Monosaccharides

<p>UDP-D-galactosamine disodium salt is a type of sugar that is a substrate for UDP-glucuronosyltransferase (UGT), which catalyzes the transfer of galactose from UDP-D-galactose to other molecules. The product of this reaction is UDP-D-galacturonic acid. It is produced in the liver, where it participates in the synthesis of glycoproteins, glycolipids, and glycosaminoglycans. In addition, it can be found in the distal tubule of the kidney and in leukemia cells. The histological analysis of rat liver tissue showed that UDP-D-galactosamine disodium salt is present in hepatocytes. This sugar also helps with protein synthesis and activates uridine, which can be used as a carbon source. Histological analysis also revealed that UDP-D-galactosamine disodium salt plays an important role in glucose metabolism, as well as</p>

<p>Inhibitor of lysosomal acid β-glucosidase (GlcCerase/glucocerebrosidase) with IC50 in nanomolar range for wildtype and mutant enzyme. It behaves as pharmacological chaperon by binding to instable GlcCerase active site at neutral pH values and facilitating the protein folding. In acidic lysosomes, isofagomine gets release from the enzyme active site. This results in increased levels of functional glucocerebrosidase and brings therapeutic benefits to patients with Gaucher disease.</p>

Gemfibrozil b-D-glucuronide-D6 is a methylated, saccharide, Polysaccharide. It is a custom synthesis of the synthetic and fluorinated gemfibrozil b-D-glucuronide. The product is purified by HPLC to >98% purity and supplied as a white powder.

<p>3,4-Di-O-benzyl-L-rhamnal is a high purity Glycosylation Oligosaccharide with a CAS No. 117249-17-9 that is synthesized by Click modification and methylation. It can be used as a raw material in the synthesis of complex carbohydrate. 3,4-Di-O-benzyl-L-rhamnal is water soluble and has an excellent stability in acidic conditions.</p>

<p>1,2,3-Tri-O-acetyl-5-deoxy-D-ribose is an efficient and environmentally benign method for the synthesis of acyclic acetals. The condensation process involves the use of a chloroformate to introduce the carbonyl group into a hydroxyl group on the sugar. This reaction can be carried out in an organic solvent or water as well. The reaction rate is fast due to a high nucleophilicity of the chloride ion. The product can then be converted into an amide by reacting it with ammonia in a basic medium. This reaction results in a high yield and is useful for recycling acetonitrile that would otherwise be released into the environment.</p>

<p>Ethyl a-D-thioglucopyranoside is an organic compound that is used as a precursor in the synthesis of complex sugars. Ethyl a-D-thioglucopyranoside is an oligosaccharide that contains a methylated and glycosylated sugar. The glycosidic bond in this product can be modified by fluorination to give ethyl 2,3,4,5-tetrafluorothioglucopyranoside.</p>

<p>Astragaloside II is a natural compound that has been shown to have anti-inflammatory effects in vitro and in vivo. Astragaloside II inhibits the production of inflammatory mediators by inhibiting phosphodiesterase and cyclooxygenase pathways. It also has a matrix effect on the cells, which may be due to its ability to activate protein kinase C. This compound also has an analytical method, which consists of HPLC with UV detection at 210 nm.</p>

<p>Please enquire for more information about Fructose-L-tryptophan including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Acetyl-5-methoxyphenyl beta-D-glucopyranoside is a flavonoid that belongs to the group of dihydroquercetin. It can be prepared by liquid chromatography. 2-Acetyl-5-methoxyphenyl beta-D-glucopyranoside inhibits tumor cells in vitro and in vivo, through the inhibition of protein synthesis and DNA replication. In addition, it has been shown to inhibit the growth of leptadenia species with a high degree of selectivity. It also exhibits an antitumor effect on mouse sarcoma 180 cells, as well as on human melanoma cells. This compound binds to macroporous adsorbents such as sephadex and tricusposide, which are used for purification purposes.</p>

<p>Ouabain is a potent inhibitor of the Na+/K+-ATPase pump in cardiac and skeletal muscles. It has been shown to inhibit signal pathways that are involved in the regulation of cellular membrane potentials, such as the michaelis–menten kinetics. Ouabain has also been found to be effective against syncytial virus infection. Ouabain inhibits viral replication by inhibiting cellular protein synthesis and reducing cell number due to its cytotoxic effects on myocardial cells. Ouabain has also been found to inhibit neuronal death induced by α1-adrenergic receptor agonists, such as p2y receptors.</p>

<p>6-O-Feruloylsucrose is a phenylpropanoid glycoside that has been shown to inhibit the growth of Gram-positive and Gram-negative bacteria. It is also hepatoprotective and has been shown to have antimicrobial activity against fungi, such as Candida albicans. The 6-O-feruloylsucrose inhibits microbial infections by binding to metal cations, which are essential for bacterial cell wall synthesis. This leads to a decrease in the production of microbial cell walls, inhibiting their growth. 6-O-Feruloylsucrose can be used as an additive in food products or as a preservative in cosmetics.</p>

<p>a-L-Fucose-1-phosphate is a Glycosylation, complex carbohydrate, Methylation, Click modification, Polysaccharide, Fluorination, saccharide, Modification, sugar, Oligosaccharide and Synthetic product. a-L-Fucose-1-phosphate is available for custom synthesis and can be ordered with high purity.</p>

<p>1,4-Dideoxy-1,4-imino-D-xylitol HCl (DDX) is a potent inhibitor of the enzyme carboxypeptidase A2. DDX has been shown to inhibit the growth of HIV in vitro and in vivo. DDX also inhibits the production of proinflammatory cytokines and neurotrophic factors from HL60 cells. It has been shown to be a potential drug target for the treatment of infectious diseases such as alphaviruses, which produce a severe neuroinvasive disease in humans. DDX binds to dna with high affinity and specificity, but does not bind to RNA or proteins. DDX inhibits mitochondrial membrane potential by binding to ATP synthase and blocking the synthesis of ATP. DDX has also been shown to have an anti-oxidative injury effect on mitochondria, which may contribute to its inhibition of viral replication.</p>

<p>2-Keto-D-galactonic acid is a chemical compound that is used as an intermediate in the synthesis of antibiotics. It has been found to inhibit the growth of bacteria, such as Erwinia carotovora and Escherichia coli. The 2-keto-d-galactonic acid can be crystallized in two forms: an amorphous form or a crystalline form.</p>

<p>Glufosfamide is a cytotoxic drug that is used in the treatment of some types of cancer. It is a prodrug that requires conversion to its active form, glufosfamid, by esterase enzymes before it can exert its genotoxic effects. Glufosfamide has shown to be active against platinum-resistant ovarian cancer and solid tumours. This drug also has been shown to inhibit the growth of prostate cancer cells and miapaca-2 cells, which are derived from pancreatic cancer. Glufosfamide has been found to have low toxicity in mice, but there may be adverse reactions when combined with other drugs such as erythromycin or ketoconazole.</p>

<p>3-Azido-2,3-dideoxy-D-ribose is a boron trifluoride etherate that has significant activity against the anomers of d-mannitol. It can be used as a stereoselective synthesis of the triflate on the corresponding anomer. Triflate is prepared by reaction with trifluoromethanesulfonic acid chloride and then reacted with sodium azide in ethanol to yield 3-azido-2,3-dideoxy-D-ribose. The product can be purified by recrystallization from acetic acid and water or by extraction with chloroform. This compound is also extracted from boric acid and dioxane using aqueous sodium hydroxide solution.</p>

<p>Naltrexone 3-D-glucuronide-D4 is a carbohydrate. It is a glycosylation product of naltrexone. The compound has been synthesized by the methylation of naltrexone and the glycosylation of the resultant product with glucose. Naltrexone 3-D-glucuronide-D4 is a high purity, custom synthesis, synthetic carbohydrate with a CAS number.</p>

<p>Methyl a-D-mannofuranoside is a synthetic sugar that has been modified by the addition of fluorine at C-1 and methylation at C-2. This modification provides the compound with desired physical properties, such as increased stability and solubility. Methyl a-D-mannofuranoside can be used in the synthesis of oligosaccharides, which are complex carbohydrates consisting of three to ten monosaccharides linked together by glycosidic bonds. It is also used for click chemistry modifications.</p>

<p>5-Deoxy-L-lyxono-1,4-lactone is a crystalline solid that belongs to the class of hydroxamic acids. This compound has been shown to react with hydroxylamine in an aldonic reaction and to inhibit the enzyme xanthin oxidase. The monoclinic crystal structure of 5-Deoxy-L-lyxono-1,4-lactone was determined by XRD analysis. This compound is synthesized from glyoxylate and malonitrile in an efficient manner. It also inhibits glucose oxidation and can be used as an additive for food products.</p>

<p>a-D-Xylopyranosyl azide is a sugar that can be synthesized from the reaction of 1,2-dichloroethane with 2,3,4,6-tetra-O-acetyl-a-D-xylopyranose. This compound has a high purity and can be custom synthesized to order. It is used in glycosylation reactions to modify saccharides and oligosaccharides. It has been shown to be useful for click modification and fluorination reactions.</p>