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Volumn 9, Issue 4, 2001, Pages 1001-1011

2′-O,4′-C-methylene bridged nucleic acid (2′,4′-BNA): Synthesis and triplex-forming properties

Author keywords

[No Author keywords available]

Indexed keywords

OLIGONUCLEOTIDE; DEOXYRIBONUCLEASE I; DNA; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; FUSED HETEROCYCLIC RINGS; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN;

EID: 0034744290     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(00)00325-4     Document Type: Article
Times cited : (153)

References (52)
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    • A part of this work appeared in a preliminary report:
    • A part of this work appeared in a preliminary report: Imanishi T., Obika S. J. Synth. Org. Chem., Jpn. 57:1999;969.
    • (1999) J. Synth. Org. Chem., Jpn , vol.57 , pp. 969
    • Imanishi, T.1    Obika, S.2
  • 9
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    • N3′-P5′ Phosphoramidate oligonucleotides are known to form a stable triplex with a homopurine·homopyrimidine tract in dsDNA. See:
    • N3′-P5′ Phosphoramidate oligonucleotides are known to form a stable triplex with a homopurine·homopyrimidine tract in dsDNA. See: Gryaznov S.M., Chen J.-K. J. Am. Chem. Soc. 116:1994;3143.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 3143
    • Gryaznov, S.M.1    Chen, J.-K.2
  • 12
    • 0030834244 scopus 로고    scopus 로고
    • Only C-rich homopyrimidine sequences of peptide nucleic acids (PNA) can bind to dsDNA to form PNA·DNA·DNA triplex. See:
    • Only C-rich homopyrimidine sequences of peptide nucleic acids (PNA) can bind to dsDNA to form PNA·DNA·DNA triplex. See: Wittung P., Nielsen P., Nordén B. Biochemistry. 36:1997;7973.
    • (1997) Biochemistry , vol.36 , pp. 7973
    • Wittung, P.1    Nielsen, P.2    Nordén, B.3
  • 14
    • 0026341239 scopus 로고
    • However, except for the C-rich sequences, the strand invasion (PNA·DNA·PNA triplex formation) was favored. See:
    • However, except for the C-rich sequences, the strand invasion (PNA·DNA·PNA triplex formation) was favored. See: Nielsen P.E., Egholm M., Berg R.H., Buchardt O. Science. 254:1991;1497.
    • (1991) Science , vol.254 , pp. 1497
    • Nielsen, P.E.1    Egholm, M.2    Berg, R.H.3    Buchardt, O.4
  • 15
    • 0003472884 scopus 로고    scopus 로고
    • Although the conformation of triplexes was believed to be A-form-like structures (N-form sugar puckering) from the X-ray fiber analysis of poly(dT)·poly(dA)·poly(dT), recent studies have shown that some triplex structures differ from the A form. See: New York: Springer-Verlag. pp 100-150
    • Although the conformation of triplexes was believed to be A-form-like structures (N-form sugar puckering) from the X-ray fiber analysis of poly(dT)·poly(dA)·poly(dT), recent studies have shown that some triplex structures differ from the A form. See: Soyfer V.N., Potaman V.N. Triple-Helical Nucleic Acids. 1996;Springer-Verlag, New York. pp 100-150.
    • (1996) Triple-Helical Nucleic Acids
    • Soyfer, V.N.1    Potaman, V.N.2
  • 16
    • 33749282063 scopus 로고    scopus 로고
    • Recent reviews for conformationally restricted or locked oligonucleotides. See
    • Recent reviews for conformationally restricted or locked oligonucleotides. See: Herdewijn, P. Liebigs Ann. Chem. 1996, 1337.
    • (1996) Liebigs Ann. Chem. , pp. 1337
    • Herdewijn, P.1
  • 34
    • 84987574125 scopus 로고
    • The stereochemistry of 5 was confirmed by the observation of NOE between the benzyliden hydrogen and 2′- or 3′-hydrogen. It is thought that the endo-isomer was selectively obtained thermodynamically. See:
    • The stereochemistry of 5 was confirmed by the observation of NOE between the benzyliden hydrogen and 2′- or 3′-hydrogen. It is thought that the endo-isomer was selectively obtained thermodynamically. See: Li C., Vasella A. Helv. Chim. Acta. 76:1993;211.
    • (1993) Helv. Chim. Acta , vol.76 , pp. 211
    • Li, C.1    Vasella, A.2
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    • 15
    • 15.
  • 42
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    • The association constants were calculated according to the literature. See:
    • The association constants were calculated according to the literature. See: Akiyama T., Hogan M.E. J. Biol. Chem. 271:1996;29126.
    • (1996) J. Biol. Chem. , vol.271 , pp. 29126
    • Akiyama, T.1    Hogan, M.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.