Triplex formation involving 2′-O,4′-C-methylene bridged nucleic acid (2′,4′-BNA) with 1-isoquinolone base analogue: Efficient and selective recognition of C:G interruption

Nucleosides, Nucleotides and Nucleic Acids

Volumn 22, Issue 5-8, 2003, Pages 1571-1573

  Torigoe, Hidetaka ^a   Hari, Yoshiyuki ^b   Obika, Satoshi ^b   Imanishi, Takeshi ^b  

^a TOKYO UNIVERSITY OF SCIENCE   (Japan)

^b OSAKA UNIVERSITY   (Japan)

Author keywords

1 Isoquinolone; 2 O, 4 C Methylene bridged nucleic acid; Triplex

Indexed keywords

1 ISOQUINOLONE; 2' O,4' C METHYLENE BRIDGED NUCLEIC ACID; CARBENE; CYTOSINE; DOUBLE STRANDED DNA; GUANINE; NUCLEIC ACID; OLIGONUCLEOTIDE; PURINE; PYRIMIDINE; QUINOLONE DERIVATIVE; UNCLASSIFIED DRUG;

BINDING AFFINITY; CHEMICAL MODIFICATION; CONFERENCE PAPER; DNA SEQUENCE; DNA STRUCTURE; MOLECULAR RECOGNITION;

BASE PAIRING; CYTOSINE; DNA; GUANINE; HYDROCARBONS; HYDROGEN BONDING; ISOQUINOLINES; METHANE; NUCLEIC ACID CONFORMATION; OLIGODEOXYRIBONUCLEOTIDES;

EID: 0141819154     PISSN: 15257770     EISSN: None     Source Type: Journal    
DOI: 10.1081/NCN-120023036     Document Type: Conference Paper

References (7)

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5. Torigoe, H.; Hari, Y.; Obika, S.; Imanishi, T. Triplex formation involving 2′,4′-BNA with 2-pyridone base analogue: efficient and selective recognition of C:G interruption. Nucleic Acids Res. 2001, Sup. 1, 281-282.
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