CAS 18354-06-8
:Uracil Arabinonucleoside 5'-Phosphate
Description:
Uracil Arabinonucleoside 5'-Phosphate, with the CAS number 18354-06-8, is a nucleoside analog that plays a significant role in biochemical research, particularly in the study of nucleic acids and their functions. This compound consists of a uracil base linked to an arabinose sugar, which is further phosphorylated at the 5' position. The presence of the arabinose sugar distinguishes it from the more common ribonucleosides, as it can influence the stability and binding properties of nucleic acid structures. Uracil Arabinonucleoside 5'-Phosphate is often utilized in the synthesis of modified RNA molecules and can serve as a substrate for various enzymatic reactions. Its structural characteristics allow it to participate in biochemical pathways, making it a valuable tool in molecular biology and pharmacology. Additionally, due to its analog nature, it may exhibit unique interactions with nucleic acid-binding proteins and enzymes, providing insights into nucleic acid metabolism and function.
Formula:C9H13N2O9P
InChI:InChI=1/C9H13N2O9P/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18)/t4-,6+,7-,8-/m1/s1
Synonyms:- 1-(5-O-Phosphono--D-arabinofuranosyl)-2,4(1H,3H)-pyrimidinedione
- 1--D-Arabinofuranosyluracil 5'-Monophosphate
- 1-(5-O-phosphono-β-D-xylofuranosyl)pyrimidine-2,4(1H,3H)-dione
- Uracil Arabinonucleoside 5'-Phosphate
- 1-b-D-Arabinofuranosyluracil 5'-monophosphate
- 2,4(1H,3H)-Pyrimidinedione, 1-(5-O-phosphono-β-D-arabinofuranosyl)-
- 1-β-D-Arabinofuranosyluracil 5'-Monophosphate
- 1-2-D-Arabinofuranosyluracil 5-Monophosphate
- Ara-uridine-5'-monophosphate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
2,4(1H,3H)-Pyrimidinedione, 1-(5-O-phosphono-β-D-arabinofuranosyl)-
CAS:Formula:C9H13N2O9PColor and Shape:SolidMolecular weight:324.18131-b-D-Arabinofuranosyluracil 5'-monophosphate
CAS:<p>1-b-D-Arabinofuranosyluracil 5'-monophosphate is a pyrimidine nucleotide analog. Because of its structural similarity to natural nucleotides, it can interact with enzymes involved in nucleic acid synthesis. It is also a metabolite of Ara-U (arabinosyluracil), which is itself a compound studied for its biological activity. Scientists could potentially use this molecule in research to study how cells process and use nucleotides, and to understand how changes in nucleotide structure can affect biological processes.</p>Formula:C9H13N2O9PPurity:Min. 95%Color and Shape:PowderMolecular weight:324.18 g/mol


