Monosaccharides

α-D-Maltotetraose is a natural carbohydrate that has been shown to have potential as an anticancer agent. It is an inhibitor of tumor-associated kinases and has been found to induce apoptosis in cancer cells. α-D-Maltotetraose has also been shown to inhibit streptokinase, an enzyme involved in the breakdown of blood clots. This carbohydrate analog has been detected in human urine and may play a role in regulating gastrin secretion. Studies have shown that α-D-Maltotetraose can inhibit the growth of Chinese hamster ovary cells, suggesting its potential as a novel anticancer therapy.

Muraglitazar acyl-b-D-glucuronide is a complex carbohydrate that has been modified with fluorination. The compound is synthesized from methylation, glycosylation, and carbamylation reactions with saccharides. The saccharide modification includes the attachment of various sugars such as glucose, galactose, and mannose. Muraglitazar acyl-b-D-glucuronide can be used in the synthesis of oligosaccharides and polysaccharides. It is also used for Click modification of sugar molecules.

Please enquire for more information about Benzyl 2-(acetylamino)-2-deoxy-3-o-[3,4,6-tri-o-acetyl-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-α-D-galactopyranoside 4,6-diaceta te including the price, delivery time and more detailed product information at the technical inquiry form on this page

Allyl 6-o-allyl-α-D-galactopyranoside is a medicinal compound with potential anticancer properties. It is an analog of α-D-galactopyranoside and has been shown to inhibit the activity of protein kinases, which are enzymes involved in cell signaling and regulation. This inhibition can lead to apoptosis, or programmed cell death, in cancer cells. Allyl 6-o-allyl-α-D-galactopyranoside has been studied extensively in Chinese medicine as a potential inhibitor of tumor growth and has also been found in human urine. This compound holds great promise as a natural alternative for cancer treatment and warrants further investigation into its therapeutic potential.

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.

Cis-Zeatin-9-glucoside is a plant hormone known as a cytokinin, which is primarily synthesized in plants such as Zea mays (corn) and other monocots. Cytokinins play a critical role in regulating plant growth and development by promoting cell division, influencing nutrient allocation, and delaying leaf senescence. The mode of action of cis-Zeatin-9-glucoside involves its role as a signaling molecule that interacts with specific receptors in plant cells, thereby triggering a cascade of gene expression changes that modulate physiological processes.

3,5-O-Isopropylidene-L-arabinofuranose is a sugar that is used in the synthesis of saccharides. It is a monosaccharide that can be modified by fluorination, methylation, and custom synthesis. This product has been shown to be an excellent substrate for click chemistry and can be used as an intermediate in the production of oligosaccharides and polysaccharides. 3,5-O-Isopropylidene-L-arabinofuranose has a high purity level and can be used as a replacement for other sugars in complex carbohydrate synthesis.

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.

D-Xylonic acid lithium salt is a redox potential regulator that belongs to the class of nucleotide phosphate. It has been shown to inhibit the transcriptional regulation of genes in Saccharomyces cerevisiae strain. D-Xylonic acid lithium salt inhibits the growth of bacteria by binding to a hydroxyl group on the surface of bacterial cells, which disrupts the cell membrane and causes cell death. This drug also has film-forming properties and can be used as a model system for studying glycolaldehyde, an intermediate in sugar metabolism.

4-Epi-daunosamine is a glycopeptide antibiotic that is used to treat infections caused by Gram-positive bacteria. It binds to the cell wall of these bacteria and inhibits the synthesis of new cell walls. This causes the cells to burst and die, which leads to bacterial death. 4-Epi-daunosamine has been shown to be effective against animal pathogens such as Streptococcus pneumoniae, Haemophilus influenzae, and Clostridium perfringens. 4-Epi-daunosamine also has a low level of toxicity in humans, but can cause adverse effects such as nausea and vomiting if taken in large doses.

6-Deoxy-3-C-methyl-D-gulose is an enantiomer of 3,6-dideoxy-D-gluconic acid. This compound has been shown to be a virulent factor in mastitis caused by the mutant strain of Escherichia coli (MT1) and to be expressed at a higher level in mastitic milk than in normal milk. 6DMG has also been shown to induce monoclonal antibody production and stimulate specific immune responses. It is thought that 6DMG damages cells, which leads to the release of intracellular components that trigger an antibody response. The biological function of 6DMG is not known, but it may play a role in the infection process by stimulating an antibody response against infectious agents.

Please enquire for more information about D-Glucose-1,3-13C2 including the price, delivery time and more detailed product information at the technical inquiry form on this page