Abstract
Previously, we reported that S-vinyl thioguanosine analogs exhibited the efficient functionality-transfer reaction with selectivity toward cytidine. This technique was applied to the inhibition and the labelling of DNA or RNA. In this study, we aimed at developing functionality-transfer oligonucleotide with the photo-inducible reactivity. This photo-induced transfer reaction proceeded only to d(m)C but not to dC and dT at the target site of the complementary ODN.
Original language | English |
---|---|
Pages (from-to) | 367-368 |
Number of pages | 2 |
Journal | Nucleic acids symposium series (2004) |
Issue number | 52 |
Publication status | Published - 2008 |
All Science Journal Classification (ASJC) codes
- Medicine(all)