H18N2O5Purity:Min. 95%Color and Shape:PowderMolecular weight:246.26 g/molIsosaccharinic acid
CAS:<p>Isosaccharinic acid is a bacterial strain that produces isosaccharinic acid as its main fatty acid. The thermodynamic data for the reaction mechanism of the conversion of glucose to isosaccharinic acid has been determined. Isosaccharinic acid formation is catalyzed by an enzyme called glycosyl-glycerate dehydrogenase, which converts glycerate to 3-hydroxypropanoic acid and then to 3-oxopropanoate before it undergoes decarboxylation and reduction to form isosaccharinic acid. Radionuclides such as TcO4 are used in chemical ionization mass spectrometry for the detection of this compound in samples. Neutral pH, high activation energies, and low binding constants are all factors that affect the stability of this molecule.</p>Formula:C6H12O6Purity:Min. 95%Molecular weight:180.16 g/molD-Idonic acid-1,4-lactone
CAS:<p>D-Idonic acid-1,4-lactone is a modification of a carbohydrate which can be custom synthesized. The product is an oligosaccharide that has a high purity and is synthetically produced. This product is composed of monosaccharides, methylation, glycosylation, polysaccharides and sugar. It also contains fluorination and saccharide.</p>Formula:C6H10O6Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:178.14 g/mol5-Thio-N-acetylglucosamine
<p>5-Thio-N-acetylglucosamine is a microtubule inhibitor that binds to o-glcnac, a posttranslational modification of proteins that regulates the morphology and cycling of stem cells. 5-Thio-N-acetylglucosamine has been shown to inhibit the transcriptional activity of o-glcnacase, an enzyme that catalyzes the conversion of o-glcnac to glucosamine. This drug also inhibits the metabolic activity of neural progenitor cells, which may be due to its ability to regulate subpopulations with concomitant expression of markers such as Oct4 and Sox2.</p>Purity:Min. 95%Sialyl Lewis X cholesterol
<p>Sialyl Lewis X Cholesterol is a synthetically modified sugar</p>Purity:Min. 95%6'-α-Sialyl-N-acetyllactosamine-sp-biotin
CAS:<p>6'-a-Sialyl-N-acetyllactosamine-sp-biotin is a recombinant modified oligosaccharide. It is an Oligosaccharide that is synthesized by the methylation of 6'-sialyllactose with acetic anhydride and triethylamine in DMF. It has a molecular weight of 805.00 Da and a CAS number of 1038746-08-5. 6'-a-Sialyl-N-acetyllactosamine-sp-biotin may be used as a monomer for click chemistry, as well as for other applications in carbohydrate chemistry, such as the synthesis of polysaccharides and complex carbohydrates. This product has high purity and can be custom synthesized to order.</p>Formula:C44H74N6O22SPurity:Min. 95%Color and Shape:White PowderMolecular weight:1,071.15 g/molGalactostatin
CAS:<p>Galactostatin is a protein synthesis inhibitor that binds to the l-tartaric acid site of the bacterial 30S ribosomal subunit. It inhibits the binding of aminoacyl-tRNA to the ribosome, preventing translation and inhibiting cell growth. Galactostatin has been shown to be effective against HIV infection in mammalian cells. This drug also has a chaperone effect that protects cells from heat or cold stress.</p>Formula:C6H13NO5Purity:Min. 95%Molecular weight:179.17 g/molNGA5B N-Glycan
CAS:<p>NGA5B N-Glycan is a custom synthesis that can be modified by fluorination, methylation, and monosaccharide. It is synthesized from natural and synthetic substances. This N-glycan is a modification of glycans that have been shown to have anti-cancer effects. The glycosylation of the saccharide has been shown to have anti-inflammatory properties.</p>Formula:C82H136N8O56Purity:Min. 95%Color and Shape:PowderMolecular weight:2,129.98 g/molBlood Group A trisaccharide, spacer-biotin conjugate
CAS:<p>Blood group A antigen conjugated to spacer arm and biotin</p>Formula:C39H67N5O18SPurity:Min. 95 Area-%Color and Shape:PowderMolecular weight:926.04 g/molLewis X trisaccharide-sp-biotin
<p>Lewis X trisaccharide-sp-biotin is a synthetic compound with fluorination, monosaccharide, and oligosaccharide. The sugar is a complex carbohydrate. It is synthesized by glycosylation and polysaccharide modification. The product has high purity and is custom synthesis for research purposes only. This product does not have CAS number because it is a custom synthesis.</p>Formula:C39H67N5O18SPurity:Min. 95 Area-%Color and Shape:White Off-White PowderMolecular weight:926.04 g/molSodium alginate, viscosity 100 - 150 mPa.s
CAS:<p>Sodium alginate is a soluble fiber that is extracted from brown seaweed. It is a natural carbohydrate that can be modified to create a variety of sugar-based derivatives, such as Oligosaccharides, Monosaccharides, and Custom Synthesis. Sodium alginate has been modified with Fluorination, Methylation, Glycosylation, and Click Modification to create high-purity products for various applications.</p>Purity:90.8 To 106.0%Color and Shape:Powder3-Deoxy-2-keto-6-phospho-D-galactonate lithium salt
CAS:<p>The enzyme aldolase, which is involved in the metabolism of carbohydrates, catalyzes the cleavage of 3-deoxy-2-keto-6-phospho-D-galactonate to form aldol and 6-phosphoglycerate. The reaction mechanism involves an initial dehydration step that converts the substrate to an enolate ion. This intermediate then reacts with water to produce aldol and 6-phosphoglycerate. The enzyme is active only at low pH levels due to its dependence on divalent cations. The enzyme is also inhibited by other substrates or products of the reaction, such as D-tagatose, D-sorbose, and maltophilia.</p>Formula:C6H11O9P·xLiPurity:Min. 95%Blood Group B trisaccharide, spacer-biotin conjugate
CAS:<p>Blood group B antigen conjugated to spacer arm and biotin</p>Formula:C37H64N4O18SPurity:Min. 95%Color and Shape:PowderMolecular weight:884.99 g/mol3-Deoxy-2-keto-D-xylonate lithium
CAS:<p>3-Deoxy-2-keto-D-xylonate lithium salt is a synthetic compound that is used in the synthesis of protamine. It is produced by the reduction of an aldehyde with borohydride. 3-Deoxy-2-keto-D-xylonate lithium salt has been shown to be active against E. cloacae, which can cause diarrhea and other gastrointestinal disorders. 3-Deoxy-2-keto-D-xylonate lithium salt inhibits the growth of E. cloacae by inhibiting glycolaldehyde reductase and aldolases, which are enzymes that are essential for glycolysis and citrate metabolism, respectively. The cleavage products formed by this reaction inhibit bacterial growth by interfering with cell wall biosynthesis, preventing protein synthesis, or blocking ATP production (oxidative phosphorylation).</p>Formula:C5H8O5•LixPurity:Min. 95%Color and Shape:PowderMolecular weight:148.11 g/mol
