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Volumn 6, Issue 12, 1996, Pages 1381-1386

Adenosine dialdehyde analogs I: Regioselective synthesis of adenosine monoaldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE 3' MONOALDEHYDE; ADENOSINE DIALDEHYDE; ADENOSINE DIALDEHYDE DERIVATIVE; ADENOSYLHOMOCYSTEINASE; UNCLASSIFIED DRUG;

EID: 0029890466     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0960-894X(96)00234-X     Document Type: Article
Times cited : (3)

References (28)
  • 10
    • 85030209794 scopus 로고    scopus 로고
    • note
    • 2O (compounds 2 and 6, respectively).
  • 11
    • 85030208563 scopus 로고    scopus 로고
    • note
    • 2-of THF).
  • 13
    • 85030210609 scopus 로고    scopus 로고
    • note
    • 2-2′).
  • 14
    • 85030200651 scopus 로고    scopus 로고
    • note
    • 28
  • 17
    • 85030203119 scopus 로고    scopus 로고
    • note
    • 2O) δ 8.37-8.16 (m, 2 H; H-2 and H-8); 6.14-5.99 (m, 1 H; H-1′); 5.17-4.70 (m, 5 H; 2 H-2′, H-4′ and 2 H-5′).
  • 21
    • 0242651290 scopus 로고
    • Usdin, E.; Borchardt, R. T.; Creveling, C. R., Eds.; Elsevier: New York
    • Hoffman, J. L. Transmethylation; Usdin, E.; Borchardt, R. T.; Creveling, C. R., Eds.; Elsevier: New York, 1979; pp 181-186.
    • (1979) Transmethylation , pp. 181-186
    • Hoffman, J.L.1
  • 23
    • 85030201586 scopus 로고    scopus 로고
    • note
    • 14C] adenosine, 54.3 mCi/mmol (New England Nuclear); and inhibitor in a final volume of 0.2 mL. The reaction was started by addition of enzyme followed by incubation at 37 °C for 2.5 min. The reaction was terminated by heating in boiling water for 2 min., followed by centrifugation. After addition of 5 μ1 each of 5 mM solutions of adenosine, inosine, and product AdoHcy as markers, aliquots (5 × 5 μ1 each) were spotted on aluminum-supported silica gel 60 F254 TLC sheets (E. Merck). Chromatograms were developed in 1-butanol : acetic acid : water (12:3:5) for 100 min. Spots containing radioactive product were visualized under UV light, cut out, and counted after addition of Scintisol fluor. Each reaction was run in duplicate. Kinetic parameters were determined by Lineweaver-Burk plots.
  • 24
    • 85030200194 scopus 로고    scopus 로고
    • note
    • Antiviral data on compounds 1, 2, 5 and 6 were obtained from the U. S. Army Medical Research Institute of Infectious Diseases, Frederick, MD, USA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.