600707-57-1Relevant articles and documents
Selective recognition of CG interruption by 2′,4′-BNA having 1-isoquinolone as a nucleobase in a pyrimidine motif triplex formation
Hari, Yoshiyuki,Obika, Satoshi,Sekiguchi, Mitsuaki,Imanishi, Takeshi
, p. 5123 - 5128 (2007/10/03)
To develop a novel nucleoside analogue for the effective recognition of CG interruption in a homopurine-homopyrimidine tract of double-stranded DNA (dsDNA), we succeeded in the synthesis of a triplex-forming oligonucleotide (TFO) containing a novel 2′,4′-