96203-41-7

Upstream product

• 96203-40-6 5'-O-[4,4'-dimethoxytrityl]-5-[3-methoxy-3-oxopropyl]-2'-deoxyuridine 
• 107-15-3 ethylenediamine 

Downstream Products

• 128900-35-6 5'-O--5-<3-<<2-<<2-<<(2,2-dimethylethoxy)carbonyl>amino>-3-<1-<(2,2-dimethylethoxy)carbonyl>-1H-imidazol-4-yl>-1-oxopropyl>amino>ethyl>amino>-3-oxopropyl>2'-deoxyuridine 
• 221209-20-7 5-<3-<<<<2-<2-pyridyldithio>ethyl>amino>ethyl>amino>-3-oxopropyl>-5'-O-DMT-2'-deoxyuridine 
• 121329-88-2 5'-Dimethoxytrityl-2'-deoxyuridine-5-<2-(N'-(trifluoroacetyl)amino)ethyl>propionamide-3'-(O-methyl(diisopropylamino))phosphoramidate 
• 161068-16-2 5'-O-[4,4'-dimethoxytrityl]-5-[3-[[2-[(S-pivaloyloxymethyl-4-thiothymin-1-ylacetyl)amino]ethyl]amino]-3-oxopropyl]-2'-deoxyuridine 
• 132776-84-2 5'-O--5-<3-oxo-3-<<2-<<1-oxo-2,6-bis<(trifluoroacetyl)amino>hexyl>amino>-ethyl>amino>propyl>-2'-deoxyuridine 
• 130699-89-7 5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine 
• 128870-16-6 5'-O--5-<3-<<2-<<2-<<(9H-fluoren-9-ylmethoxy)carbonyl>amino>-3-<1-<(9H-fluoren-9-ylmethoxy)carbonyl>-1H-imidazol-4-yl>-1-oxopropyl>amino>ethyl>amino>-3-oxopropyl>2'-deoxyuridine 
• 128870-15-5 5'-O--5-<3-<<2-<<2-<<(9H-fluoren-9-ylmethoxy)carbonyl>amino>-3-<1-<(2,2-dimethylethoxy)carbonyl>-1H-imidazol-4-yl>-1-oxopropyl>amino>ethyl>amino>-3-oxopropyl>2'-deoxyuridine 
• 132776-81-9 5'-O--5-<3-<<2<<6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<<(9H-fluoren-9-ylmethoxy)carbonyl>amino>-1-oxohexyl>amino>ethyl>-amino>-3-oxopropyl>-2'-deoxyuridine 
• 121329-87-1 5’-O-(4,4’-dimethoxytrityl)-5-[2-(trifluoroacetylamino)ethylaminocarbonylethyl]-2’-deoxyuridine 

Relevant academic research and scientific papers

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.

Binding properties of oligonucleotides containing a modified 2'-deoxyuridine with a thymine ended linker to pair with 2'-deoxyadenosine.

Oligonucleotides containing in the place of thymidine the nucleoside 2, a 2'-deoxyuridine harbouring at C-5 a thymine ended linker, were found to undergo base pairing with the opposite 2'-deoxyadenosine. However, the corresponding duplexes are significantly destabilised as compared to the fully natural ones.