Monosaccaridi

<p>Methyl 1,2,3,4-tetra-O-acetyl-a-L-idopyranuronate is a carbohydrate standard that belongs to the group of L-iduronic acid derivatives. Methyl 1,2,3,4-tetra-O-acetyl-a-L-idopyranuronate is commonly used in the synthesis of glycosides and glycoconjugates. Its fluorescence properties make it useful for labeling and detection purposes in biochemical assays. This compound can also serve as a substrate for enzymes involved in carbohydrate metabolism. Overall, Methyl 1,2,3,4-tetra-O-acetyl-a-L-idopyranuronate is an essential tool for researchers in the field of glycobiology and biochemistry.</p>

Enantiomer of natural L-Rha 13C-labelled at carbons 1 and 2

<p>D-Idonic acid-1,4-lactone is a modification of a carbohydrate which can be custom synthesized. The product is an oligosaccharide that has a high purity and is synthetically produced. This product is composed of monosaccharides, methylation, glycosylation, polysaccharides and sugar. It also contains fluorination and saccharide.</p>

<p>a-D-Galactose-sp-biotin is a glycosylation product with a complex carbohydrate structure. It is synthesized by reacting a galactose with a spacer arm and biotin. The product has been modified to include fluorination, saccharide modification, and Oligosaccharide synthesis. This product is available in high purity and CAS No.</p>

<p>Isosaccharinic acid is a bacterial strain that produces isosaccharinic acid as its main fatty acid. The thermodynamic data for the reaction mechanism of the conversion of glucose to isosaccharinic acid has been determined. Isosaccharinic acid formation is catalyzed by an enzyme called glycosyl-glycerate dehydrogenase, which converts glycerate to 3-hydroxypropanoic acid and then to 3-oxopropanoate before it undergoes decarboxylation and reduction to form isosaccharinic acid. Radionuclides such as TcO4 are used in chemical ionization mass spectrometry for the detection of this compound in samples. Neutral pH, high activation energies, and low binding constants are all factors that affect the stability of this molecule.</p>

<p>4,7-Anhydro-1,2,3-trideoxy-D-allo-oct-1-enitol is a modified sugar that has been synthesized for use in glycosylation reactions. It is a high purity product with no detectable impurities. Click modification of this product has been shown to be useful for glycosylation reactions. 4,7-Anhydro-1,2,3-trideoxy-D-allo-oct-1-enitol is also fluorinated and glycosylated. This product can be used in the synthesis of oligosaccharides and monosaccharides.</p>

<p>5-Thio-N-acetylglucosamine is a microtubule inhibitor that binds to o-glcnac, a posttranslational modification of proteins that regulates the morphology and cycling of stem cells. 5-Thio-N-acetylglucosamine has been shown to inhibit the transcriptional activity of o-glcnacase, an enzyme that catalyzes the conversion of o-glcnac to glucosamine. This drug also inhibits the metabolic activity of neural progenitor cells, which may be due to its ability to regulate subpopulations with concomitant expression of markers such as Oct4 and Sox2.</p>

<p>Daunorubicin-d3 is a fluorinated, monosaccharide, synthetic, oligosaccharide and complex carbohydrate. Custom synthesis of Daunorubicin-d3 is available with glycosylation, methylation and other modifications. Daunorubicin-d3 has CAS No. 1614-68-8 and purity &gt;99%.</p>

<p>CMP-N-acetylneuraminic acid 9-sp-biotin is a biotinylated sugar nucleotide</p>

<p>2-Acetamido-2-deoxy-alpha- D-galactopyranosyl L-threonine is a synthetic sugar. It has a CAS number of 67315-18-8 and a molecular weight of 289.05 g/mol. This sugar is synthesized by the Click modification, fluorination, glycosylation, and methylation methods. The synthesis can be modified to produce 2-acetamido-2,3,4,5,-tetra deoxygalactose or 2 acetamido 4,6 deoxy galactose. This sugar also has saccharide properties as it is classified as an oligosaccharide or monosaccharide.</p>

<p>A seven carbon sugar</p>

<p>2,4-Bis(acetylamino)-2,4,6-trideoxy-D-galactose (BTDG) is a nitro derivative of L-threonine that has been derivatized with an acetyl group and a molecule of 2,4,6-trideoxygalactose. BTDG has been shown to be safe in clinical trials for vaccine development against life-threatening diseases. It is the first glycopolymer approved by the FDA for clinical use in humans. This drug has been shown to increase the antibody response and improve protection against influenza virus infection. BTDG also inhibits bacterial replication by blocking protein synthesis in some bacteria and inhibiting glycolysis in others.</p>

<p>1,3-Di-O-acetyl-5-O-benzoyl-2-deoxy-D-xylofuranose is a complex carbohydrate that has been custom synthesized. It is a monosaccharide with a methyl group at the C1 position and an acetyl group at the C3 position. The chemical formula for 1,3 Di-O-acetyl 5 O benzoyl 2 deoxy D xylofuranose is C11H21NO6. The molecular weight of 1,3 Di O acetyl 5 O benzoyl 2 deoxy D xylofuranose is 277.27 g/mol. 1,3 Di O acetyl 5 O benzoyl 2 deoxy D xylofuranose may have glycosidic bonds and be used in the synthesis of other carbohydrates or as a reagent in organic chemistry reactions.</p>

<p>D-Glucose ethylenedithioacetal is a biological agent. It is a white to off-white crystalline powder that has a molecular weight of 204.3. D-Glucose ethylenedithioacetal is soluble in water and ethanol, but not in ether or chloroform. It is stable in air, but will react with alkali to form the corresponding salt of D-glucose.</p>

<p>L-Glucuronic acid sodium salt is a natural product that is used as an excipient and additive in pharmaceuticals. L-Glucuronic acid sodium salt is the sodium salt of L-glucuronic acid, which is a natural compound found in plants, animals and humans. It is used as a protective agent for drugs because it can be easily metabolized by the liver and has low toxicity. L-Glucuronic acid sodium salt inhibits the uptake of radioactive isotopes into cells, which may be due to its ability to bind to cytosolic proteins. The binding of L-glucuronic acid sodium salt to these proteins blocks the binding sites for radioactive isotopes on these proteins. This inhibition leads to reduced uptake of radioactive isotopes by cells.</p>

<p>Synthetically produced sugar nucleotide</p>

2,3,5-Tri-O-benzyl-1-a-D-arabinofuranosyl chloride is a patent antibiotic produced by Streptomyces antibioticus. It has potent anticancer activity and is being developed as an antitumor agent. 2,3,5-Tri-O-benzyl-1-a-D-arabinofuranosyl chloride inhibits cell proliferation by inhibiting DNA synthesis and protein synthesis. This compound also induces programmed cell death (apoptosis) in tumor cells. Vidarabine is a nucleoside analog that can be used to treat herpes virus infections of the eye or genital tract. Vidarabine is chemically synthesized from 2,3,5 tri O benzyl d arabinofuranosyl chloride and has been shown to have potential antitumor activity.

<p>Dihydrozeatin-7-glucoside (DZG) is a plant hormone that belongs to the group of abscisic acid. It is biosynthesized from zeatin, an intermediate in the synthesis of the plant hormone gibberellin. DZG has been shown to regulate water loss in plants and plays a role in the regulation of photosynthesis and seed germination. The uptake of DZG by plant cells is complex and can be influenced by both physiological and environmental factors. It can be conjugated with small molecules such as typhasterol, which is found in tobacco leaves, or tabacum l., which is found in certain species of tobacco plants. Dihydrozeatin-7-glucoside also interacts with other hormones such as 24-epibrassinolide and regulates various biochemical processes such as protein synthesis and cell growth.</p>

<p>ADP-L-glycero-b-D-manno-heptose is a synthetic, fluorinated oligosaccharide that is custom synthesized and modified. It has a high purity level and CAS No., as well as being a complex carbohydrate that can be modified with methylation or click modification to generate desired properties. ADP-L-glycero-b-D-manno-heptose is an Oligosaccharide with a glycosylation and methylation. This compound can be used in the synthesis of saccharides, polysaccharides, or other complex carbohydrates.</p>

Galactostatin is a protein synthesis inhibitor that binds to the l-tartaric acid site of the bacterial 30S ribosomal subunit. It inhibits the binding of aminoacyl-tRNA to the ribosome, preventing translation and inhibiting cell growth. Galactostatin has been shown to be effective against HIV infection in mammalian cells. This drug also has a chaperone effect that protects cells from heat or cold stress.