Autor: |
Hari, Yoshiyuki, Akabane, Masaaki, Obika, Satoshi |
Předmět: |
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Zdroj: |
Chemical Communications; 2013, Vol. 49 Issue 67, p7421-7423, 3p |
Abstrakt: |
In order to expand the target sequence used in triplex DNA formation, seven novel nucleotide analogues were synthesized and incorporated into triplex-forming oligonucleotides by post-elongation modification approaches. Among them, GPB, equipped with a suitable restricted conformation of sugar and nucleobase moieties, was found to have the highest sequence-selectivity and affinity towards CG base pairs within double-stranded DNA. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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