Oligosaccharides

Thiodiglucoside is a plant glycoside that is used as a preparative agent for the isolation of active substances from lymphocytes. It can be used in chromatographic and inhibition studies to determine the binding sites on lymphocytes. Thiodiglucoside has been shown to bind to lectins and inhibit protein synthesis in activated lymphocytes. This glycoside also inhibits the constriction of smooth muscle cells, which may be due to its inhibition of protein synthesis. The physiological function of thiodiglucoside is not yet fully understood; however, it is known that this compound binds to macropores and affects subunits within the cell membrane.

k-carrageenan derived octasaccharide alcohol tetrasulfate+(3-6 anhydrogalactose)

<p>Fully acetylated cellohexoses, part of a polymer homologous series of oligosaccharides isolated from cellulose by acetolysis followed by chromatography.</p>

Monosialyl, monofucosyllacto-N-neohexaose is a synthetic oligosaccharide. It has a molecular weight of 1205. The compound has been modified with a click modification and fluorination, and has been shown to be stable in the presence of acid, base, and heat. The compound is also high purity and can be synthesized on request. Monosialyl, monofucosyllacto-N-neohexaose is an example of a complex carbohydrate that contains both a sugar and polysaccharide component. The sugar component is composed of one monosaccharide: sialic acid. The polysaccharide component consists of six disaccharides: two lactose molecules linked with one glucose molecule each. Monosialyl, monofucosyllacto-N-neohexaose is used as an artificial sweetener in food products such as cookies or cakes

Glycyl-asialo, galactosylated biantennary is a high purity custom synthesis of sugar. Glycyl-asialo, galactosylated biantennary is custom synthesized by the click modification of glycosylation and fluorination with methylation and modification. The CAS number for glycyl-asialo, galactosylated biantennary is **********.

<p>GalNAcb(1-3)Gala(1-3)Galb(1-4)Glc-b-pNP is a synthetic glycoconjugate that is a glycosylated complex carbohydrate. It has been modified by Click chemistry and fluorination, and contains the monosaccharides galactose, galactosamine, glucose, and glucuronic acid. GalNAcb(1-3)Gala(1-3)Galb(1-4)Glc-b-pNP is used as a substrate for enzyme assays to study the activity of glycosyltransferases such as galactosyltransferase. This product can be used for research purposes in immunology, molecular biology, biochemistry and other fields.</p>

<p>5-O-β-D-Glucopyranosyl-D-xylitol is a disaccharide that is synthesized for use in research.</p>

<p>Lacto-N-difucohexaose IV is a pentasaccharide with a lacto-n-difucohexaose backbone that has been shown to have inhibitory activities against human red blood cells. This pentasaccharide is a glycosaminoglycan, which is a type of carbohydrate that consists of an oligosaccharide and protein. Lacto-N-difucohexaose IV specifically binds to the antigen on the surface of human red blood cells, inhibiting their proliferation. The pentasaccharide is also known as Hansson's hapten or Hapten IV. The pentasaccharides are found in group O blood and are not found in groups A, B, or AB.</p>

<p>Glycyl-sialyllacto-N-tetraose c is a custom synthesis of the carbohydrate polysaccharide glycyl-sialyllacto-N-tetraose. It is a complex carbohydrate that has been modified for use in biochemical research. Glycyl-sialyllacto-N-tetraose c contains four sugars, including erythrose and threose, and has been fluorinated at the C5 position. The modification of this carbohydrate was achieved through a click reaction. This product has been purified to be greater than 95% pure and is ready for use as an organic solvent or chemical reagent in laboratory experiments.</p>

<p>Lacto-N-triose I is a carbohydrate antigen that is used as an acceptor in the synthesis of trisaccharides. Lacto-N-triose I has been shown to have acidic hydrolysis and gel permeation chromatography. It can be used for the synthesis of oligosaccharides, which are important for glycosylation reactions. Lacto-N-triose I also has a glycosylation reaction that can be activated by desulfurization.</p>

<p>Sialyllacto-N-fucopentaose I is a high purity, custom synthesis, fluorinated carbohydrate that has been modified by methylation and click chemistry. This oligosaccharide is composed of a saccharide with a molecular weight of 908.5 g/mol and an enantiomeric purity of 99%. Sialyllacto-N-fucopentaose I is an Oligosaccharide with a CAS number of 61497-04-8. It is used in the synthesis of polysaccharides or as a monosaccharide or sugar substitute to produce high purity products.</p>

This mixture contains some of the lower oligosaccharides found in human milk. There are small amounts of lactose but the bulk of the mixture are tri- and tetrasaccharides. 3-Fucosyllactose, 3'-Sialyllactose, 6'-Sialyllactose, Lacto-N-tetraose, Sialyllacto-N-tetraose b, Sialyllacto-N-tetraose b and Blood Group A tetrasaccharide type V are the major components that have been found in the mixture by chromatography but there may be other minor components not mentioned here.

<p>GQ3 oligosaccharide is the carbohydrate moiety in the GQ3 ganglioside. Breast cancer cells MCF-7 were found to express a complex pattern of neutral and sialylated glycosphingolipids from the globo- and ganglio-series, including unusual tetrasialylated and pentasialylated lactosylceramide derivatives, and GQ3 (II3Neu5Ac4-Gg2Cer) (Steenackers, 2012).</p>

<p>Applications N,N’,N’’-Triacetyl Chitotriose is a multivalent glycosides with strong crosslinking activity for lectin as a specific coagulant.<br>References Bhattacharyya, L., et al.: Biochemistry, 29, 7523 (1990), Sacchettini, J., et al.: Biochemistry, 40, 3009 (2001), Maierhofer, C., et al.: Bioorg. Med. Chem., 15, 7661 (2007),<br></p>

<p>Bulk sweetener; viscosity/bodying agent; humectant; cryoprotectant</p>

<p>Synthetic MPLA analog equivalent derived from bacterial LPS</p>

2-Acetamido-3-O-(b-D-galactopyranosyl)-2-deoxy-D-thiogalactopyranose is a synthetic disaccharide analog designed for research in glycoscience and biochemistry, particularly for applications in glycosylation-related studies. This compound is synthesized in the laboratory and is not derived from natural sources, allowing for precise structural modifications that facilitate detailed analyses of glycan interactions.The mode of action of this compound involves its role as a mimic of natural glycans, enabling the examination of carbohydrate-protein interactions, enzymatic activity, and glycan recognition processes with high specificity. It can be leveraged as a probe in structural biology to elucidate the mechanisms underlying biological recognition and signaling events mediated by carbohydrate molecules.This compound finds applications in the study of enzymatic hydrolysis, as an inhibitor of glycosidases, and in the synthesis of glycan-based drugs. It is of particular interest in the field of glycobiology for developing therapeutic agents and probing molecular pathways. The high specificity and structural fidelity of 2-Acetamido-3-O-(b-D-galactopyranosyl)-2-deoxy-D-thiogalactopyranose make it an invaluable tool for advancing our understanding of the intricate roles glycans play in biology.