489-59-8 Usage
Description
Isocytidine is an isomer of cytidine, a nucleoside that is a constituent of nucleic acids. It plays a significant role in the genetic code and is involved in various metabolic processes within living organisms.
Uses
Used in Molecular Biology and Genetics:
Isocytidine is used as a research tool for studying the structure and function of nucleic acids. Its unique properties allow scientists to investigate the mechanisms of genetic information transfer and the role of nucleic acids in cellular processes.
Used in Metabolic Studies:
Isocytidine is used as a substrate in metabolic studies, particularly in Escherichia coli, where it is converted to isocytosine and uracil. This conversion helps researchers understand the metabolic pathways and the role of isocytidine in cellular metabolism.
Used in Pharmaceutical Research:
Isocytidine may have potential applications in the development of new drugs targeting nucleic acid metabolism or genetic disorders. Its unique properties and interactions with other cellular components make it a promising candidate for drug discovery and therapeutic applications.
Used in Biochemical Education:
Isocytidine can be used as an educational tool to teach students about the structure and function of nucleic acids, as well as the role of different nucleosides in genetic information transfer and cellular processes.
Check Digit Verification of cas no
The CAS Registry Mumber 489-59-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 489-59:
(5*4)+(4*8)+(3*9)+(2*5)+(1*9)=98
98 % 10 = 8
So 489-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N3O5/c10-9-11-5(14)1-2-12(9)8-7(16)6(15)4(3-13)17-8/h1-2,4,6-8,13,15-16H,3H2,(H2,10,11,14)/t4-,6-,7-,8-/m1/s1
489-59-8Relevant articles and documents
Reactions of Alkoxyuridines with Ammonia (l)
Mathews, Robert A.,Stoehrer, Gerhard
, p. 1601 - 1602 (2007/10/02)
2-Alkoxy- and 4-alkoxyuridines were converted into isocytidine and cytidine by reaction with ammonia at room temperature.Reaction with hydrogen sulfide produced 2-thio- and 4-thiouridine but the reaction was incomplete.The reaction may be helpful in the identification of alkylated pyrimidine nucleosides in DNA.
