Monossacáridos
Monossacarídeos são a forma mais simples de carboidratos e servem como building blocks fundamentais para açúcares mais complexos e polissacarídeos. Essas moléculas de açúcar único desempenham papéis críticos no metabolismo energético, na comunicação celular e nos componentes estruturais das células. Nesta seção, você encontrará uma ampla variedade de monossacarídeos essenciais para pesquisas em bioquímica, biologia molecular e glicociência. Esses compostos são cruciais para estudar vias metabólicas, processos de glicosilação e desenvolvimento de agentes terapêuticos. Na CymitQuimica, oferecemos monossacarídeos de alta qualidade para apoiar suas necessidades de pesquisa, garantindo precisão e confiabilidade em suas investigações científicas.
Subcategorias de "Monossacáridos"
- Aloses(11 produtos)
- Arabinoses(21 produtos)
- Eritroses(11 produtos)
- Frutoses(9 produtos)
- Fucoses(36 produtos)
- Galactosamina(41 produtos)
- Galactoses(261 produtos)
- Glucoses(365 produtos)
- Ácidos Glucurónicos(51 produtos)
- Glico-substratos para enzimas(77 produtos)
- Guloses(6 produtos)
- Idoses(4 produtos)
- Inositóis(15 produtos)
- Lixoses(4 produtos)
- Mannoses(65 produtos)
- O-Glicanos(48 produtos)
- Psicoses(3 produtos)
- Ramnoses(10 produtos)
- Riboses(61 produtos)
- Ácidos siálicos(100 produtos)
- Sorboses(4 produtos)
- Açúcares(173 produtos)
- Tagatoses(4 produtos)
- Taloses(8 produtos)
- Xiloses(20 produtos)
Exibir 17 mais subcategorias
Foram encontrados 6090 produtos de "Monossacáridos"
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1,6-Anhydro-β-D-mannopyranose
CAS:Produto Controlado<p>Applications Monosaccharide anhydrides, new markers of toasted oak wood used for ageing wines and distillates.<br>References Goldberg, D., et al.: J. Agric. Food Chem., 47, 3978 (1999), Fu, P., et al.: Environ. Sci. Technol., 43, 286 (2009),<br></p>Fórmula:C6H10O5Cor e Forma:Off-WhitePeso molecular:162.14Ethylmalonic Acid
CAS:<p>Applications Ethylmalonic Acid is used as a diagnostic agent used in the diagnosis of Ethylmalonic encephalopathy which is a rare autosomal recessive inborn error of metabolism.<br>References Baertling, F. et al.: Eur. J. Pediat., 173, 1719 (2014); Sudo, Y. et al.: Hu,am Genome Var., 1, 15016 (2014);<br></p>Fórmula:C5H8O4Cor e Forma:NeatPeso molecular:132.121,6-Anhydro-β-D-galactose
CAS:Produto Controlado<p>Applications 1,6-Anhydro-β-D-glucopyranose is a carbohydrate contains in liquid smoke flavorings.<br>References Kim, K., et al.: Agric. Biol. Chem., 38, 53 (1974), Guillen, M., et al.: Food Chem., 58, 97 (1997), Guillen, M., et al.: J. Agric. Food Chem., 46, 1276 (1998),<br></p>Fórmula:C6H10O5Cor e Forma:White To BeigePeso molecular:162.14L-Fucose - non animal origin
CAS:<p>L-Fucose is an aldohexose that is used as the building block for various glycoproteins and glycolipids. It is found in human serum and human pathogens. L-Fucose can be isolated from the hybridoma cell line by apical chromatography. The analytical method of L-fucose includes body formation, oligosaccharides, and glycan titration calorimetry. Structural analysis of L-fucose includes glycosylation, sugar analysis, and carbohydrate analysis. Fucose can also be used to produce oligosaccharides through enzymatic reactions with other sugars including glucose and galactose. This reaction produces a linkage between fucose and other sugars that are called glycosidic bonds.</p>Fórmula:C6H12O5Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:164.16 g/molUDP-2-deoxy-2-fluoro-D-glucose sodium salt
CAS:<p>UDP-2-deoxy-2-fluoro-D-glucose sodium salt (UDPFG) is a fluorinated analog of the sugar donor, UDP-glucose. It is an acceptor for the enzyme, glycosylation protein glucosyltransferase, which catalyzes the transfer of glucose to proteins. This compound has been shown to be an activating sugar donor in vitro and in vivo. In addition, it was found that UDFG can bind to the active site of glucosyltransferase in a hydrogen bond interaction that may be important for catalysis.</p>Fórmula:C15H21FN2O16P2·2NaPureza:Min. 95%Cor e Forma:PowderPeso molecular:568.29 g/molPropargyl β-D-glucopyranoside
CAS:<p>A beta glycoside with an alkyne handle suitable to click chemistry</p>Fórmula:C9H14O6Pureza:Min. 95%Cor e Forma:PowderPeso molecular:218.2 g/mol(2R, 4S) - 3- Fluoro- 2,4- azetidinedimethanol
<p>(2R, 4S) - 3- Fluoro- 2,4- azetidinedimethanol is a fluorinated monosaccharide. It is a synthetic compound that has been modified by methylation and Click chemistry. The fluorination of the sugar allows for high purity and modification of the carbohydrate. This compound is used in the synthesis of oligosaccharides and polysaccharides.</p>Pureza:Min. 95%Propargyl a-D-glucopyranoside
CAS:<p>Propargyl a-D-glucopyranoside is a high purity custom synthesis sugar. It is synthesized by Click modification, fluorination, and glycosylation followed by methylation. Propargyl a-D-glucopyranoside can be used for the modification of oligosaccharides and monosaccharides to produce complex carbohydrates.</p>Fórmula:C9H14O6Pureza:Min. 95%Cor e Forma:PowderPeso molecular:218.2 g/mol2-Acetamido-2-deoxy-b-D-glucopyranosyl amine
CAS:<p>2-Acetamido-2-deoxy-b-D-glucopyranosyl amine is a synthetic molecule that has shown to be an effective therapeutic agent for the treatment of juvenile idiopathic arthritis. It binds to the surface of cells and activates the immune system by generating antibodies against the disease. This drug has been shown to reduce disease activity in patients with juvenile idiopathic arthritis, as well as improve quality of life. 2-Acetamido-2-deoxy-b-D-glucopyranosyl amine is being developed for use in other autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis, and psoriasis.</p>Fórmula:C8H16N2O5Pureza:Min. 95 Area-%Cor e Forma:PowderPeso molecular:220.22 g/mol1,2,3,4,6-Penta-O-acetyl-a-D-galactopyranose
CAS:<p>1,2,3,4,6-Penta-O-acetyl-a-D-galactopyranose is a pentaacetate of glucose. This compound is transported in the blood and extracellular fluids and has been shown to be a substrate for hexaacetate transport. The transport of this compound by hexaacetate has been shown to bypass the intracellular k+ concentration gradient. It has also been shown to have anti-diabetic effects in animals and humans. 1,2,3,4,6-Penta-O-acetyl-a-D-galactopyranose can also be found in foods that contain beta d glucopyranoside (e.g., bananas). This compound is resistant to digestion and can be found in the stomach or intestines where it postulated to have an inhibitory effect on bacterial growth. 1,2,3,4,6-Penta-O-</p>Fórmula:C16H22O11Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:390.34 g/mol(-)-D-Noviose
CAS:<p>(-)-D-Noviose is a naturally occurring sulfoxide that was first isolated from the tubercles of tuberculosis patients. It is a biosynthetic precursor to tiacumicin, an antibacterial agent. In addition, (-)-D-Noviose has been shown to act as a chaperone and inhibit cancer cells in vitro. (-)-D-Noviose binds to the cysteine residues of proteins, preventing their oxidation and subsequent aggregation. This prevents the cross-linking of proteins that leads to cellular damage and death.</p>Fórmula:C8H16O5Pureza:Min. 95%Peso molecular:192.21 g/mol1,2-Dideoxy-3,5-di-O-toluoyl-D-ribose
CAS:<p>1,2-Dideoxy-3,5-di-O-toluoyl-D-ribose is a synthetic sugar that can be used in the synthesis of complex carbohydrates. It has been modified with fluorine, methylation, and click chemistry. It is also available as a high purity product. 1,2-Dideoxy-3,5-di-O-toluoyl-D-ribose is an oligosaccharide that is used in glycosylation reactions to form polysaccharides or saccharides. Click chemistry allows for the modification of this sugar with other molecules such as amino acids or peptides. This modification may be useful for studying protein interactions or for drug development.</p>Fórmula:C21H22O5Pureza:Min. 95%Peso molecular:354.4 g/molUDP-b-L-arabinopyranose
CAS:<p>UDP-b-L-arabinopyranose is a nucleotide sugar that is used in the synthesis of proteins and other macromolecules. It is synthesized from uridine and d-ribulose 5-phosphate by the enzyme ribulokinase. The reaction between UDP, b-L-arabinofuranose, and ATP, catalyzed by arabinofuranosyl transferase, produces UDP-b-L-arabinopyranose. This nucleotide sugar can be converted to UDP-b-(1→4)-glucuronate by the enzyme glucuronosyltransferase. This process plays an important role in plant physiology as well as in cell wall biosynthesis. The optimal pH for this conversion is 7.5 to 8.2.</p>Fórmula:C14H22N2O16P2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:536.28 g/molD-Glucono-1,5-lactone
CAS:<p>D-Glucono-1,5-lactone is a chemical compound that is a member of the class of compounds known as diketones. It can be used in chemical biology and polymer chemistry to probe hydrogen bonding interactions, polymer compositions, and redox potentials. D-Glucono-1,5-lactone has been shown to inhibit the growth of cells in culture by inhibiting DNA synthesis. This inhibition is due to its ability to bind with high affinity to nucleic acids and prevent the formation of the enzyme complexes required for transcription and replication. The effects are reversible.</p>Fórmula:C6H10O6Pureza:Min. 95%Cor e Forma:PowderPeso molecular:178.14 g/molepi-Inositol
CAS:<p>Epi-inositol, also known as myo-inositol, is a member of the group of molecules known as sugar alcohols. It is a naturally occurring compound that is found in the human body and can be synthesized by the human body from glucose. Epi-inositol has been shown to have a number of biological effects, including inhibition of cell proliferation and energy metabolism in ovarian cancer cells. Epi-inositol has also been used in clinical trials for treatment of mood disorders such as depression.</p>Fórmula:C6H12O6Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:180.16 g/molLentinan
CAS:<p>The polysaccharide Lentinan is isolated from the mushroom L. edodes (shitake mushroom). The primary structure is a β-(1–3)-glucose backbone with two (1–6)-β-glucose branches for each five glucose resiodues. Lentinan is clinically used for cancer treatment both in China and Japan. According to the clinical studies published in and outside of China, lentinan-based drugs are used for the treatment of various cancers, including lung, gastric, colorectal and other cancers. In addition, lentinan-based drugs are also used for treating HIV, hepatitis and malignant pleural effusion.</p>Cor e Forma:Brown Powder1,3,4-Tri-O-acetyl-2-deoxy-2-fluoro-L-fucose
CAS:Peracetylated 2-fluoro-L-fucose is the acetylated form of 2-deoxy-2-fluoro-L-fucose which is a potent inhibitor of protein fucosylation. It exhibits improved cell permeability and is rapidly deacetylated into its active form, inside the cell. It is metabolised inside the cell into a corresponding donor substrate analogue of GDP-fucose or GDP-2FF, via the salvage pathway. GDP-2FF accumulates in the cell causing a shutdown of de novo pathway which leads to the desired fucosylation inhibition. The addition of 100 uM peracetylated-2-fluoro-L-fucose to plants severely inhibits root growth by 95% compared to an untreated plant, and is more potent compared to 2-fluoro-L-fucose. The material is soluble in DMSO at 10mg/ml.Fórmula:C12H17FO7Pureza:Min. 97 Area-%Cor e Forma:White Off-White PowderPeso molecular:292.26 g/molPhenyl 2,4,6-Tri-O-acetyl-3-O-allyl-b-D-thioglucopyranoside
CAS:<p>Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-β-D-thioglucopyranoside is an enantiomer that can be synthesized from the commercially available 2,4,6-triacetylphenyl boronic acid. It has been shown to have a positive effect on insulin sensitivity and uptake in plasma glucose in diabetic patients. Phenyl 2,4,6-tri-O-acetyl-3-O-allyl β D thioglucopyranoside also has a safety profile that is similar to other antidiabetic drugs. This drug has been shown to inhibit influenza virus uptake into cells by competitive inhibition of a transporter type.</p>Fórmula:C21H26O8SPureza:Min. 98 Area-%Cor e Forma:White Off-White PowderPeso molecular:438.49 g/molD-Mannose - F (from birch)
CAS:<p>Abundant and critical component of natural glycans and glycoproteins</p>Fórmula:C6H12O6Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:180.16 g/molDL-Glyceraldehyde 3-phosphate - 45-55 mg/mL aqueous solution
CAS:<p>Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an enzyme that catalyzes the conversion of glyceraldehyde-3-phosphate to 1,3 bisphosphoglycerate. GAPDH is involved in glycolysis and the pentose phosphate pathway. It has been shown to be an important player in mediating cellular responses to hypoxia, inflammation, and oxidative stress. The glyceraldehyde-3-phosphate dehydrogenase gene has been found to be mutated in a number of cancers including breast cancer and colon cancer. This gene also has a role in inflammatory lesion development as well as energy metabolism. GAPDH also participates in the biochemical reactions that lead to neuronal death during neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease.</p>Fórmula:C3H7O6PCor e Forma:Colorless Clear LiquidPeso molecular:170.06 g/mol
