Synthesis and characterization of oligodeoxynucleotides containing a novel tetraazabenzo[cd]azulene:naphthyridine base pair

Bioorganic and Medicinal Chemistry

Volumn 19, Issue 1, 2011, Pages 352-358

  Hirama, Yasuyuki ^a   Minakawa, Noriaki ^b   Matsuda, Akira ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b UNIVERSITY OF TOKUSHIMA   (Japan)

Author keywords

Hydrogen bond; Nucleobase; Nucleoside; Oligodeoxynucleotide; Tetraazabenzo cd azulene

Indexed keywords

2 AMINO 7 HYDROXY 1,8 NAPHTHYRIDINE NUCLEOSIDE; 2,4 DIAMINO 5 [1 (METHOXYCARBONYL) 2 ETHENYL] 7 (2 DEOXY BETA DEXTRO ERYTHRO PENTOFURANOSYL)PYRROLO[2,3 D]PYRIMIDINE; 4 (4 TERT BUTYLPHENOXYACETYLAMINO) 2 (2 DEOXY 5 O 4,4' DIMETHOXYTRITYL BETA DEXTRO ERYTHRO PENTOFURANOSYL) 2,6 DIHYDRO 7H 2,3,5,6 TETRAAZABENZO[CD]AZULEN 7 ONE; 4 (4 TERT BUTYLPHENOXYACETYLAMINO) 2 (2 DEOXY BETA DEXTRO ERYTHRO PENTOFURANOSYL) 2,6 DIHYDRO 7H 2,3,5,6 TETRAAZABENZO[CD]AZULEN 7 ONE; 4 (4 TERT BUTYLPHENOXYACETYLAMINO) 2 [2 DEOXY 3 O [(N,N DIISOPROPYLAMINO) 2 CYANOETHOXYPHOSPHINO] 5 O 4,4' DIMETHOXYTRITYL BETA DEXTRO ERYTHRO PENTOFURANOSYL] 2,6 DIHYDRO 7H 2,3,5,6 TETRAAZABENZO[CD]AZULEN 7 ONE; 4 AMINO 2 (2 DEOXY 3,5 DI O TERT BUTYLDIMETHYLSILYL BETA DEXTRO ERYTHRO PENTOFURANOSYL) 2,6 DIHYDRO 7H 2,3,5,6 TETRAAZABENZO[CD]AZULENE 7 ONE; 4 AMINO 2 (2 DEOXY BETA DEXTRO ERYTHRO PENTOFURANOSYL) 2,6 DIHYDRO 7H 2,3,5,6 TETRAAZABENZO[CD]AZULEN 7 ONE; 4,7 AMINO 2,3,5,6 TETRAAZABENZO[CD]AZULENE NUCLEOSIDE; 7 AMINO IMIDAZO[5',4':4,5]PYRIDO[2,3 D]PYRIMIDIN 4(5H)ONE NUCLEOSIDE; ACRYLIC ACID METHYL ESTER; ADENINE; AZULENE DERIVATIVE; CYTOSINE; DOUBLE STRANDED DNA; GUANINE; NAPHTHYRIDINE DERIVATIVE; OLIGODEOXYNUCLEOTIDE; THYMINE; UNCLASSIFIED DRUG;

ARTICLE; BASE PAIRING; CROSS COUPLING REACTION; CYCLIZATION; DENATURATION; HYDROGEN BOND; MELTING POINT; NUCLEOTIDE METABOLISM; PROTEIN STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS; TEMPERATURE DEPENDENCE; THERMOSTABILITY;

AZULENES; BASE PAIRING; NAPHTHYRIDINES; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; OLIGODEOXYRIBONUCLEOTIDES;

EID: 78650724581     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2010.11.023     Document Type: Article

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