CAS 28225-17-4
:N4-anisoylcytidine
Description:
N4-anisoylcytidine is a modified nucleoside that features a cytidine base with an anisoyl (or anisic acid-derived) group attached at the N4 position. This modification can influence the molecule's biochemical properties, such as its stability, solubility, and interaction with nucleic acids. The presence of the anisoyl group, which is derived from anisole, may enhance the compound's hydrophobic characteristics, potentially affecting its biological activity and cellular uptake. N4-anisoylcytidine is of interest in biochemical research, particularly in studies related to nucleic acid chemistry and the development of antiviral or anticancer agents. Its structural modifications can also provide insights into the mechanisms of nucleoside analogs and their therapeutic applications. As with many nucleoside derivatives, the study of N4-anisoylcytidine may involve exploring its synthesis, reactivity, and interactions with enzymes or other biomolecules, contributing to a better understanding of nucleoside function in biological systems.
Formula:C17H19N3O7
InChI:InChI=1/C17H19N3O7/c1-26-10-4-2-9(3-5-10)15(24)18-12-6-7-20(17(25)19-12)16-14(23)13(22)11(8-21)27-16/h2-7,11,13-14,16,21-23H,8H2,1H3,(H,18,19,24,25)
SMILES:COc1ccc(cc1)C(=O)N=c1ccn(C2C(C(C(CO)O2)O)O)c(n1)O
Synonyms:- 4-{[(4-methoxyphenyl)carbonyl]amino}-1-pentofuranosylpyrimidin-2(1H)-one
- N(sup 4)anisoylcytidine
- N4-ANISOYLCYTIDINE
- Cytidine, N-(4-methoxybenzoyl)-
- N4-p-Anisoylcytidine
- N
- 4
- -Anisoylcytidine
- n-(1-((2r,3r,4s,5r)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)-4-methoxybenzamide
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Found 2 products.
N4-p-Anisoylcytidine
CAS:<p>N4-p-Anisoylcytidine is a labile, crystalline, and water soluble oligoribonucleotide. It is an intermediate in the synthesis of cytidine and phenyl ring. N4-p-Anisoylcytidine can be prepared by reacting p-anisic acid with 4-benzoylcytosine. The reaction yields a mixture of products that can be purified by recrystallization or chromatography. It is hydrolyzed by acidic conditions to yield cytidine and phenyl ring. N4-p-Anisoylcytidine has been used as an intermediate in the synthesis of cytidine, which is subsequently converted to phenyl ring by reaction with benzene. This compound also has been used as an esterification agent for orthoesters.</p>Formula:C17H19N3O7Purity:Min. 95%Molecular weight:377.35 g/mol

