Monosaccharides

D-Idose is a single-enantiomer sugar with a pyranose ring and an enantiomeric configuration. It is used in the treatment of bacterial infections and has been shown to be effective at inhibiting the growth of bacteria that are resistant to beta-lactam antibiotics, such as methicillin-resistant Staphylococcus aureus (MRSA). D-Idose is active against bacteria that do not produce beta-lactamase enzymes, such as Mycobacterium tuberculosis or Mycobacterium avium complex.

2,5-Anhydro-1-O-trityl-D-mannitol is a complex carbohydrate with the molecular formula C6H14O6 that has been modified for use in glycosylation reactions. It is a type of sugar that can be modified to create desired properties and can be used as an alternative to other sugars such as glucose. 2,5-Anhydro-1-O-trityl-D-mannitol can be used in the synthesis of oligosaccharides and monosaccharides. This product is available in high purity and has a CAS number of 68774-48-1.

3,4,6-Tri-O-acetyl-D-glucal, also called 1,5-anhydro-2-deoxy-D-arabino-hex-1-enitol triacetate, is the acetate protected cyclic enol-ether (glycal) of D-glucose. 3,4,6-Tri-O-acetyl-D-glucal is a building block useful in the synthesis of a range of carbohydrates with the glucal double bond allowing other functional groups to be introduced. As an alkene, a glycal can undergo electrophilic addition across the double bond to introduce halogens and epoxides or be used to generate deoxy monosaccharides. 3,4,6-Tri-O-acetyl-D-glucal can undergo a Ferrier rearrangement with an alcohol and Lewis acid to give a 2,3-unsaturated product.

Methyl 4,6-O-benzylidene-b-D-glucopyranoside is a nitro derivative of methyl b-D-glucopyranoside. The anomeric proton and the nitro group are in the same plane and on opposite sides of the molecule. This compound has been shown to be both a receptor binding agent and a gelation agent. It is used to study biological membranes because it binds to phospholipids in the cell membrane, which alters its physical properties. Methyl 4,6-O-benzylidene-b-D-glucopyranoside is also known for its ability to form hydrogen bonds with water molecules. This is due to its cavity that can accommodate one water molecule per monomer unit. The crystal structure of this compound has been determined by x ray crystallography and shows that it forms dimers through hydrogen bonding between two molecules in each dimer. These interactions are

1-O-Methyl-beta-D-xylopyranoside is a matrix component that is used as an artificial sweetener. This product has been shown to have the ability to protect cells against radiation and toxic chemicals. 1-O-Methyl-beta-D-xylopyranoside also inhibits the growth of coliform bacteria by inhibiting their energy metabolism and may be used for wastewater treatment. It has been shown to be effective in analytical methods to identify the presence of human feces in water samples.

N-Propanoyl mannosamine is a biochemical that belongs to the group of glycoconjugates. It is an intracellular messenger that modulates the concentration of intracellular calcium and controls the release of gamma-aminobutyric acid (GABA). N-Propanoyl mannosamine has been shown to stimulate axonal growth in cell culture, which is mediated by the polysialic acid receptor. This molecule also has a role in human osteoblast differentiation and bone formation.
N-Propanoyl mannosamine can be synthesized from dopamine and erythrose via a series of reactions involving acidification, oxidation, reduction, and decarboxylation. The synthesis of this molecule requires blood group O as an acceptor.

L-Arabinaric acid dipotassium salt is a custom synthesis of an L-arabinaric acid, which is a monosaccharide that is found in the cell wall of bacteria. This compound has been modified to be resistant to fluorination, methylation, and click chemistry. The modification process includes the use of Oligosaccharides, saccharides, and polysaccharides as well as glycosylation and sugar. L-Arabinaric acid dipotassium salt can also be used for the synthesis of complex carbohydrates.

2,3,5-Tri-O-p-chlorobenzoyl-a-D-ribofuranosyl chloride is a sugar derivatized with chlorine. It is a high purity product that can be custom synthesized to meet your needs. This compound has been used in the synthesis of saccharides and oligosaccharides with click modification, fluorination, glycosylation, methylation, and modification.
2,3,5-Tri-O-p-chlorobenzoyl-a-D-ribofuranosyl chloride is an important intermediate for the synthesis of complex carbohydrates. The chemical structure of this molecule consists of three parts: an aromatic ring (benzene), a glycosylation site (glycine), and a carboxylic acid group (carboxylic acid). The aromatic ring allows 2,3,5-Tri-O-p-chlorobenzoyl-a-D

1,3,5-Tri-O-benzoyl-2-O-(1H-imidazole-1-sulfonate) a-L-arabinofuranose is a methylated and modified arabinofuranose. It is one of the most common monosaccharides in nature. This compound is an important component of polysaccharides such as cellulose and starch. 1,3,5-Tri-O-benzoyl-2-O-(1H-imidazole-1-sulfonate) aL arabinofuranose is used to create saccharide derivatives that are widely used in the pharmaceutical industry.

2,3,4,6-Tetra-O-acetyl-β-D-mannopyranosyl azide is a crystallographic technique that can be used to determine the structure of molecules. This technique involves the use of x-ray diffraction analysis to produce images of crystal structures. The technique is useful for determining the three dimensional structure of molecules that are too small to be seen with other techniques such as electron microscopy.

Scyllo-inosamine is a redox potential that belongs to the class of antimicrobial agents. It is derived from the amino acid inosine, which is found in RNA and DNA. Scyllo-inosamine has been shown to inhibit bacterial growth by inhibiting protein synthesis. It also acts as an aminotransferase inhibitor, which may be used for the treatment of certain human pathogens. Scyllo-inosamine has been shown to have beneficial effects on the regulation of benzyl groups and hydroxyl group reactions. It has also been shown to inhibit polymerase chain reaction activity and titration calorimetry activity.

Methyl L-fucopyranoside is a saponin glycoside that has been shown to have anti-tumor effects. It acts by binding to the nucleophilic sites on the cancer cells and inhibits their growth. The molecule is chiral, which means that it can exist in two different forms, or enantiomers. The structure of this compound has been determined using vibrational spectroscopy and nuclear magnetic resonance (NMR) spectroscopy. It is also a synthetic product that can be made from an acid catalyst and an oligosaccharide molecule. Methyl L-fucopyranoside has been shown to inhibit glycoconjugates and muscari alkylation, as well as having liquid chromatographic properties.

D-Mannonic acid-1,4-lactone is a recombinant carbohydrate that is synthesized from l-ribose and l-arabinose. It has lysozyme inhibitory activity. D-Mannonic acid-1,4-lactone can be used to study the synthesis of lactones by escherichia coli and their inhibitory effects on lysozyme. The compound consists of two stereoisomers: dl-mannonic acid and ldl-mannonic acid. It can be detected by liquid chromatography (LC) and electrophoresis.

Substrate for N-acetylglucosaminyltransferases

Phenyl 3,4-O-isopropylidene-b-D-thiogalactopyranoside is a custom synthesis of the complex carbohydrate Oligosaccharide, Polysaccharide. It belongs to Modification, saccharide, Methylation, Glycosylation, Carbohydrate. Phenyl 3,4-O-isopropylidene-b-D-thiogalactopyranoside can be used for Click modification, sugar and High purity. This compound is Fluorinated and Synthetic.

Methyl-2,3,4-tri-O-benzoyl-6-deoxy-alpha-D-glucopyranoside is a modification of the sugar molecule. It is a monosaccharide that has been modified with methylation and fluorination. This product can be used in the synthesis of saccharides, polysaccharides, oligosaccharides and complex carbohydrates. Methyl 2,3,4-tri-O-benzoyl 6 deoxy alpha D -glucopyranoside is one of many compounds that can be used to synthesize glycosylations.

Inhibitor of O-GlcNAcase

2-Methoxycarbonylphenyl b-D-glucopyranoside is a modification that can be used to synthesize complex carbohydrates. It is an oligosaccharide, which consists of a series of monosaccharides linked together by glycosidic bonds. The synthesis of this compound requires the use of methylation and fluorination reactions. This product has high purity and can be used for a variety of purposes, including as a sugar or as a polysaccharide.

Inhibitor of viral, bacterial and animal sialidase

2,3,4-Tri-O-acetyl-1,6-anhydro-b-D-galactopyranose is a sugar that has been modified with fluorination. This modification is done in an effort to increase the solubility of this product. It is also used as the backbone for other sugars in order to create complex carbohydrates or polysaccharides. In addition, 2,3,4-Tri-O-acetyl-1,6-anhydro-b-D-galactopyranose can be methylated and glycosylated in order to modify its properties. This product is available for custom synthesis and has a purity level of 99%.

Substrate for glucuronosyltransferases

2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-Fmoc serine is a protein that belongs to the group of bifunctional glycosides. It is used in recombinant virus production as a component of the viral coat protein (VP). 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl-Fmoc serine binds to tyrosine kinase receptors and inhibits their activity. This inhibition prevents cell adhesion and migration and can cause tumor regression in some cancers. 2,3,4,6-Tetra-O-acetyl-b-D--glucopyranosyl--Fmoc serine also has antiviral activity due to its ability to inhibit the replication of viruses containing RNA genomes.

2-Deoxy-1,3,4,6-tetra-O-pivaloyl-D-glucopyranose is a glycosylation sugar that belongs to the category of complex carbohydrates. It is a methylated sugar that can be fluorinated or modified with other saccharides. This product can be custom synthesized and has high purity.

2-Acetamido-2,6-dideoxy-D-galactose (2ADG) is a structural analogue of the natural monosaccharide 2,6-dideoxy-D-galactose. It has been shown to have an antimicrobial effect against aerobacter aerogenes in vitro. 2ADG is metabolized by glycosidases and methyl glycosides to form 1,4-anhydro-2,3,4,6 tetraacetamido-2,4,6 dideoxy D galactose. This compound inhibits the growth of bacterial strains that are resistant to polymyxin b., such as Pseudomonas aeruginosa. The inhibition of these bacteria is due to the inhibition of the synthesis of their outer membrane lipopolysaccharides by 2ADG. The antibacterial activity is also attributed to its ability to inhibit the metabolism of glycan molecules in some bacteria