Glycoscience

<p>Galactose from plant origin, animal free production</p>

<p>2-Amino-b-L-arabinofurano[1,2:4,5]oxazoline is a custom synthesis. It is a white to off-white powder with a molecular weight of 264.50 and a melting point of about 160°C. The purity of this compound is &gt;98% by HPLC analysis. This product has been modified with glycosylation, methylation, click modification, fluorination, saccharide modification, sugar modification, and oligosaccharide modification.</p>

<p>3-O-Allyl-1,2-O-isopropylidene-α-D-galactofuranose is a synthetic glycoside that can be custom synthesized. It is a fluorinated monosaccharide that reacts with an allyl group to form an allyl glycoside. This modification increases the solubility of the molecule and can make it soluble in organic solvents. 3-O-Allyl-1,2-O-isopropylidene α D galactofuranose is used to modify saccharides or complex carbohydrates for use in research.</p>

<p>Please enquire for more information about 2-Acetamido-2-deoxy-a-D-thiogalactopyranose including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(1S) -1- [(2S, 3S,4R) -N-Butyl-4-hydroxymethyl-3- hydroxy- 1- azetidinyl] -1, 2- ethanediol is a synthetic monosaccharide that belongs to the group of complex carbohydrates. It has been modified by fluorination and methylation. This product can be synthesized according to customer specifications. The CAS number for this product is 97911-51-7. It is highly pure with a purity level of 98%. This product can be glycosylated or click modified according to customer specifications.</p>

<p>2'-Azidoethyl a-mannopyranoside is a synthetic monosaccharide that is used as a building block for the synthesis of oligosaccharides and polysaccharides. This product has been custom synthesized for your specific needs. It is an off-white powder with purity greater than 99%. The methylation of this compound can be achieved by reacting it with sodium methoxide in methanol, followed by hydrolysis with sodium hydroxide. The azido group can also be converted to an acetyl group by reaction with acetic anhydride in pyridine.</p>

<p>Isosorbide dinitrate is a drug that belongs to the class of nitrates. It is used in the treatment of angina pectoris, as well as congestive heart failure and chronic heart failure. Isosorbide dinitrate has been shown to cause caspase-independent cell death in human leukemia cells and breast cancer cells. This may be due to its ability to inhibit mitochondrial membrane potential and interfere with intracellular calcium mobilization. The optimum concentration for isosorbide dinitrate is 10 µM, which inhibits the growth of bacteria, including Mycobacterium tuberculosis and Salmonella enterica serovar Typhimurium. The drug also inhibits the production of proinflammatory cytokines such as IL-1β, IL-6, and TNF-α by inhibiting c-jun phosphorylation. Isosorbide dinitrate also has anti-inflammatory properties, which may be due to its ability to inhibit 4-hyd</p>

<p>D-Glucosamine-oxime HCl is a hydrocyanic acid derivative that contains a polyhydroxy group. It can exist as two isomers, D-glucosamine and D-glucosamine-oxime. These isomers are distinguished by the presence or absence of acetyl groups on the nitrogen atoms. D-Glucosamine-oxime HCl functions as a divalent metal ion chelator and sequestering agent that has been shown to be useful in the treatment of lead poisoning. It also has been used in the synthesis of hydrocyanic acid, which is an important chemical for organic synthesis.END&gt;</p>

<p>2,3,5-Tri-O-benzyl-L-ribonic acid-1,4-lactone (2,3,5-TRBA) is a fluorinated monosaccharide that is synthesized from D-ribose and hexafluoroisopropanol. It is also an oligosaccharide that can be custom synthesized for the synthesis of complex carbohydrates. 2,3,5-TRBA can be modified with methylation or glycosylation to yield a range of desired products. The CAS number for this compound is 103514-06-1. This compound has a purity of &gt;98%.</p>

<p>Lactose is the principal sugar in human and most other mammalian milks, ( 4-O-(β-d-galactopyranosyl)-d-glucopyranose) (Collins, 2006). Lactose undergoes mutarotation; it is a reducing sugar and is significantly less soluble in water than sucrose. Lactose is much less sweet than sucrose (at ~1% about 0.15 (sucrose=1). The enzyme lactase (β-galactosidase), which is present in the small intestine, catalyzes hydrolysis of lactose to form glucose and galactose. Anhydrous lactose is an excipient, filler, diluent, and bulking agent in a wide variety of pharmaceutical tablets, capsules, powders and other preparations. Lactose also has applications as a nutrient and multi-functional ingredient in infant formulae, geriatric, dietetic and health foods (Linko, 1982).</p>

<p>L-Arabinose diethyldithioacetal is a potassium carbonate derivative of L-arabinose that reacts with sulfur to form 1,2-dithioketals. These dithioketals are used as glycosyl donors in the synthesis of L-fucitol and d-xylose. This reaction is catalyzed by acetobacter, which converts L-arabinose and carbon dioxide into acetaldehyde and acetic acid. The reaction mechanism for this transformation includes an epimerization of the hydroxyl group on the C5 position of L-arabinose to a hydroxyl group on C6, followed by glycosidation with sulfuric acid. The glycosidic bond formed between the hydroxyl group on C6 and the carbonyl group at C1 (in this case, from L-arabinose) is called an acetal linkage. In addition to being antithrombotic</p>

<p>11-Dehydroxygrevilloside B is a natural glycoside compound, which is primarily isolated from the plant genus Grevillea. This genus is known for its rich diversity of secondary metabolites with various biological activities. The mode of action of 11-Dehydroxygrevilloside B involves interactions with specific molecular targets, potentially influencing biochemical pathways associated with inflammation, oxidative stress, or other cellular processes. Its exact mechanism is still under research, aiming to unravel its potential therapeutic or protective effects. Applications of 11-Dehydroxygrevilloside B are mainly within the realm of biochemical and pharmacological research, where it serves as a subject for in vitro or in vivo experiments to explore its efficacy and safety profile. Its study contributes to understanding how plant-derived compounds can be harnessed for medicinal purposes and augments the exploration of novel drug candidates from natural sources.</p>

<p>Dextran is a polysaccharide that is used as an antimicrobial agent and as a volume expander in the treatment of bowel disease, myocardial infarct, and other diseases. Dextran sulfate is a linear polymer with a molecular weight of 500,000 to 1,000,000. It has minimal toxicity and does not interfere with iron homeostasis or cause fluid overload. Dextran sulfate can be used for the treatment of bowel disease because it has been shown to have anti-inflammatory effects in experimental models. The mechanism by which dextran sulfate inhibits inflammation is unknown, but may involve its ability to bind to macrophages and neutrophils in the gut wall. Dextran sulfate also binds to bacteria and prevents their growth. This binding may prevent bacterial penetration into epithelial cells or block bacterial attachment to cell surfaces. The efficacy of dextran sulfate against pathogenic mechanisms such as inflammation has been demonstrated in experimental models.</p>

<p>Hexahydro-1,2,8-trihydroxy-[1S-(1a,2a,8a,8ab)]-5(1H)-indolizinone is a custom synthesis of a complex carbohydrate. It is an Oligosaccharide and Polysaccharide. The saccharide Methylation and Glycosylation are the Modification of this molecule. This product has CAS No. 96625-36-4 and Click modification is Carbohydrate sugar. This product is highly pure with Fluorination Synthetic</p>

<p>2-Acetamido-2-deoxy-5-thio-D-glucose is a custom synthesis product. It is an oligosaccharide or polysaccharide that is modified with a fluorine atom in the 2 position of the sugar. This modification can be done either by Click chemistry or by chemical oxidation. The modification of 2-acetamido-2-deoxy-5-thio-D-glucose makes it useful as a fluorescence probe for probes and as a fluorescent dye.</p>

<p>3,6-Anhydro-D-galactose is a monosaccharide of D-galactose where the 3 and 6 positions are cyclised in an ether link. 3,6-Anhydro-D-galactose is found naturally occurring in Rhodophyta (Red Algae) and is a constituent of the sulphated polysaccharide PLS, which has shown anti-inflammation activity and anti-nociceptive effects. In addition, sulphated polysaccharide is capable of inhibiting the in vitro replication of Herpes simplex virus type 1 (HSV-1) and HIV-1.<br>We also offer this product in 10% aqueous solution (MA07897).</p>

<p>1-deoxy-D-psicose is a deoxy sugar that can be used as a reagent for the conversion of 1-deoxy-d-fructose to d-psicose. It is useful in the synthesis of rhamnose, which is a precursor to pharmaceuticals and agrochemicals. 1-Deoxy-D-psicose can be used in the synthesis of l-rhamnose from d-psicose or vice versa. This process of converting one epimer to another isomerization is very efficient, with an 88% yield.</p>

<p>2-Deoxy-L-ribose-anilide is a chemical compound that has been patented for its use in the detection of magnetic fields. The patent claims that this compound can be used as an intermediate in the preparation of other compounds. 2DRA has different transition temperatures, depending on whether it is in the solid or liquid state. When 2DRA is heated, it changes from a colorless liquid to a yellow crystal at around 100°C and then becomes a white solid at around 150°C. The magnetic properties of 2DRA arise from its ability to form strong bonds with other molecules, which are broken by external magnetic fields.</p>

<p>4-Methoxyphenyl 4-O-(2,4,6-tri-O-acetyl-3-O-allyl-b-D-galactopyranosyl)-3-O-allyl-b-Dglucopyranoside is a synthetic sugar with a molecular weight of 532. This product can be used in the synthesis of oligosaccharides and monosaccharides. It is also used as an intermediate in glycosylation reactions. This product has not been assigned a CAS number yet.</p>

<p>A fucan sulphate found in brown marine algae (Phaeophyta-typically Fucus vesiculotus, Durvillea (illustrated), Alaria and Cladosiphon) and has been shown to have anticoagulant activity. The main constituents are α-1,4 and α-1,2 linked L-fucose sulphates although galactose also occurs and there are many variations of the basic structure found in different species of Phaeophyta.<br>The fucose content of this fucan is approximately 27.9% and it also contains galactose (approx. 6.2%), uronic acid (approx. 22.4%) and sulfate (approx. 21.4%).<br>The image was kindly provided by Prof Mike Guiry from Cork who runs ‘The Seaweed Site’.</p>

<p>Ethyl 2,3,4,6-tetra-O-acetyl-b-D-thiogalactopyranoside is a natural sugar that is used in the food industry as a flavoring agent.</p>

<p>A fucan sulphate found in brown marine algae (Phaeophyta-typically Fucus serratus, Ascophyllum nodosum, Laminaria japonica (illustrated) and Macrocystis pyrifyra) and has been shown to have anticoagulant activity. The main constituents are α-1,4 and α-1,2 linked L-fucose sulphates although galactose also occurs and there are many variations of the basic structure found in different species of Phaeophyta.<br>Fucoidan ≥ 95.0% Organic SO42- ≥ 20.0% Carbohydrate ≥ 70.0% L-Fucose ≥ 23.0% Alginic Acid ≤ 31.0% <br>The image was kindly provided by Prof Mike Guiry from Cork who runs ‘The Seaweed Site’.</p>

<p>6-Deoxy-6-fluoro-D-galactose is a fluorinated sugar that has been shown to inhibit the uptake of glucose by human liver cells. This sugar binds to the enzyme activity and inhibits its activity. 6-Deoxy-6-fluoro-D-galactose was found to be metabolized in a dose dependent manner, with higher doses leading to increased uptake of fluorescein and decreased uptake of glucose. 6FDG is also metabolized by chemical reactions, such as oxidation or hydration, which leads to a decrease in its inhibitory effect on glucose uptake. 6FDG has been shown to bind to sequences that are involved in sugar transport and cell culture studies have shown that this sugar can induce inhibition of cell growth at high concentrations.</p>

<p>Component of plant, especially grape, glucuronoxylans</p>

<p>1,5-Anhydro-2,3,4-tri-O-benzoyl-D-threo-pent-1-enitol is a high purity compound that is synthesized from D-threo pent 1 enitol. It is a sugar that belongs to the category of complex carbohydrates. This product can be custom synthesized and modified according to customer requirements.</p>

<p>1,4-β-D-Xylotetraose is a sugar that is found in the genus Talaromyces and is used as a sweetener. It is produced by plant cells and has been shown to have thermostability. 1,4-β-D-Xylotetraose has been found to have lipidomic activity, which may be related to its ability to bind lipids. It also has a dietary profile, which may contribute to its use as a supplement. 1,4-β-D-Xylotetraose can be used as an affinity agent for lipid profiling because it binds lipids with high affinity.</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>2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-b-D-mannopyranose is a synthetic carbohydrate. It is a modified form of the natural sugar mannose that has been fluorinated. This modification gives 2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy--b--D--mannopyranose an increased resistance to degradation by enzymes. The CAS number for this compound is 6730–10–5.</p>

<p>Methyl 4,6-O-benzylidene-a-D-mannopyranoside is a hexadecanoic acid that is mediated by the target cell. It has been shown to inhibit the growth of bacteria and cancer cells in vitro. Methyl 4,6-O-benzylidene-a-D-mannopyranoside also possesses an antibacterial activity with a low mammalian toxicity. This compound is hydrolyzed by esterases or glucuronidases, oxidized by cytochrome P450 enzymes, reduced by glutathione reductase, or conjugated with glucuronic acid. The residue of this compound has been shown to be carcinogenic in vivo and in vitro. Anticancer activity of this compound may be due to its ability to disrupt DNA synthesis and induce apoptosis of cancer cells.</p>

<p>Chitosan is the deacetylated form of chitin.  The polysaccharide is deacetylated in order to render it soluble, which is then possible at pH values of less than 7 (normally in dilute acid).  This then allows the material to be used in a number of industrial applications as a binder and film former.MW typically 10-100kDa.</p>

<p>3-Azido-3-deoxy-1,2:5,6-di-O-isopropylidene-a-D-galactofuranose is a synthetic sugar that can be used as a monosaccharide or oligosaccharide. It is a complex carbohydrate that can be modified with methylation, fluorination, and click chemistry. 3-Azido-3-deoxy-1,2:5,6-di-O-isopropylidene-a-D galactofuranose is an important compound in carbohydrate chemistry due to its ability to undergo glycosylation reactions. The chemical properties of 3ADGFP are comparable to those of other monosaccharides and carbohydrates.</p>

<p>D-Glucarate monopotassium is a pharmaceutical preparation that is used to inhibit the growth of bacteria. It inhibits the proliferation of cells by inhibiting fatty acid synthesis, which leads to decreased levels of cholesterol, and reduces the uptake of glucose. D-Glucarate monopotassium is also an oxidizing agent that converts uridine into uric acid and has been shown to have inhibitory properties against human cancer cells. D-Glucarate monopotassium can be used as an antioxidant for the prevention or treatment of chronic diseases such as atherosclerosis, diabetes, and cancer. This compound acts as an inhibitor for trypsin treatment on carbohydrates, preventing hydrolysis by this enzyme.</p>

<p>Trivalent GalNAc precursor</p>

<p>1-Octylamino-1-deoxy-D-glucitol is a natural product that is extracted from the bark of the tree Streptomyces griseorubens. It has been shown to have a diastereomeric ratio of 97:3 and an optical purity of 98%. The thermodynamic properties of this compound are determined by the reaction time, which can vary from 1 to 24 hours. The enantiomers are separated by chromatography or crystallization, and the solubility data is determined at 25°C.</p>

<p>Chitosan oligomer (Dp 12-20) is a modification of chitin, a polysaccharide. It can be synthesized by treating chitin with sodium hydroxide in an alkaline environment. Chitosan oligomer (Dp 12-20) has a high degree of saccharide modification and exhibits a variety of functions, including complex carbohydrate, custom synthesis, synthetic, high purity, CAS No., and monosaccharide methylation. This compound has been shown to inhibit the growth of bacteria such as Staphylococcus aureus and Clostridium perfringens.</p>

<p>3,5-Di-O-benzoyl-2-deoxy-2,2-difluoro-D-ribonic acid-1,4-lactone (3DBR) is a nucleoside that has been shown to have antiaging properties. It has been found to be an effective scavenger of peroxyl radicals and reactive oxygen species (ROS). 3DBR also inhibits the formation of aluminum oxide and styrene by catalyzing the salt formation reaction. This compound also has anti-tumour activity and can be used as a chemotherapeutic agent for the treatment of cancer. It is heat resistant and can be combined with gemcitabine hydrochloride in chemotherapy.</p>

<p>Galactose (Gal) is the C4 epimer of glucose with one hydroxyl group axial which by Hudsons rules makes it slightly less stable than glucose (Hudson, 1948). However, galactose is very common in plants and animals, and occurs in many polysaccharides, such as, galactomannans (e.g. Guar, Locust Bean Gum), Carrageenans , Agar (L-Galactose), Hemicellulose, Gum Arabic [link] and galactans (e.g. from Lupin) (Whistler, 1993). Galactose is one of the key mammalian monosaccharides (glucose, galactose, mannose, fucose, N-acetyl glucosamine, N-acetyl galactosamine and sialic acid) and it occurs in blood, milk, gangliosides, N- and O-linked glycans (Gabius, 2009). Like glucose, galactose exhibits mutarotation (Acree, 1968) and is optically active (dextrorotary) with L-galactose as its enantiomer (levorotary).</p>

<p>D-Galacturonic acid sodium salt is a salt form of D-galacturonic acid. It is an extract from seaweed and has been shown to have the ability to be absorbed in the intestines. This compound can be used as a diagnostic tool, such as for detecting strontium or radioactive isotopes in urine samples. The esters of this compound have been shown to have chelating activity and may be useful as reagents in analytical chemistry.</p>

<p>Used for the synthesis of 1β-O-acyl glucuronides</p>

<p>3-O-(β-D-Galactopyranosyl)-D-glucopyranose is a custom synthesis, modification, and fluorination of a monosaccharide. It is a synthetic and modified saccharide. The molecular formula for this compound is C6H10O5 and its molecular weight is 180.17 g/mol. This chemical has been assigned CAS No. 28447-38-3 and has the following structure:</p>

<p>4,6-O-(4-Methoxybenzylidene)-1,2,3-tri-O-pivaloyl-b-D-galactopyranose is a custom synthesis of a complex carbohydrate. It is an oligosaccharide that has been modified with methylation and glycosylation. The CAS number for this compound is 123097-29-2. This compound has a high purity and has been fluorinated with the click reaction. It is a synthetic sugar that is also a polysaccharide.</p>

<p>Sialyl-3-fucosyllactose is a monosaccharide that is a component of the sialyl-Lewisx oligosaccharide. The il-2 receptor binds to this oligosaccharide, which is involved in energy efficiency. 3'-Sialyl-3-fucosyllactose has been linked to cancer resistance and gene product production. It has also been found to be an important dietary nutrient for animals and humans. 3'-Sialyl-3-fucosyllactose plays an important role in the growth of cells, especially those that have been damaged or are undergoing apoptosis. It also has neurotrophic effects, which are beneficial for the development of neurons and brain function. Body mass index (BMI) is also known to be related to 3'-sialyl-3-fucosyllactose levels in plasma.</p>

<p>Thymol-b-D-glucopyranoside is a bactericidal agent that is resistant to encapsulation. It has been shown to be effective against animals and typhimurium in an incubated population and endogenous deaminase inhibitor strategy. The porcine activated food chemistry and abattoir experiments show that thymol-b-D-glucopyranoside has the potential to reduce populations of bacteria in the gastrointestinal tract by inhibiting protein synthesis.</p>

<p>3,4-O-Isopropylidene-L-arabinose (3,4-OIRA) is an isopropylidene derivative of L-arabinose. 3,4-OIRA has been shown to be a substrate for glycosylation reactions with various other sugars. It can also undergo methylation reactions and has been modified by fluorination. 3,4-OIRA is a food additive that belongs to the category of complex carbohydrates.</p>

<p>D-Galactosamine is a glycosaminoglycan (GAG) that is found in the mammalian cell. N-Thioglycolyl-D-galactosamine is a synthetic analog of D-galactosamine that was developed to study the biosynthesis of GAGs and glycoconjugates in cells. This molecule can be activated by hematopoietic cells, which leads to an increase in o-glycosylation and galnac synthesis.</p>

<p>The glucuronidation of 1-O-(trans-3-hydroxycotinine)-b-D-glucuronide ammonium salt is mediated by the enzyme UDP-glucuronosyltransferase. This reaction is catalyzed by the transfer of a glucuronic acid residue from UDP-glucuronic acid to a hydroxyl group on the side chain of 1-O-(trans-3-hydroxycotinine)-b-D-glucuronide ammonium salt. The kinetic analysis of human urine samples has shown that this reaction is significant. This metabolite can be detected in urine samples using next generation sequencing and its concentration can be used as an indicator for the consumption of tobacco or nicotine containing products. Epidemiological studies have shown that this metabolite has significant effects on cancer risk. Genotyping and genotype studies have shown that this metabolite is responsible for genetic polymorphisms that are associated with increased cancer risk.</p>

<p>Gal-b-1-3-GalNAc-b-1-4-Gal-b-1-4-Glc is a polysaccharide that is an important component of the outer membrane of Gram negative bacteria. It has been synthesized and modified with methylation, saccharide, Click modification, and glycosylation. The oligosaccharide has a high purity and is synthesized by custom synthesis. GalNAc is purified by HPLC and fluorinated to achieve complex carbohydrate.</p>

<p>2-C-Methyl-L-ribono-1,4-lactone is a crystallized carbohydrate that contains the enantiomers L and D. It is a chiral molecule with two asymmetric carbon atoms. The L form has a higher yield than the D form and can be synthesized from l-arabinose, dimethylamine, and isomerisation. This compound is also present in ketoses such as d-xylose and 1-deoxy-d-ribulose. 2CMLR1L4L acts as an inhibitor of the enzyme d-galactose dehydrogenase, which catalyzes the conversion of d-galactose to d-glucose. Cyanide can bind to this compound to form cyanohydrin adducts, which are toxic to cells.</p>

<p>1,4-Anhydro-D-glucitol is a compound that belongs to the group of monosaccharides and has biological properties. It has also been used in the production of acetate extracts from fetal bovine erythrocytes. The ester linkages are formed between 1,4-anhydro-D-glucitol and sodium salt by reaction with acetic anhydride. The reaction mechanism has been studied in detail, and it was found that hydroxyl groups on the molecule react with sodium ions to form an ester linkage. This compound is toxicologically safe at high doses, but can become toxic at lower doses due to its acid formation potential.</p>

<p>2-Acetamido-4,6-O-benzylidene-2-deoxy-D-galactopyranose is a fluorescent dye that binds to the hydroxyl group of nucleic acids. It can be used for microscopy of cells and bacteria in culture. This dye is also used for the measurement of cavitation activity. The dye is added at a concentration of 0.1% to the cell culture media. After 24 hours, it can then be observed with a microscope under UV light. 2-Acetamido-4,6-O-benzylidene-2-deoxy-D-galactopyranose has been shown to have lysis effects on cells such as agarose gels and mammalian cells, leading to cell death by apoptosis or necrosis. It's also used as an indicator in gel electrophoresis experiments because it can bind to DNA and RNA molecules, which makes</p>

<p>This gamma-cyclodextrin (γ-CD) derivative is a modified cyclic oligosaccharide composed of eight glucose units, featuring a larger cavity size than α- and β-cyclodextrins. This structural characteristic allows γ-CDs to form inclusion complexes with a wider range of guest molecules, making it particularly versatile in various industries. In the food sector, it is used as a carrier and stabilizer for flavors, fat-soluble vitamins, and polyunsaturated fatty acids, protecting volatile compounds from evaporation. In pharmaceuticals, it enhances the solubility and bioavailability of poorly water-soluble drugs and, thanks to its larger ring size, allows for the encapsulation of larger molecules or even entire drug molecules. γ-CDs and derivatives are also used for environmental remediation and, in analytical chemistry, for the extraction and concentration of target substances.</p>

<p>L-glucose is a monosaccharide that is an important source of energy for the human body. The glucose molecule consists of 6 carbon atoms, 12 hydrogen atoms and 6 oxygen atoms. Glucose enters cells with the help of insulin and ATP-sensitive potassium channels. It has been shown that L-glucose can inhibit viral replication in vitro, such as HIV and herpes simplex virus type 1 (HSV-1). L-Glucose may be used to treat squamous carcinoma by reducing the redox potential in cancer cells. L-Glucose inhibits the growth of c. glabrata by inhibiting transcription activators and enzymes involved in glycolysis. L-Glucose also has hypoglycemic effects on humans by reducing cortisol concentrations in human serum.</p>

<p>Scleroglucan is produced by the fermentation of the fungus Sclerotium rolfsii. It is a glucan with a main chain of 1,3-linked β-D-glucopyranosyl units with every third unit having a single β-D-glucopyranosyl unit linked 1,6. Scleroglucan powders disperse in water and give very viscous shear thinning solutions. Applications are in the oil industry in enhanced oil recovery, in agriculture in sprays and in the food and pharmaceutical industries.<br>The image was kindly provided by Dr. Chris Lawson.</p>

<p>Substrate for UDP-3-O-acyl-N-acetylglucosamine deacetylase (LpxC)</p>

<p>For synthesis of D-Altritol nucleosides</p>

<p>6-Methyldiosgenin acetate is a saponin that is found in the plant Balanites aegyptiaca. It has been shown to have anti-inflammatory and anti-tumor effects, as well as antioxidant properties. 6-Methyldiosgenin acetate also has been shown to stimulate the production of nitric oxide (NO) in endothelial cells, which may contribute to its anti-inflammatory effects. The chemical structure of 6-methyldiosgenin acetate is similar to that of furostanol and spirostanol, which are both saponins found in plants that can be used for the treatment of cancer. In addition, sapogenols are known to have a variety of therapeutic activities including antidiabetic, antiviral and anticancer activity.</p>

<p>Pregnanediol 3α-O-β-D-glucuronide is a glucuronide metabolite of progesterone, which is a key steroid hormone in the reproductive system. This compound is derived from the metabolic conversion of progesterone, primarily within the liver, where it undergoes glucuronidation. This process involves the addition of glucuronic acid, mediated by the enzyme UDP-glucuronosyltransferase, enhancing the compound’s solubility for renal excretion.</p>

<p>2,3,5-Tri-O-benzyl-D-ribofuranose is a carbohydrate that can be synthesized through an efficient method. It is a glycoside with an oxotitanium (oxo) group. The synthesis of this compound requires magnesium as the activating agent and o-glycosylation. The glycoconjugates of this compound are found in organisms such as fungi, yeast, and bacteria. In addition to its carbohydrate function, 2,3,5-Tri-O-benzyl-D-ribofuranose has been shown to have antimicrobial properties. This sugar has also been shown to have antiviral properties due to its ability to inhibit the enzyme ribonucleotide reductase (RNR).</p>

<p>4-O-(2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl)-1,2,3,6-tetra-O-acetyl-b-D-thioglucopyranose is a glycosylated saccharide that belongs to the group of complex carbohydrates. The glycosylation of 4-O-(2,3,4,6,-Tetra-O-acetyl b -D -glucopyranosyl)-1,2,3,6,-tetra -O -acetyl b -D -thioglucopyranose is achieved by the enzymatic reaction of an acetate donor and an acceptor molecule in the presence of glucose 1 phosphate (G1P) and UDP sugar pyrophosphorylase. It has been modified by methylation with dimethyl sulphate in the presence of</p>

<p>Inhibitor of beta-glucosidase</p>

<p>D-Allose pentaacetate is a modified oligosaccharide that can be used as a synthetic intermediate in the production of complex carbohydrates. It has been shown to have high purity and is easily synthesized in a laboratory setting. D-Allose pentaacetate is a monosaccharide with five acetate groups that can be methylated or glycosylated, which makes it an ideal candidate for modification. D-Allose pentaacetate has CAS No. 144071-49-8 and can be found on PubChem CID: 1215965.</p>

<p>b-Lactopyranosyl phenylisothiocyanate is a synthetic carbohydrate that has been modified with fluorine, methylation, glycosylation, and click chemistry. It is used in the synthesis of saccharides and oligosaccharides. This compound can also be used to modify saccharides or oligosaccharides with fluorine, methylation, glycosylations, or click chemistry.</p>

<p>a1-3-Galactobiose-biotin is a synthetic, fluorinated oligosaccharide that has been modified with 3 biotin molecules. It is synthesized by the glycosylation of 1,3-galactobiose and is used as an intermediate in the synthesis of carbohydrates. The sugar moiety can be modified with different chemical groups and reactions such as methylation or click modification to change its properties.</p>

<p>4-Methylphenyl 3-O-[(4-methoxyphenyl)methyl]-4,6-O-[(R)-phenylmethylene]-1-thio-α-D-mannopyranoside is a synthetic glycosaminoglycan. It is a complex carbohydrate that contains a saccharide and an oligosaccharide bound to each other by an aminosugar link. 4-Methylphenyl 3-O-[(4-methoxyphenyl)methyl]-4,6-O-[(R)-phenylmethylene]-1-thio-α-D mannopyranoside has been synthesized with the use of Click chemistry and fluorination. The CAS number for this compound is 1071226–24–8. This compound was custom synthesized in high purity.</p>

<p>4-Methylphenyl 4,6-O-[bis(1,1-dimethylethyl)silylene]-1-thio-β-D-galactopyranoside is a synthetic sugar that is used in the glycosylation of proteins. It is synthesized from 4-methylphenol and 1,1'-dimethylethylsilylene in the presence of trichlorosilane, followed by silylation with trimethylchlorosilane. The fluorinated site can be modified to suit your needs by following a Click chemistry protocol. This product has CAS No. 1242144-05-3 and is available for custom synthesis upon request.</p>

<p>GD1b (shown as sodium salt) is one of the major gangliosides in neuronal and glial membranes. It has a core tetrasaccharide structure (Galβ1,3GalNAcβ1,4Galβ1,4Glc) with it’s two sialic acids linked α2,3/α2,8 to the inner galactose residue and ceramide linked β to position 1 on the reducing terminal glucose residue (Ledeen, 2009). GD1b 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).</p>

<p>Hexa-guluronic acid sodium salt (1,4-linked α-L-sodium guluronohexaose) is one of a number of oligosaccharides obtained from alginate which is a polysaccharide in brown seaweeds containing: blocks of repeating mannuronic acid sequences (M-M-M-M etc), repeating guluronic acid sequences (G-G-G-G etc), and alternating M-G-M-G sequences. This oligosaccharide can be released by acid hydrolysis (Shimokawa, 1996) and a number of biological activities have been discussed in a recent review (Xing, 2020).</p>

<p>2-Amino-3,4-dihydroxybenzoic acid is an organic compound. It is a white solid that is soluble in water and polar organic solvents. 2-Amino-3,4-dihydroxybenzoic acid is used as an anti-inflammatory agent and for the treatment of arthritis.</p>

<p>2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone is an organic compound that belongs to the class of lactones. It is a chiral molecule with two asymmetric carbons and four stereogenic atoms. This compound can be used for the synthesis of optically active compounds. It is also a precursor for the synthesis of morpholines and phosphonates. 2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone can be synthesized by reacting an enolate with an aldehyde in the presence of a base and acid catalyst. The acid catalyst causes elimination of water from the enolate to produce the desired product.</p>

<p>2-Keto-L-galactonic acid is a chemical compound that belongs to the group of fatty acids. It is produced by the degradation of polyunsaturated fatty acids and has been shown to be a potential control agent for hepatic steatosis. 2-Keto-L-galactonic acid also inhibits the synthesis of dinucleotide phosphate in rat liver cells, leading to an accumulation of intracellular potassium ion. This compound inhibits the uptake of glucose by activating ATPase, which leads to an increase in intracellular pH. The uptake of 2-keto-L-galactonic acid into cells has been shown using cell culture experiments with wild type and mutant strains.</p>

<p>1,2-O-Isopropylidene-3-deoxy-3-fluoro-a-D-ribofuranose is a custom synthesis. It is a complex carbohydrate that has been modified by methylation and glycosylation. This molecule has been fluorinated to produce a high purity product with the desired properties. The 1,2-O-isopropylidene group provides for increased stability and solubility of the product.</p>

<p>Induces ulceration; used to model inflammatory bowel disease</p>

<p>Please enquire for more information about 2-Amino-1,6-anhydro-2-deoxy-β-D-glucopyranose including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>A gallotannin found in plants, with various biological activities. Its anti-cancer effect has been demonstrated in several cancer cell lines, mediated by inhibition of DNA replication, proliferation and angiogenesis. Elicits anti-inflammatory, antioxidative and anti-diabetic effects. Recently, it has been identified as an inhibitor of c-Myc in hepatocellular carcinoma and multiple myeloma cells.</p>

<p>1,2,3,4-Tetra-O-benzyl-6-O-tert-butyldiphenylsilyl-a-D-mannopyranose is a synthetic glycoside that can be used as a building block for the synthesis of complex carbohydrates. It is a fluorinated sugar that can be modified with methyl groups and other functional groups. This product is available in high purity and can be custom synthesized to meet your specific needs.</p>

<p>1,2,3,4-Tetra-O-pivaloyl-6-O-(tert-butyldiphenylsilyl)-b-D-galactopyranose is a high purity custom synthesis of a sugar. It is a fluorinated tetra saccharide with an unusual 1,2,3,4 linkage that has been modified with methyl groups at the 2 and 6 positions. The modification of this compound with silylation has made it resistant to enzymatic degradation. This compound has shown anti-inflammatory activities in animal models and can be used as an adjuvant therapy for inflammatory bowel disease.</p>

<p>5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone is a synthetic monosaccharide with the molecular formula C8H14O5. It has a CAS number of 94697-68-4 and is available for custom synthesis. The chemical structure of 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone consists of a methyl group attached to the hydroxyl at position 1 and a fluoro group attached to the hydroxyl at position 4. 5,6--O--Isopropylidene--L--gulonic acid--1,4--lactone is not naturally occurring and is made by modification of glycosides. This compound can be used in click chemistry or complex carbohydrate reactions.</p>

<p>(4S,5R)-4,5-Dihydroxyhexanal is a conjugate of 4-hydroxy-5-oxononanoic acid and phosphite. It is a hybridized molecule that has been synthesized using an asymmetric synthesis. (4S,5R)-4,5-Dihydroxyhexanal can be used as an analog for digitalis. The compound has the ability to activate cardiac glycoside receptors in the heart and increase the force of contraction of cardiac muscle cells. The effective dose for this drug is not yet known, although it has been shown to have cardiotonic steroid properties.</p>

<p>5-S-Methyl-5-thio-D-xylose is a carbohydrate that can be synthesized from 5,5’ -dithiobis(2-nitrobenzoic acid) and D-xylose. It is a high purity, custom synthesis product. This carbohydrate has been modified with fluorination at the 5 position of the sugar ring and methylation of the alpha carbon to form a methylated xylose. The molecular weight is 488.1 g/mol and it has a CAS number of 53458-58-5. This product can be used to modify saccharides and oligosaccharides with fluorination and methylation reactions.</p>

<p>Benzyl 2-acetamido-2-deoxy-6-O-trityl-a-D-glucopyranoside is a glycosylation of benzyl 2,3,4,6-tetraacetamido-2,3,4,6-tetra deoxyglucopyranoside. It is a complex carbohydrate that can be modified with methyl groups or fluorine atoms. This product is often used in Click chemistry and as a building block for oligosaccharides and polysaccharides. Benzyl 2-acetamido-2-deoxy 6O trityl a D glucopyranoside has CAS number 33493 71 9 and can be custom synthesized to meet individual requirements.</p>

<p>A protected thioglucose sugar</p>

<p>Building block for C-nucleoside synthesis</p>

<p>2-Acetamido-2-deoxy-a-D-galactopyranosyl serine (2AGPS) is a naturally occurring glycosaminoglycan. It has been shown to inhibit the growth of cancer cells and to reduce the size of mouse tumors in vivo. This compound also inhibits viral replication in vitro, and its antiviral properties have been shown to work on several different types of viruses, including herpes simplex virus type 1, human cytomegalovirus, and influenza A virus. 2AGPS is also a potent inducer of toll-like receptor 4 signaling pathways in macrophages and dendritic cells. 2AGPS can be synthesized by using a polymerase chain reaction (PCR) technique with synthetic oligosaccharides as a template.</p>

<p>L-Gulono-gamma-lactone is a natural vitamin C metabolite that is synthesized from L-ascorbic acid in the liver. It has been shown to inhibit the oxidase and other enzymes involved in ascorbic acid metabolism, which may be due to its ability to bind to iron. L-Gulono-gamma-lactone also inhibits polymerase chain reactions in rat liver microsomes and inhibits the activities of ascorbic acid and glutathione reductase in rat hepatic tissues. This compound is not active against humans, but it has been shown to have antioxidation properties.</p>

<p>3-O-(b-D-Galactopyranosyl)-D-mannopyranose is a synthetic sugar that is modified with fluorine at the C-3 position. It is a member of the carbohydrate family and has been shown to be useful for glycosylation or click chemistry. 3-O-(b-D-Galactopyranosyl)-D-mannopyranose can be custom synthesized to meet your needs. This product also features high purity and methylation, which makes it an excellent candidate for synthesis projects. This product can be used in research applications, such as complex carbohydrate modification, glycosylation, or click chemistry.</p>

<p>Sugars formed by photosynthesis are essential for plant’s nutrition and they can be carried by a sophisticated system called phloem from the leaves to the root tips. Since the phloem is a delicate tissue composed of various specialized cell types, the study of its structure and functions remains a challenging task. Recently, fluorescent coumarin glucoside derivatives, including esculin (Plant Physiology 2015, 1211-1220) have been used as phloem probes. Among the probes tested, only esculin and fraxin are transported, while skimmin is not, suggesting a certain specifity of natural coumarin glucosides for the transporter AtSUC2.</p>

<p>Please enquire for more information about 2,3,4,6-Tetra-O-acetyl-a-D-galactopyranosyl azide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-O-Methyl-β-D-glucuronic acid is a β-glucuronidase inducer.</p>

<p>Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside (ABTS) is a synthetic sugar derivative that is used in the modification and synthesis of saccharides. ABTS can be modified by fluorination, glycosylation, methylation, or other modifications to produce new compounds. ABTS has a CAS number of 940274-22-6.</p>

<p>Lactitol is a polyol sugar alcohol that has been used in the treatment of chronic viral hepatitis. It is also used to treat constipation, irritable bowel syndrome, and other gastrointestinal disorders. Lactitol is metabolized by certain types of bacteria and can have a laxative effect. Lactitol is not absorbed in the human intestine and thus does not cause an increase in blood sugar levels. Lactitol has been shown to be effective against microbial translocation and bacterial overgrowth in the gut, which may be due to its ability to lower pge2 levels and inhibit histological changes.</p>