161068-16-2

Upstream product

• 96203-41-7 5'-O-DMT-5-<3-<(2-aminoethyl)-amino>-3-oxopropyl>-2'-deoxyuridine 
• 161068-22-0 N-succinyl S-pivaloyloxymethyl-4-thiothymin-1-ylacetate 
• 134456-94-3 methyl (5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)ethanoate 
• 266358-95-6 methyl 4-thiothymin-1-ylacetate 
• 161068-21-9 S-pivaloyloxymethyl-4-thiothymin-1-ylacetic acid 
• 161068-20-8 4-thiothymin-1-ylacetic acid 
• 18997-19-8 Chloromethyl pivalate 
• 96203-40-6 5'-O-[4,4'-dimethoxytrityl]-5-[3-methoxy-3-oxopropyl]-2'-deoxyuridine 
• 161068-20-8 (4-Mercapto-5-methyl-2-oxo-2H-pyrimidin-1-yl)-acetic acid 

Relevant academic research and scientific papers

Synthesis of 4-thiothymine based photolabels as new tools for nucleic acids structural studies in solution: Formation of long-range photo-cross- links within a hammerhead ribozyme domain

The nucleosidic photolabels 2-5, able to form long-range photo-cross- links, have been used to further investigate the tertiary folding of a hammerhead ribozyme domain. These photolabels derive from 2'-deoxyuridine which is substituted at its C-5 position

Development of new nucleic acid photoaffinity probes: Synthesis of 4-thiothymine labelled nucleoside analogues

The new nucleic acid photoaffinity probes 1a, 1b, 2 and 3 in which a 4-thiothymine is linked at the end of a variable chain introduced at the C-5 position of deoxyuridine have been constructed.