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Volumn 39, Issue 7, 2000, Pages 1316-1318

Photocontrol of triple-helix formation by using azobenzene-bearing oligo(thymidine)

Author keywords

Azo compounds; DNA structures; Isomerizations; Nucleotides

Indexed keywords

AZOBENZENE DERIVATIVE; DNA; NUCLEOTIDE; THYMIDINE DERIVATIVE;

EID: 0034599413     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(20000403)39:7<1316::AID-ANIE1316>3.0.CO;2-H     Document Type: Article
Times cited : (45)

References (26)
  • 16
    • 33847542126 scopus 로고    scopus 로고
    • Augew. Chem. Int. Ed. 1999, 55, 2393-2395.
    • (1999) Augew. Chem. Int. Ed. , vol.55 , pp. 2393-2395
  • 19
    • 85003718851 scopus 로고    scopus 로고
    • note
    • 10 were used as mixtures of the two diastereomers with respect to the chirality of the X residue. The attempts to separate these two diastereomers by HPLC have been unsuccessful.
  • 20
    • 0001414917 scopus 로고
    • Nordén et al. concretely correlated the sign and magnitude of the CD, induced on the binding of small molecules to DNA, to the manner of the binding: a) M. Kubista, B. Åkerman, B. Nordén, J. Phys. Chem. 1988, 92, 2352-2356;
    • (1988) J. Phys. Chem. , vol.92 , pp. 2352-2356
    • Kubista, M.1    Åkerman, B.2    Nordén, B.3
  • 23
    • 85003733723 scopus 로고    scopus 로고
    • note
    • 13/t/a] triple helix was determined to be -0.15 Debye-Bohr magnetons (DBM). This is in marked contrast with the large positive values for the well-known groove binders dibutylproflavine (+1.77 DBM) and netropsin (+1.31 DBM) (data from ref. [6]).
  • 24
    • 85003470401 scopus 로고    scopus 로고
    • m of the triple helix, within experimental error
    • m of the triple helix, within experimental error.
  • 26
    • 85003757322 scopus 로고    scopus 로고
    • m measurement
    • m measurement.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.