CAS 54267-16-2
:1-[5-O-(hydroxy{[hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl)-alpha-D-ribofuranosyl]pyridine-2,4(1H,3H)-dione
Description:
The chemical substance known as 1-[5-O-(hydroxy{[hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl)-alpha-D-ribofuranosyl]pyridine-2,4(1H,3H)-dione, with the CAS number 54267-16-2, is a complex organic compound characterized by its intricate structure that includes a pyridine ring and multiple phosphoryl groups. This compound is a derivative of ribofuranose, which is a sugar component, and features hydroxyl and phosphonate functionalities that contribute to its biochemical reactivity. It is often studied for its potential roles in biochemical pathways, particularly in relation to nucleotides and nucleic acids. The presence of multiple phosphate groups suggests that it may participate in energy transfer or signaling processes within biological systems. Additionally, its structural complexity indicates potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Overall, this compound exemplifies the intricate interplay between organic chemistry and biochemistry, highlighting the importance of phosphorylated compounds in biological systems.
Formula:C10H16NO15P3
InChI:InChI=1/C10H16NO15P3/c12-5-1-2-11(7(13)3-5)10-9(15)8(14)6(24-10)4-23-28(19,20)26-29(21,22)25-27(16,17)18/h1-2,6,8-10,14-15H,3-4H2,(H,19,20)(H,21,22)(H2,16,17,18)/t6-,8-,9-,10+/m1/s1
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Found 2 products.
3-Deazauridine-5'-triphosphate Triethylamine Salt
CAS:Controlled ProductFormula:C10H16NO15P3•xC6H15NColor and Shape:NeatMolecular weight:483.15 + x(101.19)3-Deazauridine-5'-triphosphate triethylamine salt
CAS:<p>3-Deazauridine-5'-triphosphate triethylamine salt is a xanthosine analog that has been used as a biochemical reagent in animals and humans. It is postulated to be a potential cancer therapeutic agent because of its ability to inhibit DNA synthesis and cell division. 3-Deazauridine-5'-triphosphate triethylamine salt inhibits the biosynthesis of uridine in leukemic mice, hamster V79 cells, and mammalian cells. This drug inhibits the incorporation of uracil into RNA by competitive inhibition with respect to ATP. 3DATTP also inhibits the incorporation of thymidine into DNA by competitive inhibition with respect to dCTP.</p>Formula:C10H16NO15P3Purity:Min. 95%Molecular weight:483.15 g/mol

