Glycoscience

<p>Lewis B pentasaccharide is a custom-synthesized carbohydrate that belongs to the Modification, saccharide, Oligosaccharide, sugar category. It is an oligosaccharide with a non-reducing end and a reducing end. Lewis B pentasaccharide is a complex carbohydrate that is synthesized from monosaccharides by glycosylation and methylation reactions. This product has high purity and it can be used in research for its fluoroquinolone resistance properties.</p>

<p>Silodosin O-beta-D-glucuronide is a metabolite of silodosin, a drug used to treat benign prostatic hyperplasia. It is the glucuronide conjugate of silodosin and its presence in plasma can be quantified by high performance liquid chromatography (HPLC). The solvents used in HPLC are acetonitrile and ammonium formate. The chromatographic separation is achieved with a mobile phase consisting of an organic solvent (acetonitrile) and an ion pairing agent (ammonium formate) that interacts with the analyte and forms an ion pair. The sensitivity of HPLC for this analyte can be improved by using deuterated solvents.</p>

<p>1,4:3,6-Dianhydro-2-O-acetyl-D-glucitol is an isosorbide intermediate</p>

Inhibitor of Gal-dependent lectin binding; used for synthesis of galactoses

<p>N-Nonyldeoxygalactonojirimycin (NDGJ) is a novel antiviral agent that inhibits the activity of viral enzymes, such as polymerase chain reaction and reverse transcriptase. NDGJ has been shown to inhibit the replication of hepatitis viruses in primary cells and human macrophages. The drug also inhibits the replication of human pathogens, such as HIV-1, herpes simplex virus type 1, and cytomegalovirus in cell culture. NDGJ has an effect on hydrophobic amino acids in protein synthesis by binding to them and preventing their attachment to the ribosomal surface. This leads to cell lysis through a process called osmotic shock.</p>

<p>Neutral octasasaccharide naturally present in human breast milk</p>

Ferrous gluconate dihydrate is a fine chemical that has many applications in research and development. It is a versatile building block that can be used as a starting material for the synthesis of complex compounds, such as drugs, pesticides, and perfumes. Ferrous gluconate dihydrate can also be used as a reaction component to produce speciality chemicals, such as benzyl alcohols. In addition to its usefulness in research, ferrous gluconate dihydrate is an important reagent for the production of high-quality pharmaceuticals.

<p>Glycosaminoglycans (GAGs) are polysaccharides that are found in the extracellular matrix and on the surface of cells. GAGs consist of a linear chain of repeating disaccharide units, with one or more sugar molecules linked by a glycosidic bond. They have been shown to be important for the function and structure of tissues, including those in the gastrointestinal tract. GAGs have been shown to stimulate cellular growth, regulate inflammatory responses, and promote wound healing. They have also been shown to inhibit activity of polymorphonuclear leucocytes (PMN), which play an important role in inflammation. One type of GAG is dextran sulfate, which has been used as a biological scaffold for tissue engineering applications. Glycosaminoglycans may also play a role in regulating immune responses through interaction with toll-like receptor 4 (TLR4).</p>

<p>Chondroitin sulfate A sodium salt is a glycosaminoglycan that is derived from chondroitin. It is a complex carbohydrate with a high molecular weight and an average MW of 10,000 to 50,000 Da. The synthesis of the monosaccharide units in chondroitin sulfate A sodium salt occurs by Methylation, Click modification, Polysaccharide, or Fluorination. Chondroitin sulfate A sodium salt can be custom synthesized according to customer specifications and can be ordered as a CAS No. 39455-18-0 with high purity.</p>

<p>2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-b-D-glucopyranosyl azide is a modified carbohydrate that is used in the synthesis of glycosides. It is a synthetic molecule that is fluorinated at the alpha position of the glycosidic bond to allow for reaction with other molecules. This product has been shown to be stable in acid and base reactions and can be used for oligosaccharide synthesis or modification.</p>

<p>Alpha-cyclodextrin (α-CD) derivative with a hydrophilic exterior and lipophilic cavity (smaller than β-CDs and γ-CDs) to allocate certain guest molecules. This structural characteristic enables applications in molecular encapsulation, solubility enhancement, and stabilization across multiple industries. In pharmaceuticals, it serves as a drug delivery vehicle, enhancing the bioavailability and stability of active ingredients. The food industry utilizes it as a stabilizer for flavors, colors, and nutrients, as well as a functional ingredient for its effects on lipid metabolism. In cosmetics, it acts as a complex agent for fragrances and active components. Its applications extend to analytical chemistry for chiral separation and to materials science for developing smart materials and nanosystems.</p>

<p>Amylopectin is composed of between 2,000 to 200,000 glucose residues linked α (1→4) with α (1→6) branching. The molecule is highly branched, every 24 to 30 glucose units, resulting in a soluble molecule with many terminal residues. Starch is made of about 70% amylopectin by weight, though it varies depending on the source (higher in medium-grain rice to 100% in glutinous rice, waxy potato starch, waxy corn, and lower in long-grain rice, amylomaize, and russet potatoes).</p>

<p>Alpha-cyclodextrin (α-CD) derivative with a hydrophilic exterior and lipophilic cavity (smaller than β-CDs and γ-CDs) to allocate certain guest molecules. This structural characteristic enables applications in molecular encapsulation, solubility enhancement, and stabilization across multiple industries. In pharmaceuticals, it serves as a drug delivery vehicle, enhancing the bioavailability and stability of active ingredients. The food industry utilizes it as a stabilizer for flavors, colors, and nutrients, as well as a functional ingredient for its effects on lipid metabolism. In cosmetics, it acts as a complex agent for fragrances and active components. Its applications extend to analytical chemistry for chiral separation and to materials science for developing smart materials and nanosystems.</p>

<p>D-Glycero-D-talo-heptitol is a natural product that is found in plants and bacteria. It is an alditol, which is created by the glycosidic bond of a carbohydrate and a hydroxyl group. D-Glycero-D-talo-heptitol has shown to inhibit the activity of enzymes involved in fatty acid synthesis, such as 3-hydroxyacyl coenzyme A dehydrogenase, and carbohydrate synthesis, such as fructose 1,6 bisphosphatase. This compound also inhibits the borohydride reduction of glycan precursors. This may be due to its hydrophilic interactions with water molecules and its hydrophobic interactions with other lipid molecules.</p>

<p>Starch is an energy storing polysaccharide produced by higher plants and some algae. Pure starch is a white, tasteless and odorless powder that is insoluble in cold water or alcohol. It consists of two types of polysaccharide: the linear and helical amylose (α-1,4-linked glucose) and the branched amylopectin (α-1,4 and α-1,6-linked glucose). Depending on the plant, starch generally contains 20 to 25% amylose and 75 to 80% amylopectin by weight.</p>

2’-(N-Hexadecanoylamino)-4’-nitrophenyl-b-D-glucopyranoside is a synthetic substrate that is used in diagnostic procedures to identify the presence of lysosomal enzymes. The reaction product, resorufin, is a fluorogenic substrate that reacts with the enzyme hexanoyl coenzyme A reductase and can be detected by spectrophotometry. This experimentally insensitive compound has been used to measure the activity of hexanoyl coenzyme A reductase in skin fibroblasts from patients with ichthyosis vulgaris. Resorufin fluorescence is proportional to the amount of hexanoyl coenzyme A reductase present in cells.

<p>Cellulose is a linear polysaccharide of β 1-4 linked glucose residues. The polysaccharide chains are bundled as microfibrils in cell walls and provide the essential structural components within growing plants. Each microfibril exhibits a high degree of three-dimensional internal bonding resulting in a crystalline structure that is insoluble in water, resistant to reagents and very strong.</p>

Lipopolysaccharides are a heterogeneous group of molecules that include endotoxins, lipid A, and core oligosaccharide. They are released from the cell wall of gram-negative bacteria as a result of bacterial lysis. Lipopolysaccharides are potent activators of immune cells, inducing the secretion of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). TNF-α is also known to induce the production of other pro-inflammatory cytokines including IL-6, IL-8, IL-10, and IL-12. Lipopolysaccharides have been shown to cause liver damage in animals by increasing plasma alanine aminotransferase levels. This may also be due to their ability to induce the production of malondialdehyde and c-reactive protein.

<p>Methyl β-L-arabinopyranoside is a monomer that is used for the synthesis of polymers. It has been shown to be an effective polymerization catalyst, with long-term stability and good storage properties. Methyl β-L-arabinopyranoside has been used in gas chromatographic analysis as an analyte to identify hydroxy groups, although it may also interfere with the detection of certain other analytes. This monomer is often used in the production of plastics and rubbers because it enhances bonding between rubber molecules and plasticizers. Methyl β-L-arabinopyranoside has also been shown to have tailing enhancements and extracts that are due to hydroxy groups, which can lead to signal enhancement in gas chromatography. Additives such as ammonium acetate can be added if there is a need to increase sensitivity or reduce tailing effects.</p>

Oroxylin A 7-O-glucuronide (OA7G) is a natural compound that exhibits anti-angiogenic and anti-inflammatory effects. OA7G binds to p-hydroxybenzoic acid and inhibits the activity of glycosidases, which are enzymes that hydrolyze glycosides. OA7G has been shown to have therapeutic potential in several models of inflammatory bowel disease. In vivo studies show that OA7G may be a useful agent for the treatment of bowel disease by inhibiting angiogenesis, which is the formation of new blood vessels from pre-existing ones. Molecular docking analysis showed binding affinity between OA7G and the enzyme dextran sulfate glucuronyltransferase, suggesting a possible mechanism for its anti-inflammatory effects.

<p>An anhydro thio sugar</p>

<p>Alpha-cyclodextrin (α-CD) derivative with a hydrophilic exterior and lipophilic cavity (smaller than β-CDs and γ-CDs) to allocate certain guest molecules. This structural characteristic enables applications in molecular encapsulation, solubility enhancement, and stabilization across multiple industries. In pharmaceuticals, it serves as a drug delivery vehicle, enhancing the bioavailability and stability of active ingredients. The food industry utilizes it as a stabilizer for flavors, colors, and nutrients, as well as a functional ingredient for its effects on lipid metabolism. In cosmetics, it acts as a complex agent for fragrances and active components. Its applications extend to analytical chemistry for chiral separation and to materials science for developing smart materials and nanosystems.</p>

<p>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.</p>

<p>An anhydro thio sugar</p>

<p>Digalacturonic acid (DGA) (α-1,4 galacturonobiose), is derived from pectin or pectic acid, by enzymatic or partial acid hydrolysis. It is used in the co-crystallization of enzymes such as proteinase K. It is also used in galacturonic acid metabolism research as a substrate to identify, differentiate, and characterized endo- and exopolygalacturonase(s), and gluconase(s).</p>

<p>2,3,4,6-Tetra-O-acetyl-a-D-galactopyranosyl trichloroacetimidate is a disaccharide that is an activated glycoprotein. It is used as a hapten for the production of monoclonal antibodies and as an immunogen in stepwise immunization with bovine serum albumin. This compound has been shown to be specific for the EGF receptor on neoglycoproteins and can be used to detect this receptor. The glycosidic residue of 2,3,4,6-tetra-O-acetyl-a-D-galactopyranosyl trichloroacetimidate allows it to bind to proteins such as albumin and act as a carrier for other molecules.</p>

<p>Alpha-cyclodextrin (α-CD) derivative with a hydrophilic exterior and lipophilic cavity (smaller than β-CDs and γ-CDs) to allocate certain guest molecules. This structural characteristic enables applications in molecular encapsulation, solubility enhancement, and stabilization across multiple industries. In pharmaceuticals, it serves as a drug delivery vehicle, enhancing the bioavailability and stability of active ingredients. The food industry utilizes it as a stabilizer for flavors, colors, and nutrients, as well as a functional ingredient for its effects on lipid metabolism. In cosmetics, it acts as a complex agent for fragrances and active components. Its applications extend to analytical chemistry for chiral separation and to materials science for developing smart materials and nanosystems.</p>

<p>Tween 85 is a surface active agent that can be used to remove particulates from the air. It is a synthetic, non-ionic surfactant composed of ethylene oxide and propylene oxide. This product has been shown to inhibit particle aggregation in vitro studies. Tween 85 has also been shown to reduce bronchiolitis obliterans in mice when administered by inhalation. Tween 85 may also be useful for removal of water-soluble drugs from wastewater treatment systems and as a chitosan quaternary ammonium detergent additive.</p>

An alginate-like polysaccharide produced by the fermentation of Azotobacter vinelandii or Pseudomonas mendocina. The chemical structure consists of blocks of (1,4) linked-β-D-polymannuronic acid (poly M), (1,4) linked-α-L-polyguluronic acid (poly G) and alternating blocks of the two uronic acids (poly MG). Unlike the alginate from seaweed, this polysaccharide is partially acetylated.

Sophorolipids are produced by various yeast species, notably Starmerella bombicola. Acidic Sophorolipids are amphiphilic molecules and therefore possess the attributes of surfactants; however as bio-surfactants they have several advantages over synthetic surfactants including low toxicity, biodegradability and the potential for low cost manufacture.

<p>2-(D-Gluco-pentylhydroxypentyl)-4(R)-1,3-thiazolidine-4-carboxylic acid is a custom synthesis. It is used in the glycosylation of saccharides and oligosaccharides. This product can be modified with fluorination, methylation, or click modification. It is also used in the synthesis of complex carbohydrates.</p>

<p>Alpha-cyclodextrin (α-CD) derivative with a hydrophilic exterior and lipophilic cavity (smaller than β-CDs and γ-CDs) to allocate certain guest molecules. This structural characteristic enables applications in molecular encapsulation, solubility enhancement, and stabilization across multiple industries. In pharmaceuticals, it serves as a drug delivery vehicle, enhancing the bioavailability and stability of active ingredients. The food industry utilizes it as a stabilizer for flavors, colors, and nutrients, as well as a functional ingredient for its effects on lipid metabolism. In cosmetics, it acts as a complex agent for fragrances and active components. Its applications extend to analytical chemistry for chiral separation and to materials science for developing smart materials and nanosystems.</p>

<p>Trans-zeatin-7-glucoside is an abscisic acid (ABA) metabolite that can be found in plant tissue. It is used as a natural product to regulate growth and development. Trans-zeatin-7-glucoside has been shown to inhibit the biosynthesis of gibberellins, which are plant hormones that promote cell elongation. This compound is purified from plant tissues by chromatographic methods, such as reversed phase HPLC or ion exchange chromatography. The sample preparation involves extraction with a solvent such as methanol or chloroform followed by purification on an analytical column. Immunoaffinity chromatography is also used for sample preparation, which involves binding to antibody molecules on the surface of a solid support material. Trans-zeatin-7-glucoside can be detected using analytical methods such as gas chromatography or liquid chromatography coupled with mass spectrometry. Trans-zeatin-7-</p>

<p>Lividamine is a protein synthesis inhibitor that has biphasic responses in animal studies. Lividamine inhibits the enzyme catalysis of aminoglycosides, which are used for the treatment of bacterial infections. It also blocks the biosynthesis of polypeptides, which are essential for cell growth and division. Lividamine binds to the hydroxyl group or carboxylate group on an amino acid, cleaving it from the peptide chain and stopping protein synthesis. Lividamine has been shown to be effective against bacteria in vitro assays. Further research is required to determine its clinical properties.</p>

<p>L-Arabinose-BSA is a Glycosylation, Oligosaccharide, sugar, Synthetic, Fluorination, Custom synthesis, Methylation, Monosaccharide, Polysaccharide, saccharide. It is a Click modification. L-Arabinose-BSA has CAS No. 1590-84-3 and Modification of complex carbohydrate. This product has High purity.</p>

Drug carrier for cancer therapy & imaging, biocompatible, soluble, biodegradable

Nepetin-7-glucoside is a compound found in plants that has been shown to have anti-inflammatory and antiviral properties. Nepetin-7-glucoside inhibits the activity of enzymes such as phospholipase A2, cyclooxygenase, and lipoxygenase. It also reduces the production of inflammatory mediators such as prostaglandins and leukotrienes. Nepetin-7-glucoside may be helpful in the treatment of autoimmune diseases and other inflammatory disorders. This compound also has antiviral effects by inhibiting the replication of herpes simplex virus type 1 (HSV1) in a cell culture system. Nepetin-7-glucoside also has been shown to inhibit the expression of genes related to inflammation and other inflammatory diseases, such as rheumatoid arthritis, colitis ulcerosa, psoriasis, and Crohn's disease.

<p>Flavanone rhamnoglucoside is a specialized flavonoid compound, which is derived from various natural sources such as fruits, vegetables, and certain medicinal plants. It functions primarily as an antioxidant by scavenging free radicals, thereby protecting cells from oxidative stress. Additionally, it exhibits anti-inflammatory properties by modulating pathways involved in inflammation, such as NF-kB and COX-2.</p>

<p>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.</p>

<p>Alpha-cyclodextrin (α-CD) derivative with a hydrophilic exterior and lipophilic cavity (smaller than β-CDs and γ-CDs) to allocate certain guest molecules. This structural characteristic enables applications in molecular encapsulation, solubility enhancement, and stabilization across multiple industries. In pharmaceuticals, it serves as a drug delivery vehicle, enhancing the bioavailability and stability of active ingredients. The food industry utilizes it as a stabilizer for flavors, colors, and nutrients, as well as a functional ingredient for its effects on lipid metabolism. In cosmetics, it acts as a complex agent for fragrances and active components. Its applications extend to analytical chemistry for chiral separation and to materials science for developing smart materials and nanosystems.</p>

<p>13-cis-Retinoyl b-D-glucuronide is a synthetic compound that can be modified to create a wide range of potential products. 13-cis-Retinoyl b-D-glucuronide is an oligosaccharide with a carbohydrate that may be glycosylated or polysaccharided. It has been custom synthesized and fluorinated, methylated, and monosaccharided. This product is extremely pure and can be used for many applications in the biomedical field.</p>

Alpha-cyclodextrin (α-CD) derivative with a hydrophilic exterior and lipophilic cavity (smaller than β-CDs and γ-CDs) to allocate certain guest molecules. This structural characteristic enables applications in molecular encapsulation, solubility enhancement, and stabilization across multiple industries. In pharmaceuticals, it serves as a drug delivery vehicle, enhancing the bioavailability and stability of active ingredients. The food industry utilizes it as a stabilizer for flavors, colors, and nutrients, as well as a functional ingredient for its effects on lipid metabolism. In cosmetics, it acts as a complex agent for fragrances and active components. Its applications extend to analytical chemistry for chiral separation and to materials science for developing smart materials and nanosystems.

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.

<p>Building block for DNA-related organic synthesis</p>

The anomeric position of 2,3,4-tri-O-benzyl-L-arabinopyranose is anomeric. The yields of the two possible anomers were not determined in this experiment. Hydrogenolysis of the benzyl group in 2,3,4-tri-O-benzyl-L-arabinopyranose at room temperature resulted in a mixture of the two possible anomers.

<p>2-O-a-D-Glucopyranosyl-L-ascorbic acid is a potent antioxidant compound found in the human body. It is produced by the enzyme tyrosinase from L-ascorbic acid and has been shown to have anti-apoptotic effects on skin cells. 2-O-a-D-Glucopyranosyl-L-ascorbic acid has also been shown to enhance mitochondrial membrane potential and increase the proliferation of skin cells in vitro. The compound has been tested for its ability to prevent radiation damage in mice and was found to be more effective than vitamin C at preventing cell death.<br>2OAGA can be used as a topical treatment for skin conditions, such as acne or wrinkles, by reducing inflammation and stimulating cellular growth.</p>

<p>a-D-Glucoheptonic acid sodium salt is a compound that has been shown to modulate the immune system. It also has been used in pharmaceutical formulations as an excipient and as a carrier for diagnostic and therapeutic agents.</p>

<p>L-Sorbose-1-phosphate potassium salt is a sugar phosphate</p>

Benzoic acid-acyl-b-D-glucuronide is a β-glucuronide linker that is cleaved by β-glucuronidase enzymes. This allows controlled release of the payload to the targeted cells.

<p>Monofucosyl-para-lacto-N-hexaose IV is a trisaccharide that belongs to the group of blood group antigens. It is found in human milk and can be used as an indicator for infant nutrition. Monofucosyl-para-lacto-N-hexaose IV is found in the cells of streptococcus, lactobacillus, and clostridium. It has been shown to be a potential biomarker for inflammatory bowel disease (IBD). This molecule has been used as an antigen in immunological assays. The sequences of monofucosyl-para-lacto-N-hexaose IV have been determined using chromatograms and profiles.</p>

<p>Asialylated glycosphingolipid and precursor for ganglioside biosynthesis. The compound is a major glycosphingolipid in human neutrophils and is involved in the regulation of superoxides as well as nitric oxide. Moreover, lactosylceramide accumulates in atherosclerotic plaques and is also found elevated in familial hypercholesterolemia and polycystic kidney disease. Animal studies revealed that lactosylceramide induces hypertrophy in cardiomyocytes via signal transduction pathway that is oxygen-sensitive.</p>

<p>N-Acetyl-D-quinovosamine is a chemical compound that belongs to the group of quinovosamines. It is an acidic molecule with a pKa of 3.5 and is soluble in water, methanol, and acetic acid. N-Acetyl-D-quinovosamine has been shown to inhibit the growth of P. aeruginosa strains, which are human pathogens. This drug binds to the bacterial cell wall by competitive inhibition and prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division. N-Acetyl-D-quinovosamine also inhibits the production of hydrogen fluoride (HF) by bacteria as well as their ability to produce ammonia from nitrite or nitrate ions.</p>

<p>GM4-ganglioside (sodium salt) is a disaccharide of sialic acid linked α2,4 to galactose and ceramide linked β to position 1 on the galactose (Ledeen, 2009). Demyelinated plaques in multiple sclerosis have decreased amounts of GM4-ganglioside, localized in myelin and oligodendroglia of the central nervous system. It has been found that the myelin basic protein is capable of releasing large quantities of entrapped [14C]glucose from multilamellar liposomes containing GM4. If the conformation of GM4 ganglioside in liposomal membranes resembles that of GM4 ganglioside in its natural environment, basic protein and GM4 may be associated within the myelin sheath of the central nervous system and their interactions are altered in demyelinating diseases, such as, multiple sclerosis (Mullin, 1981).</p>

<p>2,3,4,6-Tetra-O-acetyl-4-(hydroxymethyl)phenyl-b-D-glucopyranoside is a chemical that is extracted from the rhizoma gastrodiae. It is used to treat symptoms of damaged ganglion cells in diabetic patients. 2,3,4,6-Tetra-O-acetyl-4-(hydroxymethyl)phenyl-b-D-glucopyranoside inhibits chloride channels in neurons by binding with the extracellular receptor site and thereby preventing the influx of chloride ions. This leads to reduced neuronal excitability and decreased symptoms of damaged ganglion cells in diabetic patients. 2,3,4,6 Tetra O acetyl 4 (hydroxymethyl) phenyl b D glucopyranoside has been shown to have an inhibitory effect on structural formula and environmental pollution.</p>

<p>Lactose-6'-phosphate is a sugar phosphate</p>

<p>GM2 ganglioside (sodium salt) has a core trisaccharide structure (GalNAcβ1,4Galβ1,4Glc) with sialic acid linked α2,3 to the central galactose residue and ceramide linked β to position 1 on the reducing terminal glucose residue (Ledeen, 2009). GM2 ganglioside is present on neuronal cells and plays a key role in the regulation of dendritogenesis in cortical pyramidal neurons. In lysosomal storage disorders, such as, Tay-Sachs and Sandhoff disease, where hexosaminases A and B are deficient, GM2 ganglioside accumulates in the nervous system (Cachon-Gonzalez, 2018). GM2 ganglioside is also overexpressed in melanomas and other tumours of neuro-ecto origin (Yoshida, 2020). Moreover, the sugar moiety of the GM2 ganglioside is a receptor allowing the viral infection of cells with reovirus and rotavirus (Zhu, 2018).</p>

<p>2-Hydroxypropyl-b-cyclodextrin is a water-soluble drug that is chemically stable in aqueous media. It has been shown to be safe for use in the eye, with no significant side effects. 2-Hydroxypropyl-b-cyclodextrin has been shown to have anti-inflammatory properties and will not cause hemolytic activity. 2-Hydroxypropyl-b-cyclodextrin binds to retinoic acid receptors, which are found on cells of the corneal surface and in human spermatozoa. The binding of retinoic acid inhibits the production of enzymes that break down retinoids and prevents cell proliferation. This agent also interacts with other cellular components such as proteins, lipids, carbohydrates, nucleic acids, and hormones.</p>

<p>Tetraose composed of four N-acetylglucosamine residues.</p>

<p>Fucogalactan (GFS) is a polysaccharide isolated and purified from the brown seaweed Undaria pinnatifida. The polysaccharide is a sulphated galactose containing fucan. Fucogalactan is currently under investigation for possible therapeutic indications including anti-inflammatory properties, immuno- modulating activities, inhibition of tumor growth, stem cell replentishment, antiviral activity, dementia and ulcer healing.Fucoidan ≥ 75 %<br>The image was kindly provided by Prof Mike Guiry from Cork who runs ‘The Seaweed Site’.</p>

<p>Phenyl 2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside (TTA) is a synthetic monosaccharide that is used in the synthesis of complex carbohydrates. TTA is also known as Fluorination, Monosaccharide, Synthetic, Oligosaccharide, complex carbohydrate and has CAS No. 2872-72-2. TTA can be custom synthesized for research purposes or for commercial use and can be glycosylated to form polysaccharides. TTA is modified through methylation or click chemistry and can be used to modify sugar molecules or other carbohydrates. It is also high purity with less than 1% impurities.</p>

<p>Sustainable solvent used widely in cosmetic and pharmaceutical formulations</p>

<p>2,3:4,5-Di-O-isopropylidene-b-D-fructopyranose (IDFP) is a natural compound that has been shown to have pharmacological properties. It is an inhibitor of the enzyme alpha-glucosidase and may be used as a treatment for diabetes mellitus type II. IDFP binds to the active site of the enzyme α-glucosidase, preventing access of the substrate glucose. This causes a decrease in blood glucose levels and has also been shown to reduce cholesterol levels in mice. IDFP is synthesized by reacting ethylene diamine with 2,3:4,5-di-O-isopropylidene b -D -fructofuranose. This reaction produces a heterocycle that undergoes asymmetric synthesis using sodium hydroxide solution and hydrogen fluoride as catalysts.</p>

1,2-O-Isopropylideneglycerol is an inhibitor of glycerin and glycerol dehydrogenase. It is a colorless liquid that has been shown to have a kinetic inhibitory effect on the enzyme activities of glycerin and glycerol dehydrogenase in vitro. 1,2-O-Isopropylideneglycerol has also been shown to react with light at wavelengths of 250 nm or less. This reaction produces reactive oxygen species that may lead to the degradation of the enzyme's active site. In vivo, 1,2-O-isopropylideneglycerol is converted into an acidic metabolite that can accumulate in cells. This metabolite can react with other molecules such as proteins and nucleic acids, which may result in structural changes and/or modification of their function.

<p>Octyl D-galactofuranoside is a disaccharide that is found in the plant Gossypium hirsutum. It has been shown to have antibacterial activity and can be used as an alternative to antibiotics. Octyl D-galactofuranoside has been shown to inhibit the growth of bacteria by binding to chloride ions and inhibiting bacterial cell wall synthesis. It also acts synergistically with other antibiotics, such as penicillin, ampicillin, sulfonamides, tetracycline, erythromycin, and cefadroxil. This compound has been shown to be biodegradable and o-glycosylated. Octyl D-galactofuranoside also has anti-leishmanial activity.</p>

<p>70% β-D-Lactose is used in the pharmaceutical industry to produce tablets. It acts as a nutrient and as a filler in pills. It is also utilized in the dilution of heroin and to sweeten some beers.</p>

<p>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.</p>

<p>3,4,6-Tri-O-benzyl-D-glucal is a benzyl protected, 2,3 unsaturated glucal used as a chiral intermediate. The C2-C3 double bond of the pyranose ring can be modified via a variety of reactions including: hydrogenation, oxidation, hydroxylation, and aminohydroxylation, to generate structural complexity. 3,4,6-Tri-O-benzyl-D-glucal also minimizes tedious protecting-group strategies required for fully oxygenated sugars. The products of 2,3 unsaturated glycosides as chiral intermediates have played a role in the synthesis of many biologically active compounds, such as, nucleosides and modified sugar derivatives.</p>

<p>1,3-a-1,6-a-D-Mannotriose 1-O-propylamine acetate salt is a modified oligosaccharide. It has been synthesized by the reaction of 1,3-a-1,6-a-D-mannopyranosyl bromide with proline amine acetate. This product is 98% pure and can be used as a complex carbohydrate in research or as a food additive. The CAS number for this product is 712092-14-8.</p>

<p>L-Threonic acid is a metabolite of plants that is involved in the synthesis of other molecules. It can be found in the injection solution and magnesium salts that are used for treating osteoporosis and magnesium deficiency. L-Threonic acid can also be found in caffeic acids, which are plant polyphenols that have antioxidant properties. L-Threonic acid has been shown to have structural similarity to calcium and has been shown to have a role in mitochondrial membrane potential, cellular physiology, and oxidative injury. L-Threonic acid may also play a role in energy metabolism. The toxicity of L-Threonic acid has been studied extensively with mixed results.</p>

<p>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</p>

<p>Please enquire for more information about N-Acetyl-β-D-glucosaminyl-(1→4)-N-acetylmuramoyl-L-alanyl-D-isoglutamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Melezitose is a non-reducing trisaccharide that is produced by many plant sap-consuming insects, such as aphids (e.g. Cinara pilicornis).  Melezitose is a component of honeydew which acts as an attractant for ants and also as food for bees. Partial hydrolysis of melizitose releases glucose and turanose, an isomer of sucrose.

<p>a-D-Lactose 1-phosphate barium salt is a modification of a D-lactose monosaccharide. It is a complex carbohydrate that has been synthesized using the polyol method. The CAS number for this product is 103404-65-5. This product is available in high purity and the molecular weight of this compound is 576. a-D-Lactose 1-phosphate barium salt can be used as an ingredient in pharmaceuticals, food products, and cosmetics. It has been shown to have anticariogenic activities and may be used as a substitute for sucrose in food products.</p>

<p>L-Glycero-D-manno-heptose is a polymyxin B antimicrobial agent that has been shown to have significant activity against Gram-positive bacteria, including Staphylococcus aureus and Streptococcus pneumoniae. This compound also has an inhibitory effect on the growth of Gram-negative species such as Salmonella enterica. L-Glycero-D-manno-heptose inhibits the synthesis of bacterial cell wall peptidoglycan by binding to the terminal residues of oligosaccharides, which are linked to D-alanine in the peptidoglycan chain. The terminal residues of oligosaccharides are transferred from the lipid carrier to L-glycero-D manno heptose, forming a stable acylated glycoside. This reaction mechanism is similar to that of polymyxin B, but with a difference in reactivity due to steric hindrance.</p>

<p>Competitive inhibitor of fucosyltransferases FUT3, FUT5, FUT6 and FUT7 with Ki values in low micromolar range. This fluorinated GDP-fucose analog inhibits oligosaccharide core fucosylation of N-linked glycans in animal and plant cells.</p>

<p>2-Aminophenyl b-D-glucuronide is a cytosolic drug that is metabolized by the liver to mandelonitrile, which is then excreted in urine. 2-Aminophenyl b-D-glucuronide has been shown to inhibit the growth of fungi in vivo and has been shown to have a reversible binding affinity for fungal cell walls. This drug also inhibits the production of ergosterol, an important component of fungal cell membranes, which leads to cell death.</p>

<p>Candesartan N-glucuronide is a metabolite of candesartan. It is produced by human UDP-glucuronosyltransferase, which belongs to the subfamily of uridine diphosphate (UDP)-glucuronosyltransferases. Candesartan N-glucuronide inhibits angiotensin II receptor type 1 (AT1) and has minimal effects on angiotensin II receptor type 2 (AT2). Candesartan N-glucuronide binds to the AT1 receptor and blocks its activation by angiotensin II. This binding inhibits the uptake of sodium ions into cells and causes an increase in potassium ion secretion, leading to vasodilation. Candesartan N-glucuronide also induces the expression of cytochrome P450 3A5, which results in increased metabolism of drugs such as paclitaxel.</p>

UDP-L-galactose diammonium salt is a modification of the sugar UDP-galactose. It is an oligosaccharide that is found in glycoproteins and glycolipids. It is synthesized by the addition of a methyl group to the galactose ring and a fluorine atom to the hydroxyl group on carbon 4. UDP-L-galactose diammonium salt is used as a synthetic sugar in laboratory settings, although it can also be found in nature. This compound has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.

<p>GD1b oligosaccharide (shown as ammonium salt) is the carbohydrate moiety in one of the major gangliosides in neuronal and glial membranes; it has a core tetrasaccharide structure (Galβ1,3GalNAcβ1,4Galβ1,4Glc) with its two sialic acids linked α2,3/α2,8 to the inner galactose residue (Ledeen, 2009). GD1b ganglioside acts as a receptor for BK virus as well as for heat-labile LTII-a toxin, produced by enteropathogenic E. coli. GD1b ganglioside also interacts with tetanus neurotoxin (TeNT) and is crucial for its entry into cells (Kolter, 2012). The functional significance of ammonia in the brain is not yet fully understood. However, NH4 + stimulates Na+, K+ activated ATPase causing stabilization of the neuronal membranes of which gangliosides are major structural components. Further, ammonia is known to inhibit lysosomal enzymes which include enzymes degrading gangliosides (Modi, 1994).</p>

<p>Inhibitor of α-glucosidase with applications in diabetes therapy for control of post-prandial blood glucose fluctuations. The compound inhibits the digestive breakdown of complex carbohydrates to absorbable monosaccharides and smoothens hyperglycaemic peaks in type 2 diabetes mellitus. It also possesses anti-obesity effects thanks to activation of brown adipose tissue and increasing energy expenditure.</p>

<p>Monofucosyl (1-2)-iso-lacto-N-octaose I is an oligosaccharide found in human milk</p>