188754-55-4 Usage
Uses
Used in Research Applications:
Uridine, 5-methyl-, 2'-acetate 3',5'-dibenzoate is utilized as a research compound for exploring the chemical properties and biological functions of nucleosides. Its distinctive structure allows scientists to study the effects of modifications on the behavior of nucleosides in various biochemical reactions and pathways.
Used in Biochemical Studies:
In the field of biochemistry, Uridine, 5-methyl-, 2'-acetate 3',5'-dibenzoate is employed as a specialized molecule to investigate the interactions of nucleosides with enzymes, proteins, and other biomolecules. This can provide insights into the mechanisms of RNA synthesis and regulation, as well as potential roles in disease processes.
Used in Pharmaceutical Development:
Uridine, 5-methyl-, 2'-acetate 3',5'-dibenzoate may also be used in the development of pharmaceuticals, particularly in the design of drugs targeting RNA metabolism or diseases associated with nucleoside imbalances. Its unique chemical properties could offer new avenues for drug discovery and therapeutic intervention.
Used in Diagnostic Applications:
Uridine, 5-methyl-, 2'-acetate 3',5'-dibenzoate could be applied in diagnostic assays to detect or measure the activity of enzymes involved in nucleoside metabolism, serving as a specific substrate or inhibitor in such tests.
Used in Educational Settings:
In academic and educational contexts, Uridine, 5-methyl-, 2'-acetate 3',5'-dibenzoate can be used to illustrate the principles of nucleoside chemistry and the impact of structural modifications on molecular function, providing a hands-on example for students learning about biochemistry and molecular biology.
Check Digit Verification of cas no
The CAS Registry Mumber 188754-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,5 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188754-55:
(8*1)+(7*8)+(6*8)+(5*7)+(4*5)+(3*4)+(2*5)+(1*5)=194
194 % 10 = 4
So 188754-55-4 is a valid CAS Registry Number.
188754-55-4Relevant academic research and scientific papers
Stereocontrolled Syntheses of Deoxyribonucleosides via Photoinduced Electron-Transfer Deoxygenation of Benzoyl-Protected Ribo- and Arabinonucleosides
Wang, Zhiwei,Prudhomme, Daniel R.,Buck, Jason R.,Park, Minnie,Rizzo, Carmelo J.
, p. 5969 - 5985 (2007/10/03)
The stereocontrolled, de novo syntheses of β-2′-deoxy-, α-2′-deoxy-, β-3′-deoxy-, and β-2′,3′-dideoxyribonucleosides are described. Strategically protected ribose, arabinose, and xylose glycosylation precursors were synthesized bearing C2-esters capable of directing Vorbrueggen glycosylation. The key step is the regioselective deoxygenation of the desired hydroxyl group as either the benzoyl- or 3-(trifluoromethyl)benzoyl derivative. This deoxygenation is accomplished via a photoinduced electron-transfer (PET) mechanism using carbazole derivatives as the photosensitizer. The syntheses of the desired deoxynucleoside generally proceed in three steps from a common, readily available precursor.
