108782-92-9 Usage
Uses
Used in Research Applications:
Uridine, 4-O-(2-nitrophenyl)is used as a research tool for studying the interactions and functions of uridine in various biological processes. The modification with the 2-nitrophenyl group allows researchers to investigate the effects of this alteration on the molecule's behavior and its potential impact on cellular activities.
Used in Medical Applications:
Uridine, 4-O-(2-nitrophenyl)is used as a potential therapeutic agent in the medical field. The modified uridine derivative may exhibit different properties compared to the native uridine, which could be harnessed for the development of new treatments. Studies on the effects and uses of Uridine, 4-O-(2-nitrophenyl)- may provide insights into its potential applications in medicine, such as in the treatment of certain diseases or conditions where the manipulation of uridine interactions is beneficial.
Used in Drug Development:
Uridine, 4-O-(2-nitrophenyl)is used as a starting point for the development of new drugs. The modified uridine derivative may serve as a lead compound for the synthesis of novel therapeutic agents. Researchers can explore the potential of Uridine, 4-O-(2-nitrophenyl)- in drug discovery, focusing on its unique properties and interactions with biological targets to create new medications with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 108782-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,8 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 108782-92:
(8*1)+(7*0)+(6*8)+(5*7)+(4*8)+(3*2)+(2*9)+(1*2)=149
149 % 10 = 9
So 108782-92-9 is a valid CAS Registry Number.
108782-92-9Relevant academic research and scientific papers
SITE-SPECIFIC MODIFICATION OF THE PYRIMIDINE RESIDUE DURING THE DEPROTECTION OF THE FULLY-PROTECTED DIURIDYLIC ACID.
Zhou, X-X.,Chattopadhyaya, J.
, p. 5149 - 5156 (2007/10/02)
A study of four different O-4 and N-3 protected uridine derivatives, 4 to 7, for their stabilities under different conditions versus their abilities to undergo nucleophilic substitution reaction at C-4 by an appropriate oxygen or a nitrogen nucleophile has established a general strategy for the site-specific modification of a particular pyrimidine residue in a model fully protected diuridylic acid to give either UpC, CpC or UpU, depending upon the deprotection condition.
