22886-34-6 Usage
Uses
Used in Pharmaceutical Industry:
Cytidine, uridylyl-(2'5')(9CI) is used as a research compound for studying its potential role in the immune response to viral infections. Its involvement in cellular regulation makes it a valuable tool for understanding the body's defense mechanisms against viruses.
Used in Cancer Therapy Research:
In the field of oncology, Cytidine, uridylyl-(2'5')(9CI) is used as an experimental agent for its anti-tumor effects. It is being studied for its potential to target and eliminate certain types of cancer cells, offering a novel approach to cancer treatment.
Used in Basic Research:
Cytidine, uridylyl-(2'5')(9CI) serves as a key component in basic research aimed at understanding the complex interactions and regulatory mechanisms within cells. Its role in cellular processes provides insights into the fundamental biology of cells and their response to various stimuli.
Check Digit Verification of cas no
The CAS Registry Mumber 22886-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,8 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22886-34:
(7*2)+(6*2)+(5*8)+(4*8)+(3*6)+(2*3)+(1*4)=126
126 % 10 = 6
So 22886-34-6 is a valid CAS Registry Number.
22886-34-6Relevant academic research and scientific papers
A nucleotide dimer synthesis without protecting groups using montmorillonite as catalyst
Joshi, Prakash C.,Aldersley, Michael F.,Zagorevskii, Dmitri V.,Ferris, James P.
, p. 536 - 566 (2012/10/08)
A synthesis has been developed providing nucleotide dimers comprising natural or unnatural nucleoside residues. A ribonucleoside 5-phosphorimidazolide is added to a nucleoside adsorbed on montmorillonite at neutral pH with the absence of protecting groups. Approximately 30% of the imidazolide is converted into each 2-5 dimer and 3-5 dimer with the rest hydrolyzed to the 5-monophosphate. Experiments with many combinations have suggested the limits to which this method may be applied, including heterochiral and chimeric syntheses. This greener chemistry has enabled the synthesis of dimers from activated nucleotides themselves, activated nucleotides with nucleosides, and activated nucleotides with nucleotide 5-monophosphates.
