CAS 25878-60-8
:1,2,3,4,6-penta-o-acetyl-d-galactopyranose
Description:
1,2,3,4,6-Penta-O-acetyl-D-galactopyranose is a derivative of D-galactose, a monosaccharide that plays a crucial role in various biological processes. This compound is characterized by the presence of five acetyl groups attached to the hydroxyl groups of the galactopyranose ring, which enhances its stability and solubility in organic solvents. The acetylation modifies the reactivity of the hydroxyl groups, making it less polar compared to its parent sugar. This compound typically appears as a white to off-white crystalline solid and is soluble in organic solvents like chloroform and methanol, but less so in water due to the hydrophobic nature imparted by the acetyl groups. It is often used in organic synthesis and carbohydrate chemistry as a protecting group for hydroxyl functionalities. Additionally, its structural features make it a valuable intermediate in the synthesis of more complex carbohydrates and glycosides. The compound is also of interest in the study of glycosylation reactions and carbohydrate-based drug design.
Formula:C16H22O11
InChI:InChI=1/C16H22O11/c1-7(17)22-6-12-13(23-8(2)18)14(24-9(3)19)15(25-10(4)20)16(27-12)26-11(5)21/h12-16H,6H2,1-5H3/t12-,13+,14+,15-,16?/m1/s1
Synonyms:- D-Galactopyranose Pentaacetate
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Found 6 products.
1,2,3,4,6-Penta-O-acetyl-D-galactopyranose
CAS:Formula:C16H22O11Purity:95%Color and Shape:SolidMolecular weight:390.3393(3R,4S,5S,6R)-6-(Acetoxymethyl)Tetrahydro-2H-Pyran-2,3,4,5-Tetrayl Tetraacetate
CAS:(3R,4S,5S,6R)-6-(Acetoxymethyl)Tetrahydro-2H-Pyran-2,3,4,5-Tetrayl TetraacetatePurity:95%Molecular weight:390.34g/molD-Galactose pentaacetate
CAS:<p>D-Galactose pentaacetate inhibits leucine-induced insulin release. It is used in research studies involving persistent hyperinsulinemia or insulinomas in children.</p>Formula:C16H22O11Color and Shape:SolidMolecular weight:390.34D-Galactose Pentaacetate
CAS:Controlled Product<p>Applications Used for production of fucosylated carbohydrates by enzymic fucosylation synthesis of sugar nucleotides.<br>References Muramatsu, et al.: Eur. J. Biochem., 157, 71 (1986), Phillips, et al.: Science, 250, 1130 (1990), Foster, et al.: J. Biol. Chem., 266, 3526 (1991),<br></p>Formula:C16H22O11Color and Shape:NeatMolecular weight:390.341,2,3,4,6-Penta-O-acetyl-D-galactopyranose
CAS:<p>1,2,3,4,6-Penta-O-acetyl-D-galactopyranose is an analog of the natural pentoses that binds to the mitochondrial membrane and inhibits the production of pro-inflammatory cytokines. This drug has been shown to inhibit the binding of lysophosphatidic acid (LPA) to its receptor by substituting for LPA in this binding site. 1,2,3,4,6-Penta-O-acetyl-D-galactopyranose also inhibits the expression of proinflammatory cytokines such as interleukin 6 (IL6) and IL1β in a dose dependent manner. This drug is also capable of inhibiting phosphotungstic acid from binding to a monolayer surface and can be used as a glycopolymer for cell culture. It has been shown that 1,2,3,4,6-Penta-O-acetyl</p>Formula:C16H22O11Purity:Min. 95%Color and Shape:PowderMolecular weight:390.34 g/mol





