872610-15-6

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 610766-50-2 3-(β-D-ribofuranosyl)-5-iodo-2-oxo(1H)pyridine 
• 114072-10-5 3-(β-D-ribofuranosyl)-2-oxo(1H)pyridine 

Downstream Products

• 872610-21-4 3-(2,3-di-O-acetyl-5-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl)-5-[3-(6-trifluoroacetamidohexanamido)-1-propynyl]-2-oxo(1H)pyridine 
• 872610-18-9 3-(2,3-di-O-acetyl-5-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl)-5-[3-(2,2-dichloroacetamido)-1-propynyl]-2-oxo(1H)pyridine 
• 872610-16-7 3-(2,3-di-O-acetyl-5-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl)-5-iodo-2-oxo(1H)pyridine 

Relevant academic research and scientific papers

Site-specific fluorescent labeling of RNA molecules by specific transcription using unnatural base pairs

Site-specific fluorescent labeling of RNA molecules was achieved by specific transcription using an unnatural base pair system. The unnatural base pairs between 2-amino-6-(2-thienyl)purine (s) and 2-oxo-(1H)pyridine (y), and 2-amino-6-(2-thiazolyl)purine

NOVEL NUCLEOSIDE OR NUCLEOTIDE DERIVATIVE AND USE THEREOF

The object of the present invention is to provide a nucleoside or nucleotide having a 5-substituted-2-oxo(1H)pyridin-3-yl group as a base, as well as a method using the same. In one embodiment, the nucleoside or nucleotide of the present invention has a f