Abstract
The site-specific reaction with high efficiency and specificity to DNA or RNA has become of great interests, as such modification may have possibility to induce point mutation of a genetic code. The cross-linking reagents within complementary duplexes and triplexes are one of the tools for site-specific modification by forming covalently bond. However, the existing alkylating agents still need further improvement for application in either in vitro or in vivo study. Previously, we have designed a new cross-linking motif, 2-amino-6-vinylpurine (1), toward cytosine by expecting a proximity effect within the complex resembling a natural G-C pair. In this paper, we wish to describe the development of the novel cross-linking reagents based on the structure of 1.
Original language | English |
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Pages (from-to) | 108-117 |
Number of pages | 10 |
Journal | Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry |
Volume | 69 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2011 Dec 1 |
Keywords
- Antigene
- Antisense
- Cross-linking
- DNA
- MiRNA
- Oligonucleotide
- Sequence and base specific reaction
ASJC Scopus subject areas
- Organic Chemistry