828261-38-7

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 219582-35-1 2'-deoxy-N⁴-[(phenylamino)carbonyl]cytidine 
• 144947-12-6 N-{1-{4-(acetyloxy)-5-[(acetyloxy)methyl]tetrahydrofuran-2-yl}-1,2-dihydro-2-oxo-pyrimidin-4-yl}-N'-phenylurea 
• 103-71-9 phenyl isocyanate 
• 951-77-9 2'-Deoxycytidine 
• 65919-98-4 3',5'-di-O-acetyl-2'-deoxycytidine 

Relevant academic research and scientific papers

Synthesis and hybridization affinity of oligodeoxyribonucleotides incorporating 4-N-(N-arylcarbamoyl)deoxycytidine derivatives

Modified oligodeoxynucleotides incorporating 4-N-(N-arylcarbamoyl)-dC derivatives 1a-c were synthesized. The 1H NMR spectra of 1a-c suggest that the carbamoyl group forms an intramolecular hydrogen bond with the cytosine ring nitrogen atom so t

Triplex formation by an oligonucleotide containing the novel modified nucleoside 2′-deoxy-N4-phenylcarbamoylcytidine

2′-Deoxy-N4-phenylcarbamoylcytidine (Pc) was designed for triplex recognition of the cytosine-guanine base pair at physiological pH values to assist in the development of triplex-forming oligomers. Thermal denaturation of a triplex m