Glicociência

Polysorbate 80, is a non-ionic surfactant, also known as Tween 80. It also acts as an emulsifier and a solubilizer, making it a useful tool in scientific industries such as pharmaceuticals, food and cosmetics.

6-Cyclohexylhexyl b-D-maltoside (6CHBM) is a monoclonal antibody that inhibits the acetylcholine receptor. It binds to the hydroxyl group on the acetylcholine receptor and blocks nicotinic acetylcholine binding, preventing activation of the receptor. 6CHBM is a hydrophobic molecule with a hydroxyl group that can interact with other hydrophobic molecules in the membrane bilayer, such as fatty acids. 6CHBM has been shown to be an allosteric inhibitor of acetylcholine receptors by binding to a site outside of the active site and altering conformational changes required for channel opening. 6CHBM has also been shown to inhibit cation channels.
6CHBM was developed from mouse antibodies and has shown no adverse effects in mice or rabbits.

Applications 4,6-O-Benzylidene-N-acetyl-D-galactosamine (cas# 420118-03-2) is a compound useful in organic synthesis.

Applications Propylene Glycol β-D-Glucopyranosiduronic Acid Benzyl Ester 2,3,4-Triacetate-d6 s an intermediate in the synthesis of Isotope labelled Propylene Glycol 2-Glucuronide which is a metabolite of propylene glycol, used in the synthesis of N-terminal kinase inhibitors with cellular activity. Acts as a solvent for various pharmaceutical compounds.
References Szczepankiewicz, B. et al.: J. Med. Chem., 49, 3563 (2006); Mateus, R. et al.: Int. J. Pharm., 444, 106 (2013);

Stability Temperature Sensitive, Hygroscopic - Store Refridgerated
Applications An intermediate in the synthesis of PugNAc (Cat. No. A15725), an inhibitor of glucosamidase.
References Beer, D., et al.: Helv. Chim. Acta., 73, 1918 (1990), Horsch, M., et al.: Eur. J. Biochem., 197, 815 (1991), Horsch, M., et al.: J. Enzyme Inhib., 7, 47 (1993),Horsch, M., et al.: Eur. J. Biochem., 237, 476 (1996),

Stability Hygroscopic
Applications 3-O-(α-D-Galactopyranosyl)-D-galactose (cas# 13168-24-6) is a compound useful in organic synthesis.
References Abramenko, I.V., et al.: Tsitologiya, 35 (5), 91 (1993), Kelly, R.F., et al.: Mol. Microbiol., 10 (3), 615 (1993), Stortz, C.A., et al.: J. Carbohydr. Chem., 13 (2), 235 (1994), Neethling, F.A., et al.: Transplantation, 57 (6), 959 (1994)

Applications Intermediate used in the addition of protected Glucopyranuronic Acid.

Applications Trigalacturonic Acid, is the product of polygalacturonic acid degradation. The mixture of Oligogalacturonic Acids has shown to have shoot growth in cockscomb (Celosia argentea L.) seedlings.
References Suzuki, T., et al.: J. Plant Growth Reg., 21, 209 (2003);

Impurity Capecitabine 3-O-BDR Impurity (USP)
Applications Capecitabine (C175650) impurity. Capecitabine 3-O-BDR Impurity (USP).

Applications Spiramycin Embonate is an antibiotic that is used in biological studies in the role of multidrug resistance of Strenotrophomonas maltophilia.
References Huang, Y., et al.: J. Antimicrob. Chemother., 68, 1987 (2013); Poole, K., et al.: Mol. Microbiol., 21, 713 (1996)

Applications 2-Acetamido-2-deoxy-N-[N-(benzyloxycarbonyl)-ε-aminocaproyl]-β-D-glucopyranosylamine (cas# 56146-89-5) is a compound useful in organic synthesis.

Neutral octasasaccharide naturally present in human breast milk

This beta-cyclodextrin (β-CD) derivative is a functionalized cyclic oligosaccharide composed of seven glucose units, characterized by a hydrophilic exterior and a lipophilic cavity (bigger than α-CD and smaller than γ-CDs), which allows it to encapsulate various guest molecules. This structural feature facilitates its use in multiple applications, including pharmaceuticals, food enhancement, and cosmetics. In the pharmaceutical industry, it enhances the solubility and stability of poorly water-soluble drugs, improving their bioavailability and efficacy while also masking unpleasant tastes. The food sector utilizes it as a stabilizer for flavors, colors, and nutrients, extending shelf life by protecting sensitive ingredients from degradation. In cosmetics, it serves as a complexing agent for fragrances and active components, ensuring their stability and controlled release. Its use expands to many other fields, including nanotechnology for drug delivery systems, environmental remediation for extracting organic pollutants, textiles for slow-release fragrances, and analytical chemistry for chiral separation.

6'-Sialyllactose-sp-biotin is a custom synthesis of a 6'-sialyllactose with a biotin moiety attached to the reducing end. The modification was done through fluorination, methylation, and monosaccharide synthesis. This product has CAS No. 1384441-62-6 and is an oligosaccharide saccharide that is polysaccharide containing glycosylated sugar. It is also a complex carbohydrate that contains many sugars in one molecule.

1,4-Anhydro-D-mannitol is a sugar alcohol that belongs to the group of alditols. It is a tautomer of galactitol, which is found in fetal bovine serum. The dehydrated form of this compound has been shown to have an inhibitory effect on tyrosinase activity. 1,4-Anhydro-D-mannitol may be used as an intermediate in the production of polymers or as a cosmeceutical agent due to its high water solubility and low toxicity.

An anhydro thio sugar

Sugammadex is a modified gamma-cyclodextrin specifically designed to reverse the effects of steroidal non-depolarizing neuromuscular blocking drugs, particularly rocuronium and vecuronium. In anesthesiology, it offers a novel approach to neuromuscular blockade reversal by directly encapsulating and inactivating these muscle relaxants. Sugammadex forms tight 1:1 complexes with free plasma rocuronium or vecuronium molecules, rapidly reducing their concentration at the neuromuscular junction. This mechanism allows for fast and predictable reversal of neuromuscular blockade, even from deep levels, without the need for anticholinesterases or antimuscarinic agents. Sugammadex has also shown promise in special populations, including pregnancy, pediatrics, and patients with renal or hepatic impairment.

An anhydro thio sugar

Please enquire for more information about Benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside including the price, delivery time and more detailed product information at the technical inquiry form on this page

Tetrasaccharide; tumor-associated antigen; prognostic factor

This beta-cyclodextrin (β-CD) derivative is a functionalized cyclic oligosaccharide composed of seven glucose units, characterized by a hydrophilic exterior and a lipophilic cavity (bigger than α-CD and smaller than γ-CDs), which allows it to encapsulate various guest molecules. This structural feature facilitates its use in multiple applications, including pharmaceuticals, food enhancement, and cosmetics. In the pharmaceutical industry, it enhances the solubility and stability of poorly water-soluble drugs, improving their bioavailability and efficacy while also masking unpleasant tastes. The food sector utilizes it as a stabilizer for flavors, colors, and nutrients, extending shelf life by protecting sensitive ingredients from degradation. In cosmetics, it serves as a complexing agent for fragrances and active components, ensuring their stability and controlled release. Its use expands to many other fields, including nanotechnology for drug delivery systems, environmental remediation for extracting organic pollutants, textiles for slow-release fragrances, and analytical chemistry for chiral separation.

This beta-cyclodextrin (β-CD) derivative is a functionalized cyclic oligosaccharide composed of seven glucose units, characterized by a hydrophilic exterior and a lipophilic cavity (bigger than α-CD and smaller than γ-CDs), which allows it to encapsulate various guest molecules. This structural feature facilitates its use in multiple applications, including pharmaceuticals, food enhancement, and cosmetics. In the pharmaceutical industry, it enhances the solubility and stability of poorly water-soluble drugs, improving their bioavailability and efficacy while also masking unpleasant tastes. The food sector utilizes it as a stabilizer for flavors, colors, and nutrients, extending shelf life by protecting sensitive ingredients from degradation. In cosmetics, it serves as a complexing agent for fragrances and active components, ensuring their stability and controlled release. Its use expands to many other fields, including nanotechnology for drug delivery systems, environmental remediation for extracting organic pollutants, textiles for slow-release fragrances, and analytical chemistry for chiral separation.

Rengasin-3'-O-glucoside is a fine chemical, useful building block, and research chemical. It is a versatile building block that can be used in the synthesis of complex compounds. Rengasin-3'-O-glucoside is also a useful intermediate or scaffold for reactions. This compound has been shown to react with 1,2-ethanediol and form an ester, which can be hydrolyzed to release glycerol and the original rengasin-3'-O-glucoside.

1,2,3,4-Tetra-O-acetyl-5-alkynyl-L-fucose is a per-O-acetylated version of 5-alkynyl-L-fucose, an inhibitor of the cellular fucosylation pathway. 1,2,3,4-Tetra-O-acetyl-5-alkynyl-L-fucose can pass through the eukaryotic cell membrane somewhat better than 5-alkynyl-L-fucose can itself, is deacetylated by cellular esterases and interferes with the biosynthesis of the fucosyl-donor and fucosyltransferase substrate GDP-Fuc, thus reducing fucosylation levels during glycoprotein biosynthesis (Dekkers, 2016).